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
|