Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:32176054-32176233 | Common:1; Rare:37 | ||||
chr6:32189854-32190072 | Common:3; Rare:60 | ||||
chr6:32190146-32190336 | Rare:36 | ||||
chr6:32530237-32530465 | Common:17; Rare:19 | ||||
chr6:32637252-32637439 | Common:19; Rare:13 | ||||
chr6:32666645-32666838 | Common:29; Rare:21 | ||||
chr6:32844001-32844115 | Rare:25; Clinvar:1 | ||||
chr6:32853675-32853888 | Rare:85; Clinvar:2; Clinvar (benign):2 | ||||
chr6:32853989-32854221 | Common:2; Rare:54 | ||||
chr6:32968812-32968991 | Common:5; Rare:59 | ||||
chr6:32970713-32970952 | Common:1; Rare:64 | ||||
chr6:33075752-33076013 | Common:3; Rare:32 | ||||
chr6:33200656-33200925 | Common:2; Rare:82 | ||||
chr6:33201820-33202125 | Common:4; Rare:78 | ||||
chr6:33208455-33208560 | Rare:29 |