| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:41780994-41781062 | Rare:9 | ||||
| chr6:41921099-41921234 | Rare:36 | ||||
| chr6:42050393-42050581 | Rare:76 | ||||
| chr6:42564165-42564210 | Rare:10 | ||||
| chr6:42746069-42746340 | Rare:77 | ||||
| chr6:42746839-42747002 | Rare:36 | ||||
| chr6:42929209-42929578 | Common:4; Rare:111 | ||||
| chr6:42984333-42984619 | Rare:68 | ||||
| chr6:43013869-43014280 | Common:2; Rare:90 | ||||
| chr6:43427500-43427572 | Rare:21 | ||||
| chr6:43477326-43477589 | Common:2; Rare:51 | ||||
| chr6:43516785-43517112 | Common:6; Rare:115; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575962-43576227 | Common:1; Rare:109; Clinvar:8 | ||||
| chr6:43687768-43687912 | Common:2; Rare:55 | ||||
| chr6:43770087-43770229 | Common:2; Rare:43 |