| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:97713541-97713829 | Rare:116 | ||||
| chr10:97714090-97714740 | Common:1; Rare:266 | ||||
| chr10:97714760-97715450 | Common:1; Rare:249 | ||||
| chr10:97737011-97737235 | Common:2; Rare:143 | ||||
| chr10:98134529-98134706 | Common:2; Rare:121 | ||||
| chr10:98446850-98447053 | Rare:108; Clinvar:1 | ||||
| chr10:99430602-99431143 | Common:6; Rare:218 | ||||
| chr10:99620361-99620967 | Common:5; Rare:232 | ||||
| chr10:99659246-99659565 | Common:2; Rare:154 | ||||
| chr10:99732033-99732349 | Rare:219; Clinvar:8; Clinvar (benign):1 | ||||
| chr10:99732370-99732894 | Common:5; Rare:160; Clinvar:5; Clinvar (benign):3 | ||||
| chr10:99782464-99782819 | Rare:92; Clinvar:1 | ||||
| chr10:100009844-100010273 | Common:1; Rare:162 | ||||
| chr10:100185882-100186220 | Rare:223 | ||||
| chr10:100229530-100229689 | Rare:113 |