Variant report

Variant	rs215507
Chromosome Location	chr14:79303992-79303993
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs150786	0.91[CHB][hapmap]
rs154300	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs154318	1.00[CEU][hapmap];0.95[CHB][hapmap]
rs17108313	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs215509	1.00[CEU][hapmap]
rs31354	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs31356	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs31382	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs31397	1.00[CEU][hapmap];0.96[CHB][hapmap];0.80[JPT][hapmap]
rs8007270	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79303400-79304000	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr14:79303600-79305000	Weak transcription	Brain Angular Gyrus	brain
3	chr14:79303800-79304000	Enhancers	Fetal Brain Male	brain

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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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