| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:129486254-129486558 | Common:3; Rare:62; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr6:129491708-129492054 | Common:2; Rare:79; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr6:129505058-129505322 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr6:129512271-129512449 | Rare:51; Clinvar:4; Clinvar (benign):2 | ||||
| chr6:129514273-129514468 | Rare:56; Clinvar:6; Clinvar (benign):2 | ||||
| chr6:131283799-131283926 | Common:3; Rare:21 | ||||
| chr6:131287619-131287668 | Rare:9 | ||||
| chr6:131299478-131299717 | Common:5; Rare:48 | ||||
| chr6:131325109-131325223 | Common:1; Rare:41 | ||||
| chr6:131325266-131325357 | Rare:27 | ||||
| chr6:131325391-131325770 | Common:7; Rare:110 | ||||
| chr6:131325815-131325853 | Rare:11 | ||||
| chr6:131325857-131325904 | Common:1; Rare:17 | ||||
| chr6:131326745-131326845 | Common:5; Rare:24 | ||||
| chr6:131326847-131326932 | Rare:20 |