Variant report

Variant	nsv429748
Chromosome Location	chr7:40054760-40140660
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:660)
CpG islands
(count:61)
Chromatin interactive
region (count:53)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:660 , 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	chr7:40138413-40138773	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:40135727-40135825	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:40110475-40110675	K562	blood:	n/a	n/a
4	ARID3A	chr7:40092188-40092405	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:40139011-40139191	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:40134894-40135287	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:40098322-40098610	K562	blood:	n/a	n/a
8	ATF1	chr7:40117561-40117768	K562	blood:	n/a	n/a
9	ATF3	chr7:40096977-40097167	K562	blood:	n/a	n/a
10	BACH1	chr7:40134033-40134217	K562	blood:	n/a	n/a
11	BACH1	chr7:40098245-40098605	K562	blood:	n/a	n/a
12	BACH1	chr7:40098271-40098628	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr7:40078099-40078178	K562	blood:	n/a	n/a
14	BHLHE40	chr7:40098417-40098988	K562	blood:	n/a	n/a
15	BHLHE40	chr7:40092120-40092431	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:40133785-40133889	K562	blood:	n/a	n/a
17	BHLHE40	chr7:40096875-40097314	K562	blood:	n/a	n/a
18	CBX3	chr7:40096872-40097273	K562	blood:	n/a	n/a
19	CEBPB	chr7:40104567-40104841	HepG2	liver:	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
20	CEBPB	chr7:40139526-40139586	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:40117497-40117807	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:40135562-40135794	H1-hESC	embryonic stem cell:	n/a	chr7:40135755-40135766
23	CEBPB	chr7:40117519-40117821	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr7:40124139-40124432	IMR90	lung:	n/a	chr7:40124257-40124268
25	CEBPB	chr7:40135621-40135835	HepG2	liver:	n/a	chr7:40135755-40135766
26	CEBPB	chr7:40082049-40082293	HepG2	liver:	n/a	chr7:40082133-40082144
27	CEBPB	chr7:40117517-40117829	IMR90	lung:	n/a	n/a
28	CEBPB	chr7:40082068-40082213	HepG2	liver:	n/a	chr7:40082133-40082144
29	CEBPB	chr7:40114299-40114406	Hela-S3	cervix:	n/a	chr7:40114370-40114381
30	CEBPB	chr7:40117557-40117777	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr7:40124115-40124426	HepG2	liver:	n/a	chr7:40124257-40124268
32	CEBPB	chr7:40082093-40082233	K562	blood:	n/a	chr7:40082133-40082144
33	CEBPB	chr7:40114217-40114443	A549	lung:	n/a	chr7:40114370-40114381
34	CEBPB	chr7:40134823-40135150	HepG2	liver:	n/a	n/a
35	CEBPB	chr7:40117544-40117798	K562	blood:	n/a	n/a
36	CEBPB	chr7:40104549-40104819	IMR90	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
37	CEBPB	chr7:40114215-40114498	HepG2	liver:	n/a	chr7:40114370-40114381
38	CEBPB	chr7:40117500-40117833	K562	blood:	n/a	n/a
39	CEBPB	chr7:40114213-40114488	IMR90	lung:	n/a	chr7:40114370-40114381
40	CEBPB	chr7:40134892-40135257	HepG2	liver:	n/a	n/a
41	CEBPB	chr7:40114232-40114490	K562	blood:	n/a	chr7:40114370-40114381
42	CEBPB	chr7:40138522-40138737	HepG2	liver:	n/a	chr7:40138631-40138644
43	CEBPB	chr7:40134932-40135181	HepG2	liver:	n/a	n/a
44	CEBPB	chr7:40124141-40124418	K562	blood:	n/a	chr7:40124257-40124268
45	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
46	CEBPB	chr7:40117525-40117828	A549	lung:	n/a	n/a
47	CEBPB	chr7:40117514-40117763	K562	blood:	n/a	n/a
48	CEBPB	chr7:40104587-40104830	K562	blood:	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
49	CEBPB	chr7:40081989-40082303	HepG2	liver:	n/a	chr7:40082133-40082144
50	CEBPB	chr7:40114247-40114475	H1-hESC	embryonic stem cell:	n/a	chr7:40114370-40114381

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:40098119-40098169	HepG2	liver:	n/a
2	chr7:40098119-40098169	GM12891	blood:	n/a
3	chr7:40098119-40098169	T-47D	breast:	n/a
4	chr7:40098119-40098169	RPTEC	kidney:	n/a
5	chr7:40098119-40098169	HCPEpiC	choroid plexus:	n/a
6	chr7:40098119-40098169	LNCaP	prostate:	n/a
7	chr7:40098119-40098169	HL-60	blood:	n/a
8	chr7:40098119-40098169	HRE	kidney:	n/a
9	chr7:40098119-40098169	SK-N-SH	brain:	n/a
10	chr7:40098119-40098169	HEEpiC	esophagus:	n/a
11	chr7:40098119-40098169	Jurkat	blood:	n/a
12	chr7:40098119-40098169	NHBE	bronchial:	n/a
13	chr7:40098119-40098169	BE2_C	brain:	n/a
14	chr7:40098119-40098169	NB4	blood:	n/a
15	chr7:40098119-40098169	PANC-1	pancreas:	n/a
16	chr7:40098119-40098169	HRPEpiC	eye:	n/a
17	chr7:40098119-40098169	HCT-116	colon:	n/a
