Variant report

Variant	nsv830019
Chromosome Location	chr4:101023666-101208908
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:583)
CpG islands
(count:915)
Chromatin interactive
region (count:29)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:583 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:101083345-101083949	GM12878	blood:	n/a	n/a
2	BACH1	chr4:101111799-101112380	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr4:101083355-101083728	GM12878	blood:	n/a	chr4:101083557-101083568
4	BHLHE40	chr4:101083611-101083895	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:101052145-101052340	GM12878	blood:	n/a	n/a
6	CBX3	chr4:101083149-101083634	HCT-116	colon:	n/a	n/a
7	CBX3	chr4:101178670-101179127	HCT-116	colon:	n/a	n/a
8	CBX3	chr4:101083153-101083662	HCT-116	colon:	n/a	n/a
9	CCNT2	chr4:101071732-101072017	K562	blood:	n/a	n/a
10	CEBPB	chr4:101120850-101121102	IMR90	lung:	n/a	n/a
11	CEBPB	chr4:101104285-101104507	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr4:101104179-101104479	IMR90	lung:	n/a	n/a
13	CEBPB	chr4:101099344-101099492	HepG2	liver:	n/a	chr4:101099410-101099427 chr4:101099412-101099423
14	CEBPB	chr4:101179251-101179499	HepG2	liver:	n/a	chr4:101179377-101179388
15	CEBPB	chr4:101179220-101179546	IMR90	lung:	n/a	chr4:101179377-101179388
16	CEBPB	chr4:101057737-101057966	HepG2	liver:	n/a	chr4:101057866-101057875 chr4:101057864-101057877 chr4:101057865-101057876 chr4:101057864-101057875 chr4:101057866-101057875 chr4:101057866-101057875 chr4:101057866-101057875
17	CEBPB	chr4:101111861-101112179	IMR90	lung:	n/a	n/a
18	CEBPB	chr4:101142132-101142360	HepG2	liver:	n/a	chr4:101142242-101142253
19	CEBPB	chr4:101150557-101150686	HepG2	liver:	n/a	chr4:101150628-101150639
20	CEBPB	chr4:101119961-101120304	A549	lung:	n/a	chr4:101120153-101120164 chr4:101119972-101119983 chr4:101119972-101119985
21	CEBPB	chr4:101179268-101179442	A549	lung:	n/a	chr4:101179377-101179388
22	CEBPB	chr4:101024914-101025132	HepG2	liver:	n/a	chr4:101025013-101025024
23	CEBPB	chr4:101120835-101121148	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:101119906-101120291	IMR90	lung:	n/a	chr4:101120153-101120164 chr4:101119972-101119983 chr4:101119972-101119985
25	CEBPB	chr4:101106118-101106375	HepG2	liver:	n/a	chr4:101106268-101106279
26	CEBPB	chr4:101104270-101104381	K562	blood:	n/a	n/a
27	CEBPB	chr4:101024852-101025176	IMR90	lung:	n/a	chr4:101025013-101025024
28	CEBPB	chr4:101057746-101058008	IMR90	lung:	n/a	chr4:101057866-101057875 chr4:101057864-101057877 chr4:101057865-101057876 chr4:101057864-101057875 chr4:101057866-101057875 chr4:101057866-101057875 chr4:101057866-101057875
29	CEBPB	chr4:101098891-101099522	IMR90	lung:	n/a	chr4:101099410-101099427 chr4:101099412-101099423
30	CEBPB	chr4:101111906-101112106	A549	lung:	n/a	n/a
31	CEBPB	chr4:101106248-101106282	K562	blood:	n/a	chr4:101106268-101106279
32	CEBPB	chr4:101119966-101120286	HepG2	liver:	n/a	chr4:101120153-101120164 chr4:101119972-101119983 chr4:101119972-101119985
33	CEBPB	chr4:101106185-101106405	IMR90	lung:	n/a	chr4:101106268-101106279
34	CHD1	chr4:101111873-101111896	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD1	chr4:101111175-101111176	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr4:101111889-101111902	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr4:101129926-101130319	GM12878	blood:	n/a	n/a
38	CHD2	chr4:101040085-101040199	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr4:101083874-101083934	GM12878	blood:	n/a	n/a
40	CHD2	chr4:101028197-101028441	GM12878	blood:	n/a	n/a
41	CTCF	chr4:101145080-101145230	GM12873	blood:	n/a	n/a
42	CTCF	chr4:101111120-101111270	AG09319	gingival:	n/a	n/a
43	CTCF	chr4:101088760-101088910	GM12872	blood:	n/a	chr4:101088821-101088839 chr4:101088816-101088837
44	CTCF	chr4:101187740-101187817	LNCaP	prostate:	n/a	n/a
45	CTCF	chr4:101145175-101145264	GM12892	blood:	n/a	n/a
46	CTCF	chr4:101088760-101088910	HRPEpiC	eye:	n/a	chr4:101088821-101088839 chr4:101088816-101088837
47	CTCF	chr4:101039020-101039170	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr4:101088780-101088930	GM12873	blood:	n/a	chr4:101088821-101088839 chr4:101088816-101088837
49	CTCF	chr4:101039060-101039210	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr4:101096200-101096350	HBMEC	blood vessel:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:101111927-101111977	PrEC	prostate:	n/a
2	chr4:101111617-101111667	ProgFib	skin:	n/a
3	chr4:101110248-101110298	HRE	kidney:	n/a
4	chr4:101111147-101111197	BJ	skin:	n/a
5	chr4:101111261-101111311	NT2-D1	testis:	n/a
6	chr4:101111771-101111821	HepG2	liver:	n/a
7	chr4:101111261-101111311	HAEpiC	amniotic membrane:	n/a
8	chr4:101110248-101110298	SK-N-SH_RA	brain:	n/a
