Variant report

Variant	rs62364704
Chromosome Location	chr5:94369876-94369877
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs17339969	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs67002726	0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2756469	chr5:94323268-94400017	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94349000-94377800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:94364200-94371000	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr5:94366400-94371800	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr5:94366400-94374200	Weak transcription	Primary hematopoietic stem cells	blood
5	chr5:94367200-94371600	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr5:94369000-94370400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr5:94369400-94378200	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr5:94369600-94373000	Weak transcription	HUVEC	blood vessel

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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