| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:75710860-75711015 | Common:2; Rare:113 | ||||
| chr2:84459227-84459615 | Common:6; Rare:191; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr2:84881016-84881401 | Common:3; Rare:164 | ||||
| chr2:84904907-84905350 | Common:4; Rare:124 | ||||
| chr2:84905428-84906132 | Common:5; Rare:377 | ||||
| chr2:84906997-84907380 | Common:1; Rare:115 | ||||
| chr2:84970340-84970860 | Common:3; Rare:193 | ||||
| chr2:84970920-84971386 | Common:6; Rare:252 | ||||
| chr2:85327916-85328118 | Common:4; Rare:158 | ||||
| chr2:85328180-85328640 | Common:5; Rare:111 | ||||
| chr2:85354470-85354807 | Common:2; Rare:215 | ||||
| chr2:85410307-85410489 | Rare:93 | ||||
| chr2:85413951-85414098 | Common:2; Rare:60 | ||||
| chr2:85418390-85418560 | Common:4; Rare:76 | ||||
| chr2:85418580-85418850 | Common:7; Rare:126 |