| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201118607-201118831 | Rare:34 | ||||
| chr2:201129270-201129571 | Rare:64 | ||||
| chr2:201132867-201132965 | Rare:18 | ||||
| chr2:201258185-201258348 | Common:2; Rare:52; Clinvar (benign):2 | ||||
| chr2:201260420-201260578 | Rare:34 | ||||
| chr2:201451435-201451899 | Common:3; Rare:112 | ||||
| chr2:201642643-201642743 | Rare:51 | ||||
| chr2:201643405-201643549 | Common:1; Rare:46; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:202238443-202238626 | Rare:63; Clinvar:1 | ||||
| chr2:202634795-202635019 | Common:5; Rare:84 | ||||
| chr2:202911881-202912311 | Common:2; Rare:116 | ||||
| chr2:202912474-202912568 | Common:2; Rare:31 | ||||
| chr2:203014676-203014938 | Common:1; Rare:79 | ||||
| chr2:203238751-203239040 | Common:1; Rare:100 | ||||
| chr2:203239201-203239322 | Rare:38 |