Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:147733787-147733918 | Rare:20 | ||||
chr4:147822204-147822391 | Rare:26 | ||||
chr4:148445320-148445707 | Common:3; Rare:109 | ||||
chr4:148680623-148680802 | Common:1; Rare:17 | ||||
chr4:151100679-151101161 | Common:1; Rare:93 | ||||
chr4:153684135-153684337 | Common:1; Rare:65 | ||||
chr4:158059508-158059538 | Rare:4 | ||||
chr4:168890780-168891057 | Common:1; Rare:69; Clinvar:4; Clinvar (benign):2 | ||||
chr4:168913718-168914021 | Common:2; Rare:56; Clinvar:9; Clinvar (benign):1 | ||||
chr4:168915635-168915926 | Common:1; Rare:55; Clinvar (benign):2 | ||||
chr4:168923927-168924273 | Common:1; Rare:82 | ||||
chr4:169179620-169179669 | Rare:6 | ||||
chr4:173509545-173509675 | Common:1; Rare:34 | ||||
chr4:176320505-176320633 | Rare:40 | ||||
chr4:176791632-176791766 | Rare:26 |