| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv1034445 |
chr5:49986171-50492609 |
Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
16 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv598116 |
chr5:50064292-50318550 |
Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
11 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv830286 |
chr5:50165805-50374600 |
Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
10 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv511286 |
chr5:50231548-50254200 |
Enhancers
|
TF binding regionChromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
esv3325778 |
chr5:50232395-50240693 |
Inactive region
|
TF binding regionChromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 6 |
nsv598117 |
chr5:50233199-50236505 |
Inactive region
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 7 |
nsv598118 |
chr5:50233199-50238827 |
Inactive region
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 8 |
nsv436476 |
chr5:50233884-50239735 |
Inactive region
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 9 |
esv2530506 |
chr5:50234019-50240297 |
Inactive region
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 10 |
esv2092918 |
chr5:50234218-50239675 |
Inactive region
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 11 |
esv3469213 |
chr5:50234250-50239572 |
Inactive region
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 12 |
nsv513236 |
chr5:50234284-50239696 |
Inactive region
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 13 |
esv3360478 |
chr5:50234295-50239535 |
Inactive region
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 14 |
esv3469212 |
chr5:50234306-50239538 |
Inactive region
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page:
1
