Variant report

Variant	rs73251088
Chromosome Location	chr12:10456159-10456160
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11053736	0.91[AFR][1000 genomes]
rs11838090	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34401616	1.00[AMR][1000 genomes]
rs35775301	1.00[AMR][1000 genomes]
rs55963190	1.00[AMR][1000 genomes]
rs57041498	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57989020	1.00[AMR][1000 genomes]
rs60220961	1.00[AMR][1000 genomes]
rs73252885	1.00[AMR][1000 genomes]
rs73262640	1.00[AMR][1000 genomes]
rs73262645	1.00[AMR][1000 genomes]
rs73262654	1.00[AMR][1000 genomes]
rs73262700	1.00[AMR][1000 genomes]
rs73264786	1.00[AMR][1000 genomes]
rs73266605	1.00[AMR][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	nsv898757	chr12:10229281-10614641	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv832328	chr12:10398071-10620443	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv605	chr12:10448638-10494208	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv898759	chr12:10454556-10583365	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10447800-10456600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr12:10453200-10461000	Weak transcription	Placenta	Placenta
3	chr12:10453400-10457000	Enhancers	Placenta Amnion	Placenta Amnion
4	chr12:10453800-10457200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr12:10454200-10458000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr12:10454800-10474400	Weak transcription	Left Ventricle	heart
7	chr12:10455800-10456200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr12:10456000-10457000	Weak transcription	Primary T cells fromperipheralblood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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