| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:143119617-143119841 | Rare:64 | ||||
| chr3:143848451-143848521 | Rare:8 | ||||
| chr3:143971306-143971509 | Common:1; Rare:80 | ||||
| chr3:143971654-143972269 | Common:5; Rare:252 | ||||
| chr3:143972416-143972733 | Common:1; Rare:130 | ||||
| chr3:143972773-143972808 | Rare:13 | ||||
| chr3:143973138-143973370 | Common:1; Rare:86 | ||||
| chr3:146161146-146161302 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:146469309-146469651 | Common:5; Rare:81 | ||||
| chr3:146544444-146544872 | Common:5; Rare:101 | ||||
| chr3:148991318-148991715 | Common:6; Rare:165; Clinvar (benign):1 | ||||
| chr3:148991823-148991940 | Rare:41 | ||||
| chr3:148992214-148992263 | Rare:7 | ||||
| chr3:148992276-148992365 | Common:1; Rare:24 | ||||
| chr3:149086461-149086754 | Rare:91 |