Variant report

Variant	rs10827819
Chromosome Location	chr10:38012285-38012286
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10740949	0.91[ASN][1000 genomes]
rs10764142	0.84[ASN][1000 genomes]
rs10764143	0.91[ASN][1000 genomes]
rs10764144	0.91[ASN][1000 genomes]
rs10827815	0.88[ASN][1000 genomes]
rs10827818	0.91[ASN][1000 genomes]
rs10827824	0.81[AFR][1000 genomes]
rs10827825	0.81[AFR][1000 genomes]
rs11011323	0.88[ASN][1000 genomes]
rs11011324	0.87[ASN][1000 genomes]
rs11011325	0.88[ASN][1000 genomes]
rs11011339	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11011341	0.91[ASN][1000 genomes]
rs11011346	0.96[ASN][1000 genomes]
rs11011354	0.81[EUR][1000 genomes]
rs11011355	0.81[AFR][1000 genomes]
rs11597720	0.91[ASN][1000 genomes]
rs12357413	0.88[ASN][1000 genomes]
rs12360411	0.81[AFR][1000 genomes]
rs12570943	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12776092	0.98[ASN][1000 genomes]
rs12781703	0.81[AFR][1000 genomes]
rs12783272	0.89[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs12783722	0.81[EUR][1000 genomes]
rs1779150	0.81[AFR][1000 genomes]
rs1830612	0.91[ASN][1000 genomes]
rs34185758	0.89[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs4934898	0.90[ASN][1000 genomes]
rs61858629	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs734512	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7476802	0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895030	chr10:37715737-38674609	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv1045684	chr10:37765361-38426204	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	nsv540564	chr10:37765361-38426204	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv1040704	chr10:37940024-38451917	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
5	nsv975072	chr10:37990724-38017623	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv975812	chr10:37990724-38084639	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:38011800-38012400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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