Variant report

Variant	rs231121
Chromosome Location	chr16:64805237-64805238
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs16967877	0.88[ASN][1000 genomes]
rs1862769	0.95[ASN][1000 genomes]
rs1862770	0.95[ASN][1000 genomes]
rs231076	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs231078	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs231089	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs231091	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs231097	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs231104	0.80[EUR][1000 genomes]
rs231106	0.85[AMR][1000 genomes]
rs231111	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs231119	0.88[EUR][1000 genomes]
rs8055356	0.98[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:64803600-64807400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr16:64803800-64805800	Weak transcription	Osteobl	bone
3	chr16:64805000-64805400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr16:64805000-64806000	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr16:64805200-64805600	Enhancers	Esophagus	oesophagus

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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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