| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219254562-219254609 | Rare:9 | ||||
| chr2:219277782-219278085 | Common:1; Rare:49 | ||||
| chr2:219279023-219279429 | Common:2; Rare:114 | ||||
| chr2:219279733-219279972 | Rare:64; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:219387525-219387804 | Common:2; Rare:90 | ||||
| chr2:219387807-219387848 | Rare:18 | ||||
| chr2:219387874-219388179 | Common:2; Rare:46 | ||||
| chr2:219388325-219388616 | Common:1; Rare:59 | ||||
| chr2:219498665-219499006 | Common:2; Rare:78 | ||||
| chr2:219543067-219543204 | Common:2; Rare:33 | ||||
| chr2:219543514-219543717 | Rare:60 | ||||
| chr2:219597630-219597913 | Common:1; Rare:109 | ||||
| chr2:219598016-219598280 | Common:1; Rare:85 | ||||
| chr2:221572295-221572453 | Common:2; Rare:54 | ||||
| chr2:222424158-222424211 | Rare:11 |