| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179806881-179807035 | Common:3; Rare:61 | ||||
| chr5:179858781-179858995 | Rare:119 | ||||
| chr5:179907828-179908015 | Common:2; Rare:97 | ||||
| chr5:181223118-181223306 | Rare:63 | ||||
| chr5:181243690-181243741 | Rare:12 | ||||
| chr5:181261049-181261262 | Rare:72 | ||||
| chr6:693074-693221 | Rare:43 | ||||
| chr6:3118575-3118755 | Common:2; Rare:61 | ||||
| chr6:4021213-4021415 | Rare:90 | ||||
| chr6:5004007-5004118 | Common:1; Rare:52 | ||||
| chr6:5260729-5261007 | Common:2; Rare:88; Clinvar (benign):2 | ||||
| chr6:6588491-6588801 | Common:2; Rare:85 | ||||
| chr6:7313127-7313383 | Common:4; Rare:93 | ||||
| chr6:7389740-7389868 | Common:1; Rare:38 | ||||
| chr6:8064338-8064522 | Common:4; Rare:61 |