18	chr7:40098119-40098169	SK-N-SH_RA	brain:	n/a
19	chr7:40098119-40098169	GM19239	blood:	n/a
20	chr7:40098119-40098169	HRCEpiC	kidney:	n/a
21	chr7:40098119-40098169	NT2-D1	testis:	n/a
22	chr7:40098119-40098169	A549	lung:	n/a
23	chr7:40098119-40098169	HIPEpiC	eye:	n/a
24	chr7:40098119-40098169	HCM	heart:	n/a
25	chr7:40098119-40098169	PrEC	prostate:	n/a
26	chr7:40098119-40098169	NHDF-neo	bronchial:	n/a
27	chr7:40098119-40098169	GM12892	blood:	n/a
28	chr7:40098119-40098169	AG09319	gingival:	n/a
29	chr7:40098119-40098169	GM06990	blood:	n/a
30	chr7:40098119-40098169	BJ	skin:	n/a
31	chr7:40098119-40098169	HNPCEpiC	eye:	n/a
32	chr7:40098119-40098169	AG04450	lung:	fetal
33	chr7:40098119-40098169	Caco-2	colon:	n/a
34	chr7:40098119-40098169	GM12878	blood:	n/a
35	chr7:40098119-40098169	AoSMC	blood vessel:	n/a
36	chr7:40098119-40098169	SK-N-MC	brain:	n/a
37	chr7:40098119-40098169	Hela-S3	cervix:	n/a
38	chr7:40098119-40098169	AG04449	skin:	fetal
39	chr7:40098119-40098169	ovcar-3	ovarian:	n/a
40	chr7:40098119-40098169	HUVEC	blood vessel:	n/a
41	chr7:40098119-40098169	ProgFib	skin:	n/a
42	chr7:40098119-40098169	MCF-7	breast:	n/a
43	chr7:40098119-40098169	HPAEpiC	pulmonary alveolar:	n/a
44	chr7:40098119-40098169	SKMC	muscle:	n/a
45	chr7:40098119-40098169	H1-hESC	embryonic stem cell:	embryo
46	chr7:40098119-40098169	HCF	heart:	n/a
47	chr7:40098119-40098169	SAEC	small airway:	n/a
48	chr7:40098119-40098169	MCF10A-Er-Src	breast:	n/a
49	chr7:40098119-40098169	HAEpiC	amniotic membrane:	n/a
50	chr7:40098119-40098169	PFSK-1	brain:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:40115479..40117853-chr7:40121950..40124630,2	MCF-7	breast:
2	chr7:40084993..40087566-chr7:40090698..40092927,2	K562	blood:
3	chr7:39784501..39786932-chr7:40060004..40061750,2	MCF-7	breast:
4	chr7:40139705..40142810-chr7:40143193..40146222,3	K562	blood:
5	chr7:39988058..39990368-chr7:40072620..40075295,2	K562	blood:
6	chr7:40132356..40134649-chr7:40137450..40139023,2	K562	blood:
7	chr7:40131598..40134106-chr7:40137449..40139937,2	MCF-7	breast:
8	chr7:40059026..40061512-chr7:40062237..40065156,2	MCF-7	breast:
9	chr7:40088024..40089904-chr7:40091053..40093923,2	MCF-7	breast:
10	chr7:39988254..39991540-chr7:40078571..40080480,3	MCF-7	breast:
11	chr7:40090602..40093136-chr7:40095056..40097125,2	K562	blood:
12	chr11:126173275..126173777-chr7:40061848..40062348,2	NB4	blood:
13	chr7:40055192..40057711-chr7:40058795..40061552,3	K562	blood:
14	chr7:39987621..39991955-chr7:40089379..40093722,6	MCF-7	breast:
15	chr7:40038038..40041383-chr7:40051581..40055589,3	K562	blood:
16	chr7:40109167..40111821-chr7:40114946..40117693,2	K562	blood:
17	chr7:40059026..40061512-chr7:40062237..40065156,2	MCF-7	breast:
18	chr7:40093916..40096892-chr7:40098882..40101191,2	K562	blood:
19	chr7:40090602..40093136-chr7:40095056..40097125,2	K562	blood:
20	chr7:39935762..39936421-chr7:40091763..40092363,2	K562	blood:
21	chr7:40098014..40099578-chr7:40101201..40104032,2	K562	blood:
22	chr7:39989128..39990851-chr7:40089712..40092117,2	K562	blood:
23	chr7:40080571..40083008-chr7:40084879..40087447,2	MCF-7	breast:
24	chr7:40084390..40086552-chr7:40091089..40093935,3	K562	blood:
25	chr7:40105682..40108224-chr7:40109570..40112415,2	K562	blood:
26	chr7:40048646..40050601-chr7:40053388..40055304,2	K562	blood:
27	chr7:40055192..40057711-chr7:40058795..40061552,3	K562	blood:
28	chr7:40109167..40111821-chr7:40114946..40117693,2	K562	blood:
29	chr7:40135569..40137778-chr7:40140510..40143010,2	MCF-7	breast:
30	chr7:40084390..40086552-chr7:40091089..40093935,3	K562	blood:
31	chr7:39989467..39991419-chr7:40087056..40089179,2	K562	blood:
32	chr7:39987767..39989590-chr7:40096379..40098788,2	K562	blood:
33	chr7:40038956..40041383-chr7:40052873..40055589,2	K562	blood:
34	chr7:39988782..39993568-chr7:40089798..40094373,7	MCF-7	breast:
35	chr7:39987662..39991169-chr7:40080646..40083080,4	MCF-7	breast:
36	chr7:40080571..40083008-chr7:40084879..40087447,2	MCF-7	breast:
37	chr17:59501958..59502789-chr7:40112228..40112887,2	MCF-7	breast:
38	chr7:40093916..40096892-chr7:40098882..40101191,2	K562	blood:
39	chr7:40132356..40134649-chr7:40137450..40139023,2	K562	blood:
40	chr7:40088024..40089904-chr7:40091053..40093923,2	MCF-7	breast:
41	chr7:40130215..40132846-chr7:40133657..40135422,2	K562	blood:
42	chr7:40048549..40051232-chr7:40060255..40062264,2	K562	blood:
43	chr7:39988550..39991713-chr7:40061558..40063608,3	K562	blood:
