| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:118893913-118894231 | Common:2; Rare:97 | ||||
| chr6:122471768-122471921 | Common:2; Rare:45 | ||||
| chr6:125918936-125919354 | Common:1; Rare:95 | ||||
| chr6:125986382-125986548 | Rare:54 | ||||
| chr6:127343343-127343603 | Common:1; Rare:57 | ||||
| chr6:128520566-128520757 | Rare:74 | ||||
| chr6:132814313-132814600 | Common:3; Rare:104 | ||||
| chr6:134174839-134175121 | Common:1; Rare:130 | ||||
| chr6:135497705-135497857 | Common:3; Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:136289758-136290014 | Common:1; Rare:111 | ||||
| chr6:136550414-136550687 | Common:2; Rare:75 | ||||
| chr6:143060752-143060919 | Common:6; Rare:60 | ||||
| chr6:143450654-143450929 | Common:1; Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:145964324-145964534 | Rare:66 | ||||
| chr6:148272064-148272310 | Rare:42 |