Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:58578111-58578138 | Rare:7 | ||||
chr11:58578237-58578537 | Common:3; Rare:104 | ||||
chr11:58578910-58579237 | Common:4; Rare:84 | ||||
chr11:59142705-59142940 | Common:1; Rare:41 | ||||
chr11:59668983-59669321 | Rare:117 | ||||
chr11:60906409-60906808 | Rare:99 | ||||
chr11:61332986-61333266 | Rare:96 | ||||
chr11:61361835-61361988 | Common:1; Rare:38 | ||||
chr11:61362232-61362397 | Common:2; Rare:48; Clinvar:7; Clinvar (benign):1 | ||||
chr11:61392527-61392649 | Common:2; Rare:41; Clinvar:3; Clinvar (benign):2 | ||||
chr11:61429920-61430176 | Common:1; Rare:118; Clinvar:3; Clinvar (benign):6 | ||||
chr11:61792555-61792939 | Common:6; Rare:107 | ||||
chr11:61967311-61967571 | Common:1; Rare:97; Clinvar:1 | ||||
chr11:61967580-61967790 | Common:2; Rare:82; Clinvar:3 | ||||
chr11:62123818-62124073 | Common:6; Rare:65 |