Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179882472-179882928 | Rare:221; Clinvar:9; Clinvar (benign):2 | ||||
chr1:179883007-179883196 | Common:3; Rare:67 | ||||
chr1:179954464-179955016 | Common:4; Rare:128 | ||||
chr1:180154700-180155025 | Common:4; Rare:118 | ||||
chr1:181088494-181088711 | Rare:71 | ||||
chr1:182388795-182389062 | Common:3; Rare:56 | ||||
chr1:182391269-182391489 | Rare:49 | ||||
chr1:182391535-182391593 | Rare:21 | ||||
chr1:182391666-182392001 | Common:3; Rare:121; Clinvar:5; Clinvar (benign):3 | ||||
chr1:182589203-182589317 | Rare:22 | ||||
chr1:182789528-182789804 | Common:2; Rare:93 | ||||
chr1:182794197-182794367 | Common:1; Rare:29 | ||||
chr1:182839094-182839399 | Common:1; Rare:113 | ||||
chr1:183023065-183023256 | Common:4; Rare:51 | ||||
chr1:183472248-183472538 | Common:2; Rare:99 |