Variant report

Variant	nsv888021
Chromosome Location	chr7:50538589-50610071
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1086)
CpG islands
(count:367)
Chromatin interactive
region (count:22)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1086 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:50549711-50549911	K562	blood:	n/a	n/a
2	ARID3A	chr7:50554248-50554550	K562	blood:	n/a	n/a
3	ARID3A	chr7:50596390-50596788	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:50602400-50602964	K562	blood:	n/a	n/a
5	ARID3A	chr7:50601744-50601799	K562	blood:	n/a	n/a
6	ARID3A	chr7:50564372-50565500	K562	blood:	n/a	n/a
7	ARID3A	chr7:50545345-50545545	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:50555462-50555572	K562	blood:	n/a	n/a
9	ATF1	chr7:50602377-50602983	K562	blood:	n/a	n/a
10	ATF1	chr7:50554229-50554572	K562	blood:	n/a	n/a
11	ATF1	chr7:50564633-50565134	K562	blood:	n/a	n/a
12	ATF3	chr7:50602543-50602989	K562	blood:	n/a	n/a
13	ATF3	chr7:50602445-50602991	A549	lung:	n/a	n/a
14	ATF3	chr7:50564692-50565091	K562	blood:	n/a	n/a
15	ATF3	chr7:50602433-50602845	K562	blood:	n/a	n/a
16	BACH1	chr7:50600585-50600588	K562	blood:	n/a	n/a
17	BACH1	chr7:50603356-50603556	K562	blood:	n/a	n/a
18	BACH1	chr7:50602290-50603057	K562	blood:	n/a	n/a
19	BACH1	chr7:50602473-50602960	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr7:50544710-50544993	K562	blood:	n/a	n/a
21	BATF	chr7:50599113-50599361	GM12878	blood:	n/a	chr7:50599217-50599228
22	BCL3	chr7:50602322-50603003	A549	lung:	n/a	chr7:50602744-50602753 chr7:50602767-50602776
23	BHLHE40	chr7:50601623-50602040	K562	blood:	n/a	n/a
24	BHLHE40	chr7:50569896-50570208	K562	blood:	n/a	n/a
25	BHLHE40	chr7:50564301-50564408	K562	blood:	n/a	n/a
26	BHLHE40	chr7:50564711-50565125	K562	blood:	n/a	n/a
27	BHLHE40	chr7:50560606-50560748	K562	blood:	n/a	n/a
28	BHLHE40	chr7:50545019-50545114	K562	blood:	n/a	n/a
29	BHLHE40	chr7:50576230-50576395	K562	blood:	n/a	n/a
30	BHLHE40	chr7:50602278-50602896	K562	blood:	n/a	n/a
31	BHLHE40	chr7:50603121-50603381	K562	blood:	n/a	n/a
32	BRCA1	chr7:50564843-50565049	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr7:50565585-50565895	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr7:50602435-50603426	Hela-S3	cervix:	n/a	n/a
35	CBX3	chr7:50564702-50565073	K562	blood:	n/a	n/a
36	CBX3	chr7:50581227-50581606	K562	blood:	n/a	n/a
37	CBX3	chr7:50564657-50565085	K562	blood:	n/a	n/a
38	CBX3	chr7:50602268-50603007	HCT-116	colon:	n/a	n/a
39	CBX3	chr7:50602345-50602942	K562	blood:	n/a	n/a
40	CBX3	chr7:50602259-50603567	K562	blood:	n/a	n/a
41	CCNT2	chr7:50560488-50560688	K562	blood:	n/a	n/a
42	CCNT2	chr7:50564647-50565217	K562	blood:	n/a	n/a
43	CCNT2	chr7:50554223-50554732	K562	blood:	n/a	n/a
44	CCNT2	chr7:50602449-50602862	K562	blood:	n/a	n/a
45	CEBPB	chr7:50565601-50566166	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr7:50596563-50596744	HepG2	liver:	n/a	n/a
47	CEBPB	chr7:50575828-50576159	K562	blood:	n/a	n/a
48	CEBPB	chr7:50564703-50564954	K562	blood:	n/a	n/a
49	CEBPB	chr7:50564597-50565140	K562	blood:	n/a	n/a
50	CEBPB	chr7:50602491-50603523	Hela-S3	cervix:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:50560743-50560793	CMK	blood:	n/a
2	chr7:50560743-50560793	CMK	blood:	n/a
3	chr7:50560524-50560574	Hela-S3	cervix:	n/a
4	chr7:50570049-50570099	HAEpiC	amniotic membrane:	n/a
5	chr7:50570049-50570099	NB4	blood:	n/a
6	chr7:50538740-50538790	T-47D	breast:	n/a
7	chr7:50560524-50560574	HCT-116	colon:	n/a
8	chr7:50560743-50560793	IMR90	lung:	fetal
9	chr7:50603292-50603342	NT2-D1	testis:	n/a
10	chr7:50560524-50560574	MCF-7	breast:	n/a
11	chr7:50538740-50538790	PFSK-1	brain:	n/a
12	chr7:50560743-50560793	SKMC	muscle:	n/a
13	chr7:50538740-50538790	Caco-2	colon:	n/a
14	chr7:50560524-50560574	H1-hESC	embryonic stem cell:	embryo
15	chr7:50560686-50560736	HNPCEpiC	eye:	n/a
16	chr7:50538740-50538790	NT2-D1	testis:	n/a
17	chr7:50560686-50560736	ovcar-3	ovarian:	n/a
18	chr7:50538740-50538790	BJ	skin:	n/a
19	chr7:50560524-50560574	HEK293	kidney:	embryo
20	chr7:50570049-50570099	HRCEpiC	kidney:	n/a
21	chr7:50570049-50570099	RPTEC	kidney:	n/a
22	chr7:50560743-50560793	A549	lung:	n/a
23	chr7:50538740-50538790	AG09309	skin:	n/a
24	chr7:50560743-50560793	HCT-116	colon:	n/a
25	chr7:50560743-50560793	HRPEpiC	eye:	n/a
26	chr7:50538740-50538790	HCPEpiC	choroid plexus:	n/a
27	chr7:50560686-50560736	HUVEC	blood vessel:	n/a
28	chr7:50603292-50603342	HRCEpiC	kidney:	n/a
29	chr7:50603292-50603342	SK-N-SH	brain:	n/a
