Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:140373384-140373709 | Common:3; Rare:133 | ||||
chr4:140523926-140524231 | Common:2; Rare:94 | ||||
chr4:141636567-141636649 | Rare:17 | ||||
chr4:141636769-141636898 | Common:1; Rare:32 | ||||
chr4:143184847-143184985 | Common:5; Rare:54 | ||||
chr4:143336535-143336912 | Rare:85 | ||||
chr4:143337086-143337204 | Rare:47 | ||||
chr4:143513325-143513759 | Common:3; Rare:140 | ||||
chr4:145098141-145098348 | Rare:72 | ||||
chr4:145180009-145180313 | Rare:86 | ||||
chr4:145619320-145619402 | Rare:32 | ||||
chr4:147617240-147617473 | Common:1; Rare:52 | ||||
chr4:147684081-147684302 | Common:1; Rare:87 | ||||
chr4:148442319-148442712 | Rare:111; Clinvar:4; Clinvar (benign):3 | ||||
chr4:151099560-151099748 | Common:3; Rare:84 |