| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:47380861-47381062 | Rare:52 | ||||
| chr3:47475816-47476088 | Common:3; Rare:109 | ||||
| chr3:48240991-48241118 | Common:1; Rare:37 | ||||
| chr3:48301328-48301600 | Common:3; Rare:90 | ||||
| chr3:48440035-48440312 | Common:1; Rare:103 | ||||
| chr3:48446630-48446743 | Rare:40 | ||||
| chr3:48556784-48557173 | Common:1; Rare:88 | ||||
| chr3:48635452-48635644 | Rare:57 | ||||
| chr3:48918783-48918903 | Common:2; Rare:71 | ||||
| chr3:49104712-49104948 | Rare:97; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:49120778-49121018 | Rare:67 | ||||
| chr3:49132987-49133100 | Rare:23 | ||||
| chr3:49358285-49358486 | Common:2; Rare:108 | ||||
| chr3:49411909-49412213 | Common:1; Rare:108 | ||||
| chr3:49470008-49470303 | Common:1; Rare:81 |