| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31739702-31740080 | Common:3; Rare:101 | ||||
| chr6:31763205-31763605 | Common:4; Rare:129 | ||||
| chr6:31763639-31763895 | Rare:28 | ||||
| chr6:31794903-31795185 | Common:2; Rare:82; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr6:31795691-31796036 | Common:2; Rare:75 | ||||
| chr6:31806900-31807110 | Common:5; Rare:83 | ||||
| chr6:31814479-31815543 | Common:8; Rare:310 | ||||
| chr6:31827295-31827764 | Common:4; Rare:121 | ||||
| chr6:31834575-31834964 | Common:4; Rare:104 | ||||
| chr6:31862771-31863179 | Common:3; Rare:110; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:31897646-31897820 | Rare:39 | ||||
| chr6:31901312-31901712 | Common:5; Rare:120 | ||||
| chr6:31902198-31902436 | Common:2; Rare:78 | ||||
| chr6:31958939-31959187 | Rare:69; Clinvar:5 | ||||
| chr6:31971946-31972247 | Common:2; Rare:125 |