| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:111483638-111483775 | Common:1; Rare:52 | ||||
| chr6:112087430-112087691 | Rare:83 | ||||
| chr6:116100713-116100928 | Common:1; Rare:89 | ||||
| chr6:116254058-116254242 | Common:4; Rare:49 | ||||
| chr6:116279833-116280108 | Common:2; Rare:94 | ||||
| chr6:116370679-116371060 | Common:1; Rare:90 | ||||
| chr6:116571202-116571600 | Common:3; Rare:113 | ||||
| chr6:116681002-116681262 | Common:3; Rare:76 | ||||
| chr6:117602401-117602677 | Common:4; Rare:73 | ||||
| chr6:117675292-117675498 | Common:3; Rare:57 | ||||
| chr6:118548195-118548336 | Common:1; Rare:31; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:118710069-118710228 | Rare:37 | ||||
| chr6:118893901-118894246 | Common:3; Rare:103 | ||||
| chr6:119349759-119349923 | Common:1; Rare:55 | ||||
| chr6:121334454-121334606 | Common:4; Rare:58 |