| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201642637-201642722 | Rare:43 | ||||
| chr2:202911631-202911723 | Rare:15 | ||||
| chr2:202912127-202912291 | Common:2; Rare:56 | ||||
| chr2:203014676-203014915 | Common:1; Rare:66 | ||||
| chr2:203238662-203239030 | Common:1; Rare:106 | ||||
| chr2:203239235-203239363 | Rare:47 | ||||
| chr2:203535250-203535546 | Common:3; Rare:129 | ||||
| chr2:205682356-205682703 | Rare:70 | ||||
| chr2:205682929-205683096 | Common:1; Rare:19 | ||||
| chr2:206085771-206085955 | Common:1; Rare:54 | ||||
| chr2:206159362-206159989 | Common:4; Rare:185; Clinvar (benign):1 | ||||
| chr2:206274845-206275041 | Rare:64 | ||||
| chr2:206765297-206765668 | Common:3; Rare:97; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165928-207166094 | Rare:30 | ||||
| chr2:207529571-207530104 | Common:3; Rare:140 |