| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:144518134-144518203 | Common:1; Rare:14 | ||||
| chr2:144518386-144518674 | Rare:50 | ||||
| chr2:144519938-144520533 | Common:4; Rare:121; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:144524425-144524566 | Common:2; Rare:26 | ||||
| chr2:148020681-148021109 | Common:2; Rare:99; Clinvar (benign):2 | ||||
| chr2:148021135-148021289 | Rare:37 | ||||
| chr2:148021332-148021531 | Rare:62 | ||||
| chr2:148021534-148021555 | Rare:4 | ||||
| chr2:148021571-148021658 | Rare:18 | ||||
| chr2:148644571-148644751 | Rare:64 | ||||
| chr2:149587245-149587456 | Common:2; Rare:43 | ||||
| chr2:149587685-149587849 | Common:1; Rare:46; Clinvar:1 | ||||
| chr2:151261765-151261870 | Common:1; Rare:26 | ||||
| chr2:151289609-151289938 | Common:1; Rare:65 | ||||
| chr2:151828336-151828614 | Common:3; Rare:86 |