Variant report

Variant	nsv879516
Chromosome Location	chr4:85877561-85895436
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:810)
CpG islands
(count:549)
Chromatin interactive
region (count:24)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:810 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:85892480-85892823	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:85886734-85886855	HepG2	liver:	n/a	n/a
3	ATF1	chr4:85887757-85887998	K562	blood:	n/a	n/a
4	BACH1	chr4:85886751-85887443	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:85888178-85888727	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr4:85887728-85887924	K562	blood:	n/a	n/a
7	BHLHE40	chr4:85892665-85892725	GM12878	blood:	n/a	n/a
8	BRCA1	chr4:85888159-85888550	HepG2	liver:	n/a	n/a
9	BRCA1	chr4:85887670-85887763	HepG2	liver:	n/a	n/a
10	CCNT2	chr4:85886860-85888131	K562	blood:	n/a	chr4:85887085-85887094 chr4:85887332-85887341 chr4:85886962-85886971
11	CEBPB	chr4:85892465-85892865	MCF-7	breast:	n/a	n/a
12	CEBPB	chr4:85887688-85888223	MCF-7	breast:	n/a	n/a
13	CEBPB	chr4:85892427-85892859	K562	blood:	n/a	n/a
14	CEBPB	chr4:85892417-85892768	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr4:85887786-85888596	A549	lung:	n/a	n/a
16	CEBPB	chr4:85892423-85892811	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr4:85892450-85892849	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr4:85892579-85892757	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:85892337-85892938	MCF-7	breast:	n/a	n/a
20	CEBPB	chr4:85892389-85893033	K562	blood:	n/a	n/a
21	CEBPB	chr4:85892486-85892757	K562	blood:	n/a	n/a
22	CEBPB	chr4:85887915-85888060	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:85892442-85892961	HCT-116	colon:	n/a	n/a
24	CEBPB	chr4:85892448-85892891	A549	lung:	n/a	n/a
25	CEBPB	chr4:85885621-85885865	K562	blood:	n/a	chr4:85885766-85885779 chr4:85885767-85885778 chr4:85885766-85885777
26	CEBPB	chr4:85892452-85892828	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr4:85887812-85888492	HepG2	liver:	n/a	n/a
28	CEBPB	chr4:85887829-85888098	K562	blood:	n/a	n/a
29	CEBPB	chr4:85892477-85892811	A549	lung:	n/a	n/a
30	CEBPB	chr4:85887836-85888074	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr4:85892452-85892829	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:85885696-85885820	HepG2	liver:	n/a	chr4:85885766-85885779 chr4:85885767-85885778 chr4:85885766-85885777
33	CEBPB	chr4:85892400-85892962	A549	lung:	n/a	n/a
34	CEBPB	chr4:85892440-85892826	IMR90	lung:	n/a	n/a
35	CEBPB	chr4:85892323-85892983	HCT-116	colon:	n/a	n/a
36	CEBPB	chr4:85887596-85888629	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr4:85887735-85888594	IMR90	lung:	n/a	n/a
38	CEBPD	chr4:85887750-85888145	HepG2	liver:	n/a	n/a
39	CEBPD	chr4:85886965-85887271	HepG2	liver:	n/a	n/a
40	CHD1	chr4:85887527-85887886	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr4:85886387-85887319	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr4:85885928-85885974	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD1	chr4:85892543-85892724	GM12878	blood:	n/a	n/a
44	CHD2	chr4:85887070-85887175	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr4:85887118-85888023	Hela-S3	cervix:	n/a	chr4:85887333-85887343
46	CHD2	chr4:85887874-85888425	HepG2	liver:	n/a	n/a
47	CREB1	chr4:85886950-85887668	A549	lung:	n/a	n/a
48	CTBP2	chr4:85886711-85888497	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr4:85887080-85887230	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr4:85887130-85887278	Pancreas_OC	pancreas:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:85887769-85887819	A549	lung:	n/a
2	chr4:85878805-85878855	HMEC	breast:	n/a
3	chr4:85886384-85886434	AG09309	skin:	n/a
4	chr4:85878805-85878855	NB4	blood:	n/a
5	chr4:85886830-85886880	SAEC	small airway:	n/a
6	chr4:85888263-85888313	NHBE	bronchial:	n/a
7	chr4:85887382-85887432	HCF	heart:	n/a
8	chr4:85888001-85888051	NH-A	brain:	n/a
9	chr4:85886384-85886434	HCPEpiC	choroid plexus:	n/a
10	chr4:85878805-85878855	HAEpiC	amniotic membrane:	n/a
11	chr4:85887600-85887650	K562	blood:	n/a
12	chr4:85888263-85888313	PrEC	prostate:	n/a
13	chr4:85878805-85878855	HCPEpiC	choroid plexus:	n/a
14	chr4:85887600-85887650	U87	brain:	n/a
