Variant report

Variant	rs60600614
Chromosome Location	chr2:115844811-115844812
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10184481	0.93[AMR][1000 genomes]
rs10496485	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs13397884	0.93[AMR][1000 genomes]
rs13429396	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1396919	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17044073	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2420886	0.96[ASN][1000 genomes]
rs58951820	0.96[ASN][1000 genomes]
rs62164532	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:115843200-115849800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:115844600-115845000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
3	chr2:115844600-115845600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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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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