Variant report

Variant	rs59720903
Chromosome Location	chr17:63447956-63447957
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs56146103	0.90[ASN][1000 genomes]
rs56323090	0.90[ASN][1000 genomes]
rs58768287	0.93[ASN][1000 genomes]
rs60028782	1.00[EUR][1000 genomes]
rs60529904	1.00[EUR][1000 genomes]
rs60799116	1.00[EUR][1000 genomes]
rs7208176	0.93[ASN][1000 genomes]
rs7213593	1.00[EUR][1000 genomes]
rs7219534	1.00[EUR][1000 genomes]
rs73339859	1.00[EUR][1000 genomes]
rs73339861	1.00[EUR][1000 genomes]
rs73339873	1.00[EUR][1000 genomes]
rs73339874	1.00[EUR][1000 genomes]
rs73342069	0.90[ASN][1000 genomes]
rs73342074	0.90[ASN][1000 genomes]
rs73342091	0.83[ASN][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	nsv1056195	chr17:63439524-63512389	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:63446800-63450000	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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