9	chr4:101111642-101111692	SK-N-SH_RA	brain:	n/a
10	chr4:101111147-101111197	AoSMC	blood vessel:	n/a
11	chr4:101111147-101111197	NHBE	bronchial:	n/a
12	chr4:101107472-101107522	T-47D	breast:	n/a
13	chr4:101111427-101111477	Hela-S3	cervix:	n/a
14	chr4:101111427-101111477	Caco-2	colon:	n/a
15	chr4:101090547-101090597	Jurkat	blood:	n/a
16	chr4:101111314-101111364	NHBE	bronchial:	n/a
17	chr4:101180994-101181044	GM06990	blood:	n/a
18	chr4:101111642-101111692	HepG2	liver:	n/a
19	chr4:101111261-101111311	NHDF-neo	bronchial:	n/a
20	chr4:101111872-101111922	HIPEpiC	eye:	n/a
21	chr4:101111617-101111667	H1-hESC	embryonic stem cell:	embryo
22	chr4:101115184-101115234	SK-N-SH_RA	brain:	n/a
23	chr4:101115184-101115234	GM12891	blood:	n/a
24	chr4:101115184-101115234	Hepatocyte	liver:	n/a
25	chr4:101090547-101090597	HEEpiC	esophagus:	n/a
26	chr4:101111314-101111364	Hepatocyte	liver:	n/a
27	chr4:101090547-101090597	AG09309	skin:	n/a
28	chr4:101112317-101112367	GM12891	blood:	n/a
29	chr4:101111927-101111977	PANC-1	pancreas:	n/a
30	chr4:101180994-101181044	PFSK-1	brain:	n/a
31	chr4:101111617-101111667	BJ	skin:	n/a
32	chr4:101111617-101111667	BE2_C	brain:	n/a
33	chr4:101107472-101107522	SAEC	small airway:	n/a
34	chr4:101112317-101112367	HL-60	blood:	n/a
35	chr4:101090547-101090597	HRCEpiC	kidney:	n/a
36	chr4:101112317-101112367	SK-N-SH	brain:	n/a
37	chr4:101111927-101111977	HEK293	kidney:	embryo
38	chr4:101110248-101110298	GM06990	blood:	n/a
39	chr4:101090547-101090597	HAEpiC	amniotic membrane:	n/a
40	chr4:101107472-101107522	HMEC	breast:	n/a
41	chr4:101111771-101111821	ECC-1	luminal epithelium:	n/a
42	chr4:101111427-101111477	NHBE	bronchial:	n/a
43	chr4:101111617-101111667	LNCaP	prostate:	n/a
44	chr4:101090547-101090597	NB4	blood:	n/a
45	chr4:101111617-101111667	Hepatocyte	liver:	n/a
46	chr4:101111427-101111477	HUVEC	blood vessel:	n/a
47	chr4:101111642-101111692	HUVEC	blood vessel:	n/a
48	chr4:101111927-101111977	Caco-2	colon:	n/a
49	chr4:101111617-101111667	HEK293	kidney:	embryo
50	chr4:101180994-101181044	HRCEpiC	kidney:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:101072313..101075181-chr4:101094898..101096788,2	MCF-7	breast:
2	chr4:101195701..101197890-chr4:101201002..101202970,2	K562	blood:
3	chr4:100869815..100872401-chr4:101038061..101039950,3	K562	blood:
4	chr4:101031221..101033181-chr4:101038741..101041641,2	MCF-7	breast:
5	chr4:101039108..101041675-chr4:102229054..102231223,2	K562	blood:
6	chr4:101112745..101114731-chr4:101119357..101121348,2	MCF-7	breast:
7	chr4:101160745..101163177-chr4:101167667..101169870,2	MCF-7	breast:
8	chr4:100868231..100870491-chr4:101024426..101027309,2	K562	blood:
9	chr4:101084718..101086912-chr4:101087632..101089284,2	K562	blood:
10	chr4:101031221..101033181-chr4:101038741..101041641,2	MCF-7	breast:
11	chr4:101143411..101145421-chr4:101147010..101148787,2	K562	blood:
12	chr4:101061927..101063715-chr4:101066155..101068480,2	K562	blood:
13	chr4:101143411..101145421-chr4:101147010..101148787,2	K562	blood:
14	chr4:101118797..101120878-chr4:101120967..101123129,2	MCF-7	breast:
15	chr4:101176314..101178937-chr4:101179418..101181051,2	K562	blood:
16	chr4:101195701..101197890-chr4:101201002..101202970,2	K562	blood:
17	chr3:73159958..73162068-chr4:101040564..101042084,2	MCF-7	breast:
18	chr17:41400377..41402235-chr4:101040564..101042084,3	K562	blood:
19	chr4:101176314..101178937-chr4:101179418..101181051,2	K562	blood:
20	chr4:101038045..101039843-chr4:101042215..101043823,2	MCF-7	breast:
21	chr3:73160568..73161109-chr4:101040564..101041084,2	HCT-116	colon:
22	chr2:70056434..70057117-chr4:101138315..101138816,2	HCT-116	colon:
23	chr4:101084718..101086912-chr4:101087632..101089284,2	K562	blood:
24	chr4:101072313..101075181-chr4:101094898..101096788,2	MCF-7	breast:
25	chr4:101160745..101163177-chr4:101167667..101169870,2	MCF-7	breast:
26	chr4:101118797..101120878-chr4:101120967..101123129,2	MCF-7	breast:
27	chr4:101112745..101114731-chr4:101119357..101121348,2	MCF-7	breast:
28	chr4:101038045..101039843-chr4:101042215..101043823,2	MCF-7	breast:
29	chr4:101061927..101063715-chr4:101066155..101068480,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DAPP1-3	chr4:101111190-101111231	ENSG00000249710.1
2	lnc-DAPP1-3	chr4:101136437-101136662	ENSG00000249710.1
3	lnc-DAPP1-5	chr4:101148021-101148411	l_2695_chr4:101148020-101174234_testes
4	lnc-DAPP1-3	chr4:101114123-101114206	ENSG00000249710.1
5	lnc-DDIT4L-1	chr4:101037987-101038339	expReg_chr4_4712_-
6	lnc-DAPP1-4	chr4:101090659-101092643	l_2694_NR_002799
7	lnc-DAPP1-3	chr4:101114903-101114999	ENSG00000249710.1
8	lnc-DDIT4L-2	chr4:101036953-101037201	expReg_chr4_4708_-
