| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:40453151-40453421 | Common:6; Rare:61 | ||||
| chr3:46883923-46884131 | Common:2; Rare:31 | ||||
| chr3:46895477-46895809 | Rare:69; Clinvar (benign):2 | ||||
| chr3:46899165-46899454 | Common:1; Rare:70; Clinvar:1 | ||||
| chr3:47164798-47164896 | Common:2; Rare:21 | ||||
| chr3:47870952-47871276 | Common:1; Rare:91 | ||||
| chr3:50381478-50381655 | Rare:23 | ||||
| chr3:53493981-53494103 | Common:1; Rare:31 | ||||
| chr3:61560342-61560650 | Rare:78 | ||||
| chr3:61560879-61561050 | Common:2; Rare:51 | ||||
| chr3:61743136-61743223 | Common:2; Rare:22 | ||||
| chr3:62262518-62262889 | Common:1; Rare:93 | ||||
| chr3:64560714-64561237 | Common:11; Rare:92 | ||||
| chr3:64561273-64561534 | Common:2; Rare:48 | ||||
| chr3:64565263-64565593 | Common:3; Rare:62 |