Variant report

Variant	rs13139454
Chromosome Location	chr4:47016259-47016260
allele	C/G
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]
rs13108870	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs13116355	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13140672	1.00[YRI][hapmap]
rs16859782	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs17539014	1.00[YRI][hapmap]
rs34429439	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62303743	0.91[EUR][1000 genomes]
rs62303745	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62305281	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62305283	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:47013400-47019600	Weak transcription	Hela-S3	cervix
2	chr4:47013600-47018800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr4:47013600-47028600	Weak transcription	Fetal Heart	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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