Variant report

Variant	rs10044595
Chromosome Location	chr5:52211674-52211675
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:51960655..51961277-chr5:52210932..52211824,2	MCF-7	breast:
2	chr5:52080967..52081532-chr5:52210924..52211709,2	MCF-7	breast:
3	chr5:52082232..52084006-chr5:52211443..52214627,3	MCF-7	breast:
4	chr5:52082398..52083133-chr5:52210696..52211846,7	MCF-7	breast:
5	chr5:50258548..50259403-chr5:52210902..52211872,2	K562	blood:
6	chr14:61170328..61170942-chr5:52211099..52211691,2	MCF-7	breast:
7	chr5:52082422..52083413-chr5:52210723..52211912,23	MCF-7	breast:
8	chr5:51960252..51961162-chr5:52211037..52211737,2	MCF-7	breast:
9	chr5:51989137..51989978-chr5:52210928..52211897,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000213949	Chromatin interaction
ENSG00000248898	Chromatin interaction
ENSG00000152684	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10039713	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10040519	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10043218	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10054155	0.84[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10059882	1.00[AMR][1000 genomes]
rs10076207	0.84[YRI][hapmap];1.00[AMR][1000 genomes]
rs11948400	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28691604	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6867514	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6889474	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv462187	chr5:51758804-52333420	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv598163	chr5:51758804-52333420	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv471013	chr5:51779197-52339114	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
4	nsv830295	chr5:52084532-52257696	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	nsv949005	chr5:52188028-52808229	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
6	nsv830296	chr5:52209528-52410253	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:52142000-52220200	Weak transcription	Fetal Muscle Trunk	muscle
2	chr5:52166800-52214800	Weak transcription	Spleen	Spleen
3	chr5:52181200-52214000	Weak transcription	Placenta	Placenta
4	chr5:52188800-52218200	Weak transcription	Duodenum Mucosa	Duodenum
5	chr5:52188800-52228200	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr5:52191600-52218400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr5:52192200-52218400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr5:52192200-52219600	Weak transcription	Fetal Stomach	stomach
9	chr5:52192200-52220000	Weak transcription	Lung	lung
10	chr5:52193200-52218400	Weak transcription	Fetal Kidney	kidney
11	chr5:52195200-52218400	Weak transcription	Fetal Intestine Large	intestine
12	chr5:52195200-52219000	Weak transcription	Fetal Muscle Leg	muscle
13	chr5:52198400-52213600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr5:52198400-52218200	Weak transcription	Aorta	Aorta
15	chr5:52200200-52213600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr5:52202200-52252200	Weak transcription	Small Intestine	intestine
17	chr5:52203400-52211800	Weak transcription	Stomach Smooth Muscle	stomach
18	chr5:52206200-52214800	Weak transcription	Left Ventricle	heart
19	chr5:52206400-52240800	Weak transcription	Rectal Smooth Muscle	rectum
20	chr5:52211200-52212800	Weak transcription	Colon Smooth Muscle	Colon
21	chr5:52211400-52212200	Weak transcription	Liver	Liver
22	chr5:52211400-52212400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr5:52211400-52212800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr5:52211400-52212800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr5:52211400-52212800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr5:52211400-52213400	Weak transcription	Hela-S3	cervix
27	chr5:52211400-52213600	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr5:52211400-52214400	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr5:52211400-52216600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr5:52211400-52216600	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr5:52211400-52216600	Weak transcription	NHLF	lung
32	chr5:52211400-52216600	Weak transcription	Osteobl	bone
33	chr5:52211400-52218200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr5:52211400-52218200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr5:52211400-52218200	Weak transcription	Adipose Nuclei	Adipose
36	chr5:52211400-52218400	Weak transcription	Primary T cells from cord blood	blood
37	chr5:52211400-52220200	Weak transcription	Fetal Intestine Small	intestine
38	chr5:52211400-52221200	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr5:52211400-52239400	Weak transcription	Right Ventricle	heart
40	chr5:52211400-52240200	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr5:52211600-52211800	Strong transcription	Dnd41	blood
42	chr5:52211600-52216600	Weak transcription	NHDF-Ad	bronchial
43	chr5:52211600-52218200	Weak transcription	Fetal Lung	lung
44	chr5:52211600-52218400	Weak transcription	HSMMtube	muscle
45	chr5:52211600-52244400	Weak transcription	HepG2	liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links