No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
nsv1008691 |
chr4:28051516-28193042 |
Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
2 |
nsv1005346 |
chr4:28120195-28161929 |
Enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
3 |
nsv998352 |
chr4:28120195-28162959 |
Enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
4 |
nsv1012692 |
chr4:28122071-28165368 |
Enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
5 |
nsv1002855 |
chr4:28141588-28240495 |
Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
6 |
nsv878774 |
chr4:28153349-28254938 |
Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
7 |
nsv1005382 |
chr4:28157180-28403800 |
Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers
|
Chromatin interactive regionlncRNA
|
5 gene(s)
|
inside rSNPs
|
diseases
|