Variant report

Variant	rs72731752
Chromosome Location	chr9:73641621-73641622
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1362825	0.85[ASN][1000 genomes]
rs1411164	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17520753	0.95[ASN][1000 genomes]
rs17521958	0.90[ASN][1000 genomes]
rs17593251	0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs72731745	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72731763	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs72731767	0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs72731768	0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs72731779	0.90[ASN][1000 genomes]
rs72731780	0.90[ASN][1000 genomes]
rs972386	0.90[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	nsv1042806	chr9:73613885-73686104	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:73639800-73643600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr9:73640800-73641800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:73641400-73642000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr9:73641400-73642000	Active TSS	Spleen	Spleen
5	chr9:73641600-73652600	Weak transcription	iPS DF 19.11 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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