Variant report

Variant	rs7226445
Chromosome Location	chr18:8355048-8355049
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:8353642..8356194-chr18:8356373..8359340,2	K562	blood:

Extended variants
information (count: 26 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11873504	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11873699	0.92[CEU][hapmap];0.83[CHB][hapmap];0.86[JPT][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11875935	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11876724	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11876786	0.81[ASW][hapmap];0.83[CHB][hapmap];0.96[CHD][hapmap];0.85[GIH][hapmap];0.89[JPT][hapmap];0.85[TSI][hapmap];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11877672	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12456630	0.91[CHD][hapmap];0.81[TSI][hapmap]
rs12954518	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12966511	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1542451	0.87[CEU][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17490458	0.91[CHD][hapmap];0.84[AMR][1000 genomes]
rs17490807	0.92[CEU][hapmap];0.83[CHB][hapmap];0.89[JPT][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17490828	0.81[ASW][hapmap];0.92[CEU][hapmap];0.83[CHB][hapmap];0.96[CHD][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap];0.95[MEX][hapmap];0.90[TSI][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2279074	0.81[ASW][hapmap];0.83[CHB][hapmap];0.96[CHD][hapmap];0.85[GIH][hapmap];0.89[JPT][hapmap];0.85[TSI][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2279075	0.81[ASW][hapmap];0.83[CHB][hapmap];0.96[CHD][hapmap];0.85[GIH][hapmap];0.89[JPT][hapmap];0.85[TSI][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35431779	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs36032451	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56137612	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62085046	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7244164	0.81[ASW][hapmap];0.91[CEU][hapmap];0.83[CHB][hapmap];0.96[CHD][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap];0.92[TSI][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8087223	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.97[TSI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534374	chr18:7438812-8412546	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv458018	chr18:8110805-8645907	Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv576426	chr18:8110805-8645907	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	esv3351324	chr18:8250514-8405140	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1058445	chr18:8270681-8421249	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7226445	TUBB6	cis	cerebellum	SCAN

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:8320800-8357200	Weak transcription	Thymus	Thymus
2	chr18:8329600-8358200	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr18:8329800-8365200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr18:8340200-8365600	Weak transcription	Psoas Muscle	Psoas
5	chr18:8342000-8359200	Weak transcription	Stomach Smooth Muscle	stomach
6	chr18:8342000-8362400	Weak transcription	Fetal Muscle Trunk	muscle
7	chr18:8342200-8355200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr18:8342200-8359600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr18:8342200-8366800	Weak transcription	Adipose Nuclei	Adipose
10	chr18:8342200-8367400	Weak transcription	Aorta	Aorta
11	chr18:8342600-8366400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr18:8342800-8357600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr18:8344200-8356600	Weak transcription	A549	lung
14	chr18:8344200-8367000	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr18:8345400-8358200	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr18:8346400-8366800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr18:8346600-8358200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr18:8346600-8358800	Weak transcription	Ovary	ovary
19	chr18:8348600-8359200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr18:8350200-8362000	Weak transcription	Lung	lung
21	chr18:8350200-8366200	Weak transcription	Pancreas	Pancrea
22	chr18:8350200-8367200	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr18:8350400-8359800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr18:8352000-8359400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr18:8352400-8367200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr18:8352600-8372600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr18:8353800-8356400	Enhancers	Right Ventricle	heart
28	chr18:8354200-8355400	Enhancers	Fetal Heart	heart
29	chr18:8354600-8355200	Enhancers	Gastric	stomach
30	chr18:8354600-8355400	Enhancers	Left Ventricle	heart
31	chr18:8354600-8355400	Enhancers	Right Atrium	heart
32	chr18:8354800-8366800	Weak transcription	HSMMtube	muscle
33	chr18:8355000-8355400	Enhancers	Fetal Brain Female	brain
34	chr18:8355000-8358000	Weak transcription	Fetal Brain Male	brain
35	chr18:8355000-8358000	Weak transcription	HepG2	liver

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