| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49093585-49093643 | Rare:30 | ||||
| chr3:49104616-49104910 | Common:1; Rare:120; Clinvar:3; Clinvar (benign):7 | ||||
| chr3:49120747-49121019 | Rare:77 | ||||
| chr3:49125863-49126006 | Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:49132319-49132631 | Common:1; Rare:107; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:49132969-49133143 | Rare:37; Clinvar:2 | ||||
| chr3:49166284-49166442 | Common:1; Rare:42 | ||||
| chr3:49339972-49340132 | Common:2; Rare:75 | ||||
| chr3:49358025-49358430 | Common:4; Rare:210 | ||||
| chr3:49411820-49412213 | Common:1; Rare:125 | ||||
| chr3:49412320-49412445 | Rare:44 | ||||
| chr3:49429262-49429499 | Common:1; Rare:53 | ||||
| chr3:49469997-49470319 | Common:1; Rare:98 | ||||
| chr3:49674220-49674402 | Common:1; Rare:70 | ||||
| chr3:49689460-49689605 | Rare:45 |