| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:5003603-5003836 | Common:12; Rare:136 | ||||
| chr6:5004008-5004126 | Common:2; Rare:103 | ||||
| chr6:5260668-5261064 | Common:10; Rare:265; Clinvar (benign):6 | ||||
| chr6:5261221-5261618 | Common:21; Rare:198 | ||||
| chr6:7107646-7108140 | Common:2; Rare:152 | ||||
| chr6:7108183-7108520 | Rare:129 | ||||
| chr6:7313054-7313406 | Common:10; Rare:259 | ||||
| chr6:7389146-7389530 | Common:2; Rare:153 | ||||
| chr6:7389702-7389904 | Common:3; Rare:122 | ||||
| chr6:7541383-7541769 | Rare:230; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:7590064-7590286 | Common:10; Rare:146 | ||||
| chr6:7909690-7910410 | Common:13; Rare:271 | ||||
| chr6:7910706-7910930 | Common:2; Rare:134 | ||||
| chr6:8064305-8064644 | Common:8; Rare:197 | ||||
| chr6:8102430-8102767 | Common:2; Rare:206 |