Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:128060994-128061325 | Common:1; Rare:118 | ||||
chr4:129093452-129093741 | Common:1; Rare:83 | ||||
chr4:139084304-139084573 | Common:3; Rare:117 | ||||
chr4:139301295-139301549 | Common:4; Rare:78 | ||||
chr4:139453770-139454190 | Common:3; Rare:106; Clinvar:10; Clinvar (benign):4 | ||||
chr4:140373380-140373709 | Common:3; Rare:133 | ||||
chr4:141220801-141220944 | Rare:42 | ||||
chr4:141636514-141636900 | Common:1; Rare:93 | ||||
chr4:141637081-141637113 | Rare:8 | ||||
chr4:142405389-142405516 | Rare:21 | ||||
chr4:143184652-143184986 | Common:8; Rare:133 | ||||
chr4:144645891-144646202 | Common:1; Rare:81 | ||||
chr4:145098143-145098354 | Rare:75 | ||||
chr4:145619252-145619396 | Rare:59 | ||||
chr4:147617230-147617463 | Common:1; Rare:53 |