Variant report

Variant	nsv537445
Chromosome Location	chr4:187921350-188155687
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:598)
CpG islands
(count:2444)
Chromatin interactive
region (count:26)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:598 , 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	BACH1	chr4:188068202-188068264	K562	blood:	n/a	n/a
2	BACH1	chr4:188008250-188008420	K562	blood:	n/a	n/a
3	BACH1	chr4:188129825-188130039	K562	blood:	n/a	n/a
4	BACH1	chr4:187938365-187938620	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:188009756-188009863	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:188129816-188130163	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr4:188078752-188079118	K562	blood:	n/a	n/a
8	CEBPB	chr4:187949036-187949236	HepG2	liver:	n/a	n/a
9	CEBPB	chr4:187967672-187967719	HepG2	liver:	n/a	n/a
10	CEBPB	chr4:187951805-187952024	A549	lung:	n/a	chr4:187951939-187951950
11	CEBPB	chr4:188026962-188027291	HepG2	liver:	n/a	chr4:188027103-188027114
12	CEBPB	chr4:188058554-188058744	IMR90	lung:	n/a	chr4:188058583-188058592
13	CEBPB	chr4:188023857-188024454	HepG2	liver:	n/a	chr4:188023987-188023998
14	CEBPB	chr4:188056837-188057059	A549	lung:	n/a	n/a
15	CEBPB	chr4:188011726-188011964	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:188153348-188153608	IMR90	lung:	n/a	n/a
17	CEBPB	chr4:188026969-188027265	IMR90	lung:	n/a	chr4:188027103-188027114
18	CEBPB	chr4:188020810-188020969	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:188026988-188027296	A549	lung:	n/a	chr4:188027103-188027114
20	CEBPB	chr4:188100977-188101137	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr4:188148708-188148996	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:187923457-187923475	K562	blood:	n/a	n/a
23	CEBPB	chr4:188151952-188152262	HepG2	liver:	n/a	chr4:188152090-188152101 chr4:188152090-188152103 chr4:188152092-188152103 chr4:188152230-188152243 chr4:188152092-188152101
24	CEBPB	chr4:187923364-187923655	A549	lung:	n/a	chr4:187923465-187923476
25	CEBPB	chr4:187951890-187952101	K562	blood:	n/a	chr4:187951939-187951950
26	CEBPB	chr4:187923294-187923654	IMR90	lung:	n/a	chr4:187923465-187923476
27	CEBPB	chr4:187948947-187949293	IMR90	lung:	n/a	n/a
28	CEBPB	chr4:188153426-188153626	A549	lung:	n/a	n/a
29	CEBPB	chr4:188130901-188131533	IMR90	lung:	n/a	n/a
30	CEBPB	chr4:188146558-188146694	K562	blood:	n/a	n/a
31	CEBPB	chr4:187950987-187951100	H1-hESC	embryonic stem cell:	n/a	chr4:187951044-187951061
32	CEBPB	chr4:188026960-188027208	K562	blood:	n/a	chr4:188027103-188027114
33	CEBPB	chr4:187923410-187923599	H1-hESC	embryonic stem cell:	n/a	chr4:187923465-187923476
34	CEBPB	chr4:187996652-187996971	IMR90	lung:	n/a	n/a
35	CEBPB	chr4:188148689-188148861	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr4:187949058-187949232	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr4:187951803-187952065	IMR90	lung:	n/a	chr4:187951939-187951950
38	CEBPB	chr4:188152011-188152233	IMR90	lung:	n/a	chr4:188152090-188152101 chr4:188152090-188152103 chr4:188152092-188152103 chr4:188152092-188152101
39	CEBPB	chr4:188152008-188152230	K562	blood:	n/a	chr4:188152090-188152101 chr4:188152090-188152103 chr4:188152092-188152103 chr4:188152092-188152101
40	CEBPB	chr4:188018970-188019044	HepG2	liver:	n/a	chr4:188018994-188019005
41	CEBPB	chr4:187930239-187930492	HepG2	liver:	n/a	chr4:187930359-187930370
42	CEBPB	chr4:188063266-188063464	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr4:188146498-188146805	IMR90	lung:	n/a	n/a
44	CEBPB	chr4:187923422-187923659	HepG2	liver:	n/a	chr4:187923465-187923476
45	CEBPB	chr4:187951852-187952028	HepG2	liver:	n/a	chr4:187951939-187951950
46	CEBPB	chr4:188153356-188153615	HepG2	liver:	n/a	n/a
47	CEBPB	chr4:187927557-187927886	IMR90	lung:	n/a	chr4:187927733-187927746
48	CHD2	chr4:188073936-188073939	GM12878	blood:	n/a	n/a
49	CHD2	chr4:188138090-188138332	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr4:188154260-188154452	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2444 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187984718-187984768	ovcar-3	ovarian:	n/a
2	chr4:187985253-187985303	BE2_C	brain:	n/a
