| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:157138732-157138976 | Common:1; Rare:70 | ||||
| chr7:157336790-157337083 | Common:2; Rare:136; Clinvar:2 | ||||
| chr7:158704725-158704983 | Common:1; Rare:87 | ||||
| chr7:158856403-158856703 | Common:7; Rare:103 | ||||
| chr8:232176-232487 | Common:3; Rare:131 | ||||
| chr8:233057-233127 | Rare:15 | ||||
| chr8:731154-731420 | Common:3; Rare:101 | ||||
| chr8:1755687-1756031 | Common:3; Rare:100 | ||||
| chr8:2127579-2127804 | Common:7; Rare:42 | ||||
| chr8:6406518-6406685 | Common:3; Rare:91; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6708165-6708370 | Common:3; Rare:81 | ||||
| chr8:9150610-9150848 | Common:1; Rare:78 | ||||
| chr8:9555712-9555928 | Common:5; Rare:84 | ||||
| chr8:10839784-10840100 | Common:3; Rare:106 | ||||
| chr8:11284731-11284869 | Common:2; Rare:60 |