Variant report

Variant	rs3134884
Chromosome Location	chr4:55566266-55566267
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11726190	0.85[CEU][hapmap];0.88[CHB][hapmap];0.92[JPT][hapmap];0.87[ASN][1000 genomes]
rs17240054	1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.95[TSI][hapmap];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2237017	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2237019	0.89[TSI][hapmap]
rs2237020	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2237021	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2237023	0.89[TSI][hapmap]
rs2282775	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.97[MKK][hapmap];0.98[TSI][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2703461	0.87[TSI][hapmap]
rs2703488	0.85[CEU][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];0.98[TSI][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2855777	0.93[CEU][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];0.98[TSI][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs28729669	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3020821	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3020825	0.81[GIH][hapmap];0.87[TSI][hapmap]
rs3020826	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3020827	0.81[TSI][hapmap]
rs3111791	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3111795	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3111800	0.89[TSI][hapmap]
rs34332764	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3796772	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56295037	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999400	chr4:55143598-55776995	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	esv3367952	chr4:55437113-55724644	Bivalent/Poised TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv526344	chr4:55522488-56231119	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:55545600-55575800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr4:55554600-55566400	Weak transcription	NH-A	brain
3	chr4:55555200-55573600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr4:55555600-55574400	Weak transcription	Fetal Stomach	stomach
5	chr4:55557800-55594000	Weak transcription	Aorta	Aorta
6	chr4:55559600-55569600	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr4:55560400-55568400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr4:55561000-55606600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr4:55561200-55569200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr4:55561400-55572000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
11	chr4:55561600-55567000	Strong transcription	Primary hematopoietic stem cells	blood
12	chr4:55562000-55566400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
13	chr4:55562000-55577200	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr4:55562800-55597400	Weak transcription	Fetal Muscle Trunk	muscle
15	chr4:55563200-55573400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr4:55564000-55566800	Weak transcription	Right Ventricle	heart
17	chr4:55564200-55569600	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr4:55565000-55570200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr4:55565000-55573600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr4:55565000-55574000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr4:55565000-55576000	Weak transcription	Ovary	ovary
22	chr4:55565200-55566800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr4:55565600-55575000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr4:55565600-55592800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr4:55566000-55566600	Strong transcription	HUES48 Cell Line	embryonic stem cell
26	chr4:55566200-55567800	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:55566200-55568600	Weak transcription	NHDF-Ad	bronchial
28	chr4:55566200-55569400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr4:55566200-55589600	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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