Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:94616162-94616266 | Rare:20 | ||||
chr14:95516614-95516780 | Common:2; Rare:39 | ||||
chr14:96309272-96309417 | Common:2; Rare:25 | ||||
chr14:99602286-99602441 | Common:2; Rare:34 | ||||
chr14:100321969-100322031 | Rare:14 | ||||
chr14:101731299-101731418 | Common:3; Rare:31 | ||||
chr14:101948010-101948381 | Common:2; Rare:111 | ||||
chr14:102009972-102010312 | Common:1; Rare:86; Clinvar (benign):5 | ||||
chr14:104734857-104735100 | Common:1; Rare:86 | ||||
chr14:104735609-104735737 | Common:2; Rare:22 | ||||
chr14:104766859-104767250 | Common:5; Rare:75 | ||||
chr14:105643861-105643910 | Rare:23 | ||||
chr14:105707387-105707504 | Common:1; Rare:46 | ||||
chr14:105707508-105707825 | Common:2; Rare:86 | ||||
chr14:105707986-105708093 | Common:1; Rare:43 |