Variant report

Variant	nsv522386
Chromosome Location	chr4:120009147-120115379
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:736)
CpG islands
(count:429)
Chromatin interactive
region (count:36)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:736 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:120069300-120069382	K562	blood:	n/a	n/a
2	ARID3A	chr4:120014649-120014660	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:120034563-120034635	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:120014245-120014446	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:120061121-120061568	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:120020305-120020333	K562	blood:	n/a	n/a
7	ATF1	chr4:120024459-120024838	K562	blood:	n/a	n/a
8	ATF3	chr4:120024370-120024929	A549	lung:	n/a	n/a
9	ATF3	chr4:120024490-120024806	K562	blood:	n/a	n/a
10	ATF3	chr4:120024332-120025018	HCT-116	colon:	n/a	n/a
11	ATF3	chr4:120024324-120024955	HCT-116	colon:	n/a	n/a
12	ATF3	chr4:120034410-120034782	HCT-116	colon:	n/a	n/a
13	ATF3	chr4:120024333-120024882	A549	lung:	n/a	n/a
14	BACH1	chr4:120064017-120064337	K562	blood:	n/a	n/a
15	BACH1	chr4:120043723-120043785	K562	blood:	n/a	n/a
16	BACH1	chr4:120064009-120064372	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr4:120023606-120023664	K562	blood:	n/a	n/a
18	BCL3	chr4:120023637-120024906	A549	lung:	n/a	n/a
19	BHLHE40	chr4:120045731-120045795	K562	blood:	n/a	n/a
20	BHLHE40	chr4:120023932-120024184	HepG2	liver:	n/a	n/a
21	CBX3	chr4:120024314-120025029	HCT-116	colon:	n/a	n/a
22	CBX3	chr4:120034414-120034855	HCT-116	colon:	n/a	n/a
23	CBX3	chr4:120034232-120034884	HCT-116	colon:	n/a	n/a
24	CEBPB	chr4:120023726-120025088	A549	lung:	n/a	n/a
25	CEBPB	chr4:120034470-120034729	MCF-7	breast:	n/a	chr4:120034597-120034608
26	CEBPB	chr4:120014237-120014989	A549	lung:	n/a	chr4:120014307-120014318
27	CEBPB	chr4:120034354-120034881	Hela-S3	cervix:	n/a	chr4:120034597-120034608
28	CEBPB	chr4:120026759-120027092	Hela-S3	cervix:	n/a	chr4:120026921-120026934 chr4:120026899-120026912 chr4:120026922-120026933 chr4:120026921-120026932
29	CEBPB	chr4:120024043-120025008	IMR90	lung:	n/a	n/a
30	CEBPB	chr4:120023929-120024255	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:120020255-120021096	Hela-S3	cervix:	n/a	chr4:120020578-120020589 chr4:120020578-120020591 chr4:120020909-120020920 chr4:120020578-120020591 chr4:120020908-120020921
32	CEBPB	chr4:120034471-120034710	K562	blood:	n/a	chr4:120034597-120034608
33	CEBPB	chr4:120020489-120020985	A549	lung:	n/a	chr4:120020578-120020589 chr4:120020578-120020591 chr4:120020909-120020920 chr4:120020578-120020591 chr4:120020908-120020921
34	CEBPB	chr4:120060450-120060925	Hela-S3	cervix:	n/a	chr4:120060612-120060625
35	CEBPB	chr4:120014234-120014925	A549	lung:	n/a	chr4:120014307-120014318
36	CEBPB	chr4:120034433-120034773	HepG2	liver:	n/a	chr4:120034597-120034608
37	CEBPB	chr4:120034393-120034832	IMR90	lung:	n/a	chr4:120034597-120034608
38	CEBPB	chr4:120026910-120026953	H1-hESC	embryonic stem cell:	n/a	chr4:120026921-120026934 chr4:120026922-120026933 chr4:120026921-120026932
39	CEBPB	chr4:120024426-120024900	A549	lung:	n/a	n/a
40	CEBPB	chr4:120024542-120024761	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr4:120023472-120025128	HCT-116	colon:	n/a	n/a
42	CEBPB	chr4:120034507-120034821	A549	lung:	n/a	chr4:120034597-120034608
43	CEBPB	chr4:120023818-120024305	A549	lung:	n/a	n/a
44	CEBPB	chr4:120026753-120027094	HepG2	liver:	n/a	chr4:120026921-120026934 chr4:120026899-120026912 chr4:120026922-120026933 chr4:120026921-120026932
45	CEBPB	chr4:120013801-120013836	K562	blood:	n/a	n/a
46	CEBPB	chr4:120026757-120027115	IMR90	lung:	n/a	chr4:120026921-120026934 chr4:120026899-120026912 chr4:120026922-120026933 chr4:120026921-120026932
47	CEBPB	chr4:120060440-120060928	HCT-116	colon:	n/a	chr4:120060612-120060625
48	CEBPB	chr4:120020731-120021054	HepG2	liver:	n/a	chr4:120020909-120020920 chr4:120020908-120020921
49	CEBPB	chr4:120081367-120081422	K562	blood:	n/a	chr4:120081399-120081412
50	CEBPB	chr4:120026790-120027106	A549	lung:	n/a	chr4:120026921-120026934 chr4:120026899-120026912 chr4:120026922-120026933 chr4:120026921-120026932

