| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:156081296-156081372 | Rare:17 | ||||
| chr1:156081526-156081998 | Rare:91 | ||||
| chr1:156082368-156082726 | Rare:82 | ||||
| chr1:156082876-156083022 | Rare:54 | ||||
| chr1:156106424-156106593 | Common:2; Rare:32 | ||||
| chr1:156114146-156114274 | Rare:24 | ||||
| chr1:156114496-156114805 | Rare:66; Clinvar:3; Clinvar (benign):1 | ||||
| chr1:156123505-156123731 | Common:1; Rare:42 | ||||
| chr1:156126212-156126355 | Rare:28 | ||||
| chr1:156160944-156161123 | Rare:65; Clinvar:2 | ||||
| chr1:156161411-156161533 | Rare:38; Clinvar:1 | ||||
| chr1:156193528-156193576 | Rare:9 | ||||
| chr1:156193679-156194221 | Common:3; Rare:122 | ||||
| chr1:156212804-156213424 | Common:3; Rare:189 | ||||
| chr1:156282385-156282628 | Common:1; Rare:68 |