| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:116616291-116616487 | Common:3; Rare:41 | ||||
| chr6:116680748-116681312 | Common:4; Rare:153 | ||||
| chr6:117265397-117265616 | Common:1; Rare:57 | ||||
| chr6:117602005-117602564 | Common:3; Rare:169 | ||||
| chr6:117675382-117675501 | Common:3; Rare:27 | ||||
| chr6:118548157-118548380 | Common:2; Rare:47; Clinvar:4; Clinvar (benign):2 | ||||
| chr6:118651471-118651732 | Common:3; Rare:81 | ||||
| chr6:118710069-118710210 | Rare:35 | ||||
| chr6:118893913-118894313 | Common:3; Rare:122 | ||||
| chr6:118934485-118934631 | Rare:50 | ||||
| chr6:118934944-118935063 | Common:3; Rare:36 | ||||
| chr6:119349719-119349981 | Common:3; Rare:99 | ||||
| chr6:121334426-121334549 | Common:3; Rare:57 | ||||
| chr6:121334679-121334820 | Common:1; Rare:27 | ||||
| chr6:121435497-121435830 | Rare:74; Clinvar:1; Clinvar (benign):2 |