Variant report

Variant	rs10782457
Chromosome Location	chr14:69760369-69760370
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10873218	1.00[CEU][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12586532	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12589585	0.81[CEU][hapmap]
rs1890941	0.82[YRI][hapmap]
rs4496059	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7493080	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs8006103	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.98[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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