| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33454368-33454599 | Common:1; Rare:66 | ||||
| chr6:33789108-33789155 | Rare:39 | ||||
| chr6:34248472-34248555 | Rare:11 | ||||
| chr6:34392268-34392540 | Rare:103 | ||||
| chr6:34424754-34425223 | Common:3; Rare:120; Clinvar (benign):7 | ||||
| chr6:34696536-34696592 | Rare:16 | ||||
| chr6:34696618-34696988 | Common:1; Rare:94 | ||||
| chr6:34757330-34757545 | Common:1; Rare:64 | ||||
| chr6:35058103-35058290 | Rare:35 | ||||
| chr6:35259373-35259797 | Common:3; Rare:133 | ||||
| chr6:35728015-35728245 | Rare:45 | ||||
| chr6:35728343-35728402 | Rare:7 | ||||
| chr6:35921047-35921194 | Common:1; Rare:71 | ||||
| chr6:36197203-36197387 | Rare:66 | ||||
| chr6:36442887-36443087 | Common:2; Rare:83 |