Variant report

Variant	nsv888765
Chromosome Location	chr7:97834386-97853184
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:379)
CpG islands
(count:2259)
Chromatin interactive
region (count:28)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:379 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:97841106-97841413	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:97847663-97847944	K562	blood:	n/a	n/a
3	ATF2	chr7:97848596-97849007	GM12878	blood:	n/a	n/a
4	ATF2	chr7:97849099-97849509	GM12878	blood:	n/a	n/a
5	ATF3	chr7:97841200-97841340	K562	blood:	n/a	n/a
6	BACH1	chr7:97839948-97840290	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:97840715-97840870	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr7:97848680-97848997	GM12878	blood:	n/a	n/a
9	BATF	chr7:97848653-97849003	GM12878	blood:	n/a	n/a
10	BCLAF1	chr7:97848668-97849063	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:97846978-97847938	K562	blood:	n/a	chr7:97847399-97847415
12	BHLHE40	chr7:97848682-97848872	GM12878	blood:	n/a	n/a
13	BHLHE40	chr7:97843618-97843621	K562	blood:	n/a	n/a
14	BHLHE40	chr7:97849181-97849480	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:97841083-97841121	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:97840950-97841274	K562	blood:	n/a	n/a
17	BHLHE40	chr7:97840739-97841503	HepG2	liver:	n/a	n/a
18	BRCA1	chr7:97841048-97841415	HepG2	liver:	n/a	n/a
19	CBX3	chr7:97847579-97847944	K562	blood:	n/a	n/a
20	CCNT2	chr7:97835012-97835236	K562	blood:	n/a	n/a
21	CCNT2	chr7:97841471-97841671	K562	blood:	n/a	n/a
22	CCNT2	chr7:97840716-97841121	K562	blood:	n/a	n/a
23	CCNT2	chr7:97847291-97847938	K562	blood:	n/a	n/a
24	CEBPB	chr7:97841211-97841387	HepG2	liver:	n/a	n/a
25	CEBPB	chr7:97849858-97849970	K562	blood:	n/a	n/a
26	CEBPB	chr7:97847691-97847919	K562	blood:	n/a	n/a
27	CHD2	chr7:97839942-97840021	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr7:97840957-97841477	HepG2	liver:	n/a	n/a
29	CHD2	chr7:97844910-97845001	HepG2	liver:	n/a	n/a
30	CHD2	chr7:97844264-97844285	HepG2	liver:	n/a	n/a
31	CTCF	chr7:97840565-97840717	HepG2	liver:	n/a	chr7:97840589-97840599
32	CTCF	chr7:97841157-97841208	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr7:97841217-97841244	GM12891	blood:	n/a	n/a
34	CTCF	chr7:97841120-97841270	HepG2	liver:	n/a	n/a
35	CTCF	chr7:97847719-97847901	K562	blood:	n/a	n/a
36	CUX1	chr7:97847776-97847811	GM12878	blood:	n/a	n/a
37	CUX1	chr7:97847587-97848108	K562	blood:	n/a	n/a
38	CUX1	chr7:97848816-97848871	GM12878	blood:	n/a	n/a
39	E2F6	chr7:97847207-97847342	K562	blood:	n/a	n/a
40	E2F6	chr7:97840978-97841208	K562	blood:	n/a	n/a
41	EBF1	chr7:97849175-97849368	GM12878	blood:	n/a	n/a
42	EBF1	chr7:97847550-97847822	GM12878	blood:	n/a	n/a
43	EGR1	chr7:97840946-97841568	K562	blood:	n/a	chr7:97841382-97841391 chr7:97841378-97841393 chr7:97841380-97841391 chr7:97841379-97841392 chr7:97841379-97841393 chr7:97841379-97841392
44	EGR1	chr7:97840917-97841582	MCF-7	breast:	n/a	chr7:97841382-97841391 chr7:97841378-97841393 chr7:97841380-97841391 chr7:97841379-97841392 chr7:97841379-97841393 chr7:97841379-97841392
45	EGR1	chr7:97847592-97847934	K562	blood:	n/a	n/a
46	EGR1	chr7:97840998-97841531	K562	blood:	n/a	chr7:97841382-97841391 chr7:97841378-97841393 chr7:97841380-97841391 chr7:97841379-97841392 chr7:97841379-97841393 chr7:97841379-97841392
47	ELF1	chr7:97847495-97847907	K562	blood:	n/a	chr7:97847724-97847737
48	ELK1	chr7:97847654-97847764	K562	blood:	n/a	n/a
49	EP300	chr7:97848779-97849388	GM12878	blood:	n/a	n/a
50	EP300	chr7:97840895-97841575	HepG2	liver:	n/a	chr7:97841309-97841318 chr7:97841308-97841317

(count:2259 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:97846357-97846407	ovcar-3	ovarian:	n/a
2	chr7:97842268-97842318	HCPEpiC	choroid plexus:	n/a
3	chr7:97846357-97846407	ovcar-3	ovarian:	n/a
4	chr7:97842268-97842318	HCPEpiC	choroid plexus:	n/a
5	chr7:97841440-97841490	Hepatocyte	liver:	n/a
6	chr7:97838735-97838785	IMR90	lung:	fetal
7	chr7:97852022-97852072	PrEC	prostate:	n/a
8	chr7:97837957-97838007	NB4	blood:	n/a
9	chr7:97846357-97846407	NHBE	bronchial:	n/a
10	chr7:97841001-97841051	GM12891	blood:	n/a
11	chr7:97841864-97841914	HCF	heart:	n/a
