| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:11164937-11165202 | Common:2; Rare:52 | ||||
| chr10:11165432-11165511 | Rare:26 | ||||
| chr10:12042707-12043456 | Common:3; Rare:207 | ||||
| chr10:12068817-12069031 | Common:1; Rare:87 | ||||
| chr10:12129451-12129755 | Common:1; Rare:124 | ||||
| chr10:12195814-12195984 | Rare:43 | ||||
| chr10:13099949-13100316 | Common:4; Rare:91; Clinvar:3; Clinvar (benign):7 | ||||
| chr10:13161512-13161599 | Rare:22 | ||||
| chr10:13299545-13299666 | Common:1; Rare:28 | ||||
| chr10:13300040-13300219 | Rare:64; Clinvar:1 | ||||
| chr10:13348001-13348351 | Rare:114 | ||||
| chr10:13502935-13503068 | Common:1; Rare:20 | ||||
| chr10:13586913-13587056 | Common:1; Rare:53 | ||||
| chr10:13707184-13707495 | Common:3; Rare:72 | ||||
| chr10:13707547-13707691 | Rare:34 |