Variant report

Variant	rs610293
Chromosome Location	chr11:66310380-66310381
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:66310356-66310502	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:66309086..66311433-chr11:66555544..66558511,2	K562	blood:
2	chr11:66304927..66310447-chr11:66310654..66314937,8	MCF-7	breast:
3	chr11:66297799..66301066-chr11:66306778..66311237,4	K562	blood:
4	chr11:66309047..66311384-chr11:66342148..66345525,3	K562	blood:
5	chr11:66310336..66313549-chr11:66442504..66446890,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000269990	TF binding region
ACTN3	TF binding region
ENSG00000174165	Chromatin interaction
ENSG00000173914	Chromatin interaction
ENSG00000248746	Chromatin interaction
ENSG00000173715	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1044522	0.88[ASN][1000 genomes]
rs10896126	0.94[ASN][1000 genomes]
rs11110	0.83[CHB][hapmap];0.92[JPT][hapmap]
rs1201433	0.86[ASN][1000 genomes]
rs12795774	0.85[JPT][hapmap]
rs1785640	0.89[CHB][hapmap];0.93[JPT][hapmap]
rs1791679	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1791690	0.83[YRI][hapmap]
rs1945302	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2242663	0.89[CHB][hapmap];0.92[JPT][hapmap];0.96[ASN][1000 genomes]
rs2282640	0.94[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs2511220	0.89[CHB][hapmap];0.93[JPT][hapmap]
rs2511224	0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.90[ASN][1000 genomes]
rs2511225	0.94[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs4277117	0.84[ASN][1000 genomes]
rs481296	0.85[JPT][hapmap]
rs490998	0.83[YRI][hapmap]
rs4930376	0.89[CHB][hapmap];0.92[JPT][hapmap]
rs4930381	0.81[ASN][1000 genomes]
rs4930383	0.90[ASN][1000 genomes]
rs4930384	0.95[ASN][1000 genomes]
rs544021	1.00[YRI][hapmap];0.94[AFR][1000 genomes]
rs551708	0.85[JPT][hapmap]
rs597626	1.00[YRI][hapmap];0.94[AFR][1000 genomes]
rs607736	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs624561	0.85[JPT][hapmap]
rs7123875	0.89[CHB][hapmap];0.92[JPT][hapmap]
rs7947391	0.92[JPT][hapmap]
rs7951189	0.94[CHB][hapmap];1.00[JPT][hapmap];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	nsv897771	chr11:66011280-66362997	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	124 gene(s)	inside rSNPs	diseases
2	nsv897780	chr11:66083129-66362997	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
3	nsv522277	chr11:66234023-66493825	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
4	nsv897787	chr11:66300348-66347850	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs610293	CTD-3074O7.2	cis	Muscle Skeletal	GTEx
rs610293	ACTN3	cis	Muscle Skeletal	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:66278600-66311000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr11:66278800-66312800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr11:66279000-66313000	Weak transcription	Small Intestine	intestine
4	chr11:66279200-66310400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr11:66279200-66310800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr11:66279200-66310800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr11:66279400-66311000	Weak transcription	Fetal Brain Male	brain
8	chr11:66279400-66311200	Weak transcription	Right Atrium	heart
9	chr11:66281000-66311000	Strong transcription	Fetal Stomach	stomach
10	chr11:66283400-66312800	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr11:66289000-66312800	Weak transcription	Stomach Mucosa	stomach
12	chr11:66290200-66310800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr11:66291200-66311600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr11:66291400-66311000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:66291600-66312600	Weak transcription	NHEK	skin
16	chr11:66293600-66311000	Strong transcription	Fetal Intestine Small	intestine
17	chr11:66294800-66312400	Weak transcription	Hela-S3	cervix
18	chr11:66296200-66311200	Weak transcription	Fetal Kidney	kidney
19	chr11:66299200-66311200	Weak transcription	Fetal Lung	lung
20	chr11:66302400-66312800	Weak transcription	K562	blood
21	chr11:66302600-66310600	Strong transcription	Primary T helper cells fromperipheralblood	blood
22	chr11:66302800-66310800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr11:66302800-66310800	Strong transcription	Thymus	Thymus
24	chr11:66303000-66310800	Strong transcription	Primary B cells from peripheral blood	blood
25	chr11:66303200-66310800	Strong transcription	Brain Cingulate Gyrus	brain
26	chr11:66303200-66311000	Strong transcription	Liver	Liver
27	chr11:66303200-66311000	Strong transcription	Placenta	Placenta
28	chr11:66303400-66311200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr11:66303800-66311000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr11:66303800-66312200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr11:66304800-66310400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr11:66305800-66310600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr11:66305800-66310800	Strong transcription	Fetal Thymus	thymus
34	chr11:66306000-66310400	Strong transcription	Primary neutrophils fromperipheralblood	blood
35	chr11:66306000-66310400	Strong transcription	Fetal Intestine Large	intestine
36	chr11:66306000-66310600	Strong transcription	Brain Anterior Caudate	brain
37	chr11:66306000-66310800	Strong transcription	Fetal Muscle Leg	muscle
38	chr11:66306000-66311000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr11:66306000-66311200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr11:66306000-66311200	Strong transcription	Brain Hippocampus Middle	brain
41	chr11:66306200-66310400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
42	chr11:66306200-66310400	Strong transcription	Primary T cells from cord blood	blood
43	chr11:66306200-66310400	Strong transcription	Duodenum Mucosa	Duodenum
44	chr11:66306200-66310600	Strong transcription	Primary hematopoietic stem cells	blood
45	chr11:66306200-66310600	Strong transcription	Gastric	stomach
46	chr11:66306200-66310800	Strong transcription	Pancreas	Pancrea
47	chr11:66306200-66310800	Strong transcription	Dnd41	blood
48	chr11:66306400-66310400	Strong transcription	Stomach Smooth Muscle	stomach
49	chr11:66306600-66310600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr11:66306600-66310800	Strong transcription	Colonic Mucosa	Colon

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