Variant report

Variant	rs11901645
Chromosome Location	chr2:47737218-47737219
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	chr2:47735627..47737590-chr2:47744199..47746815,2	MCF-7	breast:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10175959	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10175972	0.94[ASN][1000 genomes]
rs10188090	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10197011	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10206575	0.93[ASN][1000 genomes]
rs10206782	0.92[ASN][1000 genomes]
rs10209369	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs10495945	0.90[CHB][hapmap];0.86[JPT][hapmap];0.87[ASN][1000 genomes]
rs11684661	0.84[ASN][1000 genomes]
rs11684737	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11694689	0.80[EUR][1000 genomes]
rs11886591	0.81[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs12712994	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12991125	0.93[ASN][1000 genomes]
rs13031342	0.94[ASN][1000 genomes]
rs2059520	0.85[CEU][hapmap];0.90[CHB][hapmap];0.86[CHD][hapmap];0.81[GIH][hapmap];0.95[JPT][hapmap];0.84[MEX][hapmap];0.92[TSI][hapmap];0.83[ASN][1000 genomes]
rs2303424	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3771274	0.95[CHB][hapmap];0.91[CHD][hapmap];0.85[GIH][hapmap];0.95[JPT][hapmap];0.81[MEX][hapmap];0.81[TSI][hapmap]
rs3771280	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs3821227	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4550716	0.90[CHB][hapmap]
rs4583514	0.81[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6544990	1.00[CHB][hapmap];0.88[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap]
rs6711675	0.95[CHB][hapmap];0.95[JPT][hapmap];0.80[ASN][1000 genomes]
rs6718364	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6744097	0.85[JPT][hapmap]
rs6746426	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6754473	0.80[EUR][1000 genomes]
rs6759990	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs7585174	0.94[ASN][1000 genomes]
rs7596629	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7599880	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7601062	0.91[EUR][1000 genomes]
rs876936	0.95[CHB][hapmap];0.92[CHD][hapmap];0.91[GIH][hapmap];0.91[JPT][hapmap];0.80[MEX][hapmap];0.97[TSI][hapmap];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs876937	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs879722	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9784092	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004828	chr2:47056849-47814482	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
2	nsv531348	chr2:47433147-47827310	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv999576	chr2:47506116-47773960	Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
4	nsv998314	chr2:47720420-47959168	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:47732600-47747800	Weak transcription	Primary T cells from cord blood	blood
2	chr2:47733600-47739200	Weak transcription	Right Atrium	heart
3	chr2:47734000-47740800	Weak transcription	Brain Angular Gyrus	brain
4	chr2:47734000-47741000	Weak transcription	Brain Cingulate Gyrus	brain
5	chr2:47734000-47741400	Weak transcription	Brain Hippocampus Middle	brain
6	chr2:47734000-47747000	Weak transcription	Brain Anterior Caudate	brain
7	chr2:47734000-47747600	Weak transcription	Brain Substantia Nigra	brain
8	chr2:47734800-47738200	Enhancers	Fetal Brain Male	brain
9	chr2:47735400-47737400	Enhancers	Dnd41	blood
10	chr2:47735400-47738400	Enhancers	Fetal Brain Female	brain
11	chr2:47736800-47742800	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr2:47736800-47747400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr2:47736800-47747400	Weak transcription	Thymus	Thymus
14	chr2:47737000-47747200	Weak transcription	GM12878-XiMat	blood
15	chr2:47737200-47739200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr2:47737200-47739600	Weak transcription	HUVEC	blood vessel
17	chr2:47737200-47741200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr2:47737200-47741200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr2:47737200-47743400	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr2:47737200-47744400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:47737200-47744800	Weak transcription	Fetal Thymus	thymus

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