| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:69369985-69370088 | Rare:24 | ||||
| chr5:69560117-69560261 | Common:1; Rare:39 | ||||
| chr5:71455566-71455689 | Rare:32 | ||||
| chr5:71587137-71587420 | Common:1; Rare:95; Clinvar (benign):2 | ||||
| chr5:72107154-72107526 | Common:2; Rare:147 | ||||
| chr5:72816468-72816764 | Common:4; Rare:111 | ||||
| chr5:72848070-72848231 | Common:3; Rare:60 | ||||
| chr5:72955854-72956085 | Common:1; Rare:106 | ||||
| chr5:73498298-73498660 | Common:3; Rare:117 | ||||
| chr5:73565370-73565820 | Common:7; Rare:138 | ||||
| chr5:74685519-74685542 | Rare:4 | ||||
| chr5:74767047-74767360 | Common:3; Rare:100 | ||||
| chr5:75336902-75337290 | Common:3; Rare:135 | ||||
| chr5:75511610-75511913 | Common:1; Rare:112 | ||||
| chr5:75717372-75717663 | Common:5; Rare:73 |