Variant report

Variant	rs72856229
Chromosome Location	chr4:73707531-73707532
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11489096	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13340205	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16848681	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16848700	1.00[ASN][1000 genomes]
rs16848718	1.00[ASN][1000 genomes]
rs57295189	1.00[ASN][1000 genomes]
rs57542547	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72854292	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72854294	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72854298	1.00[ASN][1000 genomes]
rs72854302	1.00[ASN][1000 genomes]
rs72856207	1.00[ASN][1000 genomes]
rs72856214	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72856245	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72856269	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72856295	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72857531	0.80[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949371	chr4:73678470-74094500	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	esv2757068	chr4:73683018-73770378	Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv2759261	chr4:73683018-73770378	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv436952	chr4:73693532-73759117	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv437923	chr4:73699066-73758650	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:73687200-73707800	Weak transcription	Fetal Heart	heart
2	chr4:73706600-73711800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr4:73707000-73712000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:73707200-73711800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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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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