Variant report

Variant	rs7797362
Chromosome Location	chr7:21653116-21653117
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10499531	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs11765753	0.91[CEU][hapmap];0.87[EUR][1000 genomes]
rs11766011	0.91[CEU][hapmap];0.88[EUR][1000 genomes]
rs11768411	0.90[CEU][hapmap];0.90[EUR][1000 genomes]
rs11768728	0.91[CEU][hapmap];0.88[EUR][1000 genomes]
rs11773760	0.93[EUR][1000 genomes]
rs11978567	0.97[EUR][1000 genomes]
rs12669590	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs12670130	0.91[CEU][hapmap];0.88[EUR][1000 genomes]
rs12673164	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs17144781	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17745898	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs35758178	1.00[EUR][1000 genomes]
rs3810898	0.86[EUR][1000 genomes]
rs3827658	0.91[CEU][hapmap];0.87[EUR][1000 genomes]
rs55844287	0.97[EUR][1000 genomes]
rs55937657	1.00[EUR][1000 genomes]
rs56106069	0.87[EUR][1000 genomes]
rs56214809	0.96[EUR][1000 genomes]
rs62441680	0.87[EUR][1000 genomes]
rs62441682	0.85[EUR][1000 genomes]
rs62441683	0.87[EUR][1000 genomes]
rs62441720	0.85[EUR][1000 genomes]
rs62441726	0.95[EUR][1000 genomes]
rs62447776	0.97[EUR][1000 genomes]
rs62447777	0.97[EUR][1000 genomes]
rs62447778	0.97[EUR][1000 genomes]
rs62447780	0.97[EUR][1000 genomes]
rs62447782	0.97[EUR][1000 genomes]
rs6461585	0.97[EUR][1000 genomes]
rs6461587	0.93[EUR][1000 genomes]
rs6461588	0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs73070433	0.84[EUR][1000 genomes]
rs7788995	0.91[CEU][hapmap];0.88[EUR][1000 genomes]
rs7803297	0.91[CEU][hapmap];0.85[EUR][1000 genomes]
rs7805701	0.88[EUR][1000 genomes]
rs7809703	0.91[CEU][hapmap];0.88[EUR][1000 genomes]
rs8180768	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs9638787	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs9639381	0.90[CEU][hapmap];0.97[EUR][1000 genomes]
rs9639382	0.85[CHB][hapmap];0.81[JPT][hapmap];0.85[ASN][1000 genomes]
rs9639383	1.00[CEU][hapmap];0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1027302	chr7:21391598-21727016	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv538800	chr7:21391598-21727016	Enhancers Genic enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1023655	chr7:21486485-21727016	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
4	nsv538801	chr7:21486485-21727016	ZNF genes & repeats Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv830921	chr7:21489100-21688016	Strong transcription ZNF genes & repeats Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
6	nsv1030577	chr7:21548909-21681379	Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
7	nsv1025634	chr7:21566727-21686272	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 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	chr7:21651600-21657000	Weak transcription	Liver	Liver

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