| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:91923721-91923805 | Rare:30 | ||||
| chr10:92290956-92291378 | Common:5; Rare:132 | ||||
| chr10:92573743-92574129 | Common:2; Rare:120 | ||||
| chr10:92592952-92593169 | Common:3; Rare:63 | ||||
| chr10:92689600-92689955 | Common:1; Rare:105 | ||||
| chr10:92848360-92848558 | Rare:75 | ||||
| chr10:93482181-93482358 | Common:2; Rare:50 | ||||
| chr10:93757685-93758028 | Common:1; Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:93893880-93894038 | Common:1; Rare:65 | ||||
| chr10:94362875-94363034 | Common:3; Rare:64 | ||||
| chr10:94545714-94545837 | Common:2; Rare:39 | ||||
| chr10:95290853-95291168 | Common:2; Rare:121 | ||||
| chr10:95561334-95561576 | Common:3; Rare:66 | ||||
| chr10:95656499-95656765 | Common:1; Rare:80; Clinvar:5; Clinvar (benign):4 | ||||
| chr10:95693847-95694067 | Common:2; Rare:89; Clinvar (benign):3; Clinvar (pathogenic):1 |