Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:118895097-118895259 | Rare:46 | ||||
chr6:119350594-119350737 | Common:2; Rare:30 | ||||
chr6:121438512-121438676 | Rare:37 | ||||
chr6:122451676-122452053 | Common:7; Rare:104 | ||||
chr6:125197811-125197953 | Common:1; Rare:26 | ||||
chr6:125224111-125224311 | Rare:22 | ||||
chr6:129486315-129486621 | Common:4; Rare:75; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
chr6:129491738-129492076 | Common:2; Rare:79; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr6:129514131-129514591 | Common:1; Rare:128; Clinvar:11; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr6:129660288-129660393 | Rare:18 | ||||
chr6:130050309-130050628 | Rare:70 | ||||
chr6:132817023-132817202 | Common:2; Rare:58 | ||||
chr6:134296021-134296316 | Common:2; Rare:52 | ||||
chr6:134539958-134540141 | Common:1; Rare:31 | ||||
chr6:135498418-135498428 | Rare:2 |