| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177618693-177619023 | Common:7; Rare:95 | ||||
| chr2:177675689-177675716 | Rare:8 | ||||
| chr2:178450693-178450879 | Common:1; Rare:62 | ||||
| chr2:178451083-178451387 | Common:6; Rare:89; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478507-178478644 | Common:1; Rare:43 | ||||
| chr2:179264502-179264856 | Common:4; Rare:131 | ||||
| chr2:180007080-180007132 | Rare:9 | ||||
| chr2:180980832-180980963 | Rare:29 | ||||
| chr2:181891626-181892049 | Common:4; Rare:177 | ||||
| chr2:182715979-182716350 | Common:3; Rare:138 | ||||
| chr2:183078658-183078799 | Rare:29 | ||||
| chr2:183124252-183124473 | Common:4; Rare:76 | ||||
| chr2:186485966-186486457 | Common:3; Rare:140 | ||||
| chr2:186589907-186590365 | Rare:141 | ||||
| chr2:187554375-187554514 | Rare:30 |