Variant report

Variant	rs11234961
Chromosome Location	chr11:86804081-86804082
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:86803340..86806124-chr11:86810035..86812567,2	K562	blood:
2	chr11:86664322..86666678-chr11:86802389..86805418,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000174804	Chromatin interaction
ENSG00000246523	Chromatin interaction

Extended variants
information (count: 85 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10792897	0.81[EUR][1000 genomes]
rs10792906	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10792908	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10792909	0.87[CHB][hapmap];0.89[JPT][hapmap];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10792910	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10898580	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10898586	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10898587	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10898588	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10898589	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10898590	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10898593	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10898594	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10898595	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10898600	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10898603	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10898604	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10898605	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10898606	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10898607	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10898608	0.87[ASN][1000 genomes]
rs10898609	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10898610	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10898613	0.88[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs10898619	0.88[CEU][hapmap];0.83[CHB][hapmap];0.88[JPT][hapmap]
rs11234907	0.83[EUR][1000 genomes]
rs11234911	1.00[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];0.86[EUR][1000 genomes]
rs11234923	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11234925	1.00[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11234930	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11234932	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11234933	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11234937	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11234940	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11234941	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11234945	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11234946	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11234950	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11234952	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11234958	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11234962	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11234964	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11234965	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11234966	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11234968	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11234969	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11234972	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11234976	0.98[EUR][1000 genomes]
rs11234977	0.85[CEU][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11234982	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11234989	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11234991	0.84[ASN][1000 genomes]
rs11234993	0.85[ASN][1000 genomes]
rs11234996	0.88[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs11533276	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11820668	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12223784	0.87[CEU][hapmap];0.94[CHB][hapmap];0.90[JPT][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12224600	0.88[CEU][hapmap];0.88[JPT][hapmap]
rs12360980	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12363760	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1531144	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1968741	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2512325	0.81[CHB][hapmap]
rs6592334	0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs67946471	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7117731	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7124448	0.88[CEU][hapmap];0.88[CHB][hapmap];0.88[JPT][hapmap];0.80[ASN][1000 genomes]
rs7127557	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9666468	0.98[EUR][1000 genomes];0.87[ASN][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	nsv1044081	chr11:86133641-86868560	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv541118	chr11:86133641-86868560	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv1037042	chr11:86586876-86978492	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers 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	16 gene(s)	inside rSNPs	diseases
4	nsv541119	chr11:86586876-86978492	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv898058	chr11:86754948-86889284	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv898059	chr11:86754948-86949369	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1043562	chr11:86755535-87547185	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
8	nsv541120	chr11:86755535-87547185	Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
9	nsv1046288	chr11:86757573-87158571	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
10	esv1844274	chr11:86776992-86872908	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv468776	chr11:86788716-86826422	ZNF genes & repeats Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv555706	chr11:86788716-86826422	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv1045057	chr11:86794670-87033779	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
14	nsv541121	chr11:86794670-87033779	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
15	nsv468777	chr11:86794856-86985581	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
16	nsv555707	chr11:86794856-86985581	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86770400-86808200	Weak transcription	HUVEC	blood vessel
2	chr11:86774800-86806400	Weak transcription	Small Intestine	intestine
3	chr11:86776600-86815600	Weak transcription	HSMMtube	muscle
4	chr11:86783000-86814000	Weak transcription	Hela-S3	cervix
5	chr11:86787400-86819600	Weak transcription	NH-A	brain
6	chr11:86787600-86804200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr11:86787600-86825200	Weak transcription	Brain Substantia Nigra	brain
8	chr11:86787800-86817400	Weak transcription	Colon Smooth Muscle	Colon
9	chr11:86787800-86819400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr11:86788000-86804200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr11:86788000-86804200	Weak transcription	Aorta	Aorta
12	chr11:86788000-86807000	Weak transcription	Pancreas	Pancrea
13	chr11:86788000-86808600	Weak transcription	Left Ventricle	heart
14	chr11:86788200-86808400	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr11:86788200-86817800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr11:86788200-86824600	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr11:86788200-86830400	Weak transcription	Right Ventricle	heart
18	chr11:86788400-86807800	Weak transcription	Brain Hippocampus Middle	brain
19	chr11:86788600-86804200	Weak transcription	Placenta	Placenta
20	chr11:86788600-86806000	Weak transcription	A549	lung
21	chr11:86788600-86836400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr11:86789200-86805600	Weak transcription	Stomach Smooth Muscle	stomach
23	chr11:86792800-86804200	Weak transcription	Ovary	ovary
24	chr11:86792800-86808800	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr11:86793200-86806200	Weak transcription	Adipose Nuclei	Adipose
26	chr11:86793200-86808400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr11:86793800-86808400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr11:86797600-86804200	Weak transcription	Thymus	Thymus
29	chr11:86798000-86804200	Weak transcription	K562	blood
30	chr11:86798000-86804400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr11:86798000-86820000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr11:86798200-86817800	Weak transcription	Fetal Thymus	thymus
33	chr11:86798400-86804200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr11:86798400-86821600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr11:86799400-86805600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr11:86799400-86817800	Weak transcription	Psoas Muscle	Psoas
37	chr11:86799600-86821000	Weak transcription	Primary B cells from cord blood	blood
38	chr11:86800400-86808800	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr11:86800400-86808800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr11:86801000-86804200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr11:86801000-86816200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr11:86801600-86817800	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr11:86801800-86804400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr11:86802200-86804600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr11:86802200-86804600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr11:86802400-86804400	ZNF genes & repeats	Primary T cells from cord blood	blood
47	chr11:86802600-86804400	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
48	chr11:86803200-86804400	ZNF genes & repeats	Liver	Liver
49	chr11:86803200-86804400	Strong transcription	HepG2	liver
50	chr11:86803200-86804600	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood

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