| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:7389740-7390032 | Common:1; Rare:84 | ||||
| chr6:7541368-7541748 | Common:1; Rare:115; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:7541797-7542085 | Common:4; Rare:110; Clinvar:15; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr6:7910633-7910930 | Common:3; Rare:117 | ||||
| chr6:8102524-8102712 | Common:1; Rare:63 | ||||
| chr6:8435440-8435682 | Common:5; Rare:89 | ||||
| chr6:10521213-10521391 | Rare:45 | ||||
| chr6:10694603-10695001 | Common:4; Rare:109 | ||||
| chr6:10722992-10723248 | Common:3; Rare:103 | ||||
| chr6:10747582-10747869 | Common:3; Rare:110 | ||||
| chr6:11232060-11232165 | Rare:28 | ||||
| chr6:11232477-11232696 | Rare:67 | ||||
| chr6:11778676-11779254 | Common:4; Rare:109 | ||||
| chr6:12290100-12290362 | Rare:41 | ||||
| chr6:13328515-13328609 | Common:2; Rare:32 |