30	chr7:50560524-50560574	MCF10A-Er-Src	breast:	n/a
31	chr7:50560524-50560574	T-47D	breast:	n/a
32	chr7:50560743-50560793	Caco-2	colon:	n/a
33	chr7:50538740-50538790	U87	brain:	n/a
34	chr7:50560524-50560574	PANC-1	pancreas:	n/a
35	chr7:50560686-50560736	NHBE	bronchial:	n/a
36	chr7:50603292-50603342	Caco-2	colon:	n/a
37	chr7:50560524-50560574	HL-60	blood:	n/a
38	chr7:50570049-50570099	AG10803	skin:	n/a
39	chr7:50560524-50560574	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:50538740-50538790	HAEpiC	amniotic membrane:	n/a
41	chr7:50560743-50560793	SAEC	small airway:	n/a
42	chr7:50538740-50538790	PrEC	prostate:	n/a
43	chr7:50560524-50560574	HAEpiC	amniotic membrane:	n/a
44	chr7:50560524-50560574	ovcar-3	ovarian:	n/a
45	chr7:50560524-50560574	RPTEC	kidney:	n/a
46	chr7:50570049-50570099	HUVEC	blood vessel:	n/a
47	chr7:50560743-50560793	HCPEpiC	choroid plexus:	n/a
48	chr7:50560686-50560736	CMK	blood:	n/a
49	chr7:50560524-50560574	ProgFib	skin:	n/a
50	chr7:50560524-50560574	BJ	skin:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:50570130..50572623-chr7:50573822..50576522,2	K562	blood:
2	chr7:50537654..50539269-chr7:50553300..50555389,2	K562	blood:
3	chr7:50540382..50543888-chr7:50545544..50548848,3	K562	blood:
4	chr7:50565140..50566781-chr7:50570058..50572270,2	K562	blood:
5	chr7:50538202..50540101-chr7:50549374..50551291,2	K562	blood:
6	chr7:50537654..50539269-chr7:50553300..50555389,2	K562	blood:
7	chr7:50601800..50604303-chr7:50605834..50607689,2	K562	blood:
8	chr7:50546772..50548404-chr7:50551410..50554000,2	K562	blood:
9	chr7:50570130..50572623-chr7:50573822..50576522,2	K562	blood:
10	chr7:50569843..50571376-chr7:50579895..50581810,2	K562	blood:
11	chr7:50564851..50566745-chr7:50568557..50570240,2	K562	blood:
12	chr7:50564851..50566745-chr7:50568557..50570240,2	K562	blood:
13	chr7:50598241..50600922-chr7:50601073..50603965,2	K562	blood:
14	chr7:50538202..50540101-chr7:50549374..50551291,2	K562	blood:
15	chr7:50518383..50520516-chr7:50572098..50575046,2	MCF-7	breast:
16	chr7:50601800..50604303-chr7:50605834..50607689,2	K562	blood:
17	chr7:50605928..50607774-chr7:50609469..50611799,3	MCF-7	breast:
18	chr7:50605928..50607774-chr7:50609469..50611799,3	MCF-7	breast:
19	chr7:50565140..50566781-chr7:50570058..50572270,2	K562	blood:
20	chr7:50601758..50604303-chr7:50604942..50607334,2	K562	blood:
21	chr7:50601758..50604303-chr7:50604942..50607334,2	K562	blood:
22	chr7:50569843..50571376-chr7:50579895..50581810,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IKZF1-7	chr7:50576538-50576601	refGeneNc_4230_NR_033845
2	lnc-IKZF1-7	chr7:50577437-50578655	refGeneNc_4230_NR_033845
3	lnc-IKZF1-1	chr7:50599286-50599580	NONHSAT120562
4	lnc-IKZF1-1	chr7:50606812-50606865	ENSG00000226122.1
5	lnc-IKZF1-1	chr7:50599457-50599580	ENSG00000226122.1
6	lnc-IKZF1-7	chr7:50566951-50567074	refGeneNc_4230_NR_033845
7	lnc-IKZF1-1	chr7:50599969-50600290	NONHSAT120562
8	lnc-IKZF1-1	chr7:50609943-50611161	ENSG00000226122.1
9	lnc-IKZF1-1	chr7:50607529-50607843	ENSG00000226122.1
10	lnc-IKZF1-1	chr7:50609044-50609107	ENSG00000226122.1
11	lnc-IKZF1-7	chr7:50575023-50575337	refGeneNc_4230_NR_033845
12	lnc-IKZF1-7	chr7:50574306-50574359	refGeneNc_4230_NR_033845

No data

Variant related genes	Relation type
DDC	TF binding region
ENSG00000226122	TF binding region
DDC	CpG island
ENSG00000226122	CpG island
ENSG00000226122	chromatin interactions
ENSG00000132437	chromatin interactions
E2F3	miRNA target sites
TAB3	miRNA target sites

Extended variants
information (count: 3062 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:3062 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11238131	chr7:50538589-50538590	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs143426137	chr7:50538590-50538591	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143846049	chr7:50538645-50538646	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs148192170	chr7:50538692-50538693	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567846046	chr7:50538693-50538694	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187654216	chr7:50538704-50538705	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs557137495	chr7:50538723-50538724	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142028441	chr7:50538740-50538741	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566822120	chr7:50538741-50538742	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558950097	chr7:50538756-50538757	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150688776	