Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:127880806-127880913 | Rare:35 | ||||
chr4:128061002-128061325 | Common:1; Rare:116 | ||||
chr4:129093492-129093712 | Rare:70 | ||||
chr4:133149099-133149298 | Common:2; Rare:58 | ||||
chr4:138242320-138242538 | Common:1; Rare:51 | ||||
chr4:139301327-139301531 | Common:2; Rare:64 | ||||
chr4:139665748-139666026 | Common:2; Rare:62 | ||||
chr4:140373392-140373680 | Common:2; Rare:111 | ||||
chr4:143184650-143184998 | Common:8; Rare:137 | ||||
chr4:144645917-144646205 | Common:1; Rare:75 | ||||
chr4:145098141-145098343 | Rare:71 | ||||
chr4:145619235-145619416 | Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
chr4:147617225-147617462 | Common:1; Rare:56 | ||||
chr4:147684133-147684296 | Rare:66 | ||||
chr4:150581731-150581966 | Rare:49 |