Variant report

Variant	rs10873218
Chromosome Location	chr14:69760394-69760395
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10782457	1.00[CEU][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12586532	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12589585	0.81[CEU][hapmap]
rs4496059	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7493080	0.89[EUR][1000 genomes]
rs8006103	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8016064	0.98[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69735800-69771600	Weak transcription	Fetal Intestine Small	intestine
2	chr14:69750200-69760600	Weak transcription	Pancreas	Pancrea
3	chr14:69758800-69760600	Enhancers	Fetal Heart	heart
4	chr14:69759200-69765200	Weak transcription	Right Atrium	heart
5	chr14:69759400-69764800	Weak transcription	Left Ventricle	heart
6	chr14:69759400-69764800	Weak transcription	Right Ventricle	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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