Variant report

Variant	nsv1003170
Chromosome Location	chr1:155762204-155836564
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1135)
CpG islands
(count:1589)
Chromatin interactive
region (count:65)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1135 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:155827026-155827279	K562	blood:	n/a	chr1:155827066-155827074
2	ARID3A	chr1:155828770-155829179	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:155830360-155830367	K562	blood:	n/a	n/a
4	ARID3A	chr1:155826902-155827222	HepG2	liver:	n/a	chr1:155827066-155827074
5	ARID3A	chr1:155827548-155828486	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:155804174-155804585	K562	blood:	n/a	n/a
7	ATF1	chr1:155804139-155804592	K562	blood:	n/a	n/a
8	ATF1	chr1:155830118-155830643	K562	blood:	n/a	n/a
9	ATF1	chr1:155826876-155827295	K562	blood:	n/a	n/a
10	ATF1	chr1:155817745-155817914	K562	blood:	n/a	n/a
11	ATF1	chr1:155828941-155829625	K562	blood:	n/a	n/a
12	ATF2	chr1:155829859-155830808	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr1:155829958-155830802	GM12878	blood:	n/a	n/a
14	ATF2	chr1:155826702-155827264	GM12878	blood:	n/a	n/a
15	ATF2	chr1:155829865-155831034	GM12878	blood:	n/a	n/a
16	ATF2	chr1:155829807-155830789	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr1:155828867-155829402	GM12878	blood:	n/a	n/a
18	ATF2	chr1:155826868-155827286	GM12878	blood:	n/a	n/a
19	ATF2	chr1:155826800-155827292	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr1:155826725-155827302	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF3	chr1:155804057-155804675	K562	blood:	n/a	n/a
22	ATF3	chr1:155830075-155830594	K562	blood:	n/a	chr1:155830257-155830268 chr1:155830460-155830480 chr1:155830255-155830269 chr1:155830459-155830472 chr1:155830461-155830469
23	ATF3	chr1:155826743-155827317	A549	lung:	n/a	chr1:155827039-155827048
24	ATF3	chr1:155826795-155827336	K562	blood:	n/a	chr1:155827039-155827048
25	ATF3	chr1:155826775-155827145	K562	blood:	n/a	chr1:155827039-155827048
26	BACH1	chr1:155828954-155829215	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr1:155826601-155826607	K562	blood:	n/a	n/a
28	BCL3	chr1:155826614-155827270	A549	lung:	n/a	chr1:155827041-155827054
29	BCL3	chr1:155826690-155827273	A549	lung:	n/a	chr1:155827041-155827054
30	BCLAF1	chr1:155830028-155830640	GM12878	blood:	n/a	chr1:155830078-155830091
31	BHLHE40	chr1:155828858-155830514	GM12878	blood:	n/a	n/a
32	BHLHE40	chr1:155829427-155829463	K562	blood:	n/a	n/a
33	BHLHE40	chr1:155827155-155827224	K562	blood:	n/a	n/a
34	BHLHE40	chr1:155829790-155830501	K562	blood:	n/a	n/a
35	BHLHE40	chr1:155826788-155827229	GM12878	blood:	n/a	n/a
36	BHLHE40	chr1:155828247-155828537	GM12878	blood:	n/a	n/a
37	BRCA1	chr1:155830512-155830639	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr1:155826850-155827252	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr1:155826966-155827016	HepG2	liver:	n/a	n/a
40	CBX3	chr1:155826718-155827346	K562	blood:	n/a	n/a
41	CBX3	chr1:155830018-155830639	K562	blood:	n/a	n/a
42	CBX3	chr1:155826854-155827357	K562	blood:	n/a	n/a
43	CCNT2	chr1:155826846-155827159	K562	blood:	n/a	n/a
44	CCNT2	chr1:155830202-155830521	K562	blood:	n/a	chr1:155830402-155830411
45	CCNT2	chr1:155771119-155771267	K562	blood:	n/a	n/a
46	CCNT2	chr1:155804593-155804751	K562	blood:	n/a	n/a
47	CEBPB	chr1:155828712-155829025	ECC-1	luminal epithelium:	n/a	chr1:155828813-155828824
48	CEBPB	chr1:155826906-155827149	HepG2	liver:	n/a	n/a
49	CEBPB	chr1:155828657-155829711	HepG2	liver:	n/a	chr1:155828813-155828824
50	CEBPB	chr1:155830279-155830635	IMR90	lung:	n/a	n/a