15	chr4:85886384-85886434	HEEpiC	esophagus:	n/a
16	chr4:85888001-85888051	ProgFib	skin:	n/a
17	chr4:85887382-85887432	AG09319	gingival:	n/a
18	chr4:85887769-85887819	ECC-1	luminal epithelium:	n/a
19	chr4:85887769-85887819	AG04449	skin:	fetal
20	chr4:85878805-85878855	H1-hESC	embryonic stem cell:	embryo
21	chr4:85886830-85886880	IMR90	lung:	fetal
22	chr4:85886384-85886434	SK-N-SH_RA	brain:	n/a
23	chr4:85888263-85888313	AG10803	skin:	n/a
24	chr4:85886830-85886880	MCF10A-Er-Src	breast:	n/a
25	chr4:85888362-85888412	H1-hESC	embryonic stem cell:	embryo
26	chr4:85886384-85886434	MCF-7	breast:	n/a
27	chr4:85888001-85888051	SKMC	muscle:	n/a
28	chr4:85888001-85888051	HepG2	liver:	n/a
29	chr4:85888362-85888412	AG04450	lung:	fetal
30	chr4:85886830-85886880	HL-60	blood:	n/a
31	chr4:85886830-85886880	GM12892	blood:	n/a
32	chr4:85888001-85888051	HRPEpiC	eye:	n/a
33	chr4:85888263-85888313	MCF-7	breast:	n/a
34	chr4:85886384-85886434	Hela-S3	cervix:	n/a
35	chr4:85887600-85887650	HCPEpiC	choroid plexus:	n/a
36	chr4:85888362-85888412	Caco-2	colon:	n/a
37	chr4:85888263-85888313	SKMC	muscle:	n/a
38	chr4:85888001-85888051	HUVEC	blood vessel:	n/a
39	chr4:85888263-85888313	HCPEpiC	choroid plexus:	n/a
40	chr4:85888001-85888051	MCF10A-Er-Src	breast:	n/a
41	chr4:85886830-85886880	HEK293	kidney:	embryo
42	chr4:85886384-85886434	HUVEC	blood vessel:	n/a
43	chr4:85888362-85888412	HPAEpiC	pulmonary alveolar:	n/a
44	chr4:85878805-85878855	SK-N-MC	brain:	n/a
45	chr4:85887382-85887432	HPAEpiC	pulmonary alveolar:	n/a
46	chr4:85887769-85887819	NB4	blood:	n/a
47	chr4:85887600-85887650	H1-hESC	embryonic stem cell:	embryo
48	chr4:85887600-85887650	Hela-S3	cervix:	n/a
49	chr4:85887600-85887650	AG04449	skin:	fetal
50	chr4:85888001-85888051	GM12891	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:85840711..85842530-chr4:85882246..85885030,2	MCF-7	breast:
2	chr4:85879778..85882729-chr4:85884440..85887298,2	K562	blood:
3	chr4:85877154..85880144-chr4:85883390..85884959,2	MCF-7	breast:
4	chr4:85671021..85672424-chr4:85892203..85893136,7	MCF-7	breast:
5	chr4:85876909..85884375-chr4:85886007..85890757,11	MCF-7	breast:
6	chr4:85879778..85882729-chr4:85884440..85887298,2	K562	blood:
7	chr4:85883700..85885216-chr4:85886284..85888198,2	MCF-7	breast:
8	chr4:84565742..84566425-chr4:85892168..85893103,2	K562	blood:
9	chr4:85790487..85793474-chr4:85885792..85887497,2	MCF-7	breast:
10	chr4:85820113..85822349-chr4:85884941..85887197,2	MCF-7	breast:
11	chr4:85881229..85883388-chr4:85885235..85887298,2	K562	blood:
12	chr4:85671072..85672068-chr4:85893422..85894309,2	MCF-7	breast:
13	chr4:85871120..85875052-chr4:85876385..85879344,3	MCF-7	breast:
14	chr4:85669778..85672132-chr4:85890342..85893925,3	MCF-7	breast:
15	chr4:85877992..85883015-chr4:85885939..85888953,5	MCF-7	breast:
16	chr4:85503502..85505436-chr4:85887662..85889953,2	MCF-7	breast:
17	chr4:85881229..85883388-chr4:85885235..85887298,2	K562	blood:
18	chr4:85888138..85888639-chr7:132287182..132287682,2	Hela-S3	cervix:
19	chr4:85503339..85505737-chr4:85885750..85887907,3	MCF-7	breast:
20	chr4:85648671..85650306-chr4:85882299..85884684,2	MCF-7	breast:
21	chr4:85671238..85672086-chr4:85892384..85893145,4	MCF-7	breast:
22	chr4:85671137..85672231-chr4:85892144..85893141,6	K562	blood:
23	chr4:85877154..85880144-chr4:85883390..85884959,2	MCF-7	breast:
24	chr4:85673481..85676586-chr4:85887682..85889836,3	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDS1-2	chr4:85890893-85891029	NONHSAT097257
2	lnc-CDS1-2	chr4:85890940-85891029	NONHSAT097258
3	lnc-CDS1-2	chr4:85888763-85888799	NONHSAT097251
4	lnc-CDS1-2	chr4:85890874-85891029	NONHSAT097256
5	lnc-CDS1-2	chr4:85887429-85888280	NONHSAT097251
6	lnc-CDS1-2	chr4:85890878-85891029	ENSG00000180769
7	lnc-CDS1-2	chr4:85887539-85887960	NONHSAT097253
8	lnc-CDS1-2	chr4:85887538-85888280	ENSG00000180769
9	lnc-CDS1-2	chr4:85890878-85891029	ENSG00000180769
10	lnc-CDS1-2	chr4:85887971-85888280	NR_015359
11	lnc-CDS1-2	chr4:85887946-85888280	ENSG00000180769
12	lnc-CDS1-2	chr4:85890878-85891029	NR_015359
13	lnc-CDS1-2	chr4:85887971-85888280	NONHSAT097255

No data

Variant related genes	Relation type
WDFY3	TF binding region
WDFY3-AS2	TF binding region
WDFY3	CpG island
WDFY3-AS2	CpG island
ENSG00000163624	chromatin interactions
