Variant report

Variant	nsv872267
Chromosome Location	chr1:147143887-147185251
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:425)
CpG islands
(count:122)
Chromatin interactive
region (count:44)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:425 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:147172208-147172529	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:147148435-147149188	HepG2	liver:	n/a	n/a
3	BACH1	chr1:147148616-147148633	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr1:147148952-147148963	HepG2	liver:	n/a	n/a
5	CBX3	chr1:147149749-147150232	K562	blood:	n/a	n/a
6	CEBPB	chr1:147164386-147164682	A549	lung:	n/a	chr1:147164489-147164500
7	CEBPB	chr1:147148297-147149213	MCF-7	breast:	n/a	n/a
8	CEBPB	chr1:147148340-147149140	A549	lung:	n/a	n/a
9	CEBPB	chr1:147164330-147164662	IMR90	lung:	n/a	chr1:147164489-147164500
10	CEBPB	chr1:147148535-147148695	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr1:147148465-147149063	A549	lung:	n/a	n/a
12	CEBPB	chr1:147148068-147149223	MCF-7	breast:	n/a	n/a
13	CEBPB	chr1:147164335-147164622	K562	blood:	n/a	chr1:147164489-147164500
14	CEBPB	chr1:147148450-147149131	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:147148500-147149074	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:147148176-147149150	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr1:147169118-147169276	HepG2	liver:	n/a	chr1:147169153-147169164
18	CEBPB	chr1:147164359-147164668	HepG2	liver:	n/a	chr1:147164489-147164500
19	CTCF	chr1:147172121-147172387	HepG2	liver:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
20	CTCF	chr1:147171680-147171830	HFF-Myc	foreskin:	n/a	n/a
21	CTCF	chr1:147172160-147172310	HA-sp	spinal cord:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
22	CTCF	chr1:147172200-147172350	BJ	skin:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
23	CTCF	chr1:147172106-147172375	K562	blood:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
24	CTCF	chr1:147172119-147172360	GM10248	blood:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
25	CTCF	chr1:147172140-147172290	GM12867	blood:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
26	CTCF	chr1:147172140-147172290	A549	lung:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
27	CTCF	chr1:147172200-147172350	HCT-116	colon:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
28	CTCF	chr1:147172200-147172350	WI-38	lung:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
29	CTCF	chr1:147172180-147172330	AG09309	skin:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
30	CTCF	chr1:147172160-147172310	BE2_C	brain:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
31	CTCF	chr1:147172160-147172310	GM12878	blood:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
32	CTCF	chr1:147172482-147172492	NHEK	skin:	n/a	n/a
33	CTCF	chr1:147172120-147172270	HFF-Myc	foreskin:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
34	CTCF	chr1:147172240-147172390	AG04450	lung:	n/a	n/a
35	CTCF	chr1:147172089-147172405	Spleen_OC	spleen:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
36	CTCF	chr1:147172097-147172362	HepG2	liver:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
37	CTCF	chr1:147171720-147171870	HA-sp	spinal cord:	n/a	n/a
38	CTCF	chr1:147172114-147172397	ProgFib	skin:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
39	CTCF	chr1:147165971-147166098	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr1:147172151-147172349	GM20000	blood:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
41	CTCF	chr1:147172580-147172730	RPTEC	kidney:	n/a	n/a
42	CTCF	chr1:147172160-147172310	HCFaa	heart:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
43	CTCF	chr1:147172180-147172330	HRPEpiC	eye:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
44	CTCF	chr1:147165980-147166130	HMEC	breast:	n/a	n/a
45	CTCF	chr1:147172180-147172330	HEK293	kidney:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
46	CTCF	chr1:147172180-147172330	GM12870	blood:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
47	CTCF	chr1:147172200-147172350	HRPEpiC	eye:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
48	CTCF	chr1:147171982-147172457	HCT-116	colon:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
49	CTCF	chr1:147172160-147172310	AG04450	lung:	n/a	chr1:147172233-147172251 chr1:147172235-147172256
50	CTCF	chr1:147172180-147172330	WERI-Rb-1	eye:	n/a	chr1:147172233-147172251 chr1:147172235-147172256

