Variant report

Variant	rs17799604
Chromosome Location	chr8:104229824-104229825
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:104220760..104222737-chr8:104228002..104230540,2	MCF-7	breast:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1138873	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12541167	1.00[CHB][hapmap];0.89[JPT][hapmap];0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12543038	1.00[CHB][hapmap];0.89[JPT][hapmap];0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12548629	0.81[ASN][1000 genomes]
rs13275377	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs13278361	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs13278540	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13279226	0.92[ASN][1000 genomes]
rs1353212	0.95[CHB][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1353213	0.94[CHB][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1403293	0.80[AMR][1000 genomes]
rs1494278	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1522707	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs16870243	0.88[ASN][1000 genomes]
rs16870245	0.88[ASN][1000 genomes]
rs16870249	0.88[ASN][1000 genomes]
rs17205332	1.00[CHB][hapmap];0.95[JPT][hapmap];0.85[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1982892	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1982893	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2220825	0.94[CHB][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs3104031	0.80[AMR][1000 genomes]
rs3107646	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3116457	0.83[AMR][1000 genomes]
rs3133824	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs34185273	0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs34201011	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs34273148	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs34337822	0.88[ASN][1000 genomes]
rs4734693	0.86[ASN][1000 genomes]
rs4734695	0.83[ASN][1000 genomes]
rs56666894	0.81[AFR][1000 genomes]
rs7002269	0.95[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs9656787	1.00[CHB][hapmap];0.91[ASN][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	nsv831413	chr8:104085141-104269789	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
2	nsv429931	chr8:104097396-104878014	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
3	esv1848810	chr8:104128496-104369288	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
4	esv1844303	chr8:104128696-104369090	Genic enhancers Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
5	esv14660	chr8:104182119-104245529	ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv1015965	chr8:104192086-104361108	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104222400-104240800	Weak transcription	Gastric	stomach
2	chr8:104222400-104241200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr8:104222800-104240800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr8:104222800-104241000	Weak transcription	NHDF-Ad	bronchial
5	chr8:104223600-104231600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:104225400-104240400	Weak transcription	Brain Angular Gyrus	brain
7	chr8:104225600-104233000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr8:104226400-104242800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr8:104226600-104234800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr8:104226800-104232400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr8:104227000-104230800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr8:104227400-104237800	Weak transcription	Aorta	Aorta
13	chr8:104227600-104242200	Weak transcription	Fetal Brain Female	brain
14	chr8:104227600-104245400	Weak transcription	Fetal Brain Male	brain
15	chr8:104228000-104232000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr8:104228000-104241600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr8:104228200-104233800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr8:104228400-104230600	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr8:104228800-104230000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr8:104228800-104231000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr8:104229000-104230000	Enhancers	H1 Cell Line	embryonic stem cell
22	chr8:104229000-104230400	Weak transcription	Primary hematopoietic stem cells	blood
23	chr8:104229000-104230600	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr8:104229000-104230800	Enhancers	Brain Hippocampus Middle	brain
25	chr8:104229000-104231000	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr8:104229200-104230000	Enhancers	Brain Substantia Nigra	brain
27	chr8:104229200-104230200	Enhancers	Brain Anterior Caudate	brain
28	chr8:104229400-104230000	Enhancers	Brain Cingulate Gyrus	brain
29	chr8:104229400-104230000	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr8:104229400-104230600	Enhancers	H9 Cell Line	embryonic stem cell
31	chr8:104229400-104231200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr8:104229400-104231200	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr8:104229400-104233200	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr8:104229600-104232000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr8:104229800-104230800	Enhancers	Fetal Stomach	stomach
36	chr8:104229800-104233200	Weak transcription	HUES48 Cell Line	embryonic stem cell

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