Variant report

Variant	rs895911
Chromosome Location	chr14:85787747-85787748
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs12436591	0.87[EUR][1000 genomes]
rs12436824	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17201916	0.81[EUR][1000 genomes]
rs2034018	0.93[AFR][1000 genomes]
rs60463145	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6574813	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7140796	0.87[EUR][1000 genomes]
rs7154757	0.91[ASN][1000 genomes]
rs7159595	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72689116	0.87[EUR][1000 genomes]
rs72689118	0.87[EUR][1000 genomes]
rs72689121	0.87[EUR][1000 genomes]
rs72689126	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72689127	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:85785000-85798800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr14:85785600-85787800	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr14:85786800-85789000	Weak transcription	Pancreas	Pancrea

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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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