| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:51975013-51975144 | Common:1; Rare:46 | ||||
| chr3:52197983-52198165 | Rare:78 | ||||
| chr3:52239069-52239202 | Common:2; Rare:46 | ||||
| chr3:52455414-52455638 | Common:2; Rare:72 | ||||
| chr3:52495257-52495398 | Common:1; Rare:37 | ||||
| chr3:52685926-52686086 | Common:2; Rare:66 | ||||
| chr3:52705570-52706212 | Common:4; Rare:204 | ||||
| chr3:53347525-53347725 | Common:1; Rare:62 | ||||
| chr3:53891801-53892021 | Common:2; Rare:71 | ||||
| chr3:56557076-56557238 | Common:2; Rare:63 | ||||
| chr3:57079252-57079363 | Rare:39 | ||||
| chr3:57227600-57227913 | Common:3; Rare:107 | ||||
| chr3:57555996-57556321 | Rare:81 | ||||
| chr3:57597331-57597778 | Common:4; Rare:131 | ||||
| chr3:58433810-58433939 | Rare:50; Clinvar (benign):2 |