| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:85449905-85450140 | Common:1; Rare:69 | ||||
| chr6:87155268-87155588 | Rare:85 | ||||
| chr6:87589965-87590165 | Common:2; Rare:83; Clinvar (benign):3 | ||||
| chr6:93419552-93419824 | Common:1; Rare:73 | ||||
| chr6:100881287-100881480 | Common:5; Rare:86 | ||||
| chr6:105179924-105180085 | Common:4; Rare:43 | ||||
| chr6:110958512-110958775 | Common:5; Rare:85 | ||||
| chr6:110981975-110982093 | Common:1; Rare:60 | ||||
| chr6:112087474-112087635 | Rare:40 | ||||
| chr6:116279899-116280114 | Common:1; Rare:64 | ||||
| chr6:118893913-118894224 | Common:2; Rare:93 | ||||
| chr6:122471768-122471921 | Common:2; Rare:45 | ||||
| chr6:128520569-128520747 | Rare:68 | ||||
| chr6:136289779-136290008 | Common:1; Rare:99 | ||||
| chr6:143450689-143450921 | Common:1; Rare:83; Clinvar:4; Clinvar (benign):1 |