Variant report

Variant	rs16842834
Chromosome Location	chr2:210221944-210221945
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:210209759..210211803-chr2:210221775..210224209,2	MCF-7	breast:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11892351	0.86[YRI][hapmap]
rs12986778	1.00[CEU][hapmap]
rs12998272	1.00[CEU][hapmap];0.96[YRI][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12999670	0.86[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12999884	1.00[CEU][hapmap]
rs13002012	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13006419	0.80[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs13007765	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13012322	0.81[EUR][1000 genomes]
rs13022552	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13023112	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13032445	0.86[YRI][hapmap]
rs13032935	0.81[EUR][1000 genomes]
rs13036037	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1374338	0.82[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs1374339	0.82[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs16842843	0.86[YRI][hapmap]
rs16842895	1.00[CEU][hapmap]
rs16842899	1.00[CEU][hapmap]
rs16842900	1.00[CEU][hapmap];0.89[GIH][hapmap];1.00[TSI][hapmap]
rs16842904	1.00[CEU][hapmap];0.89[GIH][hapmap];1.00[TSI][hapmap]
rs16842906	1.00[CEU][hapmap];0.89[GIH][hapmap];1.00[TSI][hapmap]
rs1992772	0.80[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs2167933	1.00[CEU][hapmap]
rs34445752	0.94[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34565674	0.93[EUR][1000 genomes]
rs34578885	0.93[EUR][1000 genomes]
rs34811576	0.83[AMR][1000 genomes]
rs34884270	0.83[AMR][1000 genomes]
rs35216876	0.81[EUR][1000 genomes]
rs35347413	0.87[EUR][1000 genomes]
rs35382863	0.80[EUR][1000 genomes]
rs35955770	0.86[EUR][1000 genomes]
rs35978314	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs36035019	0.80[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs59984943	0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs67917650	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]

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	nsv875761	chr2:209912108-210222004	Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1000214	chr2:209987607-210308626	Strong transcription Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv536133	chr2:209987607-210308626	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv1003864	chr2:210063871-210308626	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv875764	chr2:210195717-210240990	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv834518	chr2:210204958-210372744	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
7	nsv1014900	chr2:210205050-210235562	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
8	nsv1006636	chr2:210207332-210235562	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:210221600-210222400	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr2:210221600-210222800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr2:210221600-210223200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr2:210221800-210222000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
5	chr2:210221800-210222200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr2:210221800-210222800	Enhancers	H1 Cell Line	embryonic stem cell
7	chr2:210221800-210222800	Enhancers	H9 Cell Line	embryonic stem cell
8	chr2:210221800-210222800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr2:210221800-210222800	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr2:210221800-210223200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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