Variant report

Variant	nsv538326
Chromosome Location	chr6:78352231-79003866
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:78635944-78636263	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:78544192-78545206	HepG2	liver:	n/a	n/a
3	ATF2	chr6:78359867-78360364	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr6:78359807-78360307	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr6:78360044-78360429	H1-hESC	embryonic stem cell:	n/a	chr6:78360299-78360308
6	BACH1	chr6:78830228-78830262	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:78803262-78803267	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr6:78359692-78360430	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr6:78927907-78927947	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr6:78961745-78962001	GM12878	blood:	n/a	chr6:78961848-78961859 chr6:78961849-78961859
11	BHLHE40	chr6:78360002-78360490	K562	blood:	n/a	chr6:78360383-78360392
12	BHLHE40	chr6:78963305-78963665	GM12878	blood:	n/a	n/a
13	BRCA1	chr6:78359694-78360209	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr6:78944978-78945317	Hela-S3	cervix:	n/a	n/a
15	CCNT2	chr6:78564324-78564562	K562	blood:	n/a	n/a
16	CEBPB	chr6:78953223-78953650	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr6:78646654-78646963	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:78772716-78773097	IMR90	lung:	n/a	chr6:78772899-78772912 chr6:78772901-78772910 chr6:78772899-78772910 chr6:78772901-78772910 chr6:78772901-78772910
19	CEBPB	chr6:78387761-78388091	A549	lung:	n/a	chr6:78387921-78387930 chr6:78387919-78387930 chr6:78387919-78387932 chr6:78387921-78387930 chr6:78387921-78387930 chr6:78387916-78387933
20	CEBPB	chr6:78772707-78773078	A549	lung:	n/a	chr6:78772899-78772912 chr6:78772901-78772910 chr6:78772899-78772910 chr6:78772901-78772910 chr6:78772901-78772910
21	CEBPB	chr6:78544334-78544618	HepG2	liver:	n/a	n/a
22	CEBPB	chr6:78917590-78917813	HepG2	liver:	n/a	chr6:78917649-78917660
23	CEBPB	chr6:78870070-78870306	K562	blood:	n/a	n/a
24	CEBPB	chr6:78876347-78876480	A549	lung:	n/a	n/a
25	CEBPB	chr6:78643089-78643174	A549	lung:	n/a	n/a
26	CEBPB	chr6:78685530-78685797	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr6:78945069-78945269	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr6:78387768-78388109	MCF-7	breast:	n/a	chr6:78387921-78387930 chr6:78387919-78387930 chr6:78387919-78387932 chr6:78387921-78387930 chr6:78387921-78387930 chr6:78387916-78387933
29	CEBPB	chr6:78387750-78388121	Hela-S3	cervix:	n/a	chr6:78387921-78387930 chr6:78387919-78387930 chr6:78387919-78387932 chr6:78387921-78387930 chr6:78387921-78387930 chr6:78387916-78387933
30	CEBPB	chr6:78772693-78773088	A549	lung:	n/a	chr6:78772899-78772912 chr6:78772901-78772910 chr6:78772899-78772910 chr6:78772901-78772910 chr6:78772901-78772910
31	CEBPB	chr6:78787710-78787720	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr6:78567713-78567950	HepG2	liver:	n/a	chr6:78567824-78567833
33	CEBPB	chr6:78772723-78773147	ECC-1	luminal epithelium:	n/a	chr6:78772899-78772912 chr6:78772901-78772910 chr6:78772899-78772910 chr6:78772901-78772910 chr6:78772901-78772910
34	CEBPB	chr6:78387745-78388103	HepG2	liver:	n/a	chr6:78387921-78387930 chr6:78387919-78387930 chr6:78387919-78387932 chr6:78387921-78387930 chr6:78387921-78387930 chr6:78387916-78387933
35	CEBPB	chr6:78535525-78535565	A549	lung:	n/a	n/a
36	CEBPB	chr6:78772714-78773194	MCF-7	breast:	n/a	chr6:78772899-78772912 chr6:78772901-78772910 chr6:78772899-78772910 chr6:78772901-78772910 chr6:78772901-78772910
37	CEBPB	chr6:78357174-78357455	HepG2	liver:	n/a	chr6:78357309-78357320
38	CEBPB	chr6:78956506-78956776	HepG2	liver:	n/a	chr6:78956645-78956656
39	CEBPB	chr6:78945030-78945340	IMR90	lung:	n/a	n/a
40	CEBPB	chr6:78772718-78773090	K562	blood:	n/a	chr6:78772899-78772912 chr6:78772901-78772910 chr6:78772899-78772910 chr6:78772901-78772910 chr6:78772901-78772910
41	CEBPB	chr6:78359811-78360322	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr6:78387746-78388115	IMR90	lung:	n/a	chr6:78387921-78387930 chr6:78387919-78387930 chr6:78387919-78387932 chr6:78387921-78387930 chr6:78387921-78387930 chr6:78387916-78387933
43	CEBPB	chr6:78944886-78945498	HCT-116	colon:	n/a	n/a
44	CEBPB	chr6:78917584-78917793	IMR90	lung:	n/a	chr6:78917649-78917660
