Variant report

Variant	rs11165851
Chromosome Location	chr1:97845577-97845578
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10783061	0.89[ASW][hapmap];1.00[CEU][hapmap];0.89[LWK][hapmap];0.93[MKK][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10875074	0.92[LWK][hapmap];0.91[MKK][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs11165802	1.00[CEU][hapmap]
rs11799304	1.00[CEU][hapmap]
rs11800171	1.00[CEU][hapmap]
rs11804848	1.00[EUR][1000 genomes]
rs11805694	1.00[CEU][hapmap]
rs11806147	1.00[CEU][hapmap]
rs11810136	1.00[EUR][1000 genomes]
rs11811238	1.00[CEU][hapmap]
rs11812084	1.00[CEU][hapmap]
rs12032674	1.00[CEU][hapmap]
rs12081472	1.00[CEU][hapmap]
rs12124566	0.91[LWK][hapmap];0.89[MKK][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1607778	0.94[LWK][hapmap];0.91[YRI][hapmap]
rs17116566	1.00[CEU][hapmap]
rs17116766	1.00[CEU][hapmap]
rs17116821	1.00[CEU][hapmap]
rs17116854	1.00[CEU][hapmap]
rs17116860	1.00[CEU][hapmap]
rs17116923	1.00[EUR][1000 genomes]
rs17116940	1.00[EUR][1000 genomes]
rs17116949	1.00[EUR][1000 genomes]
rs17116957	1.00[EUR][1000 genomes]
rs17116962	1.00[EUR][1000 genomes]
rs2068642	1.00[CEU][hapmap]
rs2786514	1.00[CEU][hapmap]
rs2786525	1.00[CEU][hapmap]
rs2786526	1.00[CEU][hapmap]
rs2786527	1.00[CEU][hapmap]
rs2786528	1.00[CEU][hapmap]
rs2786531	1.00[CEU][hapmap]
rs2786532	1.00[CEU][hapmap]
rs2786535	1.00[CEU][hapmap]
rs2786538	1.00[CEU][hapmap]
rs2786539	1.00[CEU][hapmap]
rs2811161	1.00[CEU][hapmap]
rs2811162	1.00[CEU][hapmap]
rs2811163	1.00[CEU][hapmap]
rs2811164	1.00[CEU][hapmap]
rs2811165	1.00[CEU][hapmap]
rs2811166	1.00[CEU][hapmap]
rs2811217	1.00[CEU][hapmap]
rs3120632	1.00[CEU][hapmap]
rs35728010	1.00[EUR][1000 genomes]
rs4128472	1.00[CEU][hapmap]
rs4949950	1.00[CEU][hapmap];0.86[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6593647	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6681743	1.00[CEU][hapmap]
rs6700063	0.89[LWK][hapmap];0.80[MKK][hapmap];0.91[YRI][hapmap]
rs74104366	1.00[EUR][1000 genomes]
rs74105265	1.00[EUR][1000 genomes]
rs7414298	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7512345	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7521567	1.00[ASW][hapmap];1.00[CEU][hapmap];0.82[LWK][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7522200	1.00[CEU][hapmap]
rs7540621	1.00[CEU][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	nsv491816	chr1:97266403-98223619	Enhancers Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS 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
2	nsv530048	chr1:97457175-98031501	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1007950	chr1:97466488-98021146	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv533039	chr1:97665736-98343102	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv546865	chr1:97838887-97874663	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv933115	chr1:97839250-97848477	Weak transcription Enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:97794600-97848200	Weak transcription	Left Ventricle	heart
2	chr1:97802200-97848600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr1:97805800-97846800	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr1:97820200-97848200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr1:97823800-97845600	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr1:97824000-97846800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr1:97824200-97846800	Weak transcription	Fetal Intestine Small	intestine
8	chr1:97824200-97848000	Weak transcription	Ovary	ovary
9	chr1:97824400-97855000	Weak transcription	Lung	lung
10	chr1:97827600-97847200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr1:97828800-97849800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr1:97829200-97851000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr1:97830400-97848400	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr1:97831000-97874800	Weak transcription	HSMM	muscle
15	chr1:97832800-97846200	Weak transcription	Primary B cells from cord blood	blood
16	chr1:97832800-97847800	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr1:97832800-97861200	Weak transcription	Primary hematopoietic stem cells	blood
18	chr1:97833400-97846000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr1:97837200-97877600	Weak transcription	Adipose Nuclei	Adipose
20	chr1:97839200-97846000	Weak transcription	Fetal Stomach	stomach
21	chr1:97841200-97848400	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr1:97841800-97847600	Weak transcription	Stomach Smooth Muscle	stomach
23	chr1:97841800-97850000	Weak transcription	HSMMtube	muscle
24	chr1:97842000-97847400	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr1:97843000-97846000	Enhancers	NHLF	lung
26	chr1:97843200-97845600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr1:97843200-97846200	Strong transcription	Primary T cells from cord blood	blood
28	chr1:97843200-97846600	Strong transcription	Liver	Liver
29	chr1:97843600-97846400	Weak transcription	Spleen	Spleen
30	chr1:97843600-97848200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr1:97843600-97851400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr1:97843800-97846400	Enhancers	NHDF-Ad	bronchial
33	chr1:97844000-97845600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr1:97844200-97846200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:97844400-97849200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr1:97844800-97846400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr1:97844800-97849200	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr1:97845000-97845800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr1:97845000-97845800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr1:97845200-97846600	Strong transcription	Dnd41	blood
41	chr1:97845400-97849200	Weak transcription	NH-A	brain
42	chr1:97845400-97849200	Weak transcription	Osteobl	bone
43	chr1:97845400-97850000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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