Variant report

Variant	rs7696063
Chromosome Location	chr4:107445649-107445650
allele	A/T
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]
rs1522218	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2049206	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2049207	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2648047	0.84[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2648048	0.87[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2686290	0.83[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs2686308	0.86[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs28449210	0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs4956258	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6830270	0.84[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs7671573	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7696513	0.84[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9996119	0.99[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:107415200-107450200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:107445000-107450800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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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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