Variant report

Variant	nsv1027981
Chromosome Location	chr7:112577657-112613212
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:655)
CpG islands
(count:672)
Chromatin interactive
region (count:26)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:655 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:112579802-112580571	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:112578133-112578400	HepG2	liver:	n/a	n/a
3	ATF1	chr7:112579830-112580980	K562	blood:	n/a	n/a
4	ATF1	chr7:112599838-112599896	K562	blood:	n/a	n/a
5	ATF1	chr7:112610852-112610969	K562	blood:	n/a	n/a
6	ATF1	chr7:112591210-112591392	K562	blood:	n/a	n/a
7	ATF2	chr7:112580038-112580496	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr7:112579800-112580535	GM12878	blood:	n/a	n/a
9	ATF3	chr7:112580043-112580580	K562	blood:	n/a	chr7:112580257-112580270
10	BHLHE40	chr7:112579032-112579293	K562	blood:	n/a	n/a
11	BHLHE40	chr7:112579184-112579293	GM12878	blood:	n/a	n/a
12	BHLHE40	chr7:112579659-112580648	GM12878	blood:	n/a	n/a
13	BHLHE40	chr7:112579565-112580648	K562	blood:	n/a	n/a
14	CBX3	chr7:112579913-112580953	K562	blood:	n/a	n/a
15	CBX3	chr7:112579498-112580946	K562	blood:	n/a	n/a
16	CCNT2	chr7:112579172-112580391	K562	blood:	n/a	chr7:112579458-112579467 chr7:112579397-112579406
17	CEBPB	chr7:112581584-112581784	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:112580045-112580514	K562	blood:	n/a	n/a
19	CEBPB	chr7:112607411-112607467	K562	blood:	n/a	n/a
20	CEBPB	chr7:112579965-112580122	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr7:112607905-112608244	K562	blood:	n/a	n/a
22	CEBPB	chr7:112607909-112608293	K562	blood:	n/a	n/a
23	CEBPB	chr7:112607913-112608165	K562	blood:	n/a	n/a
24	CEBPB	chr7:112598065-112598107	HepG2	liver:	n/a	n/a
25	CEBPB	chr7:112579977-112580010	A549	lung:	n/a	n/a
26	CEBPD	chr7:112580088-112580457	HepG2	liver:	n/a	n/a
27	CEBPD	chr7:112579622-112579996	HepG2	liver:	n/a	n/a
28	CHD1	chr7:112579462-112579597	GM12878	blood:	n/a	n/a
29	CHD1	chr7:112579250-112579700	H1-hESC	embryonic stem cell:	n/a	chr7:112579459-112579469
30	CHD1	chr7:112580191-112580486	GM12878	blood:	n/a	n/a
31	CHD2	chr7:112579621-112580347	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr7:112579811-112580620	K562	blood:	n/a	n/a
33	CHD2	chr7:112579214-112580775	GM12878	blood:	n/a	chr7:112579459-112579469
34	CHD2	chr7:112579591-112580402	HepG2	liver:	n/a	n/a
35	CHD2	chr7:112579799-112580440	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr7:112579684-112580648	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr7:112579759-112581102	K562	blood:	n/a	n/a
38	CREB1	chr7:112579538-112580681	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr7:112579464-112580650	GM12878	blood:	n/a	n/a
40	CREB1	chr7:112579385-112580823	K562	blood:	n/a	n/a
41	CREB1	chr7:112579684-112580483	A549	lung:	n/a	n/a
42	CREB1	chr7:112579519-112580715	HepG2	liver:	n/a	n/a
43	CTCF	chr7:112610940-112611090	GM12864	blood:	n/a	n/a
44	CTCF	chr7:112610940-112611090	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr7:112579612-112579706	GM12892	blood:	n/a	n/a
46	CTCF	chr7:112610900-112611050	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr7:112610980-112611130	HMEC	breast:	n/a	n/a
48	CTCF	chr7:112610960-112611110	GM12874	blood:	n/a	n/a
49	CTCF	chr7:112610920-112611070	HCT-116	colon:	n/a	n/a
50	CTCF	chr7:112611000-112611150	A549	lung:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:112580216-112580266	HAEpiC	amniotic membrane:	n/a
2	chr7:112580216-112580266	HAEpiC	amniotic membrane:	n/a
3	chr7:112579992-112580042	T-47D	breast:	n/a
4	chr7:112582716-112582766	SK-N-MC	brain:	n/a
5	chr7:112582716-112582766	ovcar-3	ovarian:	n/a
6	chr7:112579757-112579807	Hela-S3	cervix:	n/a
7	chr7:112580216-112580266	HRE	kidney:	n/a
8	chr7:112579509-112579559	HIPEpiC	eye:	n/a
9	chr7:112580077-112580127	GM06990	blood:	n/a
10	chr7:112579757-112579807	SAEC	small airway:	n/a
11	chr7:112580216-112580266	AoSMC	blood vessel:	n/a
12	chr7:112579927-112579977	HPAEpiC	pulmonary alveolar:	n/a
13	chr7:112582716-112582766	Hela-S3	cervix:	n/a
14	chr7:112579509-112579559	IMR90	lung:	fetal
15	chr7:112579137-112579187	HEEpiC	esophagus:	n/a
16	chr7:112580528-112580578	NHDF-neo	bronchial:	n/a
17	chr7:112579509-112579559	SK-N-MC	brain:	n/a
18	chr7:112579998-112580048	NT2-D1	testis:	n/a
19	chr7:112579137-112579187	HL-60	blood:	n/a
