Variant report

Variant	rs34590963
Chromosome Location	chr3:18091958-18091959
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs2203242	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4130063	0.95[ASN][1000 genomes]
rs4132218	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4688898	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4688899	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4688913	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6790525	1.00[EUR][1000 genomes]
rs7627583	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7645289	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9809015	0.91[ASN][1000 genomes]
rs9846000	0.95[ASN][1000 genomes]
rs9857811	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9859212	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9861146	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:18086000-18092800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:18086000-18096000	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr3:18086800-18113400	Weak transcription	Fetal Thymus	thymus
4	chr3:18088400-18095600	Weak transcription	Primary hematopoietic stem cells	blood

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