| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:85615931-85616192 | Rare:84 | ||||
| chr2:86105855-86106277 | Common:3; Rare:125 | ||||
| chr2:86195407-86195651 | Common:4; Rare:76 | ||||
| chr2:86199366-86199522 | Common:1; Rare:57 | ||||
| chr2:88055736-88055958 | Common:1; Rare:83 | ||||
| chr2:88691474-88691703 | Common:2; Rare:77 | ||||
| chr2:95121736-95122098 | Common:1; Rare:125 | ||||
| chr2:95165397-95165420 | Rare:2 | ||||
| chr2:95165651-95165817 | Rare:49 | ||||
| chr2:95207431-95207590 | Rare:63 | ||||
| chr2:95402462-95402750 | Rare:89 | ||||
| chr2:96208264-96208403 | Rare:71 | ||||
| chr2:96208823-96208950 | Common:3; Rare:45 | ||||
| chr2:96265978-96266287 | Common:2; Rare:94 | ||||
| chr2:96305439-96305657 | Common:2; Rare:86; Clinvar:3; Clinvar (benign):2 |