| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:98423654-98423780 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:99696619-99696699 | Rare:13 | ||||
| chr10:99715715-99715961 | Common:1; Rare:32 | ||||
| chr10:99718472-99718774 | Rare:64 | ||||
| chr10:99725704-99725846 | Common:1; Rare:22 | ||||
| chr10:99750189-99750338 | Rare:21 | ||||
| chr10:99891150-99891296 | Common:2; Rare:63 | ||||
| chr10:99930737-99931029 | Common:2; Rare:76 | ||||
| chr10:99977088-99977314 | Common:2; Rare:31 | ||||
| chr10:99984276-99984576 | Common:1; Rare:40 | ||||
| chr10:100006292-100006544 | Common:2; Rare:35 | ||||
| chr10:100112513-100112677 | Rare:26 | ||||
| chr10:100241083-100241288 | Common:1; Rare:33 | ||||
| chr10:100347905-100348038 | Rare:36 | ||||
| chr10:100371331-100371587 | Common:1; Rare:58 |