Variant report

Variant	rs60313866
Chromosome Location	chr5:94291838-94291839
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs11135416	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs159012	0.81[AMR][1000 genomes]
rs17084334	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56894814	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94288200-94294600	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr5:94288600-94296600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr5:94289000-94304800	Weak transcription	HUVEC	blood vessel
4	chr5:94289200-94300800	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr5:94290200-94292200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr5:94291000-94292200	ZNF genes & repeats	Primary hematopoietic stem cells	blood

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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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