| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:155325166-155325566 | Common:2; Rare:186 | ||||
| chr1:155561770-155563046 | Common:12; Rare:1693 | ||||
| chr1:155563000-155563490 | Common:1; Rare:715 | ||||
| chr1:155609592-155610401 | Common:29; Rare:765; Clinvar (pathogenic):2 | ||||
| chr1:155687644-155687960 | Common:2; Rare:57 | ||||
| chr1:155688299-155688570 | Common:2; Rare:171 | ||||
| chr1:155688588-155689340 | Common:19; Rare:1023 | ||||
| chr1:155857137-155857448 | Common:1; Rare:350 | ||||
| chr1:155857403-155857803 | Common:5; Rare:81 | ||||
| chr1:155858918-155859801 | Common:17; Rare:497 | ||||
| chr1:155910463-155910863 | Common:2; Rare:107; Clinvar:1; Clinvar (benign):7 | ||||
| chr1:155910859-155911079 | Common:4; Rare:94; Clinvar:1 | ||||
| chr1:155911242-155911740 | Common:7; Rare:410; Clinvar (benign):2 | ||||
| chr1:155933903-155934303 | Common:1; Rare:78 | ||||
| chr1:155934334-155934760 | Common:12; Rare:842 |