12	chr7:97841001-97841051	HCT-116	colon:	n/a
13	chr7:97834891-97834941	HEK293	kidney:	embryo
14	chr7:97838735-97838785	HAEpiC	amniotic membrane:	n/a
15	chr7:97846988-97847038	Jurkat	blood:	n/a
16	chr7:97844473-97844523	HCF	heart:	n/a
17	chr7:97841941-97841991	AoSMC	blood vessel:	n/a
18	chr7:97844910-97844960	SK-N-SH	brain:	n/a
19	chr7:97852022-97852072	HRCEpiC	kidney:	n/a
20	chr7:97834674-97834724	AG09309	skin:	n/a
21	chr7:97840014-97840064	AG04449	skin:	fetal
22	chr7:97840113-97840163	HMEC	breast:	n/a
23	chr7:97846790-97846840	AG04450	lung:	fetal
24	chr7:97840113-97840163	H1-hESC	embryonic stem cell:	embryo
25	chr7:97844473-97844523	HCM	heart:	n/a
26	chr7:97834623-97834673	HCM	heart:	n/a
27	chr7:97838663-97838713	SKMC	muscle:	n/a
28	chr7:97834674-97834724	GM19239	blood:	n/a
29	chr7:97834623-97834673	AoSMC	blood vessel:	n/a
30	chr7:97834891-97834941	T-47D	breast:	n/a
31	chr7:97836563-97836613	AG09319	gingival:	n/a
32	chr7:97838735-97838785	HMEC	breast:	n/a
33	chr7:97844947-97844997	AG10803	skin:	n/a
34	chr7:97841334-97841384	HUVEC	blood vessel:	n/a
35	chr7:97838659-97838709	GM12892	blood:	n/a
36	chr7:97835841-97835891	PANC-1	pancreas:	n/a
37	chr7:97841001-97841051	NB4	blood:	n/a
38	chr7:97838659-97838709	HMEC	breast:	n/a
39	chr7:97841334-97841384	Caco-2	colon:	n/a
40	chr7:97844947-97844997	IMR90	lung:	fetal
41	chr7:97841334-97841384	HRCEpiC	kidney:	n/a
42	chr7:97840113-97840163	PANC-1	pancreas:	n/a
43	chr7:97834623-97834673	Hepatocyte	liver:	n/a
44	chr7:97841502-97841552	NHDF-neo	bronchial:	n/a
45	chr7:97852022-97852072	SAEC	small airway:	n/a
46	chr7:97836563-97836613	SK-N-SH_RA	brain:	n/a
47	chr7:97834674-97834724	GM12878	blood:	n/a
48	chr7:97841071-97841121	HUVEC	blood vessel:	n/a
49	chr7:97841502-97841552	NH-A	brain:	n/a
50	chr7:97841941-97841991	AG09319	gingival:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:97843013..97845825-chr7:97853837..97855430,2	MCF-7	breast:
2	chr7:97840856..97842377-chr7:97845637..97848224,2	MCF-7	breast:
3	chr7:97842812..97845120-chr7:97865672..97868033,2	K562	blood:
4	chr7:97844672..97846998-chr7:97849549..97852989,3	K562	blood:
5	chr7:97840856..97842377-chr7:97845637..97848224,2	MCF-7	breast:
6	chr7:97844651..97846802-chr7:97859229..97862130,2	MCF-7	breast:
7	chr7:97843965..97846398-chr7:97856911..97858412,2	K562	blood:
8	chr7:97852333..97858295-chr7:97859641..97865309,7	MCF-7	breast:
9	chr7:97848875..97850795-chr7:97850910..97852902,2	K562	blood:
10	chr7:97841230..97842751-chr7:97851743..97853660,2	K562	blood:
11	chr7:97840173..97842487-chr7:97845725..97848039,2	MCF-7	breast:
12	chr7:97829526..97831904-chr7:97833458..97836322,3	K562	blood:
13	chr7:97844457..97846470-chr7:97865336..97867376,2	MCF-7	breast:
14	chr7:97844672..97846262-chr7:97850164..97852989,2	K562	blood:
15	chr7:97845652..97847962-chr7:97851352..97854034,2	MCF-7	breast:
16	chr7:97845652..97847962-chr7:97851352..97854034,2	MCF-7	breast:
17	chr7:97839660..97842920-chr7:97872632..97874833,3	K562	blood:
18	chr7:97852038..97854221-chr7:97858720..97861626,2	K562	blood:
19	chr10:8099641..8101523-chr7:97840811..97843007,2	MCF-7	breast:
20	chr7:97839794..97841701-chr7:97843448..97845628,2	MCF-7	breast:
21	chr7:97834447..97836459-chr7:97921103..97922884,2	K562	blood:
22	chr7:97846624..97850033-chr7:97850682..97852457,3	MCF-7	breast:
23	chr7:97840173..97842487-chr7:97845725..97848039,2	MCF-7	breast:
24	chr7:97841230..97842751-chr7:97851743..97853660,2	K562	blood:
25	chr7:97847018..97848537-chr7:97878984..97881844,2	K562	blood:
26	chr7:97826253..97828518-chr7:97833038..97835255,2	K562	blood:
27	chr7:97846624..97850033-chr7:97850682..97852457,3	MCF-7	breast:
28	chr7:97851992..97854043-chr7:98027877..98030619,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BHLHA15-1	chr7:97841568-97841603	NONHSAT122177
2	lnc-BHLHA15-1	chr7:97842411-97844754	NONHSAT122177
3	lnc-BHLHA15-1	chr7:97840778-97840810	NONHSAT122177

No data

Variant related genes	Relation type
BHLHA15	TF binding region
TECPR1	TF binding region
BHLHA15	CpG island
TECPR1	CpG island
ENSG00000006453	chromatin interactions
ENSG00000180535	chromatin interactions
ENSG00000164713	chromatin interactions
ENSG00000205356	chromatin interactions
