Variant report

Variant	rs4716012
Chromosome Location	chr6:15933610-15933611
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1418671	0.82[EUR][1000 genomes]
rs1935785	0.90[EUR][1000 genomes]
rs2103644	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28394795	0.90[EUR][1000 genomes]
rs58093807	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6459431	0.88[EUR][1000 genomes]
rs6900771	0.84[EUR][1000 genomes]
rs6933513	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6941696	0.90[EUR][1000 genomes]
rs6942060	0.90[EUR][1000 genomes]
rs9296994	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15928000-15936400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:15933200-15935000	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr6:15933600-15934200	Enhancers	Esophagus	oesophagus

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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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