| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv1020899 |
chr5:151412785-151516788 |
Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
esv2760935 |
chr5:151463117-151586051 |
Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv883039 |
chr5:151471642-151540888 |
Enhancers Weak transcription Bivalent Enhancer Active TSS
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv883040 |
chr5:151471642-151596273 |
Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv5072 |
chr5:151490271-151530419 |
Enhancers Weak transcription Active TSS Bivalent Enhancer
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 6 |
nsv1023452 |
chr5:151508200-151518339 |
Bivalent Enhancer Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
nsv600040 |
chr5:151508799-151518270 |
Bivalent Enhancer Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
nsv600041 |
chr5:151508799-151518810 |
Bivalent Enhancer Weak transcription Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
nsv600042 |
chr5:151508799-151522878 |
Enhancers Weak transcription Bivalent Enhancer
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
nsv883041 |
chr5:151508799-151522878 |
Enhancers Weak transcription Bivalent Enhancer
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv3415842 |
chr5:151510881-151514802 |
Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv3390294 |
chr5:151510978-151514714 |
Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
esv3471394 |
chr5:151511002-151514698 |
Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv3471395 |
chr5:151511016-151514697 |
Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
nsv1032207 |
chr5:151511045-151522383 |
Enhancers Weak transcription Bivalent Enhancer
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
nsv1016168 |
chr5:151511636-151522383 |
Enhancers Weak transcription Bivalent Enhancer
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page:
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