Variant report

Variant	rs10277308
Chromosome Location	chr7:13581020-13581021
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10238802	0.99[ASN][1000 genomes]
rs10239716	0.96[ASN][1000 genomes]
rs10257130	0.83[ASN][1000 genomes]
rs10807767	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10950471	0.88[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12699516	0.99[ASN][1000 genomes]
rs12699517	0.98[ASN][1000 genomes]
rs12699518	0.98[ASN][1000 genomes]
rs12699519	0.98[ASN][1000 genomes]
rs12699520	0.98[ASN][1000 genomes]
rs1357975	0.95[ASN][1000 genomes]
rs1357976	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1357977	0.95[ASN][1000 genomes]
rs1404931	0.97[ASN][1000 genomes]
rs1404933	0.98[ASN][1000 genomes]
rs16877874	0.99[ASN][1000 genomes]
rs1852177	0.84[ASN][1000 genomes]
rs1880631	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1880632	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1880633	0.85[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs2204478	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2222619	0.99[ASN][1000 genomes]
rs28463916	0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs28538412	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4721236	0.94[ASN][1000 genomes]
rs6949896	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6955341	0.97[ASN][1000 genomes]
rs6962321	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6962489	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6973078	0.97[ASN][1000 genomes]
rs6979093	0.98[ASN][1000 genomes]
rs7810495	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9638695	0.98[ASN][1000 genomes]
rs9638696	0.98[ASN][1000 genomes]
rs9638697	0.98[ASN][1000 genomes]
rs9638698	0.98[ASN][1000 genomes]
rs9638699	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9638700	0.98[ASN][1000 genomes]
rs9638701	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9638702	0.99[ASN][1000 genomes]
rs9639158	0.97[ASN][1000 genomes]
rs9639160	0.98[ASN][1000 genomes]
rs9639161	0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019173	chr7:13063854-13585360	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv538737	chr7:13063854-13585360	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1023580	chr7:13403531-13624975	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr7:13580200-13581200	Enhancers	Muscle Satellite Cultured Cells	--
2	chr7:13580800-13582600	Weak transcription	HUES6 Cell Line	embryonic stem cell

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