Variant report

Variant	rs10818669
Chromosome Location	chr9:101006443-101006444
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:100818546..100820662-chr9:101005577..101007101,2	MCF-7	breast:
2	chr9:101005587..101007898-chr9:101011469..101013243,2	MCF-7	breast:
3	chr9:101000479..101004519-chr9:101004686..101007074,4	MCF-7	breast:
4	chr9:100683384..100686138-chr9:101006133..101008454,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000095380	Chromatin interaction
ENSG00000136932	Chromatin interaction

Extended variants
information (count: 23 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10985441	0.83[AMR][1000 genomes]
rs10985666	0.85[ASN][1000 genomes]
rs12343641	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1435261	0.89[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs1469800	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1469802	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2023361	0.83[AMR][1000 genomes]
rs2417893	0.86[AMR][1000 genomes]
rs2900463	0.86[AMR][1000 genomes]
rs3739664	0.86[AMR][1000 genomes]
rs3780449	0.82[AMR][1000 genomes]
rs3780450	0.83[AMR][1000 genomes]
rs4743186	0.86[AMR][1000 genomes]
rs4743193	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7021760	0.86[AMR][1000 genomes]
rs733040	0.85[AMR][1000 genomes]
rs7850360	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7855855	0.88[AMR][1000 genomes]
rs942166	0.86[AMR][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	nsv430085	chr9:100928245-101339645	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv831663	chr9:100941048-101109492	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1045780	chr9:100943318-101080389	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv540180	chr9:100943318-101080389	Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10818669	TBC1D2	cis	Thyroid	GTEx

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:100968600-101010400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr9:100968800-101011000	Weak transcription	Primary B cells from peripheral blood	blood
3	chr9:100974800-101010600	Weak transcription	Colon Smooth Muscle	Colon
4	chr9:100980200-101010200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr9:100981800-101010400	Weak transcription	Fetal Thymus	thymus
6	chr9:100983000-101007200	Weak transcription	Fetal Brain Male	brain
7	chr9:100989600-101016000	Weak transcription	Rectal Smooth Muscle	rectum
8	chr9:100991400-101010600	Weak transcription	Brain Cingulate Gyrus	brain
9	chr9:100991400-101015400	Weak transcription	Brain Anterior Caudate	brain
10	chr9:100991800-101011400	Weak transcription	Right Ventricle	heart
11	chr9:100992200-101012800	Weak transcription	Brain Substantia Nigra	brain
12	chr9:100992200-101016000	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr9:100993200-101010200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr9:100993400-101012600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr9:100993600-101010400	Weak transcription	Left Ventricle	heart
16	chr9:100995000-101016600	Weak transcription	Brain Angular Gyrus	brain
17	chr9:100995200-101010200	Weak transcription	NHDF-Ad	bronchial
18	chr9:100995400-101010400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr9:100995800-101010400	Weak transcription	Adipose Nuclei	Adipose
20	chr9:100995800-101011200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr9:100996000-101010600	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr9:100996000-101010600	Weak transcription	Stomach Smooth Muscle	stomach
23	chr9:100996000-101012400	Weak transcription	Fetal Stomach	stomach
24	chr9:100996000-101016000	Weak transcription	Pancreas	Pancrea
25	chr9:100996200-101017200	Weak transcription	Ovary	ovary
26	chr9:100996600-101010600	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr9:100996600-101011200	Weak transcription	Thymus	Thymus
28	chr9:100996800-101006800	Strong transcription	Osteobl	bone
29	chr9:100996800-101011000	Weak transcription	Liver	Liver
30	chr9:100997200-101008800	Weak transcription	Aorta	Aorta
31	chr9:100999600-101008400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr9:101001600-101006600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr9:101001600-101007000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr9:101002600-101006600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr9:101003600-101008800	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr9:101003800-101008800	Weak transcription	Primary hematopoietic stem cells	blood
37	chr9:101003800-101010400	Weak transcription	Spleen	Spleen
38	chr9:101003800-101011200	Weak transcription	Gastric	stomach
39	chr9:101004000-101006600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr9:101004000-101010400	Weak transcription	Colonic Mucosa	Colon
41	chr9:101004000-101011000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr9:101004200-101006600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr9:101004200-101010200	Weak transcription	Primary T helper cells PMA-I stimulated	--
44	chr9:101004200-101011000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr9:101004200-101015800	Weak transcription	Brain Hippocampus Middle	brain
46	chr9:101004200-101017200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr9:101004400-101006600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr9:101004400-101006800	Genic enhancers	Monocytes-CD14+_RO01746	blood
49	chr9:101004400-101008000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr9:101004400-101010400	Weak transcription	NHLF	lung

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