| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:93893910-93894014 | Common:1; Rare:45 | ||||
| chr10:93993780-93993949 | Common:1; Rare:46 | ||||
| chr10:94545668-94545891 | Common:4; Rare:75 | ||||
| chr10:95290819-95291163 | Common:2; Rare:130 | ||||
| chr10:95693846-95694256 | Common:5; Rare:133; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr10:95755965-95756176 | Common:1; Rare:40 | ||||
| chr10:95756441-95756597 | Common:1; Rare:36 | ||||
| chr10:95907826-95907939 | Common:1; Rare:34 | ||||
| chr10:95908160-95908315 | Rare:20 | ||||
| chr10:96129969-96130067 | Common:1; Rare:32 | ||||
| chr10:96130189-96130536 | Common:2; Rare:119 | ||||
| chr10:96833467-96833693 | Common:1; Rare:55 | ||||
| chr10:97318945-97319272 | Common:6; Rare:89 | ||||
| chr10:97334694-97334740 | Common:1; Rare:29 | ||||
| chr10:97426052-97426298 | Common:2; Rare:103 |