Variant report

Variant	rs1147477
Chromosome Location	chr14:69777855-69777856
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10141602	0.90[CHB][hapmap];0.98[ASN][1000 genomes]
rs10146252	0.98[ASN][1000 genomes]
rs12880330	0.89[EUR][1000 genomes]
rs1378286	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1954119	1.00[CHB][hapmap];0.94[JPT][hapmap];0.82[YRI][hapmap];0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs35613673	0.96[ASN][1000 genomes]
rs4902713	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs56107218	0.90[ASN][1000 genomes]
rs745781	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8017671	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs8021760	0.98[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69770200-69778400	Weak transcription	Left Ventricle	heart
2	chr14:69777600-69778000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr14:69777600-69783200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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