20	chr7:112579927-112579977	HEEpiC	esophagus:	n/a
21	chr7:112580305-112580355	Caco-2	colon:	n/a
22	chr7:112579509-112579559	HEEpiC	esophagus:	n/a
23	chr7:112580077-112580127	Caco-2	colon:	n/a
24	chr7:112579137-112579187	HCPEpiC	choroid plexus:	n/a
25	chr7:112579998-112580048	ECC-1	luminal epithelium:	n/a
26	chr7:112580216-112580266	AG09309	skin:	n/a
27	chr7:112582716-112582766	HCPEpiC	choroid plexus:	n/a
28	chr7:112580216-112580266	HCM	heart:	n/a
29	chr7:112579927-112579977	AG04450	lung:	fetal
30	chr7:112579927-112579977	HCPEpiC	choroid plexus:	n/a
31	chr7:112580077-112580127	T-47D	breast:	n/a
32	chr7:112580305-112580355	RPTEC	kidney:	n/a
33	chr7:112582716-112582766	HL-60	blood:	n/a
34	chr7:112580077-112580127	Hela-S3	cervix:	n/a
35	chr7:112580216-112580266	PFSK-1	brain:	n/a
36	chr7:112582716-112582766	AG09309	skin:	n/a
37	chr7:112579992-112580042	LNCaP	prostate:	n/a
38	chr7:112579509-112579559	SK-N-SH	brain:	n/a
39	chr7:112582716-112582766	Caco-2	colon:	n/a
40	chr7:112580077-112580127	GM19239	blood:	n/a
41	chr7:112579757-112579807	Jurkat	blood:	n/a
42	chr7:112580077-112580127	ProgFib	skin:	n/a
43	chr7:112579509-112579559	HUVEC	blood vessel:	n/a
44	chr7:112580305-112580355	BE2_C	brain:	n/a
45	chr7:112579137-112579187	A549	lung:	n/a
46	chr7:112580216-112580266	HUVEC	blood vessel:	n/a
47	chr7:112580077-112580127	NH-A	brain:	n/a
48	chr7:112580216-112580266	HEK293	kidney:	embryo
49	chr7:112579927-112579977	AG09319	gingival:	n/a
50	chr7:112579992-112580042	GM12892	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:129642024..129642655-chr7:112579975..112580488,2	MCF-7	breast:
2	chr7:112578366..112581242-chr7:112590311..112591816,2	MCF-7	breast:
3	chr7:112580392..112582093-chr7:112599898..112601408,2	MCF-7	breast:
4	chr7:112428924..112430644-chr7:112579193..112581843,2	K562	blood:
5	chr7:112608892..112612012-chr7:112612504..112614943,3	MCF-7	breast:
6	chr7:112578476..112580812-chr7:112583356..112586040,2	MCF-7	breast:
7	chr7:112578925..112581917-chr7:112594123..112596440,2	MCF-7	breast:
8	chr7:112601365..112604036-chr7:112606772..112610926,4	K562	blood:
9	chr7:112583353..112585564-chr7:112597999..112600804,2	MCF-7	breast:
10	chr7:112602086..112604534-chr7:112611738..112613298,2	K562	blood:
11	chr7:112574893..112577839-chr7:112578042..112580398,5	K562	blood:
12	chr7:112605934..112608716-chr7:112610889..112612705,2	K562	blood:
13	chr7:112577667..112580375-chr7:112582881..112584475,2	MCF-7	breast:
14	chr7:112430077..112432189-chr7:112593600..112595306,2	MCF-7	breast:
15	chr7:112605934..112608716-chr7:112610889..112612705,2	K562	blood:
16	chr7:112579376..112581874-chr7:112583714..112588388,6	K562	blood:
17	chr7:112569158..112571513-chr7:112600317..112602732,2	MCF-7	breast:
18	chr7:112442436..112445188-chr7:112575668..112578638,2	K562	blood:
19	chr7:112477234..112479370-chr7:112580510..112582070,2	K562	blood:
20	chr7:112602086..112604534-chr7:112611738..112613298,2	K562	blood:
21	chr7:112601365..112604036-chr7:112606772..112610926,4	K562	blood:
22	chr7:112609190..112612964-chr7:112622640..112627113,4	K562	blood:
23	chr7:112583353..112585564-chr7:112597999..112600804,2	MCF-7	breast:
24	chr7:112608892..112612012-chr7:112612504..112614943,3	MCF-7	breast:
25	chr7:112580392..112582093-chr7:112599898..112601408,2	MCF-7	breast:
26	chr7:112579425..112581874-chr7:112585299..112587492,4	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C7orf60-1	chr7:112593368-112593811	NONHSAT122804
2	lnc-C7orf60-1	chr7:112593368-112593811	NONHSAT122806
3	lnc-C7orf60-1	chr7:112596577-112596766	NONHSAT122806
4	lnc-C7orf60-1	chr7:112596577-112596766	NONHSAT122804
5	lnc-C7orf60-1	chr7:112594718-112594823	NONHSAT122808
6	lnc-C7orf60-1	chr7:112594658-112594823	NONHSAT122804
7	lnc-C7orf60-1	chr7:112593368-112593811	NONHSAT122805
8	lnc-C7orf60-1	chr7:112596577-112596757	ENSG00000234520
9	lnc-C7orf60-1	chr7:112594690-112594823	NR_110162
10	lnc-C7orf60-1	chr7:112594658-112594823	NONHSAT122805
11	lnc-C7orf60-1	chr7:112594701-112594823	ENSG00000234520
12	lnc-C7orf60-1	chr7:112593368-112593811	NONHSAT122803
13	lnc-C7orf60-1	chr7:112596577-112596766	NONHSAT122805
14	lnc-C7orf60-1	chr7:112594658-112594823	NONHSAT122803
15	lnc-C7orf60-1	chr7:112596577-112596768	NONHSAT122808
16	lnc-C7orf60-1	chr7:112594658-112594823	NONHSAT122806
17	lnc-C7orf60-1	chr7:112596577-112596757	NR_110162
