Variant report

Variant	rs9955272
Chromosome Location	chr18:12601850-12601851
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr18:12600695..12603563-chr18:12609773..12612258,2	K562	blood:
2	chr18:12601083..12604521-chr18:12605372..12609062,5	MCF-7	breast:
3	chr18:12594070..12599084-chr18:12599553..12605396,7	K562	blood:
4	chr18:12601660..12604327-chr18:12604536..12607212,2	K562	blood:

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs28458340	1.00[AMR][1000 genomes]
rs8085567	1.00[AMR][1000 genomes]
rs9945047	1.00[AMR][1000 genomes]
rs9945963	1.00[AMR][1000 genomes]
rs9949515	1.00[AMR][1000 genomes]
rs9961266	1.00[AMR][1000 genomes]
rs9962448	1.00[AMR][1000 genomes]
rs9963004	1.00[AMR][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	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	esv3528039	chr18:12396582-12851293	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
4	esv3528041	chr18:12396641-12851245	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
5	nsv523743	chr18:12474505-12742809	Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12597000-12605800	Weak transcription	Gastric	stomach
2	chr18:12597000-12605800	Weak transcription	K562	blood
3	chr18:12597000-12606800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr18:12597800-12610800	Weak transcription	Right Ventricle	heart
5	chr18:12597800-12634600	Weak transcription	Aorta	Aorta
6	chr18:12598000-12606600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr18:12598000-12607000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr18:12598000-12607200	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr18:12598000-12610000	Weak transcription	Lung	lung
10	chr18:12598200-12606800	Weak transcription	Brain Anterior Caudate	brain
11	chr18:12598600-12608600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr18:12598800-12606000	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr18:12598800-12606000	Weak transcription	Left Ventricle	heart
14	chr18:12598800-12606800	Weak transcription	Brain Cingulate Gyrus	brain
15	chr18:12598800-12607000	Weak transcription	Brain Angular Gyrus	brain
16	chr18:12598800-12609000	Weak transcription	Right Atrium	heart
17	chr18:12599000-12606800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr18:12599000-12606800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr18:12599800-12606200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr18:12599800-12607000	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr18:12600000-12604600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr18:12600000-12606200	Weak transcription	A549	lung
23	chr18:12600000-12607400	Weak transcription	Pancreas	Pancrea
24	chr18:12600200-12607000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr18:12600400-12604600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr18:12600400-12605800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr18:12600400-12605800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr18:12600400-12605800	Weak transcription	Hela-S3	cervix
29	chr18:12600400-12606600	Weak transcription	HepG2	liver
30	chr18:12600400-12606800	Weak transcription	HSMM	muscle
31	chr18:12600400-12607000	Weak transcription	NHLF	lung
32	chr18:12600400-12608600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr18:12600600-12602000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr18:12600600-12605000	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr18:12600600-12606000	Weak transcription	NHEK	skin
36	chr18:12600600-12606400	Weak transcription	HSMMtube	muscle
37	chr18:12600600-12606800	Weak transcription	NHDF-Ad	bronchial
38	chr18:12600800-12604800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr18:12601600-12602600	Enhancers	Primary hematopoietic stem cells	blood
40	chr18:12601600-12602800	Enhancers	Primary T cells from cord blood	blood
41	chr18:12601600-12602800	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr18:12601600-12602800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr18:12601600-12603000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr18:12601800-12602000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr18:12601800-12602000	Genic enhancers	Fetal Brain Female	brain
46	chr18:12601800-12602000	Enhancers	Spleen	Spleen
47	chr18:12601800-12602200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr18:12601800-12602200	Enhancers	Fetal Brain Male	brain
49	chr18:12601800-12602400	Enhancers	Brain Hippocampus Middle	brain
50	chr18:12601800-12602600	Enhancers	Fetal Thymus	thymus

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