| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv886764 |
chr6:150114745-150393683 |
Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
40 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv517022 |
chr6:150145001-150426272 |
Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
39 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv886765 |
chr6:150198491-150288722 |
Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
21 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv981194 |
chr6:150276068-150281801 |
Bivalent Enhancer Bivalent/Poised TSS Enhancers
|
TF binding regionCpG islandChromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page:
1
