Variant report

Variant	rs6437966
Chromosome Location	chr3:110956340-110956341
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs11715652	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12490607	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12493629	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13086151	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13323922	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1471989	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1906703	0.83[CHB][hapmap]
rs2932051	0.98[ASN][1000 genomes]
rs2958068	0.98[ASN][1000 genomes]
rs2971350	0.98[ASN][1000 genomes]
rs4682243	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4682248	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4682254	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4682255	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4682256	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62276307	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6414249	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6437964	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6437965	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6437969	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7371938	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7373383	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7427713	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7430044	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7431784	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7432243	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7433817	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7615671	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7619144	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7629508	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7631076	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9714275	0.81[AMR][1000 genomes]
rs9816038	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9819170	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9826558	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9827344	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9828332	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9833532	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9836183	0.87[ASN][1000 genomes]
rs9854607	0.91[ASN][1000 genomes]
rs9860277	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9883993	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]

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	nsv1003106	chr3:110264476-111105943	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv460821	chr3:110637471-111501097	Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv591275	chr3:110637471-111501097	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv829675	chr3:110885605-111101858	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv877339	chr3:110889974-111070554	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv3945	chr3:110922029-110967244	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:110930400-110961000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:110953000-110956400	Weak transcription	Primary T cells from cord blood	blood
3	chr3:110954800-110956400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr3:110955400-110956800	Enhancers	NHDF-Ad	bronchial
5	chr3:110955600-110956600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr3:110955600-110956600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr3:110955600-110956800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr3:110955600-110956800	Enhancers	Muscle Satellite Cultured Cells	--
9	chr3:110955600-110958200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr3:110955800-110956600	Enhancers	NH-A	brain
11	chr3:110955800-110956800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr3:110955800-110956800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr3:110955800-110956800	Enhancers	HMEC	breast
14	chr3:110955800-110956800	Enhancers	Osteobl	bone
15	chr3:110955800-110957000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr3:110956000-110956400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr3:110956000-110956400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr3:110956000-110956800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr3:110956000-110956800	Enhancers	HSMM	muscle
20	chr3:110956000-110958400	Enhancers	Primary T helper naive cells from peripheral blood	blood
21	chr3:110956200-110956400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr3:110956200-110956600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr3:110956200-110956600	Enhancers	NHLF	lung
24	chr3:110956200-110957000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr3:110956200-110957200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr3:110956200-110958400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr3:110956200-110958400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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