Variant report

Variant	rs5011191
Chromosome Location	chr6:54877581-54877582
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs60139657	0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72957255	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72966310	0.88[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs72966320	0.88[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs72970757	0.86[EUR][1000 genomes]
rs72978508	0.85[EUR][1000 genomes]
rs72978515	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9464190	0.85[EUR][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:54876600-54877600	Enhancers	Placenta Amnion	Placenta Amnion
2	chr6:54876800-54879000	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr6:54877000-54878400	Weak transcription	Fetal Lung	lung
4	chr6:54877200-54881200	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr6:54877400-54877600	Enhancers	Fetal Brain Male	brain

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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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