Variant report

Variant	rs1849011
Chromosome Location	chr5:107614397-107614398
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:107596085..107596926-chr5:107614295..107614996,3	MCF-7	breast:

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10036343	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs10041907	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs10063449	0.90[EUR][1000 genomes]
rs10063866	0.88[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.90[EUR][1000 genomes]
rs10071595	0.89[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs10072270	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10075907	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs10463586	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11743651	0.96[CEU][hapmap];0.90[EUR][1000 genomes]
rs11744374	0.88[EUR][1000 genomes]
rs13178456	0.89[EUR][1000 genomes]
rs2029104	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs2044709	0.85[EUR][1000 genomes]
rs2044710	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs2112306	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs2122158	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs2167001	0.92[EUR][1000 genomes]
rs2416188	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs28497144	0.86[EUR][1000 genomes]
rs286764	0.96[CEU][hapmap];0.92[CHB][hapmap];0.94[JPT][hapmap];0.91[EUR][1000 genomes]
rs286767	0.90[EUR][1000 genomes]
rs2922423	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs2922424	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs2922426	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs2922427	0.91[EUR][1000 genomes]
rs2922428	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs2922429	0.92[EUR][1000 genomes]
rs2922430	0.84[EUR][1000 genomes]
rs2922433	0.88[EUR][1000 genomes]
rs2966795	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs2966797	0.92[EUR][1000 genomes]
rs2966799	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs34298471	0.96[EUR][1000 genomes]
rs4541643	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs4957553	0.96[CEU][hapmap];0.89[EUR][1000 genomes]
rs4957751	1.00[CEU][hapmap];0.92[CHB][hapmap];0.88[JPT][hapmap];0.93[YRI][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4957753	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs4957756	0.83[CHB][hapmap]
rs55896795	0.90[EUR][1000 genomes]
rs57222565	0.96[EUR][1000 genomes]
rs6596770	0.88[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6596771	0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6596777	0.92[EUR][1000 genomes]
rs6875297	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6883082	0.89[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7708996	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs7713705	0.92[CHB][hapmap];0.94[JPT][hapmap]
rs7717747	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs7726298	1.00[CEU][hapmap];0.87[YRI][hapmap];0.90[EUR][1000 genomes]
rs9326725	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs962680	0.91[EUR][1000 genomes]
rs989001	1.00[CEU][hapmap];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534281	chr5:107357579-107674981	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv830441	chr5:107450392-107614557	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv882683	chr5:107476501-107769095	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	nsv882684	chr5:107521677-107695558	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv830442	chr5:107539150-107697020	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv882685	chr5:107564746-107695558	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv882686	chr5:107564746-107769095	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
8	nsv4950	chr5:107587778-107637348	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv882687	chr5:107595383-107695558	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv882688	chr5:107595383-107715746	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
11	nsv882689	chr5:107595383-108299744	Enhancers ZNF genes & repeats Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
12	esv2755544	chr5:107614101-107748101	Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:107575400-107617600	Weak transcription	Primary B cells from cord blood	blood
2	chr5:107577000-107616000	Weak transcription	Primary T cells from cord blood	blood
3	chr5:107585000-107617800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr5:107596600-107616000	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr5:107602200-107615800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr5:107604800-107644400	Weak transcription	Fetal Intestine Small	intestine
7	chr5:107607400-107617600	Weak transcription	Primary hematopoietic stem cells	blood
8	chr5:107607600-107614400	Weak transcription	Lung	lung
9	chr5:107611600-107617800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr5:107612400-107624600	Weak transcription	Aorta	Aorta
11	chr5:107612800-107614600	Enhancers	Fetal Heart	heart
12	chr5:107613400-107615000	Enhancers	Liver	Liver
13	chr5:107613400-107616400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr5:107613600-107614800	Enhancers	Right Ventricle	heart
15	chr5:107613600-107615000	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr5:107613800-107615000	Enhancers	Left Ventricle	heart
17	chr5:107613800-107616000	Enhancers	Skeletal Muscle Female	skeletal muscle
18	chr5:107614000-107614800	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr5:107614000-107614800	Enhancers	Gastric	stomach
20	chr5:107614000-107615000	Enhancers	Psoas Muscle	Psoas
21	chr5:107614000-107615000	Enhancers	Right Atrium	heart
22	chr5:107614000-107615000	Genic enhancers	Sigmoid Colon	Sigmoid Colon
23	chr5:107614000-107617200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr5:107614200-107614600	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:107614200-107614600	Enhancers	Primary T cells fromperipheralblood	blood
26	chr5:107614200-107615800	Weak transcription	Colon Smooth Muscle	Colon

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