(count:1589 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155826844-155826894	HRPEpiC	eye:	n/a
2	chr1:155828174-155828224	HRE	kidney:	n/a
3	chr1:155828926-155828976	GM19239	blood:	n/a
4	chr1:155826844-155826894	HRPEpiC	eye:	n/a
5	chr1:155828174-155828224	HRE	kidney:	n/a
6	chr1:155828926-155828976	GM19239	blood:	n/a
7	chr1:155828174-155828224	PFSK-1	brain:	n/a
8	chr1:155829285-155829335	HCM	heart:	n/a
9	chr1:155826844-155826894	HCT-116	colon:	n/a
10	chr1:155827082-155827132	HPAEpiC	pulmonary alveolar:	n/a
11	chr1:155830797-155830847	Jurkat	blood:	n/a
12	chr1:155829206-155829256	GM12892	blood:	n/a
13	chr1:155828926-155828976	Hela-S3	cervix:	n/a
14	chr1:155827042-155827092	HIPEpiC	eye:	n/a
15	chr1:155831789-155831839	HNPCEpiC	eye:	n/a
16	chr1:155829126-155829176	BE2_C	brain:	n/a
17	chr1:155830264-155830314	HRPEpiC	eye:	n/a
18	chr1:155764892-155764942	AG09319	gingival:	n/a
19	chr1:155830294-155830344	HRPEpiC	eye:	n/a
20	chr1:155826954-155827004	PFSK-1	brain:	n/a
21	chr1:155829430-155829480	ProgFib	skin:	n/a
22	chr1:155827042-155827092	SK-N-SH_RA	brain:	n/a
23	chr1:155831789-155831839	AG09319	gingival:	n/a
24	chr1:155830294-155830344	HCT-116	colon:	n/a
25	chr1:155829430-155829480	GM12878	blood:	n/a
26	chr1:155827042-155827092	NHBE	bronchial:	n/a
27	chr1:155830797-155830847	BJ	skin:	n/a
28	chr1:155830477-155830527	U87	brain:	n/a
29	chr1:155830264-155830314	HCF	heart:	n/a
30	chr1:155829126-155829176	HL-60	blood:	n/a
31	chr1:155829263-155829313	HAEpiC	amniotic membrane:	n/a
32	chr1:155829126-155829176	NT2-D1	testis:	n/a
33	chr1:155830264-155830314	K562	blood:	n/a
34	chr1:155828357-155828407	HEK293	kidney:	embryo
35	chr1:155830294-155830344	IMR90	lung:	fetal
36	chr1:155829549-155829599	LNCaP	prostate:	n/a
37	chr1:155829206-155829256	NT2-D1	testis:	n/a
38	chr1:155826954-155827004	BJ	skin:	n/a
39	chr1:155828357-155828407	NHBE	bronchial:	n/a
40	chr1:155826844-155826894	HepG2	liver:	n/a
41	chr1:155829285-155829335	HMEC	breast:	n/a
42	chr1:155829126-155829176	GM12891	blood:	n/a
43	chr1:155829549-155829599	Jurkat	blood:	n/a
44	chr1:155830477-155830527	SK-N-SH_RA	brain:	n/a
45	chr1:155829206-155829256	HEEpiC	esophagus:	n/a
46	chr1:155826954-155827004	AG04449	skin:	fetal
47	chr1:155829126-155829176	MCF-7	breast:	n/a
48	chr1:155814285-155814335	ECC-1	luminal epithelium:	n/a
49	chr1:155826954-155827004	HEK293	kidney:	embryo
50	chr1:155828174-155828224	Caco-2	colon:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:155804226..155806022-chr1:155818533..155820531,2	K562	blood:
2	chr1:155799410..155800938-chr1:155802704..155804564,2	K562	blood:
3	chr1:155836334..155839218-chr1:155841025..155842829,2	K562	blood:
4	chr1:155828307..155831270-chr1:155832837..155834825,2	K562	blood:
5	chr1:155829582..155831880-chr1:155833605..155835699,2	MCF-7	breast:
6	chr1:155803309..155806039-chr1:155809985..155811724,2	K562	blood:
7	chr1:155814935..155817841-chr1:155818057..155819869,2	K562	blood:
8	chr1:155806684..155808221-chr1:155825084..155827215,2	MCF-7	breast:
9	chr1:155804226..155806022-chr1:155818351..155820531,3	K562	blood:
