| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201071620-201072078 | Rare:99 | ||||
| chr2:201140060-201140183 | Common:3; Rare:39 | ||||
| chr2:201451444-201451907 | Common:3; Rare:112 | ||||
| chr2:201642427-201642806 | Common:3; Rare:130; Clinvar (benign):1 | ||||
| chr2:201643449-201643555 | Rare:29; Clinvar:3 | ||||
| chr2:201780887-201781227 | Common:2; Rare:106; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:202238443-202238687 | Common:1; Rare:86; Clinvar:1 | ||||
| chr2:202265650-202265826 | Rare:70 | ||||
| chr2:202634651-202635024 | Common:6; Rare:122 | ||||
| chr2:202871637-202871859 | Common:1; Rare:76 | ||||
| chr2:203014626-203014933 | Common:1; Rare:98 | ||||
| chr2:203238774-203239054 | Common:2; Rare:101 | ||||
| chr2:203239222-203239373 | Rare:53 | ||||
| chr2:203327998-203328538 | Common:2; Rare:181 | ||||
| chr2:203535169-203535553 | Common:3; Rare:150 |