Variant report

Variant	nsv830011
Chromosome Location	chr4:95947560-96103934
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1739)
CpG islands
(count:550)
Chromatin interactive
region (count:47)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1739 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:96028813-96029127	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:96087112-96087434	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:96077355-96077648	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:96009257-96009440	K562	blood:	n/a	n/a
5	ATF1	chr4:96009321-96009510	K562	blood:	n/a	n/a
6	ATF1	chr4:96015817-96016032	K562	blood:	n/a	n/a
7	ATF3	chr4:96050951-96051511	A549	lung:	n/a	chr4:96051361-96051374
8	ATF3	chr4:96016460-96016817	A549	lung:	n/a	n/a
9	ATF3	chr4:96051030-96051575	A549	lung:	n/a	chr4:96051361-96051374
10	BACH1	chr4:96079844-96080146	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:96071182-96071218	K562	blood:	n/a	n/a
12	BACH1	chr4:96009288-96009544	K562	blood:	n/a	n/a
13	BCL3	chr4:96005516-96006289	A549	lung:	n/a	n/a
14	BCL3	chr4:96006382-96007008	A549	lung:	n/a	n/a
15	BCL3	chr4:96005564-96006173	A549	lung:	n/a	n/a
16	BCL3	chr4:96050969-96051663	A549	lung:	n/a	n/a
17	BCL3	chr4:95966549-95967073	A549	lung:	n/a	n/a
18	BCL3	chr4:96050906-96051514	A549	lung:	n/a	n/a
19	BHLHE40	chr4:95983001-95983312	K562	blood:	n/a	n/a
20	BHLHE40	chr4:96102659-96103176	K562	blood:	n/a	n/a
21	BRCA1	chr4:96062650-96062762	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr4:96051080-96051522	HCT-116	colon:	n/a	n/a
23	CCNT2	chr4:95989697-95989789	K562	blood:	n/a	n/a
24	CEBPB	chr4:96016531-96016786	MCF-7	breast:	n/a	n/a
25	CEBPB	chr4:96039025-96039363	HepG2	liver:	n/a	chr4:96039184-96039193 chr4:96039184-96039193 chr4:96039182-96039195 chr4:96039184-96039193
26	CEBPB	chr4:96077673-96077926	A549	lung:	n/a	n/a
27	CEBPB	chr4:96077437-96077943	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr4:96088968-96089314	K562	blood:	n/a	n/a
29	CEBPB	chr4:95999169-95999391	HepG2	liver:	n/a	chr4:95999294-95999305
30	CEBPB	chr4:95949053-95949376	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr4:96028745-96029133	A549	lung:	n/a	n/a
32	CEBPB	chr4:96039052-96039334	H1-hESC	embryonic stem cell:	n/a	chr4:96039184-96039193 chr4:96039184-96039193 chr4:96039182-96039195 chr4:96039184-96039193
33	CEBPB	chr4:96007741-96008042	MCF-7	breast:	n/a	n/a
34	CEBPB	chr4:96016475-96016848	A549	lung:	n/a	n/a
35	CEBPB	chr4:96016483-96016873	A549	lung:	n/a	n/a
36	CEBPB	chr4:96050894-96051665	HCT-116	colon:	n/a	chr4:96051299-96051308
37	CEBPB	chr4:96051090-96051496	K562	blood:	n/a	chr4:96051299-96051308
38	CEBPB	chr4:96050934-96051756	A549	lung:	n/a	chr4:96051299-96051308
39	CEBPB	chr4:96012178-96013026	A549	lung:	n/a	chr4:96012907-96012920
40	CEBPB	chr4:96016562-96016798	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr4:96012468-96012729	MCF-7	breast:	n/a	n/a
42	CEBPB	chr4:96050896-96051829	Hela-S3	cervix:	n/a	chr4:96051299-96051308
43	CEBPB	chr4:96051022-96051598	HCT-116	colon:	n/a	chr4:96051299-96051308
44	CEBPB	chr4:96028608-96029259	HCT-116	colon:	n/a	n/a
45	CEBPB	chr4:96012122-96012959	A549	lung:	n/a	chr4:96012907-96012920
46	CEBPB	chr4:96012403-96012830	A549	lung:	n/a	n/a
47	CEBPB	chr4:95964692-95964997	A549	lung:	n/a	chr4:95964860-95964871 chr4:95964859-95964872 chr4:95964859-95964872
48	CEBPB	chr4:96051132-96051451	K562	blood:	n/a	chr4:96051299-96051308
49	CEBPB	chr4:96051053-96051496	MCF-7	breast:	n/a	chr4:96051299-96051308
50	CEBPB	chr4:95949058-95949430	ECC-1	luminal epithelium:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:96090330-96090380	HEK293	kidney:	embryo
2	chr4:96090330-96090380	HEK293	kidney:	embryo
3	chr4:96025493-96025543	PrEC	prostate:	n/a
4	chr4:96012317-96012367	LNCaP	prostate:	n/a
5	chr4:96051461-96051511	NHDF-neo	bronchial:	n/a
6	chr4:96077623-96077673	ovcar-3	ovarian:	n/a
7	chr4:95960149-95960199	PANC-1	pancreas:	n/a
8	chr4:96102203-96102253	HCPEpiC	choroid plexus:	n/a
9	chr4:96011175-96011225	MCF-7	breast:	n/a
10	chr4:96012317-96012367	NHDF-neo	bronchial:	n/a
11	chr4:95960149-95960199	SKMC	muscle:	n/a
12	chr4:96080181-96080231	SK-N-MC	brain:	n/a
13	chr4:96090330-96090380	Hela-S3	cervix:	n/a
14	chr4:96077623-96077673	HMEC	breast:	n/a
15	chr4:96051461-96051511	BE2_C	brain:	n/a
16	chr4:95960149-95960199	SK-N-SH_RA	brain:	n/a
