| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31897673-31897782 | Rare:20 | ||||
| chr6:31933609-31933958 | Rare:114 | ||||
| chr6:31943436-31943711 | Rare:66; Clinvar:2 | ||||
| chr6:31943918-31944223 | Common:1; Rare:78; Clinvar (benign):2 | ||||
| chr6:31945559-31945972 | Rare:54; Clinvar:1 | ||||
| chr6:31945981-31946292 | Common:2; Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:31947000-31947521 | Common:5; Rare:148; Clinvar:2; Clinvar (benign):5 | ||||
| chr6:31947735-31948096 | Common:3; Rare:94; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:31949990-31950953 | Common:4; Rare:277; Clinvar:1; Clinvar (benign):5 | ||||
| chr6:31951036-31951473 | Common:3; Rare:110; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr6:31958906-31959204 | Rare:98; Clinvar:8 | ||||
| chr6:31995959-31996323 | Common:1; Rare:97 | ||||
| chr6:32117678-32117977 | Common:2; Rare:69 | ||||
| chr6:32153851-32154047 | Common:1; Rare:32 | ||||
| chr6:32154749-32155047 | Rare:60 |