| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49104705-49104887 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):5 | ||||
| chr3:49132998-49133145 | Rare:34; Clinvar:1 | ||||
| chr3:49166293-49166409 | Common:1; Rare:31 | ||||
| chr3:49339919-49340149 | Common:2; Rare:96 | ||||
| chr3:49340618-49340907 | Common:2; Rare:56 | ||||
| chr3:49358285-49358469 | Common:2; Rare:95 | ||||
| chr3:49411894-49412427 | Common:2; Rare:197 | ||||
| chr3:49470008-49470320 | Common:1; Rare:91 | ||||
| chr3:49674222-49674398 | Common:1; Rare:66 | ||||
| chr3:49689451-49689593 | Rare:46 | ||||
| chr3:49803074-49803313 | Common:3; Rare:79 | ||||
| chr3:49813828-49813991 | Common:1; Rare:25 | ||||
| chr3:50299284-50299692 | Common:1; Rare:99 | ||||
| chr3:50340823-50340912 | Rare:30 | ||||
| chr3:50350705-50350905 | Common:1; Rare:31 |