Variant report

Variant	nsv537447
Chromosome Location	chr4:187979722-188159706
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:505)
CpG islands
(count:2503)
Chromatin interactive
region (count:26)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:505 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:188129825-188130039	K562	blood:	n/a	n/a
2	BACH1	chr4:188129816-188130163	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:188008250-188008420	K562	blood:	n/a	n/a
4	BACH1	chr4:188009756-188009863	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:188068202-188068264	K562	blood:	n/a	n/a
6	BHLHE40	chr4:188078752-188079118	K562	blood:	n/a	n/a
7	CEBPB	chr4:188152008-188152230	K562	blood:	n/a	chr4:188152090-188152101 chr4:188152090-188152103 chr4:188152092-188152103 chr4:188152092-188152101
8	CEBPB	chr4:188056837-188057059	A549	lung:	n/a	n/a
9	CEBPB	chr4:188158488-188158792	HepG2	liver:	n/a	n/a
10	CEBPB	chr4:188158514-188158784	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr4:188153356-188153615	HepG2	liver:	n/a	n/a
12	CEBPB	chr4:188058554-188058744	IMR90	lung:	n/a	chr4:188058583-188058592
13	CEBPB	chr4:188020810-188020969	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:188026962-188027291	HepG2	liver:	n/a	chr4:188027103-188027114
15	CEBPB	chr4:188158501-188158795	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:188130901-188131533	IMR90	lung:	n/a	n/a
17	CEBPB	chr4:187996652-187996971	IMR90	lung:	n/a	n/a
18	CEBPB	chr4:188158510-188158761	A549	lung:	n/a	n/a
19	CEBPB	chr4:188146558-188146694	K562	blood:	n/a	n/a
20	CEBPB	chr4:188011726-188011964	IMR90	lung:	n/a	n/a
21	CEBPB	chr4:188026960-188027208	K562	blood:	n/a	chr4:188027103-188027114
22	CEBPB	chr4:188026969-188027265	IMR90	lung:	n/a	chr4:188027103-188027114
23	CEBPB	chr4:188063266-188063464	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr4:188152011-188152233	IMR90	lung:	n/a	chr4:188152090-188152101 chr4:188152090-188152103 chr4:188152092-188152103 chr4:188152092-188152101
25	CEBPB	chr4:188151952-188152262	HepG2	liver:	n/a	chr4:188152090-188152101 chr4:188152090-188152103 chr4:188152092-188152103 chr4:188152230-188152243 chr4:188152092-188152101
26	CEBPB	chr4:188148708-188148996	IMR90	lung:	n/a	n/a
27	CEBPB	chr4:188157115-188157171	HepG2	liver:	n/a	chr4:188157139-188157150
28	CEBPB	chr4:188146498-188146805	IMR90	lung:	n/a	n/a
29	CEBPB	chr4:188148689-188148861	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr4:188026988-188027296	A549	lung:	n/a	chr4:188027103-188027114
31	CEBPB	chr4:188153426-188153626	A549	lung:	n/a	n/a
32	CEBPB	chr4:188018970-188019044	HepG2	liver:	n/a	chr4:188018994-188019005
33	CEBPB	chr4:188153348-188153608	IMR90	lung:	n/a	n/a
34	CEBPB	chr4:188100977-188101137	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr4:188023857-188024454	HepG2	liver:	n/a	chr4:188023987-188023998
36	CHD2	chr4:188154260-188154452	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr4:188154257-188154438	K562	blood:	n/a	n/a
38	CHD2	chr4:188073936-188073939	GM12878	blood:	n/a	n/a
39	CHD2	chr4:188138083-188138363	K562	blood:	n/a	n/a
40	CHD2	chr4:188138090-188138332	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr4:188096420-188096570	Caco-2	colon:	n/a	chr4:188096537-188096546
42	CTCF	chr4:187985302-187985470	T-47D	breast:	n/a	chr4:187985404-187985417
43	CTCF	chr4:188096440-188096590	HPAF	blood vessel:	n/a	chr4:188096537-188096546
44	CTCF	chr4:188096400-188096550	BE2_C	brain:	n/a	chr4:188096537-188096546
45	CTCF	chr4:188096500-188096650	HEEpiC	esophagus:	n/a	chr4:188096537-188096546
46	CTCF	chr4:188096541-188096602	Fibrobl	skin:	n/a	n/a
47	CTCF	chr4:188096460-188096610	HAc	cerebellar:	n/a	chr4:188096537-188096546
48	CTCF	chr4:188096480-188096630	HFF	foreskin:	n/a	chr4:188096537-188096546
49	CTCF	chr4:188096540-188096690	HMEC	breast:	n/a	n/a
50	CTCF	chr4:188015478-188015535	LNCaP	prostate:	n/a	n/a

