| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:93482153-93482456 | Common:2; Rare:79 | ||||
| chr10:93702380-93702683 | Common:5; Rare:98 | ||||
| chr10:93757683-93758034 | Common:1; Rare:59; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:93893867-93894033 | Common:1; Rare:67 | ||||
| chr10:93993773-93994108 | Common:5; Rare:98; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:94324194-94324423 | Common:1; Rare:49; Clinvar:1 | ||||
| chr10:94362892-94363034 | Common:3; Rare:58 | ||||
| chr10:94683658-94683988 | Common:1; Rare:83 | ||||
| chr10:95193793-95194267 | Rare:60 | ||||
| chr10:95290853-95291170 | Common:2; Rare:122 | ||||
| chr10:95561320-95561611 | Common:4; Rare:89 | ||||
| chr10:95656622-95656765 | Common:1; Rare:48; Clinvar:5; Clinvar (benign):2 | ||||
| chr10:95693846-95694006 | Common:2; Rare:75; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr10:95755649-95755757 | Rare:22 | ||||
| chr10:95756051-95756203 | Common:2; Rare:49 |