Variant report

Variant	nsv606708
Chromosome Location	chr7:40021044-40157040
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:932)
CpG islands
(count:183)
Chromatin interactive
region (count:77)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:932 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:40135727-40135825	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:40092188-40092405	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:40134894-40135287	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:40048432-40048455	K562	blood:	n/a	n/a
5	ARID3A	chr7:40110475-40110675	K562	blood:	n/a	n/a
6	ARID3A	chr7:40098322-40098610	K562	blood:	n/a	n/a
7	ARID3A	chr7:40139011-40139191	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:40138413-40138773	HepG2	liver:	n/a	n/a
9	ATF1	chr7:40117561-40117768	K562	blood:	n/a	n/a
10	ATF3	chr7:40096977-40097167	K562	blood:	n/a	n/a
11	BACH1	chr7:40078099-40078178	K562	blood:	n/a	n/a
12	BACH1	chr7:40134033-40134217	K562	blood:	n/a	n/a
13	BACH1	chr7:40098245-40098605	K562	blood:	n/a	n/a
14	BACH1	chr7:40098271-40098628	H1-hESC	embryonic stem cell:	n/a	n/a
15	BHLHE40	chr7:40092120-40092431	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:40096875-40097314	K562	blood:	n/a	n/a
17	BHLHE40	chr7:40098417-40098988	K562	blood:	n/a	n/a
18	BHLHE40	chr7:40133785-40133889	K562	blood:	n/a	n/a
19	BRCA1	chr7:40030603-40030622	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr7:40096872-40097273	K562	blood:	n/a	n/a
21	CCNT2	chr7:40143597-40143730	K562	blood:	n/a	n/a
22	CEBPB	chr7:40145690-40146048	IMR90	lung:	n/a	chr7:40145861-40145872
23	CEBPB	chr7:40135562-40135794	H1-hESC	embryonic stem cell:	n/a	chr7:40135755-40135766
24	CEBPB	chr7:40114217-40114443	A549	lung:	n/a	chr7:40114370-40114381
25	CEBPB	chr7:40082049-40082293	HepG2	liver:	n/a	chr7:40082133-40082144
26	CEBPB	chr7:40114247-40114475	H1-hESC	embryonic stem cell:	n/a	chr7:40114370-40114381
27	CEBPB	chr7:40052800-40053114	IMR90	lung:	n/a	chr7:40052935-40052946
28	CEBPB	chr7:40117514-40117763	K562	blood:	n/a	n/a
29	CEBPB	chr7:40104584-40104827	A549	lung:	n/a	chr7:40104687-40104700 chr7:40104689-40104698 chr7:40104687-40104698 chr7:40104687-40104700 chr7:40104689-40104698 chr7:40104689-40104698 chr7:40104689-40104698 chr7:40104686-40104703 chr7:40104688-40104699
30	CEBPB	chr7:40028054-40028261	A549	lung:	n/a	n/a
31	CEBPB	chr7:40028548-40028593	IMR90	lung:	n/a	n/a
32	CEBPB	chr7:40052756-40053137	K562	blood:	n/a	chr7:40052935-40052946
33	CEBPB	chr7:40114213-40114488	IMR90	lung:	n/a	chr7:40114370-40114381
34	CEBPB	chr7:40145810-40145976	A549	lung:	n/a	chr7:40145861-40145872
35	CEBPB	chr7:40114215-40114498	HepG2	liver:	n/a	chr7:40114370-40114381
36	CEBPB	chr7:40145718-40146009	K562	blood:	n/a	chr7:40145861-40145872
37	CEBPB	chr7:40028089-40028276	HepG2	liver:	n/a	n/a
38	CEBPB	chr7:40117525-40117828	A549	lung:	n/a	n/a
39	CEBPB	chr7:40124141-40124418	K562	blood:	n/a	chr7:40124257-40124268
40	CEBPB	chr7:40023285-40023485	HepG2	liver:	n/a	chr7:40023439-40023450
41	CEBPB	chr7:40117544-40117798	K562	blood:	n/a	n/a
42	CEBPB	chr7:40046274-40046386	K562	blood:	n/a	n/a
43	CEBPB	chr7:40047766-40048133	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr7:40135621-40135835	HepG2	liver:	n/a	chr7:40135755-40135766
45	CEBPB	chr7:40124139-40124432	IMR90	lung:	n/a	chr7:40124257-40124268
46	CEBPB	chr7:40114299-40114406	Hela-S3	cervix:	n/a	chr7:40114370-40114381
47	CEBPB	chr7:40145755-40146018	H1-hESC	embryonic stem cell:	n/a	chr7:40145861-40145872
48	CEBPB	chr7:40117497-40117807	HepG2	liver:	n/a	n/a
49	CEBPB	chr7:40023284-40023543	K562	blood:	n/a	chr7:40023439-40023450
50	CEBPB	chr7:40028039-40028275	IMR90	lung:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:40047674-40047724	HMEC	breast:	n/a
2	chr7:40098119-40098169	HRE	kidney:	n/a
3	chr7:40047674-40047724	HCF	heart:	n/a
4	chr7:40098119-40098169	SK-N-SH	brain:	n/a
5	chr7:40026390-40026440	Hela-S3	cervix:	n/a
6	chr7:40047674-40047724	SKMC	muscle:	n/a
7	chr7:40026390-40026440	HNPCEpiC	eye:	n/a
8	chr7:40047674-40047724	H1-hESC	embryonic stem cell:	embryo
9	chr7:40026390-40026440	SK-N-MC	brain:	n/a
10	chr7:40047674-40047724	Caco-2	colon:	n/a
11	chr7:40047674-40047724	Jurkat	blood:	n/a
12	chr7:40026390-40026440	HRCEpiC	kidney:	n/a
13	chr7:40047674-40047724	GM06990	blood:	n/a
14	chr7:40047674-40047724	HL-60	blood:	n/a
15	chr7:40047674-40047724	Hepatocyte	liver:	n/a
16	chr7:40098119-40098169	HAEpiC	amniotic membrane:	n/a
17	chr7:40026390-40026440	GM06990	blood:	n/a
18	chr7:40098119-40098169	AG10803	skin:	n/a
