| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31739743-31740034 | Common:3; Rare:72 | ||||
| chr6:31777082-31777331 | Common:3; Rare:45 | ||||
| chr6:31795691-31796054 | Common:2; Rare:75 | ||||
| chr6:31815333-31815592 | Common:1; Rare:96 | ||||
| chr6:31827546-31827826 | Common:5; Rare:115 | ||||
| chr6:31827828-31827941 | Common:3; Rare:64 | ||||
| chr6:31877253-31877355 | Rare:18 | ||||
| chr6:31877628-31878022 | Rare:56 | ||||
| chr6:31878946-31879102 | Common:2; Rare:41 | ||||
| chr6:31897661-31897796 | Rare:27 | ||||
| chr6:31945789-31946124 | Common:1; Rare:42; Clinvar (benign):1 | ||||
| chr6:31946188-31946431 | Common:3; Rare:44; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:31958891-31959398 | Rare:166; Clinvar:9 | ||||
| chr6:32109295-32109651 | Common:1; Rare:55 | ||||
| chr6:32128172-32128435 | Common:2; Rare:70 |