| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:110958591-110958781 | Common:4; Rare:69 | ||||
| chr6:110981959-110982100 | Common:2; Rare:68 | ||||
| chr6:111483295-111483611 | Rare:116 | ||||
| chr6:111605827-111606150 | Common:2; Rare:57 | ||||
| chr6:112087452-112087684 | Rare:71 | ||||
| chr6:116100695-116100893 | Common:1; Rare:71 | ||||
| chr6:116254068-116254232 | Common:4; Rare:42 | ||||
| chr6:116279846-116280110 | Common:2; Rare:89 | ||||
| chr6:116370753-116370982 | Rare:60 | ||||
| chr6:117602451-117602638 | Common:3; Rare:56 | ||||
| chr6:117675279-117675498 | Common:3; Rare:58 | ||||
| chr6:118548157-118548336 | Common:1; Rare:39; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:118893908-118894313 | Common:3; Rare:123 | ||||
| chr6:119349759-119349936 | Common:2; Rare:63 | ||||
| chr6:121334468-121334537 | Common:2; Rare:26 |