Variant report

Variant	rs10898479
Chromosome Location	chr11:86104460-86104461
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs11234629	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56019070	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61906693	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61906694	0.98[ASN][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86086000-86106200	Weak transcription	Aorta	Aorta
2	chr11:86095200-86106200	Weak transcription	Fetal Brain Female	brain
3	chr11:86097600-86105000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr11:86098200-86105000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr11:86099600-86105000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr11:86102000-86105000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr11:86102200-86105200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr11:86102400-86106400	Weak transcription	HUVEC	blood vessel

Quick Search:

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

what's new

Quick links