| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:101034561-101034712 | Rare:40 | ||||
| chr10:101588205-101588329 | Rare:50 | ||||
| chr10:101694899-101695244 | Rare:81; Clinvar:2 | ||||
| chr10:102152089-102152406 | Common:3; Rare:102 | ||||
| chr10:102394354-102394570 | Rare:60 | ||||
| chr10:102421474-102421617 | Common:1; Rare:44 | ||||
| chr10:102502652-102502744 | Rare:42 | ||||
| chr10:102644978-102645127 | Rare:34 | ||||
| chr10:102714271-102714669 | Common:2; Rare:129 | ||||
| chr10:102743625-102743937 | Common:3; Rare:79 | ||||
| chr10:102854214-102854285 | Rare:28 | ||||
| chr10:103193248-103193421 | Common:5; Rare:55; Clinvar (benign):1 | ||||
| chr10:103396419-103396722 | Rare:106 | ||||
| chr10:103452273-103452441 | Rare:49 | ||||
| chr10:103554997-103555390 | Rare:107 |