Variant report

Variant	rs9442956
Chromosome Location	chr6:74455832-74455833
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10455283	0.83[EUR][1000 genomes]
rs10805974	0.89[GIH][hapmap]
rs12197682	0.96[AMR][1000 genomes]
rs12203043	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1392913	0.93[GIH][hapmap];0.96[MEX][hapmap];0.81[EUR][1000 genomes]
rs1501191	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1875367	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1973480	0.83[MEX][hapmap]
rs2033736	1.00[MEX][hapmap]
rs2134016	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2164755	1.00[MEX][hapmap]
rs2173853	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2351528	1.00[MEX][hapmap]
rs35027042	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4235875	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4706553	0.81[AMR][1000 genomes]
rs4708077	0.91[CEU][hapmap];0.89[CHB][hapmap];0.83[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];0.83[MEX][hapmap];0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4708082	1.00[MEX][hapmap]
rs5023688	1.00[MEX][hapmap]
rs6453700	1.00[MEX][hapmap]
rs6901628	0.83[CHB][hapmap];0.87[CHD][hapmap];0.85[GIH][hapmap];0.90[JPT][hapmap];0.96[YRI][hapmap];0.89[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6923034	0.83[CEU][hapmap];0.83[CHB][hapmap];0.89[GIH][hapmap];0.82[TSI][hapmap]
rs7742217	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7767106	0.82[EUR][1000 genomes]
rs7771585	1.00[MEX][hapmap]
rs7774119	0.93[ASW][hapmap];0.82[CEU][hapmap];0.83[CHB][hapmap];0.84[CHD][hapmap];0.93[GIH][hapmap];1.00[MEX][hapmap];0.83[YRI][hapmap];0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9293937	0.83[CEU][hapmap]
rs9442953	0.82[CHB][hapmap];0.81[AMR][1000 genomes]
rs9442954	0.81[EUR][1000 genomes]
rs9442955	0.81[EUR][1000 genomes]
rs9442961	1.00[MEX][hapmap]
rs9446995	0.84[EUR][1000 genomes]
rs9447001	0.87[CEU][hapmap];0.83[CHB][hapmap];0.86[EUR][1000 genomes]
rs9447019	1.00[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1027968	chr6:74155378-74521923	Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
2	nsv538305	chr6:74155378-74521923	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
3	nsv1023250	chr6:74189642-74605976	Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	172 gene(s)	inside rSNPs	diseases
4	nsv538306	chr6:74189642-74605976	Strong transcription Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	172 gene(s)	inside rSNPs	diseases
5	nsv463154	chr6:74412048-74775904	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	nsv603695	chr6:74412048-74775904	Flanking Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74414800-74474600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr6:74425200-74475800	Weak transcription	Hela-S3	cervix
3	chr6:74425400-74483200	Weak transcription	A549	lung
4	chr6:74433000-74456400	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr6:74433000-74456400	Weak transcription	HSMM	muscle
6	chr6:74433400-74456400	Weak transcription	NHLF	lung
7	chr6:74435800-74475400	Weak transcription	Primary T cells from cord blood	blood
8	chr6:74438400-74527200	Weak transcription	Esophagus	oesophagus
9	chr6:74441400-74473200	Weak transcription	HUVEC	blood vessel
10	chr6:74441400-74544400	Weak transcription	Aorta	Aorta
11	chr6:74442200-74473400	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr6:74442400-74493400	Weak transcription	Fetal Muscle Trunk	muscle
13	chr6:74443400-74484000	Weak transcription	Left Ventricle	heart
14	chr6:74444000-74498600	Weak transcription	Fetal Muscle Leg	muscle
15	chr6:74444400-74474600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr6:74445400-74456200	Weak transcription	Osteobl	bone
17	chr6:74447200-74456000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr6:74448800-74456400	Weak transcription	Adipose Nuclei	Adipose
19	chr6:74448800-74483400	Weak transcription	NHEK	skin
20	chr6:74452200-74456200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr6:74452200-74456600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr6:74453600-74479400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr6:74453800-74456000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr6:74453800-74456000	Weak transcription	Primary hematopoietic stem cells	blood
25	chr6:74454000-74456000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr6:74454200-74457400	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr6:74454600-74456600	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr6:74454800-74458400	Weak transcription	Rectal Smooth Muscle	rectum
29	chr6:74455200-74456400	Weak transcription	GM12878-XiMat	blood
30	chr6:74455200-74457200	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr6:74455200-74458200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr6:74455400-74456000	Weak transcription	HMEC	breast
33	chr6:74455400-74456400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr6:74455400-74456400	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr6:74455400-74460000	Weak transcription	Colon Smooth Muscle	Colon
36	chr6:74455600-74456000	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr6:74455800-74456000	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr6:74455800-74456400	Enhancers	NHDF-Ad	bronchial
39	chr6:74455800-74456600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr6:74455800-74456600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr6:74455800-74457600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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