| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv1031592 |
chr4:173112542-173662991 |
Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
5 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv537359 |
chr4:173112542-173662991 |
Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
5 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv534293 |
chr4:173121379-173606082 |
Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
5 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv1031327 |
chr4:173306405-173465248 |
Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS
|
TF binding regionCpG islandChromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv508333 |
chr4:173369686-173447675 |
ZNF genes & repeats Enhancers Weak transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 6 |
nsv948856 |
chr4:173388217-173967546 |
Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh
|
Chromatin interactive regionlncRNA
|
9 gene(s)
|
inside rSNPs
|
diseases
|
| 7 |
nsv4607 |
chr4:173406293-173457588 |
ZNF genes & repeats Enhancers Weak transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 8 |
nsv870205 |
chr4:173409062-173436383 |
Weak transcription Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
nsv1026882 |
chr4:173410691-173441120 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
nsv1016549 |
chr4:173411663-173441120 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
nsv1023134 |
chr4:173412218-173455427 |
Enhancers ZNF genes & repeats Weak transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 12 |
nsv1021404 |
chr4:173413885-173458833 |
Enhancers Weak transcription ZNF genes & repeats
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
n/a
|
| 13 |
nsv263 |
chr4:173418319-173438806 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 14 |
esv1838024 |
chr4:173422260-173441120 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 15 |
esv1813301 |
chr4:173422510-173441120 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 16 |
esv3464632 |
chr4:173423077-173435475 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 17 |
esv1811294 |
chr4:173423656-173439265 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 18 |
esv1814617 |
chr4:173423656-173439265 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 19 |
esv2439458 |
chr4:173424507-173435431 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 20 |
nsv10613 |
chr4:173424734-173436613 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 21 |
nsv596216 |
chr4:173425609-173438438 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 22 |
esv1804232 |
chr4:173425609-173439265 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 23 |
esv1805934 |
chr4:173425609-173439265 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 24 |
esv1808400 |
chr4:173425609-173439265 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 25 |
nsv596221 |
chr4:173426583-173435062 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 26 |
esv1809547 |
chr4:173427242-173437677 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page:
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