| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:102854304-102854329 | Rare:12 | ||||
| chr10:102854461-102854539 | Rare:20 | ||||
| chr10:103193240-103193442 | Common:5; Rare:64; Clinvar (benign):1 | ||||
| chr10:103350925-103351215 | Common:2; Rare:115 | ||||
| chr10:103367815-103367981 | Common:3; Rare:30 | ||||
| chr10:103396386-103396730 | Rare:122 | ||||
| chr10:103452262-103452441 | Rare:55 | ||||
| chr10:103917753-103917870 | Rare:23 | ||||
| chr10:103918114-103918523 | Common:5; Rare:112 | ||||
| chr10:103966985-103967096 | Common:1; Rare:35 | ||||
| chr10:104121621-104122193 | Common:4; Rare:184 | ||||
| chr10:104232319-104232490 | Common:1; Rare:45 | ||||
| chr10:104254546-104254968 | Common:5; Rare:93 | ||||
| chr10:104268887-104269308 | Common:4; Rare:111 | ||||
| chr10:104338369-104338574 | Rare:55 |