| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:101694834-101694976 | Common:1; Rare:31; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:101694920-101695680 | Common:2; Rare:178; Clinvar:1 | ||||
| chr10:101783281-101783472 | Rare:92 | ||||
| chr10:101818338-101818842 | Common:2; Rare:244 | ||||
| chr10:102056088-102056391 | Common:4; Rare:142 | ||||
| chr10:102065173-102065488 | Common:2; Rare:223 | ||||
| chr10:102114941-102115078 | Common:2; Rare:46 | ||||
| chr10:102120328-102120638 | Common:4; Rare:201 | ||||
| chr10:102132846-102133077 | Common:1; Rare:103 | ||||
| chr10:102152062-102152469 | Common:7; Rare:221 | ||||
| chr10:102241449-102242004 | Common:2; Rare:223 | ||||
| chr10:102245183-102245615 | Common:2; Rare:151 | ||||
| chr10:102394299-102394611 | Common:1; Rare:82 | ||||
| chr10:102395536-102395981 | Common:2; Rare:202 | ||||
| chr10:102420733-102420879 | Rare:60 |