Variant report

Variant	rs10734067
Chromosome Location	chr10:19023660-19023661
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10764702	0.83[ASN][1000 genomes]
rs10764710	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10764711	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10826350	0.85[ASW][hapmap];1.00[CEU][hapmap];0.95[GIH][hapmap];0.83[JPT][hapmap];0.92[MEX][hapmap];0.80[MKK][hapmap];0.98[TSI][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10829264	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10829307	0.84[EUR][1000 genomes]
rs1387837	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1873313	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2009241	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2451515	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35201297	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs35840835	0.81[ASN][1000 genomes]
rs7097370	0.81[EUR][1000 genomes]
rs7097952	0.86[EUR][1000 genomes]
rs7912040	0.80[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	nsv894915	chr10:18984571-19257664	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr10:19019400-19024200	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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