Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:43076512-43076888 | Common:2; Rare:80 | ||||
chr6:43516804-43517130 | Common:5; Rare:123; Clinvar:2; Clinvar (benign):1 | ||||
chr6:43575939-43576341 | Common:1; Rare:143; Clinvar:10 | ||||
chr6:43629229-43629493 | Common:1; Rare:62 | ||||
chr6:43770541-43770872 | Common:2; Rare:91; Clinvar:1 | ||||
chr6:43778079-43778179 | Rare:16 | ||||
chr6:44126872-44126919 | Rare:12 | ||||
chr6:44127371-44127657 | Common:4; Rare:83 | ||||
chr6:49463149-49463433 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
chr6:52576885-52577307 | Common:7; Rare:151 | ||||
chr6:52670969-52671174 | Rare:68 | ||||
chr6:53065580-53065608 | Rare:6 | ||||
chr6:53348876-53349227 | Common:2; Rare:135 | ||||
chr6:56462480-56462725 | Common:2; Rare:40 | ||||
chr6:56542882-56543078 | Common:1; Rare:29 |