Variant report

Variant	rs1423861
Chromosome Location	chr16:76116546-76116547
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:76109470..76111074-chr16:76115250..76116774,2	MCF-7	breast:

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs11149863	0.82[EUR][1000 genomes]
rs11149864	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs11149868	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs11149869	0.87[ASN][1000 genomes]
rs11149870	0.85[ASN][1000 genomes]
rs11149872	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11149873	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11149874	0.81[ASN][1000 genomes]
rs11643060	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs11645633	0.81[ASN][1000 genomes]
rs11648269	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs11648313	0.87[ASN][1000 genomes]
rs12443612	0.91[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs12446660	0.84[EUR][1000 genomes]
rs13331826	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs13332847	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1364133	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1364134	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1498057	0.82[EUR][1000 genomes]
rs1593153	0.84[ASN][1000 genomes]
rs1833976	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1834067	0.82[ASN][1000 genomes]
rs2113187	0.89[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs2278056	0.87[ASN][1000 genomes]
rs2454144	0.96[ASN][1000 genomes]
rs28417077	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2866267	0.86[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs4313827	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4424937	0.83[ASN][1000 genomes]
rs55957576	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6564307	0.97[ASN][1000 genomes]
rs7189202	0.86[ASN][1000 genomes]
rs8050473	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs8050585	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs8053596	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs918691	0.83[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs9635566	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9635567	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs977044	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9922334	0.82[ASN][1000 genomes]
rs9922420	0.82[ASN][1000 genomes]
rs9924757	0.80[ASN][1000 genomes]
rs9925205	0.82[ASN][1000 genomes]
rs9926025	0.81[EUR][1000 genomes]
rs9926814	0.82[ASN][1000 genomes]
rs9933460	0.82[ASN][1000 genomes]
rs9935238	0.81[ASN][1000 genomes]
rs9935609	0.82[ASN][1000 genomes]
rs9935708	0.82[ASN][1000 genomes]
rs9936194	0.81[EUR][1000 genomes]
rs9937270	0.84[ASN][1000 genomes]
rs9938010	0.82[ASN][1000 genomes]
rs9938314	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532562	chr16:75614947-76371158	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv1064607	chr16:75787129-76449101	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1065794	chr16:75792288-76434118	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv542961	chr16:75792288-76434118	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
5	nsv1059162	chr16:75929348-76730816	Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv572995	chr16:75935025-76708417	Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv572996	chr16:75935025-76735249	Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	nsv817220	chr16:75939705-76735383	ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
9	nsv1056021	chr16:75955522-76729765	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
10	nsv542962	chr16:75955522-76729765	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
11	nsv906935	chr16:76031737-76453110	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
12	nsv906936	chr16:76031737-76768178	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
13	nsv833284	chr16:76057741-76205989	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv817549	chr16:76067068-76582099	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
15	nsv906937	chr16:76077294-76163049	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76114400-76116800	Enhancers	Brain Hippocampus Middle	brain
2	chr16:76115000-76116600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr16:76115800-76116600	Enhancers	Brain Angular Gyrus	brain
4	chr16:76116000-76116600	Active TSS	Brain Substantia Nigra	brain
5	chr16:76116000-76117000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr16:76116200-76116600	Enhancers	Brain Anterior Caudate	brain
7	chr16:76116200-76116600	Active TSS	Brain Inferior Temporal Lobe	brain
8	chr16:76116200-76117600	Enhancers	HMEC	breast
9	chr16:76116400-76116800	Enhancers	Cortex derived primary cultured neurospheres	brain

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