Variant report

Variant	rs3751066
Chromosome Location	chr11:8947283-8947284
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	chr11:8941546..8948177-chr11:8950032..8955141,6	MCF-7	breast:
2	chr11:8940620..8943003-chr11:8946457..8949397,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000176029	Chromatin interaction

Extended variants
information (count: 89 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs10219366	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10279	0.83[YRI][hapmap]
rs10734639	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10743094	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10769974	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10769976	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10769977	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10840150	0.89[AMR][1000 genomes]
rs10840151	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10840153	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10840154	0.92[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10840155	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10840156	0.92[CEU][hapmap];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11042127	0.92[YRI][hapmap]
rs11042128	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11042129	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11042131	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12798311	0.83[EUR][1000 genomes]
rs1347016	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2016844	0.91[CEU][hapmap];0.83[EUR][1000 genomes]
rs2043218	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2056903	0.91[CEU][hapmap];0.83[EUR][1000 genomes]
rs2116510	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2116511	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2163625	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2246878	0.83[EUR][1000 genomes]
rs2247038	0.83[EUR][1000 genomes]
rs2316523	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2316541	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2568034	0.92[CEU][hapmap]
rs2568042	0.91[CEU][hapmap]
rs2568069	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2568074	0.83[EUR][1000 genomes]
rs2568075	0.83[EUR][1000 genomes]
rs2568077	0.83[EUR][1000 genomes]
rs2568079	0.91[CEU][hapmap];0.81[EUR][1000 genomes]
rs2568081	0.96[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2568086	0.82[AMR][1000 genomes]
rs2568087	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2568088	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2653556	0.87[CEU][hapmap]
rs2653565	0.91[CEU][hapmap]
rs2653590	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2653594	0.89[EUR][1000 genomes]
rs2653597	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2653601	0.91[CEU][hapmap];0.83[EUR][1000 genomes]
rs2653604	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2653611	0.81[EUR][1000 genomes]
rs2742486	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2742487	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2742488	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2742489	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2742491	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2742493	0.96[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2742494	0.85[EUR][1000 genomes]
rs2742495	0.92[CEU][hapmap];0.80[EUR][1000 genomes]
rs2742496	0.91[CEU][hapmap]
rs2742497	0.91[CEU][hapmap];0.81[EUR][1000 genomes]
rs2742504	0.81[EUR][1000 genomes]
rs2742505	0.81[EUR][1000 genomes]
rs2742512	0.83[EUR][1000 genomes]
rs2742513	0.83[EUR][1000 genomes]
rs2742514	1.00[CEU][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2742519	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2742521	0.92[CEU][hapmap]
rs3751063	0.91[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3751064	0.84[YRI][hapmap]
rs3751065	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3751068	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3763911	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3763912	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3763913	0.82[YRI][hapmap]
rs3763914	0.91[YRI][hapmap]
rs4909951	0.91[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4910179	0.81[AFR][1000 genomes]
rs4910181	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6486061	0.84[JPT][hapmap]
rs7106152	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7932377	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7942026	0.84[EUR][1000 genomes]
rs7951226	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs909464	0.83[EUR][1000 genomes]
rs9300096	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs982273	0.88[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758256	chr11:8784813-9009573	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	esv2759803	chr11:8784813-9009573	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv435923	chr11:8839325-9000602	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv832062	chr11:8849295-9009472	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
5	esv3413845	chr11:8887279-9285127	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs3751066	C11orf17	cis	multi-tissue	Pritchard
rs3751066	C11orf17	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8933400-8947800	Weak transcription	Small Intestine	intestine
2	chr11:8934000-8952200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr11:8934200-8948800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr11:8936400-8951200	Weak transcription	Right Atrium	heart
5	chr11:8936600-8948600	Strong transcription	Fetal Thymus	thymus
6	chr11:8936600-8949000	Strong transcription	Fetal Stomach	stomach
7	chr11:8936600-8954000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr11:8936800-8947600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr11:8937000-8947600	Strong transcription	Cortex derived primary cultured neurospheres	brain
10	chr11:8937000-8948200	Strong transcription	Fetal Brain Female	brain
11	chr11:8937200-8947400	Strong transcription	Thymus	Thymus
12	chr11:8937800-8947400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr11:8938000-8947400	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr11:8938000-8947600	Strong transcription	Brain Cingulate Gyrus	brain
15	chr11:8939000-8947400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr11:8939000-8947600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr11:8939000-8948200	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr11:8939400-8948200	Strong transcription	Skeletal Muscle Male	skeletal muscle
19	chr11:8939400-8948800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr11:8939800-8947600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr11:8939800-8947600	Strong transcription	Lung	lung
22	chr11:8940000-8948400	Strong transcription	Spleen	Spleen
23	chr11:8940200-8948600	Strong transcription	Stomach Smooth Muscle	stomach
24	chr11:8940200-8949200	Weak transcription	Primary B cells from cord blood	blood
25	chr11:8940800-8947400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr11:8940800-8949200	Weak transcription	Fetal Heart	heart
27	chr11:8941200-8953400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr11:8941200-8956200	Weak transcription	K562	blood
29	chr11:8942000-8948800	Weak transcription	Rectal Smooth Muscle	rectum
30	chr11:8942400-8950200	Weak transcription	Esophagus	oesophagus
31	chr11:8942400-8959000	Weak transcription	Fetal Kidney	kidney
32	chr11:8942600-8948800	Weak transcription	Colonic Mucosa	Colon
33	chr11:8943200-8950000	Weak transcription	GM12878-XiMat	blood
34	chr11:8943200-8950800	Weak transcription	Primary T cells from cord blood	blood
35	chr11:8943800-8969200	Weak transcription	Primary hematopoietic stem cells	blood
36	chr11:8944000-8952200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr11:8944200-8956400	Weak transcription	HUVEC	blood vessel
38	chr11:8944600-8950000	Weak transcription	HMEC	breast
39	chr11:8944600-8950000	Weak transcription	HSMMtube	muscle
40	chr11:8944600-8950800	Weak transcription	HepG2	liver
41	chr11:8944600-8985000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr11:8944800-8949000	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr11:8944800-8949200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr11:8944800-8949600	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr11:8944800-8950200	Weak transcription	Placenta	Placenta
46	chr11:8944800-8954000	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr11:8944800-8956400	Weak transcription	Fetal Intestine Large	intestine
48	chr11:8945000-8948000	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr11:8945000-8948000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr11:8945000-8948600	Weak transcription	Left Ventricle	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links