| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:118893908-118894292 | Common:3; Rare:115 | ||||
| chr6:121334462-121334529 | Common:2; Rare:24 | ||||
| chr6:122399351-122399737 | Common:6; Rare:148 | ||||
| chr6:122471768-122471952 | Common:4; Rare:62 | ||||
| chr6:125781058-125781201 | Rare:24 | ||||
| chr6:125956661-125956861 | Common:1; Rare:58 | ||||
| chr6:125986343-125986548 | Common:1; Rare:67 | ||||
| chr6:127343337-127343408 | Rare:11 | ||||
| chr6:131628178-131628456 | Common:2; Rare:73 | ||||
| chr6:132513014-132513221 | Common:1; Rare:53 | ||||
| chr6:132763402-132763560 | Rare:19 | ||||
| chr6:133952907-133953246 | Common:2; Rare:87 | ||||
| chr6:135054784-135054991 | Common:6; Rare:62 | ||||
| chr6:135497604-135497665 | Rare:14 | ||||
| chr6:135497710-135497854 | Common:3; Rare:61; Clinvar:1; Clinvar (benign):1 |