| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:151289040-151289490 | Common:5; Rare:126 | ||||
| chr2:151289581-151289739 | Common:2; Rare:76 | ||||
| chr2:151409652-151410011 | Common:12; Rare:262 | ||||
| chr2:151410031-151410431 | Common:1; Rare:172 | ||||
| chr2:151410440-151410960 | Common:8; Rare:278 | ||||
| chr2:151828334-151828691 | Common:9; Rare:288 | ||||
| chr2:152098610-152099150 | Common:1; Rare:180; Clinvar:6; Clinvar (benign):7 | ||||
| chr2:152175300-152175653 | Rare:281 | ||||
| chr2:152175604-152176250 | Common:7; Rare:394 | ||||
| chr2:152335134-152335276 | Common:1; Rare:46 | ||||
| chr2:152715763-152716633 | Common:8; Rare:305 | ||||
| chr2:152716916-152717316 | Common:1; Rare:158 | ||||
| chr2:152717349-152717757 | Common:4; Rare:202 | ||||
| chr2:152717789-152718356 | Common:2; Rare:529 | ||||
| chr2:152718404-152718856 | Common:4; Rare:436; Clinvar:1 |