| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69436850-69437395 | Common:4; Rare:268; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:69437347-69437715 | Common:6; Rare:645; Clinvar:26; Clinvar (benign):19 | ||||
| chr2:69642720-69643519 | Common:8; Rare:355 | ||||
| chr2:69643558-69644351 | Common:15; Rare:898 | ||||
| chr2:69644268-69644996 | Common:10; Rare:175 | ||||
| chr2:69741671-69742184 | Common:7; Rare:303 | ||||
| chr2:69828960-69829360 | Common:6; Rare:107 | ||||
| chr2:69829380-69829834 | Common:8; Rare:798 | ||||
| chr2:69893601-69894240 | Common:4; Rare:324 | ||||
| chr2:69914424-69915880 | Common:13; Rare:1059 | ||||
| chr2:70086833-70087242 | Common:11; Rare:924 | ||||
| chr2:70087285-70087912 | Common:14; Rare:1177 | ||||
| chr2:70190340-70190860 | Common:14; Rare:464 | ||||
| chr2:70190880-70191320 | Common:15; Rare:417 | ||||
| chr2:70248411-70249490 | Common:56; Rare:1454; Clinvar:1 |