| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49104640-49105028 | Common:1; Rare:351; Clinvar:4; Clinvar (benign):14 | ||||
| chr3:49120718-49120977 | Rare:178 | ||||
| chr3:49120879-49121008 | Rare:35 | ||||
| chr3:49132290-49132570 | Common:2; Rare:171; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr3:49132553-49132671 | Rare:46; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:49132790-49133172 | Rare:164; Clinvar:7 | ||||
| chr3:49166229-49166456 | Common:2; Rare:104 | ||||
| chr3:49171471-49171633 | Common:4; Rare:71 | ||||
| chr3:49276810-49277180 | Common:4; Rare:236 | ||||
| chr3:49339951-49340327 | Common:7; Rare:276 | ||||
| chr3:49340434-49340880 | Common:3; Rare:140 | ||||
| chr3:49411826-49412482 | Common:6; Rare:637 | ||||
| chr3:49412531-49413692 | Common:13; Rare:384 | ||||
| chr3:49429228-49429461 | Common:2; Rare:143 | ||||
| chr3:49468839-49469329 | Common:4; Rare:152 |