Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:39114137-39114334 | Common:2; Rare:61 | ||||
chr14:39170249-39170471 | Common:3; Rare:66 | ||||
chr14:39174873-39175289 | Common:6; Rare:138 | ||||
chr14:39267037-39267448 | Common:2; Rare:150 | ||||
chr14:39432418-39432618 | Common:6; Rare:66 | ||||
chr14:44961892-44962255 | Common:3; Rare:105 | ||||
chr14:45135723-45135979 | Common:1; Rare:48 | ||||
chr14:45253059-45253294 | Rare:64 | ||||
chr14:45253509-45253567 | Common:1; Rare:23 | ||||
chr14:49586289-49586776 | Common:1; Rare:247; Clinvar (benign):1 | ||||
chr14:49598675-49598996 | Common:1; Rare:127 | ||||
chr14:49620561-49620818 | Common:2; Rare:102; Clinvar:1 | ||||
chr14:49688209-49688266 | Rare:17 | ||||
chr14:49892895-49893125 | Rare:97 | ||||
chr14:50312152-50312376 | Rare:98 |