Variant report

Variant	rs17610248
Chromosome Location	chr10:18618034-18618035
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs12240995	0.81[EUR][1000 genomes]
rs12359226	1.00[YRI][hapmap]
rs17610062	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17610159	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17683651	0.88[EUR][1000 genomes]
rs2357929	0.81[EUR][1000 genomes]
rs4748456	0.83[EUR][1000 genomes]
rs56177813	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs56346389	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56346888	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18615600-18621600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr10:18615800-18620400	Weak transcription	Liver	Liver
3	chr10:18615800-18620800	Weak transcription	Ovary	ovary
4	chr10:18615800-18620800	Weak transcription	Pancreas	Pancrea
5	chr10:18616000-18622600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr10:18616800-18620600	Weak transcription	Right Atrium	heart

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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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