| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:18560147-18560284 | Common:1; Rare:67 | ||||
| chr2:18560418-18560853 | Rare:308 | ||||
| chr2:19358617-19358768 | Rare:65 | ||||
| chr2:19901574-19901766 | Common:3; Rare:164 | ||||
| chr2:19901914-19902091 | Common:3; Rare:96 | ||||
| chr2:19989497-19989897 | Common:3; Rare:136 | ||||
| chr2:19990025-19990235 | Rare:109 | ||||
| chr2:20012644-20012820 | Common:6; Rare:75; Clinvar (benign):2 | ||||
| chr2:20013053-20013423 | Common:7; Rare:98 | ||||
| chr2:20051543-20051874 | Common:2; Rare:164 | ||||
| chr2:20051930-20052240 | Common:3; Rare:122 | ||||
| chr2:20224993-20225224 | Common:2; Rare:110 | ||||
| chr2:20225340-20225526 | Common:2; Rare:97 | ||||
| chr2:20350180-20350470 | Common:4; Rare:128 | ||||
| chr2:20350607-20351101 | Common:4; Rare:356 |