| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:89332261-89332537 | Common:3; Rare:45 | ||||
| chr10:89414664-89414785 | Common:3; Rare:60 | ||||
| chr10:89643927-89644147 | Rare:43 | ||||
| chr10:89701409-89701623 | Common:1; Rare:57 | ||||
| chr10:91923732-91923811 | Rare:28 | ||||
| chr10:92290997-92291393 | Common:5; Rare:126 | ||||
| chr10:92573789-92574111 | Common:2; Rare:103 | ||||
| chr10:92592972-92593169 | Common:3; Rare:60 | ||||
| chr10:93482199-93482341 | Common:2; Rare:43 | ||||
| chr10:93600394-93600819 | Common:3; Rare:115; Clinvar (pathogenic):1 | ||||
| chr10:93601169-93601396 | Common:3; Rare:49 | ||||
| chr10:95290902-95291149 | Common:2; Rare:98 | ||||
| chr10:95384045-95384392 | Common:3; Rare:90 | ||||
| chr10:95561345-95561605 | Common:4; Rare:78 | ||||
| chr10:95693902-95694058 | Common:2; Rare:56; Clinvar (benign):1 |