Variant report

Variant	rs1482473
Chromosome Location	chr10:44707598-44707599
allele	C/G
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:16)

rs_ID	r²[population]
rs10899997	0.82[EUR][1000 genomes]
rs1509929	0.82[EUR][1000 genomes]
rs1623851	0.82[EUR][1000 genomes]
rs1627329	0.82[EUR][1000 genomes]
rs1680641	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17155641	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1746052	0.95[CHB][hapmap]
rs1905150	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs487465	0.95[CHB][hapmap]
rs573141	0.95[CHB][hapmap]
rs607363	0.95[CHB][hapmap]
rs620356	0.91[CHB][hapmap]
rs620828	0.91[CHB][hapmap]
rs634963	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs694425	0.91[CHB][hapmap]
rs7909598	0.82[EUR][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	nsv1038511	chr10:44596885-44870030	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 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	chr10:44706200-44710400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr10:44707400-44707600	Enhancers	iPS-18 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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