| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:95472762-95472980 | Common:1; Rare:41 | ||||
| chr10:95517606-95517741 | Common:1; Rare:26 | ||||
| chr10:96656768-96657127 | Common:1; Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:96673493-96673677 | Common:2; Rare:32 | ||||
| chr10:96673794-96673910 | Common:3; Rare:13 | ||||
| chr10:99612562-99612698 | Common:1; Rare:46 | ||||
| chr10:102435566-102435771 | Rare:23 | ||||
| chr10:102436493-102436605 | Common:1; Rare:27 | ||||
| chr10:110399528-110399761 | Common:1; Rare:36 | ||||
| chr10:110460225-110460313 | Rare:20 | ||||
| chr10:112272007-112272295 | Common:5; Rare:39 | ||||
| chr10:112821778-112822009 | Common:1; Rare:42 | ||||
| chr10:114632015-114632294 | Rare:70 | ||||
| chr10:114822902-114823090 | Common:1; Rare:21 | ||||
| chr10:122304135-122304229 | Rare:15 |