Variant report

Variant	rs11031062
Chromosome Location	chr11:4151334-4151335
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:4146273..4149774-chr11:4150555..4152860,3	K562	blood:
2	chr11:4149701..4154222-chr11:4154719..4157955,5	K562	blood:

Extended variants
information (count: 23 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1015998	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11030980	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11031043	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11031070	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1662173	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs183484	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1980412	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2284452	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs232054	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2735689	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2735691	0.82[EUR][1000 genomes]
rs34356743	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3794049	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9937	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv896896	chr11:4010409-4185595	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	esv2758253	chr11:4055945-4510188	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
3	esv2759797	chr11:4055945-4510188	Active TSS Flanking Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
4	nsv428248	chr11:4055945-4510188	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
5	nsv832053	chr11:4096527-4330263	Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Enhancers ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv1053189	chr11:4123119-4359044	Strong transcription Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv1048590	chr11:4133055-4225100	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv540911	chr11:4133055-4225100	Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv1053482	chr11:4138062-4276133	Strong transcription Flanking Active TSS Genic enhancers Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11031062	RRM1	cis	Artery Tibial	GTEx

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4117600-4153000	Weak transcription	Stomach Mucosa	stomach
2	chr11:4117800-4160200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr11:4118000-4159200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr11:4118400-4156200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr11:4119400-4157600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr11:4121000-4159400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr11:4122400-4158000	Strong transcription	Dnd41	blood
8	chr11:4122800-4158000	Strong transcription	Fetal Thymus	thymus
9	chr11:4123000-4152000	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr11:4123000-4157600	Strong transcription	HUES64 Cell Line	embryonic stem cell
11	chr11:4123000-4157600	Strong transcription	Primary T helper cells fromperipheralblood	blood
12	chr11:4123000-4157800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr11:4123200-4158000	Strong transcription	Primary T cells fromperipheralblood	blood
14	chr11:4124000-4157600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
15	chr11:4124000-4157800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr11:4126600-4166600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr11:4127600-4158000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
18	chr11:4131000-4157400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
19	chr11:4132200-4151600	Strong transcription	Primary hematopoietic stem cells	blood
20	chr11:4137400-4156600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr11:4137800-4158000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr11:4138200-4160600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr11:4138400-4155600	Strong transcription	Hela-S3	cervix
24	chr11:4138600-4157600	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr11:4138600-4158000	Strong transcription	Primary B cells from peripheral blood	blood
26	chr11:4138800-4157400	Strong transcription	Primary T helper cells PMA-I stimulated	--
27	chr11:4138800-4158000	Strong transcription	HUES6 Cell Line	embryonic stem cell
28	chr11:4138800-4160400	Strong transcription	Placenta	Placenta
29	chr11:4139400-4155000	Strong transcription	HUVEC	blood vessel
30	chr11:4139600-4153800	Strong transcription	HSMM	muscle
31	chr11:4139600-4157400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr11:4139800-4158000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr11:4140200-4154200	Strong transcription	A549	lung
34	chr11:4140400-4157400	Strong transcription	Fetal Lung	lung
35	chr11:4140400-4157600	Strong transcription	K562	blood
36	chr11:4140400-4158000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
37	chr11:4141000-4155600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr11:4141000-4156200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr11:4143200-4159400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr11:4144000-4159400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr11:4144200-4158000	Strong transcription	GM12878-XiMat	blood
42	chr11:4144600-4152800	Weak transcription	Brain Angular Gyrus	brain
43	chr11:4144800-4160800	Weak transcription	Colonic Mucosa	Colon
44	chr11:4145400-4158200	Weak transcription	Esophagus	oesophagus
45	chr11:4145600-4152400	Weak transcription	Right Ventricle	heart
46	chr11:4145600-4157400	Weak transcription	Small Intestine	intestine
47	chr11:4145600-4159400	Weak transcription	Fetal Heart	heart
48	chr11:4147200-4158200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr11:4147400-4156400	Weak transcription	Fetal Kidney	kidney
50	chr11:4147600-4155200	Strong transcription	NH-A	brain

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