| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27771650-27771771 | Common:1; Rare:47 | ||||
| chr2:27890662-27890825 | Rare:44 | ||||
| chr2:28392626-28392917 | Rare:104 | ||||
| chr2:28395222-28395446 | Common:5; Rare:43 | ||||
| chr2:28395474-28395735 | Common:1; Rare:50 | ||||
| chr2:28751687-28752197 | Common:2; Rare:209 | ||||
| chr2:28870243-28870425 | Rare:79 | ||||
| chr2:30146639-30147061 | Common:5; Rare:139 | ||||
| chr2:30147886-30148199 | Common:2; Rare:85 | ||||
| chr2:30447068-30447314 | Common:4; Rare:85 | ||||
| chr2:32010283-32010338 | Rare:12 | ||||
| chr2:32039747-32039858 | Rare:35 | ||||
| chr2:32063895-32064152 | Common:1; Rare:129; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:32165745-32165903 | Common:1; Rare:61 | ||||
| chr2:32627934-32628119 | Rare:56 |