| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:80536001-80536124 | Common:4; Rare:34 | ||||
| chr10:84173120-84173210 | Common:1; Rare:18 | ||||
| chr10:84196332-84196519 | Common:1; Rare:37; Clinvar:3 | ||||
| chr10:86955598-86955778 | Rare:29 | ||||
| chr10:86970415-86970526 | Common:4; Rare:46 | ||||
| chr10:87136858-87137047 | Common:1; Rare:37 | ||||
| chr10:87342264-87342949 | Common:6; Rare:209 | ||||
| chr10:87862258-87862575 | Rare:151; Clinvar:1 | ||||
| chr10:91807500-91807691 | Rare:38 | ||||
| chr10:95289657-95289889 | Common:1; Rare:38 | ||||
| chr10:95503037-95503342 | Common:1; Rare:35 | ||||
| chr10:96750312-96750614 | Common:3; Rare:88 | ||||
| chr10:96794987-96795327 | Common:2; Rare:64 | ||||
| chr10:97430765-97431134 | Rare:109 | ||||
| chr10:99727036-99727345 | Common:1; Rare:81; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 |