Variant report

Variant	rs11003243
Chromosome Location	chr10:54644056-54644057
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	chr10:54577745..54578264-chr10:54643756..54644460,2	MCF-7	breast:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10508976	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10762898	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10824822	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10824823	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10824828	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10824829	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11003227	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11003232	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11003234	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11003235	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11003241	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11003242	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11003245	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11003246	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11814215	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12570523	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12775588	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1891645	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1935933	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2211446	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35037013	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35256266	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35483275	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4935366	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4935367	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4935368	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4935369	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61846796	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs67316945	0.84[AMR][1000 genomes]
rs7900222	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7905883	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7918475	0.80[EUR][1000 genomes]
rs7920023	0.83[ASN][1000 genomes]
rs7922561	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532194	chr10:53746620-54735550	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv831876	chr10:54492511-54649392	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv895404	chr10:54545590-54850707	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv831877	chr10:54565135-54764638	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv467200	chr10:54585401-54726056	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv550905	chr10:54585401-54726056	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1041940	chr10:54621342-54737528	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:54640000-54644200	Weak transcription	Fetal Brain Female	brain
2	chr10:54641000-54653600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr10:54641200-54644600	Enhancers	HUVEC	blood vessel
4	chr10:54642600-54647000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr10:54643000-54644600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr10:54643200-54644400	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr10:54643200-54644600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr10:54643800-54644200	Enhancers	Stomach Mucosa	stomach
9	chr10:54643800-54644200	Flanking Active TSS	A549	lung
10	chr10:54643800-54644200	Enhancers	Hela-S3	cervix
11	chr10:54643800-54644600	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr10:54643800-54644600	Enhancers	H1 Cell Line	embryonic stem cell
13	chr10:54643800-54644600	Enhancers	H9 Cell Line	embryonic stem cell
14	chr10:54643800-54644600	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr10:54643800-54644600	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr10:54643800-54644600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr10:54643800-54644600	Enhancers	Liver	Liver
18	chr10:54643800-54644600	Enhancers	Fetal Heart	heart
19	chr10:54643800-54644600	Enhancers	Placenta Amnion	Placenta Amnion
20	chr10:54643800-54644600	Flanking Active TSS	NHEK	skin
21	chr10:54643800-54645200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr10:54644000-54644200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
23	chr10:54644000-54644200	Active TSS	Brain Substantia Nigra	brain
24	chr10:54644000-54644200	Weak transcription	Fetal Kidney	kidney
25	chr10:54644000-54644200	Flanking Active TSS	Fetal Lung	lung
26	chr10:54644000-54644200	Enhancers	Fetal Stomach	stomach
27	chr10:54644000-54644200	Enhancers	Ovary	ovary
28	chr10:54644000-54644200	Flanking Active TSS	HepG2	liver
29	chr10:54644000-54644200	Flanking Active TSS	NH-A	brain
30	chr10:54644000-54644400	Active TSS	Breast Myoepithelial Primary Cells	Breast
31	chr10:54644000-54644400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr10:54644000-54644400	Active TSS	Brain Angular Gyrus	brain
33	chr10:54644000-54644400	Active TSS	Brain Cingulate Gyrus	brain
34	chr10:54644000-54644400	Active TSS	Fetal Intestine Large	intestine
35	chr10:54644000-54644400	Active TSS	Fetal Intestine Small	intestine
36	chr10:54644000-54644400	Weak transcription	Rectal Smooth Muscle	rectum
37	chr10:54644000-54644400	Active TSS	Stomach Smooth Muscle	stomach
38	chr10:54644000-54644600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr10:54644000-54644600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr10:54644000-54644600	Enhancers	Fetal Brain Male	brain
41	chr10:54644000-54644600	Flanking Active TSS	HMEC	breast

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