Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:71866074-71866219 | Rare:20 | ||||
chr13:72971510-72971586 | Common:1; Rare:13 | ||||
chr13:73063214-73063274 | Rare:14 | ||||
chr13:73194392-73194585 | Common:3; Rare:30 | ||||
chr13:95786831-95787134 | Rare:56 | ||||
chr13:98709572-98709774 | Common:1; Rare:55 | ||||
chr13:98745357-98745590 | Common:1; Rare:43 | ||||
chr13:98748946-98749190 | Common:1; Rare:38 | ||||
chr13:103050411-103050602 | Common:1; Rare:41 | ||||
chr13:103054775-103054826 | Rare:12 | ||||
chr13:103057914-103057950 | Rare:10 | ||||
chr13:103057989-103058039 | Rare:8 | ||||
chr13:103065843-103066156 | Common:3; Rare:130; Clinvar:18; Clinvar (benign):2 | ||||
chr13:110449493-110449786 | Common:4; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
chr13:110524636-110524766 | Common:2; Rare:24 |