variants: 4297776
Data license: Apache License 2.0
This data as json
| rowid | Variant_ID | RSID | Chromosome | Position | Reference_Allele | Alternate_Allele | Joint_AF | African_AF | Admixed_American_AF | Ashkenazi_Jewish_AF | East_Asian_AF | Finnish_AF | Middle_Eastern_AF | Non_Finnish_European_AF | South_Asian_AF | ENCODE_cCRE_Annotation | Repeat_Name | Repeat_Class | Repeat_Family | Functional_Annotation | Gene | Gene_Detail | Exonic_Function | Amino_Acid_Change | PhastCons_100way | PhyloP_100way | Evo2_7B_NoRC_Ref | Evo2_7B_NoRC_Alt | Evo2_7B_NoRC_Delta | Evo2_7B_AvgRC_Ref | Evo2_7B_AvgRC_Alt | Evo2_7B_AvgRC_Delta | Evo2_7B_WeightedRC_Ref | Evo2_7B_WeightedRC_Alt | Evo2_7B_WeightedRC_Delta | Evo2_40B_NoRC_Ref | Evo2_40B_NoRC_Alt | Evo2_40B_NoRC_Delta | Evo2_40B_AvgRC_Ref | Evo2_40B_AvgRC_Alt | Evo2_40B_AvgRC_Delta | Evo2_40B_WeightedRC_Ref | Evo2_40B_WeightedRC_Alt | Evo2_40B_WeightedRC_Delta | MAF_tier | AF_bin | SCREEN_V4_Classes | SCREEN_V4_Accessions | SCREEN_V4_Overlap_Count |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4297776 | 4:16393345:C:T | rs368728684 | 4 | 16393345 | C | T | 0.110845 | 0.0904768 | 0.135723 | 0.104947 | 0.142379 | 0.0481224 | 0.15625 | 0.12412 | 0.0998201 | Intronic | SVA_D | Retroposon | SVA | ncRNA_intronic | ENSG00000293014 | -31912.796875 | -31939.2890625 | -26.4921875 | -31795.224609375 | -31835.564453125 | -40.33984375 | -34368.0018466264 | -34405.500613588 | -37.4987669616094 | -20463.84765625 | -16030.71875 | 4433.12890625 | -18007.75 | -15675.22265625 | 2332.52734375 | -20134.5944906047 | -16630.2058763757 | 3504.38861422899 | Q2_20-40% | AF_0-0.2 | CA | EH38E4328148 | 1 |