Variant report

Variant	nsv606194
Chromosome Location	chr7:11042905-11144078
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:267)
CpG islands
(count:183)
Chromatin interactive
region (count:66)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:11122472-11122755	HepG2	liver:	n/a	n/a
2	ATF1	chr7:11128773-11128831	K562	blood:	n/a	n/a
3	ATF2	chr7:11122404-11123057	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:11052516-11052565	K562	blood:	n/a	n/a
5	BACH1	chr7:11102229-11102429	K562	blood:	n/a	n/a
6	BACH1	chr7:11071316-11071425	K562	blood:	n/a	n/a
7	BATF	chr7:11118139-11118345	GM12878	blood:	n/a	chr7:11118255-11118265
8	BATF	chr7:11118081-11118314	GM12878	blood:	n/a	chr7:11118255-11118265
9	CEBPB	chr7:11115611-11115936	K562	blood:	n/a	n/a
10	CEBPB	chr7:11115583-11115943	HepG2	liver:	n/a	n/a
11	CEBPB	chr7:11122659-11123159	A549	lung:	n/a	n/a
12	CEBPB	chr7:11108099-11108373	A549	lung:	n/a	chr7:11108241-11108252
13	CEBPB	chr7:11108116-11108371	HepG2	liver:	n/a	chr7:11108241-11108252
14	CEBPB	chr7:11115591-11115952	IMR90	lung:	n/a	n/a
15	CEBPB	chr7:11049383-11049522	H1-hESC	embryonic stem cell:	n/a	chr7:11049444-11049457 chr7:11049444-11049457
16	CEBPB	chr7:11108137-11108367	K562	blood:	n/a	chr7:11108241-11108252
17	CEBPB	chr7:11059645-11059822	HepG2	liver:	n/a	chr7:11059669-11059680
18	CEBPB	chr7:11043669-11043961	HepG2	liver:	n/a	chr7:11043824-11043835
19	CEBPB	chr7:11115589-11115882	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr7:11124794-11124970	HepG2	liver:	n/a	chr7:11124881-11124894
21	CEBPB	chr7:11122652-11122903	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:11124748-11125014	K562	blood:	n/a	chr7:11124881-11124894
23	CEBPB	chr7:11115581-11115979	MCF-7	breast:	n/a	n/a
24	CEBPB	chr7:11059524-11059769	A549	lung:	n/a	chr7:11059669-11059680
25	CEBPB	chr7:11115586-11115929	A549	lung:	n/a	n/a
26	CEBPB	chr7:11108217-11108264	H1-hESC	embryonic stem cell:	n/a	chr7:11108241-11108252
27	CEBPB	chr7:11115591-11115931	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr7:11061140-11061290	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr7:11065700-11065850	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr7:11114300-11114450	GM12871	blood:	n/a	n/a
31	CTCF	chr7:11057521-11057553	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr7:11110120-11110270	BJ	skin:	n/a	n/a
33	CTCF	chr7:11095112-11095126	K562	blood:	n/a	n/a
34	E2F4	chr7:11096537-11096779	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr7:11101787-11101981	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr7:11070455-11070655	MCF10A-Er-Src	breast:	n/a	n/a
37	EBF1	chr7:11100715-11100725	GM12878	blood:	n/a	n/a
38	EP300	chr7:11122365-11123187	A549	lung:	n/a	chr7:11122422-11122436
39	EP300	chr7:11117349-11117907	SK-N-SH	brain:	n/a	chr7:11117808-11117815
40	EP300	chr7:11065920-11067061	SK-N-SH	brain:	n/a	chr7:11066677-11066687
41	EP300	chr7:11122440-11122781	HepG2	liver:	n/a	n/a
42	EP300	chr7:11130432-11130758	SK-N-SH_RA	brain:	n/a	chr7:11130586-11130595
43	EP300	chr7:11065649-11067031	SK-N-SH_RA	brain:	n/a	chr7:11066677-11066687
44	EP300	chr7:11143284-11143367	K562	blood:	n/a	n/a
45	EP300	chr7:11122384-11122731	H1-hESC	embryonic stem cell:	n/a	chr7:11122422-11122436
46	EP300	chr7:11076616-11076714	K562	blood:	n/a	n/a
47	EP300	chr7:11065541-11067235	SK-N-SH	brain:	n/a	chr7:11066677-11066687
48	EP300	chr7:11065659-11067097	SK-N-SH_RA	brain:	n/a	chr7:11066677-11066687
