| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:13299990-13300232 | Rare:171; Clinvar:4 | ||||
| chr10:13301995-13302208 | Common:2; Rare:67 | ||||
| chr10:13302260-13302620 | Common:1; Rare:138 | ||||
| chr10:13346862-13347445 | Common:15; Rare:321 | ||||
| chr10:13347668-13347858 | Common:4; Rare:87 | ||||
| chr10:13347820-13348530 | Common:1; Rare:506 | ||||
| chr10:13528926-13529194 | Common:3; Rare:150 | ||||
| chr10:13586770-13587061 | Common:3; Rare:101 | ||||
| chr10:13707160-13707375 | Common:8; Rare:91 | ||||
| chr10:13707405-13707801 | Common:4; Rare:160 | ||||
| chr10:13707790-13708030 | Rare:63 | ||||
| chr10:14604257-14604592 | Common:11; Rare:272 | ||||
| chr10:14837931-14838431 | Common:10; Rare:378 | ||||
| chr10:14878491-14878963 | Common:8; Rare:335 | ||||
| chr10:14953690-14953978 | Common:1; Rare:85; Clinvar (pathogenic):1 |