Variant report

Variant	rs9962240
Chromosome Location	chr18:12334203-12334204
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr18:12304979..12308873-chr18:12332783..12336926,3	K562	blood:
2	chr18:12333793..12335382-chr18:12358022..12359784,2	K562	blood:
3	chr18:12334089..12335746-chr18:12343294..12345170,2	K562	blood:
4	chr18:12327453..12330082-chr18:12330908..12334376,4	K562	blood:
5	chr18:12333547..12336346-chr18:12375267..12377221,2	K562	blood:
6	chr18:12327453..12329462-chr18:12331955..12334376,2	K562	blood:

Variant related genes	Relation type
ENSG00000176014	Chromatin interaction
ENSG00000141385	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs9945568	1.00[AFR][1000 genomes]
rs9946027	1.00[AMR][1000 genomes]
rs9950999	1.00[AFR][1000 genomes]
rs9961298	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9961477	1.00[AFR][1000 genomes]
rs9962634	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9964600	1.00[AMR][1000 genomes]
rs9964653	1.00[AMR][1000 genomes]
rs9965144	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063125	chr18:12046892-12918251	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	130 gene(s)	inside rSNPs	diseases
2	nsv491873	chr18:12159445-12739784	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
3	nsv909400	chr18:12201374-12585545	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
4	esv2758471	chr18:12240681-12499525	Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
5	esv2758714	chr18:12240681-12499525	Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
6	nsv576496	chr18:12247872-12490502	Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
7	nsv1060808	chr18:12302792-12514417	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
8	esv3442047	chr18:12331977-12334525	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	esv3408066	chr18:12332052-12334450	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9962240	TUBB6	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12314400-12342600	Weak transcription	Small Intestine	intestine
2	chr18:12318400-12334800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr18:12319000-12336800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr18:12320800-12348200	Strong transcription	Fetal Intestine Small	intestine
5	chr18:12323400-12342800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr18:12324800-12337000	Strong transcription	Liver	Liver
7	chr18:12324800-12338800	Strong transcription	Rectal Mucosa Donor 29	rectum
8	chr18:12324800-12339400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr18:12325200-12335800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr18:12326000-12343200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr18:12326200-12366400	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr18:12326800-12334400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr18:12328000-12335400	Weak transcription	Psoas Muscle	Psoas
14	chr18:12328000-12335600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr18:12328400-12334600	Weak transcription	Stomach Mucosa	stomach
16	chr18:12329600-12336800	Weak transcription	NHDF-Ad	bronchial
17	chr18:12331400-12334600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr18:12331400-12336800	Weak transcription	HUVEC	blood vessel
19	chr18:12333000-12336400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr18:12333000-12336800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr18:12333200-12336200	Strong transcription	Duodenum Mucosa	Duodenum
22	chr18:12333200-12339600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr18:12333200-12362200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr18:12333200-12370800	Strong transcription	Fetal Muscle Trunk	muscle
25	chr18:12333200-12371200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
26	chr18:12333400-12334600	Strong transcription	Pancreas	Pancrea
27	chr18:12333400-12334800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr18:12333400-12335600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr18:12333400-12335800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr18:12333400-12335800	Strong transcription	Skeletal Muscle Male	skeletal muscle
31	chr18:12333400-12336400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr18:12333400-12336400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr18:12333400-12337000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr18:12333400-12339000	Enhancers	H1 Cell Line	embryonic stem cell
35	chr18:12333400-12339000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr18:12333400-12339000	Strong transcription	Colonic Mucosa	Colon
37	chr18:12333400-12339200	Strong transcription	Primary T helper cells fromperipheralblood	blood
38	chr18:12333400-12339600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr18:12333400-12339600	Strong transcription	Thymus	Thymus
40	chr18:12333400-12340800	Strong transcription	Primary monocytes fromperipheralblood	blood
41	chr18:12333400-12366600	Strong transcription	Sigmoid Colon	Sigmoid Colon
42	chr18:12333400-12370200	Strong transcription	Fetal Thymus	thymus
43	chr18:12333400-12370800	Strong transcription	Fetal Muscle Leg	muscle
44	chr18:12333400-12371400	Strong transcription	Fetal Stomach	stomach
45	chr18:12333600-12334400	Strong transcription	Fetal Brain Male	brain
46	chr18:12333600-12334400	Strong transcription	Fetal Intestine Large	intestine
47	chr18:12333600-12334400	Strong transcription	Fetal Kidney	kidney
48	chr18:12333600-12334400	ZNF genes & repeats	Lung	lung
49	chr18:12333600-12334400	Strong transcription	HMEC	breast
50	chr18:12333600-12334600	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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