| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74198819-74199786 | Common:7; Rare:194 | ||||
| chr2:74391594-74391776 | Common:3; Rare:57 | ||||
| chr2:74391788-74392214 | Common:2; Rare:183 | ||||
| chr2:74421507-74421793 | Rare:89 | ||||
| chr2:74422100-74422220 | Rare:56 | ||||
| chr2:74440336-74440395 | Rare:9 | ||||
| chr2:74440397-74440702 | Rare:76 | ||||
| chr2:74454652-74454709 | Rare:9 | ||||
| chr2:74454757-74455151 | Rare:93 | ||||
| chr2:74457865-74457933 | Rare:23 | ||||
| chr2:74458010-74458525 | Common:1; Rare:159 | ||||
| chr2:74458706-74459015 | Common:1; Rare:88 | ||||
| chr2:74465157-74465277 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:74465312-74465563 | Common:2; Rare:66; Clinvar:1 | ||||
| chr2:74472167-74472292 | Rare:46 |