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:120055608-120055658	SK-N-MC	brain:	n/a
2	chr4:120055608-120055658	PFSK-1	brain:	n/a
3	chr4:120055608-120055658	SK-N-MC	brain:	n/a
4	chr4:120055608-120055658	PFSK-1	brain:	n/a
5	chr4:120038219-120038269	T-47D	breast:	n/a
6	chr4:120055608-120055658	NHBE	bronchial:	n/a
7	chr4:120061211-120061261	AG04450	lung:	fetal
8	chr4:120056829-120056879	U87	brain:	n/a
9	chr4:120038219-120038269	AG09309	skin:	n/a
10	chr4:120057110-120057160	HRE	kidney:	n/a
11	chr4:120015469-120015519	AoSMC	blood vessel:	n/a
12	chr4:120056829-120056879	ovcar-3	ovarian:	n/a
13	chr4:120038219-120038269	HNPCEpiC	eye:	n/a
14	chr4:120038219-120038269	HCT-116	colon:	n/a
15	chr4:120038219-120038269	MCF-7	breast:	n/a
16	chr4:120038219-120038269	K562	blood:	n/a
17	chr4:120061211-120061261	MCF-7	breast:	n/a
18	chr4:120057110-120057160	HRCEpiC	kidney:	n/a
19	chr4:120038219-120038269	SK-N-MC	brain:	n/a
20	chr4:120038219-120038269	NT2-D1	testis:	n/a
21	chr4:120057110-120057160	LNCaP	prostate:	n/a
22	chr4:120056829-120056879	AoSMC	blood vessel:	n/a
23	chr4:120057818-120057868	SAEC	small airway:	n/a
24	chr4:120061211-120061261	HCM	heart:	n/a
25	chr4:120057110-120057160	SK-N-SH_RA	brain:	n/a
26	chr4:120015469-120015519	K562	blood:	n/a
27	chr4:120015469-120015519	PrEC	prostate:	n/a
28	chr4:120055608-120055658	AG09309	skin:	n/a
29	chr4:120038219-120038269	AG04449	skin:	fetal
30	chr4:120055608-120055658	T-47D	breast:	n/a
31	chr4:120061211-120061261	GM12891	blood:	n/a
32	chr4:120057818-120057868	GM12878	blood:	n/a
33	chr4:120015469-120015519	GM19239	blood:	n/a
34	chr4:120056829-120056879	IMR90	lung:	fetal
35	chr4:120056829-120056879	NT2-D1	testis:	n/a
36	chr4:120056829-120056879	Caco-2	colon:	n/a
37	chr4:120061211-120061261	HNPCEpiC	eye:	n/a
38	chr4:120057818-120057868	NB4	blood:	n/a
39	chr4:120038219-120038269	HMEC	breast:	n/a
40	chr4:120015469-120015519	RPTEC	kidney:	n/a
41	chr4:120056829-120056879	PrEC	prostate:	n/a
42	chr4:120056829-120056879	HIPEpiC	eye:	n/a
43	chr4:120055608-120055658	AG04449	skin:	fetal
44	chr4:120057110-120057160	HMEC	breast:	n/a
45	chr4:120038219-120038269	HEK293	kidney:	embryo
46	chr4:120015469-120015519	HEK293	kidney:	embryo
47	chr4:120055608-120055658	RPTEC	kidney:	n/a
48	chr4:120038219-120038269	HAEpiC	amniotic membrane:	n/a
49	chr4:120057818-120057868	H1-hESC	embryonic stem cell:	embryo
50	chr4:120057818-120057868	HCT-116	colon:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:120059391..120062207-chr4:120131058..120133617,2	MCF-7	breast:
2	chr4:120072229..120075010-chr4:120089681..120092174,2	K562	blood:
3	chr4:120021974..120023552-chr4:120133050..120134987,2	MCF-7	breast:
4	chr4:120060909..120063531-chr4:120066181..120067927,2	MCF-7	breast:
5	chr4:120021896..120024544-chr4:120027887..120030777,2	MCF-7	breast:
6	chr4:120033457..120035928-chr4:120042450..120044760,2	MCF-7	breast:
7	chr4:120107053..120109251-chr4:120131734..120133629,2	MCF-7	breast:
