Variant report

Variant	nsv872469
Chromosome Location	chr1:155743310-155810293
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:237)
CpG islands
(count:62)
Chromatin interactive
region (count:34)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:237 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:155804174-155804585	K562	blood:	n/a	n/a
2	ATF1	chr1:155746378-155746503	K562	blood:	n/a	n/a
3	ATF1	chr1:155804139-155804592	K562	blood:	n/a	n/a
4	ATF3	chr1:155746257-155746513	K562	blood:	n/a	n/a
5	ATF3	chr1:155746267-155746595	HCT-116	colon:	n/a	n/a
6	ATF3	chr1:155804057-155804675	K562	blood:	n/a	n/a
7	CCNT2	chr1:155804593-155804751	K562	blood:	n/a	n/a
8	CCNT2	chr1:155771119-155771267	K562	blood:	n/a	n/a
9	CEBPB	chr1:155781834-155782163	HepG2	liver:	n/a	chr1:155782005-155782016
10	CEBPB	chr1:155746212-155746591	K562	blood:	n/a	chr1:155746397-155746408
11	CEBPB	chr1:155781856-155782132	A549	lung:	n/a	chr1:155782005-155782016
12	CEBPB	chr1:155746195-155746540	K562	blood:	n/a	chr1:155746397-155746408
13	CEBPB	chr1:155746231-155746480	K562	blood:	n/a	chr1:155746397-155746408
14	CEBPB	chr1:155746230-155746571	A549	lung:	n/a	chr1:155746397-155746408
15	CEBPB	chr1:155764578-155764611	K562	blood:	n/a	chr1:155764598-155764609
16	CEBPB	chr1:155804053-155804635	K562	blood:	n/a	n/a
17	CEBPB	chr1:155781856-155782139	IMR90	lung:	n/a	chr1:155782005-155782016
18	CEBPB	chr1:155746223-155746568	HepG2	liver:	n/a	chr1:155746397-155746408
19	CEBPB	chr1:155764437-155764738	MCF-7	breast:	n/a	chr1:155764665-155764673 chr1:155764598-155764609
20	CEBPB	chr1:155799154-155799511	MCF-7	breast:	n/a	n/a
21	CEBPB	chr1:155746081-155746687	HCT-116	colon:	n/a	chr1:155746171-155746183 chr1:155746397-155746408
22	CEBPB	chr1:155781859-155782144	K562	blood:	n/a	chr1:155782005-155782016
23	CEBPB	chr1:155764533-155764724	HepG2	liver:	n/a	chr1:155764665-155764673 chr1:155764598-155764609
24	CEBPB	chr1:155746233-155746707	HCT-116	colon:	n/a	chr1:155746397-155746408
25	CEBPB	chr1:155804185-155804618	K562	blood:	n/a	n/a
26	CEBPB	chr1:155746204-155746595	Hela-S3	cervix:	n/a	chr1:155746397-155746408
27	CEBPB	chr1:155746236-155746580	ECC-1	luminal epithelium:	n/a	chr1:155746397-155746408
28	CEBPB	chr1:155746279-155746534	MCF-7	breast:	n/a	chr1:155746397-155746408
29	CEBPB	chr1:155746229-155746571	IMR90	lung:	n/a	chr1:155746397-155746408
30	CEBPB	chr1:155781913-155782114	Hela-S3	cervix:	n/a	chr1:155782005-155782016
31	CEBPB	chr1:155764416-155764805	IMR90	lung:	n/a	chr1:155764665-155764673 chr1:155764598-155764609
32	CEBPB	chr1:155746265-155746490	A549	lung:	n/a	chr1:155746397-155746408
33	CTCF	chr1:155780340-155780490	GM12867	blood:	n/a	n/a
34	CTCF	chr1:155790905-155790981	GM20000	blood:	n/a	n/a
35	CTCF	chr1:155789202-155789281	GM13976	blood:	n/a	n/a
36	CUX1	chr1:155804132-155804487	K562	blood:	n/a	n/a
37	E2F4	chr1:155807658-155807664	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F6	chr1:155804258-155804639	H1-hESC	embryonic stem cell:	n/a	n/a
39	E2F6	chr1:155804331-155804552	K562	blood:	n/a	n/a
40	ELF1	chr1:155804206-155804683	K562	blood:	n/a	n/a
41	ELK1	chr1:155804384-155804664	K562	blood:	n/a	n/a
42	EP300	chr1:155770808-155771372	SK-N-SH	brain:	n/a	chr1:155771212-155771221 chr1:155770979-155770988
43	EP300	chr1:155746364-155746501	K562	blood:	n/a	n/a
44	EP300	chr1:155791870-155791895	GM12878	blood:	n/a	n/a
45	EP300	chr1:155804337-155804487	GM12878	blood:	n/a	n/a
46	EP300	chr1:155804085-155804584	K562	blood:	n/a	n/a
47	EP300	chr1:155746257-155746422	Hela-S3	cervix:	n/a	n/a
48	EP300	chr1:155804037-155804719	K562	blood:	n/a	n/a
49	ESR1	chr1:155788192-155788551	ECC-1	luminal epithelium:	n/a	n/a
50	FOS	chr1:155746290-155746563	MCF10A-Er-Src	breast:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155764892-155764942	HEEpiC	esophagus:	n/a
2	chr1:155764892-155764942	HEEpiC	esophagus:	n/a
3	chr1:155764892-155764942	HUVEC	blood vessel:	n/a
4	chr1:155764892-155764942	AG04449	skin:	fetal
5	chr1:155764892-155764942	GM12878	blood:	n/a
6	chr1:155764892-155764942	PrEC	prostate:	n/a
7	chr1:155764892-155764942	HMEC	breast:	n/a
8	chr1:155764892-155764942	NT2-D1	testis:	n/a
9	chr1:155764892-155764942	Caco-2	colon:	n/a
10	chr1:155764892-155764942	BE2_C	brain:	n/a
11	chr1:155764892-155764942	PFSK-1	brain:	n/a
12	chr1:155764892-155764942	ECC-1	luminal epithelium:	n/a
13	chr1:155764892-155764942	HRE	kidney:	n/a
14	chr1:155764892-155764942	CMK	blood:	n/a
15	chr1:155764892-155764942	HAEpiC	amniotic membrane:	n/a
