| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52533768-52533980 | Common:10; Rare:125 | ||||
| chr3:52536357-52536752 | Common:5; Rare:234 | ||||
| chr3:52685460-52685800 | Common:1; Rare:160 | ||||
| chr3:52685825-52686086 | Common:3; Rare:182 | ||||
| chr3:52705501-52706210 | Common:8; Rare:392 | ||||
| chr3:52770460-52770820 | Common:1; Rare:128 | ||||
| chr3:52770887-52771105 | Common:7; Rare:105 | ||||
| chr3:52830670-52830786 | Common:1; Rare:22 | ||||
| chr3:52897514-52897757 | Rare:88 | ||||
| chr3:53045892-53046132 | Common:2; Rare:117 | ||||
| chr3:53130385-53130570 | Common:2; Rare:128; Clinvar:2; Clinvar (benign):6 | ||||
| chr3:53161088-53161265 | Common:8; Rare:76 | ||||
| chr3:53255877-53256188 | Common:6; Rare:201 | ||||
| chr3:53347488-53347798 | Common:4; Rare:190 | ||||
| chr3:53846298-53846588 | Common:1; Rare:162 |