Variant report

Variant	rs72883021
Chromosome Location	chr4:107472596-107472597
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs17036797	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17036798	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2866896	1.00[AMR][1000 genomes]
rs4339286	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57241247	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59948578	0.84[AFR][1000 genomes]
rs72877537	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72877540	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72877562	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72883014	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72883049	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7676756	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7681916	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:107470400-107485800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:107472400-107473800	Enhancers	HUES6 Cell Line	embryonic stem cell

Quick Search:

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

what's new

Quick links