Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:35046017-35046481 | Common:2; Rare:145 | ||||
chr14:35121925-35122780 | Common:4; Rare:245 | ||||
chr14:35403721-35403880 | Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
chr14:35404416-35404779 | Common:3; Rare:129; Clinvar:1; Clinvar (benign):5 | ||||
chr14:35826071-35826410 | Rare:72 | ||||
chr14:39114195-39114332 | Common:2; Rare:45 | ||||
chr14:39170306-39170471 | Common:2; Rare:51 | ||||
chr14:39174904-39175271 | Common:5; Rare:127 | ||||
chr14:39267056-39267431 | Common:2; Rare:136 | ||||
chr14:39432129-39432225 | Common:2; Rare:31 | ||||
chr14:44961892-44962223 | Common:2; Rare:93 | ||||
chr14:45253057-45253310 | Rare:69 | ||||
chr14:49598694-49599010 | Common:2; Rare:118 | ||||
chr14:49620595-49620830 | Common:2; Rare:85; Clinvar:3 | ||||
chr14:49892898-49893118 | Rare:90 |