| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:55572312-55572561 | Common:1; Rare:100 | ||||
| chr7:56051429-56051884 | Common:1; Rare:173; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56064112-56064319 | Common:2; Rare:115 | ||||
| chr7:56106363-56106710 | Common:9; Rare:125 | ||||
| chr7:66114764-66114905 | Common:1; Rare:70 | ||||
| chr7:66115194-66115353 | Rare:35 | ||||
| chr7:66628676-66628969 | Common:2; Rare:106; Clinvar:3 | ||||
| chr7:66682005-66682192 | Common:6; Rare:91 | ||||
| chr7:66921130-66921276 | Rare:48 | ||||
| chr7:66995365-66995674 | Rare:102; Clinvar (pathogenic):3 | ||||
| chr7:66996557-66996888 | Common:2; Rare:77 | ||||
| chr7:72828130-72828483 | Common:1; Rare:100 | ||||
| chr7:73308776-73308890 | Rare:46 | ||||
| chr7:73557100-73557383 | Common:2; Rare:102 | ||||
| chr7:73557566-73557750 | Common:2; Rare:64 |