Variant report

Variant	rs72723577
Chromosome Location	chr14:56327847-56327848
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs17128859	0.89[EUR][1000 genomes]
rs17832491	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2342841	0.91[EUR][1000 genomes]
rs4901608	0.83[EUR][1000 genomes]
rs4901613	0.89[EUR][1000 genomes]
rs58176451	0.86[EUR][1000 genomes]
rs67462753	0.83[EUR][1000 genomes]
rs72622474	0.81[EUR][1000 genomes]
rs72622477	0.93[EUR][1000 genomes]
rs72723579	0.84[EUR][1000 genomes]
rs72723580	0.81[EUR][1000 genomes]
rs72723583	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv901966	chr14:56160904-56436203	Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv901977	chr14:56213392-56492996	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr14:56327400-56328000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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