| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177552755-177552838 | Common:1; Rare:31 | ||||
| chr2:178450727-178450881 | Rare:51 | ||||
| chr2:178451083-178451304 | Common:5; Rare:67; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478515-178478658 | Common:1; Rare:44 | ||||
| chr2:180980279-180980545 | Common:1; Rare:86 | ||||
| chr2:180980862-180981220 | Rare:95 | ||||
| chr2:181891669-181891996 | Common:4; Rare:131 | ||||
| chr2:182426990-182427108 | Rare:21 | ||||
| chr2:182522626-182522858 | Common:2; Rare:46 | ||||
| chr2:183078658-183078799 | Rare:29 | ||||
| chr2:183124252-183124452 | Common:4; Rare:67 | ||||
| chr2:186485997-186486344 | Common:3; Rare:97 | ||||
| chr2:186693890-186694221 | Common:1; Rare:129 | ||||
| chr2:187448142-187448396 | Rare:39 | ||||
| chr2:188974526-188974559 | Rare:11 |