Variant report

Variant	rs10211913
Chromosome Location	chr21:41526864-41526865
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1011765	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11911749	0.86[CEU][hapmap];0.82[EUR][1000 genomes]
rs13046032	0.81[EUR][1000 genomes]
rs13046959	0.80[EUR][1000 genomes]
rs2837465	0.96[EUR][1000 genomes]
rs8130732	0.80[EUR][1000 genomes]
rs8132673	0.80[CEU][hapmap];0.84[EUR][1000 genomes]
rs9978731	0.91[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9983013	0.86[AFR][1000 genomes];0.96[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:41517200-41528800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr21:41525400-41534000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr21:41525800-41527000	Enhancers	Brain Germinal Matrix	brain
4	chr21:41526400-41527400	Enhancers	Fetal Brain Female	brain
5	chr21:41526400-41527800	Enhancers	Fetal Muscle Leg	muscle
6	chr21:41526800-41527000	Enhancers	Fetal Stomach	stomach

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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