| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:119491166-119491360 | Common:2; Rare:31 | ||||
| chr6:129505021-129505322 | Common:1; Rare:83; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr6:131581060-131581360 | Common:3; Rare:80; Clinvar:2; Clinvar (pathogenic):4 | ||||
| chr6:132749162-132749335 | Common:3; Rare:31 | ||||
| chr6:132817022-132817121 | Common:1; Rare:36 | ||||
| chr6:133891627-133891734 | Common:1; Rare:29 | ||||
| chr6:135498418-135498511 | Rare:20 | ||||
| chr6:136290433-136290449 | Rare:2 | ||||
| chr6:136756343-136756593 | Common:1; Rare:52 | ||||
| chr6:136783852-136784144 | Common:2; Rare:47 | ||||
| chr6:136785398-136785543 | Rare:21 | ||||
| chr6:136793109-136793140 | Common:1; Rare:8 | ||||
| chr6:137217451-137217519 | Rare:13 | ||||
| chr6:137218002-137218029 | Rare:4 | ||||
| chr6:137218039-137218071 | Rare:5 |