Variant report

Variant	nsv1627
Chromosome Location	chr15:78683761-78728604
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:820)
CpG islands
(count:244)
Chromatin interactive
region (count:65)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:820 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:78707822-78708051	K562	blood:	n/a	n/a
2	ARID3A	chr15:78715137-78715516	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:78721870-78722218	HepG2	liver:	n/a	n/a
4	ATF2	chr15:78687493-78688091	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr15:78715245-78715548	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr15:78696514-78696751	GM12878	blood:	n/a	n/a
7	BATF	chr15:78725105-78725336	GM12878	blood:	n/a	n/a
8	BCL3	chr15:78726503-78726839	GM12878	blood:	n/a	n/a
9	BHLHE40	chr15:78711819-78712024	K562	blood:	n/a	n/a
10	BHLHE40	chr15:78715213-78715458	GM12878	blood:	n/a	n/a
11	BHLHE40	chr15:78725117-78725211	GM12878	blood:	n/a	n/a
12	BHLHE40	chr15:78707663-78707812	GM12878	blood:	n/a	n/a
13	BHLHE40	chr15:78726523-78726801	K562	blood:	n/a	n/a
14	BHLHE40	chr15:78726572-78726808	HepG2	liver:	n/a	n/a
15	BRCA1	chr15:78711659-78712027	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr15:78715270-78715564	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr15:78720144-78720588	K562	blood:	n/a	n/a
18	CBX3	chr15:78711593-78711954	K562	blood:	n/a	n/a
19	CEBPB	chr15:78684894-78685010	H1-hESC	embryonic stem cell:	n/a	chr15:78684947-78684955
20	CEBPB	chr15:78689360-78689698	HepG2	liver:	n/a	n/a
21	CEBPB	chr15:78691461-78691950	A549	lung:	n/a	chr15:78691572-78691583 chr15:78691911-78691924
22	CEBPB	chr15:78715179-78715562	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr15:78685040-78685058	A549	lung:	n/a	n/a
24	CEBPB	chr15:78699678-78699833	IMR90	lung:	n/a	n/a
25	CEBPB	chr15:78689530-78689561	IMR90	lung:	n/a	n/a
26	CEBPB	chr15:78687017-78687184	K562	blood:	n/a	n/a
27	CEBPB	chr15:78691465-78691648	Hela-S3	cervix:	n/a	chr15:78691572-78691583
28	CEBPB	chr15:78703386-78704085	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr15:78687045-78687214	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr15:78689332-78689758	MCF-7	breast:	n/a	n/a
31	CEBPB	chr15:78699666-78699856	K562	blood:	n/a	n/a
32	CEBPB	chr15:78691523-78691917	K562	blood:	n/a	chr15:78691572-78691583
33	CEBPB	chr15:78711459-78712098	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr15:78691450-78691710	HepG2	liver:	n/a	chr15:78691572-78691583
35	CEBPB	chr15:78697885-78698153	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr15:78689340-78689684	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr15:78687011-78687141	A549	lung:	n/a	n/a
38	CEBPB	chr15:78702883-78703137	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr15:78710631-78710962	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr15:78715246-78715515	Hela-S3	cervix:	n/a	n/a
41	CTBP2	chr15:78687383-78687953	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr15:78707900-78708050	A549	lung:	n/a	n/a
43	CTCF	chr15:78715300-78715450	GM12869	blood:	n/a	chr15:78715367-78715385 chr15:78715373-78715382 chr15:78715362-78715383 chr15:78715369-78715382
44	CTCF	chr15:78715264-78715522	T-47D	breast:	n/a	chr15:78715367-78715385 chr15:78715373-78715382 chr15:78715362-78715383 chr15:78715369-78715382
45	CTCF	chr15:78707840-78707990	HA-sp	spinal cord:	n/a	n/a
46	CTCF	chr15:78708140-78708290	Caco-2	colon:	n/a	n/a
47	CTCF	chr15:78715042-78715126	MCF-7	breast:	n/a	n/a
48	CTCF	chr15:78715221-78715526	K562	blood:	n/a	chr15:78715367-78715385 chr15:78715373-78715382 chr15:78715362-78715383 chr15:78715369-78715382
49	CTCF	chr15:78715360-78715510	HAc	cerebellar:	n/a	chr15:78715367-78715385 chr15:78715373-78715382 chr15:78715362-78715383 chr15:78715369-78715382
50	CTCF	chr15:78715236-78715561	A549	lung:	n/a	chr15:78715367-78715385 chr15:78715373-78715382 chr15:78715362-78715383 chr15:78715369-78715382

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:78697933-78697983	SKMC	muscle:	n/a
2	chr15:78689050-78689100	HEEpiC	esophagus:	n/a
3	chr15:78726576-78726626	GM12878	blood:	n/a
4	chr15:78707683-78707733	AoSMC	blood vessel:	n/a
5	chr15:78707683-78707733	BE2_C	brain:	n/a
6	chr15:78697933-78697983	HRPEpiC	eye:	n/a
7	chr15:78697933-78697983	NHBE	bronchial:	n/a
8	chr15:78697933-78697983	NT2-D1	testis:	n/a
9	chr15:78707683-78707733	NHDF-neo	bronchial:	n/a
10	chr15:78689050-78689100	GM19239	blood:	n/a
11	chr15:78726576-78726626	AG04450	lung:	fetal
12	chr15:78697933-78697983	PFSK-1	brain:	n/a
13	chr15:78697933-78697983	HCT-116	colon:	n/a
14	chr15:78697933-78697983	Caco-2	colon:	n/a
