Variant report

Variant	rs1016829
Chromosome Location	chr13:53787598-53787599
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1322949	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs1322951	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs1322952	0.92[ASN][1000 genomes]
rs1322955	0.94[ASN][1000 genomes]
rs1322956	0.94[ASN][1000 genomes]
rs1322958	0.80[ASN][1000 genomes]
rs1322961	0.91[ASN][1000 genomes]
rs1322962	0.86[ASN][1000 genomes]
rs1407686	0.87[ASN][1000 genomes]
rs1853369	0.92[ASN][1000 genomes]
rs1909648	0.99[ASN][1000 genomes]
rs1923771	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2015677	0.96[ASN][1000 genomes]
rs2038649	0.93[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs2093599	0.80[ASN][1000 genomes]
rs2491124	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2759706	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2759708	0.95[ASN][1000 genomes]
rs2759709	0.88[ASN][1000 genomes]
rs2759712	0.94[ASN][1000 genomes]
rs2759716	0.86[ASN][1000 genomes]
rs2806936	0.88[ASN][1000 genomes]
rs2806939	0.88[ASN][1000 genomes]
rs2806941	0.90[ASN][1000 genomes]
rs2806956	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2806960	1.00[ASN][1000 genomes]
rs2806963	0.98[ASN][1000 genomes]
rs2806964	0.99[ASN][1000 genomes]
rs2806966	0.99[ASN][1000 genomes]
rs4886270	0.94[ASN][1000 genomes]
rs7984963	0.96[ASN][1000 genomes]
rs7994915	0.92[ASN][1000 genomes]
rs8002513	0.86[ASN][1000 genomes]
rs912052	0.94[ASN][1000 genomes]
rs912054	0.84[ASN][1000 genomes]
rs927518	0.96[CHB][hapmap];0.95[JPT][hapmap];1.00[ASN][1000 genomes]
rs9527057	1.00[CHB][hapmap];0.86[JPT][hapmap];0.88[ASN][1000 genomes]
rs9536378	1.00[CHB][hapmap]
rs9568813	0.81[ASN][1000 genomes]
rs9568826	0.86[ASN][1000 genomes]
rs959222	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050969	chr13:53665927-54064861	Bivalent Enhancer Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv1840677	chr13:53774627-53791895	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription	Chromatin interactive region	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	chr13:53786400-53788400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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