Variant report

Variant	rs11024619
Chromosome Location	chr11:18333247-18333248
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:18331161..18334022-chr11:18415783..18418512,2	MCF-7	breast:
2	chr11:18331919..18334523-chr11:18342136..18345007,3	MCF-7	breast:
3	chr11:18315973..18319669-chr11:18330694..18333662,3	K562	blood:

Variant related genes	Relation type
ENSG00000110756	Chromatin interaction
ENSG00000110768	Chromatin interaction
ENSG00000134333	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10832918	0.80[ASN][1000 genomes]
rs11024605	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11024607	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11024609	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11024610	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11024611	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11024612	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11024615	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11024621	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11024625	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11024632	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12221676	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12224608	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1869786	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1869787	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3781944	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4150530	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4150572	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4150626	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4150635	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4150656	0.83[AFR][1000 genomes]
rs4150658	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4237721	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4344464	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4366463	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4586132	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4756938	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4757639	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4757642	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4757646	0.89[AMR][1000 genomes]
rs60677587	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7113249	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7122032	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7128017	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7128146	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73430865	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73430866	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73430881	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73430888	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73430894	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73432712	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73434649	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9783296	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[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	nsv949248	chr11:17791822-18692687	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
2	nsv428569	chr11:18194030-18350869	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv933836	chr11:18300254-18440933	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
4	nsv553633	chr11:18311701-19058451	Weak transcription Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18287600-18334000	Weak transcription	Right Atrium	heart
2	chr11:18298200-18333800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:18299600-18334200	Strong transcription	HUES6 Cell Line	embryonic stem cell
4	chr11:18300000-18334400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr11:18300200-18333600	Strong transcription	Primary T helper cells fromperipheralblood	blood
6	chr11:18300200-18334000	Strong transcription	HUES64 Cell Line	embryonic stem cell
7	chr11:18300200-18334800	Strong transcription	HUES48 Cell Line	embryonic stem cell
8	chr11:18300200-18336000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr11:18300600-18334000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr11:18301000-18334400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr11:18303000-18334800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr11:18303200-18334800	Strong transcription	Primary T helper cells PMA-I stimulated	--
13	chr11:18303400-18335000	Strong transcription	Primary T cells fromperipheralblood	blood
14	chr11:18305600-18335000	Strong transcription	Primary T cells from cord blood	blood
15	chr11:18310800-18334000	Weak transcription	Esophagus	oesophagus
16	chr11:18311800-18343000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr11:18312800-18334400	Strong transcription	Duodenum Smooth Muscle	Duodenum
18	chr11:18316200-18333800	Weak transcription	Fetal Heart	heart
19	chr11:18317200-18342200	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr11:18319000-18334000	Weak transcription	NHLF	lung
21	chr11:18320600-18337400	Weak transcription	Gastric	stomach
22	chr11:18321200-18334400	Strong transcription	Fetal Thymus	thymus
23	chr11:18324200-18333600	Strong transcription	Fetal Muscle Trunk	muscle
24	chr11:18324400-18334400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr11:18324400-18334400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr11:18325400-18333600	Strong transcription	Fetal Muscle Leg	muscle
27	chr11:18327000-18333600	Strong transcription	Fetal Intestine Large	intestine
28	chr11:18327800-18334200	Strong transcription	K562	blood
29	chr11:18327800-18342200	Weak transcription	Colon Smooth Muscle	Colon
30	chr11:18327800-18342200	Weak transcription	HUVEC	blood vessel
31	chr11:18328200-18333400	Strong transcription	NHDF-Ad	bronchial
32	chr11:18329600-18333800	Strong transcription	Brain Germinal Matrix	brain
33	chr11:18329600-18334800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr11:18329800-18333600	Strong transcription	Fetal Stomach	stomach
35	chr11:18329800-18333800	Weak transcription	Stomach Mucosa	stomach
36	chr11:18330200-18333400	Weak transcription	Pancreas	Pancrea
37	chr11:18330200-18340000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr11:18330200-18340800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr11:18331000-18341000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr11:18331000-18341600	Weak transcription	Fetal Lung	lung
41	chr11:18331000-18342200	Weak transcription	Right Ventricle	heart
42	chr11:18331600-18335000	Genic enhancers	Primary B cells from peripheral blood	blood
43	chr11:18331600-18341600	Weak transcription	Psoas Muscle	Psoas
44	chr11:18331800-18333800	Weak transcription	Fetal Intestine Small	intestine
45	chr11:18331800-18334000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr11:18331800-18335600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr11:18331800-18335600	Weak transcription	Aorta	Aorta
48	chr11:18331800-18336600	Weak transcription	Spleen	Spleen
49	chr11:18332000-18333400	Genic enhancers	GM12878-XiMat	blood
50	chr11:18332000-18341800	Weak transcription	Sigmoid Colon	Sigmoid Colon

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