9	lnc-DAPP1-2	chr4:101116222-101116256	ENSG00000245322.2
10	lnc-DAPP1-5	chr4:101177708-101178141	l_2695_chr4:101148020-101174234_testes
11	lnc-DAPP1-5	chr4:101174114-101174234	l_2695_chr4:101148020-101174234_testes
12	lnc-DAPP1-3	chr4:101115080-101115156	ENSG00000249710.1
13	lnc-DAPP1-5	chr4:101165462-101165507	l_2695_chr4:101148020-101174234_testes

No data

Variant related genes	Relation type
ENSG00000222196	TF binding region
DDIT4L	TF binding region
ENSG00000249710	TF binding region
ENSG00000222196	CpG island
DDIT4L	CpG island
ENSG00000249710	CpG island
ENSG00000245322	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000087338	chromatin interactions
ENSG00000164032	chromatin interactions

Extended variants
information (count: 4252 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:4252 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545388435	chr4:101023775-101023776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs181823558	chr4:101023785-101023786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575736655	chr4:101023874-101023875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542753062	chr4:101023877-101023878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs55728175	chr4:101023900-101023901	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs528635280	chr4:101023930-101023931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540822956	chr4:101023951-101023952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs565209472	chr4:101023989-101023990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532681530	chr4:101024009-101024010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550894177	chr4:101024027-101024028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs77210459	chr4:101024056-101024057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562118979	chr4:101024112-101024113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529685823	chr4:101024144-101024145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs55915722	chr4:101024148-101024149	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs566568001	chr4:101024168-101024169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185407122	chr4:101024173-101024174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs562496502	chr4:101024266-101024267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189968691	chr4:101024304-101024305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs180813610	chr4:101024328-101024329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570696617	chr4:101024333-101024334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs75727994	chr4:101024362-101024363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556544897	chr4:101024370-101024371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146135012	chr4:101024393-101024394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534879840	chr4:101024511-101024512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536659456	chr4:101024519-101024520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554718418	chr4:101024547-101024548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186726265	chr4:101024567-101024568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540437347	chr4:101024619-101024620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574878896	chr4:101024648-101024649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs191172204	chr4:101024762-101024763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183697351	chr4:101024764-101024765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs148742374	chr4:101024795-101024796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs78691248	chr4:101024883-101024884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187241578	chr4:101024912-101024913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs562882019	chr4:101024979-101024980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs529614092	chr4:101025008-101025009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190947528	chr4:101025044-101025045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs557339291	chr4:101025065-101025066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs141468852	chr4:101025110-101025111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs200613677	chr4:101025179-101025180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs59270722	chr4:101025216-101025217	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs561687298	chr4:101025240-101025241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs150812991	chr4:101025269-101025270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs56120109	chr4:101025298-101025299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183139160	chr4:101025335-101025336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs200399331	chr4:101025341-101025342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs139261654	chr4:101025352-101025353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs201953459	chr4:101025403-101025404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145281139	chr4:101025411-101025412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs113554240	chr4:101025495-101025496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
