Variant report

Variant	rs1367048
Chromosome Location	chr2:209442596-209442597
allele	G/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]
rs10198932	0.87[ASN][1000 genomes]
rs1074572	0.88[ASN][1000 genomes]
rs12472161	0.84[ASN][1000 genomes]
rs13006919	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13420044	0.86[ASN][1000 genomes]
rs1835303	0.87[ASN][1000 genomes]
rs1882373	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2115771	0.87[ASN][1000 genomes]
rs2195574	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34707921	0.87[ASN][1000 genomes]
rs34776990	0.87[ASN][1000 genomes]
rs4673415	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6756807	0.87[ASN][1000 genomes]
rs930121	0.85[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209438800-209459400	Weak transcription	K562	blood

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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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