Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156061078-156061232 | Rare:34 | ||||
chr1:156114544-156114887 | Common:1; Rare:77; Clinvar:4; Clinvar (benign):3 | ||||
chr1:156135032-156135309 | Common:2; Rare:63; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr1:156193817-156194126 | Common:3; Rare:77 | ||||
chr1:156212869-156213049 | Common:1; Rare:51 | ||||
chr1:156282777-156282941 | Common:1; Rare:48 | ||||
chr1:156338152-156338585 | Common:2; Rare:158 | ||||
chr1:156591678-156591986 | Common:5; Rare:139; Clinvar (pathogenic):1 | ||||
chr1:156601410-156601511 | Common:1; Rare:42 | ||||
chr1:156728388-156728489 | Common:1; Rare:20 | ||||
chr1:156729080-156729155 | Rare:32 | ||||
chr1:156741029-156741396 | Common:1; Rare:101 | ||||
chr1:156747487-156747587 | Rare:24 | ||||
chr1:156751347-156751597 | Rare:61 | ||||
chr1:156751830-156751975 | Rare:42 |