19	chr7:40047674-40047724	AG09309	skin:	n/a
20	chr7:40098119-40098169	K562	blood:	n/a
21	chr7:40098119-40098169	IMR90	lung:	fetal
22	chr7:40047674-40047724	HCT-116	colon:	n/a
23	chr7:40026390-40026440	ProgFib	skin:	n/a
24	chr7:40098119-40098169	HNPCEpiC	eye:	n/a
25	chr7:40026390-40026440	K562	blood:	n/a
26	chr7:40098119-40098169	CMK	blood:	n/a
27	chr7:40026390-40026440	A549	lung:	n/a
28	chr7:40047674-40047724	HRE	kidney:	n/a
29	chr7:40047674-40047724	AG09319	gingival:	n/a
30	chr7:40047674-40047724	SAEC	small airway:	n/a
31	chr7:40047674-40047724	GM19239	blood:	n/a
32	chr7:40026390-40026440	HCF	heart:	n/a
33	chr7:40026390-40026440	HCT-116	colon:	n/a
34	chr7:40026390-40026440	RPTEC	kidney:	n/a
35	chr7:40026390-40026440	HIPEpiC	eye:	n/a
36	chr7:40098119-40098169	HL-60	blood:	n/a
37	chr7:40026390-40026440	IMR90	lung:	fetal
38	chr7:40047674-40047724	HEEpiC	esophagus:	n/a
39	chr7:40098119-40098169	Hepatocyte	liver:	n/a
40	chr7:40098119-40098169	AG09319	gingival:	n/a
41	chr7:40098119-40098169	T-47D	breast:	n/a
42	chr7:40098119-40098169	AG04450	lung:	fetal
43	chr7:40098119-40098169	Jurkat	blood:	n/a
44	chr7:40026390-40026440	T-47D	breast:	n/a
45	chr7:40026390-40026440	U87	brain:	n/a
46	chr7:40047674-40047724	AG04450	lung:	fetal
47	chr7:40026390-40026440	MCF-7	breast:	n/a
48	chr7:40026390-40026440	GM12891	blood:	n/a
49	chr7:40047674-40047724	RPTEC	kidney:	n/a
50	chr7:40098119-40098169	ECC-1	luminal epithelium:	n/a

(count:77 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:39988605..39990899-chr7:40070252..40072464,2	K562	blood:
2	chr7:39987662..39991169-chr7:40080646..40083080,4	MCF-7	breast:
3	chr7:40109167..40111821-chr7:40114946..40117693,2	K562	blood:
4	chr17:59501958..59502789-chr7:40112228..40112887,2	MCF-7	breast:
5	chr7:39989128..39990851-chr7:40089712..40092117,2	K562	blood:
6	chr7:39935762..39936421-chr7:40091763..40092363,2	K562	blood:
7	chr7:40031268..40032823-chr7:40035953..40037510,2	MCF-7	breast:
8	chr7:40084390..40086552-chr7:40091089..40093935,3	K562	blood:
9	chr7:39987621..39991955-chr7:40089379..40093722,6	MCF-7	breast:
10	chr7:40135569..40137778-chr7:40140510..40143010,2	MCF-7	breast:
11	chr7:40115479..40117853-chr7:40121950..40124630,2	MCF-7	breast:
12	chr7:40084390..40086552-chr7:40091089..40093935,3	K562	blood:
13	chr7:40139705..40142810-chr7:40143193..40146222,3	K562	blood:
14	chr7:40139705..40142810-chr7:40143193..40146222,3	K562	blood:
15	chr7:40084993..40087566-chr7:40090698..40092927,2	K562	blood:
16	chr7:39988058..39990368-chr7:40072620..40075295,2	K562	blood:
17	chr7:40080571..40083008-chr7:40084879..40087447,2	MCF-7	breast:
18	chr7:39988360..39989993-chr7:40043124..40045978,3	MCF-7	breast:
19	chr7:40098014..40099578-chr7:40101201..40104032,2	K562	blood:
20	chr7:40059026..40061512-chr7:40062237..40065156,2	MCF-7	breast:
21	chr7:40025445..40027288-chr7:40029164..40032016,2	K562	blood:
22	chr7:39989467..39991419-chr7:40087056..40089179,2	K562	blood:
23	chr7:39986663..39989008-chr7:40035472..40037902,2	K562	blood:
24	chr7:39987353..39988943-chr7:40114287..40116137,2	K562	blood:
25	chr7:39619647..39620204-chr7:40092201..40092766,2	K562	blood:
26	chr7:40038956..40041383-chr7:40052873..40055589,2	K562	blood:
27	chr7:40048646..40050601-chr7:40053388..40055304,2	K562	blood:
28	chr7:40109257..40111529-chr7:40116739..40118703,2	K562	blood:
29	chr7:39988482..39990728-chr7:40029986..40032615,2	MCF-7	breast:
30	chr7:40055192..40057711-chr7:40058795..40061552,3	K562	blood:
31	chr7:40105682..40108224-chr7:40109570..40112415,2	K562	blood:
32	chr7:40131598..40134106-chr7:40137449..40139937,2	MCF-7	breast:
33	chr7:40048549..40051232-chr7:40060255..40062264,2	K562	blood:
34	chr7:39995562..39997587-chr7:40034318..40036710,2	MCF-7	breast:
35	chr7:40132356..40134649-chr7:40137450..40139023,2	K562	blood:
36	chr7:40115479..40117853-chr7:40121950..40124630,2	MCF-7	breast:
37	chr7:40048549..40051232-chr7:40060255..40062264,2	K562	blood:
38	chr7:40038038..40041383-chr7:40051581..40055589,3	K562	blood:
39	chr7:39988080..39990398-chr7:40022100..40025071,3	K562	blood:
40	chr7:40090602..40093136-chr7:40095056..40097125,2	K562	blood:
41	chr7:39987767..39989590-chr7:40096379..40098788,2	K562	blood:
42	chr7:40025445..40027288-chr7:40029164..40032016,2	K562	blood:
43	chr7:40109167..40111821-chr7:40114946..40117693,2	K562	blood:
44	chr7:40059026..40061512-chr7:40062237..40065156,2	MCF-7	breast:
45	chr7:39988550..39991713-chr7:40061558..40063608,3	K562	blood:
46	chr7:40030873..40032517-chr7:40032744..40035272,2	MCF-7	breast:
