Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:139453766-139454204 | Common:3; Rare:114; Clinvar:10; Clinvar (benign):4 | ||||
chr4:140373380-140373717 | Common:3; Rare:135 | ||||
chr4:141220782-141220978 | Rare:67 | ||||
chr4:141636785-141636991 | Common:1; Rare:41 | ||||
chr4:142405383-142405550 | Rare:25 | ||||
chr4:143184657-143184985 | Common:8; Rare:129 | ||||
chr4:143337034-143337191 | Rare:60 | ||||
chr4:143337236-143337468 | Common:1; Rare:78 | ||||
chr4:143513865-143513940 | Rare:33 | ||||
chr4:144645917-144646172 | Common:1; Rare:69 | ||||
chr4:145098136-145098354 | Rare:75 | ||||
chr4:145619313-145619396 | Rare:36 | ||||
chr4:145938821-145938981 | Rare:40 | ||||
chr4:147684081-147684346 | Common:1; Rare:106 | ||||
chr4:151099508-151099713 | Common:3; Rare:86 |