8	chr4:120026582..120029647-chr4:120131891..120134886,3	MCF-7	breast:
9	chr4:120109943..120112104-chr4:120116524..120118250,2	MCF-7	breast:
10	chr4:120021896..120024544-chr4:120027887..120030777,2	MCF-7	breast:
11	chr4:120060909..120063531-chr4:120066181..120067927,2	MCF-7	breast:
12	chr4:120110664..120112250-chr4:120132207..120134016,2	K562	blood:
13	chr4:120014220..120018464-chr4:120020403..120024000,3	MCF-7	breast:
14	chr4:120072229..120075010-chr4:120089681..120092174,2	K562	blood:
15	chr4:120060171..120063563-chr4:120128883..120130877,3	MCF-7	breast:
16	chr4:120026501..120028052-chr4:120132868..120134580,2	MCF-7	breast:
17	chr4:120032730..120035461-chr4:120133316..120136122,2	MCF-7	breast:
18	chr4:120096520..120098803-chr4:120098872..120101479,2	K562	blood:
19	chr4:120100153..120102490-chr4:120128940..120130617,2	MCF-7	breast:
20	chr4:120001166..120004043-chr4:120014693..120016511,3	MCF-7	breast:
21	chr4:120035133..120037765-chr4:120132862..120135100,2	MCF-7	breast:
22	chr4:120033922..120036234-chr4:120037431..120039972,2	K562	blood:
23	chr4:120015958..120018191-chr4:120019171..120021900,2	MCF-7	breast:
24	chr4:119989699..119991632-chr4:120032879..120034725,2	MCF-7	breast:
25	chr4:120105848..120109387-chr4:120131964..120134946,3	MCF-7	breast:
26	chr4:120033091..120034925-chr4:120132885..120135454,2	MCF-7	breast:
27	chr4:120013479..120014990-chr4:120129629..120131701,2	MCF-7	breast:
28	chr4:119964664..119967824-chr4:120028894..120031199,3	MCF-7	breast:
29	chr4:120082797..120084965-chr4:120133823..120135965,2	MCF-7	breast:
30	chr4:120096520..120098803-chr4:120098872..120101479,2	K562	blood:
31	chr4:120015958..120018191-chr4:120019171..120021900,2	MCF-7	breast:
32	chr4:120033922..120036234-chr4:120037431..120039972,2	K562	blood:
33	chr4:120014220..120018464-chr4:120020403..120024000,3	MCF-7	breast:
34	chr4:120033457..120035928-chr4:120042450..120044760,2	MCF-7	breast:
35	chr4:119967207..119969277-chr4:120017510..120021674,3	MCF-7	breast:
36	chr4:120018111..120021033-chr4:120132660..120135354,3	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-455G16.1.1-1	chr4:120038634-120039855	XLOC_004054
2	lnc-RP11-455G16.1.1-1	chr4:120043362-120043513	XLOC_004054
3	lnc-RP11-455G16.1.1-1	chr4:120040688-120040908	XLOC_004054
4	lnc-RP11-455G16.1.1-1	chr4:120038634-120039855	XLOC_004054
5	lnc-RP11-455G16.1.1-1	chr4:120038634-120039855	XLOC_004054
6	lnc-RP11-455G16.1.1-3	chr4:120114843-120115546	NONHSAT098035
7	lnc-RP11-455G16.1.1-1	chr4:120040688-120040847	XLOC_004054
8	lnc-RP11-455G16.1.1-1	chr4:120049353-120049505	XLOC_004054
9	lnc-RP11-455G16.1.1-1	chr4:120049353-120049505	XLOC_004054
10	lnc-RP11-455G16.1.1-1	chr4:120038634-120039855	XLOC_004054
11	lnc-RP11-455G16.1.1-1	chr4:120042792-120043419	XLOC_004054
12	lnc-RP11-455G16.1.1-1	chr4:120040688-120040847	XLOC_004054
13	lnc-RP11-455G16.1.1-1	chr4:120040678-120040984	XLOC_004054
14	lnc-RP11-455G16.1.1-1	chr4:120040688-120040990	XLOC_004054

