Variant report

Variant	rs4752013
Chromosome Location	chr10:118568883-118568884
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10787730	0.88[CHB][hapmap];0.85[YRI][hapmap];0.86[ASN][1000 genomes]
rs10886014	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs11197835	0.82[JPT][hapmap]
rs11591751	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11596173	0.86[ASN][1000 genomes]
rs1614092	0.88[ASN][1000 genomes]
rs1626678	0.88[ASN][1000 genomes]
rs1637556	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1637558	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1681721	0.83[ASN][1000 genomes]
rs1681723	0.88[ASN][1000 genomes]
rs1681725	0.85[ASN][1000 genomes]
rs1681748	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2291316	0.85[ASN][1000 genomes]
rs726525	0.86[JPT][hapmap]
rs740363	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9420210	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9421242	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:118560600-118586200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr10:118563400-118575400	Weak transcription	Brain Angular Gyrus	brain
3	chr10:118568400-118569800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:118568600-118570400	Enhancers	H1 Cell Line	embryonic stem cell
5	chr10:118568800-118569000	Bivalent Enhancer	Adipose Nuclei	Adipose
6	chr10:118568800-118569000	Bivalent Enhancer	Osteobl	bone
7	chr10:118568800-118569600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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