| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:101060698-101060891 | Common:1; Rare:47 | ||||
| chr10:101067643-101067768 | Common:1; Rare:17 | ||||
| chr10:101221655-101222014 | Common:1; Rare:69 | ||||
| chr10:101569732-101569980 | Rare:62 | ||||
| chr10:101589055-101589114 | Rare:14 | ||||
| chr10:101693760-101693922 | Common:1; Rare:26 | ||||
| chr10:101693991-101694292 | Rare:59 | ||||
| chr10:101694295-101694671 | Common:4; Rare:119; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:101819163-101819250 | Rare:11 | ||||
| chr10:101819282-101819318 | Rare:5 | ||||
| chr10:101819390-101819597 | Rare:29 | ||||
| chr10:101840608-101840911 | Common:1; Rare:50 | ||||
| chr10:101938436-101938655 | Rare:37 | ||||
| chr10:101939289-101939606 | Common:2; Rare:59 | ||||
| chr10:102055563-102055606 | Rare:9 |