Variant report

Variant	rs13174779
Chromosome Location	chr5:61675396-61675397
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:61671360..61674176-chr5:61674605..61678360,3	MCF-7	breast:
2	chr5:61675162..61677074-chr5:61689964..61691890,2	MCF-7	breast:
3	chr5:61671218..61675836-chr5:61680639..61684816,8	K562	blood:

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs1108158	0.83[ASN][1000 genomes]
rs11740652	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11742167	0.80[ASN][1000 genomes]
rs11747516	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12655562	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13155253	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13156073	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13156695	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13169321	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13170425	0.83[ASN][1000 genomes]
rs13176923	0.80[ASN][1000 genomes]
rs13178729	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13189446	0.89[ASN][1000 genomes]
rs13190153	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs153864	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs16875037	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16890613	0.89[ASN][1000 genomes]
rs16890618	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16890628	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16890634	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16890651	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2059162	0.83[ASN][1000 genomes]
rs2063255	0.83[ASN][1000 genomes]
rs2272291	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs246198	0.82[ASN][1000 genomes]
rs27090	0.80[ASN][1000 genomes]
rs34220654	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34596001	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35238667	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35311093	0.89[ASN][1000 genomes]
rs35572300	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35699711	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35744020	0.89[ASN][1000 genomes]
rs35746052	0.89[ASN][1000 genomes]
rs35794032	0.83[ASN][1000 genomes]
rs35808056	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35815430	0.86[EUR][1000 genomes]
rs35842742	0.89[ASN][1000 genomes]
rs36105063	0.89[ASN][1000 genomes]
rs3776612	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3776614	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3822487	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4289514	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71617426	0.89[ASN][1000 genomes]
rs71617427	0.89[ASN][1000 genomes]
rs71617428	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7446543	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs971965	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024090	chr5:61258759-61921150	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	esv2757996	chr5:61403138-61687817	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	esv2759345	chr5:61403138-61748912	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv1020255	chr5:61451792-62031365	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	nsv1027539	chr5:61457762-62000008	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
6	nsv881726	chr5:61556730-61676911	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
7	nsv881727	chr5:61578041-61700970	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	23 gene(s)	inside rSNPs	diseases
8	nsv1033578	chr5:61606610-61911153	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
9	nsv1025145	chr5:61624735-61824265	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
10	nsv1029708	chr5:61625813-61877628	Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
11	nsv881728	chr5:61630879-61857577	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
12	esv2757117	chr5:61649403-61748912	Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
13	nsv598348	chr5:61650843-61895124	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
14	esv35035	chr5:61657943-61792243	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:61622400-61676000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:61629200-61676400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr5:61631200-61676000	Weak transcription	Lung	lung
4	chr5:61639800-61684200	Weak transcription	Psoas Muscle	Psoas
5	chr5:61641400-61682400	Weak transcription	Fetal Heart	heart
6	chr5:61642400-61697400	Strong transcription	HUES64 Cell Line	embryonic stem cell
7	chr5:61642600-61688400	Weak transcription	Right Ventricle	heart
8	chr5:61642600-61696000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr5:61642600-61699200	Weak transcription	Gastric	stomach
10	chr5:61643000-61697000	Strong transcription	HUES48 Cell Line	embryonic stem cell
11	chr5:61643800-61680600	Strong transcription	Placenta	Placenta
12	chr5:61644000-61689000	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr5:61645400-61689200	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr5:61647000-61690000	Weak transcription	Spleen	Spleen
15	chr5:61647600-61698000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr5:61656200-61698000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr5:61656800-61687800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:61658400-61691800	Strong transcription	Dnd41	blood
19	chr5:61659800-61695800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr5:61661000-61678600	Strong transcription	Fetal Thymus	thymus
21	chr5:61661800-61680000	Weak transcription	Colonic Mucosa	Colon
22	chr5:61661800-61698000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr5:61662000-61697800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr5:61662000-61697800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr5:61664200-61678400	Strong transcription	Fetal Intestine Large	intestine
26	chr5:61664600-61689200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr5:61664800-61675800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr5:61665400-61699000	Weak transcription	Esophagus	oesophagus
29	chr5:61665600-61688000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr5:61666600-61678600	Strong transcription	Primary T cells from cord blood	blood
31	chr5:61666600-61679000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr5:61666800-61679200	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr5:61666800-61698000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
34	chr5:61667000-61691200	Strong transcription	Primary monocytes fromperipheralblood	blood
35	chr5:61667000-61691600	Strong transcription	Monocytes-CD14+_RO01746	blood
36	chr5:61667000-61697200	Strong transcription	Primary B cells from peripheral blood	blood
37	chr5:61667400-61677800	Strong transcription	GM12878-XiMat	blood
38	chr5:61667400-61678400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
39	chr5:61667400-61697200	Strong transcription	HUES6 Cell Line	embryonic stem cell
40	chr5:61667600-61697800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr5:61667600-61698000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
42	chr5:61667800-61681400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr5:61668000-61677400	Strong transcription	HSMM	muscle
44	chr5:61668000-61698000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr5:61668200-61678400	Strong transcription	Rectal Mucosa Donor 31	rectum
46	chr5:61668400-61685600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr5:61668600-61697000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
48	chr5:61669200-61690200	Strong transcription	HUVEC	blood vessel
49	chr5:61669400-61677400	Strong transcription	NHDF-Ad	bronchial
50	chr5:61669400-61677800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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