16	chr1:155764892-155764942	NB4	blood:	n/a
17	chr1:155764892-155764942	HCM	heart:	n/a
18	chr1:155764892-155764942	HCF	heart:	n/a
19	chr1:155764892-155764942	SKMC	muscle:	n/a
20	chr1:155764892-155764942	NHBE	bronchial:	n/a
21	chr1:155764892-155764942	SK-N-SH	brain:	n/a
22	chr1:155764892-155764942	HL-60	blood:	n/a
23	chr1:155764892-155764942	HNPCEpiC	eye:	n/a
24	chr1:155764892-155764942	AG09319	gingival:	n/a
25	chr1:155764892-155764942	GM12892	blood:	n/a
26	chr1:155764892-155764942	H1-hESC	embryonic stem cell:	embryo
27	chr1:155764892-155764942	GM19239	blood:	n/a
28	chr1:155764892-155764942	LNCaP	prostate:	n/a
29	chr1:155764892-155764942	ProgFib	skin:	n/a
30	chr1:155764892-155764942	AG09309	skin:	n/a
31	chr1:155764892-155764942	NH-A	brain:	n/a
32	chr1:155764892-155764942	MCF-7	breast:	n/a
33	chr1:155764892-155764942	HPAEpiC	pulmonary alveolar:	n/a
34	chr1:155764892-155764942	BJ	skin:	n/a
35	chr1:155764892-155764942	Jurkat	blood:	n/a
36	chr1:155764892-155764942	PANC-1	pancreas:	n/a
37	chr1:155764892-155764942	HCT-116	colon:	n/a
38	chr1:155764892-155764942	AG04450	lung:	fetal
39	chr1:155764892-155764942	U87	brain:	n/a
40	chr1:155764892-155764942	SAEC	small airway:	n/a
41	chr1:155764892-155764942	AG10803	skin:	n/a
42	chr1:155764892-155764942	ovcar-3	ovarian:	n/a
43	chr1:155764892-155764942	RPTEC	kidney:	n/a
44	chr1:155764892-155764942	GM12891	blood:	n/a
45	chr1:155764892-155764942	T-47D	breast:	n/a
46	chr1:155764892-155764942	Hela-S3	cervix:	n/a
47	chr1:155764892-155764942	K562	blood:	n/a
48	chr1:155764892-155764942	HIPEpiC	eye:	n/a
49	chr1:155764892-155764942	IMR90	lung:	fetal
50	chr1:155764892-155764942	NHDF-neo	bronchial:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:155798918..155800713-chr1:155804117..155806724,2	K562	blood:
2	chr1:155806357..155807904-chr1:155825456..155826957,2	K562	blood:
3	chr1:155804416..155805981-chr1:155807253..155809729,2	K562	blood:
4	chr1:155802875..155805310-chr1:155826870..155828666,2	K562	blood:
5	chr1:155799410..155800938-chr1:155802704..155804564,2	K562	blood:
6	chr1:155803309..155806039-chr1:155809985..155811724,2	K562	blood:
7	chr1:155779007..155780786-chr1:155785874..155788055,2	K562	blood:
8	chr1:155802913..155806826-chr1:155828788..155831078,3	K562	blood:
9	chr1:155802842..155805913-chr1:155879338..155883111,3	K562	blood:
10	chr1:155792045..155793835-chr1:155813657..155816008,2	MCF-7	breast:
11	chr1:155762196..155764672-chr1:155783747..155785750,2	K562	blood:
12	chr1:155755387..155757428-chr1:155757554..155759146,2	K562	blood:
13	chr1:155792548..155794810-chr1:155798321..155800474,2	K562	blood:
14	chr1:155792548..155794810-chr1:155798321..155800474,2	K562	blood:
15	chr1:155774997..155776767-chr1:155793865..155796563,2	K562	blood:
16	chr1:155758116..155760937-chr1:155763404..155765348,3	K562	blood:
17	chr1:155798918..155800713-chr1:155804117..155806724,2	K562	blood:
18	chr1:155804226..155806022-chr1:155818533..155820531,2	K562	blood:
19	chr1:155804226..155806022-chr1:155818351..155820531,3	K562	blood:
20	chr1:155803309..155806039-chr1:155809985..155811724,2	K562	blood:
21	chr1:155774997..155776767-chr1:155793865..155796563,2	K562	blood:
22	chr1:155698585..155701344-chr1:155765274..155767942,2	K562	blood:
23	chr1:155769410..155771297-chr1:155796541..155800799,3	K562	blood:
24	chr1:155740846..155742471-chr1:155753287..155755087,2	K562	blood:
25	chr1:155755387..155757428-chr1:155757554..155759146,2	K562	blood:
26	chr1:155804416..155805981-chr1:155807253..155809729,2	K562	blood:
27	chr1:155758116..155760937-chr1:155763404..155765348,3	K562	blood:
28	chr1:155769410..155771297-chr1:155796541..155800799,3	K562	blood:
29	chr1:155779007..155780786-chr1:155785874..155788055,2	K562	blood:
30	chr1:155799410..155800938-chr1:155802704..155804564,2	K562	blood:
31	chr1:155762196..155764672-chr1:155783747..155785750,2	K562	blood:
32	chr1:155806737..155811312-chr1:155812674..155817487,5	K562	blood:
33	chr1:155806684..155808221-chr1:155825084..155827215,2	MCF-7	breast:
34	chr1:155798865..155802623-chr1:155880941..155882734,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RIT1-3	chr1:155796628-155796819	NONHSAT006769
2	lnc-RIT1-3	chr1:155802623-155802741	NONHSAT006769
3	lnc-RIT1-3	chr1:155792238-155792267	NONHSAT006769

No data

Variant related genes	Relation type
GON4L	TF binding region
ENSG00000234937	TF binding region
GON4L	CpG island
ENSG00000234937	CpG island
ENSG00000116580	chromatin interactions