ENSG00000107485	chromatin interactions

Extended variants
information (count: 870 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:870 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17169440	chr7:97834386-97834387	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs558446965	chr7:97834401-97834402	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573601226	chr7:97834416-97834417	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540994159	chr7:97834465-97834466	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553038618	chr7:97834483-97834484	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574471200	chr7:97834568-97834569	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs181386986	chr7:97834624-97834625	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs541599627	chr7:97834646-97834647	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs563406479	chr7:97834673-97834674	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs530571878	chr7:97834686-97834687	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs111793232	chr7:97834697-97834698	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs35428901	chr7:97834704-97834705	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs144863486	chr7:97834734-97834735	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs369293299	chr7:97834751-97834752	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs372382281	chr7:97834790-97834791	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs139107740	chr7:97834801-97834802	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs562187963	chr7:97834817-97834818	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs375712279	chr7:97834822-97834823	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs370532122	chr7:97834824-97834825	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs376834738	chr7:97834827-97834828	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs546565959	chr7:97834833-97834834	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs568165039	chr7:97834865-97834866	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs529380796	chr7:97834906-97834907	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs149900508	chr7:97834913-97834914	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs146490139	chr7:97834967-97834968	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs539618085	chr7:97834994-97834995	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs369721658	chr7:97835017-97835018	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs558400597	chr7:97835066-97835067	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs567157180	chr7:97835070-97835071	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372338349	chr7:97835071-97835072	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs118058169	chr7:97835078-97835079	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574310549	chr7:97835087-97835088	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs541812536	chr7:97835114-97835115	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs140980138	chr7:97835132-97835133	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575310742	chr7:97835135-97835136	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs576760122	chr7:97835188-97835189	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544052221	chr7:97835189-97835190	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs563965608	chr7:97835241-97835242	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs377284122	chr7:97835256-97835257	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2291749	chr7:97835276-97835277	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs143489811	chr7:97835304-97835305	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562027927	chr7:97835377-97835378	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs367936182	chr7:97835379-97835380	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs529228733	chr7:97835627-97835628	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs2291748	chr7:97835640-97835641	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs117092885	chr7:97835695-97835696	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs533501638	