| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:103396395-103396739 | Rare:118 | ||||
| chr10:103452264-103452429 | Rare:50 | ||||
| chr10:103918120-103918548 | Common:5; Rare:115 | ||||
| chr10:103967006-103967080 | Common:1; Rare:22 | ||||
| chr10:104121681-104122234 | Common:4; Rare:194 | ||||
| chr10:104254826-104254955 | Rare:37 | ||||
| chr10:104268902-104269223 | Common:4; Rare:79 | ||||
| chr10:107164205-107164299 | Rare:29 | ||||
| chr10:109923423-109923665 | Common:2; Rare:93 | ||||
| chr10:110006023-110006113 | Rare:18 | ||||
| chr10:110007661-110008023 | Rare:109 | ||||
| chr10:110304851-110305065 | Common:2; Rare:71 | ||||
| chr10:110567280-110567828 | Common:4; Rare:184; Clinvar:2; Clinvar (benign):5 | ||||
| chr10:110567921-110568020 | Rare:25 | ||||
| chr10:110871628-110872016 | Rare:132 |