18	lnc-C7orf60-1	chr7:112596577-112596757	NONHSAT122803

No data

Variant related genes	Relation type
C7orf60	TF binding region
C7orf60	CpG island
ENSG00000146802	chromatin interactions
ENSG00000164603	chromatin interactions

Extended variants
information (count: 1167 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1167 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192739636	chr7:112577697-112577698	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs578119141	chr7:112577707-112577708	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs73718135	chr7:112577752-112577753	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs545159833	chr7:112577764-112577765	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs184168242	chr7:112577819-112577820	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs189945248	chr7:112577821-112577822	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs543011130	chr7:112577865-112577866	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs561592108	chr7:112577931-112577932	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs144999369	chr7:112577955-112577956	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs368894970	chr7:112577998-112577999	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs142209880	chr7:112578047-112578048	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs571740326	chr7:112578088-112578089	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs113652487	chr7:112578125-112578126	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs538516445	chr7:112578135-112578136	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs562675064	chr7:112578148-112578149	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs73718136	chr7:112578163-112578164	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs536662880	chr7:112578291-112578292	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554913218	chr7:112578322-112578323	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567248945	chr7:112578387-112578388	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534587652	chr7:112578426-112578427	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs114826451	chr7:112578430-112578431	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs577756458	chr7:112578453-112578454	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs369233241	chr7:112578535-112578536	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs545150341	chr7:112578549-112578550	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs181208392	chr7:112578550-112578551	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs575782989	chr7:112578576-112578577	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs184464280	chr7:112578594-112578595	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs147785116	chr7:112578613-112578614	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs552031046	chr7:112578629-112578630	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs528836758	chr7:112578672-112578673	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs66988577	chr7:112578675-112578676	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs565526713	chr7:112578684-112578685	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs538235397	chr7:112578701-112578702	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs141248816	chr7:112578706-112578707	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538849026	chr7:112578732-112578733	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs554669606	chr7:112578750-112578751	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs143426621	chr7:112578760-112578761	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs147989686	chr7:112578762-112578763	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs548602163	chr7:112578775-112578776	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs566911622	chr7:112578795-112578796	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs534644846	chr7:112578810-112578811	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552992796	chr7:112578836-112578837	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571488304	chr7:112578985-112578986	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs28722087	chr7:112579002-112579003	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs141990805	chr7:112579003-112579004	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199884920	chr7:112579018-112579019	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188909016	chr7:112579073-112579074	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs28560010	chr7:112579135-112579136	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs555049139	chr7:112579145-112579146	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573277681	chr7:112579155-112579156	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21248843	CNVD