3	chr4:187984633-187984683	GM12892	blood:	n/a
4	chr4:188078670-188078720	T-47D	breast:	n/a
5	chr4:187984718-187984768	ovcar-3	ovarian:	n/a
6	chr4:187985253-187985303	BE2_C	brain:	n/a
7	chr4:187984633-187984683	GM12892	blood:	n/a
8	chr4:188078670-188078720	T-47D	breast:	n/a
9	chr4:188046520-188046570	HPAEpiC	pulmonary alveolar:	n/a
10	chr4:188047315-188047365	GM12878	blood:	n/a
11	chr4:188045495-188045545	GM12891	blood:	n/a
12	chr4:187998952-187999002	HAEpiC	amniotic membrane:	n/a
13	chr4:187984412-187984462	GM19239	blood:	n/a
14	chr4:187984506-187984556	HUVEC	blood vessel:	n/a
15	chr4:188097683-188097733	ECC-1	luminal epithelium:	n/a
16	chr4:188149410-188149460	NHDF-neo	bronchial:	n/a
17	chr4:188047315-188047365	HMEC	breast:	n/a
18	chr4:187984633-187984683	BE2_C	brain:	n/a
19	chr4:187984633-187984683	LNCaP	prostate:	n/a
20	chr4:187988456-187988506	ovcar-3	ovarian:	n/a
21	chr4:187981566-187981616	HRE	kidney:	n/a
22	chr4:188104526-188104576	PANC-1	pancreas:	n/a
23	chr4:188149410-188149460	SAEC	small airway:	n/a
24	chr4:188097967-188098017	ECC-1	luminal epithelium:	n/a
25	chr4:188101115-188101165	T-47D	breast:	n/a
26	chr4:188131622-188131672	AG04450	lung:	fetal
27	chr4:188034964-188035014	ovcar-3	ovarian:	n/a
28	chr4:187998952-187999002	AG09319	gingival:	n/a
29	chr4:188078789-188078839	AG10803	skin:	n/a
30	chr4:187992866-187992916	GM12892	blood:	n/a
31	chr4:187927166-187927216	HIPEpiC	eye:	n/a
32	chr4:188045368-188045418	ECC-1	luminal epithelium:	n/a
33	chr4:188140291-188140341	BE2_C	brain:	n/a
34	chr4:188045368-188045418	T-47D	breast:	n/a
35	chr4:187984506-187984556	CMK	blood:	n/a
36	chr4:188097774-188097824	HCF	heart:	n/a
37	chr4:187984506-187984556	SKMC	muscle:	n/a
38	chr4:187981566-187981616	HPAEpiC	pulmonary alveolar:	n/a
39	chr4:188139877-188139927	HRE	kidney:	n/a
40	chr4:188097967-188098017	GM06990	blood:	n/a
41	chr4:188139877-188139927	Hela-S3	cervix:	n/a
42	chr4:187959224-187959274	IMR90	lung:	fetal
43	chr4:187959224-187959274	HCM	heart:	n/a
44	chr4:187985253-187985303	ECC-1	luminal epithelium:	n/a
45	chr4:187982852-187982902	PrEC	prostate:	n/a
46	chr4:188078789-188078839	U87	brain:	n/a
47	chr4:187984718-187984768	GM12892	blood:	n/a
48	chr4:188101115-188101165	AG09319	gingival:	n/a
49	chr4:187982852-187982902	A549	lung:	n/a
50	chr4:187987293-187987343	U87	brain:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:188127890..188131303-chr4:188136198..188140053,3	K562	blood:
2	chr4:188021348..188024236-chr4:188025948..188027821,2	K562	blood:
3	chr4:188100330..188101980-chr4:188105667..188107214,2	K562	blood:
4	chr4:187939165..187941494-chr4:187941726..187943652,2	K562	blood:
5	chr4:187987739..187989795-chr4:187999500..188002033,2	MCF-7	breast:
6	chr4:188127890..188130779-chr4:188137377..188140053,2	K562	blood:
7	chr4:188066477..188068496-chr4:188071988..188074466,2	K562	blood:
8	chr4:188127890..188130779-chr4:188137377..188140053,2	K562	blood:
9	chr4:188083083..188085833-chr4:188087348..188090241,2	MCF-7	breast:
10	chr4:188127890..188131303-chr4:188136198..188140053,3	K562	blood:
11	chr4:188056141..188059135-chr4:188062494..188064650,2	K562	blood:
12	chr4:188082742..188084382-chr4:188084801..188086705,2	K562	blood:
13	chr4:188021348..188024236-chr4:188025948..188027821,2	K562	blood:
14	chr4:188016055..188017615-chr4:188020801..188022830,2	MCF-7	breast:
15	chr4:187645367..187647070-chr4:188073656..188075512,2	K562	blood:
16	chr4:188066477..188068496-chr4:188071988..188074466,2	K562	blood:
17	chr4:187987739..187989795-chr4:187999500..188002033,2	MCF-7	breast:
18	chr4:188083083..188085833-chr4:188087348..188090241,2	MCF-7	breast:
19	chr4:188082742..188084382-chr4:188084801..188086705,2	K562	blood:
20	chr4:187647654..187649416-chr4:188063013..188065311,2	MCF-7	breast:
21	chr4:188077660..188079789-chr4:188085671..188087696,2	K562	blood:
22	chr4:188136808..188139497-chr4:188168223..188169981,2	K562	blood:
23	chr4:188100330..188101980-chr4:188105667..188107214,2	K562	blood:
24	chr4:188016055..188017615-chr4:188020801..188022830,2	MCF-7	breast:
25	chr4:188056141..188059135-chr4:188062494..188064650,2	K562	blood:
26	chr4:188077660..188079789-chr4:188085671..188087696,2	K562	blood:

(count:27 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP42-7	chr4:188123187-188123296	XLOC_003825
2	lnc-ZFP42-7	chr4:188129941-188130201	XLOC_003825
3	lnc-ZFP42-7	chr4:188133984-188134139	NONHSAT099688
4	lnc-ZFP42-7	chr4:188133530-188134139	XLOC_003825
5	lnc-FAT1-2	chr4:188119427-188119745	XLOC_004216
6	lnc-ZFP42-7	chr4:188130341-188130500	XLOC_003825
7	lnc-ZFP42-7	chr4:188123140-188123296	XLOC_003825
8	lnc-FAT1-1	chr4:187943080-187943127	XLOC_004215
9	lnc-ZFP42-7	chr4:188133499-188133581	NONHSAT099688
10	lnc-ZFP42-7	chr4:188134283-188134810	XLOC_003825
11	lnc-ZFP42-7	chr4:188123178-188123296	XLOC_003825
12	lnc-ZFP42-7	chr4:188123217-188123296	XLOC_003825
13	lnc-ZFP42-7	chr4:188133530-188134139	XLOC_003825
14	lnc-F11-3	chr4:187981371-187981417	NONHSAT099680
15	lnc-F11-3	chr4:187980278-187980644	NONHSAT099680
16	lnc-ZFP42-7	chr4:188134283-188135298	XLOC_003825
17	lnc-F11-4	chr4:187981829-187982084	XLOC_003824
18	lnc-ZFP42-7	chr4:188134283-188134753	NONHSAT099688
19	lnc-F11-4	chr4:187981253-187981417	XLOC_003824
20	lnc-ZFP42-7	chr4:188124136-188124768	XLOC_003825
21	lnc-ZFP42-7	chr4:188129941-188130201	XLOC_003825
22	lnc-F11-3	chr4:187980348-187980402	XLOC_003823
23	lnc-FAT1-2	chr4:188122781-188123084	XLOC_004216
24	lnc-ZFP42-7	chr4:188123145-188123296	XLOC_003825
25	lnc-F11-3	chr4:187981829-187982019	NONHSAT099680
26	lnc-ZFP42-7	chr4:188133530-188133630	XLOC_003825
27	lnc-F11-3	chr4:187980530-187980856	XLOC_003823

No data

Variant related genes	Relation type
ENSG00000249747	TF binding region
ENSG00000250971	TF binding region
ENSG00000249742	TF binding region
ENSG00000249747	CpG island
ENSG00000250971	CpG island
ENSG00000249742	CpG island
ENSG00000249742	chromatin interactions
ENSG00000083857	chromatin interactions
UBXN1	miRNA target sites
CCND1	miRNA target sites
LMNB1	miRNA target sites
ZFYVE26	miRNA target sites
ANKRD57	miRNA target sites
OSBPL1A	miRNA target sites

Extended variants
information (count: 8087 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:8087 , 50 per page) page: 1 2 3 4 5 6 7 ... 162