No data

Variant related genes	Relation type
MYOZ2	TF binding region
MYOZ2	CpG island
ENSG00000249356	chromatin interactions
ENSG00000178636	chromatin interactions
ENSG00000145390	chromatin interactions
BCL2L11	miRNA target sites

Extended variants
information (count: 4002 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:4002 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11732628	chr4:120009147-120009148	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs550162117	chr4:120009156-120009157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs10857064	chr4:120009168-120009169	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs6856723	chr4:120009192-120009193	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs553121028	chr4:120009214-120009215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs28528945	chr4:120009232-120009233	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs185099962	chr4:120009254-120009255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs11942178	chr4:120009273-120009274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs189165529	chr4:120009329-120009330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs192423315	chr4:120009355-120009356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs578009155	chr4:120009358-120009359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143162077	chr4:120009374-120009375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558194733	chr4:120009403-120009404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371092843	chr4:120009418-120009419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs578119954	chr4:120009419-120009420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540752938	chr4:120009428-120009429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563503439	chr4:120009434-120009435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528279896	chr4:120009441-120009442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528980344	chr4:120009461-120009462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs527371216	chr4:120009474-120009475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11421748	chr4:120009475-120009476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs34347911	chr4:120009484-120009485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369750839	chr4:120009486-120009487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79585860	chr4:120009494-120009495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs147508890	chr4:120009509-120009510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530721727	chr4:120009521-120009522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs550124944	chr4:120009563-120009564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183852441	chr4:120009623-120009624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10011228	chr4:120009641-120009642	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs556293252	chr4:120009717-120009718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532790447	chr4:120009757-120009758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188123519	chr4:120009760-120009761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566489139	chr4:120009767-120009768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140231936	chr4:120009813-120009814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181289945	chr4:120009834-120009835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs371834912	chr4:120009928-120009929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569495552	chr4:120009989-120009990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538555276	chr4:120010007-120010008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs537538554	chr4:120010050-120010051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142966872	chr4:120010095-120010096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4472122	chr4:120010107-120010108	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs528039751	chr4:120010124-120010125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534226237	chr4:120010150-120010151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372311947	chr4:120010158-120010159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554235893	chr4:120010167-120010168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574051857	chr4:120010212-120010213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541966169	chr4:120010213-120010214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561746518	chr4:120010219-120010220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375472979	chr4:120010242-120010243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10002119	chr4:120010314-120010315	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:73)

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
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
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1053 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120003400-120014200	Weak transcription	Left Ventricle	heart
2	chr4:120003400-120014400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr4:120003600-120014600	Weak transcription	Right Atrium	heart
4	chr4:120004200-120013200	Weak transcription	HepG2	liver
5	chr4:120007400-120009200	Enhancers	Stomach Mucosa	stomach
6	chr4:120007800-120009200	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr4:120007800-120009400	Enhancers	A549	lung
8	chr4:120008000-120009200	Enhancers	Fetal Intestine Large	intestine
9	chr4:120008600-120009200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr4:120008600-120009400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:120008600-120009400	Enhancers	NHEK	skin
12	chr4:120009000-120009200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr4:120009000-120017600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr4:120009200-120013000	Weak transcription	Stomach Mucosa	stomach
15	chr4:120009200-120014200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr4:120009200-120014200	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr4:120009200-120019000	Weak transcription	Fetal Intestine Large	intestine
18	chr4:120009400-120014400	Weak transcription	NHEK	skin
19	chr4:120009400-120014600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr4:120012400-120013600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr4:120012600-120013000	Enhancers	Psoas Muscle	Psoas
22	chr4:120012800-120013200	Enhancers	Sigmoid Colon	Sigmoid Colon
23	chr4:120012800-120013600	Enhancers	Pancreas	Pancrea
24	chr4:120013000-120015400	Enhancers	Stomach Mucosa	stomach
25	chr4:120013200-120013400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr4:120013200-120013400	Weak transcription	A549	lung
27	chr4:120013200-120014400	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr4:120013200-120015200	Enhancers	HepG2	liver
29	chr4:120013400-120013600	Enhancers	A549	lung
30	chr4:120013400-120014600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr4:120013600-120014000	Weak transcription	Pancreas	Pancrea
32	chr4:120013600-120014200	Weak transcription	A549	lung
33	chr4:120014000-120015000	Enhancers	Pancreas	Pancrea
34	chr4:120014200-120014400	Enhancers	Left Ventricle	heart
35	chr4:120014200-120014400	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr4:120014200-120014400	Enhancers	A549	lung
37	chr4:120014200-120014600	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr4:120014200-120015000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr4:120014200-120016000	Enhancers	HUVEC	blood vessel
40	chr4:120014400-120014800	Weak transcription	Left Ventricle	heart
41	chr4:120014400-120014800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
42	chr4:120014400-120014800	Enhancers	NHEK	skin
43	chr4:120014400-120015000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr4:120014400-120015000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr4:120014400-120015000	Enhancers	Muscle Satellite Cultured Cells	--
46	chr4:120014400-120015000	Enhancers	Colonic Mucosa	Colon
47	chr4:120014400-120015000	Enhancers	Sigmoid Colon	Sigmoid Colon
48	chr4:120014400-120015000	Enhancers	HSMM	muscle
49	chr4:120014400-120015000	Enhancers	NH-A	brain
50	chr4:120014400-120015000	Enhancers	Osteobl	bone

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