Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:142946255-142946610 | Common:3; Rare:88 | ||||
chr6:142947180-142947317 | Common:1; Rare:34 | ||||
chr6:142947512-142947751 | Common:2; Rare:61 | ||||
chr6:143059716-143059961 | Rare:33 | ||||
chr6:144284827-144285094 | Common:1; Rare:69 | ||||
chr6:144286211-144286552 | Common:4; Rare:69 | ||||
chr6:148501167-148501525 | Common:1; Rare:53 | ||||
chr6:148507834-148508474 | Common:7; Rare:114 | ||||
chr6:148508483-148508689 | Rare:33 | ||||
chr6:148508746-148508802 | Common:1; Rare:10 | ||||
chr6:148509854-148509914 | Rare:8 | ||||
chr6:150683353-150683697 | Common:2; Rare:60 | ||||
chr6:151045917-151045932 | Rare:1 | ||||
chr6:152129794-152129871 | Rare:8 | ||||
chr6:152242415-152242469 | Rare:18; Clinvar:1; Clinvar (benign):2 |