| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:38168312-38168538 | Common:2; Rare:44 | ||||
| chr6:38192546-38192752 | Rare:44 | ||||
| chr6:38608203-38608266 | Rare:11 | ||||
| chr6:39877918-39878242 | Common:2; Rare:58 | ||||
| chr6:39896976-39897281 | Common:3; Rare:76 | ||||
| chr6:41936559-41936942 | Common:2; Rare:90 | ||||
| chr6:42046293-42046318 | Rare:4 | ||||
| chr6:42046707-42046936 | Common:2; Rare:44 | ||||
| chr6:42077347-42077544 | Common:1; Rare:37 | ||||
| chr6:42093273-42093314 | Rare:8 | ||||
| chr6:42783735-42783937 | Rare:53 | ||||
| chr6:43042899-43043113 | Common:2; Rare:59; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:44126174-44126401 | Rare:38 | ||||
| chr6:44149953-44150305 | Common:1; Rare:80 | ||||
| chr6:44248406-44248776 | Common:2; Rare:121 |