10	chr1:155802875..155805310-chr1:155826870..155828666,2	K562	blood:
11	chr1:155815806..155819878-chr1:155826192..155829116,4	MCF-7	breast:
12	chr1:155802842..155805913-chr1:155879338..155883111,3	K562	blood:
13	chr1:155798918..155800713-chr1:155804117..155806724,2	K562	blood:
14	chr1:155769410..155771297-chr1:155796541..155800799,3	K562	blood:
15	chr1:155813223..155816752-chr1:155827638..155829227,3	K562	blood:
16	chr1:155779007..155780786-chr1:155785874..155788055,2	K562	blood:
17	chr1:155806357..155807904-chr1:155825456..155826957,2	K562	blood:
18	chr1:155815137..155817015-chr1:156023954..156025530,2	K562	blood:
19	chr1:155818345..155820226-chr1:155822747..155824958,2	K562	blood:
20	chr1:155825171..155830547-chr1:155878470..155884979,12	K562	blood:
21	chr1:155825653..155829252-chr1:155877943..155882760,5	MCF-7	breast:
22	chr1:155811208..155813165-chr1:155827065..155829841,2	K562	blood:
23	chr1:155827023..155830284-chr1:156022724..156025393,4	K562	blood:
24	chr1:155792548..155794810-chr1:155798321..155800474,2	K562	blood:
25	chr1:155762196..155764672-chr1:155783747..155785750,2	K562	blood:
26	chr1:155802913..155806826-chr1:155828788..155831078,3	K562	blood:
27	chr1:155821775..155825361-chr1:155825507..155828654,6	MCF-7	breast:
28	chr1:155828023..155830433-chr1:155835894..155838034,4	MCF-7	breast:
29	chr1:155799410..155800938-chr1:155802704..155804564,2	K562	blood:
30	chr1:155698585..155701344-chr1:155765274..155767942,2	K562	blood:
31	chr1:155798865..155802623-chr1:155880941..155882734,3	K562	blood:
32	chr1:155824896..155829386-chr1:155902844..155905236,4	MCF-7	breast:
33	chr1:155806357..155807904-chr1:155825456..155826957,2	K562	blood:
34	chr1:155821549..155823556-chr1:155827690..155829206,2	K562	blood:
35	chr1:155813223..155816752-chr1:155827638..155829227,3	K562	blood:
36	chr1:155762196..155764672-chr1:155783747..155785750,2	K562	blood:
37	chr1:155818594..155821262-chr1:155827766..155829417,2	K562	blood:
38	chr1:155821775..155825361-chr1:155825507..155828654,6	MCF-7	breast:
39	chr1:155817444..155818042-chr13:53712458..53713136,2	MCF-7	breast:
40	chr1:155829582..155831880-chr1:155833605..155835699,2	MCF-7	breast:
41	chr1:155774997..155776767-chr1:155793865..155796563,2	K562	blood:
42	chr1:155804226..155806022-chr1:155818351..155820531,3	K562	blood:
43	chr1:155656761..155658571-chr1:155822378..155824933,2	K562	blood:
44	chr1:155821549..155823556-chr1:155827690..155829206,2	K562	blood:
45	chr1:155806737..155811312-chr1:155812674..155817487,5	K562	blood:
46	chr1:155811458..155814834-chr1:155821359..155824319,3	K562	blood:
47	chr1:155798918..155800713-chr1:155804117..155806724,2	K562	blood:
48	chr1:155804226..155806022-chr1:155818533..155820531,2	K562	blood:
49	chr1:155827720..155829517-chr1:156180623..156183701,3	K562	blood:
50	chr1:155803309..155806039-chr1:155809985..155811724,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RIT1-3	chr1:155802623-155802741	NONHSAT006769
2	lnc-RIT1-3	chr1:155792238-155792267	NONHSAT006769
3	lnc-RIT1-3	chr1:155823067-155823196	NONHSAT006769
4	lnc-RIT1-3	chr1:155796628-155796819	NONHSAT006769

