| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171999807-171999972 | Common:1; Rare:69 | ||||
| chr2:173354602-173354900 | Common:1; Rare:89 | ||||
| chr2:174248454-174248742 | Common:1; Rare:87 | ||||
| chr2:174395623-174395800 | Common:2; Rare:58 | ||||
| chr2:174487037-174487407 | Common:2; Rare:91 | ||||
| chr2:175168122-175168497 | Common:2; Rare:99 | ||||
| chr2:175181654-175181872 | Common:3; Rare:70 | ||||
| chr2:176104254-176104582 | Common:1; Rare:73 | ||||
| chr2:176269353-176269505 | Common:1; Rare:64 | ||||
| chr2:177212430-177212802 | Common:4; Rare:152 | ||||
| chr2:177263432-177263658 | Common:1; Rare:51 | ||||
| chr2:177264640-177264892 | Common:2; Rare:79 | ||||
| chr2:177392638-177393059 | Common:3; Rare:144; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552760-177552838 | Common:1; Rare:29 | ||||
| chr2:177618688-177618984 | Common:7; Rare:89 |