Variant report

Variant	rs16937569
Chromosome Location	chr10:38030639-38030640
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10508859	0.81[EUR][1000 genomes]
rs10508861	0.86[ASW][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.83[MEX][hapmap];0.86[MKK][hapmap];0.91[YRI][hapmap];0.85[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs10764138	0.82[ASN][1000 genomes]
rs10827802	0.82[ASN][1000 genomes]
rs12243792	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.91[YRI][hapmap];0.99[ASN][1000 genomes]
rs12265979	0.90[YRI][hapmap]
rs12412402	0.99[ASN][1000 genomes]
rs12413854	1.00[ASN][1000 genomes]
rs16937571	1.00[ASN][1000 genomes]
rs200907	0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs200909	0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs200913	0.93[ASN][1000 genomes]
rs200944	0.87[CHB][hapmap];0.80[CHD][hapmap];0.95[JPT][hapmap]
rs2208317	0.82[ASN][1000 genomes]
rs2224372	0.82[ASN][1000 genomes]
rs2295647	0.85[EUR][1000 genomes]
rs289637	0.82[ASN][1000 genomes]
rs289640	0.82[ASN][1000 genomes]
rs55637824	0.89[EUR][1000 genomes]
rs55738335	0.99[ASN][1000 genomes]
rs55742761	0.98[ASN][1000 genomes]
rs56343162	0.81[EUR][1000 genomes]
rs56905472	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58379893	0.85[EUR][1000 genomes]
rs58906790	0.83[EUR][1000 genomes]
rs59486180	0.98[ASN][1000 genomes]
rs67011531	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7068885	0.99[ASN][1000 genomes]
rs72789877	0.85[EUR][1000 genomes]
rs72789892	0.89[EUR][1000 genomes]
rs72789899	0.89[EUR][1000 genomes]
rs72791703	0.85[EUR][1000 genomes]
rs7906186	1.00[CEU][hapmap]
rs9418274	0.81[EUR][1000 genomes]
rs9787710	0.82[ASN][1000 genomes]
rs995141	0.82[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	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
6	nsv947607	chr10:38021929-38040760	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs16937569	ZNF37A	Cis_1M	lymphoblastoid	RTeQTL
rs16937569	ZNF25	cis	cerebellum	SCAN
rs16937569	CUL2	cis	parietal	SCAN
rs16937569	HSD17B7///HSD17B7P2///LOC730412	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:38022200-38037000	Weak transcription	HSMM	muscle
2	chr10:38030400-38031000	Enhancers	Gastric	stomach

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