Variant report

Variant	esv1847591
Chromosome Location	chr5:7917101-7923683
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr5:7918663-7918695	GM12878	blood:	n/a	n/a
2	CEBPB	chr5:7917486-7917794	Hela-S3	cervix:	n/a	chr5:7917640-7917651
3	CEBPB	chr5:7917518-7917789	A549	lung:	n/a	chr5:7917640-7917651
4	CEBPB	chr5:7917463-7917820	IMR90	lung:	n/a	chr5:7917640-7917651
5	CEBPB	chr5:7917466-7917815	HepG2	liver:	n/a	chr5:7917640-7917651
6	CEBPB	chr5:7917491-7917819	K562	blood:	n/a	chr5:7917640-7917651
7	EP300	chr5:7918006-7918047	K562	blood:	n/a	n/a
8	FOXA2	chr5:7920040-7920268	A549	lung:	n/a	n/a
9	IRF1	chr5:7920575-7920740	K562	blood:	n/a	n/a
10	IRF1	chr5:7918658-7918797	K562	blood:	n/a	n/a
11	MAFF	chr5:7917902-7918187	HepG2	liver:	n/a	chr5:7917995-7918013 chr5:7918033-7918051
12	MAFF	chr5:7917890-7918184	K562	blood:	n/a	chr5:7917995-7918013 chr5:7918033-7918051
13	MAFK	chr5:7917898-7918155	HepG2	liver:	n/a	chr5:7918035-7918050
14	MAFK	chr5:7917984-7918089	K562	blood:	n/a	chr5:7918035-7918050
15	MAFK	chr5:7917863-7918214	IMR90	lung:	n/a	chr5:7918035-7918050
16	MAFK	chr5:7917905-7918186	HepG2	liver:	n/a	chr5:7918035-7918050
17	POLR2A	chr5:7921838-7922007	MCF10A-Er-Src	breast:	n/a	n/a
18	POLR2A	chr5:7917267-7917631	MCF10A-Er-Src	breast:	n/a	n/a
19	POLR2A	chr5:7922217-7922347	K562	blood:	n/a	n/a
20	RAD21	chr5:7917670-7917673	HepG2	liver:	n/a	n/a
21	RCOR1	chr5:7917834-7917961	K562	blood:	n/a	n/a
22	RFX5	chr5:7921468-7921605	K562	blood:	n/a	n/a
23	WRNIP1	chr5:7919207-7919210	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:7908992..7910576-chr5:7919203..7920908,2	K562	blood:
2	chr5:7913593..7916151-chr5:7918931..7921579,2	K562	blood:
3	chr5:7921024..7923404-chr5:7924962..7926484,2	K562	blood:

Variant related genes	Relation type
ENSG00000251168	TF binding region

Extended variants
information (count: 57 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:57 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142434421	chr5:7917132-7917133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs116357701	chr5:7917133-7917134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs2388771	chr5:7917137-7917138	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs575498736	chr5:7917149-7917150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540079828	chr5:7917173-7917174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs553686891	chr5:7917203-7917204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183194807	chr5:7917204-7917205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370169757	chr5:7917214-7917215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555303775	chr5:7917251-7917252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187490917	chr5:7917309-7917310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575135950	chr5:7917350-7917351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12186809	chr5:7917360-7917361	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs150901748	chr5:7917361-7917362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577755489	chr5:7917400-7917401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191988608	chr5:7917436-7917437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559939525	chr5:7917516-7917517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574793447	chr5:7917534-7917535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529119922	chr5:7917571-7917572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12189183	chr5:7917580-7917581	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs183378006	chr5:7917601-7917602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530854375	chr5:7917737-7917738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs76231165	chr5:7917739-7917740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145532675	chr5:7917741-7917742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs147807567	chr5:7917767-7917768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141197386	chr5:7917781-7917782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567081157	chr5:7917813-7917814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs187759577	chr5:7917836-7917837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192463357	chr5:7917839-7917840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540424280	chr5:7917882-7917883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs162273	chr5:7917934-7917935	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs28829123	chr5:7917953-7917954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs148099112	chr5:7917989-7917990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374983505	chr5:7920044-7920045	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs557748709	chr5:7920077-7920078	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs562895254	chr5:7920214-7920215	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs186061911	chr5:7920247-7920248	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs545366538	chr5:7920248-7920249	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs191344144	chr5:7920255-7920256	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs573984136	chr5:7920587-7920588	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs369511260	chr5:7920651-7920652	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs70940767	chr5:7920682-7920683	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs398108567	chr5:7920691-7920692	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs80145706	chr5:7920692-7920693	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs190700940	chr5:7920700-7920701	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs182983424	chr5:7920716-7920717	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs77056991	chr5:7921478-7921479	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs188403610	chr5:7921553-7921554	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs543378117	chr5:7921596-7921597	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs558671768	chr5:7921842-7921843	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs572290456	chr5:7921849-7921850	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Lung cancer	21911935	CNVD
Cri-du chat syndrome	21549014	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Melanoma	22183965	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Ovarian cancer	19193619	CNVD
Hepatocellular carcinoma	16785998	CNVD
Cancer	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intellectual disability	22102821	CNVD
early-passage human iPS cells	21368824	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:7909800-7917600	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr5:7915400-7917200	Enhancers	Osteobl	bone
3	chr5:7917600-7918000	Enhancers	Rectal Mucosa Donor 31	rectum

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