45	CEBPB	chr6:78636105-78636242	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr6:78928070-78928710	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr6:78944764-78945468	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr6:78400421-78400492	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr6:78590222-78590599	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr6:78402763-78403015	HepG2	liver:	n/a	chr6:78402884-78402895 chr6:78402886-78402897 chr6:78402886-78402895

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:78360341-78360391	MCF10A-Er-Src	breast:	n/a
2	chr6:78360341-78360391	MCF10A-Er-Src	breast:	n/a
3	chr6:78446060-78446110	HL-60	blood:	n/a
4	chr6:78360341-78360391	U87	brain:	n/a
5	chr6:78446107-78446157	SK-N-SH_RA	brain:	n/a
6	chr6:78362377-78362427	PANC-1	pancreas:	n/a
7	chr6:78446060-78446110	HepG2	liver:	n/a
8	chr6:78446107-78446157	T-47D	breast:	n/a
9	chr6:78360046-78360096	U87	brain:	n/a
10	chr6:78446107-78446157	AG04450	lung:	fetal
11	chr6:78362057-78362107	BE2_C	brain:	n/a
12	chr6:78446107-78446157	HEEpiC	esophagus:	n/a
13	chr6:78446107-78446157	Hela-S3	cervix:	n/a
14	chr6:78446107-78446157	HL-60	blood:	n/a
15	chr6:78446107-78446157	ECC-1	luminal epithelium:	n/a
16	chr6:78357241-78357291	SK-N-SH	brain:	n/a
17	chr6:78362377-78362427	HRPEpiC	eye:	n/a
18	chr6:78362057-78362107	BJ	skin:	n/a
19	chr6:78357241-78357291	RPTEC	kidney:	n/a
20	chr6:78446107-78446157	GM12891	blood:	n/a
21	chr6:78446060-78446110	GM19239	blood:	n/a
22	chr6:78357241-78357291	HNPCEpiC	eye:	n/a
23	chr6:78446107-78446157	K562	blood:	n/a
24	chr6:78357241-78357291	SK-N-SH_RA	brain:	n/a
25	chr6:78362377-78362427	Caco-2	colon:	n/a
26	chr6:78360341-78360391	NT2-D1	testis:	n/a
27	chr6:78446060-78446110	MCF10A-Er-Src	breast:	n/a
28	chr6:78446060-78446110	NHDF-neo	bronchial:	n/a
29	chr6:78360046-78360096	NH-A	brain:	n/a
30	chr6:78362377-78362427	AoSMC	blood vessel:	n/a
31	chr6:78360341-78360391	PFSK-1	brain:	n/a
32	chr6:78360046-78360096	T-47D	breast:	n/a
33	chr6:78446107-78446157	SK-N-SH	brain:	n/a
34	chr6:78446060-78446110	SK-N-SH	brain:	n/a
35	chr6:78359965-78360015	HRCEpiC	kidney:	n/a
36	chr6:78360341-78360391	NHDF-neo	bronchial:	n/a
37	chr6:78357241-78357291	AG10803	skin:	n/a
38	chr6:78446107-78446157	HEK293	kidney:	embryo
39	chr6:78359965-78360015	ECC-1	luminal epithelium:	n/a
40	chr6:78360341-78360391	PrEC	prostate:	n/a
41	chr6:78362057-78362107	HRE	kidney:	n/a
42	chr6:78359965-78360015	GM12891	blood:	n/a
43	chr6:78360046-78360096	IMR90	lung:	fetal
44	chr6:78446107-78446157	ProgFib	skin:	n/a
45	chr6:78360341-78360391	Jurkat	blood:	n/a
46	chr6:78362377-78362427	RPTEC	kidney:	n/a
47	chr6:78362057-78362107	A549	lung:	n/a
48	chr6:78362377-78362427	AG09319	gingival:	n/a
49	chr6:78362377-78362427	PrEC	prostate:	n/a
50	chr6:78362057-78362107	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr6:78884216..78887143-chr6:79140755..79143140,2	K562	blood:
2	chr6:78449866..78450562-chr6:79223273..79224176,3	MCF-7	breast:
3	chr6:78357150..78359352-chr6:78388533..78390499,2	K562	blood:
4	chr6:78871979..78874445-chr6:78875354..78878214,2	K562	blood:
5	chr6:78871979..78874445-chr6:78875354..78878214,2	K562	blood:
6	chr3:63179133..63179654-chr6:78736848..78737349,2	MCF-7	breast:
7	chr6:78922819..78924778-chr6:78931253..78933629,2	K562	blood:
8	chr6:78356313..78359113-chr6:78364118..78365918,2	MCF-7	breast:
9	chr6:78357150..78359352-chr6:78388533..78390499,2	K562	blood:
10	chr6:78175755..78176369-chr6:78410019..78410778,2	MCF-7	breast:
11	chr6:78922819..78924778-chr6:78931253..78933629,2	K562	blood:
12	chr6:78588151..78590093-chr6:78592344..78594893,2	K562	blood:
13	chr6:78588151..78590093-chr6:78592344..78594893,2	K562	blood:
14	chr6:78356313..78359113-chr6:78364118..78365918,2	MCF-7	breast:
15	chr6:78450229..78450915-chr6:79519607..79520138,2	MCF-7	breast:
16	chr6:78449862..78450824-chr6:78635645..78636377,3	MCF-7	breast:
17	chr17:59487700..59489361-chr6:78782419..78783949,2	MCF-7	breast:
18	chr6:78449862..78450824-chr6:78635645..78636377,3	MCF-7	breast:
19	chr6:78409901..78411994-chr6:78412184..78414411,2	MCF-7	breast:
20	chr6:78966571..78967392-chr6:79036188..79036778,2	MCF-7	breast:
21	chr6:78409901..78411994-chr6:78412184..78414411,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IRAK1BP1-5	chr6:78527566-78528101	l_3208_chr6:78417002-78689824_testes
2	lnc-IRAK1BP1-5	chr6:78595367-78595498	l_3208_chr6:78417002-78689824_testes
3	lnc-IRAK1BP1-2	chr6:78470847-78470871	ENSG00000214481
4	lnc-IRAK1BP1-5	chr6:78457094-78457339	l_3208_chr6:78417002-78689824_testes
