Variant report

Variant	rs12449073
Chromosome Location	chr16:72171004-72171005
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 94 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs10400963	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10492813	0.81[YRI][hapmap]
rs10492814	0.81[YRI][hapmap]
rs1050361	0.84[YRI][hapmap]
rs1050362	0.87[YRI][hapmap]
rs1050363	0.81[YRI][hapmap]
rs10852511	0.95[JPT][hapmap]
rs11075922	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11075924	0.90[JPT][hapmap]
rs11643192	0.90[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs12325142	0.87[YRI][hapmap]
rs12325266	0.86[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs12444701	0.81[ASN][1000 genomes]
rs12708928	0.87[YRI][hapmap]
rs12924413	0.84[YRI][hapmap]
rs12928732	0.85[JPT][hapmap];0.83[ASN][1000 genomes]
rs12929749	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12932845	0.86[JPT][hapmap];0.81[YRI][hapmap]
rs12933838	0.86[ASN][1000 genomes]
rs13334151	0.82[CHB][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs16973716	0.96[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2070937	0.86[JPT][hapmap]
rs2070939	0.86[JPT][hapmap]
rs2072141	0.84[YRI][hapmap]
rs2072142	0.87[YRI][hapmap]
rs2074626	0.84[JPT][hapmap];0.87[YRI][hapmap]
rs2074627	0.87[YRI][hapmap]
rs217181	0.81[YRI][hapmap]
rs2240243	0.87[YRI][hapmap]
rs2241411	0.90[JPT][hapmap]
rs2241412	0.93[YRI][hapmap]
rs2288000	0.81[JPT][hapmap]
rs2288002	0.85[JPT][hapmap]
rs2303285	0.81[YRI][hapmap]
rs2550035	0.81[YRI][hapmap]
rs2550868	0.85[JPT][hapmap]
rs28432692	0.86[ASN][1000 genomes]
rs2854956	0.81[JPT][hapmap]
rs34714490	0.85[ASN][1000 genomes]
rs35460163	0.85[ASN][1000 genomes]
rs3764311	0.84[YRI][hapmap]
rs3764312	0.85[JPT][hapmap]
rs3764314	0.81[YRI][hapmap]
rs3812984	0.91[JPT][hapmap]
rs3812986	0.86[JPT][hapmap]
rs3812987	0.81[JPT][hapmap];0.80[ASN][1000 genomes]
rs3844425	0.95[JPT][hapmap];0.81[YRI][hapmap]
rs3852782	0.95[JPT][hapmap];0.89[YRI][hapmap];0.81[ASN][1000 genomes]
rs3852784	0.95[JPT][hapmap]
rs3902135	0.81[CHB][hapmap];0.85[JPT][hapmap];0.85[ASN][1000 genomes]
rs3909541	0.90[JPT][hapmap]
rs3909543	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4238964	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4788609	0.95[JPT][hapmap]
rs4788610	0.95[JPT][hapmap]
rs56960650	0.83[ASN][1000 genomes]
rs6499562	0.96[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6680	0.81[YRI][hapmap]
rs7184169	0.81[ASN][1000 genomes]
rs7188058	0.82[CHB][hapmap];0.86[JPT][hapmap];0.88[ASN][1000 genomes]
rs7190995	0.81[JPT][hapmap];0.89[YRI][hapmap]
rs7191127	0.81[JPT][hapmap];0.89[YRI][hapmap]
rs7192848	0.85[CHB][hapmap];0.95[JPT][hapmap];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7198572	0.81[CHB][hapmap];0.85[JPT][hapmap];0.85[ASN][1000 genomes]
rs7201225	0.83[CEU][hapmap];0.85[CHB][hapmap];0.95[JPT][hapmap];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7201643	0.86[JPT][hapmap]
rs7203426	0.86[JPT][hapmap]
rs7203821	0.86[JPT][hapmap]
rs7940	0.91[JPT][hapmap];0.84[YRI][hapmap]
rs8044868	0.96[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8045481	0.80[ASN][1000 genomes]
rs8050238	0.82[ASN][1000 genomes]
rs8051882	0.93[YRI][hapmap]
rs8052338	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8052408	0.95[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8059437	0.90[JPT][hapmap];0.81[YRI][hapmap]
rs8061282	0.81[ASN][1000 genomes]
rs8061459	0.81[ASN][1000 genomes]
rs9923344	0.83[ASN][1000 genomes]
rs9924964	0.85[JPT][hapmap];0.83[YRI][hapmap]
rs9926156	0.80[JPT][hapmap];0.94[YRI][hapmap]
rs9926927	0.81[YRI][hapmap]
rs9927526	0.91[JPT][hapmap]
rs9928157	0.91[JPT][hapmap];0.83[YRI][hapmap]
rs9932951	0.90[JPT][hapmap];0.87[YRI][hapmap]
rs9933009	0.84[ASN][1000 genomes]
rs9936642	0.83[CEU][hapmap];0.85[CHB][hapmap];0.95[JPT][hapmap];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948468	chr16:71727571-72651914	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
2	esv2758430	chr16:71976344-72274347	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
3	esv2758654	chr16:71976344-72274347	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	nsv428329	chr16:71976344-72274347	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
5	nsv1060983	chr16:72074832-72791629	Genic enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
6	nsv534588	chr16:72078262-72287230	ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
7	nsv1060804	chr16:72078486-72791629	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats 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	58 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	chr16:72147000-72172200	Weak transcription	Dnd41	blood
2	chr16:72160000-72172400	Weak transcription	Fetal Intestine Small	intestine
3	chr16:72160000-72173400	Weak transcription	Pancreas	Pancrea
4	chr16:72160600-72171400	Weak transcription	HepG2	liver
5	chr16:72160600-72171600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr16:72166800-72171400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr16:72170800-72171400	Weak transcription	Thymus	Thymus
8	chr16:72170800-72172400	Weak transcription	Duodenum Mucosa	Duodenum
9	chr16:72170800-72172400	Weak transcription	Fetal Stomach	stomach

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