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:147146108-147146158	T-47D	breast:	n/a
2	chr1:147146108-147146158	HPAEpiC	pulmonary alveolar:	n/a
3	chr1:147144052-147144102	Jurkat	blood:	n/a
4	chr1:147144052-147144102	AG10803	skin:	n/a
5	chr1:147146108-147146158	MCF10A-Er-Src	breast:	n/a
6	chr1:147144052-147144102	MCF-7	breast:	n/a
7	chr1:147146108-147146158	NHBE	bronchial:	n/a
8	chr1:147146108-147146158	HCM	heart:	n/a
9	chr1:147144052-147144102	HCF	heart:	n/a
10	chr1:147146108-147146158	Caco-2	colon:	n/a
11	chr1:147144052-147144102	HMEC	breast:	n/a
12	chr1:147146108-147146158	HAEpiC	amniotic membrane:	n/a
13	chr1:147144052-147144102	ProgFib	skin:	n/a
14	chr1:147146108-147146158	AG04449	skin:	fetal
15	chr1:147146108-147146158	ProgFib	skin:	n/a
16	chr1:147144052-147144102	HCM	heart:	n/a
17	chr1:147146108-147146158	ECC-1	luminal epithelium:	n/a
18	chr1:147144052-147144102	GM12878	blood:	n/a
19	chr1:147144052-147144102	IMR90	lung:	fetal
20	chr1:147144052-147144102	U87	brain:	n/a
21	chr1:147144052-147144102	PANC-1	pancreas:	n/a
22	chr1:147144052-147144102	HCPEpiC	choroid plexus:	n/a
23	chr1:147146108-147146158	HRCEpiC	kidney:	n/a
24	chr1:147144052-147144102	ECC-1	luminal epithelium:	n/a
25	chr1:147146108-147146158	AG04450	lung:	fetal
26	chr1:147146108-147146158	HMEC	breast:	n/a
27	chr1:147146108-147146158	PANC-1	pancreas:	n/a
28	chr1:147144052-147144102	Hela-S3	cervix:	n/a
29	chr1:147146108-147146158	HUVEC	blood vessel:	n/a
30	chr1:147144052-147144102	AG04450	lung:	fetal
31	chr1:147144052-147144102	PrEC	prostate:	n/a
32	chr1:147146108-147146158	U87	brain:	n/a
33	chr1:147146108-147146158	AoSMC	blood vessel:	n/a
34	chr1:147144052-147144102	AG04449	skin:	fetal
35	chr1:147146108-147146158	SK-N-SH	brain:	n/a
36	chr1:147144052-147144102	SAEC	small airway:	n/a
37	chr1:147144052-147144102	K562	blood:	n/a
38	chr1:147146108-147146158	NH-A	brain:	n/a
39	chr1:147144052-147144102	HIPEpiC	eye:	n/a
40	chr1:147146108-147146158	AG09319	gingival:	n/a
41	chr1:147144052-147144102	MCF10A-Er-Src	breast:	n/a
42	chr1:147146108-147146158	HNPCEpiC	eye:	n/a
43	chr1:147146108-147146158	AG09309	skin:	n/a
44	chr1:147146108-147146158	HepG2	liver:	n/a
45	chr1:147146108-147146158	GM12892	blood:	n/a
46	chr1:147144052-147144102	HL-60	blood:	n/a
47	chr1:147144052-147144102	HEEpiC	esophagus:	n/a
48	chr1:147146108-147146158	GM12878	blood:	n/a
49	chr1:147146108-147146158	IMR90	lung:	fetal
50	chr1:147146108-147146158	NT2-D1	testis:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:147161905..147163561-chr1:147163570..147165401,2	MCF-7	breast:
2	chr1:147147634..147149833-chr1:147151618..147153954,3	MCF-7	breast:
3	chr1:147170971..147171789-chr1:147362560..147363129,2	MCF-7	breast:
4	chr1:147117692..147123079-chr1:147140177..147144336,6	MCF-7	breast:
5	chr1:147166855..147168994-chr1:147171581..147173810,2	MCF-7	breast:
6	chr1:147112261..147114414-chr1:147171374..147172710,13	MCF-7	breast:
7	chr1:146966531..146967185-chr1:147171603..147172737,5	MCF-7	breast:
8	chr1:147161905..147163561-chr1:147163570..147165401,2	MCF-7	breast:
9	chr1:147141877..147143649-chr1:147185214..147187551,2	MCF-7	breast:
10	chr1:147070814..147072677-chr1:147153568..147155234,2	MCF-7	breast:
11	chr1:147113548..147114186-chr1:147171660..147172586,3	MCF-7	breast:
12	chr1:147171806..147172479-chr11:131293629..131294129,2	MCF-7	breast:
13	chr1:147147058..147150070-chr1:147171054..147173663,4	MCF-7	breast:
14	chr1:147111649..147114275-chr1:147172459..147174573,2	MCF-7	breast:
15	chr1:147140560..147142453-chr1:147171932..147174495,4	MCF-7	breast:
16	chr1:147137432..147138178-chr1:147171799..147172305,2	MCF-7	breast:
17	chr1:147147327..147149122-chr1:147153111..147156100,2	MCF-7	breast:
18	chr1:147147058..147150070-chr1:147171054..147173663,4	MCF-7	breast:
19	chr1:147110556..147114398-chr1:147147907..147150571,4	MCF-7	breast:
20	chr1:147168228..147170950-chr1:147171328..147174157,2	K562	blood:
21	chr1:147146897..147149618-chr1:147162782..147165410,2	MCF-7	breast:
22	chr1:147145076..147146578-chr1:147155568..147158263,2	MCF-7	breast:
23	chr1:147166855..147168994-chr1:147171581..147173810,2	MCF-7	breast:
24	chr1:147171855..147172726-chr1:147363952..147364477,2	MCF-7	breast:
25	chr1:147140871..147143916-chr1:147171046..147173260,3	MCF-7	breast:
26	chr1:147146472..147149099-chr1:147166493..147169316,2	MCF-7	breast:
27	chr1:147146897..147149618-chr1:147162782..147165410,2	MCF-7	breast:
28	chr1:147171861..147172372-chr1:147364428..147364944,2	MCF-7	breast:
29	chr1:147153898..147154477-chr20:52555683..52556390,2	MCF-7	breast:
30	chr1:147144341..147147074-chr1:147149551..147151735,2	K562	blood:
31	chr1:147147327..147149122-chr1:147153111..147156100,2	MCF-7	breast:
32	chr1:147141080..147150089-chr1:147182806..147195488,19	MCF-7	breast:
33	chr1:147150082..147152712-chr1:147162501..147165490,3	MCF-7	breast:
34	chr1:147137689..147138269-chr1:147171665..147172341,3	MCF-7	breast:
35	chr1:147119055..147120579-chr1:147144435..147146976,2	MCF-7	breast:
36	chr1:147146472..147149099-chr1:147166493..147169316,2	MCF-7	breast:
37	chr1:147126285..147129281-chr1:147147303..147149764,2	MCF-7	breast:
38	chr1:147147634..147149833-chr1:147151618..147153954,3	MCF-7	breast:
39	chr1:147171945..147172815-chr1:147362037..147362997,6	MCF-7	breast:
40	chr1:147145076..147146578-chr1:147155568..147158263,2	MCF-7	breast:
41	chr1:147112629..147113302-chr1:147171801..147172749,4	MCF-7	breast:
42	chr1:147150082..147152712-chr1:147162501..147165490,3	MCF-7	breast:
43	chr1:147172045..147172666-chr1:147364545..147365473,2	MCF-7	breast:
44	chr1:147144341..147147074-chr1:147149551..147151735,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BCL9-3	chr1:147161375-147161681	NONHSAT006039
2	lnc-BCL9-1	chr1:147169914-147169969	XLOC_000386
3	lnc-BCL9-1	chr1:147171072-147171461	XLOC_000386

