Variant report

Variant	rs66789646
Chromosome Location	chr5:94331535-94331536
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs13360791	1.00[ASN][1000 genomes]
rs1426099	0.95[EUR][1000 genomes]
rs55682625	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56281733	1.00[EUR][1000 genomes]
rs56386135	0.95[EUR][1000 genomes]
rs66816988	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67223139	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67482451	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs722722	1.00[ASN][1000 genomes]
rs72777358	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72777361	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72777365	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72777369	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72777390	1.00[EUR][1000 genomes]
rs72777398	1.00[EUR][1000 genomes]
rs72777399	0.95[EUR][1000 genomes]
rs72777401	0.95[EUR][1000 genomes]
rs72779403	0.95[EUR][1000 genomes]
rs72779406	0.90[EUR][1000 genomes]
rs72779407	0.90[EUR][1000 genomes]
rs72779408	0.90[EUR][1000 genomes]
rs72779410	0.88[EUR][1000 genomes]
rs72779411	0.88[EUR][1000 genomes]
rs73138010	1.00[ASN][1000 genomes]
rs977577	1.00[ASN][1000 genomes]
rs977578	1.00[ASN][1000 genomes]
rs998822	1.00[ASN][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:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94301200-94337600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:94313800-94337000	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr5:94319800-94346600	Weak transcription	HUVEC	blood vessel
4	chr5:94320400-94348000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr5:94322400-94334200	Weak transcription	Gastric	stomach
6	chr5:94325600-94337600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr5:94325800-94337400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr5:94326000-94339400	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr5:94327000-94339200	Weak transcription	Primary T cells from cord blood	blood
10	chr5:94327200-94339000	Weak transcription	Primary hematopoietic stem cells	blood
11	chr5:94330000-94331600	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr5:94330200-94332200	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr5:94330400-94334200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr5:94330400-94336600	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr5:94330600-94331600	Enhancers	H1 Cell Line	embryonic stem cell
16	chr5:94330800-94332200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr5:94331000-94332200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr5:94331200-94331600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr5:94331200-94332000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr5:94331200-94333000	Weak transcription	Stomach Mucosa	stomach
21	chr5:94331400-94331600	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr5:94331400-94331800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr5:94331400-94334400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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