Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:108218339-108218538 | Rare:75 | ||||
chr13:110306958-110307526 | Common:7; Rare:176; Clinvar:3; Clinvar (benign):10 | ||||
chr13:110506152-110506530 | Common:4; Rare:120; Clinvar:1; Clinvar (benign):3 | ||||
chr13:110507755-110508080 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):4 | ||||
chr13:110561612-110561893 | Common:5; Rare:96 | ||||
chr13:110713008-110713266 | Common:2; Rare:114 | ||||
chr13:110713487-110713628 | Common:2; Rare:58 | ||||
chr13:111153594-111153721 | Common:2; Rare:60 | ||||
chr13:113208627-113208769 | Rare:81 | ||||
chr13:113297152-113297479 | Common:4; Rare:101 | ||||
chr13:113490683-113491145 | Common:4; Rare:174 | ||||
chr13:113759051-113759297 | Common:2; Rare:63 | ||||
chr13:113863831-113864189 | Common:3; Rare:88 | ||||
chr13:114281526-114281650 | Common:1; Rare:67 | ||||
chr14:20343171-20343637 | Common:13; Rare:275 |