Variant report

Variant	rs13251779
Chromosome Location	chr8:59099191-59099192
allele	A/G
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]
rs10100258	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10808689	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11782856	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13251766	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2939974	0.85[ASN][1000 genomes]
rs2977384	0.82[ASN][1000 genomes]
rs2977386	0.85[ASN][1000 genomes]
rs2977390	0.85[ASN][1000 genomes]
rs2977391	0.85[ASN][1000 genomes]
rs35764763	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs36094668	0.80[EUR][1000 genomes]
rs4373508	0.83[ASN][1000 genomes]
rs4398899	0.83[ASN][1000 genomes]
rs7815202	0.86[ASN][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:59084200-59099800	Weak transcription	Fetal Brain Female	brain
2	chr8:59093200-59103200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:59093400-59105600	Weak transcription	HMEC	breast
4	chr8:59098400-59099600	Weak transcription	Fetal Brain Male	brain
5	chr8:59098600-59104000	Weak transcription	Cortex derived primary cultured neurospheres	brain

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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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