Variant report

Variant	rs16950733
Chromosome Location	chr18:44814305-44814306
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]
rs10163633	0.95[ASN][1000 genomes]
rs1347340	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.90[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs28391188	0.81[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs28417368	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28650321	0.81[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs8087053	0.85[AFR][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44810400-44819200	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr18:44813400-44815400	Weak transcription	Pancreas	Pancrea
3	chr18:44813800-44814600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr18:44814200-44814400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr18:44814200-44814400	Enhancers	Brain Hippocampus Middle	brain
6	chr18:44814200-44815200	Enhancers	Brain Cingulate Gyrus	brain
7	chr18:44814200-44815600	Bivalent Enhancer	Brain Germinal Matrix	brain

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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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