Variant report

Variant	rs73348359
Chromosome Location	chr6:4899825-4899826
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:4898972..4902632-chr6:4903535..4907874,4	MCF-7	breast:
2	chr6:4894595..4897390-chr6:4897999..4900907,2	MCF-7	breast:
3	chr6:4849119..4850755-chr6:4898473..4900044,2	MCF-7	breast:
4	chr6:4897821..4901952-chr6:4908622..4912007,3	MCF-7	breast:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11967088	1.00[ASN][1000 genomes]
rs1630478	1.00[ASN][1000 genomes]
rs6933949	1.00[ASN][1000 genomes]
rs6938896	1.00[ASN][1000 genomes]
rs73348363	1.00[ASN][1000 genomes]
rs7761022	1.00[ASN][1000 genomes]
rs7769900	1.00[ASN][1000 genomes]
rs7771142	1.00[ASN][1000 genomes]
rs7771355	1.00[ASN][1000 genomes]
rs808590	1.00[ASN][1000 genomes]
rs808594	1.00[ASN][1000 genomes]
rs808595	1.00[ASN][1000 genomes]
rs808596	1.00[ASN][1000 genomes]
rs808597	1.00[ASN][1000 genomes]
rs808599	1.00[ASN][1000 genomes]
rs808601	1.00[ASN][1000 genomes]
rs808602	1.00[ASN][1000 genomes]
rs808604	1.00[ASN][1000 genomes]
rs808618	1.00[ASN][1000 genomes]
rs808625	1.00[ASN][1000 genomes]
rs808626	1.00[ASN][1000 genomes]
rs808627	1.00[ASN][1000 genomes]
rs808628	1.00[ASN][1000 genomes]
rs808630	1.00[ASN][1000 genomes]
rs808632	1.00[ASN][1000 genomes]
rs809471	1.00[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	nsv1023527	chr6:4729592-5387176	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	esv2422499	chr6:4745428-5073222	Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv830577	chr6:4834567-5050544	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv970734	chr6:4898790-4906391	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4878200-4905200	Weak transcription	Colon Smooth Muscle	Colon
2	chr6:4879600-4906200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr6:4880400-4907800	Weak transcription	Small Intestine	intestine
4	chr6:4882800-4909000	Weak transcription	Brain Anterior Caudate	brain
5	chr6:4884800-4903800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr6:4885000-4908200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr6:4887200-4901400	Weak transcription	HSMMtube	muscle
8	chr6:4888000-4906400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr6:4889200-4906400	Weak transcription	NHLF	lung
10	chr6:4890200-4901800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr6:4890600-4913800	Weak transcription	Hela-S3	cervix
12	chr6:4890800-4900600	Weak transcription	NH-A	brain
13	chr6:4891200-4905600	Weak transcription	Fetal Kidney	kidney
14	chr6:4891200-4907400	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr6:4891400-4900400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr6:4891400-4906400	Weak transcription	Fetal Heart	heart
17	chr6:4892800-4906400	Weak transcription	HUVEC	blood vessel
18	chr6:4892800-4906600	Weak transcription	Osteobl	bone
19	chr6:4893200-4912600	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr6:4893400-4903400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr6:4893400-4903400	Weak transcription	Brain Cingulate Gyrus	brain
22	chr6:4893400-4906600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr6:4893400-4906600	Weak transcription	Thymus	Thymus
24	chr6:4893400-4909000	Weak transcription	Brain Angular Gyrus	brain
25	chr6:4893600-4901200	Weak transcription	Pancreas	Pancrea
26	chr6:4893600-4905000	Weak transcription	Colonic Mucosa	Colon
27	chr6:4893600-4910200	Weak transcription	Esophagus	oesophagus
28	chr6:4893600-4914000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr6:4894600-4904000	Weak transcription	Brain Hippocampus Middle	brain
30	chr6:4894600-4905600	Weak transcription	Right Ventricle	heart
31	chr6:4894800-4901200	Weak transcription	Liver	Liver
32	chr6:4894800-4906600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr6:4895000-4917000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr6:4895200-4901800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr6:4895200-4909000	Weak transcription	Adipose Nuclei	Adipose
36	chr6:4896000-4906600	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr6:4896400-4903400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr6:4896600-4900000	Strong transcription	Primary T helper cells fromperipheralblood	blood
39	chr6:4896600-4900400	Strong transcription	HUES64 Cell Line	embryonic stem cell
40	chr6:4896800-4902000	Weak transcription	Gastric	stomach
41	chr6:4896800-4903800	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr6:4896800-4906600	Weak transcription	Spleen	Spleen
43	chr6:4896800-4907200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr6:4897000-4906400	Weak transcription	Fetal Thymus	thymus
45	chr6:4897000-4906600	Weak transcription	Aorta	Aorta
46	chr6:4897600-4900000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr6:4897800-4900400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
48	chr6:4897800-4906200	Weak transcription	Duodenum Mucosa	Duodenum
49	chr6:4898000-4900200	Strong transcription	Fetal Intestine Large	intestine
50	chr6:4898000-4907000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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