| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:47475812-47476027 | Common:3; Rare:96 | ||||
| chr3:47781668-47782010 | Rare:122 | ||||
| chr3:48088781-48089082 | Rare:100 | ||||
| chr3:48301351-48301449 | Common:1; Rare:27 | ||||
| chr3:48440061-48440309 | Common:1; Rare:95 | ||||
| chr3:48446696-48446743 | Rare:15 | ||||
| chr3:48504090-48504317 | Common:2; Rare:72 | ||||
| chr3:48556794-48557175 | Common:1; Rare:85 | ||||
| chr3:48918748-48918903 | Common:2; Rare:88 | ||||
| chr3:49007086-49007409 | Common:2; Rare:123 | ||||
| chr3:49022009-49022154 | Rare:47; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49025156-49025386 | Rare:51 | ||||
| chr3:49028311-49028489 | Rare:56 | ||||
| chr3:49029316-49029616 | Common:2; Rare:200 | ||||
| chr3:49104729-49104910 | Rare:75; Clinvar (benign):3 |