No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
nsv869066 |
chr6:139777114-140639695 |
Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA
|
26 gene(s)
|
inside rSNPs
|
diseases
|
2 |
nsv1016532 |
chr6:140174639-141029988 |
Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA
|
17 gene(s)
|
inside rSNPs
|
diseases
|
3 |
nsv1015293 |
chr6:140544956-140798437 |
Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
4 |
nsv817390 |
chr6:140558103-141166039 |
Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA
|
5 gene(s)
|
inside rSNPs
|
diseases
|
5 |
esv3325984 |
chr6:140597059-140600457 |
Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|