| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185775228-185775597 | Common:4; Rare:68 | ||||
| chr4:185775701-185776028 | Common:1; Rare:47 | ||||
| chr4:185810845-185810874 | Rare:8 | ||||
| chr4:185811675-185811897 | Common:1; Rare:47 | ||||
| chr4:185811902-185812248 | Common:1; Rare:63 | ||||
| chr4:186191459-186191826 | Common:6; Rare:124; Clinvar:2; Clinvar (benign):5 | ||||
| chr4:189940588-189940991 | Common:13; Rare:135 | ||||
| chr5:218112-218415 | Common:3; Rare:121; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr5:443084-443280 | Common:10; Rare:91 | ||||
| chr5:612180-612357 | Rare:72 | ||||
| chr5:892647-892929 | Common:5; Rare:99 | ||||
| chr5:1799785-1800022 | Common:9; Rare:112 | ||||
| chr5:1801281-1801473 | Common:4; Rare:100; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:5422304-5422677 | Common:3; Rare:128 | ||||
| chr5:6378452-6378699 | Rare:102 |