Variant report

Variant	rs73832855
Chromosome Location	chr4:100600830-100600831
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1352776	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17029305	1.00[AMR][1000 genomes]
rs17029309	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55747704	1.00[AMR][1000 genomes]
rs57550482	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59023023	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59104387	1.00[AMR][1000 genomes]
rs6818086	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72901505	1.00[AMR][1000 genomes]
rs72901515	1.00[AMR][1000 genomes]
rs72901556	1.00[AMR][1000 genomes]
rs72917485	1.00[AMR][1000 genomes]
rs72917501	1.00[AMR][1000 genomes]
rs73832844	1.00[AMR][1000 genomes]
rs73832846	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73832848	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73832852	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73832853	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73832854	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73832856	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73832859	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73832861	0.89[AFR][1000 genomes]
rs7670745	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7678005	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933074	chr4:100460951-100630600	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100598600-100601400	Weak transcription	Aorta	Aorta
2	chr4:100599600-100601600	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr4:100599600-100601600	Enhancers	Ovary	ovary
4	chr4:100599800-100601400	Weak transcription	Left Ventricle	heart
5	chr4:100600400-100601000	Enhancers	Fetal Heart	heart
6	chr4:100600400-100601000	Enhancers	Stomach Smooth Muscle	stomach
7	chr4:100600400-100601200	Active TSS	Skeletal Muscle Male	skeletal muscle
8	chr4:100600400-100601400	Enhancers	Skeletal Muscle Female	skeletal muscle
9	chr4:100600400-100601600	Enhancers	Fetal Muscle Leg	muscle
10	chr4:100600400-100601600	Enhancers	Psoas Muscle	Psoas
11	chr4:100600600-100601200	Enhancers	HSMMtube	muscle
12	chr4:100600600-100601600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr4:100600600-100601600	Enhancers	Liver	Liver
14	chr4:100600800-100605000	Weak transcription	Fetal Lung	lung

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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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