44	chr7:40105682..40108224-chr7:40109570..40112415,2	K562	blood:
45	chr7:40098014..40099578-chr7:40101201..40104032,2	K562	blood:
46	chr7:39987746..39990922-chr7:40055976..40057979,3	K562	blood:
47	chr7:40115479..40117853-chr7:40121950..40124630,2	MCF-7	breast:
48	chr7:39988605..39990899-chr7:40070252..40072464,2	K562	blood:
49	chr7:39619647..39620204-chr7:40092201..40092766,2	K562	blood:
50	chr7:40135569..40137778-chr7:40140510..40143010,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	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
CDK13	CpG island
ENSG00000065883	chromatin interactions
ENSG00000110063	chromatin interactions
ENSG00000259826	chromatin interactions

Extended variants
information (count: 3292 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:3292 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188594823	chr7:40054764-40054765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs1403381	chr7:40054784-40054785	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs561510639	chr7:40054809-40054810	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs527309458	chr7:40054815-40054816	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540691614	chr7:40054817-40054818	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560803982	chr7:40054900-40054901	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532864296	chr7:40054925-40054926	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs191945880	chr7:40054968-40054969	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544983143	chr7:40055018-40055019	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs773413	chr7:40055082-40055083	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs531825471	chr7:40055116-40055117	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs548692389	chr7:40055128-40055129	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs112172597	chr7:40055144-40055145	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs568485738	chr7:40055156-40055157	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs17537936	chr7:40055192-40055193	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs17171644	chr7:40055254-40055255	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs184318063	chr7:40055268-40055269	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs539393441	chr7:40055296-40055297	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs555928084	chr7:40055349-40055350	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs575864813	chr7:40055350-40055351	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs535154942	chr7:40055358-40055359	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs79836303	chr7:40055359-40055360	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs17496415	chr7:40055360-40055361	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs149242026	chr7:40055377-40055378	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs112767564	chr7:40055380-40055381	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs371603557	chr7:40055385-40055386	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs546554435	chr7:40055417-40055418	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563051641	chr7:40055428-40055429	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531915178	chr7:40055448-40055449	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187270020	chr7:40055490-40055491	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs562174010	chr7:40055504-40055505	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113426541	chr7:40055550-40055551	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs527789663	chr7:40055552-40055553	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189373964	chr7:40055558-40055559	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570549427	chr7:40055602-40055603	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567053705	chr7:40055626-40055627	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs143618819	chr7:40055720-40055721	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549690014	chr7:40055751-40055752	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569635481	chr7:40055757-40055758	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs117049063	chr7:40055759-40055760	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555280860	chr7:40055787-40055788	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572060303	