| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv873148 |
chr1:210665583-210994339 |
Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh
|
Chromatin interactive regionlncRNAmiRNA target site
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv873149 |
chr1:210749312-210793972 |
Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription
|
Chromatin interactive regionlncRNA
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv522480 |
chr1:210779936-210848344 |
Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers
|
Chromatin interactive regionlncRNAmiRNA target site
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
esv1825229 |
chr1:210789477-210854976 |
Enhancers ZNF genes & repeats Weak transcription Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer
|
Chromatin interactive regionlncRNAmiRNA target site
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
nsv523712 |
chr1:210789920-210790214 |
Weak transcription Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
