| 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 |
nsv528106 |
chr6:69581991-69610281 |
Enhancers Weak transcription ZNF genes & repeats Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
nsv470831 |
chr6:69581991-69654650 |
Weak transcription Enhancers ZNF genes & repeats Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
nsv886136 |
chr6:69598297-69654650 |
Weak transcription Strong transcription ZNF genes & repeats Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv3325770 |
chr6:69607364-69607596 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv3369451 |
chr6:69607517-69607973 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv3419155 |
chr6:69607518-69607867 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
