| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:156591828-156592228 | Common:2; Rare:135; Clinvar (pathogenic):2 | ||||
| chr1:156601018-156601418 | Common:1; Rare:90 | ||||
| chr1:156601369-156601582 | Common:7; Rare:257 | ||||
| chr1:156624337-156625078 | Common:18; Rare:492 | ||||
| chr1:156646448-156646904 | Common:14; Rare:244 | ||||
| chr1:156677140-156677720 | Rare:265 | ||||
| chr1:156705444-156705844 | Common:6; Rare:114 | ||||
| chr1:156705951-156706351 | Common:4; Rare:132 | ||||
| chr1:156725809-156726209 | Common:3; Rare:192 | ||||
| chr1:156726554-156726954 | Common:1; Rare:90 | ||||
| chr1:156728270-156728660 | Common:11; Rare:415 | ||||
| chr1:156728620-156729090 | Rare:615 | ||||
| chr1:156737924-156738521 | Common:3; Rare:166 | ||||
| chr1:156740344-156740811 | Common:1; Rare:313 | ||||
| chr1:156740984-156741452 | Common:6; Rare:637 |