17	chr4:95960149-95960199	RPTEC	kidney:	n/a
18	chr4:96011175-96011225	K562	blood:	n/a
19	chr4:96011175-96011225	U87	brain:	n/a
20	chr4:96012317-96012367	SKMC	muscle:	n/a
21	chr4:96102203-96102253	AG10803	skin:	n/a
22	chr4:96102203-96102253	PANC-1	pancreas:	n/a
23	chr4:96011175-96011225	NHDF-neo	bronchial:	n/a
24	chr4:96012317-96012367	HNPCEpiC	eye:	n/a
25	chr4:96080181-96080231	BJ	skin:	n/a
26	chr4:96025493-96025543	RPTEC	kidney:	n/a
27	chr4:95960149-95960199	HCPEpiC	choroid plexus:	n/a
28	chr4:95960149-95960199	AG04450	lung:	fetal
29	chr4:96102203-96102253	GM12878	blood:	n/a
30	chr4:96025493-96025543	HPAEpiC	pulmonary alveolar:	n/a
31	chr4:96090330-96090380	Hepatocyte	liver:	n/a
32	chr4:96080181-96080231	HCT-116	colon:	n/a
33	chr4:96051461-96051511	SK-N-SH	brain:	n/a
34	chr4:96077623-96077673	AG10803	skin:	n/a
35	chr4:96077623-96077673	HEK293	kidney:	embryo
36	chr4:96077623-96077673	NT2-D1	testis:	n/a
37	chr4:96077623-96077673	NH-A	brain:	n/a
38	chr4:96025493-96025543	PFSK-1	brain:	n/a
39	chr4:96080181-96080231	LNCaP	prostate:	n/a
40	chr4:96011175-96011225	NB4	blood:	n/a
41	chr4:96077623-96077673	BE2_C	brain:	n/a
42	chr4:96012317-96012367	PFSK-1	brain:	n/a
43	chr4:96025493-96025543	AG04450	lung:	fetal
44	chr4:96077623-96077673	T-47D	breast:	n/a
45	chr4:96025493-96025543	AG04449	skin:	fetal
46	chr4:96025493-96025543	SK-N-SH_RA	brain:	n/a
47	chr4:96012317-96012367	MCF10A-Er-Src	breast:	n/a
48	chr4:96012317-96012367	T-47D	breast:	n/a
49	chr4:96102203-96102253	AG04449	skin:	fetal
50	chr4:96090330-96090380	PrEC	prostate:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:96002491..96004992-chr4:96012725..96014797,2	MCF-7	breast:
2	chr4:96002491..96004992-chr4:96012725..96014797,2	MCF-7	breast:
3	chr4:95915803..95916373-chr4:96014810..96015711,2	MCF-7	breast:
4	chr4:96021956..96024897-chr4:96031645..96034367,2	K562	blood:
5	chr4:95970827..95973009-chr4:96005064..96008963,3	MCF-7	breast:
6	chr4:96011040..96013524-chr4:96016284..96018224,2	MCF-7	breast:
7	chr4:96020247..96022763-chr4:96027128..96028704,2	K562	blood:
8	chr4:95966448..95968999-chr4:96005215..96007562,2	MCF-7	breast:
9	chr4:95944191..95946450-chr4:96004489..96006768,3	MCF-7	breast:
10	chr4:96076258..96078033-chr4:96079736..96082501,2	K562	blood:
11	chr4:95679588..95681847-chr4:96013272..96015095,2	MCF-7	breast:
12	chr4:96022993..96023975-chr4:96045463..96046631,4	MCF-7	breast:
13	chr4:95987134..95989766-chr4:96003420..96005657,2	MCF-7	breast:
14	chr4:96029649..96031586-chr4:96035562..96037521,2	MCF-7	breast:
15	chr4:96029649..96031586-chr4:96035562..96037521,2	MCF-7	breast:
16	chr4:95679956..95681773-chr4:96032755..96034458,2	MCF-7	breast:
17	chr4:96020247..96024806-chr4:96024955..96029503,5	K562	blood:
18	chr4:96103609..96107002-chr4:96107202..96110546,3	MCF-7	breast:
19	chr4:95988285..95990355-chr4:96023182..96024954,2	K562	blood:
20	chr4:95944007..95945865-chr4:95974454..95976433,2	MCF-7	breast:
21	chr4:95677494..95679995-chr4:96034542..96036779,2	MCF-7	breast:
22	chr4:95996849..95998848-chr4:96004803..96006629,2	K562	blood:
23	chr4:96022993..96023975-chr4:96045463..96046631,4	MCF-7	breast:
24	chr4:95912061..95914592-chr4:96007501..96009488,2	MCF-7	breast:
25	chr4:95961918..95964431-chr4:96005630..96007431,2	MCF-7	breast:
26	chr4:95961918..95964431-chr4:96005630..96007431,2	MCF-7	breast:
27	chr4:96089863..96090822-chr4:96121996..96122543,2	MCF-7	breast:
28	chr4:96086744..96087935-chr4:96125403..96126613,4	MCF-7	breast:
29	chr4:95678022..95682059-chr4:96013803..96017357,5	MCF-7	breast:
30	chr4:96020247..96022763-chr4:96027128..96028704,2	K562	blood:
31	chr4:95988285..95990355-chr4:96023182..96024954,2	K562	blood:
32	chr4:96103428..96105512-chr4:96106717..96108756,2	K562	blood:
33	chr4:96026041..96029034-chr4:96031060..96033692,2	K562	blood:
34	chr4:95678678..95680883-chr4:96023985..96026151,2	MCF-7	breast:
35	chr4:95531315..95533011-chr4:96007833..96010068,2	MCF-7	breast:
36	chr4:95987134..95989766-chr4:96003420..96005657,2	MCF-7	breast:
37	chr4:96086828..96087500-chr4:96465795..96466540,3	MCF-7	breast:
38	chr4:96103400..96106252-chr4:96114809..96117645,2	K562	blood:
39	chr4:96021956..96024897-chr4:96031645..96034367,2	K562	blood:
40	chr4:95996849..95998848-chr4:96004803..96006629,2	K562	blood:
41	chr4:95966448..95968999-chr4:96005215..96007562,2	MCF-7	breast:
42	chr4:96004208..96009283-chr4:96010834..96014104,5	MCF-7	breast:
