Variant report

Variant	rs4536111
Chromosome Location	chr10:4360511-4360512
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10904225	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10904226	0.84[ASN][1000 genomes]
rs10904227	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11252451	0.84[AMR][1000 genomes]
rs11252457	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11252458	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11252459	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12765847	0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12769562	0.81[AMR][1000 genomes]
rs12773994	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12777785	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1926786	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2182584	0.84[AMR][1000 genomes]
rs4307624	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4579834	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4584477	0.89[AMR][1000 genomes]
rs4881314	0.89[AMR][1000 genomes]
rs4881316	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7093134	0.80[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][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	nsv894785	chr10:4306421-4372629	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4357000-4360600	Enhancers	Fetal Lung	lung
2	chr10:4358800-4361600	Weak transcription	Ovary	ovary
3	chr10:4359000-4362800	Weak transcription	Fetal Muscle Leg	muscle
4	chr10:4359000-4373400	Weak transcription	Right Atrium	heart
5	chr10:4359400-4364600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr10:4359800-4366200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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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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