Variant report

Variant	rs6921618
Chromosome Location	chr6:11676108-11676109
allele	C/T
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]
rs28591255	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6917332	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs6920857	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs7773628	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs9461990	0.89[AMR][1000 genomes]
rs9462005	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs9469796	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11657000-11682200	Weak transcription	HSMMtube	muscle
2	chr6:11675400-11676200	Enhancers	Fetal Intestine Large	intestine
3	chr6:11675400-11676200	Enhancers	Fetal Intestine Small	intestine
4	chr6:11675400-11682000	Weak transcription	HSMM	muscle
5	chr6:11675600-11676200	Enhancers	Rectal Mucosa Donor 31	rectum

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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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