Variant report

Variant	rs565017235
Chromosome Location	chr9:95895062-95895063
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:95763574..95766256-chr9:95893886..95895628,2	MCF-7	breast:
2	chr9:95870960..95873239-chr9:95894940..95897821,4	MCF-7	breast:
3	chr9:95881490..95886849-chr9:95891631..95895235,6	K562	blood:
4	chr9:95895042..95899051-chr9:95945154..95949540,5	MCF-7	breast:
5	chr9:95818120..95822805-chr9:95894646..95898384,4	K562	blood:
6	chr9:95525332..95528852-chr9:95893539..95896445,3	MCF-7	breast:
7	chr9:95893830..95897202-chr9:96212872..96217148,4	MCF-7	breast:
8	chr9:95892565..95895144-chr9:96051454..96053767,2	MCF-7	breast:
9	chr9:95893411..95895771-chr9:96236357..96238197,2	MCF-7	breast:
10	chr9:95856253..95862485-chr9:95892353..95899486,12	MCF-7	breast:
11	chr9:95733025..95737240-chr9:95894074..95898257,5	MCF-7	breast:
12	chr9:95895047..95897771-chr9:96069097..96071737,2	MCF-7	breast:
13	chr9:95819594..95823966-chr9:95894549..95897415,5	MCF-7	breast:
14	chr9:95894765..95898074-chr9:96066261..96068998,4	MCF-7	breast:
15	chr9:95894803..95898160-chr9:96337820..96340366,3	MCF-7	breast:
16	chr9:95893768..95895658-chr9:95897377..95900133,3	K562	blood:
17	chr9:95894917..95896473-chr9:96212218..96213888,2	MCF-7	breast:
18	chr9:95871458..95873101-chr9:95893633..95895517,2	K562	blood:
19	chr9:95855662..95862507-chr9:95894736..95899302,16	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000165238	Chromatin interaction
ENSG00000165233	Chromatin interaction
ENSG00000127084	Chromatin interaction
ENSG00000048828	Chromatin interaction
ENSG00000157303	Chromatin interaction
ENSG00000197724	Chromatin interaction
ENSG00000223446	Chromatin interaction
ENSG00000185963	Chromatin interaction
ENSG00000188938	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

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	nsv526296	chr9:95708192-96030392	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv1035230	chr9:95770249-95934982	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv893576	chr9:95789960-96158277	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	esv1824329	chr9:95811604-95921347	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS 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
5	nsv893579	chr9:95855100-95923091	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
6	nsv893580	chr9:95855100-96099377	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
7	nsv893581	chr9:95872216-95930334	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
8	nsv614879	chr9:95883363-95897564	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
9	nsv824982	chr9:95895045-95897753	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95870000-95895400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr9:95885000-95895400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr9:95886800-95895400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
4	chr9:95888600-95895200	Enhancers	Left Ventricle	heart
5	chr9:95889200-95895400	Weak transcription	Thymus	Thymus
6	chr9:95889600-95895200	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr9:95889800-95895200	Weak transcription	Fetal Kidney	kidney
8	chr9:95890000-95895600	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr9:95890400-95896600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
10	chr9:95890800-95896000	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
11	chr9:95891400-95895800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr9:95892400-95895200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr9:95892600-95895200	Enhancers	Fetal Thymus	thymus
14	chr9:95892800-95895800	Flanking Active TSS	Rectal Smooth Muscle	rectum
15	chr9:95893000-95895200	Enhancers	Fetal Lung	lung
16	chr9:95893000-95896200	Flanking Active TSS	Adipose Nuclei	Adipose
17	chr9:95893200-95895400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr9:95893200-95896000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr9:95893200-95896000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
20	chr9:95893200-95896000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
21	chr9:95893200-95896000	Flanking Active TSS	Stomach Smooth Muscle	stomach
22	chr9:95893400-95895200	Enhancers	Gastric	stomach
23	chr9:95893400-95895800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
24	chr9:95893600-95895200	Enhancers	Right Ventricle	heart
25	chr9:95893600-95895600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr9:95893600-95895600	Flanking Active TSS	Colon Smooth Muscle	Colon
27	chr9:95893600-95895800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
28	chr9:95893800-95895400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr9:95893800-95895600	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr9:95893800-95895600	Enhancers	Small Intestine	intestine
31	chr9:95893800-95896000	Flanking Active TSS	Brain Hippocampus Middle	brain
32	chr9:95893800-95896000	Flanking Active TSS	Brain Substantia Nigra	brain
33	chr9:95893800-95896000	Flanking Active TSS	Placenta	Placenta
34	chr9:95893800-95896000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
35	chr9:95893800-95896400	Flanking Active TSS	Primary B cells from cord blood	blood
36	chr9:95894000-95895600	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
37	chr9:95894000-95896000	Flanking Active TSS	Duodenum Mucosa	Duodenum
38	chr9:95894200-95895200	Enhancers	Dnd41	blood
39	chr9:95894200-95895800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr9:95894200-95896000	Flanking Active TSS	Fetal Intestine Large	intestine
41	chr9:95894200-95896000	Flanking Active TSS	GM12878-XiMat	blood
42	chr9:95894400-95895400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr9:95894400-95895800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
44	chr9:95894400-95895800	Flanking Active TSS	Liver	Liver
45	chr9:95894400-95895800	Flanking Active TSS	Hela-S3	cervix
46	chr9:95894400-95896000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
47	chr9:95894400-95896000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr9:95894400-95896000	Flanking Active TSS	Colonic Mucosa	Colon
49	chr9:95894400-95896000	Flanking Active TSS	Fetal Muscle Leg	muscle
50	chr9:95894600-95895200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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