5	lnc-IRAK1BP1-2	chr6:78400542-78400620	ENSG00000214481
6	lnc-IRAK1BP1-5	chr6:78419459-78419528	l_3208_chr6:78417002-78689824_testes
7	lnc-IRAK1BP1-5	chr6:78417003-78417143	l_3208_chr6:78417002-78689824_testes
8	lnc-IRAK1BP1-5	chr6:78689525-78690012	l_3208_chr6:78417002-78689824_testes

Variant related genes	Relation type
MEI4	TF binding region
ENSG00000252932	TF binding region
MEI4	CpG island
ENSG00000252932	CpG island
ENSG00000267280	chromatin interactions
ENSG00000187013	chromatin interactions

Extended variants
information (count: 5774 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:5774 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549455120	chr6:78352241-78352242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566375288	chr6:78352326-78352327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533509636	chr6:78352330-78352331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547389784	chr6:78352333-78352334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570526212	chr6:78352368-78352369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539572055	chr6:78352414-78352415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372431673	chr6:78352444-78352445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370888633	chr6:78352445-78352446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs78473792	chr6:78352565-78352566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376866400	chr6:78352567-78352568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560973334	chr6:78352608-78352609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149613905	chr6:78352624-78352625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs9448125	chr6:78352766-78352767	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs535730629	chr6:78352819-78352820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs377529078	chr6:78352846-78352847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146108143	chr6:78352889-78352890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572306328	chr6:78352943-78352944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs34517093	chr6:78352974-78352975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs35139014	chr6:78352994-78352995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201225780	chr6:78352995-78352996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370332523	chr6:78353029-78353030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541033896	chr6:78353061-78353062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139209216	chr6:78353103-78353104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142421319	chr6:78353104-78353105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2504285	chr6:78353105-78353106	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs200274064	chr6:78353173-78353174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148605783	chr6:78353179-78353180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369188618	chr6:78353187-78353188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12527300	chr6:78353201-78353202	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs559765857	chr6:78353223-78353224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528795517	chr6:78353253-78353254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547059773	chr6:78353258-78353259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201910115	chr6:78353282-78353283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112616834	chr6:78353292-78353293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533056808	chr6:78353337-78353338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2504284	chr6:78353362-78353363	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs151219166	chr6:78353381-78353382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535247942	chr6:78353478-78353479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181325583	chr6:78353485-78353486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185308320	chr6:78353632-78353633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs73759101	chr6:78353699-78353700	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs557726972	chr6:78353731-78353732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577659342	chr6:78353749-78353750	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74421779	