| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:101831052-101831152 | Rare:24 | ||||
| chr10:101840758-101840904 | Common:1; Rare:31 | ||||
| chr10:102117890-102118033 | Common:1; Rare:28 | ||||
| chr10:102121438-102121705 | Common:2; Rare:43 | ||||
| chr10:102133920-102133948 | Rare:4 | ||||
| chr10:102151509-102151636 | Rare:26 | ||||
| chr10:102153575-102153619 | Common:1; Rare:8 | ||||
| chr10:102230474-102230709 | Rare:89 | ||||
| chr10:102399352-102399410 | Rare:21 | ||||
| chr10:102399545-102399740 | Rare:60; Clinvar (benign):1 | ||||
| chr10:102431834-102432020 | Common:4; Rare:33 | ||||
| chr10:102449821-102449974 | Rare:27 | ||||
| chr10:102450356-102450739 | Common:1; Rare:164 | ||||
| chr10:102456009-102456152 | Rare:33 | ||||
| chr10:102579466-102579521 | Rare:7 |