| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:191678560-191678603 | Rare:20 | ||||
| chr2:191847034-191847143 | Rare:19 | ||||
| chr2:196068801-196068900 | Common:1; Rare:23 | ||||
| chr2:196171470-196171921 | Common:1; Rare:136 | ||||
| chr2:197434970-197435192 | Rare:75 | ||||
| chr2:197453227-197453563 | Rare:116 | ||||
| chr2:197499799-197500007 | Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197500101-197500427 | Common:1; Rare:134 | ||||
| chr2:197515873-197516089 | Common:1; Rare:86 | ||||
| chr2:200509907-200510263 | Common:2; Rare:121 | ||||
| chr2:200609105-200609326 | Rare:55 | ||||
| chr2:200811385-200811598 | Common:1; Rare:75 | ||||
| chr2:200864228-200864255 | Rare:8 | ||||
| chr2:200864562-200864788 | Common:1; Rare:83 | ||||
| chr2:200888994-200889439 | Common:3; Rare:142 |