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
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
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	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
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Acute myeloid leukemia	18000384	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:957 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:101007800-101028000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:101021600-101024000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr4:101022600-101027600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr4:101022600-101027800	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr4:101022600-101027800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr4:101022600-101027800	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr4:101022600-101027800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr4:101022600-101027800	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr4:101022600-101028000	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr4:101022600-101028000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr4:101022600-101028000	Weak transcription	Fetal Thymus	thymus
12	chr4:101022600-101030200	Weak transcription	Fetal Intestine Large	intestine
13	chr4:101022800-101027800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr4:101022800-101028000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr4:101022800-101028000	Weak transcription	GM12878-XiMat	blood
16	chr4:101023000-101027600	Weak transcription	Dnd41	blood
17	chr4:101023000-101027800	Weak transcription	Primary hematopoietic stem cells	blood
18	chr4:101023200-101023800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr4:101023400-101027400	Weak transcription	Primary B cells from peripheral blood	blood
20	chr4:101023800-101024000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr4:101024000-101027600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr4:101024600-101025600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr4:101026600-101027600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr4:101027400-101030000	Enhancers	Primary B cells from peripheral blood	blood
25	chr4:101027600-101028000	Enhancers	Dnd41	blood
26	chr4:101027600-101028600	Enhancers	Primary T cells from cord blood	blood
27	chr4:101027600-101028600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr4:101027600-101028800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr4:101027600-101030200	Enhancers	Primary B cells from cord blood	blood
30	chr4:101027800-101028200	Enhancers	Primary hematopoietic stem cells	blood
31	chr4:101027800-101028400	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr4:101027800-101028400	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr4:101027800-101028400	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr4:101027800-101028600	Enhancers	Primary T cells fromperipheralblood	blood
35	chr4:101027800-101028600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr4:101027800-101028600	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr4:101027800-101028600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr4:101027800-101028800	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr4:101028000-101028400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr4:101028000-101028400	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr4:101028000-101028400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr4:101028000-101028400	Flanking Active TSS	Dnd41	blood
43	chr4:101028000-101028400	Enhancers	GM12878-XiMat	blood
44	chr4:101028000-101028600	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr4:101028000-101028600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
46	chr4:101028000-101028600	Enhancers	Fetal Thymus	thymus
47	chr4:101028000-101028800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr4:101028200-101028600	Enhancers	Thymus	Thymus
49	chr4:101028400-101029200	Enhancers	Dnd41	blood
50	chr4:101028600-101030000	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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