(count:2503 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188046520-188046570	HEK293	kidney:	embryo
2	chr4:188034964-188035014	HIPEpiC	eye:	n/a
3	chr4:188046520-188046570	HEK293	kidney:	embryo
4	chr4:188034964-188035014	HIPEpiC	eye:	n/a
5	chr4:188046444-188046494	SK-N-SH	brain:	n/a
6	chr4:188009477-188009527	PrEC	prostate:	n/a
7	chr4:188034964-188035014	PrEC	prostate:	n/a
8	chr4:187985452-187985502	BJ	skin:	n/a
9	chr4:187998952-187999002	HCPEpiC	choroid plexus:	n/a
10	chr4:188097774-188097824	HMEC	breast:	n/a
11	chr4:188140291-188140341	SK-N-SH_RA	brain:	n/a
12	chr4:188046350-188046400	AG04449	skin:	fetal
13	chr4:188149410-188149460	Hela-S3	cervix:	n/a
14	chr4:187984958-187985008	Hela-S3	cervix:	n/a
15	chr4:187987293-187987343	AG10803	skin:	n/a
16	chr4:188156703-188156753	HEK293	kidney:	embryo
17	chr4:187992866-187992916	PFSK-1	brain:	n/a
18	chr4:188149410-188149460	SK-N-SH	brain:	n/a
19	chr4:187985472-187985522	SKMC	muscle:	n/a
20	chr4:187985377-187985427	AoSMC	blood vessel:	n/a
21	chr4:188046520-188046570	AG04449	skin:	fetal
22	chr4:188047315-188047365	ECC-1	luminal epithelium:	n/a
23	chr4:188046350-188046400	U87	brain:	n/a
24	chr4:188009477-188009527	HL-60	blood:	n/a
25	chr4:187985472-187985522	MCF-7	breast:	n/a
26	chr4:187998952-187999002	HCM	heart:	n/a
27	chr4:187985452-187985502	GM12891	blood:	n/a
28	chr4:187984718-187984768	AG10803	skin:	n/a
29	chr4:188034964-188035014	ProgFib	skin:	n/a
30	chr4:188156675-188156725	SK-N-SH	brain:	n/a
31	chr4:188097683-188097733	HMEC	breast:	n/a
32	chr4:188156703-188156753	HAEpiC	amniotic membrane:	n/a
33	chr4:188046350-188046400	HMEC	breast:	n/a
34	chr4:188140291-188140341	GM12892	blood:	n/a
35	chr4:187985253-187985303	GM19239	blood:	n/a
36	chr4:187985472-187985522	AG09309	skin:	n/a
37	chr4:188140291-188140341	HUVEC	blood vessel:	n/a
38	chr4:187988456-187988506	H1-hESC	embryonic stem cell:	embryo
39	chr4:188045689-188045739	Hela-S3	cervix:	n/a
40	chr4:187984633-187984683	NH-A	brain:	n/a
41	chr4:188046444-188046494	HepG2	liver:	n/a
42	chr4:188156675-188156725	HMEC	breast:	n/a
43	chr4:188156675-188156725	SAEC	small airway:	n/a
44	chr4:187987206-187987256	BE2_C	brain:	n/a
45	chr4:188156675-188156725	AG04450	lung:	fetal
46	chr4:188047315-188047365	HPAEpiC	pulmonary alveolar:	n/a
47	chr4:187998952-187999002	CMK	blood:	n/a
48	chr4:188046444-188046494	HUVEC	blood vessel:	n/a
49	chr4:188101115-188101165	GM06990	blood:	n/a
50	chr4:187985253-187985303	U87	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:188066477..188068496-chr4:188071988..188074466,2	K562	blood:
2	chr4:187646533..187648100-chr4:188156626..188159035,2	MCF-7	breast:
3	chr4:188056141..188059135-chr4:188062494..188064650,2	K562	blood:
4	chr4:188082742..188084382-chr4:188084801..188086705,2	K562	blood:
5	chr4:187987739..187989795-chr4:187999500..188002033,2	MCF-7	breast:
6	chr4:188021348..188024236-chr4:188025948..188027821,2	K562	blood:
7	chr4:188083083..188085833-chr4:188087348..188090241,2	MCF-7	breast:
8	chr4:188077660..188079789-chr4:188085671..188087696,2	K562	blood:
9	chr4:188016055..188017615-chr4:188020801..188022830,2	MCF-7	breast:
10	chr4:188056141..188059135-chr4:188062494..188064650,2	K562	blood:
11	chr4:188082742..188084382-chr4:188084801..188086705,2	K562	blood:
12	chr4:187987739..187989795-chr4:187999500..188002033,2	MCF-7	breast:
13	chr4:187645367..187647070-chr4:188073656..188075512,2	K562	blood:
14	chr4:188083083..188085833-chr4:188087348..188090241,2	MCF-7	breast:
15	chr4:188066477..188068496-chr4:188071988..188074466,2	K562	blood:
16	chr4:188136808..188139497-chr4:188168223..188169981,2	K562	blood:
17	chr4:188016055..188017615-chr4:188020801..188022830,2	MCF-7	breast:
18	chr4:188127890..188131303-chr4:188136198..188140053,3	K562	blood:
19	chr4:188127890..188131303-chr4:188136198..188140053,3	K562	blood:
20	chr4:188127890..188130779-chr4:188137377..188140053,2	K562	blood:
21	chr4:187647654..187649416-chr4:188063013..188065311,2	MCF-7	breast:
22	chr4:188021348..188024236-chr4:188025948..188027821,2	K562	blood:
23	chr4:188077660..188079789-chr4:188085671..188087696,2	K562	blood:
24	chr4:188100330..188101980-chr4:188105667..188107214,2	K562	blood:
25	chr4:188127890..188130779-chr4:188137377..188140053,2	K562	blood:
26	chr4:188100330..188101980-chr4:188105667..188107214,2	K562	blood:

