Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:139301197-139301583 | Common:6; Rare:113 | ||||
chr4:139302436-139302559 | Rare:27 | ||||
chr4:139453668-139453697 | Common:1; Rare:13 | ||||
chr4:139453707-139454225 | Common:4; Rare:148; Clinvar:10; Clinvar (benign):4 | ||||
chr4:139556383-139556611 | Rare:34 | ||||
chr4:140373353-140373709 | Common:3; Rare:141 | ||||
chr4:140523895-140524231 | Common:2; Rare:99 | ||||
chr4:141220791-141221041 | Rare:82 | ||||
chr4:141636315-141637005 | Common:4; Rare:153 | ||||
chr4:142405389-142405539 | Rare:24 | ||||
chr4:143184851-143185159 | Common:5; Rare:110 | ||||
chr4:143336362-143336960 | Rare:141 | ||||
chr4:143337044-143337114 | Rare:21 | ||||
chr4:143337116-143337216 | Rare:44 | ||||
chr4:143337224-143337259 | Rare:11 |