Variant report

Variant	rs4475832
Chromosome Location	chr10:4351582-4351583
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10795151	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10795152	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10795155	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4881315	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7071086	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7086185	0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7096543	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7901676	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9423528	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[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:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4345400-4352400	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr10:4348200-4357200	Weak transcription	Fetal Muscle Leg	muscle
3	chr10:4349400-4357800	Weak transcription	Ovary	ovary
4	chr10:4349400-4357800	Weak transcription	Psoas Muscle	Psoas
5	chr10:4349800-4353800	Enhancers	Fetal Heart	heart
6	chr10:4350200-4351600	Enhancers	Left Ventricle	heart
7	chr10:4350400-4352400	Weak transcription	Brain Germinal Matrix	brain
8	chr10:4350400-4355600	Weak transcription	Fetal Brain Male	brain
9	chr10:4350400-4355800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr10:4350400-4357200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr10:4350600-4355200	Weak transcription	Fetal Lung	lung
12	chr10:4350800-4353400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr10:4350800-4358600	Weak transcription	Right Atrium	heart
14	chr10:4351400-4351600	Enhancers	Skeletal Muscle Female	skeletal muscle

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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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