| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:105371110-105371124 | Common:1; Rare:2 | ||||
| chr2:105371456-105371679 | Common:3; Rare:36 | ||||
| chr2:105372936-105373230 | Common:2; Rare:55 | ||||
| chr2:105373300-105373327 | Rare:3 | ||||
| chr2:105373338-105373729 | Rare:110; Clinvar:3; Clinvar (benign):4 | ||||
| chr2:105375313-105375577 | Common:1; Rare:53 | ||||
| chr2:105375701-105375764 | Common:1; Rare:7 | ||||
| chr2:105377127-105377324 | Rare:42 | ||||
| chr2:105377679-105377778 | Rare:23 | ||||
| chr2:105379625-105379732 | Common:2; Rare:18 | ||||
| chr2:105380741-105381014 | Common:4; Rare:46 | ||||
| chr2:105381439-105381444 | |||||
| chr2:105383236-105383436 | Common:1; Rare:30 | ||||
| chr2:105383657-105383705 | Common:1; Rare:8 | ||||
| chr2:105384094-105384323 | Common:1; Rare:38 |