Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:143184646-143185046 | Common:9; Rare:154 | ||||
chr4:143513349-143513544 | Common:2; Rare:70 | ||||
chr4:144645931-144646162 | Common:1; Rare:62 | ||||
chr4:145098144-145098350 | Rare:73 | ||||
chr4:145619313-145619406 | Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
chr4:147617217-147617479 | Common:1; Rare:60 | ||||
chr4:147684081-147684239 | Common:1; Rare:57 | ||||
chr4:148442307-148442749 | Rare:131; Clinvar:4; Clinvar (benign):3 | ||||
chr4:150581729-150581932 | Rare:39 | ||||
chr4:151015201-151015377 | Rare:47 | ||||
chr4:151015709-151015848 | Rare:68 | ||||
chr4:151099479-151099709 | Common:3; Rare:93 | ||||
chr4:151408861-151409267 | Common:5; Rare:129 | ||||
chr4:151409359-151409452 | Common:1; Rare:17 | ||||
chr4:152536079-152536378 | Common:2; Rare:111 |