Variant report

Variant	rs7988217
Chromosome Location	chr13:90702032-90702033
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs12427571	0.98[ASN][1000 genomes]
rs12428396	0.86[ASN][1000 genomes]
rs12429307	0.98[ASN][1000 genomes]
rs12429707	0.98[ASN][1000 genomes]
rs1491029	0.99[ASN][1000 genomes]
rs1491031	0.99[ASN][1000 genomes]
rs1491032	0.99[ASN][1000 genomes]
rs1491033	0.97[ASN][1000 genomes]
rs1491034	0.99[ASN][1000 genomes]
rs1565523	0.99[ASN][1000 genomes]
rs1565524	0.99[ASN][1000 genomes]
rs1602408	0.99[ASN][1000 genomes]
rs1602409	0.99[ASN][1000 genomes]
rs1907428	0.97[ASN][1000 genomes]
rs1907431	0.97[ASN][1000 genomes]
rs2130836	0.99[ASN][1000 genomes]
rs2130840	0.99[ASN][1000 genomes]
rs2637379	0.96[ASN][1000 genomes]
rs2637380	0.99[ASN][1000 genomes]
rs2637381	0.99[ASN][1000 genomes]
rs2637383	0.99[ASN][1000 genomes]
rs2637384	0.98[ASN][1000 genomes]
rs2637386	0.97[ASN][1000 genomes]
rs2637398	0.87[ASN][1000 genomes]
rs2637483	0.99[ASN][1000 genomes]
rs2637484	0.99[ASN][1000 genomes]
rs2637485	0.97[ASN][1000 genomes]
rs2637487	0.98[ASN][1000 genomes]
rs2805635	0.86[ASN][1000 genomes]
rs2805636	0.86[ASN][1000 genomes]
rs2805637	0.86[ASN][1000 genomes]
rs2805639	0.86[ASN][1000 genomes]
rs2805666	0.97[ASN][1000 genomes]
rs2805667	0.97[ASN][1000 genomes]
rs2805668	0.97[ASN][1000 genomes]
rs2805672	0.99[ASN][1000 genomes]
rs2805673	0.99[ASN][1000 genomes]
rs2805674	0.99[ASN][1000 genomes]
rs72641506	0.84[ASN][1000 genomes]
rs7331246	1.00[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap]
rs7331447	0.98[ASN][1000 genomes]
rs7984840	0.94[ASN][1000 genomes]
rs9555968	0.96[ASN][1000 genomes]
rs9560530	0.98[ASN][1000 genomes]
rs9560531	0.98[ASN][1000 genomes]
rs9560546	0.97[ASN][1000 genomes]
rs9560554	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422378	chr13:90280619-90799585	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	esv3330508	chr13:90401807-90835334	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv1039817	chr13:90425965-90884271	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
4	nsv1054500	chr13:90427793-90879758	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
5	nsv541867	chr13:90427793-90879758	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
6	nsv456064	chr13:90429193-90886078	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
7	nsv562644	chr13:90429193-90886078	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
8	nsv1036137	chr13:90509098-90772092	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv541868	chr13:90509098-90772092	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv1047307	chr13:90509098-90849504	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
11	nsv541869	chr13:90509098-90849504	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
12	nsv1044540	chr13:90509098-91497974	Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
13	nsv541870	chr13:90509098-91497974	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
14	nsv1035856	chr13:90653288-91490014	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
15	nsv900869	chr13:90684520-90736264	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
16	nsv900870	chr13:90684520-90746594	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
17	nsv900871	chr13:90684520-90754699	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
18	nsv832677	chr13:90687286-90848836	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
19	nsv826741	chr13:90688393-90849153	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
20	nsv562646	chr13:90689775-90823859	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
21	nsv433272	chr13:90690778-90710793	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
22	nsv900872	chr13:90695255-90754699	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:90701200-90702400	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr13:90701400-90703400	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr13:90701400-90703400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr13:90701600-90703000	Enhancers	iPS-15b Cell Line	embryonic stem cell

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