15	chr15:78707683-78707733	HEEpiC	esophagus:	n/a
16	chr15:78689050-78689100	BJ	skin:	n/a
17	chr15:78689050-78689100	Hela-S3	cervix:	n/a
18	chr15:78697933-78697983	SK-N-SH_RA	brain:	n/a
19	chr15:78707683-78707733	HCF	heart:	n/a
20	chr15:78689050-78689100	AG09309	skin:	n/a
21	chr15:78726576-78726626	HMEC	breast:	n/a
22	chr15:78726576-78726626	NHDF-neo	bronchial:	n/a
23	chr15:78707683-78707733	Hepatocyte	liver:	n/a
24	chr15:78689050-78689100	LNCaP	prostate:	n/a
25	chr15:78689050-78689100	AG09319	gingival:	n/a
26	chr15:78697933-78697983	SAEC	small airway:	n/a
27	chr15:78697933-78697983	CMK	blood:	n/a
28	chr15:78697933-78697983	Hepatocyte	liver:	n/a
29	chr15:78707683-78707733	HRCEpiC	kidney:	n/a
30	chr15:78689050-78689100	AG04449	skin:	fetal
31	chr15:78707683-78707733	SKMC	muscle:	n/a
32	chr15:78726576-78726626	Hepatocyte	liver:	n/a
33	chr15:78697933-78697983	AG09309	skin:	n/a
34	chr15:78726576-78726626	HIPEpiC	eye:	n/a
35	chr15:78726576-78726626	HRE	kidney:	n/a
36	chr15:78697933-78697983	HMEC	breast:	n/a
37	chr15:78689050-78689100	NT2-D1	testis:	n/a
38	chr15:78697933-78697983	HRCEpiC	kidney:	n/a
39	chr15:78689050-78689100	GM12892	blood:	n/a
40	chr15:78707683-78707733	HCM	heart:	n/a
41	chr15:78697933-78697983	Hela-S3	cervix:	n/a
42	chr15:78697933-78697983	HCPEpiC	choroid plexus:	n/a
43	chr15:78726576-78726626	ECC-1	luminal epithelium:	n/a
44	chr15:78726576-78726626	AG09319	gingival:	n/a
45	chr15:78707683-78707733	ECC-1	luminal epithelium:	n/a
46	chr15:78726576-78726626	HEK293	kidney:	embryo
47	chr15:78697933-78697983	NB4	blood:	n/a
48	chr15:78697933-78697983	MCF10A-Er-Src	breast:	n/a
49	chr15:78726576-78726626	BE2_C	brain:	n/a
50	chr15:78726576-78726626	K562	blood:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:78640272..78641260-chr15:78688964..78689871,3	MCF-7	breast:
2	chr15:78715399..78718078-chr15:78719259..78720829,2	MCF-7	breast:
3	chr15:78699345..78701033-chr15:78728598..78731908,3	K562	blood:
4	chr15:78705837..78708183-chr15:78712525..78714255,2	K562	blood:
5	chr15:78720134..78723465-chr15:78728938..78732082,4	MCF-7	breast:
6	chr15:78714083..78716832-chr15:78721303..78723382,2	MCF-7	breast:
7	chr15:78715399..78718078-chr15:78719259..78720829,2	MCF-7	breast:
8	chr15:78691109..78692723-chr15:78696041..78697844,2	K562	blood:
9	chr15:78600505..78601390-chr15:78714866..78715903,8	MCF-7	breast:
10	chr15:78592572..78594896-chr15:78724415..78726176,2	K562	blood:
11	chr15:78689276..78690993-chr15:78695129..78697565,2	K562	blood:
12	chr15:78714909..78715620-chr15:78730027..78730764,2	K562	blood:
13	chr15:78587653..78594388-chr15:78727556..78733158,9	MCF-7	breast:
14	chr15:78600493..78601405-chr15:78707405..78708425,10	MCF-7	breast:
15	chr15:78681164..78684060-chr15:78688806..78691444,2	K562	blood:
16	chr15:78686256..78688855-chr15:78690068..78692853,2	K562	blood:
17	chr15:78686256..78688855-chr15:78690068..78692853,2	K562	blood:
18	chr15:78688849..78689413-chr15:78707506..78708008,2	MCF-7	breast:
19	chr15:78589125..78595669-chr15:78728604..78731599,7	K562	blood:
20	chr15:78609276..78610228-chr15:78689311..78689907,2	MCF-7	breast:
21	chr15:78714083..78716832-chr15:78721303..78723382,2	MCF-7	breast:
22	chr15:78694489..78696482-chr15:78729566..78731569,2	K562	blood:
23	chr15:78681164..78684060-chr15:78688806..78691444,2	K562	blood:
24	chr15:78690617..78693319-chr15:78700290..78702195,2	MCF-7	breast:
25	chr15:78705902..78708809-chr15:78708917..78710787,2	K562	blood:
26	chr15:78627296..78629815-chr15:78701487..78704015,2	MCF-7	breast:
27	chr15:78631534..78633106-chr15:78696326..78697874,2	MCF-7	breast:
28	chr15:78688934..78689473-chr15:78707850..78708354,2	MCF-7	breast:
29	chr15:78657024..78658991-chr15:78692775..78694718,2	K562	blood:
30	chr15:78711992..78713531-chr15:78829665..78831624,2	K562	blood:
31	chr15:78722314..78725378-chr15:78725474..78727729,3	MCF-7	breast:
32	chr15:78582861..78585350-chr15:78727780..78730750,2	MCF-7	breast:
33	chr15:78600454..78601279-chr15:78707435..78708437,6	MCF-7	breast:
34	chr15:78609337..78610241-chr15:78707562..78708403,2	MCF-7	breast:
35	chr15:78599674..78600430-chr15:78707799..78708454,3	MCF-7	breast:
36	chr15:78689388..78691661-chr15:78857643..78859305,2	MCF-7	breast:
37	chr15:78665803..78668679-chr15:78697732..78701698,4	MCF-7	breast:
38	chr15:78705837..78708183-chr15:78712525..78714255,2	K562	blood:
39	chr15:78718625..78720309-chr15:78729352..78732262,2	K562	blood:
40	chr15:78705902..78708809-chr15:78708917..78710787,2	K562	blood:
41	chr15:78714000..78716972-chr15:78729600..78732275,2	K562	blood:
