Variant report

Variant	rs8109507
Chromosome Location	chr19:41411234-41411235
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:41283761..41286182-chr19:41409909..41411443,2	K562	blood:

Variant related genes	Relation type
ENSG00000167578	Chromatin interaction
ENSG00000171570	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10402037	1.00[CHB][hapmap]
rs10403140	1.00[CHB][hapmap]
rs10403268	1.00[CHB][hapmap]
rs10409701	1.00[CHB][hapmap]
rs10410347	1.00[CHB][hapmap]
rs10422282	1.00[CHB][hapmap]
rs10422729	1.00[CHB][hapmap]
rs10423743	1.00[CHB][hapmap]
rs10521014	1.00[ASW][hapmap];0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11083592	0.82[CEU][hapmap];1.00[CHB][hapmap]
rs11667976	1.00[CHB][hapmap]
rs11668664	0.87[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs11878463	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11880938	1.00[CHB][hapmap];1.00[GIH][hapmap];0.92[TSI][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12974293	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12981337	0.85[EUR][1000 genomes]
rs12982060	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12984358	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16974961	1.00[CHB][hapmap]
rs2644890	1.00[CHB][hapmap]
rs28475084	0.82[EUR][1000 genomes]
rs34050311	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35809263	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71358943	0.82[EUR][1000 genomes]
rs71358948	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73555357	0.93[EUR][1000 genomes];1.00[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	esv2758500	chr19:41291627-41546068	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	esv2758762	chr19:41291627-41546068	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv1066637	chr19:41309211-41597896	Weak transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	esv3337314	chr19:41388910-41534583	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv960838	chr19:41401531-41413740	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv437830	chr19:41408746-41515702	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41403000-41414200	Weak transcription	Lung	lung
2	chr19:41411200-41413400	Weak transcription	K562	blood
3	chr19:41411200-41414400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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