Variant report

Variant	rs1504437
Chromosome Location	chr13:90149956-90149957
allele	C/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:40)

rs_ID	r²[population]
rs1113478	0.81[EUR][1000 genomes]
rs1158015	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1158016	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1199479	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12584227	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12874844	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1394321	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1504438	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1504439	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17395268	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2047905	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34294912	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35003959	0.99[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3736408	0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4773474	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4773475	0.89[AMR][1000 genomes]
rs515212	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs572497	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs574402	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs617470	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs618484	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs620909	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs633976	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs657998	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs669093	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs671140	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7318774	0.82[EUR][1000 genomes]
rs7332656	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7996556	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8001088	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8001305	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9555901	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9555902	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9555906	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9560339	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9560340	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9560341	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9560355	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9560356	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9560374	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	nsv1044807	chr13:89991827-90263328	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1039775	chr13:89995537-90260944	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv900860	chr13:90008941-90259291	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv428613	chr13:90012119-90165711	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv533455	chr13:90041897-90255725	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1053657	chr13:90100510-90578568	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv900864	chr13:90110725-90173515	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:90149800-90150000	Enhancers	Fetal Heart	heart

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