| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:50569389-50569504 | Rare:24 | ||||
| chr3:50611676-50611883 | Rare:50 | ||||
| chr3:51385025-51385345 | Common:2; Rare:97 | ||||
| chr3:51499948-51500325 | Common:1; Rare:77 | ||||
| chr3:51941931-51942409 | Common:2; Rare:119 | ||||
| chr3:51975001-51975138 | Common:1; Rare:49 | ||||
| chr3:51983349-51983541 | Rare:39 | ||||
| chr3:51995740-51995975 | Common:2; Rare:79 | ||||
| chr3:52239079-52239257 | Common:2; Rare:65 | ||||
| chr3:52287759-52287859 | Common:2; Rare:41 | ||||
| chr3:52288005-52288085 | Rare:29 | ||||
| chr3:52452785-52453164 | Common:3; Rare:59 | ||||
| chr3:52453990-52454148 | Rare:40; Clinvar (pathogenic):1 | ||||
| chr3:52455406-52455650 | Common:2; Rare:79 | ||||
| chr3:52685536-52685831 | Common:2; Rare:78 |