| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58475993-58476180 | Common:1; Rare:74 | ||||
| chr19:58499194-58499743 | Common:3; Rare:195; Clinvar:8; Clinvar (benign):2 | ||||
| chr19:58519767-58519883 | Rare:26 | ||||
| chr19:58554939-58555266 | Common:2; Rare:115 | ||||
| chr19:58558310-58558676 | Rare:117 | ||||
| chr19:58558872-58559126 | Common:1; Rare:80 | ||||
| chr19:58573276-58573597 | Common:1; Rare:81 | ||||
| chr2:46500-46713 | Common:1; Rare:60 | ||||
| chr2:263971-264149 | Common:2; Rare:63 | ||||
| chr2:264547-265006 | Common:4; Rare:180 | ||||
| chr2:677352-677557 | Common:1; Rare:87 | ||||
| chr2:1373660-1373941 | Common:3; Rare:61 | ||||
| chr2:3377774-3377905 | Rare:42 | ||||
| chr2:3379611-3379868 | Common:2; Rare:98 | ||||
| chr2:3519368-3519674 | Common:3; Rare:88 |