Variant report

Variant	rs11119797
Chromosome Location	chr1:211889042-211889043
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12123627	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12130915	0.80[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12145195	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12145981	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56230302	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7512315	0.85[EUR][1000 genomes]
rs7525086	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7543710	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7545954	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211879200-211913600	Weak transcription	Right Atrium	heart
2	chr1:211884800-211889400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr1:211885400-211889200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:211888800-211889600	Enhancers	Adipose Nuclei	Adipose
5	chr1:211889000-211889600	Enhancers	Fetal Muscle Trunk	muscle
6	chr1:211889000-211889800	Enhancers	Fetal Muscle Leg	muscle
7	chr1:211889000-211889800	Enhancers	Left Ventricle	heart

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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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