Variant report

Variant	rs2813705
Chromosome Location	chr1:216866976-216866977
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10442689	0.97[ASN][1000 genomes]
rs12728283	0.97[ASN][1000 genomes]
rs1339341	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1932494	0.80[ASN][1000 genomes]
rs1948639	0.82[ASN][1000 genomes]
rs2211118	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2813693	0.92[AFR][1000 genomes]
rs2813699	0.86[EUR][1000 genomes]
rs2820884	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2820885	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3862956	0.83[AFR][1000 genomes]
rs3900668	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3929878	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4085154	0.86[AFR][1000 genomes]
rs4846649	0.87[AFR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:216856400-216869800	Weak transcription	Psoas Muscle	Psoas
2	chr1:216864000-216873200	Weak transcription	Fetal Heart	heart
3	chr1:216866800-216867600	Weak transcription	Placenta	Placenta

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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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