| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:91409448-91409724 | Common:1; Rare:80 | ||||
| chr10:91632998-91633386 | Common:3; Rare:113 | ||||
| chr10:91923643-91923836 | Common:1; Rare:74 | ||||
| chr10:92291022-92291392 | Common:5; Rare:117 | ||||
| chr10:92573947-92574129 | Common:1; Rare:62 | ||||
| chr10:92592972-92593145 | Common:2; Rare:51 | ||||
| chr10:92689737-92689955 | Common:1; Rare:71 | ||||
| chr10:93482108-93482257 | Common:2; Rare:53 | ||||
| chr10:93482260-93482340 | Rare:16 | ||||
| chr10:93702432-93702714 | Common:5; Rare:99 | ||||
| chr10:93757735-93758020 | Common:1; Rare:47; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:95290842-95291175 | Common:2; Rare:131 | ||||
| chr10:95384236-95384321 | Common:1; Rare:21 | ||||
| chr10:95561320-95561613 | Common:4; Rare:89 | ||||
| chr10:95693858-95694207 | Common:5; Rare:115; Clinvar (benign):3; Clinvar (pathogenic):1 |