ENSG00000180769	chromatin interactions
ENSG00000163625	chromatin interactions
GNPDA2	miRNA target sites
MED23	miRNA target sites
FSTL3	miRNA target sites
INPP5B	miRNA target sites

Extended variants
information (count: 603 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:603 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7699226	chr4:85877561-85877562	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147847422	chr4:85877575-85877576	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs563743228	chr4:85877580-85877581	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs531202516	chr4:85877640-85877641	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs552618814	chr4:85877688-85877689	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs571154975	chr4:85877711-85877712	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs76555165	chr4:85877742-85877743	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs113891259	chr4:85877756-85877757	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs74455521	chr4:85877776-85877777	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs535563122	chr4:85877785-85877786	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs189024122	chr4:85877807-85877808	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs553234564	chr4:85877816-85877817	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs181614115	chr4:85877870-85877871	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs371020676	chr4:85877911-85877912	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs537280526	chr4:85877941-85877942	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs186391376	chr4:85877962-85877963	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs576613175	chr4:85878005-85878006	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs577108897	chr4:85878100-85878101	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs191597109	chr4:85878108-85878109	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs4487328	chr4:85878120-85878121	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs7654035	chr4:85878124-85878125	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs574546577	chr4:85878126-85878127	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs74843482	chr4:85878131-85878132	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs571594170	chr4:85878134-85878135	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs77929820	chr4:85878135-85878136	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs541964311	chr4:85878195-85878196	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs561943401	chr4:85878258-85878259	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs573925096	chr4:85878345-85878346	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs563879878	chr4:85878364-85878365	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs149018066	chr4:85878412-85878413	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs11938778	chr4:85878421-85878422	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs546416297	chr4:85878422-85878423	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs564619059	chr4:85878423-85878424	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs370791017	chr4:85878424-85878425	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs11938780	chr4:85878425-85878426	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs372149907	chr4:85878429-85878430	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs546547904	chr4:85878533-85878534	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs561761804	chr4:85878623-85878624	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs529317905	chr4:85878671-85878672	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs550774993	chr4:85878737-85878738	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs569369406	chr4:85878743-85878744	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs181273156	chr4:85878806-85878807	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs147602036	chr4:85878814-85878815	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs541112236	chr4:85878883-85878884	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs558902002	chr4:85879045-85879046	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs113780728	chr4:85879070-85879071	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs570608666	chr4:85879082-85879083	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs139625634	chr4:85879090-85879091	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs185431430	chr4:85879112-85879113	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs574509649	chr4:85879118-85879119	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	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
