Variant report

Variant	rs72911724
Chromosome Location	chr2:188994431-188994432
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:188994299..188994907-chr2:189145390..189145988,2	MCF-7	breast:

Extended variants
information (count: 99 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs11674292	1.00[EUR][1000 genomes]
rs11678294	0.80[EUR][1000 genomes]
rs11678501	1.00[EUR][1000 genomes]
rs11678729	0.80[EUR][1000 genomes]
rs11679720	1.00[EUR][1000 genomes]
rs11680235	1.00[EUR][1000 genomes]
rs11683340	0.80[EUR][1000 genomes]
rs11685495	1.00[EUR][1000 genomes]
rs11686476	1.00[EUR][1000 genomes]
rs11687577	1.00[EUR][1000 genomes]
rs11689113	0.86[EUR][1000 genomes]
rs11691788	1.00[EUR][1000 genomes]
rs11692575	1.00[EUR][1000 genomes]
rs11695469	1.00[EUR][1000 genomes]
rs12151778	1.00[EUR][1000 genomes]
rs12185535	1.00[EUR][1000 genomes]
rs12185546	1.00[EUR][1000 genomes]
rs12185596	1.00[EUR][1000 genomes]
rs12185714	1.00[EUR][1000 genomes]
rs12989776	1.00[EUR][1000 genomes]
rs13393442	0.86[EUR][1000 genomes]
rs72895717	1.00[EUR][1000 genomes]
rs72895720	1.00[EUR][1000 genomes]
rs72895723	1.00[EUR][1000 genomes]
rs72895727	1.00[EUR][1000 genomes]
rs72895728	1.00[EUR][1000 genomes]
rs72895740	1.00[EUR][1000 genomes]
rs72895757	1.00[EUR][1000 genomes]
rs72897930	1.00[EUR][1000 genomes]
rs72897939	1.00[EUR][1000 genomes]
rs72901578	1.00[EUR][1000 genomes]
rs72901590	1.00[EUR][1000 genomes]
rs72901594	1.00[EUR][1000 genomes]
rs72903509	0.86[EUR][1000 genomes]
rs72903511	0.86[EUR][1000 genomes]
rs72903524	0.86[EUR][1000 genomes]
rs72903526	0.86[EUR][1000 genomes]
rs72903527	0.86[EUR][1000 genomes]
rs72903532	0.86[EUR][1000 genomes]
rs72903537	0.86[EUR][1000 genomes]
rs72903560	0.86[EUR][1000 genomes]
rs72903582	0.86[EUR][1000 genomes]
rs72903583	0.86[EUR][1000 genomes]
rs72903592	0.86[EUR][1000 genomes]
rs72903876	1.00[EUR][1000 genomes]
rs72903884	1.00[EUR][1000 genomes]
rs72903890	1.00[EUR][1000 genomes]
rs72903892	1.00[EUR][1000 genomes]
rs72903902	1.00[EUR][1000 genomes]
rs72905529	0.86[EUR][1000 genomes]
rs72905551	0.80[EUR][1000 genomes]
rs72905569	0.86[EUR][1000 genomes]
rs72905578	0.86[EUR][1000 genomes]
rs72905586	0.86[EUR][1000 genomes]
rs72905596	0.86[EUR][1000 genomes]
rs72905601	0.86[EUR][1000 genomes]
rs72907612	0.86[EUR][1000 genomes]
rs72907614	0.86[EUR][1000 genomes]
rs72907632	0.86[EUR][1000 genomes]
rs72907664	0.86[EUR][1000 genomes]
rs72907686	0.86[EUR][1000 genomes]
rs72907691	0.86[EUR][1000 genomes]
rs72907958	1.00[EUR][1000 genomes]
rs72907969	1.00[EUR][1000 genomes]
rs72907970	1.00[EUR][1000 genomes]
rs72907987	1.00[EUR][1000 genomes]
rs72909876	1.00[EUR][1000 genomes]
rs72909889	1.00[EUR][1000 genomes]
rs72909891	1.00[EUR][1000 genomes]
rs72909893	1.00[EUR][1000 genomes]
rs72909895	1.00[EUR][1000 genomes]
rs72911709	1.00[EUR][1000 genomes]
rs72911710	1.00[EUR][1000 genomes]
rs72911713	1.00[EUR][1000 genomes]
rs72911720	1.00[EUR][1000 genomes]
rs72911722	1.00[EUR][1000 genomes]
rs72911729	1.00[EUR][1000 genomes]
rs72911733	1.00[EUR][1000 genomes]
rs72911739	1.00[EUR][1000 genomes]
rs72911740	1.00[EUR][1000 genomes]
rs72911751	1.00[EUR][1000 genomes]
rs72911762	1.00[EUR][1000 genomes]
rs72911775	1.00[EUR][1000 genomes]
rs72911777	1.00[EUR][1000 genomes]
rs72911779	1.00[EUR][1000 genomes]
rs72911782	1.00[EUR][1000 genomes]
rs72911793	1.00[EUR][1000 genomes]
rs9288154	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533353	chr2:188498301-189024655	Weak transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv875602	chr2:188923773-189016215	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv875603	chr2:188923773-189025977	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv584044	chr2:188928433-189016215	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv1002714	chr2:188934297-189025084	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv584045	chr2:188949715-189003106	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv875604	chr2:188957640-189043137	Enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv584046	chr2:188967163-189006890	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv821852	chr2:188985216-189000907	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv821853	chr2:188985216-189001154	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv1010394	chr2:188994398-189284092	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:188979000-189001200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:188979400-189013600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr2:188994400-188996400	Enhancers	Fetal Heart	heart
4	chr2:188994400-189003000	Strong transcription	HUES6 Cell Line	embryonic stem cell

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