No data

Variant related genes	Relation type
SYT11	TF binding region
GON4L	TF binding region
ENSG00000234937	TF binding region
SYT11	CpG island
GON4L	CpG island
ENSG00000234937	CpG island
ENSG00000160785	chromatin interactions
ENSG00000203761	chromatin interactions
ENSG00000160783	chromatin interactions
ENSG00000201614	chromatin interactions
ENSG00000143622	chromatin interactions
ENSG00000116586	chromatin interactions
ENSG00000132680	chromatin interactions
ENSG00000160803	chromatin interactions
ENSG00000163374	chromatin interactions
ENSG00000234937	chromatin interactions
ENSG00000132718	chromatin interactions
ENSG00000116580	chromatin interactions
ENSG00000260238	chromatin interactions
ENSG00000132676	chromatin interactions

Extended variants
information (count: 2674 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:2674 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531878254	chr1:155762239-155762240	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs78315870	chr1:155762258-155762259	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs76848781	chr1:155762259-155762260	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192948522	chr1:155762272-155762273	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544267392	chr1:155762394-155762395	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs562942271	chr1:155762400-155762401	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184643247	chr1:155762413-155762414	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548369990	chr1:155762415-155762416	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376253537	chr1:155762432-155762433	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370896155	chr1:155762494-155762495	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs4612618	chr1:155762509-155762510	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs527965086	chr1:155762519-155762520	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546251677	chr1:155762529-155762530	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564479790	chr1:155762584-155762585	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189481097	chr1:155762590-155762591	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs550209502	chr1:155762604-155762605	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568455093	chr1:155762621-155762622	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs180710991	chr1:155762656-155762657	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374529115	chr1:155762730-155762731	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547961424	chr1:155762818-155762819	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566464124	chr1:155762829-155762830	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560205601	chr1:155762835-155762836	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377564934	chr1:155762857-155762858	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373603642	chr1:155762885-155762886	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558152321	chr1:155762887-155762888	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147321619	chr1:155762888-155762889	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537552980	chr1:155762923-155762924	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs556262012	chr1:155762958-155762959	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370163727	chr1:155763026-155763027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs822485	chr1:155763032-155763033	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs548079429	chr1:155763060-155763061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542466946	chr1:155763103-155763104	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs59293055	chr1:155763203-155763204	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs572801284	chr1:155763246-155763247	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546476474	chr1:155763256-155763257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570760883	chr1:155763322-155763323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570714192	chr1:155763334-155763335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532177686	chr1:155763386-155763387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs199846506	chr1:155763387-155763388	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184836435	chr1:155763393-155763394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538267329	chr1:155763409-155763410	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531773314	chr1:155763449-155763450	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543450157	chr1:155763494-155763495	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562238671	chr1:155763534-155763535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115676478	chr1:155763556-155763557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547997560	chr1:155763572-155763573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566302712	chr1:155763577-155763578	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs527582659	chr1:155763600-155763601	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552405872	chr1:155763615-155763616	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570644616	chr1:155763668-155763669	Weak transcription Strong transcription	n/a	n/a	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
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3273 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

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	chr1:155717400-155795800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr1:155720200-155798200	Strong transcription	Fetal Thymus	thymus
7	chr1:155720200-155803600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr1:155720400-155796800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr1:155730400-155764200	Weak transcription	Psoas Muscle	Psoas
10	chr1:155732200-155789200	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr1:155737200-155772200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr1:155743000-155763400	Weak transcription	HMEC	breast
13	chr1:155743200-155773400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr1:155746400-155774000	Weak transcription	Pancreas	Pancrea
15	chr1:155746400-155791400	Weak transcription	Stomach Mucosa	stomach
16	chr1:155746600-155763400	Weak transcription	Spleen	Spleen
17	chr1:155747000-155763000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr1:155747000-155764200	Weak transcription	Brain Substantia Nigra	brain
19	chr1:155747200-155763400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr1:155747400-155763200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr1:155747600-155764000	Weak transcription	Brain Hippocampus Middle	brain
22	chr1:155747600-155764200	Weak transcription	A549	lung
23	chr1:155747600-155764400	Weak transcription	Ovary	ovary
24	chr1:155747600-155776200	Weak transcription	Right Ventricle	heart
25	chr1:155747600-155787200	Weak transcription	Esophagus	oesophagus
26	chr1:155747800-155762600	Weak transcription	NHLF	lung
27	chr1:155747800-155764400	Weak transcription	NHEK	skin
28	chr1:155747800-155785600	Weak transcription	Fetal Brain Male	brain
29	chr1:155747800-155791200	Weak transcription	Fetal Heart	heart
30	chr1:155748000-155789400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr1:155748800-155771600	Weak transcription	Rectal Smooth Muscle	rectum
32	chr1:155749800-155766400	Strong transcription	Primary neutrophils fromperipheralblood	blood
33	chr1:155751800-155765600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr1:155751800-155777600	Strong transcription	Monocytes-CD14+_RO01746	blood
35	chr1:155752000-155765800	Strong transcription	Adipose Nuclei	Adipose
36	chr1:155752000-155771000	Strong transcription	Fetal Muscle Leg	muscle
37	chr1:155752200-155763600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr1:155752800-155762600	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr1:155754800-155762800	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr1:155754800-155770600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr1:155755000-155762400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr1:155755000-155762600	Weak transcription	Left Ventricle	heart
43	chr1:155755000-155762800	Weak transcription	Brain Cingulate Gyrus	brain
44	chr1:155755000-155763200	Weak transcription	Fetal Lung	lung
45	chr1:155755000-155772600	Weak transcription	Gastric	stomach
46	chr1:155755200-155762400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr1:155755200-155762400	Weak transcription	NH-A	brain
48	chr1:155755200-155763200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr1:155755200-155763400	Weak transcription	Aorta	Aorta
50	chr1:155755200-155763400	Weak transcription	Brain Inferior Temporal Lobe	brain

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