Variant report

Variant	rs601032
Chromosome Location	chr3:138349332-138349333
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	chr3:138324541..138329357-chr3:138346474..138351112,6	MCF-7	breast:
2	chr3:138337140..138340391-chr3:138349263..138352301,3	K562	blood:

Variant related genes	Relation type
ENSG00000158234	Chromatin interaction

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs1066197	1.00[ASN][1000 genomes]
rs1068104	1.00[ASN][1000 genomes]
rs1068685	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10804658	1.00[CHB][hapmap]
rs1091528	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11720178	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs13069296	1.00[ASN][1000 genomes]
rs13433948	0.90[ASN][1000 genomes]
rs1663554	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1673597	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs191714	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs191775	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2607109	0.84[AMR][1000 genomes]
rs2607796	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2881900	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs361057	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs361059	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs361060	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs361061	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs361062	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs361063	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs361066	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs361067	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs361071	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs361072	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs361073	1.00[CHB][hapmap]
rs361074	1.00[CHB][hapmap]
rs361075	1.00[CHB][hapmap]
rs361076	1.00[CHB][hapmap]
rs361077	1.00[CHB][hapmap]
rs361080	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs361082	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs361087	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs361088	1.00[CHB][hapmap];0.90[ASN][1000 genomes]
rs361089	1.00[ASN][1000 genomes]
rs361092	1.00[ASN][1000 genomes]
rs361096	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs385254	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs413147	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs4305444	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs470359	1.00[ASN][1000 genomes]
rs484698	1.00[CHB][hapmap]
rs493152	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs497900	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs500687	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs520904	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs523975	1.00[CHB][hapmap]
rs524164	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs531577	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs537894	1.00[CHB][hapmap]
rs550768	1.00[ASN][1000 genomes]
rs558905	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs559160	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs564455	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs600590	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs603723	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs618457	1.00[ASN][1000 genomes]
rs621204	1.00[ASN][1000 genomes]
rs624099	1.00[CHB][hapmap]
rs635592	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs643620	1.00[CHB][hapmap]
rs6784610	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs7641106	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7643722	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs773045	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs773184	1.00[ASN][1000 genomes]
rs774015	1.00[CHB][hapmap]
rs811322	1.00[CHB][hapmap]
rs9822714	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9834963	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9879784	1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530057	chr3:138014877-138734390	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv1013074	chr3:138213166-138737688	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv1002612	chr3:138213274-138831792	Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
4	nsv536726	chr3:138213274-138831792	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
5	nsv1009726	chr3:138219923-138737688	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv869205	chr3:138248190-138775288	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv868955	chr3:138248190-138848947	Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv591854	chr3:138348081-138764229	Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers 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:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:138328400-138350200	Weak transcription	Lung	lung
2	chr3:138328400-138353200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr3:138328400-138355000	Weak transcription	Esophagus	oesophagus
4	chr3:138328600-138349400	Weak transcription	Ovary	ovary
5	chr3:138328600-138358000	Weak transcription	Psoas Muscle	Psoas
6	chr3:138328800-138358000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr3:138329000-138350000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr3:138329000-138354200	Weak transcription	Fetal Lung	lung
9	chr3:138335400-138368000	Weak transcription	Right Ventricle	heart
10	chr3:138337000-138360400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr3:138337800-138353600	Weak transcription	Colonic Mucosa	Colon
12	chr3:138338000-138353400	Weak transcription	Colon Smooth Muscle	Colon
13	chr3:138338200-138350000	Weak transcription	Rectal Smooth Muscle	rectum
14	chr3:138338600-138350400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr3:138339000-138351600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr3:138340400-138393800	Weak transcription	Fetal Brain Male	brain
17	chr3:138341000-138350600	Weak transcription	HepG2	liver
18	chr3:138341200-138351600	Weak transcription	Fetal Kidney	kidney
19	chr3:138341200-138355800	Weak transcription	Dnd41	blood
20	chr3:138341400-138349600	Weak transcription	Stomach Smooth Muscle	stomach
21	chr3:138341400-138354600	Weak transcription	Brain Angular Gyrus	brain
22	chr3:138341800-138355200	Weak transcription	Primary B cells from cord blood	blood
23	chr3:138342400-138362200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr3:138342600-138356400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr3:138343200-138352200	Weak transcription	Primary T cells from cord blood	blood
26	chr3:138343600-138352200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr3:138344800-138354000	Weak transcription	Duodenum Mucosa	Duodenum
28	chr3:138345000-138354800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr3:138345000-138356600	Weak transcription	HSMMtube	muscle
30	chr3:138345000-138367800	Weak transcription	HSMM	muscle
31	chr3:138345200-138357600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr3:138345200-138357600	Weak transcription	Spleen	Spleen
33	chr3:138345400-138350600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr3:138345400-138352800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr3:138345400-138354200	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr3:138345400-138355600	Weak transcription	NH-A	brain
37	chr3:138345400-138361600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr3:138345400-138368000	Weak transcription	NHLF	lung
39	chr3:138345600-138356600	Weak transcription	Brain Substantia Nigra	brain
40	chr3:138345600-138367400	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr3:138345800-138351000	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr3:138345800-138354200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr3:138345800-138368000	Weak transcription	HMEC	breast
44	chr3:138346000-138354600	Weak transcription	NHEK	skin
45	chr3:138346400-138349400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr3:138346400-138350000	Strong transcription	Fetal Muscle Trunk	muscle
47	chr3:138346600-138356200	Weak transcription	Primary hematopoietic stem cells	blood
48	chr3:138346600-138357800	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr3:138347200-138352800	Weak transcription	Placenta	Placenta
50	chr3:138348000-138349400	Strong transcription	Primary B cells from peripheral blood	blood

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