43	chr4:95667629..95668340-chr4:96016619..96017181,2	K562	blood:
44	chr4:95930676..95931407-chr4:96015895..96017114,4	MCF-7	breast:
45	chr4:96077419..96078385-chr4:96283655..96284313,2	K562	blood:
46	chr4:96076258..96078033-chr4:96079736..96082501,2	K562	blood:
47	chr4:96026041..96029034-chr4:96031060..96033692,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HPGDS-5	chr4:96083659-96088750	NONHSAT097459

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	BMPR1B	hsa-miR-125b-5p	chr4:96077253-96077274
2	BMPR1B	hsa-miR-125b-5p	chr4:96075965-96075972

Variant related genes	Relation type
BMPR1B	TF binding region
BMPR1B	CpG island
ENSG00000249599	chromatin interactions
ENSG00000138696	chromatin interactions

Extended variants
information (count: 6281 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:6281 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143468033	chr4:95947587-95947588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs116554376	chr4:95947631-95947632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs34618711	chr4:95947643-95947644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs532199517	chr4:95947645-95947646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370851622	chr4:95947699-95947700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs199578352	chr4:95947834-95947835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs58113438	chr4:95947855-95947856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552379290	chr4:95947871-95947872	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375313899	chr4:95947878-95947879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs77701570	chr4:95948038-95948039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372895242	chr4:95948082-95948083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76557660	chr4:95948083-95948084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs72891468	chr4:95948107-95948108	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs151229795	chr4:95948116-95948117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs140090430	chr4:95948131-95948132	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs578152571	chr4:95948183-95948184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs28663472	chr4:95948204-95948205	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs570234991	chr4:95948242-95948243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189471489	chr4:95948248-95948249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs72891471	chr4:95948269-95948270	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs11736371	chr4:95948292-95948293	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs561214392	chr4:95948294-95948295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554618851	chr4:95948342-95948343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs574498949	chr4:95948412-95948413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs543474844	chr4:95948435-95948436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs113808097	chr4:95948461-95948462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs17345417	chr4:95948486-95948487	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs550463682	chr4:95948495-95948496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs150308000	chr4:95948525-95948526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs17022883	chr4:95948609-95948610	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs536188654	chr4:95948621-95948622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539323504	chr4:95948632-95948633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs17022885	chr4:95948640-95948641	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs137914491	chr4:95948643-95948644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530543427	chr4:95948650-95948651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs149046846	chr4:95948675-95948676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs566463991	chr4:95948684-95948685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185042720	chr4:95948737-95948738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539581567	chr4:95948770-95948771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149169240	chr4:95948807-95948808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552490752	