Variant report

Variant	rs7919474
Chromosome Location	chr10:52064431-52064432
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:52040531..52043332-chr10:52062739..52065495,2	K562	blood:
2	chr10:52058612..52061385-chr10:52062063..52064503,2	K562	blood:
3	chr10:52063071..52064625-chr10:52072402..52074193,2	MCF-7	breast:
4	chr10:52064205..52066621-chr10:52082912..52084606,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs12569679	1.00[EUR][1000 genomes]
rs1436210	0.90[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs17179735	1.00[EUR][1000 genomes]
rs17179784	1.00[EUR][1000 genomes]
rs17179881	1.00[EUR][1000 genomes]
rs2140407	0.89[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2304444	1.00[ASW][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap]
rs2574978	0.90[CHB][hapmap];0.81[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs2574980	0.90[CHB][hapmap];0.81[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2688880	0.84[ASN][1000 genomes]
rs2688881	0.89[CHB][hapmap];0.95[JPT][hapmap];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2688886	0.84[ASN][1000 genomes]
rs2842087	0.90[CHB][hapmap];0.81[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2842088	0.83[ASN][1000 genomes]
rs2842089	0.89[CHB][hapmap];0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs2842090	0.84[CHB][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs2842091	0.90[CHB][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs2842092	0.84[ASN][1000 genomes]
rs2842093	0.88[JPT][hapmap];0.84[ASN][1000 genomes]
rs2842094	0.90[CHB][hapmap];0.95[JPT][hapmap];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2842095	0.84[ASN][1000 genomes]
rs2842097	0.90[CHB][hapmap];0.81[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4540795	1.00[EUR][1000 genomes]
rs59510112	1.00[EUR][1000 genomes]
rs72634643	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv518071	chr10:51595893-52157935	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv1054775	chr10:51595893-52392361	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv1053903	chr10:51886486-52163991	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv1040661	chr10:51886486-52164585	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv1051028	chr10:51886486-52164585	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	nsv1037118	chr10:51886486-52167442	Enhancers ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
7	nsv1051087	chr10:51886486-52447295	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
8	nsv916214	chr10:51886486-52458983	Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv918212	chr10:51886486-52465482	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
10	nsv817412	chr10:51911034-52432990	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
11	esv2830205	chr10:51978430-52135215	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
12	nsv1053293	chr10:51981959-52102649	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
13	nsv1046850	chr10:52009869-52135542	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
14	nsv540625	chr10:52009869-52135542	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
15	esv2762864	chr10:52030945-52107415	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
16	nsv521273	chr10:52051645-52197847	Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52051800-52066400	Weak transcription	Brain Substantia Nigra	brain
2	chr10:52055000-52069200	Weak transcription	Fetal Intestine Small	intestine
3	chr10:52055000-52069200	Weak transcription	HSMMtube	muscle
4	chr10:52056000-52066400	Weak transcription	NHDF-Ad	bronchial
5	chr10:52057800-52066800	Weak transcription	Aorta	Aorta
6	chr10:52059000-52068200	Weak transcription	Primary B cells from cord blood	blood
7	chr10:52059400-52066800	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr10:52061000-52066600	Weak transcription	Left Ventricle	heart
9	chr10:52061400-52080400	Weak transcription	Psoas Muscle	Psoas
10	chr10:52061600-52065400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr10:52062000-52065600	Weak transcription	Fetal Lung	lung
12	chr10:52062000-52066600	Weak transcription	Brain Anterior Caudate	brain
13	chr10:52062200-52075000	Weak transcription	HUVEC	blood vessel
14	chr10:52062400-52065800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr10:52062400-52066400	Weak transcription	Brain Hippocampus Middle	brain
16	chr10:52062400-52066400	Weak transcription	Fetal Muscle Leg	muscle
17	chr10:52062400-52066600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr10:52062400-52066600	Weak transcription	HSMM	muscle
19	chr10:52062400-52066800	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr10:52062400-52070600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr10:52062600-52066600	Weak transcription	Primary B cells from peripheral blood	blood
22	chr10:52062600-52070200	Weak transcription	Small Intestine	intestine
23	chr10:52062800-52064600	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr10:52062800-52064600	Weak transcription	Liver	Liver
25	chr10:52062800-52066400	Weak transcription	Duodenum Mucosa	Duodenum
26	chr10:52063000-52066600	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr10:52063000-52069200	Weak transcription	Fetal Stomach	stomach
28	chr10:52063200-52065400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr10:52063200-52065600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr10:52063200-52066800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr10:52063200-52076600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr10:52063400-52066600	Weak transcription	Osteobl	bone
33	chr10:52063800-52064600	Enhancers	HMEC	breast
34	chr10:52064000-52064600	Enhancers	K562	blood
35	chr10:52064000-52065600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr10:52064000-52066200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr10:52064000-52073400	Strong transcription	Monocytes-CD14+_RO01746	blood
38	chr10:52064200-52066400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr10:52064200-52066400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr10:52064200-52066400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr10:52064200-52066400	Weak transcription	GM12878-XiMat	blood
42	chr10:52064200-52066600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr10:52064200-52070000	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr10:52064400-52066200	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr10:52064400-52066200	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr10:52064400-52066400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr10:52064400-52066400	Weak transcription	Adipose Nuclei	Adipose
48	chr10:52064400-52066600	Weak transcription	Fetal Intestine Large	intestine
49	chr10:52064400-52066600	Weak transcription	NHEK	skin
50	chr10:52064400-52069600	Weak transcription	Cortex derived primary cultured neurospheres	brain

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