| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:51975062-51975151 | Common:1; Rare:32 | ||||
| chr3:52197994-52198197 | Common:1; Rare:86 | ||||
| chr3:52239075-52239245 | Common:2; Rare:61 | ||||
| chr3:52278637-52278777 | Rare:48 | ||||
| chr3:52287753-52287844 | Common:2; Rare:38 | ||||
| chr3:52455465-52455638 | Common:2; Rare:61 | ||||
| chr3:52534967-52535151 | Common:2; Rare:42 | ||||
| chr3:52536377-52536703 | Common:2; Rare:106 | ||||
| chr3:52685772-52686086 | Common:3; Rare:115 | ||||
| chr3:52705782-52706270 | Common:2; Rare:175 | ||||
| chr3:52770899-52771045 | Common:3; Rare:38 | ||||
| chr3:53130410-53130545 | Common:1; Rare:40; Clinvar (benign):2 | ||||
| chr3:53255952-53256180 | Common:3; Rare:97 | ||||
| chr3:53347525-53347763 | Common:1; Rare:76 | ||||
| chr3:53891794-53892075 | Common:4; Rare:94 |