| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52287999-52288108 | Rare:39 | ||||
| chr3:52455425-52455713 | Common:2; Rare:96 | ||||
| chr3:52524973-52525250 | Common:9; Rare:124 | ||||
| chr3:52536330-52536736 | Common:2; Rare:127 | ||||
| chr3:52685533-52686202 | Common:4; Rare:220 | ||||
| chr3:52705569-52706261 | Common:4; Rare:225 | ||||
| chr3:52770913-52771057 | Common:2; Rare:33 | ||||
| chr3:53130398-53130533 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53255940-53256180 | Common:3; Rare:101 | ||||
| chr3:53347504-53347768 | Common:2; Rare:87 | ||||
| chr3:53882066-53882368 | Common:4; Rare:106 | ||||
| chr3:53891789-53892225 | Common:6; Rare:135 | ||||
| chr3:54123421-54123538 | Rare:36 | ||||
| chr3:56467159-56467348 | Rare:52 | ||||
| chr3:56468310-56468740 | Common:3; Rare:114 |