| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:73912030-73912316 | Common:2; Rare:79; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:75230814-75230963 | Common:1; Rare:41 | ||||
| chr10:79331857-79332033 | Common:1; Rare:43 | ||||
| chr10:79826309-79826567 | Common:3; Rare:81 | ||||
| chr10:80207232-80207463 | Common:1; Rare:47 | ||||
| chr10:87342311-87342425 | Common:2; Rare:36 | ||||
| chr10:87342598-87342907 | Common:1; Rare:80 | ||||
| chr10:87862245-87862575 | Rare:159; Clinvar:1 | ||||
| chr10:89283725-89283750 | Rare:1 | ||||
| chr10:91807531-91807691 | Rare:27 | ||||
| chr10:96090182-96090309 | Common:1; Rare:53 | ||||
| chr10:100373346-100373600 | Common:3; Rare:60 | ||||
| chr10:102777121-102777309 | Common:2; Rare:31 | ||||
| chr10:103192382-103192637 | Rare:58 | ||||
| chr10:103678211-103678391 | Common:1; Rare:34 |