chr6:78353757-78353758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556991007	chr6:78353767-78353768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574103183	chr6:78353807-78353808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs139170188	chr6:78353856-78353857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs559928701	chr6:78353887-78353888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531996675	chr6:78353890-78353891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs9448126	chr6:78353992-78353993	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21990379	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19036926	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD

Chromatin state (count:470 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:78350400-78353800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr6:78353600-78354400	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr6:78353800-78354400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
4	chr6:78353800-78354600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr6:78353800-78354600	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr6:78353800-78355000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr6:78353800-78355000	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr6:78354400-78355600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr6:78354400-78355600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr6:78354600-78355400	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr6:78355000-78362400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr6:78355400-78356000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr6:78355600-78356000	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr6:78355600-78356200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr6:78355800-78356200	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr6:78356000-78359400	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr6:78356000-78359600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr6:78356200-78359200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr6:78356200-78359800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr6:78358200-78359400	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr6:78358600-78359200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr6:78358600-78359400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr6:78358800-78359000	Enhancers	Fetal Intestine Small	intestine
24	chr6:78358800-78359600	Enhancers	Fetal Heart	heart
25	chr6:78358800-78359800	Enhancers	Placenta Amnion	Placenta Amnion
26	chr6:78359000-78359800	Weak transcription	Fetal Intestine Small	intestine
27	chr6:78359200-78359400	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr6:78359200-78359400	Flanking Active TSS	Primary hematopoietic stem cells	blood
29	chr6:78359200-78359400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr6:78359200-78359400	Enhancers	Fetal Kidney	kidney
31	chr6:78359200-78360200	Active TSS	HUES48 Cell Line	embryonic stem cell
32	chr6:78359200-78360200	Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr6:78359200-78360400	Active TSS	iPS-15b Cell Line	embryonic stem cell
34	chr6:78359400-78359600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr6:78359400-78359600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr6:78359400-78359600	Flanking Active TSS	HUVEC	blood vessel
37	chr6:78359400-78359800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
38	chr6:78359400-78360200	Active TSS	HUES64 Cell Line	embryonic stem cell
39	chr6:78359400-78360200	Active TSS	iPS-18 Cell Line	embryonic stem cell
40	chr6:78359400-78360200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
41	chr6:78359400-78360200	Active TSS	Primary hematopoietic stem cells	blood
42	chr6:78359400-78360200	Active TSS	Fetal Kidney	kidney
43	chr6:78359400-78360400	Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr6:78359400-78360400	Active TSS	Monocytes-CD14+_RO01746	blood
45	chr6:78359600-78359800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr6:78359600-78359800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr6:78359600-78359800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr6:78359600-78359800	Enhancers	Placenta	Placenta
49	chr6:78359600-78359800	Active TSS	Fetal Stomach	stomach
50	chr6:78359600-78359800	Bivalent/Poised TSS	HUVEC	blood vessel

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