chr7:97835763-97835764	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs551982900	chr7:97835766-97835767	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185085102	chr7:97835807-97835808	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs534400670	chr7:97835818-97835819	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myoclonus-dystonia	17898012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164920	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Chronic myeloid leukemia	21384125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:960 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97765800-97840800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:97782400-97839800	Weak transcription	Fetal Brain Male	brain
3	chr7:97793400-97841000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr7:97808600-97839800	Weak transcription	Right Atrium	heart
5	chr7:97812000-97841000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr7:97816000-97839200	Weak transcription	Psoas Muscle	Psoas
7	chr7:97816600-97839800	Weak transcription	NH-A	brain
8	chr7:97819200-97834800	Weak transcription	HUVEC	blood vessel
9	chr7:97822400-97841000	Weak transcription	K562	blood
10	chr7:97822800-97837600	Weak transcription	Fetal Kidney	kidney
11	chr7:97823000-97851000	Weak transcription	HSMMtube	muscle
12	chr7:97823800-97834400	Weak transcription	Brain Substantia Nigra	brain
13	chr7:97823800-97840000	Weak transcription	Small Intestine	intestine
14	chr7:97824000-97835600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr7:97824400-97834600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr7:97824400-97839800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr7:97824600-97839800	Weak transcription	Osteobl	bone
18	chr7:97824600-97840800	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr7:97824800-97834600	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr7:97824800-97834800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr7:97824800-97835000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr7:97824800-97839800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr7:97824800-97839800	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr7:97824800-97840000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr7:97825000-97835000	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr7:97825000-97836000	Weak transcription	Brain Angular Gyrus	brain
27	chr7:97825200-97835600	Weak transcription	Rectal Smooth Muscle	rectum
28	chr7:97825200-97851000	Weak transcription	Fetal Lung	lung
29	chr7:97825800-97835200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr7:97827200-97834400	Weak transcription	Left Ventricle	heart
31	chr7:97828800-97835200	Weak transcription	Hela-S3	cervix
32	chr7:97831600-97839200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr7:97831800-97837400	Strong transcription	Sigmoid Colon	Sigmoid Colon
34	chr7:97832000-97836600	Strong transcription	Rectal Mucosa Donor 31	rectum
35	chr7:97832000-97836800	Strong transcription	Fetal Muscle Trunk	muscle
36	chr7:97832000-97837400	Strong transcription	Fetal Stomach	stomach
37	chr7:97832000-97837800	Weak transcription	NHEK	skin
38	chr7:97832200-97836400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr7:97832200-97836600	Strong transcription	Fetal Muscle Leg	muscle
40	chr7:97832200-97836800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr7:97832200-97836800	Strong transcription	Stomach Smooth Muscle	stomach
42	chr7:97832200-97837600	Strong transcription	Liver	Liver
43	chr7:97832200-97837800	Strong transcription	Cortex derived primary cultured neurospheres	brain
44	chr7:97832200-97839200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr7:97832200-97839600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr7:97832200-97839600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr7:97832200-97840600	Weak transcription	HMEC	breast
48	chr7:97832400-97836800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr7:97832400-97836800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr7:97832400-97837200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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