| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171999818-171999964 | Common:1; Rare:64 | ||||
| chr2:172084619-172084809 | Rare:45 | ||||
| chr2:172086319-172086459 | Rare:23 | ||||
| chr2:173354564-173354942 | Common:1; Rare:117 | ||||
| chr2:173965276-173965525 | Common:1; Rare:92 | ||||
| chr2:174248456-174248725 | Common:1; Rare:82 | ||||
| chr2:174395629-174395833 | Common:1; Rare:69 | ||||
| chr2:174486962-174487393 | Common:2; Rare:102 | ||||
| chr2:175168100-175168515 | Common:2; Rare:107 | ||||
| chr2:175181654-175181762 | Common:3; Rare:48 | ||||
| chr2:176002225-176002407 | Common:3; Rare:78 | ||||
| chr2:176269386-176269500 | Common:1; Rare:48 | ||||
| chr2:177212416-177212817 | Common:4; Rare:162 | ||||
| chr2:177264651-177264887 | Common:2; Rare:76 | ||||
| chr2:177392638-177393059 | Common:3; Rare:144; Clinvar:6; Clinvar (benign):4 |