chr7:50538758-50538759	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541481733	chr7:50538802-50538803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561346156	chr7:50538811-50538812	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574911606	chr7:50538812-50538813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550475111	chr7:50538841-50538842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191574308	chr7:50538848-50538849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563928636	chr7:50538876-50538877	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532655309	chr7:50538879-50538880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143770354	chr7:50538909-50538910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146336938	chr7:50538919-50538920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528058069	chr7:50538933-50538934	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547818490	chr7:50538980-50538981	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139580692	chr7:50538984-50538985	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537174800	chr7:50539032-50539033	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs550453408	chr7:50539034-50539035	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs149984502	chr7:50539036-50539037	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs539293665	chr7:50539126-50539127	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs11974997	chr7:50539138-50539139	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs370519193	chr7:50539141-50539142	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs183483201	chr7:50539168-50539169	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534999948	chr7:50539231-50539232	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555018175	chr7:50539242-50539243	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs145220507	chr7:50539260-50539261	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188427952	chr7:50539264-50539265	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563671983	chr7:50539273-50539274	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577366698	chr7:50539275-50539276	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546617433	chr7:50539299-50539300	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs546016751	chr7:50539337-50539338	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs191558283	chr7:50539355-50539356	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149136028	chr7:50539377-50539378	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs142240061	chr7:50539397-50539398	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562563098	chr7:50539422-50539423	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs182620534	chr7:50539424-50539425	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs561730317	chr7:50539433-50539434	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186598353	chr7:50539448-50539449	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs568729708	chr7:50539471-50539472	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550637904	chr7:50539491-50539492	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147845218	chr7:50539495-50539496	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs539618759	chr7:50539516-50539517	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141358215	chr7:50539539-50539540	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:124)

Disease	PMID	Source
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Biliary cancer	19435499	CNVD
Wilms tumour	21544195	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	17237825	CNVD
Gastric cancer	24379144	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal cancer	21851588	CNVD
Non-small cell lung cancer	17643093	CNVD
Ovarian cancer	18182111	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17369134	CNVD
Barrett''s esophagus	18559552	CNVD
head and neck squamous cell carcinoma	16943533	CNVD
Anaplastic thyroid cancer	17079354	CNVD
Basal-like breast cancer	17875215	CNVD
Colorectal cancer	16882699	CNVD
Colorectal cancer	18794099	CNVD
Gastrointestinal stromal cancer	17643098	CNVD
Lung cancer	18381415	CNVD
Metastatic colorectal cancer	17664472	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	17673923	CNVD
Non-small cell lung cancer	17975165	CNVD
Non-small cell lung cancer	19622585	CNVD
Ovarian cancer	16607561	CNVD
Squamous cell cancer	19670535	CNVD
head and neck squamous cell carcinoma	16818711	CNVD
