Variant report

Variant	rs11014990
Chromosome Location	chr10:18870101-18870102
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs10828973	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11014520	1.00[AMR][1000 genomes]
rs11014582	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11014594	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11014660	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11014696	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11014721	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11014733	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11014797	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11014800	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11014805	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11014825	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11014831	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11014961	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11014985	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11015001	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11015020	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs11015022	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11015033	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11015034	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11015046	1.00[EUR][1000 genomes]
rs11015060	1.00[EUR][1000 genomes]
rs11015065	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11015066	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11015089	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11015091	0.94[EUR][1000 genomes]
rs11015100	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs11015104	0.94[EUR][1000 genomes]
rs11015180	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11015185	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11015366	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11015514	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11015519	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11015533	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11015540	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11015592	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11492557	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11511205	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11516859	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12354739	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12355360	0.89[AMR][1000 genomes]
rs12355664	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12355670	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12356125	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12356280	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12356286	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12356533	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs12357063	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12357123	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12357491	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12358173	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12360352	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17620201	0.89[AMR][1000 genomes]
rs17622004	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17622211	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs17622520	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4279920	0.94[EUR][1000 genomes]
rs4466722	0.94[EUR][1000 genomes]
rs4497294	1.00[EUR][1000 genomes]
rs45452100	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4570480	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];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	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	esv1835982	chr10:18833550-18872699	Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	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
11	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
12	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
13	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
14	esv1845973	chr10:18841795-18872699	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
15	esv1793359	chr10:18841795-18872872	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
16	esv1801825	chr10:18853581-18872699	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 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	chr10:18844000-18871000	Weak transcription	Fetal Heart	heart
3	chr10:18846200-18899200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr10:18848400-18915800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr10:18849800-18910800	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr10:18861000-18883200	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr10:18862200-18894600	Weak transcription	HSMM	muscle
8	chr10:18862400-18878400	Strong transcription	Liver	Liver
9	chr10:18862600-18876600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr10:18863000-18894600	Weak transcription	A549	lung
11	chr10:18863000-18910800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr10:18863200-18876400	Weak transcription	Spleen	Spleen
13	chr10:18863600-18875200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr10:18863800-18902200	Weak transcription	Brain Anterior Caudate	brain
15	chr10:18864800-18870800	Strong transcription	Ovary	ovary
16	chr10:18864800-18898000	Weak transcription	Fetal Kidney	kidney
17	chr10:18865600-18870600	Strong transcription	Primary T helper cells PMA-I stimulated	--
18	chr10:18865600-18885000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr10:18866600-18899400	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr10:18866800-18870200	Strong transcription	Primary T helper cells fromperipheralblood	blood
21	chr10:18866800-18872000	Strong transcription	Left Ventricle	heart
22	chr10:18867000-18870600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr10:18867200-18871400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr10:18867200-18871600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr10:18867200-18872400	Strong transcription	Rectal Mucosa Donor 29	rectum
26	chr10:18867400-18871600	Strong transcription	Primary T cells fromperipheralblood	blood
27	chr10:18867400-18875200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr10:18867400-18876800	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr10:18867400-18877400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
30	chr10:18867600-18870600	Strong transcription	Thymus	Thymus
31	chr10:18867600-18871200	Strong transcription	Fetal Stomach	stomach
32	chr10:18867600-18894400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr10:18867600-18899600	Weak transcription	Placenta	Placenta
34	chr10:18867800-18871400	Weak transcription	NH-A	brain
35	chr10:18867800-18871600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
36	chr10:18867800-18871600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr10:18867800-18871600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr10:18867800-18871600	Weak transcription	Fetal Thymus	thymus
39	chr10:18867800-18871800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr10:18867800-18872800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr10:18867800-18874400	Weak transcription	Brain Cingulate Gyrus	brain
42	chr10:18867800-18878200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr10:18867800-18900400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr10:18867800-18916400	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr10:18868000-18872000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr10:18868000-18872200	Weak transcription	GM12878-XiMat	blood
47	chr10:18868000-18896400	Weak transcription	NHEK	skin
48	chr10:18868000-18902200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr10:18868000-18916200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr10:18868200-18870200	Weak transcription	HUES64 Cell Line	embryonic stem cell

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