Variant report

Variant	rs9793716
Chromosome Location	chr1:47493584-47493585
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:47489896..47492133-chr1:47492275..47494697,2	K562	blood:

Extended variants
information (count: 93 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs1021827	0.82[GIH][hapmap]
rs10890443	0.86[YRI][hapmap];0.81[AMR][1000 genomes]
rs10890444	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs10890445	0.82[GIH][hapmap]
rs10890446	1.00[CEU][hapmap];1.00[GIH][hapmap];0.97[TSI][hapmap];0.93[YRI][hapmap];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10890447	1.00[CEU][hapmap];0.93[YRI][hapmap];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10890449	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10890452	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10890453	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10890454	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10890455	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10890457	0.83[CEU][hapmap];0.86[TSI][hapmap]
rs10890460	0.83[CEU][hapmap];0.84[TSI][hapmap]
rs10890464	0.83[CEU][hapmap];0.84[TSI][hapmap]
rs1117514	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11211421	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11211422	1.00[CEU][hapmap];0.98[GIH][hapmap];0.87[TSI][hapmap]
rs11211423	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11211435	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11211439	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.95[TSI][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11211442	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11211446	0.83[CEU][hapmap]
rs11211451	0.83[CEU][hapmap];0.84[TSI][hapmap]
rs11211457	0.83[CEU][hapmap]
rs12022635	0.95[CEU][hapmap];1.00[GIH][hapmap];0.97[TSI][hapmap];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12037014	0.83[TSI][hapmap]
rs12564635	1.00[CEU][hapmap];1.00[GIH][hapmap];0.95[TSI][hapmap];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12567857	0.85[AMR][1000 genomes]
rs12568064	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12732488	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12734327	0.83[CEU][hapmap];0.84[TSI][hapmap]
rs12736235	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1393659	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1393667	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.97[TSI][hapmap];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1502908	0.85[AMR][1000 genomes]
rs1553391	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1827474	0.82[YRI][hapmap]
rs1847222	0.83[CEU][hapmap];0.84[TSI][hapmap]
rs1847223	0.82[CEU][hapmap]
rs1967757	0.83[CEU][hapmap];0.84[TSI][hapmap]
rs2016160	0.83[CEU][hapmap]
rs2055500	1.00[CEU][hapmap]
rs2134471	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2202219	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2405580	1.00[CEU][hapmap];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2405588	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4314923	0.81[AMR][1000 genomes]
rs4375314	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4926773	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4926785	0.83[CEU][hapmap];0.84[TSI][hapmap];0.82[AMR][1000 genomes]
rs4926786	0.81[AMR][1000 genomes]
rs4926788	0.81[AMR][1000 genomes]
rs4926793	0.83[CEU][hapmap];0.84[TSI][hapmap];0.81[AMR][1000 genomes]
rs4926797	0.81[AMR][1000 genomes]
rs4926804	0.81[AMR][1000 genomes]
rs4926809	0.81[AMR][1000 genomes]
rs6664392	0.83[CEU][hapmap];0.84[TSI][hapmap]
rs6664496	0.83[CEU][hapmap]
rs6669621	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6675902	0.81[AMR][1000 genomes]
rs6683137	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6690005	0.83[CEU][hapmap];0.84[TSI][hapmap];0.81[AMR][1000 genomes]
rs6693145	0.82[AMR][1000 genomes]
rs6701611	0.82[AMR][1000 genomes]
rs7540264	0.81[AMR][1000 genomes]
rs7545399	0.84[TSI][hapmap]
rs9326151	0.82[GIH][hapmap]
rs9326152	0.82[GIH][hapmap]
rs9326153	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9659815	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9699932	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9701154	1.00[CEU][hapmap];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9701868	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9701886	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9701899	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9728169	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9729662	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9793202	1.00[CEU][hapmap];1.00[GIH][hapmap];0.97[TSI][hapmap]
rs9793471	0.95[CEU][hapmap];0.88[TSI][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9793711	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv871958	chr1:47350374-47517123	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1009338	chr1:47358532-47555253	Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	esv2763300	chr1:47358532-47628774	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv870695	chr1:47363893-47502714	Bivalent/Poised TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv871288	chr1:47363893-47507808	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv871377	chr1:47363893-47517123	Bivalent Enhancer ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv546166	chr1:47407739-47495605	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv870674	chr1:47416441-47517123	Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv916813	chr1:47435635-47666179	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
10	nsv871717	chr1:47449486-47524264	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv461428	chr1:47487585-47524264	Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv546167	chr1:47487585-47524264	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	nsv871080	chr1:47489786-47517123	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47490000-47496600	Weak transcription	Esophagus	oesophagus
2	chr1:47490000-47496600	Weak transcription	Right Atrium	heart
3	chr1:47490400-47495800	Weak transcription	Adipose Nuclei	Adipose
4	chr1:47490400-47500400	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr1:47490600-47494800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr1:47490600-47498600	Weak transcription	Brain Anterior Caudate	brain
7	chr1:47491000-47496000	Weak transcription	Psoas Muscle	Psoas
8	chr1:47491000-47501600	Weak transcription	Gastric	stomach
9	chr1:47491200-47494800	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr1:47491200-47495200	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr1:47491200-47495800	Weak transcription	Aorta	Aorta
12	chr1:47491600-47495600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr1:47491600-47517200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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