No data

Variant related genes	Relation type
ACP6	TF binding region
ENSG00000227139	TF binding region
RN7SL261P	TF binding region
ACP6	CpG island
ENSG00000227139	CpG island
RN7SL261P	CpG island
ENSG00000116128	chromatin interactions
ENSG00000227139	chromatin interactions
ENSG00000162836	chromatin interactions
CDK14	miRNA target sites
CDK13	miRNA target sites

Extended variants
information (count: 751 )
Associated
traits (count: 145 )

Variant overlapped rSNPs/rCNVs (count:751 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17160530	chr1:147143887-147143888	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs587631907	chr1:147143920-147143921	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs587681304	chr1:147143931-147143932	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs113431390	chr1:147143950-147143951	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs587747070	chr1:147143951-147143952	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs587620517	chr1:147143961-147143962	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs587702291	chr1:147144035-147144036	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs12119687	chr1:147144053-147144054	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs7521629	chr1:147144127-147144128	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs376510324	chr1:147144137-147144138	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs370273431	chr1:147144140-147144141	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs7535145	chr1:147144228-147144229	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs7530666	chr1:147144260-147144261	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs188767443	chr1:147144274-147144275	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs587744591	chr1:147144303-147144304	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs181908646	chr1:147144333-147144334	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs114509078	chr1:147144340-147144341	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs142191471	chr1:147144341-147144342	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs7521822	chr1:147144364-147144365	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs35870345	chr1:147144366-147144367	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs34694375	chr1:147144384-147144385	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs587659996	chr1:147144474-147144475	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs373828604	chr1:147144477-147144478	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs146366149	chr1:147144489-147144490	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs4950467	chr1:147144592-147144593	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs72700360	chr1:147144639-147144640	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs187631434	chr1:147144687-147144688	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs587603986	chr1:147144757-147144758	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs117540534	chr1:147144764-147144765	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs587746848	chr1:147144850-147144851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs587622514	chr1:147144865-147144866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs587704150	chr1:147144898-147144899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs587737059	chr1:147144922-147144923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs587613787	chr1:147144943-147144944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs587687232	chr1:147144973-147144974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs116292306	chr1:147144992-147144993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs587641402	chr1:147145004-147145005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191945450	chr1:147145009-147145010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs150066520	chr1:147145020-147145021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs11803092	chr1:147145068-147145069	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs587660355	chr1:147145106-147145107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs587740020	chr1:147145144-147145145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs587598183	chr1:147145147-147145148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs587652588	chr1:147145163-147145164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs4430387	chr1:147145180-147145181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs182953652	chr1:147145202-147145203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185882526	chr1:147145206-147145207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs145393543	chr1:147145208-147145209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs587747128	chr1:147145271-147145272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs587604972	chr1:147145294-147145295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:145)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Tetralogy of Fallot	22912587	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Lung squamous cell carcinoma	20842114	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20369283	CNVD
Oral cancer	21386901	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Pancreatic cancer	17952125	CNVD
Obesity	21131291	CNVD

Chromatin state (count:201 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:147143000-147147400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:147143000-147147400	Weak transcription	HSMM	muscle
3	chr1:147143200-147144000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr1:147143200-147144000	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr1:147143200-147144200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr1:147143200-147144200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr1:147143200-147144200	Weak transcription	Osteobl	bone
8	chr1:147143200-147144400	Enhancers	K562	blood
9	chr1:147143200-147145000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr1:147143200-147146600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr1:147143200-147147000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr1:147143200-147147200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:147143200-147147200	Weak transcription	HUVEC	blood vessel
14	chr1:147143200-147147400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr1:147143200-147147400	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr1:147143200-147147400	Weak transcription	HMEC	breast
17	chr1:147143200-147147800	Weak transcription	NH-A	brain
18	chr1:147143200-147148000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr1:147143200-147148000	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr1:147143200-147148200	Weak transcription	A549	lung
21	chr1:147143200-147148800	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr1:147143400-147144400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr1:147143400-147147000	Weak transcription	Hela-S3	cervix
24	chr1:147143800-147144600	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr1:147143800-147147400	Weak transcription	HepG2	liver
26	chr1:147144000-147144200	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr1:147144000-147144400	Enhancers	H9 Cell Line	embryonic stem cell
28	chr1:147144200-147144400	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr1:147144200-147144600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr1:147144200-147144600	Enhancers	Osteobl	bone
31	chr1:147144200-147147000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr1:147144600-147147000	Weak transcription	Osteobl	bone
33	chr1:147145000-147146200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr1:147146200-147147800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr1:147146600-147149000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr1:147147000-147147200	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr1:147147000-147149200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr1:147147000-147149400	Enhancers	Hela-S3	cervix
39	chr1:147147000-147149400	Enhancers	Osteobl	bone
40	chr1:147147200-147147800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr1:147147200-147149200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr1:147147200-147149400	Enhancers	HUVEC	blood vessel
43	chr1:147147400-147148400	Enhancers	Muscle Satellite Cultured Cells	--
44	chr1:147147400-147149000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr1:147147400-147149200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr1:147147400-147149200	Enhancers	HMEC	breast
47	chr1:147147400-147149200	Enhancers	HSMM	muscle
48	chr1:147147400-147149400	Enhancers	HepG2	liver
49	chr1:147147800-147148000	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr1:147147800-147148400	Enhancers	NH-A	brain

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