Chromatin state (count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:112541400-112578800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:112551600-112578600	Weak transcription	Fetal Muscle Trunk	muscle
3	chr7:112551600-112579400	Weak transcription	Spleen	Spleen
4	chr7:112553800-112578800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr7:112555400-112578000	Weak transcription	Adipose Nuclei	Adipose
6	chr7:112557000-112578600	Weak transcription	Primary B cells from peripheral blood	blood
7	chr7:112563200-112578200	Weak transcription	HUVEC	blood vessel
8	chr7:112565200-112578600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr7:112568400-112578200	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr7:112570400-112578400	Weak transcription	NH-A	brain
11	chr7:112571200-112577800	Weak transcription	Thymus	Thymus
12	chr7:112571200-112577800	Weak transcription	K562	blood
13	chr7:112571200-112578200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr7:112571200-112578200	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr7:112571400-112578800	Weak transcription	Psoas Muscle	Psoas
16	chr7:112571600-112578200	Weak transcription	Fetal Muscle Leg	muscle
17	chr7:112571600-112578200	Weak transcription	Rectal Smooth Muscle	rectum
18	chr7:112571600-112578800	Weak transcription	Small Intestine	intestine
19	chr7:112571800-112578200	Weak transcription	Brain Substantia Nigra	brain
20	chr7:112572200-112578400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr7:112573200-112578200	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr7:112573200-112578200	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr7:112573200-112578800	Weak transcription	Primary T cells fromperipheralblood	blood
24	chr7:112573200-112578800	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr7:112573400-112578200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr7:112573800-112578400	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr7:112574000-112578200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr7:112574000-112578200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr7:112574600-112577800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr7:112575200-112578200	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr7:112575600-112578600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr7:112575600-112579200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr7:112575800-112578000	Active TSS	GM12878-XiMat	blood
34	chr7:112575800-112578800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr7:112576000-112578600	Weak transcription	Placenta	Placenta
36	chr7:112576200-112577800	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr7:112576200-112578200	Enhancers	Primary T killer memory cells from peripheral blood	blood
38	chr7:112576200-112578600	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr7:112576200-112578600	Enhancers	Primary T helper cells fromperipheralblood	blood
40	chr7:112576400-112578200	Enhancers	Fetal Heart	heart
41	chr7:112576400-112578200	Enhancers	Fetal Intestine Small	intestine
42	chr7:112576400-112578200	Enhancers	Fetal Lung	lung
43	chr7:112576400-112578600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr7:112576400-112578800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr7:112576600-112578200	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr7:112576600-112578200	Enhancers	Fetal Intestine Large	intestine
47	chr7:112576600-112578400	Enhancers	Primary T helper naive cells from peripheral blood	blood
48	chr7:112576600-112578400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr7:112576600-112578600	Weak transcription	Ovary	ovary
50	chr7:112576600-112578800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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