| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:97714169-97714530 | Rare:100 | ||||
| chr10:97714903-97715020 | Rare:25 | ||||
| chr10:97736966-97737235 | Common:2; Rare:91 | ||||
| chr10:97849590-97850010 | Common:2; Rare:93 | ||||
| chr10:98134522-98134947 | Common:3; Rare:145 | ||||
| chr10:98268142-98268542 | Common:4; Rare:114 | ||||
| chr10:98415120-98415318 | Common:2; Rare:64 | ||||
| chr10:98446247-98446375 | Rare:22 | ||||
| chr10:98446874-98447067 | Rare:53 | ||||
| chr10:99430581-99431187 | Common:4; Rare:139 | ||||
| chr10:99620283-99620862 | Common:2; Rare:144 | ||||
| chr10:99620896-99621192 | Common:1; Rare:72 | ||||
| chr10:99659154-99659565 | Common:1; Rare:104 | ||||
| chr10:99732024-99732390 | Rare:140; Clinvar:6; Clinvar (benign):1 | ||||
| chr10:99732481-99732590 | Common:2; Rare:16; Clinvar:1; Clinvar (benign):1 |