Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:102798895-102799180 | Common:1; Rare:59 | ||||
chr13:106567594-106567747 | Rare:52 | ||||
chr13:106568085-106568258 | Rare:56 | ||||
chr13:108218339-108218511 | Rare:66 | ||||
chr13:110307143-110307476 | Common:5; Rare:106; Clinvar (benign):6 | ||||
chr13:112588130-112588265 | Rare:30 | ||||
chr13:113208625-113208712 | Rare:54 | ||||
chr13:113297045-113297395 | Common:3; Rare:119 | ||||
chr13:113490685-113491141 | Common:4; Rare:170 | ||||
chr13:113863957-113864142 | Common:1; Rare:51 | ||||
chr14:20343415-20343635 | Common:6; Rare:102 | ||||
chr14:20454884-20455337 | Common:4; Rare:115 | ||||
chr14:20684431-20684595 | Common:2; Rare:25; Clinvar (benign):2 | ||||
chr14:20989672-20990014 | Common:7; Rare:80 | ||||
chr14:21211553-21211858 | Common:3; Rare:77 |