Variant report

Variant	rs7003883
Chromosome Location	chr8:118595986-118595987
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1115177	1.00[ASN][1000 genomes]
rs1480167	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1480168	1.00[ASN][1000 genomes]
rs3886841	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3937768	0.82[AFR][1000 genomes]
rs6994539	1.00[ASN][1000 genomes]
rs72672150	1.00[ASN][1000 genomes]
rs72672160	1.00[ASN][1000 genomes]
rs72672165	1.00[ASN][1000 genomes]
rs72672166	1.00[ASN][1000 genomes]
rs72672167	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72672168	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72672169	1.00[ASN][1000 genomes]
rs922588	1.00[ASN][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:118591600-118615000	Weak transcription	Aorta	Aorta
2	chr8:118594800-118600000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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