| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100167668-100167755 | Common:1; Rare:12 | ||||
| chr10:100185442-100185473 | Rare:7 | ||||
| chr10:100327080-100327280 | Common:1; Rare:38 | ||||
| chr10:100339306-100339525 | Common:1; Rare:37 | ||||
| chr10:100347942-100347967 | Rare:6 | ||||
| chr10:100373254-100373636 | Common:3; Rare:81 | ||||
| chr10:100373970-100374123 | Rare:27 | ||||
| chr10:101042683-101043231 | Common:1; Rare:109 | ||||
| chr10:101060590-101061065 | Common:2; Rare:113 | ||||
| chr10:101067508-101067783 | Common:2; Rare:50 | ||||
| chr10:101067848-101068028 | Common:1; Rare:47 | ||||
| chr10:101121421-101121514 | Common:1; Rare:24 | ||||
| chr10:101690524-101690617 | Rare:15 | ||||
| chr10:101693753-101693887 | Common:1; Rare:23 | ||||
| chr10:101694076-101694685 | Common:4; Rare:161; Clinvar:4; Clinvar (benign):5 |