Variant report

Variant	rs4532850
Chromosome Location	chr1:56996104-56996105
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:56967555..56969959-chr1:56994759..56997021,2	K562	blood:
2	chr1:56968459..56970187-chr1:56994690..56997021,2	K562	blood:

Extended variants
information (count: 22 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10888977	0.83[ASW][hapmap];0.83[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.95[LWK][hapmap];0.88[MKK][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs11206833	0.89[CEU][hapmap];0.83[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.89[TSI][hapmap];0.82[EUR][1000 genomes]
rs12082242	0.94[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs1759750	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1759752	0.88[CEU][hapmap];0.92[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1777274	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1777277	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1810930	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1930760	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs1930762	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4628	0.89[CEU][hapmap]
rs4912314	0.81[JPT][hapmap]
rs4912377	0.84[CEU][hapmap];0.92[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs55798508	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7515808	0.81[JPT][hapmap]
rs7529520	0.86[EUR][1000 genomes]
rs7535757	0.84[ASW][hapmap];0.85[CEU][hapmap];0.82[MKK][hapmap];0.93[TSI][hapmap];0.89[YRI][hapmap];0.85[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs7556056	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs953856	0.96[YRI][hapmap];0.94[AFR][1000 genomes]
rs993075	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869295	chr1:56894955-57656562	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	esv3372563	chr1:56996027-56996357	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs4532850	PCSK9	cis	cerebellum	SCAN
rs4532850	ACOT11	cis	cerebellum	SCAN

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:56967000-57002000	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr1:56977800-56999200	Weak transcription	A549	lung
3	chr1:56983400-57000800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr1:56987000-57015000	Genic enhancers	NHDF-Ad	bronchial
5	chr1:56990000-57004000	Genic enhancers	Liver	Liver
6	chr1:56990200-56998600	Enhancers	Brain Substantia Nigra	brain
7	chr1:56990400-56996200	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr1:56990600-56996600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
9	chr1:56990600-56997800	Enhancers	Brain Anterior Caudate	brain
10	chr1:56990800-56996600	Genic enhancers	NHLF	lung
11	chr1:56990800-56997000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr1:56990800-56997200	Enhancers	Brain Cingulate Gyrus	brain
13	chr1:56990800-56997400	Enhancers	Brain Hippocampus Middle	brain
14	chr1:56991000-56996200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr1:56991200-56996600	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr1:56991800-56996800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr1:56992000-57001200	Weak transcription	Spleen	Spleen
18	chr1:56992600-56997400	Weak transcription	Lung	lung
19	chr1:56992800-56997800	Weak transcription	HSMMtube	muscle
20	chr1:56992800-56998600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr1:56992800-56998800	Weak transcription	Gastric	stomach
22	chr1:56992800-57011200	Weak transcription	Stomach Mucosa	stomach
23	chr1:56993000-56998800	Enhancers	Ovary	ovary
24	chr1:56993000-56999800	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr1:56993000-57004600	Weak transcription	Hela-S3	cervix
26	chr1:56993200-57001400	Enhancers	Right Atrium	heart
27	chr1:56993600-57007800	Weak transcription	Primary B cells from cord blood	blood
28	chr1:56993800-56998000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr1:56993800-56998200	Weak transcription	Primary B cells from peripheral blood	blood
30	chr1:56993800-57004200	Weak transcription	NH-A	brain
31	chr1:56994000-56997800	Weak transcription	Esophagus	oesophagus
32	chr1:56994000-56997800	Weak transcription	Thymus	Thymus
33	chr1:56994000-56998600	Weak transcription	Colonic Mucosa	Colon
34	chr1:56994000-56999000	Weak transcription	Aorta	Aorta
35	chr1:56994000-57000000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr1:56994000-57001200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr1:56994000-57004000	Weak transcription	HUVEC	blood vessel
38	chr1:56994000-57012400	Weak transcription	Fetal Brain Male	brain
39	chr1:56994000-57012800	Weak transcription	Fetal Brain Female	brain
40	chr1:56994200-56998000	Weak transcription	Stomach Smooth Muscle	stomach
41	chr1:56994200-56998800	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr1:56994200-56999400	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr1:56994200-57001200	Weak transcription	Dnd41	blood
44	chr1:56994200-57004400	Strong transcription	Muscle Satellite Cultured Cells	--
45	chr1:56994400-56997000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr1:56994400-56998400	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr1:56994400-57002600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr1:56994600-56996400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr1:56994600-56997000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr1:56994600-56997000	Strong transcription	Fetal Lung	lung

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