Variant report

Variant	rs927992
Chromosome Location	chr13:51619095-51619096
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11148205	0.87[CHB][hapmap]
rs11842080	0.94[CHB][hapmap];0.85[JPT][hapmap];0.85[ASN][1000 genomes]
rs12859216	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12871332	0.94[CHB][hapmap]
rs12877403	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3790015	0.87[CHB][hapmap];0.85[JPT][hapmap];0.81[ASN][1000 genomes]
rs3790017	0.81[ASN][1000 genomes]
rs3803198	0.93[CHB][hapmap];0.85[JPT][hapmap]
rs3803199	0.93[CHB][hapmap];0.85[JPT][hapmap]
rs3803200	0.93[CHB][hapmap];0.85[JPT][hapmap]
rs913467	0.94[CHB][hapmap];0.84[ASN][1000 genomes]
rs9526717	0.93[CHB][hapmap];0.85[JPT][hapmap];0.86[ASN][1000 genomes]
rs9563015	0.94[CHB][hapmap]
rs9563018	0.87[CHB][hapmap]
rs9568502	0.93[CHB][hapmap];0.85[JPT][hapmap]
rs9568503	0.93[CHB][hapmap];0.85[JPT][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51614600-51619400	Enhancers	Fetal Brain Female	brain
2	chr13:51617200-51620000	Enhancers	Brain Germinal Matrix	brain
3	chr13:51617800-51621800	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr13:51618200-51619800	Enhancers	Fetal Muscle Trunk	muscle
5	chr13:51618400-51619400	Enhancers	Fetal Muscle Leg	muscle
6	chr13:51619000-51619400	Enhancers	Spleen	Spleen

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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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