Variant report

Variant	rs10006167
Chromosome Location	chr4:118767115-118767116
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs12640486	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12646271	1.00[CHB][hapmap];0.85[JPT][hapmap];0.82[EUR][1000 genomes]
rs28791500	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4392571	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4429786	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs4833553	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:118766200-118767600	Enhancers	Rectal Mucosa Donor 31	rectum
2	chr4:118766600-118767200	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr4:118766600-118769400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr4:118766600-118769400	Weak transcription	Sigmoid Colon	Sigmoid Colon

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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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