Variant report

Variant	rs28888757
Chromosome Location	chr16:72386626-72386627
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10492820	0.91[AFR][1000 genomes]
rs11075927	0.91[AFR][1000 genomes]
rs11075928	0.91[AFR][1000 genomes]
rs11860511	0.96[AFR][1000 genomes]
rs11860913	0.80[AFR][1000 genomes]
rs11861074	0.95[AFR][1000 genomes]
rs13333424	0.80[AFR][1000 genomes]
rs13333480	0.95[AFR][1000 genomes]
rs13338269	0.93[AFR][1000 genomes]
rs13338313	0.93[AFR][1000 genomes]
rs1429069	0.80[AFR][1000 genomes]
rs1429070	0.82[AFR][1000 genomes]
rs16970828	0.92[AFR][1000 genomes]
rs16970897	0.84[AFR][1000 genomes]
rs16970929	0.80[AFR][1000 genomes]
rs1864230	0.80[AFR][1000 genomes]
rs2017748	0.80[AFR][1000 genomes]
rs2053234	0.81[AFR][1000 genomes]
rs28393088	0.93[AFR][1000 genomes]
rs28473657	0.80[AFR][1000 genomes]
rs28634932	0.82[AFR][1000 genomes]
rs28679760	0.95[AFR][1000 genomes]
rs28706881	0.95[AFR][1000 genomes]
rs28712432	0.95[AFR][1000 genomes]
rs28882790	0.85[AFR][1000 genomes]
rs35917623	0.93[AFR][1000 genomes]
rs4788635	0.85[AFR][1000 genomes]
rs55806458	0.82[AFR][1000 genomes]
rs59875457	0.93[AFR][1000 genomes]
rs7187532	0.89[AFR][1000 genomes]
rs7187674	0.89[AFR][1000 genomes]
rs7188632	0.93[AFR][1000 genomes]
rs7197250	0.91[AFR][1000 genomes]
rs7198345	0.90[AFR][1000 genomes]
rs7198450	0.93[AFR][1000 genomes]
rs7200007	0.93[AFR][1000 genomes]
rs726887	0.91[AFR][1000 genomes]
rs73585209	0.80[AFR][1000 genomes]
rs73587415	0.95[AFR][1000 genomes]
rs8046891	0.89[AFR][1000 genomes]
rs8051595	0.91[AFR][1000 genomes]
rs8052117	0.89[AFR][1000 genomes]
rs8053288	0.92[AFR][1000 genomes]
rs8063144	0.92[AFR][1000 genomes]
rs9302636	0.94[AFR][1000 genomes]
rs9889208	0.87[AFR][1000 genomes]
rs9921281	0.95[AFR][1000 genomes]
rs9921921	0.91[AFR][1000 genomes]
rs9922597	0.93[AFR][1000 genomes]
rs9922853	0.83[AFR][1000 genomes]
rs9926141	0.92[AFR][1000 genomes]
rs9927677	0.81[AFR][1000 genomes]
rs9928119	0.96[AFR][1000 genomes]
rs9929864	0.93[AFR][1000 genomes]
rs9930862	0.93[AFR][1000 genomes]
rs9934365	0.95[AFR][1000 genomes]
rs9934457	0.91[AFR][1000 genomes]
rs9937973	0.95[AFR][1000 genomes]
rs9938153	0.89[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948468	chr16:71727571-72651914	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
2	nsv1060983	chr16:72074832-72791629	Genic enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
3	nsv1060804	chr16:72078486-72791629	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
4	nsv534039	chr16:72287171-72851170	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
5	nsv1063172	chr16:72342110-72537808	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv542947	chr16:72342110-72537808	ZNF genes & repeats Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv1067525	chr16:72342110-72602796	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
8	nsv542948	chr16:72342110-72602796	ZNF genes & repeats Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
9	nsv1867	chr16:72352262-72397339	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
10	nsv1057127	chr16:72375524-72509686	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	nsv542949	chr16:72375524-72509686	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
12	esv3524113	chr16:72385001-72386899	Weak transcription	n/a	n/a	inside rSNPs	n/a
13	esv3524114	chr16:72385001-72386899	Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:72367200-72389200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr16:72367200-72405000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr16:72367200-72423600	Weak transcription	Thymus	Thymus
4	chr16:72370200-72399600	Weak transcription	Primary B cells from cord blood	blood

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