| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:91162694-91163073 | Common:3; Rare:105 | ||||
| chr10:91410240-91410486 | Common:2; Rare:88 | ||||
| chr10:91632954-91633272 | Common:3; Rare:96 | ||||
| chr10:91923716-91923858 | Common:1; Rare:59 | ||||
| chr10:92243237-92243365 | Rare:29 | ||||
| chr10:92290978-92291358 | Common:5; Rare:122 | ||||
| chr10:92574003-92574122 | Common:1; Rare:38 | ||||
| chr10:92592952-92593205 | Common:3; Rare:72 | ||||
| chr10:93482203-93482334 | Common:2; Rare:41 | ||||
| chr10:93702432-93702690 | Common:5; Rare:92 | ||||
| chr10:93757721-93757971 | Common:1; Rare:46; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:95290853-95291194 | Common:2; Rare:132 | ||||
| chr10:95561323-95561605 | Common:4; Rare:86 | ||||
| chr10:95693891-95694067 | Common:2; Rare:66; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr10:95755637-95755753 | Common:1; Rare:24 |