chr4:95948910-95948911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566263760	chr4:95948927-95948928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs534963388	chr4:95948934-95948935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs190925571	chr4:95948952-95948953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533536549	chr4:95948987-95948988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs574825180	chr4:95948992-95948993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566333506	chr4:95949000-95949001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554992310	chr4:95949010-95949011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2114535	chr4:95949098-95949099	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs576924019	chr4:95949105-95949106	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1366 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:95941400-95949000	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr4:95945200-95948000	Weak transcription	A549	lung
3	chr4:95947800-95948200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:95947800-95949800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr4:95948000-95948200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:95948000-95949600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr4:95948000-95949800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:95948000-95949800	Enhancers	A549	lung
9	chr4:95948200-95949200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:95948200-95966600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:95948400-95949600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:95948600-95949600	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr4:95948600-95949600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr4:95948600-95949600	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr4:95948600-95949600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr4:95948800-95949200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr4:95949000-95949400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr4:95949000-95949400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr4:95949000-95949400	Enhancers	Fetal Heart	heart
20	chr4:95949000-95949600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr4:95949000-95949600	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr4:95949200-95949600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr4:95949800-95952400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr4:95949800-95956800	Weak transcription	A549	lung
25	chr4:95952400-95953000	Enhancers	Aorta	Aorta
26	chr4:95956800-95957200	ZNF genes & repeats	A549	lung
27	chr4:95957000-95972400	Weak transcription	Psoas Muscle	Psoas
28	chr4:95957200-95963600	Weak transcription	A549	lung
29	chr4:95958200-95958400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:95958200-95959600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr4:95958200-95960000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr4:95958200-95960000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr4:95958400-95959400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:95959000-95959600	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr4:95959400-95959600	Enhancers	Brain Cingulate Gyrus	brain
36	chr4:95959400-95959800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:95959400-95960400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr4:95959600-95964400	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr4:95959800-95965200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr4:95960000-95963400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr4:95960800-95965600	Weak transcription	Brain Cingulate Gyrus	brain
42	chr4:95963400-95965600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr4:95963600-95964600	Enhancers	A549	lung
44	chr4:95963800-95964000	ZNF genes & repeats	Fetal Kidney	kidney
45	chr4:95963800-95968200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr4:95964000-95964800	Weak transcription	Fetal Kidney	kidney
47	chr4:95964400-95966200	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr4:95964600-95965000	Flanking Active TSS	A549	lung
49	chr4:95964600-95965600	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr4:95964600-95967000	Enhancers	Brain Angular Gyrus	brain

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