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

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

No data

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

Extended variants
information (count: 6670 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:6670 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116422742	chr4:187980301-187980302	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs139865615	chr4:187980314-187980315	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs534704359	chr4:187980332-187980333	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs557523513	chr4:187980374-187980375	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs186730239	chr4:187980403-187980404	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs528348819	chr4:187980416-187980417	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs10019973	chr4:187980423-187980424	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs190188833	chr4:187980476-187980477	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs78511104	chr4:187980488-187980489	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs143225614	chr4:187980500-187980501	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs368179381	chr4:187980505-187980506	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs562055142	chr4:187980541-187980542	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs572309855	chr4:187980606-187980607	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs150670580	chr4:187980656-187980657	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs564395297	chr4:187980686-187980687	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs3923586	chr4:187980711-187980712	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs549945954	chr4:187980721-187980722	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs117705658	chr4:187980791-187980792	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs139851573	chr4:187980817-187980818	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs374581074	chr4:187980834-187980835	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs77029919	chr4:187980864-187980865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs4241838	chr4:187980880-187980881	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs181695534	chr4:187980948-187980949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185993811	chr4:187980970-187980971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115332257	chr4:187981011-187981012	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571241439	chr4:187981012-187981013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570909092	chr4:187981031-187981032	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557190008	chr4:187981032-187981033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567607810	chr4:187981036-187981037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377288155	chr4:187981053-187981054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553256903	chr4:187981056-187981057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201177193	chr4:187981068-187981069	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs5865028	chr4:187981092-187981093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs33917704	chr4:187981093-187981094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs397976460	chr4:187981100-187981101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191106706	chr4:187981107-187981108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541032041	chr4:187981237-187981238	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs4862758	chr4:187981262-187981263	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs200223862	chr4:187981267-187981268	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs149346394	chr4:187981272-187981273	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs149858936	chr4:187981293-187981294	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs115464757	chr4:187981327-187981328	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs183859561	chr4:187981329-187981330	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs529404496	chr4:187981331-187981332	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs542937960	chr4:187981337-187981338	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs559763585	chr4:187981394-187981395	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs188753304	chr4:187981417-187981418	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs191179679	chr4:187981434-187981435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546880258	chr4:187981441-187981442	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs117997406	chr4:187981560-187981561	Enhancers 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:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187980400-187980600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:187980400-187980600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:187980400-187982000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:187981000-187981800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr4:187982000-187991800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr4:187982000-187995200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr4:187984600-187985600	Bivalent Enhancer	Placenta	Placenta
8	chr4:187984800-187985800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:187985000-187985200	Enhancers	H1 Cell Line	embryonic stem cell
10	chr4:187985200-187986600	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr4:187985800-187986000	Enhancers	Rectal Smooth Muscle	rectum
12	chr4:187985800-187990600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr4:187986000-187987000	Weak transcription	Rectal Smooth Muscle	rectum
14	chr4:187986200-187986400	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr4:187986200-187986600	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr4:187986200-187986800	Enhancers	Brain Germinal Matrix	brain
17	chr4:187986200-187987000	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr4:187986200-187987200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr4:187986200-187987600	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr4:187986400-187987000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr4:187986600-187986800	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr4:187986600-187987400	Enhancers	H1 Cell Line	embryonic stem cell
23	chr4:187986600-187991800	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr4:187987000-187987200	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr4:187987000-187987200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
26	chr4:187987000-187987400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:187987000-187987400	Enhancers	Rectal Smooth Muscle	rectum
28	chr4:187987000-187987400	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr4:187987000-187993000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr4:187987200-187987400	Enhancers	Fetal Muscle Trunk	muscle
31	chr4:187987200-187987800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr4:187987200-187990600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr4:187987400-187990600	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr4:187987400-187990600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr4:187987400-187990600	Weak transcription	Fetal Muscle Trunk	muscle
36	chr4:187987600-187991800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr4:187990200-187990600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr4:187990400-187991200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr4:187990600-187991000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr4:187990600-187991000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr4:187990600-187991000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr4:187990600-187991000	Active TSS	Adipose Nuclei	Adipose
43	chr4:187990600-187991000	Enhancers	Fetal Muscle Trunk	muscle
44	chr4:187990600-187991000	Enhancers	Fetal Muscle Leg	muscle
45	chr4:187990600-187991000	Enhancers	NHDF-Ad	bronchial
46	chr4:187990600-187991000	Enhancers	Osteobl	bone
47	chr4:187990600-187991200	Enhancers	H1 Cell Line	embryonic stem cell
48	chr4:187990600-187991200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr4:187990600-187991200	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr4:187990600-187992000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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