Variant report

Variant	rs3777491
Chromosome Location	chr6:131590766-131590767
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10046185	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs10080261	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap]
rs10484763	1.00[JPT][hapmap]
rs10484764	0.91[CHB][hapmap];0.89[JPT][hapmap];1.00[ASN][1000 genomes]
rs1190802	1.00[JPT][hapmap]
rs12525492	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12526166	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs12660246	0.89[ASN][1000 genomes]
rs12662825	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12664060	0.90[ASN][1000 genomes]
rs1322596	1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs17060099	0.91[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs17060119	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs17060127	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1746469	1.00[JPT][hapmap]
rs17574609	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.86[EUR][1000 genomes]
rs17651884	0.86[EUR][1000 genomes]
rs2224637	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs28706329	0.86[EUR][1000 genomes]
rs28841032	1.00[ASN][1000 genomes]
rs3756773	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs3777469	0.91[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs3777470	0.91[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs3777471	0.90[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs3777473	0.91[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs3777477	1.00[JPT][hapmap]
rs3777479	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs3777481	0.93[ASN][1000 genomes]
rs3777482	0.94[ASN][1000 genomes]
rs3777484	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs3777495	1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[JPT][hapmap];0.99[ASN][1000 genomes]
rs3777496	1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[JPT][hapmap];0.91[MKK][hapmap];0.81[YRI][hapmap];0.88[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3777497	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs3777498	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs3777499	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs3822867	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs59991654	0.86[EUR][1000 genomes]
rs9321279	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs9483231	0.86[EUR][1000 genomes]
rs9483232	0.86[EUR][1000 genomes]
rs9483234	0.86[EUR][1000 genomes]
rs9483235	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs9483240	0.86[EUR][1000 genomes]
rs9492863	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs9492872	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs9492876	0.86[EUR][1000 genomes]
rs9492885	0.86[EUR][1000 genomes]
rs9492888	1.00[ASN][1000 genomes]
rs9492889	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032955	chr6:131298803-131818502	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv538443	chr6:131298803-131818502	Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv886664	chr6:131443843-131754930	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv886665	chr6:131518894-131611309	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
5	nsv830808	chr6:131521115-131735320	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
6	esv1835599	chr6:131554291-131590766	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv886666	chr6:131573433-131666295	Weak transcription Genic enhancers Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:131571800-131591400	Weak transcription	Psoas Muscle	Psoas
2	chr6:131571800-131592600	Weak transcription	Fetal Thymus	thymus
3	chr6:131571800-131596800	Weak transcription	Lung	lung
4	chr6:131571800-131603000	Weak transcription	Esophagus	oesophagus
5	chr6:131571800-131614400	Weak transcription	Gastric	stomach
6	chr6:131572200-131613000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr6:131573400-131591200	Weak transcription	Liver	Liver
8	chr6:131573600-131610400	Weak transcription	Rectal Smooth Muscle	rectum
9	chr6:131574200-131601600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr6:131574200-131601600	Weak transcription	Brain Cingulate Gyrus	brain
11	chr6:131574400-131591000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr6:131575600-131602400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr6:131577000-131591400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr6:131577000-131601600	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr6:131577400-131590800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr6:131577400-131601400	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr6:131579000-131597600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr6:131579200-131590800	Weak transcription	Fetal Brain Female	brain
19	chr6:131580600-131591200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr6:131580600-131602400	Weak transcription	Small Intestine	intestine
21	chr6:131580600-131602600	Weak transcription	Right Ventricle	heart
22	chr6:131580600-131606000	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr6:131580800-131605000	Weak transcription	Fetal Heart	heart
24	chr6:131581200-131596600	Weak transcription	Pancreas	Pancrea
25	chr6:131583400-131590800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr6:131583400-131591800	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr6:131587000-131592000	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr6:131587400-131614400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr6:131587600-131591000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr6:131587600-131591000	Weak transcription	Brain Hippocampus Middle	brain
31	chr6:131587600-131602800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr6:131589000-131590800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr6:131589400-131601400	Weak transcription	Brain Angular Gyrus	brain
34	chr6:131589600-131590800	Strong transcription	Duodenum Mucosa	Duodenum
35	chr6:131590200-131590800	Strong transcription	Fetal Stomach	stomach
36	chr6:131590200-131591000	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr6:131590200-131591400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr6:131590200-131591400	Strong transcription	Fetal Intestine Large	intestine
39	chr6:131590200-131591400	Strong transcription	Ovary	ovary
40	chr6:131590200-131591800	Strong transcription	Rectal Mucosa Donor 29	rectum
41	chr6:131590200-131592000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
42	chr6:131590400-131590800	Strong transcription	Primary T helper cells fromperipheralblood	blood
43	chr6:131590400-131591000	Strong transcription	Fetal Muscle Trunk	muscle
44	chr6:131590400-131591000	Strong transcription	Fetal Muscle Leg	muscle
45	chr6:131590400-131591200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr6:131590400-131591200	Strong transcription	Primary B cells from cord blood	blood
47	chr6:131590400-131591200	ZNF genes & repeats	Aorta	Aorta
48	chr6:131590400-131591200	Strong transcription	Left Ventricle	heart
49	chr6:131590400-131591400	Strong transcription	Primary hematopoietic stem cells	blood
50	chr6:131590400-131591400	Strong transcription	Cortex derived primary cultured neurospheres	brain

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