Variant report

Variant	rs2167178
Chromosome Location	chr3:150065289-150065290
allele	A/G
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:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:150058583..150074355-chr3:150124068..150134356,51	MCF-7	breast:
2	chr3:150063831..150066264-chr3:150212112..150214058,2	MCF-7	breast:
3	chr3:150061653..150065321-chr3:150319922..150322637,3	MCF-7	breast:
4	chr3:149955913..149960046-chr3:150062431..150067841,6	MCF-7	breast:
5	chr3:149965841..149967659-chr3:150065156..150067376,2	MCF-7	breast:
6	chr3:150063236..150065719-chr3:150124332..150126127,2	K562	blood:
7	chr3:150024822..150026384-chr3:150064779..150066444,2	MCF-7	breast:
8	chr3:150064599..150068049-chr3:150092339..150097012,5	MCF-7	breast:
9	chr3:150064573..150066847-chr3:150070283..150072225,2	K562	blood:
10	chr3:150059766..150072041-chr3:150122033..150133129,50	MCF-7	breast:
11	chr3:150064573..150066917-chr3:150070283..150073113,2	K562	blood:
12	chr3:150061806..150067641-chr3:150085085..150089827,11	MCF-7	breast:
13	chr3:150064216..150066943-chr3:150260287..150264340,3	MCF-7	breast:
14	chr11:1753546..1755772-chr3:150063275..150066246,2	MCF-7	breast:
15	chr3:150023976..150025654-chr3:150064585..150066377,2	MCF-7	breast:
16	chr3:150028795..150040018-chr3:150059749..150069074,18	MCF-7	breast:
17	chr3:150033272..150039330-chr3:150061780..150068166,12	MCF-7	breast:
18	chr3:150063392..150066331-chr3:150098048..150099992,2	MCF-7	breast:
19	chr3:150047065..150050412-chr3:150064915..150067808,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000198843	Chromatin interaction
ENSG00000244541	Chromatin interaction
ENSG00000196428	Chromatin interaction
ENSG00000120742	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11924208	1.00[CHB][hapmap];0.92[JPT][hapmap];0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11929253	0.82[ASN][1000 genomes]
rs1962345	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60243617	0.84[ASN][1000 genomes]
rs62271370	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7633948	0.85[JPT][hapmap];0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7639816	0.82[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829755	chr3:149992023-150156001	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:150053000-150066600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:150058200-150067600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr3:150058400-150066000	Weak transcription	Aorta	Aorta
4	chr3:150058400-150067400	Weak transcription	Right Atrium	heart
5	chr3:150060800-150067400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr3:150060800-150067400	Weak transcription	Fetal Muscle Trunk	muscle
7	chr3:150061800-150065400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr3:150061800-150065400	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr3:150061800-150065600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr3:150061800-150065600	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr3:150061800-150065600	Enhancers	Fetal Lung	lung
12	chr3:150061800-150065800	Enhancers	Fetal Kidney	kidney
13	chr3:150061800-150071000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr3:150061800-150071000	Enhancers	HMEC	breast
15	chr3:150062600-150067600	Weak transcription	Fetal Stomach	stomach
16	chr3:150062800-150068000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr3:150063200-150066600	Enhancers	Hela-S3	cervix
18	chr3:150063400-150066000	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr3:150063400-150067800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr3:150063600-150065400	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr3:150064000-150066200	Flanking Active TSS	NHDF-Ad	bronchial
22	chr3:150064000-150066600	Enhancers	HSMM	muscle
23	chr3:150064200-150066200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr3:150064200-150066400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr3:150064200-150068000	Enhancers	Placenta Amnion	Placenta Amnion
26	chr3:150064400-150066200	Enhancers	NH-A	brain
27	chr3:150064400-150066400	Flanking Active TSS	A549	lung
28	chr3:150064400-150066800	Enhancers	Fetal Heart	heart
29	chr3:150064400-150067200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr3:150064400-150069400	Enhancers	HSMMtube	muscle
31	chr3:150064600-150065400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr3:150064600-150065600	Enhancers	Placenta	Placenta
33	chr3:150064600-150065600	Enhancers	Stomach Smooth Muscle	stomach
34	chr3:150064600-150066200	Flanking Active TSS	NHEK	skin
35	chr3:150064600-150067400	Enhancers	NHLF	lung
36	chr3:150064800-150065400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
37	chr3:150064800-150065400	Enhancers	Fetal Intestine Large	intestine
38	chr3:150064800-150065600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr3:150064800-150065600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr3:150064800-150065600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr3:150064800-150065800	Enhancers	H9 Cell Line	embryonic stem cell
42	chr3:150064800-150065800	Enhancers	Left Ventricle	heart
43	chr3:150064800-150068000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr3:150064800-150068000	Enhancers	Adipose Nuclei	Adipose
45	chr3:150064800-150068600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr3:150065000-150066000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr3:150065000-150066200	Enhancers	Sigmoid Colon	Sigmoid Colon
48	chr3:150065000-150066600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr3:150065000-150068800	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr3:150065200-150065400	Bivalent Enhancer	Small Intestine	intestine

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