47	chr7:40135569..40137778-chr7:40140510..40143010,2	MCF-7	breast:
48	chr7:39988882..39991588-chr7:40039057..40040636,2	K562	blood:
49	chr7:40088024..40089904-chr7:40091053..40093923,2	MCF-7	breast:
50	chr7:40132356..40134649-chr7:40137450..40139023,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDK13-3	chr7:40155284-40155542	NONHSAT120244
2	lnc-C7orf10-5	chr7:40135564-40136731	NONHSAT120243

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CDK13	hsa-miR-133b	chr7:40134927-40134933
2	CDK13	hsa-miR-133b	chr7:40134910-40134934

Variant related genes	Relation type
CDK13	TF binding region
ENSG00000270577	TF binding region
ENSG00000273444	TF binding region
CDK13	CpG island
ENSG00000270577	CpG island
ENSG00000273444	CpG island
ENSG00000270577	chromatin interactions
ENSG00000110063	chromatin interactions
ENSG00000259826	chromatin interactions
ENSG00000065883	chromatin interactions

Extended variants
information (count: 5158 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:5158 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs773424	chr7:40021044-40021045	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs563139719	chr7:40021094-40021095	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs191172410	chr7:40021164-40021165	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs559149450	chr7:40021218-40021219	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs74493740	chr7:40021224-40021225	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs533830061	chr7:40021275-40021276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs111486282	chr7:40021340-40021341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534296829	chr7:40021353-40021354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545024171	chr7:40021392-40021393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373924527	chr7:40021409-40021410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551335645	chr7:40021421-40021422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs6970705	chr7:40021483-40021484	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs540118959	chr7:40021484-40021485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113259426	chr7:40021529-40021530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570219031	chr7:40021531-40021532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs6970838	chr7:40021539-40021540	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs555867394	chr7:40021551-40021552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11359193	chr7:40021558-40021559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572547348	chr7:40021570-40021571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112829224	chr7:40021571-40021572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs13239783	chr7:40021579-40021580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10273977	chr7:40021588-40021589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10258217	chr7:40021589-40021590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10273981	chr7:40021606-40021607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10258223	chr7:40021607-40021608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182664437	chr7:40021611-40021612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150132409	chr7:40021616-40021617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs773425	chr7:40021648-40021649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563249878	chr7:40021662-40021663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs546847148	chr7:40021685-40021686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201635021	chr7:40021701-40021702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529020925	chr7:40021718-40021719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372975385	chr7:40021761-40021762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187765387	chr7:40021762-40021763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs13308930	chr7:40021763-40021764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528175609	chr7:40021863-40021864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551230848	chr7:40022029-40022030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571219988	chr7:40022051-40022052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530430656	chr7:40022064-40022065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550458427	chr7:40022085-40022086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376956162	chr7:40022141-40022142	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs111668507	