| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:110700624-110700925 | Rare:41 | ||||
| chr6:111321481-111321638 | Rare:24 | ||||
| chr6:111329656-111329856 | Rare:45 | ||||
| chr6:111336240-111336547 | Common:1; Rare:43 | ||||
| chr6:111340582-111340805 | Common:1; Rare:37 | ||||
| chr6:111354790-111354827 | Common:1; Rare:5 | ||||
| chr6:111394620-111394724 | Common:1; Rare:14 | ||||
| chr6:111412953-111413200 | Common:1; Rare:38 | ||||
| chr6:111413344-111413468 | Common:1; Rare:27 | ||||
| chr6:111416398-111416651 | Rare:52 | ||||
| chr6:111424709-111424840 | Rare:18 | ||||
| chr6:111451434-111451470 | Rare:6 | ||||
| chr6:111559643-111559889 | Common:1; Rare:46 | ||||
| chr6:111604085-111604384 | Rare:55 | ||||
| chr6:112122136-112122459 | Rare:71; Clinvar:1; Clinvar (benign):2 |