Variant report

Variant	rs9493611
Chromosome Location	chr6:133687766-133687767
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1414980	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1414981	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2031596	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9373052	0.99[ASN][1000 genomes]
rs9375959	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9402506	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9402508	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9493613	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9493614	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133674000-133689800	Weak transcription	A549	lung
2	chr6:133684400-133688200	Weak transcription	Psoas Muscle	Psoas
3	chr6:133684600-133717800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr6:133686000-133688400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr6:133687200-133687800	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr6:133687200-133688400	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr6:133687400-133688000	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr6:133687600-133687800	Enhancers	Dnd41	blood
9	chr6:133687600-133690800	Enhancers	Hela-S3	cervix

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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

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