| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179347606-179347743 | Common:1; Rare:30 | ||||
| chr3:179604581-179604838 | Common:2; Rare:97 | ||||
| chr3:180912393-180912691 | Common:1; Rare:106 | ||||
| chr3:181711736-181711987 | Rare:77 | ||||
| chr3:181712252-181712363 | Common:1; Rare:33; Clinvar (benign):1 | ||||
| chr3:184017876-184018121 | Common:1; Rare:77 | ||||
| chr3:184135221-184135385 | Common:2; Rare:48; Clinvar:5 | ||||
| chr3:184248885-184249021 | Rare:68; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249451-184249741 | Common:1; Rare:81 | ||||
| chr3:184711970-184712243 | Common:1; Rare:92 | ||||
| chr3:184812042-184812193 | Common:1; Rare:36 | ||||
| chr3:185586000-185586343 | Common:1; Rare:76 | ||||
| chr3:185937966-185938188 | Common:1; Rare:96 | ||||
| chr3:186806416-186806550 | Rare:43 | ||||
| chr3:192917836-192918014 | Common:2; Rare:82 |