Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:71864659-71864869 | Common:1; Rare:53 | ||||
chr13:87671195-87671392 | Common:1; Rare:58 | ||||
chr13:91111446-91111724 | Common:2; Rare:69 | ||||
chr13:99087944-99088236 | Common:3; Rare:58 | ||||
chr13:102394493-102394660 | Common:1; Rare:63 | ||||
chr13:110304580-110304843 | Common:1; Rare:43 | ||||
chr13:110308500-110308634 | Common:2; Rare:29 | ||||
chr13:110424698-110425009 | Common:4; Rare:93; Clinvar:3; Clinvar (benign):2 | ||||
chr13:110503868-110504264 | Common:4; Rare:131; Clinvar:1; Clinvar (benign):3 | ||||
chr14:22773704-22773870 | Common:1; Rare:46 | ||||
chr14:27613066-27613358 | Rare:51 | ||||
chr14:31109574-31109640 | Rare:15 | ||||
chr14:39175855-39176147 | Common:4; Rare:72 | ||||
chr14:41605314-41605598 | Common:4; Rare:58 | ||||
chr14:49633932-49634070 | Common:1; Rare:56; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 |