Variant report

Variant	rs11719936
Chromosome Location	chr3:151021983-151021984
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:151021027..151023183-chr3:151044316..151046639,2	MCF-7	breast:
2	chr3:150999410..151001887-chr3:151020524..151022989,3	K562	blood:
3	chr3:151021234..151025100-chr3:151041293..151045950,7	MCF-7	breast:
4	chr3:151017110..151019943-chr3:151020802..151024030,3	MCF-7	breast:
5	chr3:151011307..151016157-chr3:151019117..151025599,7	MCF-7	breast:

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs1048408	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10513392	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11714714	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11717955	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs12330831	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12488267	0.88[ASN][1000 genomes]
rs12494865	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs1317465	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1352886	0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs1472122	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1565574	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16863323	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs16863334	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs16863336	0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs1844924	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1882014	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1882015	1.00[CEU][hapmap];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1882016	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1882017	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1920396	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1980143	0.90[CEU][hapmap]
rs28371419	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28497341	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2904430	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4076581	0.85[CHB][hapmap];0.95[JPT][hapmap]
rs4475010	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4679772	0.90[CEU][hapmap]
rs4679783	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4680254	0.82[CEU][hapmap]
rs4680257	0.90[CEU][hapmap]
rs4680260	0.82[CEU][hapmap]
rs56105302	0.94[ASN][1000 genomes]
rs56367650	0.85[AFR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs58334126	0.96[ASN][1000 genomes]
rs62283021	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6765215	0.95[ASN][1000 genomes]
rs6768130	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6782313	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6807308	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6809692	0.88[CEU][hapmap]
rs7617677	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7621113	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7621183	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7621211	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7623448	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7653603	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8180086	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9757688	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9810067	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9815520	0.90[CEU][hapmap]
rs9827619	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9828553	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9829753	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9870740	0.93[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9875152	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[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	nsv460894	chr3:150770614-151095093	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv592045	chr3:150770614-151095093	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	esv2754555	chr3:150968302-151054302	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:150984400-151022400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr3:151002600-151044000	Weak transcription	Primary hematopoietic stem cells	blood
3	chr3:151010200-151022200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr3:151014400-151022400	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr3:151014400-151022600	Weak transcription	Esophagus	oesophagus
6	chr3:151017000-151022600	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr3:151018200-151022000	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr3:151019000-151022400	Genic enhancers	NHEK	skin
9	chr3:151020000-151022400	Weak transcription	NHLF	lung
10	chr3:151020200-151022000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr3:151020200-151022600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr3:151020200-151022600	Weak transcription	NHDF-Ad	bronchial
13	chr3:151020600-151022200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr3:151020600-151022400	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr3:151020600-151022800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr3:151020800-151022000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr3:151020800-151022400	Weak transcription	Hela-S3	cervix
18	chr3:151021000-151022800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr3:151021600-151022000	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr3:151021600-151022400	Enhancers	HMEC	breast
21	chr3:151021600-151022600	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr3:151021600-151024600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr3:151021600-151025800	Enhancers	Placenta	Placenta
24	chr3:151021600-151026600	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr3:151021800-151022000	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr3:151021800-151022600	Enhancers	Brain Anterior Caudate	brain
27	chr3:151021800-151022600	Enhancers	NH-A	brain
28	chr3:151021800-151023200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr3:151021800-151023400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr3:151021800-151023400	Enhancers	HepG2	liver
31	chr3:151021800-151024000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr3:151021800-151024200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr3:151021800-151024600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr3:151021800-151024800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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