Variant report

Variant	rs10213482
Chromosome Location	chr4:81234226-81234227
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10009812	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs10020144	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10032770	0.91[ASN][1000 genomes]
rs10033567	1.00[JPT][hapmap]
rs10034513	0.89[ASN][1000 genomes]
rs10434062	0.89[ASN][1000 genomes]
rs17004882	0.91[ASN][1000 genomes]
rs1845691	0.82[ASN][1000 genomes]
rs28680678	0.93[ASN][1000 genomes]
rs3816574	0.95[ASN][1000 genomes]
rs6853244	0.95[ASN][1000 genomes]
rs731658	0.89[ASN][1000 genomes]
rs7655270	0.95[ASN][1000 genomes]
rs7680580	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:81231000-81235000	Enhancers	NHDF-Ad	bronchial
2	chr4:81231400-81235800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:81231400-81239200	Weak transcription	HSMM	muscle
4	chr4:81231600-81243400	Weak transcription	NH-A	brain
5	chr4:81232200-81242200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr4:81233800-81235000	Enhancers	Muscle Satellite Cultured Cells	--
7	chr4:81234000-81234800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr4:81234200-81234600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:81234200-81235000	Enhancers	Osteobl	bone

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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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