Variant report

Variant	esv3446473
Chromosome Location	chr1:227165851-227166035
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EGR1	chr1:227165754-227165959	K562	blood:	n/a	n/a
2	EGR1	chr1:227165660-227165994	K562	blood:	n/a	n/a
3	POLR2A	chr1:227165366-227166192	HepG2	liver:	n/a	n/a
4	POLR2A	chr1:227164382-227167024	HL-60	blood:	n/a	n/a
5	POLR2A	chr1:227165510-227166014	K562	blood:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:227159722..227162799-chr1:227165393..227168885,3	K562	blood:
2	chr1:227139663..227142101-chr1:227165412..227167064,2	K562	blood:
3	chr1:227165601..227167978-chr1:227173311..227176266,3	MCF-7	breast:
4	chr1:227163376..227165158-chr1:227165776..227167614,2	K562	blood:
5	chr1:227127948..227129868-chr1:227162930..227165927,2	MCF-7	breast:

No data

Variant related genes	Relation type
ADCK3	TF binding region
ENSG00000163050	chromatin interactions

Extended variants
information (count: 15 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532874730	chr1:227165860-227165861	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs548135320	chr1:227165866-227165867	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs559789716	chr1:227165869-227165870	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs371021243	chr1:227165879-227165880	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs548246323	chr1:227165881-227165882	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs140678488	chr1:227165890-227165891	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs530697821	chr1:227165926-227165927	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs111162994	chr1:227165929-227165930	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs193051768	chr1:227165935-227165936	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs199762444	chr1:227165937-227165938	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs370823000	chr1:227165941-227165942	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs534488059	chr1:227165969-227165970	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs553280019	chr1:227165980-227165981	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs376014691	chr1:227165995-227165996	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs574635523	chr1:227166002-227166003	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:227131000-227171800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:227147000-227177000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr1:227148600-227180800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr1:227154400-227294200	Weak transcription	Hela-S3	cervix
5	chr1:227154800-227176800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr1:227158400-227173200	Weak transcription	K562	blood
7	chr1:227158400-227174600	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr1:227158400-227183000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr1:227159000-227175800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr1:227159800-227174000	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr1:227160000-227173600	Weak transcription	A549	lung
12	chr1:227160000-227174400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr1:227160000-227174400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr1:227160000-227174800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr1:227160000-227177200	Weak transcription	GM12878-XiMat	blood
16	chr1:227160600-227175600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr1:227160800-227181800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr1:227162200-227166600	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr1:227162200-227169400	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr1:227162200-227176000	Strong transcription	Primary T cells from cord blood	blood
21	chr1:227162400-227173600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr1:227162400-227174200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr1:227162400-227174200	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr1:227162400-227175200	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr1:227162400-227181600	Weak transcription	NHEK	skin
26	chr1:227162600-227174200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr1:227162600-227174200	Weak transcription	Aorta	Aorta
28	chr1:227162600-227175800	Strong transcription	Primary T helper cells fromperipheralblood	blood
29	chr1:227162600-227176600	Strong transcription	Thymus	Thymus
30	chr1:227162800-227172000	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr1:227162800-227173600	Weak transcription	NHLF	lung
32	chr1:227162800-227174000	Weak transcription	Osteobl	bone
33	chr1:227162800-227174200	Weak transcription	NHDF-Ad	bronchial
34	chr1:227163000-227166000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr1:227163000-227166800	Weak transcription	Esophagus	oesophagus
36	chr1:227163000-227167800	Strong transcription	Lung	lung
37	chr1:227163000-227173400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr1:227163000-227173600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr1:227163000-227174200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr1:227163000-227180000	Weak transcription	HSMM	muscle
41	chr1:227163200-227170400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr1:227163200-227172800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr1:227163200-227174000	Weak transcription	Small Intestine	intestine
44	chr1:227163200-227175400	Strong transcription	Fetal Intestine Small	intestine
45	chr1:227163400-227191200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr1:227163800-227166600	Weak transcription	Brain Angular Gyrus	brain
47	chr1:227163800-227166800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr1:227163800-227167600	Weak transcription	Placenta	Placenta
49	chr1:227163800-227176200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:227163800-227180400	Weak transcription	Fetal Brain Male	brain

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