chr7:40055830-40055831	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534460493	chr7:40055834-40055835	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs117485121	chr7:40055849-40055850	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577743506	chr7:40055877-40055878	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138180653	chr7:40055878-40055879	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs143648797	chr7:40055917-40055918	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542365563	chr7:40055926-40055927	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549818011	chr7:40055933-40055934	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560025959	chr7:40055962-40055963	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Gastric cancer	22014070	CNVD

Chromatin state (count:2027 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:40020400-40077600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr7:40025600-40055400	Weak transcription	Rectal Smooth Muscle	rectum
3	chr7:40025800-40054800	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr7:40025800-40055400	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr7:40025800-40055400	Weak transcription	Fetal Heart	heart
6	chr7:40025800-40055400	Weak transcription	Stomach Mucosa	stomach
7	chr7:40025800-40059600	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr7:40025800-40062800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr7:40025800-40082200	Weak transcription	Spleen	Spleen
10	chr7:40026000-40071200	Weak transcription	Brain Germinal Matrix	brain
11	chr7:40026600-40096800	Weak transcription	Right Ventricle	heart
12	chr7:40027800-40054800	Weak transcription	Aorta	Aorta
13	chr7:40027800-40055400	Weak transcription	Fetal Brain Female	brain
14	chr7:40028000-40077800	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr7:40028000-40127800	Weak transcription	Colonic Mucosa	Colon
16	chr7:40028200-40073000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr7:40034400-40072200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr7:40042600-40055400	Weak transcription	Psoas Muscle	Psoas
19	chr7:40042800-40070400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr7:40043000-40061600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr7:40043400-40054800	Weak transcription	Gastric	stomach
22	chr7:40043600-40057800	Weak transcription	HUVEC	blood vessel
23	chr7:40043600-40058000	Weak transcription	Fetal Brain Male	brain
24	chr7:40043600-40059800	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr7:40043600-40067000	Weak transcription	K562	blood
26	chr7:40043600-40071600	Weak transcription	Stomach Smooth Muscle	stomach
27	chr7:40043600-40076000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr7:40043600-40079800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr7:40043600-40095200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr7:40043600-40127800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr7:40043800-40055400	Weak transcription	Colon Smooth Muscle	Colon
32	chr7:40043800-40055400	Weak transcription	Fetal Lung	lung
33	chr7:40044400-40096000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr7:40045800-40054800	Weak transcription	GM12878-XiMat	blood
35	chr7:40047600-40102600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr7:40048000-40054800	Weak transcription	Brain Anterior Caudate	brain
37	chr7:40048000-40102400	Weak transcription	HMEC	breast
38	chr7:40048000-40102400	Weak transcription	NHEK	skin
39	chr7:40048200-40055400	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr7:40048200-40058400	Weak transcription	Hela-S3	cervix
41	chr7:40048200-40059200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr7:40048400-40054800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr7:40048400-40055400	Weak transcription	HSMMtube	muscle
44	chr7:40048400-40066600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr7:40048600-40055400	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr7:40048600-40074800	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr7:40049000-40055400	Weak transcription	Brain Cingulate Gyrus	brain
48	chr7:40049000-40055400	Weak transcription	Brain Hippocampus Middle	brain
49	chr7:40049000-40085600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr7:40049000-40085800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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