| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:174310397-174310616 | Common:1; Rare:31 | ||||
| chr2:174639086-174639346 | Rare:35 | ||||
| chr2:174750166-174750172 | Rare:3; Clinvar (benign):1 | ||||
| chr2:174926421-174926471 | Rare:5 | ||||
| chr2:175048373-175048415 | Rare:11 | ||||
| chr2:175048841-175049120 | Common:1; Rare:55 | ||||
| chr2:175167169-175167630 | Common:1; Rare:101 | ||||
| chr2:175180799-175180951 | Common:1; Rare:32 | ||||
| chr2:175995556-175995787 | Common:1; Rare:40 | ||||
| chr2:176134872-176135112 | Common:1; Rare:45 | ||||
| chr2:176139659-176140112 | Common:5; Rare:107 | ||||
| chr2:176149181-176149366 | Rare:35 | ||||
| chr2:176150139-176150491 | Common:1; Rare:79 | ||||
| chr2:176155878-176155977 | Rare:16 | ||||
| chr2:176173221-176173287 | Common:1; Rare:9 |