Variant report

Variant	rs9859192
Chromosome Location	chr3:121680681-121680682
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs1136995	0.89[EUR][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	esv33139	chr3:121500400-122091831	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs9859192	GOLGB1	cis	multi-tissue	Pritchard
rs9859192	EAF2	Cis_1M	lymphoblastoid	RTeQTL
rs9859192	SLC15A2	Cis_1M	lymphoblastoid	RTeQTL
rs9859192	IQCB1	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:121670400-121686800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:121677200-121681200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr3:121677200-121681600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr3:121677200-121682000	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr3:121678200-121681000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr3:121678800-121693400	Weak transcription	Primary B cells from cord blood	blood

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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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