| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:148020681-148021125 | Common:2; Rare:105; Clinvar (benign):2 | ||||
| chr2:148021571-148021674 | Rare:20 | ||||
| chr2:149330344-149330616 | Common:1; Rare:117 | ||||
| chr2:149587685-149587826 | Common:1; Rare:40; Clinvar:1 | ||||
| chr2:150485382-150485509 | Rare:30 | ||||
| chr2:151289619-151289757 | Common:1; Rare:35 | ||||
| chr2:151828419-151828793 | Common:2; Rare:107 | ||||
| chr2:152175882-152176142 | Common:1; Rare:64 | ||||
| chr2:152717829-152717947 | Rare:47 | ||||
| chr2:152717959-152718315 | Common:1; Rare:123 | ||||
| chr2:152718490-152718650 | Rare:61 | ||||
| chr2:156332676-156332870 | Rare:58; Clinvar:3 | ||||
| chr2:158968485-158968688 | Rare:64 | ||||
| chr2:159136009-159136287 | Common:15; Rare:104 | ||||
| chr2:159615225-159615343 | Common:2; Rare:28 |