42	chr15:78722314..78725378-chr15:78725474..78727729,3	MCF-7	breast:
43	chr15:78609393..78610006-chr15:78707681..78708343,2	MCF-7	breast:
44	chr15:78690617..78693319-chr15:78700290..78702195,2	MCF-7	breast:
45	chr15:78600767..78601452-chr15:78715022..78715549,2	K562	blood:
46	chr15:78724540..78726628-chr15:78727492..78730355,3	K562	blood:
47	chr15:78688934..78689473-chr15:78707850..78708354,2	MCF-7	breast:
48	chr15:78679630..78681837-chr15:78689698..78692156,2	MCF-7	breast:
49	chr15:78686576..78687529-chr15:78715271..78715854,2	K562	blood:
50	chr15:78686576..78687529-chr15:78715271..78715854,2	K562	blood:

No data

Variant related genes	Relation type
IREB2	TF binding region
IREB2	CpG island
ENSG00000166426	chromatin interactions
ENSG00000268838	chromatin interactions
ENSG00000169684	chromatin interactions
ENSG00000136381	chromatin interactions
ENSG00000140395	chromatin interactions
ENSG00000259562	chromatin interactions

Extended variants
information (count: 1674 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1674 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73459270	chr15:78683813-78683814	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571583260	chr15:78683814-78683815	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs532697879	chr15:78683826-78683827	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs577500931	chr15:78683833-78683834	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs547571599	chr15:78683877-78683878	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs540105389	chr15:78683901-78683902	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs566184358	chr15:78683925-78683926	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs536747948	chr15:78683971-78683972	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs554718812	chr15:78684012-78684013	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs145775962	chr15:78684044-78684045	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs11630879	chr15:78684051-78684052	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs183293489	chr15:78684088-78684089	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs573709865	chr15:78684122-78684123	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs577187246	chr15:78684162-78684163	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs148951153	chr15:78684213-78684214	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs553120904	chr15:78684230-78684231	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs372791672	chr15:78684266-78684267	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs574590369	chr15:78684294-78684295	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs542007175	chr15:78684298-78684299	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs75387534	chr15:78684315-78684316	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs186864281	chr15:78684375-78684376	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs78634525	chr15:78684422-78684423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545373975	chr15:78684455-78684456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563775049	chr15:78684490-78684491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562438689	chr15:78684514-78684515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs62010380	chr15:78684517-78684518	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs547823132	chr15:78684536-78684537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189780011	chr15:78684575-78684576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs11631252	chr15:78684614-78684615	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs548779343	chr15:78684700-78684701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs182111776	chr15:78684709-78684710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs376279321	chr15:78684735-78684736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs186582583	chr15:78684749-78684750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577687265	chr15:78684757-78684758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs138434843	chr15:78684767-78684768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs570897703	chr15:78684806-78684807	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs75856821	chr15:78684831-78684832	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs112791883	chr15:78684849-78684850	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs370645448	chr15:78684861-78684862	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs115834806	chr15:78684871-78684872	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs547267065	