| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:19358556-19358777 | Rare:49 | ||||
| chr2:19901435-19901830 | Common:6; Rare:148 | ||||
| chr2:19901922-19902273 | Common:5; Rare:98 | ||||
| chr2:19902277-19902304 | Rare:5 | ||||
| chr2:19990046-19990412 | Common:1; Rare:105 | ||||
| chr2:20012419-20012607 | Common:1; Rare:57; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:20012653-20012843 | Common:3; Rare:50; Clinvar (benign):1 | ||||
| chr2:20051556-20051942 | Common:2; Rare:100 | ||||
| chr2:20051988-20052229 | Common:3; Rare:56 | ||||
| chr2:20223432-20223501 | Rare:12 | ||||
| chr2:20223929-20224026 | Common:1; Rare:20 | ||||
| chr2:20224211-20224360 | Common:1; Rare:45 | ||||
| chr2:20224983-20225321 | Common:1; Rare:85 | ||||
| chr2:20225340-20225482 | Common:1; Rare:46 | ||||
| chr2:20350134-20350252 | Common:1; Rare:27 |