| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv889384 |
chr7:145541783-146239545 |
Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv1020950 |
chr7:145683419-146264304 |
Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
5 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv889387 |
chr7:145903862-146239545 |
Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS
|
Chromatin interactive regionlncRNA
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv533345 |
chr7:145934546-146134958 |
Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer
|
Chromatin interactive regionlncRNA
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv917027 |
chr7:146069317-146194011 |
Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
nsv1024679 |
chr7:146091479-146248268 |
Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats
|
Chromatin interactive regionlncRNA
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 7 |
nsv1017138 |
chr7:146102286-146318562 |
Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS
|
Chromatin interactive regionlncRNA
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 8 |
nsv889390 |
chr7:146111034-146239545 |
Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
nsv5994 |
chr7:146131977-146151284 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv2522287 |
chr7:146133141-146140099 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv2028241 |
chr7:146133600-146139699 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv2491993 |
chr7:146133606-146139851 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
esv3476916 |
chr7:146133623-146139637 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv3476914 |
chr7:146133677-146139605 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
esv3476917 |
chr7:146133688-146139598 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
esv3476915 |
chr7:146133708-146139560 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
esv12522 |
chr7:146133751-146139658 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
esv3476918 |
chr7:146133766-146139530 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
nsv514456 |
chr7:146133851-146139403 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 20 |
esv1808742 |
chr7:146133867-146139908 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 21 |
esv1812009 |
chr7:146133867-146139908 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 22 |
esv2421508 |
chr7:146133867-146139908 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 23 |
nsv442075 |
chr7:146133867-146139908 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 24 |
esv1809542 |
chr7:146133926-146138085 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 25 |
esv1811338 |
chr7:146133926-146138085 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 26 |
esv1811557 |
chr7:146133926-146138085 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 27 |
esv1813044 |
chr7:146133926-146138085 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 28 |
esv1809662 |
chr7:146133926-146138550 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 29 |
esv1804899 |
chr7:146133926-146139175 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 30 |
esv1810858 |
chr7:146133926-146139175 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 31 |
esv1814926 |
chr7:146133926-146139175 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:31 , 50 per page) page:
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