Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:139556181-139556532 | Rare:66 | ||||
chr4:139556779-139556947 | Rare:29 | ||||
chr4:140153052-140153058 | Rare:1 | ||||
chr4:140154071-140154291 | Common:1; Rare:86 | ||||
chr4:140373333-140373717 | Common:3; Rare:151 | ||||
chr4:140524386-140524502 | Common:1; Rare:36 | ||||
chr4:140756029-140756434 | Common:1; Rare:88 | ||||
chr4:141220780-141220966 | Rare:59 | ||||
chr4:142846287-142846352 | Rare:12 | ||||
chr4:143184600-143184998 | Common:10; Rare:159 | ||||
chr4:143513329-143514101 | Common:5; Rare:283 | ||||
chr4:145098099-145098361 | Rare:84 | ||||
chr4:145180481-145180853 | Common:1; Rare:109 | ||||
chr4:145482845-145483002 | Rare:24 | ||||
chr4:145619328-145619429 | Rare:40; Clinvar:3; Clinvar (benign):1 |