Variant report

Variant	rs1404734
Chromosome Location	chr7:147417929-147417930
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs12112619	0.81[EUR][1000 genomes]
rs1404735	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1525255	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2373177	0.92[EUR][1000 genomes]
rs6464836	0.92[EUR][1000 genomes]
rs7786758	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs851721	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:147414200-147419000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr7:147414200-147419400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:147417200-147420600	Weak transcription	Brain Anterior Caudate	brain
4	chr7:147417600-147421800	Weak transcription	Brain Substantia Nigra	brain

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