| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100009860-100010092 | Common:1; Rare:69 | ||||
| chr10:100185895-100186198 | Rare:113 | ||||
| chr10:100229535-100229704 | Common:1; Rare:65 | ||||
| chr10:100267562-100267725 | Common:3; Rare:62 | ||||
| chr10:100286603-100286761 | Common:5; Rare:88 | ||||
| chr10:100346485-100346671 | Common:3; Rare:43 | ||||
| chr10:100347003-100347532 | Common:4; Rare:126 | ||||
| chr10:100519780-100519983 | Rare:71 | ||||
| chr10:100529803-100529947 | Rare:49 | ||||
| chr10:100535839-100535961 | Common:6; Rare:54 | ||||
| chr10:100912648-100913238 | Common:1; Rare:190 | ||||
| chr10:100913293-100913476 | Common:1; Rare:56 | ||||
| chr10:100969340-100969562 | Common:3; Rare:46 | ||||
| chr10:100987090-100987431 | Rare:118 | ||||
| chr10:100987439-100987685 | Common:2; Rare:85; Clinvar:2; Clinvar (benign):2 |