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Prostate cancer	16573809	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:817 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:85845600-85882800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr4:85865200-85886400	Weak transcription	Fetal Muscle Trunk	muscle
3	chr4:85865800-85885400	Weak transcription	Fetal Muscle Leg	muscle
4	chr4:85866000-85886200	Weak transcription	Fetal Intestine Small	intestine
5	chr4:85866400-85879200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:85866800-85884600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:85867800-85878600	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr4:85869600-85879800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr4:85869800-85879200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr4:85870200-85879200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr4:85870400-85879200	Weak transcription	Adipose Nuclei	Adipose
12	chr4:85870400-85880800	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr4:85871000-85879200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr4:85872000-85886600	Weak transcription	Lung	lung
15	chr4:85873200-85877600	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr4:85873200-85879200	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr4:85873200-85879200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr4:85873400-85878600	Weak transcription	Stomach Mucosa	stomach
19	chr4:85873400-85879200	Weak transcription	Pancreas	Pancrea
20	chr4:85873400-85879600	Weak transcription	Gastric	stomach
21	chr4:85873400-85886600	Weak transcription	Esophagus	oesophagus
22	chr4:85873600-85878600	Weak transcription	Liver	Liver
23	chr4:85873800-85878800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr4:85873800-85879000	Weak transcription	NH-A	brain
25	chr4:85873800-85880600	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr4:85873800-85884800	Weak transcription	HSMM	muscle
27	chr4:85873800-85885400	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr4:85873800-85885800	Weak transcription	Osteobl	bone
29	chr4:85874000-85884600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr4:85874200-85879200	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr4:85874400-85878600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr4:85874600-85878600	Weak transcription	NHDF-Ad	bronchial
33	chr4:85874600-85879400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr4:85874600-85886200	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr4:85875000-85878000	Enhancers	Brain Angular Gyrus	brain
36	chr4:85875000-85880000	Enhancers	Brain Cingulate Gyrus	brain
37	chr4:85875200-85877600	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr4:85875200-85877600	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr4:85875200-85878000	Enhancers	Brain Substantia Nigra	brain
40	chr4:85875200-85878600	Weak transcription	Fetal Intestine Large	intestine
41	chr4:85875200-85881600	Enhancers	Brain Anterior Caudate	brain
42	chr4:85875800-85877600	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr4:85875800-85877600	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr4:85875800-85877600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:85876000-85877600	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr4:85876000-85877600	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr4:85876000-85877600	Enhancers	Colon Smooth Muscle	Colon
48	chr4:85876000-85882000	Enhancers	Brain Hippocampus Middle	brain
49	chr4:85876400-85877600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr4:85876400-85878000	Enhancers	Fetal Heart	heart

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