Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:113857229-113857428 | Common:1; Rare:52 | ||||
chr6:116100727-116100886 | Rare:59 | ||||
chr6:116254073-116254222 | Common:4; Rare:39 | ||||
chr6:116279841-116280038 | Common:1; Rare:74 | ||||
chr6:116571187-116571593 | Common:3; Rare:115 | ||||
chr6:116681126-116681228 | Rare:24 | ||||
chr6:117482565-117482879 | Common:2; Rare:100 | ||||
chr6:117602401-117602677 | Common:4; Rare:73 | ||||
chr6:117675318-117675498 | Common:3; Rare:49 | ||||
chr6:118893908-118894259 | Common:3; Rare:105 | ||||
chr6:121435518-121435766 | Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
chr6:122471768-122471921 | Common:2; Rare:45 | ||||
chr6:122610308-122610513 | Rare:52 | ||||
chr6:125780836-125781121 | Common:1; Rare:51 | ||||
chr6:125956651-125956790 | Common:1; Rare:47 |