| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:173965710-173966130 | Rare:185 | ||||
| chr2:174248451-174248779 | Common:1; Rare:106 | ||||
| chr2:174395615-174395816 | Common:3; Rare:112 | ||||
| chr2:174487069-174487416 | Common:4; Rare:156 | ||||
| chr2:175167840-175168010 | Common:1; Rare:37 | ||||
| chr2:175167998-175168604 | Common:5; Rare:278 | ||||
| chr2:175181626-175181821 | Common:7; Rare:136 | ||||
| chr2:176002231-176002414 | Common:5; Rare:141 | ||||
| chr2:176269349-176269533 | Common:2; Rare:121 | ||||
| chr2:177212400-177212892 | Common:9; Rare:353 | ||||
| chr2:177263398-177263716 | Common:1; Rare:112 | ||||
| chr2:177263759-177264159 | Common:4; Rare:174 | ||||
| chr2:177264646-177264867 | Common:4; Rare:135 | ||||
| chr2:177265109-177265277 | Common:2; Rare:80 | ||||
| chr2:177392618-177392823 | Common:3; Rare:100; Clinvar:2; Clinvar (benign):1 |