Variant report

Variant	rs6718207
Chromosome Location	chr2:180518926-180518927
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10199992	0.81[ASN][1000 genomes]
rs1033213	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10497548	0.87[ASN][1000 genomes]
rs10803927	0.87[ASN][1000 genomes]
rs13035546	0.91[ASN][1000 genomes]
rs1515286	0.95[ASN][1000 genomes]
rs1515291	0.81[ASN][1000 genomes]
rs17821260	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1877941	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2037112	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2276573	0.95[ASN][1000 genomes]
rs3106718	0.87[ASN][1000 genomes]
rs3106720	0.88[ASN][1000 genomes]
rs3112932	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3112935	0.88[ASN][1000 genomes]
rs34227133	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62175185	0.81[ASN][1000 genomes]
rs62175186	0.87[ASN][1000 genomes]
rs7557247	0.86[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180517400-180521400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:180518400-180519400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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