Variant report

Variant	rs1027913
Chromosome Location	chr16:59362913-59362914
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1019571	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1022099	0.89[EUR][1000 genomes]
rs10431930	0.89[EUR][1000 genomes]
rs12447529	0.87[EUR][1000 genomes]
rs12709025	0.97[EUR][1000 genomes]
rs12925044	0.95[EUR][1000 genomes]
rs12928697	0.86[EUR][1000 genomes]
rs12929739	0.85[EUR][1000 genomes]
rs1303842	0.86[EUR][1000 genomes]
rs1582588	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1593112	0.95[EUR][1000 genomes]
rs1593146	0.87[EUR][1000 genomes]
rs1593148	0.87[EUR][1000 genomes]
rs1610077	0.96[EUR][1000 genomes]
rs1813437	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1828343	0.86[EUR][1000 genomes]
rs1834058	0.97[EUR][1000 genomes]
rs1834064	0.84[EUR][1000 genomes]
rs2036805	0.96[EUR][1000 genomes]
rs2036806	0.95[EUR][1000 genomes]
rs2036807	0.86[EUR][1000 genomes]
rs2081226	0.89[EUR][1000 genomes]
rs2081227	0.89[EUR][1000 genomes]
rs2089727	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2098731	0.89[EUR][1000 genomes]
rs2406766	0.87[EUR][1000 genomes]
rs2406779	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3958621	0.96[EUR][1000 genomes]
rs4146209	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4784076	0.89[EUR][1000 genomes]
rs4785028	0.97[EUR][1000 genomes]
rs4785029	0.96[EUR][1000 genomes]
rs4785030	0.87[EUR][1000 genomes]
rs4785034	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6500029	0.87[EUR][1000 genomes]
rs6500031	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6500033	0.81[EUR][1000 genomes]
rs7195264	0.88[EUR][1000 genomes]
rs7198374	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7198887	0.94[EUR][1000 genomes]
rs7201230	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7202206	0.81[EUR][1000 genomes]
rs7202693	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7204255	0.94[EUR][1000 genomes]
rs8043584	0.99[EUR][1000 genomes]
rs8056029	0.89[EUR][1000 genomes]
rs907053	0.87[EUR][1000 genomes]
rs9927205	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9927985	0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833249	chr16:59282950-59461023	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv906745	chr16:59323025-59408342	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv906746	chr16:59323025-59423982	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:59355000-59363000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr16:59355200-59363000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr16:59359400-59364200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr16:59362400-59363600	Enhancers	Fetal Brain Male	brain
5	chr16:59362400-59364600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr16:59362600-59363400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr16:59362600-59363600	Enhancers	Brain Germinal Matrix	brain
8	chr16:59362800-59364600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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