Variant report

Variant	rs11042831
Chromosome Location	chr11:10497967-10497968
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	chr11:10495930..10498423-chr11:10500094..10502413,3	K562	blood:
2	chr11:10493608..10495918-chr11:10496985..10499261,2	K562	blood:

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11042827	0.89[EUR][1000 genomes]
rs11042828	1.00[CEU][hapmap];0.85[CHB][hapmap];0.97[EUR][1000 genomes]
rs11042829	0.97[EUR][1000 genomes]
rs11042832	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11042833	1.00[CEU][hapmap];0.86[CHB][hapmap];0.84[JPT][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11042842	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12221503	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12295125	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs16907858	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3741043	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7107588	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430319	chr11:10027543-10711224	Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv896990	chr11:10458596-10514707	Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:10473200-10512000	Weak transcription	Aorta	Aorta
2	chr11:10478400-10500000	Weak transcription	Fetal Intestine Small	intestine
3	chr11:10478400-10502800	Weak transcription	Pancreas	Pancrea
4	chr11:10478800-10511600	Weak transcription	Psoas Muscle	Psoas
5	chr11:10479000-10502800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr11:10479800-10519400	Weak transcription	Rectal Smooth Muscle	rectum
7	chr11:10483400-10500600	Weak transcription	Stomach Smooth Muscle	stomach
8	chr11:10484200-10509600	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr11:10484200-10514800	Weak transcription	Colonic Mucosa	Colon
10	chr11:10485000-10515200	Weak transcription	Liver	Liver
11	chr11:10485200-10501000	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr11:10485400-10498600	Weak transcription	GM12878-XiMat	blood
13	chr11:10485600-10500400	Weak transcription	Adipose Nuclei	Adipose
14	chr11:10485600-10500800	Weak transcription	Fetal Muscle Leg	muscle
15	chr11:10485600-10508200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr11:10485800-10498400	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr11:10485800-10511600	Weak transcription	Osteobl	bone
18	chr11:10486000-10504800	Weak transcription	Duodenum Mucosa	Duodenum
19	chr11:10486200-10501200	Weak transcription	NHEK	skin
20	chr11:10486600-10498800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr11:10486600-10502600	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr11:10486800-10509600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr11:10486800-10515600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr11:10487200-10503000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr11:10487200-10506200	Weak transcription	Dnd41	blood
26	chr11:10487400-10500400	Weak transcription	Esophagus	oesophagus
27	chr11:10488600-10498200	Weak transcription	Fetal Stomach	stomach
28	chr11:10488600-10498400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr11:10489000-10512600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr11:10489200-10500000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr11:10494200-10510000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr11:10494400-10500200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr11:10494600-10509600	Strong transcription	Primary T cells fromperipheralblood	blood
34	chr11:10494800-10498000	Strong transcription	Monocytes-CD14+_RO01746	blood
35	chr11:10494800-10498400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
36	chr11:10495000-10509600	Strong transcription	Primary B cells from cord blood	blood
37	chr11:10495000-10528000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr11:10495200-10498000	Strong transcription	Thymus	Thymus
39	chr11:10495200-10510800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr11:10495200-10530800	Strong transcription	Primary T cells from cord blood	blood
41	chr11:10495400-10498400	Weak transcription	K562	blood
42	chr11:10495400-10509800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr11:10495400-10511800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr11:10495600-10498200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr11:10495600-10510600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr11:10495600-10516400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr11:10495800-10500200	Weak transcription	Gastric	stomach
48	chr11:10495800-10529800	Strong transcription	Primary T helper cells fromperipheralblood	blood
49	chr11:10496000-10503000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr11:10496200-10509800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood

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