Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:102596773-102597028 | Common:1; Rare:116 | ||||
chr13:102798924-102799182 | Common:1; Rare:54 | ||||
chr13:106568111-106568267 | Rare:48 | ||||
chr13:108218307-108218513 | Rare:77 | ||||
chr13:110307128-110307371 | Common:4; Rare:87; Clinvar (benign):5 | ||||
chr13:112588130-112588169 | Rare:8 | ||||
chr13:113208632-113208741 | Rare:63 | ||||
chr13:113490685-113491141 | Common:4; Rare:170 | ||||
chr13:113759128-113759226 | Common:1; Rare:29 | ||||
chr13:113863949-113864195 | Common:2; Rare:64 | ||||
chr14:20454861-20455328 | Common:4; Rare:115 | ||||
chr14:20461739-20462016 | Common:2; Rare:64 | ||||
chr14:20684438-20684639 | Common:2; Rare:34; Clinvar (benign):2 | ||||
chr14:21476882-21477245 | Common:1; Rare:112 | ||||
chr14:22766512-22766726 | Common:1; Rare:116 |