| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:110958681-110958769 | Common:1; Rare:36 | ||||
| chr6:112087468-112087641 | Rare:48 | ||||
| chr6:116279864-116280084 | Common:1; Rare:73 | ||||
| chr6:116370686-116371004 | Common:1; Rare:78 | ||||
| chr6:116571187-116571563 | Common:2; Rare:105 | ||||
| chr6:117602460-117602683 | Common:3; Rare:63 | ||||
| chr6:118893908-118894200 | Common:2; Rare:91 | ||||
| chr6:122471779-122471921 | Common:2; Rare:39 | ||||
| chr6:124963088-124963227 | Common:1; Rare:46 | ||||
| chr6:125781059-125781156 | Rare:18 | ||||
| chr6:125956661-125956784 | Common:1; Rare:43 | ||||
| chr6:127266795-127266884 | Common:1; Rare:31 | ||||
| chr6:127343346-127343415 | Rare:10 | ||||
| chr6:128520553-128520747 | Rare:71 | ||||
| chr6:135497710-135497810 | Common:3; Rare:46; Clinvar:1; Clinvar (benign):1 |