| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:53348894-53349222 | Common:2; Rare:120 | ||||
| chr6:53545098-53545239 | Rare:40 | ||||
| chr6:54846677-54846772 | Rare:23 | ||||
| chr6:56542754-56543051 | Common:2; Rare:52 | ||||
| chr6:57089904-57090227 | Rare:119 | ||||
| chr6:57172204-57172319 | Rare:36 | ||||
| chr6:57172518-57172793 | Common:1; Rare:85 | ||||
| chr6:57317539-57317647 | Rare:30 | ||||
| chr6:69796546-69796656 | Common:1; Rare:21 | ||||
| chr6:69796856-69797118 | Rare:85; Clinvar:4; Clinvar (benign):2 | ||||
| chr6:70413222-70413613 | Common:2; Rare:110 | ||||
| chr6:70566852-70566976 | Common:1; Rare:49 | ||||
| chr6:70667707-70667996 | Common:3; Rare:105 | ||||
| chr6:73263158-73263279 | Common:3; Rare:31 | ||||
| chr6:73310153-73310304 | Common:1; Rare:34 |