| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:96043463-96043583 | Rare:42 | ||||
| chr10:96586526-96586636 | Common:2; Rare:32 | ||||
| chr10:96586859-96587272 | Common:3; Rare:161 | ||||
| chr10:97334683-97334856 | Common:2; Rare:73 | ||||
| chr10:97426055-97426256 | Common:2; Rare:73 | ||||
| chr10:97445961-97446299 | Common:1; Rare:92 | ||||
| chr10:97633493-97633638 | Rare:37 | ||||
| chr10:98446312-98446375 | Rare:9 | ||||
| chr10:99430622-99430936 | Common:3; Rare:70 | ||||
| chr10:99659273-99659547 | Common:1; Rare:69 | ||||
| chr10:99732063-99732310 | Rare:89; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:100185935-100186102 | Rare:67 | ||||
| chr10:100286605-100286730 | Common:4; Rare:73 | ||||
| chr10:100346507-100346816 | Common:4; Rare:66 | ||||
| chr10:100987409-100987610 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):2 |