Variant report

Variant	rs1013593
Chromosome Location	chr2:76245086-76245087
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]
rs10195421	0.95[CEU][hapmap];0.83[CHB][hapmap]
rs1524215	0.82[JPT][hapmap]
rs2422409	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs317234	0.85[ASN][1000 genomes]
rs367949	0.84[ASN][1000 genomes]
rs379732	0.85[ASN][1000 genomes]
rs381100	0.85[ASN][1000 genomes]
rs3931110	0.81[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs450596	0.94[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs6755642	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:76243800-76245200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:76244200-76245800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr2:76244600-76246200	Weak transcription	H9 Derived Neuron 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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