small cell lung cancer	18829487	CNVD
Breast cancer	17661082	CNVD
Adenocarcinoma	19260752	CNVD
Esophageal cancer	16575012	CNVD
Lung adenocarcinoma	19138956	CNVD
Lung adenocarcinoma	18379350	CNVD
Lung adenocarcinoma	18258923	CNVD
Lung cancer	19138956	CNVD
Lung cancer	18379350	CNVD
Lung cancer	18258923	CNVD
Non-small cell lung cancer	18304967	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	19260752	CNVD
Non-small cell lung cancer	17079354	CNVD
Non-small cell lung cancer	18559607	CNVD
Rectal cancer	19506820	CNVD
Triple-negative breast cancer	18950515	CNVD
head and neck squamous cell carcinoma	18813952	CNVD
Non-small cell lung cancer	17504988	CNVD
Non-small cell lung cancer	16943533	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	17538160	CNVD
Colorectal cancer	19712476	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19671679	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
small cell lung cancer	20016488	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:728 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:50535800-50539000	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr7:50535800-50540800	Weak transcription	Duodenum Mucosa	Duodenum
3	chr7:50535800-50546800	Weak transcription	Pancreas	Pancrea
4	chr7:50535800-50553200	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr7:50536000-50542800	Weak transcription	Colonic Mucosa	Colon
6	chr7:50536200-50541400	Weak transcription	HepG2	liver
7	chr7:50536200-50542200	Strong transcription	Fetal Intestine Small	intestine
8	chr7:50536200-50545400	Weak transcription	Right Atrium	heart
9	chr7:50536400-50541400	Weak transcription	Colon Smooth Muscle	Colon
10	chr7:50536400-50541600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr7:50536400-50541800	Strong transcription	Fetal Intestine Large	intestine
12	chr7:50536600-50543000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr7:50537800-50538600	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr7:50538200-50538800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr7:50538600-50538800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr7:50538600-50538800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr7:50538600-50540800	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr7:50539000-50539600	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr7:50539000-50540000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr7:50539600-50540800	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr7:50540600-50542800	Enhancers	Stomach Smooth Muscle	stomach
22	chr7:50540800-50542200	Enhancers	Psoas Muscle	Psoas
23	chr7:50540800-50543400	Strong transcription	Duodenum Mucosa	Duodenum
24	chr7:50540800-50543400	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr7:50540800-50543400	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr7:50541400-50542200	Enhancers	Rectal Smooth Muscle	rectum
27	chr7:50541400-50542200	Strong transcription	HepG2	liver
28	chr7:50541400-50542800	Enhancers	Colon Smooth Muscle	Colon
29	chr7:50541600-50542600	Enhancers	Placenta	Placenta
30	chr7:50541600-50543200	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr7:50541800-50542200	Enhancers	Esophagus	oesophagus
32	chr7:50541800-50542400	Weak transcription	Lung	lung
33	chr7:50541800-50543600	Enhancers	Liver	Liver
34	chr7:50541800-50543800	Weak transcription	Fetal Intestine Large	intestine
35	chr7:50542000-50543000	Enhancers	Adipose Nuclei	Adipose
36	chr7:50542000-50543400	Enhancers	Spleen	Spleen
37	chr7:50542000-50549600	Weak transcription	Stomach Mucosa	stomach
38	chr7:50542200-50542400	Weak transcription	Psoas Muscle	Psoas
39	chr7:50542200-50542800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr7:50542200-50543400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr7:50542200-50545000	Weak transcription	HepG2	liver
42	chr7:50542200-50546000	Genic enhancers	Fetal Intestine Small	intestine
43	chr7:50542600-50543000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr7:50542600-50543000	Enhancers	Fetal Muscle Leg	muscle
45	chr7:50542800-50543000	Enhancers	Ovary	ovary
46	chr7:50542800-50543400	Enhancers	Lung	lung
47	chr7:50542800-50544200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr7:50542800-50544200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:50543000-50543200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
50	chr7:50543000-50543400	Bivalent Enhancer	Fetal Muscle Leg	muscle

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