Variant report

Variant	rs10429569
Chromosome Location	chr9:85294473-85294474
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10125742	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10217175	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10512134	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10780550	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10867869	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10867870	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1412523	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs565634	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs569518	0.82[EUR][1000 genomes]
rs631785	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs654629	0.82[EUR][1000 genomes]
rs6559681	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs667567	0.82[EUR][1000 genomes]
rs7856840	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs944681	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][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	nsv831641	chr9:85145561-85309589	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv428539	chr9:85240027-85402367	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	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	chr9:85291200-85295000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr9:85293000-85297400	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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