Variant report

Variant	rs62230293
Chromosome Location	chr3:25155041-25155042
allele	G/T
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]
rs34155045	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs41441147	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs41530749	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56023574	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56098835	0.92[AMR][1000 genomes]
rs62230277	0.90[AMR][1000 genomes]
rs62230292	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62230297	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73047766	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:25147800-25157600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:25155000-25155800	Enhancers	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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