| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49029378-49029564 | Common:2; Rare:131 | ||||
| chr3:49104615-49104891 | Common:1; Rare:111; Clinvar:3; Clinvar (benign):7 | ||||
| chr3:49120810-49121115 | Rare:81 | ||||
| chr3:49132918-49133161 | Rare:44; Clinvar:2 | ||||
| chr3:49411882-49412213 | Common:1; Rare:114 | ||||
| chr3:49674284-49674395 | Rare:48 | ||||
| chr3:49689461-49689613 | Rare:47 | ||||
| chr3:49723943-49724233 | Common:8; Rare:101 | ||||
| chr3:49786501-49786769 | Rare:87 | ||||
| chr3:50267404-50267674 | Common:2; Rare:84 | ||||
| chr3:50268880-50269214 | Common:1; Rare:79 | ||||
| chr3:50299336-50299656 | Common:1; Rare:80 | ||||
| chr3:50350687-50350894 | Common:1; Rare:30 | ||||
| chr3:50569421-50569510 | Rare:18 | ||||
| chr3:51385030-51385329 | Rare:83 |