ENSG00000132718	chromatin interactions
ENSG00000132676	chromatin interactions
ENSG00000234937	chromatin interactions
ENSG00000143622	chromatin interactions

Extended variants
information (count: 2492 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:2492 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs708611	chr1:155743310-155743311	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs563432703	chr1:155743323-155743324	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs555463785	chr1:155743326-155743327	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs574290880	chr1:155743329-155743330	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs541692711	chr1:155743330-155743331	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs559888088	chr1:155743476-155743477	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs543810112	chr1:155743527-155743528	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187656695	chr1:155743545-155743546	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545663185	chr1:155743581-155743582	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs149977965	chr1:155743728-155743729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542806251	chr1:155743798-155743799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs78675472	chr1:155743856-155743857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549068808	chr1:155743872-155743873	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113176887	chr1:155743952-155743953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561092443	chr1:155743976-155743977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs114075499	chr1:155744005-155744006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs202220926	chr1:155744099-155744100	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564146859	chr1:155744116-155744117	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs59844793	chr1:155744117-155744118	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547309388	chr1:155744138-155744139	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565843683	chr1:155744139-155744140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539374466	chr1:155744193-155744194	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551620105	chr1:155744246-155744247	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532806673	chr1:155744247-155744248	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372109900	chr1:155744254-155744255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192607439	chr1:155744288-155744289	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555400011	chr1:155744289-155744290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528745205	chr1:155744302-155744303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573820953	chr1:155744342-155744343	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534701482	chr1:155744350-155744351	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553320060	chr1:155744389-155744390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375497288	chr1:155744410-155744411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183374731	chr1:155744448-155744449	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2686257	chr1:155744486-155744487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143645681	chr1:155744487-155744488	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112412750	chr1:155744509-155744510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs4021860	chr1:155744590-155744591	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2363018	chr1:155744591-155744592	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187714270	chr1:155744592-155744593	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4021861	chr1:155744593-155744594	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1756235	chr1:155744606-155744607	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112697362	chr1:155744611-155744612	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560929185	chr1:155744617-155744618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192308057	chr1:155744635-155744636	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs369911447	chr1:155744716-155744717	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs2363019	chr1:155744717-155744718	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs540693061	chr1:155744765-155744766	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs559300852	chr1:155744798-155744799	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs532952211	chr1:155744840-155744841	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs370318949	chr1:155744866-155744867	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	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
