| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:92349390-92349754 | Rare:83 | ||||
| chr10:92592957-92593162 | Common:3; Rare:62 | ||||
| chr10:92689718-92689952 | Common:1; Rare:76 | ||||
| chr10:93482165-93482257 | Common:2; Rare:36 | ||||
| chr10:93482261-93482452 | Rare:40 | ||||
| chr10:93702353-93702461 | Rare:20 | ||||
| chr10:95290829-95291167 | Common:2; Rare:129 | ||||
| chr10:95693862-95694207 | Common:5; Rare:114; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr10:96043425-96043606 | Common:1; Rare:64 | ||||
| chr10:96130006-96130075 | Common:1; Rare:23 | ||||
| chr10:96586737-96586810 | Common:1; Rare:25 | ||||
| chr10:96586924-96587244 | Rare:126 | ||||
| chr10:96832177-96832308 | Rare:45 | ||||
| chr10:97426049-97426257 | Common:2; Rare:79 | ||||
| chr10:97445971-97446242 | Common:1; Rare:71 |