| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:101694680-101694731 | Rare:5 | ||||
| chr10:101726033-101726216 | Common:1; Rare:35 | ||||
| chr10:101730109-101730253 | Rare:27 | ||||
| chr10:101818979-101819122 | Rare:32 | ||||
| chr10:101819178-101819262 | Rare:14 | ||||
| chr10:102055551-102055604 | Rare:10 | ||||
| chr10:102066034-102066072 | Rare:16 | ||||
| chr10:102119647-102119917 | Common:1; Rare:51 | ||||
| chr10:102133541-102133836 | Common:1; Rare:71 | ||||
| chr10:102134008-102134078 | Rare:18 | ||||
| chr10:102368200-102368307 | Rare:21 | ||||
| chr10:102399513-102399794 | Rare:87; Clinvar (benign):1 | ||||
| chr10:102401878-102402103 | Common:2; Rare:61; Clinvar (benign):1 | ||||
| chr10:102422721-102422920 | Rare:60 | ||||
| chr10:102431733-102432013 | Common:3; Rare:50 |