| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:104268893-104269320 | Common:4; Rare:111 | ||||
| chr10:104274788-104274944 | Common:1; Rare:42 | ||||
| chr10:104275090-104275197 | Rare:25 | ||||
| chr10:104329273-104329617 | Common:1; Rare:50 | ||||
| chr10:104338177-104338789 | Rare:148 | ||||
| chr10:104353519-104353845 | Common:2; Rare:79 | ||||
| chr10:109923389-109923710 | Common:2; Rare:119 | ||||
| chr10:110007596-110008016 | Rare:134 | ||||
| chr10:110207415-110207661 | Rare:50 | ||||
| chr10:110225711-110226232 | Common:2; Rare:138 | ||||
| chr10:110304851-110305235 | Common:2; Rare:120 | ||||
| chr10:110497476-110497977 | Common:5; Rare:158 | ||||
| chr10:110567238-110567761 | Common:4; Rare:166; Clinvar:2; Clinvar (benign):5 | ||||
| chr10:110643590-110644100 | Common:6; Rare:115 | ||||
| chr10:110644120-110644480 | Common:1; Rare:93; Clinvar (benign):4 |