| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:50624504-50624681 | Common:1; Rare:74 | ||||
| chr10:50625161-50625216 | Rare:19 | ||||
| chr10:50739906-50739982 | Rare:16 | ||||
| chr10:51074029-51074353 | Common:5; Rare:77 | ||||
| chr10:51074377-51074588 | Common:1; Rare:49; Clinvar (benign):2 | ||||
| chr10:51153000-51153329 | Common:1; Rare:63; Clinvar:9; Clinvar (benign):5 | ||||
| chr10:51699521-51699982 | Common:7; Rare:131 | ||||
| chr10:55628243-55628333 | Common:2; Rare:17 | ||||
| chr10:56361193-56361520 | Common:7; Rare:127 | ||||
| chr10:58267874-58268066 | Common:1; Rare:56 | ||||
| chr10:58268815-58269231 | Common:6; Rare:114 | ||||
| chr10:58385291-58385634 | Common:3; Rare:116 | ||||
| chr10:58385952-58386238 | Common:4; Rare:71 | ||||
| chr10:59709656-59709890 | Common:2; Rare:56 | ||||
| chr10:59906281-59906343 | Rare:36 |