| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219041485-219041572 | Rare:32 | ||||
| chr2:219160534-219160587 | Common:2; Rare:12 | ||||
| chr2:219160793-219160935 | Common:1; Rare:38 | ||||
| chr2:219176887-219177118 | Common:4; Rare:69 | ||||
| chr2:219178095-219178556 | Common:7; Rare:167 | ||||
| chr2:219206674-219206936 | Rare:95 | ||||
| chr2:219229149-219229430 | Common:2; Rare:63 | ||||
| chr2:219229549-219229914 | Common:2; Rare:115 | ||||
| chr2:219245378-219245537 | Common:1; Rare:47 | ||||
| chr2:219253914-219254056 | Common:1; Rare:48 | ||||
| chr2:219254532-219254660 | Common:1; Rare:26 | ||||
| chr2:219254710-219254852 | Rare:19 | ||||
| chr2:219279017-219279069 | Rare:8 | ||||
| chr2:219279225-219279545 | Common:3; Rare:100; Clinvar (benign):1 | ||||
| chr2:219387786-219388118 | Common:2; Rare:76 |