Variant report

Variant	rs314578
Chromosome Location	chr13:89908325-89908326
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs1023806	0.85[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs1034231	0.85[EUR][1000 genomes]
rs11069920	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12877053	0.84[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs12877418	0.82[ASN][1000 genomes]
rs1334201	0.85[EUR][1000 genomes]
rs1334202	0.82[EUR][1000 genomes]
rs1334206	0.85[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs1334207	0.93[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs1413463	0.85[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs1504153	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2044348	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs2102238	0.85[EUR][1000 genomes]
rs2134801	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2348654	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2348655	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs314528	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs314530	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs314531	0.87[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs314562	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs314563	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs314565	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs314570	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs314572	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs314574	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs314576	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs314579	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4773459	0.91[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6492425	0.82[EUR][1000 genomes]
rs6492426	0.82[EUR][1000 genomes]
rs6492427	0.82[EUR][1000 genomes]
rs7139784	0.85[EUR][1000 genomes]
rs7317403	0.85[EUR][1000 genomes]
rs7325345	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7332403	0.85[EUR][1000 genomes]
rs7332816	0.85[EUR][1000 genomes]
rs734050	0.84[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs9522488	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs9522502	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9522506	0.82[EUR][1000 genomes]
rs9522507	0.82[EUR][1000 genomes]
rs9522509	0.82[EUR][1000 genomes]
rs9522512	0.85[EUR][1000 genomes]
rs9522513	0.85[EUR][1000 genomes]
rs9522514	0.85[EUR][1000 genomes]
rs9522516	0.85[EUR][1000 genomes]
rs9522517	0.85[EUR][1000 genomes]
rs991342	0.82[EUR][1000 genomes]
rs991343	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv900821	chr13:89302824-89941209	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv915862	chr13:89408920-90118030	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1040210	chr13:89584630-90156186	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv1048574	chr13:89650680-90232894	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv900844	chr13:89721607-89944833	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv832675	chr13:89772410-89926955	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv900851	chr13:89797903-89941209	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv900856	chr13:89824076-89922393	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv900857	chr13:89824076-89934019	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	esv3436529	chr13:89906000-89928585	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 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	chr13:89908000-89909000	Enhancers	Fetal Heart	heart

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