| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv886132 |
chr6:69487204-69610281 |
Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer
|
Chromatin interactive region
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv886133 |
chr6:69549897-69610281 |
Weak transcription Enhancers ZNF genes & repeats Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
nsv1020792 |
chr6:69555181-69578740 |
Weak transcription Enhancers Strong transcription ZNF genes & repeats
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
nsv1025548 |
chr6:69555181-69589956 |
Enhancers Weak transcription ZNF genes & repeats Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
nsv886134 |
chr6:69571053-69605682 |
Weak transcription Enhancers ZNF genes & repeats Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
nsv886135 |
chr6:69571053-69606748 |
Weak transcription Strong transcription Enhancers ZNF genes & repeats
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
nsv5337 |
chr6:69575123-69581074 |
Enhancers ZNF genes & repeats Strong transcription Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
