| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:101354514-101354640 | Rare:35 | ||||
| chr10:101570233-101570456 | Common:1; Rare:67 | ||||
| chr10:101587993-101588575 | Common:1; Rare:198; Clinvar:1 | ||||
| chr10:101694788-101695262 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:101695274-101695357 | Common:1; Rare:24 | ||||
| chr10:101782094-101782348 | Common:1; Rare:86 | ||||
| chr10:101782988-101783136 | Rare:32 | ||||
| chr10:101783306-101783506 | Rare:88 | ||||
| chr10:101817507-101817855 | Common:1; Rare:90 | ||||
| chr10:101818333-101818845 | Common:1; Rare:135 | ||||
| chr10:101818956-101819089 | Rare:30 | ||||
| chr10:101830507-101830778 | Common:4; Rare:59 | ||||
| chr10:101830887-101831120 | Common:2; Rare:56 | ||||
| chr10:101839706-101839956 | Rare:84 | ||||
| chr10:102055763-102055880 | Rare:32 |