| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69012917-69013623 | Common:17; Rare:261 | ||||
| chr2:69387124-69387452 | Rare:181; Clinvar:4 | ||||
| chr2:69437427-69437583 | Rare:113; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:69643613-69643892 | Rare:134 | ||||
| chr2:69643920-69644260 | Common:7; Rare:57 | ||||
| chr2:69741806-69742154 | Common:3; Rare:136 | ||||
| chr2:69829508-69829748 | Common:1; Rare:181 | ||||
| chr2:69893876-69894019 | Rare:39 | ||||
| chr2:69914489-69915136 | Common:3; Rare:295 | ||||
| chr2:70086904-70087118 | Common:1; Rare:108 | ||||
| chr2:70087248-70088159 | Common:5; Rare:463 | ||||
| chr2:70190627-70190870 | Common:2; Rare:91 | ||||
| chr2:70190940-70191147 | Common:2; Rare:96 | ||||
| chr2:70248544-70248805 | Common:8; Rare:183 | ||||
| chr2:70257977-70258183 | Common:2; Rare:134 |