| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:99430525-99431147 | Common:4; Rare:153 | ||||
| chr10:99620777-99620858 | Rare:27 | ||||
| chr10:99620870-99621680 | Common:3; Rare:184 | ||||
| chr10:99659130-99659567 | Common:1; Rare:108 | ||||
| chr10:99732027-99732329 | Rare:113; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:99732670-99732729 | Rare:10 | ||||
| chr10:100009894-100010009 | Common:1; Rare:40 | ||||
| chr10:100185864-100186369 | Common:2; Rare:152 | ||||
| chr10:100229538-100229737 | Common:1; Rare:68 | ||||
| chr10:100267606-100267808 | Common:4; Rare:57 | ||||
| chr10:100286048-100286479 | Rare:102 | ||||
| chr10:100286605-100286804 | Common:5; Rare:101 | ||||
| chr10:100346448-100346674 | Common:3; Rare:48 | ||||
| chr10:100346875-100347398 | Common:1; Rare:120 | ||||
| chr10:100529797-100529975 | Rare:55 |