chr15:78684882-78684883	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs567161990	chr15:78684910-78684911	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs557150113	chr15:78684928-78684929	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs574981651	chr15:78684962-78684963	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs545535632	chr15:78685008-78685009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529079188	chr15:78685032-78685033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572460441	chr15:78685047-78685048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs371792071	chr15:78685134-78685135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77218112	chr15:78685147-78685148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540232406	chr15:78685165-78685166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:556 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78667600-78704400	Weak transcription	Lung	lung
2	chr15:78680200-78683800	Enhancers	Placenta	Placenta
3	chr15:78680200-78684800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr15:78680400-78684800	Weak transcription	Fetal Brain Female	brain
5	chr15:78681200-78684400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr15:78681600-78683800	Enhancers	NHDF-Ad	bronchial
7	chr15:78681800-78688800	Weak transcription	Spleen	Spleen
8	chr15:78682000-78684600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr15:78682000-78684800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr15:78682200-78683800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr15:78682200-78684200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr15:78682200-78684400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr15:78682200-78684600	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr15:78682200-78684600	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr15:78682200-78687400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr15:78682200-78687400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr15:78682200-78687400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr15:78682200-78687600	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr15:78682400-78684600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr15:78682400-78686000	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr15:78682400-78686200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr15:78682400-78686200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
23	chr15:78682400-78686400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr15:78682400-78687000	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr15:78682800-78683800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr15:78683200-78684200	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr15:78683800-78687400	Weak transcription	Placenta	Placenta
28	chr15:78684200-78685000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr15:78684600-78684800	Enhancers	Fetal Intestine Large	intestine
30	chr15:78684600-78685000	Enhancers	Brain Germinal Matrix	brain
31	chr15:78684600-78685200	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr15:78684600-78685200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr15:78684600-78685200	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr15:78684600-78685200	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr15:78684600-78685400	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr15:78684800-78685000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr15:78684800-78685000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr15:78684800-78685000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr15:78684800-78685000	Enhancers	Fetal Brain Male	brain
40	chr15:78684800-78685000	Enhancers	Fetal Brain Female	brain
41	chr15:78684800-78685200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr15:78684800-78686600	Weak transcription	Fetal Intestine Large	intestine
43	chr15:78685000-78686000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr15:78685000-78686200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr15:78685200-78686200	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr15:78685200-78686400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr15:78685200-78686600	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr15:78685200-78687200	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr15:78685200-78687400	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr15:78685200-78687400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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