| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201260420-201260578 | Rare:34 | ||||
| chr2:201451444-201451874 | Common:3; Rare:108 | ||||
| chr2:201642641-201642743 | Rare:52 | ||||
| chr2:201643384-201643553 | Common:2; Rare:53; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:202238498-202238604 | Rare:35 | ||||
| chr2:202376992-202377119 | Rare:34; Clinvar:1 | ||||
| chr2:202912151-202912291 | Common:1; Rare:51 | ||||
| chr2:203014665-203014933 | Common:1; Rare:81 | ||||
| chr2:203238945-203239042 | Rare:36 | ||||
| chr2:203328119-203328465 | Common:2; Rare:124 | ||||
| chr2:203535250-203535546 | Common:3; Rare:129 | ||||
| chr2:206085919-206085981 | Rare:19 | ||||
| chr2:206086065-206086235 | Rare:24 | ||||
| chr2:206159362-206159689 | Common:3; Rare:103; Clinvar (benign):1 | ||||
| chr2:206274909-206275057 | Common:1; Rare:52 |