Variant report

Variant	rs2759695
Chromosome Location	chr13:53694093-53694094
allele	A/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:18)

rs_ID	r²[population]
rs2476029	1.00[AFR][1000 genomes]
rs2491126	1.00[AMR][1000 genomes]
rs2759683	1.00[AMR][1000 genomes]
rs2759684	1.00[AMR][1000 genomes]
rs2759685	1.00[AMR][1000 genomes]
rs2759686	1.00[AMR][1000 genomes]
rs2759687	1.00[AMR][1000 genomes]
rs2759692	1.00[AMR][1000 genomes]
rs2759693	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2759699	0.92[AFR][1000 genomes]
rs2806986	1.00[AFR][1000 genomes]
rs2806987	1.00[AFR][1000 genomes]
rs2806989	1.00[AMR][1000 genomes]
rs2806991	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2806993	1.00[AMR][1000 genomes]
rs2806997	1.00[AMR][1000 genomes]
rs2807003	1.00[AMR][1000 genomes]
rs2807005	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050969	chr13:53665927-54064861	Bivalent Enhancer Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:53681800-53695000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:53691000-53694800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr13:53692000-53694600	Weak transcription	H1 Cell Line	embryonic stem cell

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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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