Variant report

Variant	rs559259215
Chromosome Location	chr18:9223432-9223433
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:9212963..9214485-chr18:9221786..9224318,2	K562	blood:
2	chr18:9216476..9220254-chr18:9222451..9224440,3	K562	blood:

Variant related genes	Relation type
ENSG00000101745	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

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	nsv916373	chr18:9026803-9592201	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv431971	chr18:9081185-9326852	Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv1056407	chr18:9144345-9553764	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv1055696	chr18:9191679-9309805	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	esv3338337	chr18:9223152-9227450	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:9174600-9233600	Weak transcription	Spleen	Spleen
2	chr18:9174800-9233600	Weak transcription	Pancreas	Pancrea
3	chr18:9183800-9225600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr18:9184600-9233800	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr18:9185200-9233800	Weak transcription	Right Ventricle	heart
6	chr18:9185600-9232400	Weak transcription	Colonic Mucosa	Colon
7	chr18:9188400-9233600	Weak transcription	Esophagus	oesophagus
8	chr18:9188600-9233600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr18:9189200-9233800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr18:9192200-9233600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr18:9192200-9284000	Weak transcription	NHEK	skin
12	chr18:9193400-9224800	Weak transcription	Lung	lung
13	chr18:9193400-9230600	Weak transcription	Fetal Stomach	stomach
14	chr18:9199200-9224800	Weak transcription	Fetal Intestine Small	intestine
15	chr18:9201000-9232000	Weak transcription	Brain Substantia Nigra	brain
16	chr18:9201200-9232800	Weak transcription	Gastric	stomach
17	chr18:9202200-9234000	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr18:9202600-9229400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr18:9203400-9228800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr18:9207600-9226800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr18:9207800-9225200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr18:9207800-9231000	Strong transcription	Primary T helper cells fromperipheralblood	blood
23	chr18:9208000-9228600	Strong transcription	Liver	Liver
24	chr18:9208400-9227000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr18:9208800-9226400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr18:9209400-9228200	Strong transcription	Primary B cells from cord blood	blood
27	chr18:9210600-9228000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
28	chr18:9210800-9224000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr18:9210800-9228200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr18:9211000-9224600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr18:9211000-9228600	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr18:9211200-9231600	Strong transcription	Monocytes-CD14+_RO01746	blood
33	chr18:9211800-9254800	Weak transcription	NH-A	brain
34	chr18:9212200-9224800	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr18:9212200-9254200	Weak transcription	Hela-S3	cervix
36	chr18:9213200-9232200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr18:9214200-9224400	Strong transcription	Duodenum Mucosa	Duodenum
38	chr18:9214200-9228200	Strong transcription	Primary T cells fromperipheralblood	blood
39	chr18:9214200-9228600	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr18:9214200-9231200	Strong transcription	Primary B cells from peripheral blood	blood
41	chr18:9214400-9224000	Strong transcription	Muscle Satellite Cultured Cells	--
42	chr18:9214400-9224600	Strong transcription	Fetal Intestine Large	intestine
43	chr18:9214400-9226600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr18:9214600-9225600	Weak transcription	A549	lung
45	chr18:9214800-9232000	Weak transcription	HSMMtube	muscle
46	chr18:9215200-9232200	Weak transcription	Brain Cingulate Gyrus	brain
47	chr18:9215800-9233800	Weak transcription	Aorta	Aorta
48	chr18:9216000-9250000	Weak transcription	Small Intestine	intestine
49	chr18:9216000-9289600	Weak transcription	HMEC	breast
50	chr18:9216400-9223800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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