chr7:40022295-40022296	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs536180634	chr7:40022378-40022379	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs192634316	chr7:40022451-40022452	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs566180381	chr7:40022500-40022501	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs535114820	chr7:40022517-40022518	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs557972148	chr7:40022533-40022534	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs572649497	chr7:40022621-40022622	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs182965446	chr7:40022646-40022647	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs111486838	chr7:40022665-40022666	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	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
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Gastric cancer	22014070	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:3092 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39993600-40048200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr7:39994200-40027200	Weak transcription	HSMM	muscle
3	chr7:39995200-40042600	Weak transcription	K562	blood
4	chr7:39997800-40027400	Weak transcription	Duodenum Mucosa	Duodenum
5	chr7:39998000-40027200	Weak transcription	Hela-S3	cervix
6	chr7:40006800-40031200	Weak transcription	Fetal Stomach	stomach
7	chr7:40007200-40027200	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr7:40007600-40027200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr7:40009400-40027200	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr7:40009400-40027400	Weak transcription	Osteobl	bone
11	chr7:40009600-40027400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr7:40009800-40027200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr7:40010000-40024600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr7:40010000-40026800	Weak transcription	NHEK	skin
15	chr7:40010200-40025000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr7:40010400-40027200	Weak transcription	Esophagus	oesophagus
17	chr7:40011200-40023600	Weak transcription	Lung	lung
18	chr7:40011200-40025400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr7:40011400-40027400	Weak transcription	Fetal Muscle Trunk	muscle
20	chr7:40014200-40021200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
21	chr7:40014800-40021200	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr7:40015000-40023600	Weak transcription	Fetal Intestine Small	intestine
23	chr7:40016800-40027200	Weak transcription	A549	lung
24	chr7:40017400-40027400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr7:40017600-40024400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr7:40017800-40026800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr7:40017800-40027400	Weak transcription	Liver	Liver
28	chr7:40018000-40025000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr7:40018000-40025200	Weak transcription	Small Intestine	intestine
30	chr7:40018400-40024600	Weak transcription	Brain Cingulate Gyrus	brain
31	chr7:40018400-40024600	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr7:40018400-40027200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr7:40018400-40027400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr7:40018600-40023200	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr7:40018600-40023200	Weak transcription	Rectal Smooth Muscle	rectum
36	chr7:40018600-40023400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr7:40018600-40023800	Weak transcription	Psoas Muscle	Psoas
38	chr7:40018600-40024400	Weak transcription	Right Ventricle	heart
39	chr7:40018600-40047800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr7:40018800-40023200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr7:40018800-40025200	Weak transcription	Adipose Nuclei	Adipose
42	chr7:40018800-40027400	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr7:40019200-40023800	Weak transcription	Spleen	Spleen
44	chr7:40019200-40025000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr7:40019200-40025200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr7:40019400-40024800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr7:40019400-40025200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr7:40019400-40025200	Weak transcription	Dnd41	blood
49	chr7:40019400-40025400	Weak transcription	Pancreas	Pancrea
50	chr7:40019400-40027200	Weak transcription	Primary hematopoietic stem cells	blood

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