Variant report

Variant	rs10484668
Chromosome Location	chr6:133703698-133703699
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs17062414	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3777804	0.96[YRI][hapmap];0.84[AFR][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133684600-133717800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr6:133699400-133705600	Weak transcription	Hela-S3	cervix
3	chr6:133701200-133703800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr6:133701800-133703800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr6:133701800-133710000	Weak transcription	Psoas Muscle	Psoas
6	chr6:133703200-133703800	Enhancers	HSMMtube	muscle

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