Variant report

Variant	rs9326370
Chromosome Location	chr11:65992008-65992009
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:65985243..65987105-chr11:65991157..65993460,2	K562	blood:
2	chr11:65983052..65986048-chr11:65987938..65993154,6	K562	blood:
3	chr11:65991713..65994038-chr11:66048544..66051109,2	K562	blood:
4	chr11:65990668..65992905-chr11:66012040..66014914,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000174871	Chromatin interaction
ENSG00000175115	Chromatin interaction
ENSG00000255320	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10791865	1.00[GIH][hapmap]
rs10896104	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1115508	0.94[EUR][1000 genomes]
rs1151537	0.94[EUR][1000 genomes]
rs1151539	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1151540	1.00[CEU][hapmap];1.00[GIH][hapmap];0.95[MEX][hapmap];0.98[TSI][hapmap];0.94[EUR][1000 genomes]
rs1203798	0.96[EUR][1000 genomes]
rs1717669	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1892939	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2508657	0.93[EUR][1000 genomes]
rs3016319	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs474005	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs521109	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs524859	0.89[GIH][hapmap]
rs528842	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs555360	0.95[EUR][1000 genomes]
rs556595	1.00[CEU][hapmap];0.87[CHB][hapmap];0.97[GIH][hapmap];0.80[JPT][hapmap];1.00[MEX][hapmap];0.86[TSI][hapmap];0.87[EUR][1000 genomes]
rs708471	0.94[EUR][1000 genomes]
rs708472	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs801731	0.93[EUR][1000 genomes]
rs801734	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs801735	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs801736	0.95[EUR][1000 genomes]
rs801737	0.94[EUR][1000 genomes]
rs801739	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs801741	1.00[CEU][hapmap];0.92[GIH][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3335923	chr11:65741698-66175759	Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
2	esv1819302	chr11:65787660-66007018	Active TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
3	esv3407551	chr11:65794503-66158322	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
4	esv3392427	chr11:65981489-66273695	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs9326370	RAB1B	cis	parietal	SCAN
rs9326370	C11orf2	cis	parietal	SCAN
rs9326370	SNX32	cis	parietal	SCAN
rs9326370	PACS1	cis	parietal	SCAN
rs9326370	MRGPRF	cis	parietal	SCAN
rs9326370	RAB1B	cis	cerebellum	SCAN

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65961400-66011200	Weak transcription	Psoas Muscle	Psoas
2	chr11:65976600-66006000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr11:65976800-65996000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr11:65977200-65996000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr11:65977400-66010600	Strong transcription	Fetal Stomach	stomach
6	chr11:65977600-66018600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr11:65978000-65993000	Strong transcription	Primary neutrophils fromperipheralblood	blood
8	chr11:65979800-66001200	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr11:65980000-65994000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr11:65982200-65995800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr11:65984600-66024200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr11:65984800-66000400	Weak transcription	HMEC	breast
13	chr11:65985200-65998800	Weak transcription	NHDF-Ad	bronchial
14	chr11:65985800-66017800	Weak transcription	Fetal Heart	heart
15	chr11:65987000-65992200	Weak transcription	HSMMtube	muscle
16	chr11:65987600-65992200	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr11:65987800-66003400	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr11:65988200-66001200	Weak transcription	Small Intestine	intestine
19	chr11:65988400-65992400	Weak transcription	HUVEC	blood vessel
20	chr11:65988400-65995800	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr11:65988600-65995200	Weak transcription	Brain Angular Gyrus	brain
22	chr11:65988600-65995200	Weak transcription	NHLF	lung
23	chr11:65988600-65997800	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr11:65988800-65992200	Weak transcription	Aorta	Aorta
25	chr11:65988800-65992400	Weak transcription	Brain Hippocampus Middle	brain
26	chr11:65988800-65992400	Weak transcription	Fetal Lung	lung
27	chr11:65988800-65992400	Weak transcription	Left Ventricle	heart
28	chr11:65988800-65992400	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr11:65988800-65994600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr11:65988800-65995000	Weak transcription	Liver	Liver
31	chr11:65988800-65997800	Weak transcription	Pancreas	Pancrea
32	chr11:65988800-65998400	Weak transcription	Brain Substantia Nigra	brain
33	chr11:65988800-65998800	Weak transcription	Colonic Mucosa	Colon
34	chr11:65989000-65995200	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr11:65989000-65997800	Weak transcription	Right Ventricle	heart
36	chr11:65989400-65992400	Weak transcription	Brain Cingulate Gyrus	brain
37	chr11:65989600-66024200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr11:65989800-65992200	Weak transcription	Spleen	Spleen
39	chr11:65990000-65995200	Weak transcription	Gastric	stomach
40	chr11:65990000-66002600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr11:65990200-65995200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr11:65990200-65995200	Weak transcription	Esophagus	oesophagus
43	chr11:65990200-65995800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr11:65990200-65995800	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr11:65990200-65996200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr11:65990200-65998600	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr11:65990200-65999200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr11:65990200-65999200	Weak transcription	Stomach Mucosa	stomach
49	chr11:65990200-66003000	Weak transcription	HepG2	liver
50	chr11:65990200-66007600	Weak transcription	H1 Cell Line	embryonic stem cell

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