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547368631	chr4:187921355-187921356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs188797451	chr4:187921370-187921371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181171334	chr4:187921410-187921411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547687747	chr4:187921411-187921412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557735921	chr4:187921423-187921424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573043615	chr4:187921436-187921437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs570199696	chr4:187921471-187921472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145911773	chr4:187921478-187921479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555819371	chr4:187921486-187921487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs7660345	chr4:187921499-187921500	Weak transcription	n/a	n/a	Overlapped CNVs	disease
11	rs561975238	chr4:187921531-187921532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573892255	chr4:187921555-187921556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs9884149	chr4:187921568-187921569	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs187037566	chr4:187921604-187921605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138470606	chr4:187921607-187921608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs75657502	chr4:187921627-187921628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191425764	chr4:187921659-187921660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs138074303	chr4:187921664-187921665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs377339496	chr4:187921666-187921667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374377813	chr4:187921675-187921676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113808548	chr4:187921796-187921797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs71595129	chr4:187921815-187921816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs76979856	chr4:187921833-187921834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs397880129	chr4:187921834-187921835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576196633	chr4:187921840-187921841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542783121	chr4:187921843-187921844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs181849369	chr4:187921847-187921848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528381858	chr4:187921880-187921881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187377637	chr4:187921894-187921895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs544589229	chr4:187921898-187921899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564151589	chr4:187921902-187921903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371624566	chr4:187921910-187921911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376888590	chr4:187921916-187921917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4861734	chr4:187921918-187921919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533236986	chr4:187921936-187921937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529498587	chr4:187921942-187921943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558174942	chr4:187921952-187921953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12640228	chr4:187921955-187921956	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs374741901	chr4:187921961-187921962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574580467	chr4:187921977-187921978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565694510	chr4:187922000-187922001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541853109	chr4:187922001-187922002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560216758	chr4:187922004-187922005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558451163	chr4:187922005-187922006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571303496	chr4:187922016-187922017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377587333	chr4:187922018-187922019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148287780	chr4:187922037-187922038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369815953	chr4:187922039-187922040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527847897	chr4:187922084-187922085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556804716	chr4:187922092-187922093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
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
Acute lymphoblastic leukemia	20067559	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
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Oral cancer	21386901	CNVD
Pancreatic cancer	17952125	CNVD
Oral cancer	17325662	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:654 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187911800-187942600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:187920800-187921400	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr4:187924000-187925400	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr4:187925400-187927000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr4:187926000-187928200	Enhancers	Fetal Kidney	kidney
6	chr4:187926400-187927800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr4:187926400-187928200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr4:187927000-187927400	Enhancers	HMEC	breast
9	chr4:187927000-187927800	Enhancers	Fetal Stomach	stomach
10	chr4:187927000-187928200	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr4:187927000-187928200	Enhancers	Fetal Lung	lung
12	chr4:187927000-187928400	Enhancers	NHEK	skin
13	chr4:187927000-187928800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr4:187927200-187927800	Enhancers	Rectal Smooth Muscle	rectum
15	chr4:187927200-187928000	Enhancers	Osteobl	bone
16	chr4:187927200-187928200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr4:187927400-187927800	Flanking Active TSS	HMEC	breast
18	chr4:187927600-187928200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr4:187927800-187928400	Enhancers	HMEC	breast
20	chr4:187928000-187931200	Weak transcription	Osteobl	bone
21	chr4:187928200-187931000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr4:187931000-187931800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr4:187931200-187932000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr4:187931200-187932000	Enhancers	Osteobl	bone
25	chr4:187938000-187938600	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr4:187938200-187938600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr4:187938200-187938600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr4:187938200-187938600	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr4:187938200-187938800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr4:187938200-187939000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr4:187938400-187938600	Enhancers	H1 Cell Line	embryonic stem cell
32	chr4:187938400-187938600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr4:187938400-187938600	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr4:187938600-187939000	Enhancers	Fetal Kidney	kidney
35	chr4:187938600-187941000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr4:187938600-187941000	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr4:187938800-187940800	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr4:187939000-187941000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr4:187939000-187942600	Weak transcription	Fetal Kidney	kidney
40	chr4:187940800-187941200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr4:187940800-187941600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr4:187940800-187941600	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr4:187941000-187941400	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr4:187941000-187941400	Enhancers	H9 Cell Line	embryonic stem cell
45	chr4:187941000-187941400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr4:187941000-187941400	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr4:187941000-187941400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
48	chr4:187941000-187941600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr4:187941000-187941600	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr4:187941000-187941600	Enhancers	HUES6 Cell Line	embryonic stem cell

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