| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:56542748-56543117 | Common:2; Rare:62 | ||||
| chr6:56843645-56843928 | Common:9; Rare:64 | ||||
| chr6:56851604-56851956 | Rare:78 | ||||
| chr6:57172542-57172810 | Common:1; Rare:82 | ||||
| chr6:57222250-57222409 | Rare:67 | ||||
| chr6:63636053-63636149 | Rare:31 | ||||
| chr6:68634930-68635479 | Common:3; Rare:142 | ||||
| chr6:68635770-68635983 | Rare:44 | ||||
| chr6:69796847-69797146 | Common:1; Rare:93; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:69866548-69866619 | Rare:11 | ||||
| chr6:70413222-70413577 | Common:2; Rare:98 | ||||
| chr6:70667713-70668032 | Common:4; Rare:123 | ||||
| chr6:73262946-73263284 | Common:5; Rare:93 | ||||
| chr6:73310134-73310232 | Common:1; Rare:26 | ||||
| chr6:73461686-73461814 | Common:1; Rare:41; Clinvar (benign):1 |