Variant report

Variant	rs10000726
Chromosome Location	chr4:120210764-120210765
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:120210640..120212674-chr4:120212958..120216371,3	MCF-7	breast:

Extended variants
information (count: 24 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10006850	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10010174	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10034661	0.95[CHB][hapmap];0.96[CHD][hapmap];0.84[GIH][hapmap];0.84[JPT][hapmap];0.82[TSI][hapmap];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1011052	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10857065	0.94[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11737086	0.81[ASW][hapmap]
rs12644843	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1511016	0.82[ASW][hapmap];0.86[CHB][hapmap];0.97[CHD][hapmap];0.84[JPT][hapmap];0.82[ASN][1000 genomes]
rs1799883	0.95[CHB][hapmap];0.96[CHD][hapmap];0.81[GIH][hapmap];0.84[JPT][hapmap];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4496567	0.82[ASN][1000 genomes]
rs4834765	1.00[ASW][hapmap];0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6823331	0.82[ASW][hapmap];0.87[CHD][hapmap];0.82[ASN][1000 genomes]
rs6841872	0.88[ASW][hapmap];0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7356185	1.00[ASW][hapmap];0.95[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7656644	0.95[CHB][hapmap];0.82[JPT][hapmap];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7676969	0.82[ASN][1000 genomes]
rs7681373	0.95[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs925387	0.81[CEU][hapmap]
rs953966	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9683450	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916641	chr4:119780023-120777320	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv1012868	chr4:120014630-120464880	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
3	nsv537232	chr4:120014630-120464880	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv428769	chr4:120205572-120363323	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10000726	SEMA6A	trans	cerebellum	SCAN

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120136200-120219200	Weak transcription	Brain Angular Gyrus	brain
2	chr4:120148200-120213600	Weak transcription	Fetal Muscle Leg	muscle
3	chr4:120177000-120213600	Weak transcription	Lung	lung
4	chr4:120177000-120220200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr4:120177000-120220200	Weak transcription	Pancreas	Pancrea
6	chr4:120177200-120213600	Weak transcription	Esophagus	oesophagus
7	chr4:120177800-120211400	Weak transcription	HepG2	liver
8	chr4:120178200-120213400	Weak transcription	Primary B cells from peripheral blood	blood
9	chr4:120178200-120213600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr4:120178200-120213800	Weak transcription	Primary B cells from cord blood	blood
11	chr4:120178600-120217600	Weak transcription	Fetal Stomach	stomach
12	chr4:120187000-120219200	Weak transcription	Right Ventricle	heart
13	chr4:120193000-120217600	Weak transcription	Psoas Muscle	Psoas
14	chr4:120193000-120219200	Weak transcription	Fetal Brain Male	brain
15	chr4:120193200-120212600	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr4:120193800-120213600	Weak transcription	Left Ventricle	heart
17	chr4:120194600-120213400	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr4:120195000-120211800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr4:120201200-120212400	Weak transcription	Placenta	Placenta
20	chr4:120201200-120220200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr4:120201200-120220200	Weak transcription	Gastric	stomach
22	chr4:120201400-120220200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr4:120201800-120213600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr4:120201800-120213800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr4:120202000-120213400	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr4:120202000-120213600	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr4:120202000-120220200	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr4:120202400-120211800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr4:120203000-120213600	Weak transcription	Primary T cells from cord blood	blood
30	chr4:120206400-120211600	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr4:120206400-120213200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr4:120206400-120213400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr4:120206400-120213400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr4:120206400-120213400	Weak transcription	Ovary	ovary
35	chr4:120206400-120217400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr4:120206400-120217600	Weak transcription	Brain Cingulate Gyrus	brain
37	chr4:120206400-120217600	Weak transcription	Fetal Intestine Small	intestine
38	chr4:120206400-120218200	Weak transcription	Aorta	Aorta
39	chr4:120206400-120219200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr4:120206400-120219600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr4:120206400-120219800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
42	chr4:120206400-120219800	Weak transcription	Brain Substantia Nigra	brain
43	chr4:120206400-120220000	Weak transcription	Colonic Mucosa	Colon
44	chr4:120206600-120212000	Weak transcription	Fetal Kidney	kidney
45	chr4:120206600-120212000	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr4:120206600-120213400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr4:120206600-120213600	Weak transcription	Brain Anterior Caudate	brain
48	chr4:120206600-120213600	Weak transcription	Fetal Intestine Large	intestine
49	chr4:120206600-120213800	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr4:120206600-120216600	Weak transcription	Stomach Smooth Muscle	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links