| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:173354566-173354890 | Common:1; Rare:96 | ||||
| chr2:173965299-173965510 | Common:1; Rare:75 | ||||
| chr2:174395618-174395800 | Common:2; Rare:59 | ||||
| chr2:174486994-174487144 | Common:1; Rare:40 | ||||
| chr2:175181629-175181762 | Common:4; Rare:59 | ||||
| chr2:176002221-176002414 | Common:3; Rare:85 | ||||
| chr2:177212607-177212802 | Common:1; Rare:83 | ||||
| chr2:177263427-177263687 | Common:1; Rare:63 | ||||
| chr2:177264651-177264905 | Common:2; Rare:77 | ||||
| chr2:177392627-177393005 | Common:3; Rare:129; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552761-177552838 | Common:1; Rare:29 | ||||
| chr2:178451083-178451378 | Common:6; Rare:86; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178702659-178702898 | Rare:46; Clinvar (benign):2 | ||||
| chr2:179049986-179050201 | Rare:47 | ||||
| chr2:180980246-180980545 | Common:1; Rare:94 |