| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:36598068-36598309 | Common:30; Rare:193 | ||||
| chr2:36965920-36966370 | Common:1; Rare:213 | ||||
| chr2:36966436-36967078 | Common:18; Rare:592 | ||||
| chr2:37084244-37084604 | Common:12; Rare:335 | ||||
| chr2:37156912-37157167 | Common:6; Rare:163 | ||||
| chr2:37196394-37196607 | Common:3; Rare:116 | ||||
| chr2:37231435-37231805 | Common:15; Rare:405; Clinvar:2; Clinvar (benign):13 | ||||
| chr2:37323992-37324136 | Rare:40 | ||||
| chr2:37324642-37324971 | Common:1; Rare:200 | ||||
| chr2:37344621-37344726 | Common:1; Rare:45 | ||||
| chr2:37344628-37344779 | Common:1; Rare:59 | ||||
| chr2:37671600-37671888 | Common:13; Rare:227 | ||||
| chr2:37672014-37672890 | Common:35; Rare:550 | ||||
| chr2:37924810-37925095 | Common:5; Rare:128 | ||||
| chr2:37925270-37925700 | Common:15; Rare:496 |