Variant report

Variant	rs7618596
Chromosome Location	chr3:160515742-160515743
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	chr3:160513259..160516252-chr3:160518883..160520924,2	MCF-7	breast:

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs1455870	0.94[EUR][1000 genomes]
rs1455871	0.94[EUR][1000 genomes]
rs16831442	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs16831457	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16831467	0.82[AFR][1000 genomes]
rs16831471	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16831473	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs16831516	0.94[EUR][1000 genomes]
rs16831520	0.94[EUR][1000 genomes]
rs17236620	0.94[EUR][1000 genomes]
rs17236641	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17236648	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17236655	1.00[EUR][1000 genomes]
rs17236662	0.94[EUR][1000 genomes]
rs17826352	0.94[EUR][1000 genomes]
rs17826358	0.94[EUR][1000 genomes]
rs17826364	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17826370	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17826376	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2068817	0.94[EUR][1000 genomes]
rs34035435	0.97[EUR][1000 genomes]
rs3907061	0.94[EUR][1000 genomes]
rs4549318	0.97[EUR][1000 genomes]
rs4627794	1.00[EUR][1000 genomes]
rs55891037	1.00[EUR][1000 genomes]
rs55905728	1.00[EUR][1000 genomes]
rs55923270	0.94[EUR][1000 genomes]
rs55997050	1.00[EUR][1000 genomes]
rs56083575	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56141155	1.00[EUR][1000 genomes]
rs56157815	1.00[EUR][1000 genomes]
rs56180903	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56331465	1.00[EUR][1000 genomes]
rs57828617	0.94[EUR][1000 genomes]
rs58891820	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6771910	0.94[EUR][1000 genomes]
rs6779461	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6793062	0.82[AFR][1000 genomes]
rs73877952	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73877966	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7618082	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7629154	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7633401	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532666	chr3:159777847-160703202	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
2	nsv1009249	chr3:160496237-160627378	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv536780	chr3:160496237-160627378	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:160498400-160522600	Weak transcription	Right Ventricle	heart
2	chr3:160509000-160522600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr3:160509600-160519000	Weak transcription	Stomach Smooth Muscle	stomach
4	chr3:160511400-160518400	Weak transcription	Primary T cells from cord blood	blood
5	chr3:160511800-160519800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr3:160512800-160519400	Weak transcription	Colon Smooth Muscle	Colon
7	chr3:160513400-160519000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr3:160513400-160522600	Weak transcription	Pancreas	Pancrea
9	chr3:160513800-160519600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr3:160514200-160520000	Weak transcription	Left Ventricle	heart
11	chr3:160514400-160522600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr3:160514800-160519200	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr3:160515000-160515800	Enhancers	Brain Cingulate Gyrus	brain
14	chr3:160515000-160518400	Weak transcription	Fetal Heart	heart
15	chr3:160515200-160515800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr3:160515200-160519200	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr3:160515200-160519200	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr3:160515400-160516000	Enhancers	Psoas Muscle	Psoas
19	chr3:160515400-160519000	Weak transcription	Liver	Liver
20	chr3:160515400-160526400	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr3:160515600-160518400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr3:160515600-160518600	Weak transcription	Adipose Nuclei	Adipose
23	chr3:160515600-160518800	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr3:160515600-160519000	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr3:160515600-160519000	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr3:160515600-160519000	Weak transcription	Stomach Mucosa	stomach
27	chr3:160515600-160519200	Weak transcription	Right Atrium	heart

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