Variant report

Variant	rs72720295
Chromosome Location	chr1:95574598-95574599
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1336437	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72720233	0.83[AFR][1000 genomes]
rs72720235	0.83[AFR][1000 genomes]
rs72722107	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72722127	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72722131	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72722140	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72722148	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72722161	1.00[EUR][1000 genomes]
rs72722168	1.00[EUR][1000 genomes]
rs72722178	1.00[EUR][1000 genomes]
rs72723805	1.00[EUR][1000 genomes]
rs72723823	1.00[EUR][1000 genomes]
rs72723860	1.00[AMR][1000 genomes];1.00[EUR][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	nsv830636	chr1:95495849-95703126	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:95573400-95574800	Enhancers	Liver	Liver
2	chr1:95574400-95576000	Weak transcription	K562	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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