Variant report

Variant	rs2881587
Chromosome Location	chr2:47211163-47211164
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:47166581..47170403-chr2:47208479..47213858,6	MCF-7	breast:
2	chr2:47209484..47211730-chr2:47212313..47214032,2	MCF-7	breast:
3	chr2:47210245..47211992-chr2:47348391..47350564,2	K562	blood:
4	chr2:47188341..47190485-chr2:47209167..47212158,2	MCF-7	breast:
5	chr2:47209205..47217024-chr2:47399516..47404811,13	MCF-7	breast:
6	chr2:47194084..47197081-chr2:47210689..47213163,3	MCF-7	breast:
7	chr2:47210303..47217706-chr2:47402135..47406405,13	MCF-7	breast:

Variant related genes	Relation type
ENSG00000180398	Chromatin interaction
ENSG00000143933	Chromatin interaction
ENSG00000068724	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10183233	1.00[CEU][hapmap];0.82[CHB][hapmap];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11125106	1.00[CEU][hapmap];0.88[CHB][hapmap];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11125107	0.88[CHB][hapmap]
rs11125108	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11680029	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11681157	0.81[ASN][1000 genomes]
rs11685605	0.94[CHB][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs11883507	0.80[ASN][1000 genomes]
rs12052808	0.94[CHB][hapmap];0.91[ASN][1000 genomes]
rs12712983	0.93[CHB][hapmap]
rs13002842	0.95[CEU][hapmap];0.88[CHB][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13014374	0.83[CHB][hapmap]
rs13395498	0.94[CHB][hapmap];0.89[ASN][1000 genomes]
rs13406452	0.92[ASN][1000 genomes]
rs1433772	0.88[ASN][1000 genomes]
rs1433773	0.94[CHB][hapmap];0.82[ASN][1000 genomes]
rs17480779	0.94[CHB][hapmap];0.95[ASN][1000 genomes]
rs1865262	0.83[CHB][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2347260	0.84[CEU][hapmap];0.87[CHB][hapmap];0.82[ASN][1000 genomes]
rs35779609	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4952858	0.82[CHB][hapmap]
rs6716882	0.81[CEU][hapmap];0.84[ASN][1000 genomes]
rs6731862	0.84[CEU][hapmap];0.94[CHB][hapmap];0.84[ASN][1000 genomes]
rs6731875	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6734201	1.00[CEU][hapmap];0.89[CHB][hapmap];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs736683	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs746915	1.00[CHB][hapmap];0.94[JPT][hapmap];0.82[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs7558171	0.94[CHB][hapmap]
rs7558196	0.89[CHB][hapmap]
rs7560371	0.84[CEU][hapmap];0.94[CHB][hapmap];0.82[ASN][1000 genomes]
rs877048	0.83[CHB][hapmap]
rs892381	0.94[CHB][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs993847	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817517	chr2:46819371-47715140	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
2	nsv457352	chr2:47004788-47325973	Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv581749	chr2:47004788-47325973	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv1004828	chr2:47056849-47814482	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
5	nsv524970	chr2:47162739-47302095	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
6	nsv1000377	chr2:47189386-47344029	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv581750	chr2:47207665-47229953	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
8	nsv525197	chr2:47210747-47297973	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:47169800-47214600	Weak transcription	Fetal Kidney	kidney
2	chr2:47174400-47212400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr2:47195600-47212800	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr2:47196400-47211800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr2:47196600-47227800	Strong transcription	Dnd41	blood
6	chr2:47200800-47216400	Genic enhancers	Fetal Thymus	thymus
7	chr2:47201600-47211800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr2:47201600-47213200	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr2:47201800-47211600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr2:47202000-47211400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr2:47202000-47214800	Genic enhancers	Primary monocytes fromperipheralblood	blood
12	chr2:47202200-47212600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr2:47203600-47212800	Genic enhancers	Placenta	Placenta
14	chr2:47203800-47213000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr2:47204600-47211800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr2:47206200-47211200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr2:47206200-47213000	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr2:47206400-47212000	Strong transcription	Fetal Stomach	stomach
19	chr2:47206600-47211800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr2:47206600-47213800	Weak transcription	Fetal Lung	lung
21	chr2:47206800-47211200	Weak transcription	Colon Smooth Muscle	Colon
22	chr2:47206800-47213800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr2:47207000-47212000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr2:47207000-47212000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr2:47207000-47212000	Weak transcription	Liver	Liver
26	chr2:47207200-47211800	Enhancers	Pancreas	Pancrea
27	chr2:47207200-47213800	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr2:47207200-47214200	Genic enhancers	Primary T cells from cord blood	blood
29	chr2:47207200-47214400	Weak transcription	Brain Germinal Matrix	brain
30	chr2:47207600-47211400	Weak transcription	Aorta	Aorta
31	chr2:47207600-47213800	Weak transcription	Fetal Brain Male	brain
32	chr2:47207800-47211600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr2:47208000-47217400	Enhancers	Stomach Mucosa	stomach
34	chr2:47208200-47212000	Weak transcription	Rectal Smooth Muscle	rectum
35	chr2:47208200-47212600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr2:47208200-47214600	Weak transcription	Fetal Brain Female	brain
37	chr2:47208400-47212400	Genic enhancers	Fetal Muscle Trunk	muscle
38	chr2:47208400-47214800	Enhancers	HUVEC	blood vessel
39	chr2:47208600-47211200	Genic enhancers	A549	lung
40	chr2:47208600-47211800	Genic enhancers	Lung	lung
41	chr2:47208600-47216000	Enhancers	Brain Substantia Nigra	brain
42	chr2:47208600-47219200	Enhancers	Brain Inferior Temporal Lobe	brain
43	chr2:47208800-47212000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr2:47209000-47211400	Enhancers	Right Ventricle	heart
45	chr2:47209000-47212400	Weak transcription	Fetal Heart	heart
46	chr2:47209000-47213400	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr2:47209400-47211400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr2:47209400-47211600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr2:47209400-47211600	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
50	chr2:47209400-47211600	Genic enhancers	NHDF-Ad	bronchial

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