Variant report

Variant	rs211630
Chromosome Location	chr6:133688284-133688285
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs150532	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs211601	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs211602	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs211604	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs211610	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap]
rs211619	0.80[EUR][1000 genomes]
rs211620	1.00[CEU][hapmap]
rs212813	1.00[CEU][hapmap];0.81[EUR][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133674000-133689800	Weak transcription	A549	lung
2	chr6:133684600-133717800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr6:133686000-133688400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr6:133687200-133688400	Enhancers	Skeletal Muscle Female	skeletal muscle
5	chr6:133687600-133690800	Enhancers	Hela-S3	cervix
6	chr6:133687800-133690400	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr6:133688000-133689200	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr6:133688200-133688400	Enhancers	Psoas Muscle	Psoas

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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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