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Dihydropyrimidine dehydrogenase deficiency	18421352	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2003 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155715400-155789200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:155715600-155764600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr1:155716000-155793400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:155716600-155781800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:155717200-155761000	Strong transcription	Fetal Stomach	stomach
6	chr1:155717400-155795800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr1:155717600-155750200	Strong transcription	Primary T helper cells PMA-I stimulated	--
8	chr1:155720200-155745400	Strong transcription	Fetal Muscle Leg	muscle
9	chr1:155720200-155748600	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr1:155720200-155748800	Strong transcription	Duodenum Mucosa	Duodenum
11	chr1:155720200-155748800	Strong transcription	Rectal Mucosa Donor 29	rectum
12	chr1:155720200-155749000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr1:155720200-155749600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr1:155720200-155750200	Strong transcription	Primary T cells from cord blood	blood
15	chr1:155720200-155750600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr1:155720200-155755800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr1:155720200-155756200	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr1:155720200-155756600	Strong transcription	HUES6 Cell Line	embryonic stem cell
19	chr1:155720200-155798200	Strong transcription	Fetal Thymus	thymus
20	chr1:155720200-155803600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr1:155720400-155750200	Strong transcription	Adipose Nuclei	Adipose
22	chr1:155720400-155750400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr1:155720400-155750600	Strong transcription	Dnd41	blood
24	chr1:155720400-155755600	Strong transcription	Placenta	Placenta
25	chr1:155720400-155756400	Strong transcription	Liver	Liver
26	chr1:155720400-155760800	Strong transcription	Primary T cells fromperipheralblood	blood
27	chr1:155720400-155796800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr1:155720600-155743600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr1:155720600-155757200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr1:155720800-155747600	Strong transcription	Fetal Muscle Trunk	muscle
31	chr1:155720800-155749000	Strong transcription	HUES64 Cell Line	embryonic stem cell
32	chr1:155721000-155748800	Strong transcription	Skeletal Muscle Female	skeletal muscle
33	chr1:155725000-155748600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr1:155726000-155747400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr1:155727200-155754200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr1:155728600-155747600	Strong transcription	Brain Inferior Temporal Lobe	brain
37	chr1:155729400-155747600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
38	chr1:155730400-155764200	Weak transcription	Psoas Muscle	Psoas
39	chr1:155730800-155748000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
40	chr1:155731000-155748800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr1:155732200-155789200	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr1:155732400-155755600	Strong transcription	Fetal Intestine Large	intestine
43	chr1:155732600-155748800	Strong transcription	Primary B cells from peripheral blood	blood
44	chr1:155733800-155743400	Strong transcription	Skeletal Muscle Male	skeletal muscle
45	chr1:155734000-155748800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr1:155734400-155746200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr1:155734400-155747800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr1:155734600-155743800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr1:155734600-155748000	Strong transcription	Sigmoid Colon	Sigmoid Colon
50	chr1:155734600-155748000	Strong transcription	Osteobl	bone

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