Variant report

Variant	rs4632419
Chromosome Location	chr20:11232115-11232116
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 92 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs1473700	0.98[ASN][1000 genomes]
rs1473701	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1473702	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1473703	0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2015108	0.88[ASN][1000 genomes]
rs2076643	0.97[ASN][1000 genomes]
rs2076644	0.96[ASN][1000 genomes]
rs2076645	0.96[ASN][1000 genomes]
rs2076646	0.88[ASN][1000 genomes]
rs2076647	0.89[ASN][1000 genomes]
rs2143857	0.88[ASN][1000 genomes]
rs2143859	0.89[ASN][1000 genomes]
rs2179827	0.89[ASN][1000 genomes]
rs2207098	0.88[ASN][1000 genomes]
rs2207099	0.85[ASN][1000 genomes]
rs2207100	0.87[ASN][1000 genomes]
rs2223858	0.99[ASN][1000 genomes]
rs2327366	0.98[ASN][1000 genomes]
rs2327368	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2876220	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2876221	0.93[ASN][1000 genomes]
rs4384859	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4435520	0.97[ASN][1000 genomes]
rs4449208	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4643605	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4813966	0.89[ASN][1000 genomes]
rs4813967	0.89[ASN][1000 genomes]
rs4813968	0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4813969	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4813970	0.98[ASN][1000 genomes]
rs4813971	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4813972	0.98[ASN][1000 genomes]
rs6033062	0.83[ASN][1000 genomes]
rs6033063	0.89[ASN][1000 genomes]
rs6033066	0.98[ASN][1000 genomes]
rs6033067	0.94[ASN][1000 genomes]
rs6033068	0.98[ASN][1000 genomes]
rs6033069	0.98[ASN][1000 genomes]
rs6033070	0.98[ASN][1000 genomes]
rs6033071	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6033072	0.99[ASN][1000 genomes]
rs6040442	0.86[ASN][1000 genomes]
rs6040446	0.88[ASN][1000 genomes]
rs6040447	0.88[ASN][1000 genomes]
rs6040450	0.89[ASN][1000 genomes]
rs6040451	0.89[ASN][1000 genomes]
rs6040452	0.89[ASN][1000 genomes]
rs6040456	0.89[ASN][1000 genomes]
rs6040458	0.98[ASN][1000 genomes]
rs6040459	0.98[ASN][1000 genomes]
rs6040460	0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6040461	0.98[ASN][1000 genomes]
rs6040463	0.98[ASN][1000 genomes]
rs6040464	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6040465	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6040466	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6040469	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6040470	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6040471	0.85[AFR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6040472	0.99[ASN][1000 genomes]
rs6040473	0.99[ASN][1000 genomes]
rs6040474	0.99[ASN][1000 genomes]
rs6040475	0.99[ASN][1000 genomes]
rs6040477	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6040479	0.91[ASN][1000 genomes]
rs6040480	0.85[AFR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6040481	0.85[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs6040482	0.91[ASN][1000 genomes]
rs6040486	0.88[ASN][1000 genomes]
rs6040487	0.88[ASN][1000 genomes]
rs6078105	0.98[ASN][1000 genomes]
rs6078109	0.85[AFR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6104726	0.83[ASN][1000 genomes]
rs6108870	0.88[ASN][1000 genomes]
rs6108871	0.88[ASN][1000 genomes]
rs6108872	0.89[ASN][1000 genomes]
rs6108876	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6108882	0.90[ASN][1000 genomes]
rs714690	0.89[ASN][1000 genomes]
rs714691	0.89[ASN][1000 genomes]
rs714692	0.89[ASN][1000 genomes]
rs761471	0.88[ASN][1000 genomes]
rs761472	0.89[ASN][1000 genomes]
rs926725	0.89[ASN][1000 genomes]
rs983251	0.88[ASN][1000 genomes]
rs983252	0.88[ASN][1000 genomes]
rs983342	0.88[ASN][1000 genomes]
rs983343	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1065969	chr20:10850562-11464172	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv544181	chr20:10850562-11464172	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv585415	chr20:11134907-11383327	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv819382	chr20:11231079-11232630	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:11216200-11238800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr20:11227400-11235000	Weak transcription	Fetal Kidney	kidney
3	chr20:11230800-11232200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr20:11232000-11233000	Weak transcription	Cortex derived primary cultured neurospheres	brain

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