Variant report

Variant	rs7093907
Chromosome Location	chr10:18876154-18876155
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10732437	0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10741086	0.83[CEU][hapmap];1.00[CHB][hapmap]
rs10741120	0.89[CEU][hapmap];0.92[EUR][1000 genomes]
rs10741131	0.81[EUR][1000 genomes]
rs10764584	0.85[YRI][hapmap];0.85[AMR][1000 genomes]
rs10764587	1.00[CHB][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10764661	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10828834	0.94[CEU][hapmap];0.86[YRI][hapmap]
rs10828879	0.83[AMR][1000 genomes]
rs10828906	0.90[YRI][hapmap];0.85[AMR][1000 genomes]
rs10829156	1.00[CHB][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10829157	0.82[AFR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10829199	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11014830	0.81[AMR][1000 genomes]
rs11014852	0.81[AMR][1000 genomes]
rs1917209	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1917823	0.94[CEU][hapmap];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4316423	0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4328135	0.81[AMR][1000 genomes]
rs4338439	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4456162	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs4475830	1.00[ASN][1000 genomes]
rs4484992	1.00[CHB][hapmap]
rs4606373	1.00[ASN][1000 genomes]
rs4634984	1.00[ASN][1000 genomes]
rs4636555	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs4747348	0.89[CEU][hapmap]
rs4747353	0.91[YRI][hapmap];0.84[AMR][1000 genomes]
rs4748476	0.83[CEU][hapmap];1.00[CHB][hapmap]
rs4748479	1.00[ASN][1000 genomes]
rs4748493	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs4748494	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs4748502	0.89[EUR][1000 genomes]
rs4748504	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4748507	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62636215	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6482534	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6482545	0.89[ASN][1000 genomes]
rs6482546	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6482565	0.94[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs6482567	0.88[CEU][hapmap];0.94[YRI][hapmap];0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7075678	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7077786	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7081435	1.00[CHB][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7082235	1.00[CHB][hapmap];0.95[YRI][hapmap];0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7090926	0.89[ASN][1000 genomes]
rs7092437	1.00[CHB][hapmap]
rs7095666	0.88[CEU][hapmap];1.00[CHB][hapmap];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7097534	0.80[EUR][1000 genomes]
rs7098721	1.00[ASN][1000 genomes]
rs7099307	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7100884	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7895709	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7895775	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7904365	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7908550	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7909552	0.89[CEU][hapmap];1.00[CHB][hapmap];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7911922	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7918933	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7923072	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[YRI][hapmap];0.91[AFR][1000 genomes];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8181345	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9731044	0.96[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv550042	chr10:18683267-18994583	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	esv34545	chr10:18821185-18908294	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	esv1793653	chr10:18827828-18888369	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	esv1794817	chr10:18827828-18888369	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
5	esv1811259	chr10:18827828-18888369	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	esv1840241	chr10:18827828-18888369	Enhancers Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
7	esv1841068	chr10:18827828-18888369	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
8	esv1851495	chr10:18827828-18888369	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
9	esv2757371	chr10:18835325-18906507	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
10	esv2759736	chr10:18835325-18906507	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
11	nsv466760	chr10:18839350-18905935	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
12	nsv550044	chr10:18839350-18905935	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18842000-18886400	Weak transcription	Colon Smooth Muscle	Colon
2	chr10:18846200-18899200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr10:18848400-18915800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr10:18849800-18910800	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr10:18861000-18883200	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr10:18862200-18894600	Weak transcription	HSMM	muscle
7	chr10:18862400-18878400	Strong transcription	Liver	Liver
8	chr10:18862600-18876600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr10:18863000-18894600	Weak transcription	A549	lung
10	chr10:18863000-18910800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr10:18863200-18876400	Weak transcription	Spleen	Spleen
12	chr10:18863800-18902200	Weak transcription	Brain Anterior Caudate	brain
13	chr10:18864800-18898000	Weak transcription	Fetal Kidney	kidney
14	chr10:18865600-18885000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr10:18866600-18899400	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr10:18867400-18876800	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr10:18867400-18877400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr10:18867600-18894400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr10:18867600-18899600	Weak transcription	Placenta	Placenta
20	chr10:18867800-18878200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr10:18867800-18900400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr10:18867800-18916400	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr10:18868000-18896400	Weak transcription	NHEK	skin
24	chr10:18868000-18902200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr10:18868000-18916200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr10:18868200-18876800	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr10:18868200-18896600	Weak transcription	Small Intestine	intestine
28	chr10:18868200-18904800	Weak transcription	HSMMtube	muscle
29	chr10:18868400-18879200	Weak transcription	Stomach Mucosa	stomach
30	chr10:18868800-18896600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr10:18869200-18877000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr10:18869800-18910800	Weak transcription	Right Ventricle	heart
33	chr10:18870000-18884000	Weak transcription	Aorta	Aorta
34	chr10:18870200-18876400	Weak transcription	Pancreas	Pancrea
35	chr10:18870200-18892000	Weak transcription	HepG2	liver
36	chr10:18870200-18900600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr10:18870400-18884000	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr10:18870400-18884000	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr10:18870400-18894400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr10:18870600-18876400	Weak transcription	Brain Hippocampus Middle	brain
41	chr10:18870600-18884000	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr10:18870600-18884000	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr10:18870600-18908400	Weak transcription	Brain Substantia Nigra	brain
44	chr10:18870600-18916000	Weak transcription	Rectal Smooth Muscle	rectum
45	chr10:18871000-18896400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr10:18871400-18895000	Weak transcription	Fetal Brain Male	brain
47	chr10:18871600-18910000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr10:18872000-18887200	Weak transcription	Fetal Heart	heart
49	chr10:18872200-18876400	Weak transcription	Thymus	Thymus
50	chr10:18872200-18878200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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