Variant report

Variant	rs2160364
Chromosome Location	chr2:40357323-40357324
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10205502	1.00[CEU][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10208777	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10221571	1.00[JPT][hapmap]
rs12712682	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2110923	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2110924	0.95[YRI][hapmap];0.99[AFR][1000 genomes];0.88[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2110925	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2110927	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2160365	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2373793	1.00[CEU][hapmap];0.80[YRI][hapmap];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2373794	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs417614	1.00[JPT][hapmap]
rs429648	0.81[JPT][hapmap]
rs432188	0.81[JPT][hapmap]
rs435923	1.00[JPT][hapmap]
rs444999	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs448517	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs4614975	0.81[JPT][hapmap]
rs4952490	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs4952491	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs6739058	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6746919	1.00[JPT][hapmap]
rs6755509	1.00[JPT][hapmap]
rs7572256	1.00[JPT][hapmap]
rs7586346	1.00[CEU][hapmap];0.90[YRI][hapmap];0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs759444	0.93[CEU][hapmap];0.81[JPT][hapmap];0.95[YRI][hapmap];0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs888073	1.00[CEU][hapmap];0.90[YRI][hapmap];0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9309051	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs985991	1.00[CEU][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833892	chr2:40188785-40363480	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv529606	chr2:40206280-40896881	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv873902	chr2:40231282-40466268	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1004092	chr2:40264608-40451701	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1000572	chr2:40271958-40458911	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv535654	chr2:40271958-40458911	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv581502	chr2:40273903-40459645	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv873903	chr2:40285145-40382712	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv873904	chr2:40292289-40466268	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv873905	chr2:40341847-40364895	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv873906	chr2:40341847-40385045	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv873907	chr2:40349094-40381369	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
13	nsv1005758	chr2:40349403-40381369	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
14	nsv873908	chr2:40351453-40371095	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40328000-40365600	Weak transcription	Brain Germinal Matrix	brain
2	chr2:40342800-40357600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr2:40349800-40358200	Enhancers	Osteobl	bone
4	chr2:40349800-40359600	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr2:40350200-40358000	Enhancers	Muscle Satellite Cultured Cells	--
6	chr2:40351000-40358200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr2:40351200-40358000	Enhancers	NHDF-Ad	bronchial
8	chr2:40351600-40360400	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr2:40352800-40358000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr2:40354000-40358600	Enhancers	Colon Smooth Muscle	Colon
11	chr2:40354400-40357400	Genic enhancers	Fetal Heart	heart
12	chr2:40354400-40358800	Enhancers	Rectal Smooth Muscle	rectum
13	chr2:40354600-40357800	Enhancers	Left Ventricle	heart
14	chr2:40354600-40358000	Enhancers	HSMM	muscle
15	chr2:40354600-40366600	Weak transcription	Lung	lung
16	chr2:40355000-40366200	Weak transcription	Fetal Muscle Trunk	muscle
17	chr2:40355200-40357600	Weak transcription	Dnd41	blood
18	chr2:40355400-40383800	Weak transcription	Small Intestine	intestine
19	chr2:40355800-40357400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr2:40355800-40357400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr2:40355800-40357600	Enhancers	HSMMtube	muscle
22	chr2:40355800-40357800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr2:40355800-40365600	Weak transcription	Fetal Muscle Leg	muscle
24	chr2:40355800-40370000	Weak transcription	Fetal Brain Male	brain
25	chr2:40356000-40367400	Weak transcription	Fetal Brain Female	brain
26	chr2:40356400-40357800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr2:40356600-40358400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr2:40356800-40358000	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr2:40356800-40358000	Enhancers	Duodenum Smooth Muscle	Duodenum
30	chr2:40356800-40358000	Enhancers	Ovary	ovary
31	chr2:40356800-40358200	Enhancers	Stomach Smooth Muscle	stomach
32	chr2:40356800-40358200	Enhancers	NHLF	lung
33	chr2:40356800-40359000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr2:40356800-40375000	Strong transcription	Primary monocytes fromperipheralblood	blood
35	chr2:40357000-40357800	Enhancers	Fetal Stomach	stomach
36	chr2:40357000-40358000	Enhancers	Aorta	Aorta
37	chr2:40357000-40358000	Enhancers	Fetal Lung	lung
38	chr2:40357000-40358000	Enhancers	NH-A	brain
39	chr2:40357000-40358200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr2:40357000-40359000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr2:40357200-40357600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr2:40357200-40357600	Weak transcription	Right Ventricle	heart
43	chr2:40357200-40357800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr2:40357200-40357800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr2:40357200-40358000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr2:40357200-40358000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr2:40357200-40358400	Weak transcription	Right Atrium	heart

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