| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:12195773-12196005 | Rare:56 | ||||
| chr10:12196076-12196296 | Rare:73 | ||||
| chr10:12349521-12349730 | Common:1; Rare:54 | ||||
| chr10:13099958-13100198 | Common:2; Rare:63; Clinvar:2; Clinvar (benign):4 | ||||
| chr10:13161312-13161609 | Common:1; Rare:82 | ||||
| chr10:13299530-13299720 | Common:1; Rare:41 | ||||
| chr10:13299914-13300222 | Rare:107; Clinvar:2 | ||||
| chr10:13302145-13302224 | Common:2; Rare:11 | ||||
| chr10:13302307-13302566 | Rare:54 | ||||
| chr10:13347454-13347773 | Common:2; Rare:128 | ||||
| chr10:13348228-13348563 | Common:1; Rare:97 | ||||
| chr10:13348667-13348865 | Common:1; Rare:38 | ||||
| chr10:13586763-13587047 | Common:3; Rare:94 | ||||
| chr10:13707680-13707845 | Common:1; Rare:35 | ||||
| chr10:14604292-14604609 | Common:6; Rare:138 |