Variant report

Variant	rs10733002
Chromosome Location	chr1:179669906-179669907
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10157699	0.95[YRI][hapmap]
rs10798704	0.95[YRI][hapmap]
rs1328595	1.00[YRI][hapmap]
rs1410594	1.00[YRI][hapmap]
rs1999069	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs4391629	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4422967	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4443850	0.96[YRI][hapmap]
rs4628468	1.00[YRI][hapmap]
rs4651044	0.95[YRI][hapmap]
rs4652417	0.81[AMR][1000 genomes]
rs4652421	1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4652423	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7514875	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7534216	1.00[YRI][hapmap]
rs7549258	0.95[YRI][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179669800-179672200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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