49	EP300	chr7:11122400-11123163	A549	lung:	n/a	chr7:11122422-11122436
50	EP300	chr7:11130437-11130686	SK-N-SH_RA	brain:	n/a	chr7:11130586-11130595

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:11066024-11066074	NHBE	bronchial:	n/a
2	chr7:11091695-11091745	HPAEpiC	pulmonary alveolar:	n/a
3	chr7:11101436-11101486	NHDF-neo	bronchial:	n/a
4	chr7:11066024-11066074	U87	brain:	n/a
5	chr7:11066024-11066074	AG10803	skin:	n/a
6	chr7:11101436-11101486	HNPCEpiC	eye:	n/a
7	chr7:11101436-11101486	HCT-116	colon:	n/a
8	chr7:11101436-11101486	AG04450	lung:	fetal
9	chr7:11066024-11066074	LNCaP	prostate:	n/a
10	chr7:11091695-11091745	ovcar-3	ovarian:	n/a
11	chr7:11066024-11066074	HRE	kidney:	n/a
12	chr7:11091695-11091745	Caco-2	colon:	n/a
13	chr7:11091695-11091745	BE2_C	brain:	n/a
14	chr7:11066024-11066074	SAEC	small airway:	n/a
15	chr7:11091695-11091745	HCT-116	colon:	n/a
16	chr7:11066024-11066074	ProgFib	skin:	n/a
17	chr7:11101436-11101486	HRPEpiC	eye:	n/a
18	chr7:11091695-11091745	AG10803	skin:	n/a
19	chr7:11091695-11091745	IMR90	lung:	fetal
20	chr7:11066024-11066074	HEK293	kidney:	embryo
21	chr7:11066024-11066074	Jurkat	blood:	n/a
22	chr7:11101436-11101486	HCF	heart:	n/a
23	chr7:11066024-11066074	BE2_C	brain:	n/a
24	chr7:11101436-11101486	SKMC	muscle:	n/a
25	chr7:11066024-11066074	Caco-2	colon:	n/a
26	chr7:11091695-11091745	NHBE	bronchial:	n/a
27	chr7:11091695-11091745	SK-N-SH	brain:	n/a
28	chr7:11066024-11066074	GM12878	blood:	n/a
29	chr7:11091695-11091745	HIPEpiC	eye:	n/a
30	chr7:11066024-11066074	HAEpiC	amniotic membrane:	n/a
31	chr7:11091695-11091745	BJ	skin:	n/a
32	chr7:11066024-11066074	AG04450	lung:	fetal
33	chr7:11066024-11066074	K562	blood:	n/a
34	chr7:11091695-11091745	ProgFib	skin:	n/a
35	chr7:11091695-11091745	MCF10A-Er-Src	breast:	n/a
36	chr7:11091695-11091745	HRCEpiC	kidney:	n/a
37	chr7:11066024-11066074	HRPEpiC	eye:	n/a
38	chr7:11066024-11066074	AG09319	gingival:	n/a
39	chr7:11101436-11101486	NB4	blood:	n/a
40	chr7:11091695-11091745	T-47D	breast:	n/a
41	chr7:11101436-11101486	MCF10A-Er-Src	breast:	n/a
42	chr7:11091695-11091745	HL-60	blood:	n/a
43	chr7:11066024-11066074	MCF10A-Er-Src	breast:	n/a
44	chr7:11091695-11091745	U87	brain:	n/a
45	chr7:11101436-11101486	HEEpiC	esophagus:	n/a
46	chr7:11091695-11091745	AoSMC	blood vessel:	n/a
47	chr7:11091695-11091745	SKMC	muscle:	n/a
48	chr7:11101436-11101486	AG09319	gingival:	n/a
49	chr7:11101436-11101486	GM12892	blood:	n/a
50	chr7:11066024-11066074	HNPCEpiC	eye:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:11080726..11082742-chr7:11094808..11097463,2	K562	blood:
2	chr7:11050410..11053088-chr7:11054274..11057224,2	K562	blood:
3	chr7:10978704..10980840-chr7:11097948..11100485,2	MCF-7	breast:
4	chr7:11076840..11078456-chr7:11079311..11081268,2	MCF-7	breast:
5	chr7:11060572..11062361-chr7:11064593..11066272,2	MCF-7	breast:
6	chr7:11124384..11127270-chr7:11131542..11136731,4	K562	blood:
7	chr7:11120505..11122093-chr7:11122139..11123895,2	K562	blood:
8	chr7:11012908..11015544-chr7:11049769..11053521,4	MCF-7	breast:
9	chr7:11108681..11111650-chr7:11117427..11119548,2	K562	blood:
10	chr7:11130768..11133783-chr7:11134322..11137393,4	K562	blood:
11	chr7:11013556..11016152-chr7:11041534..11043076,2	MCF-7	breast:
12	chr7:11013088..11016193-chr7:11045661..11047742,3	MCF-7	breast:
13	chr7:11121527..11123973-chr7:11131499..11134132,2	K562	blood:
14	chr7:11140028..11142682-chr7:11145035..11147597,3	K562	blood:
15	chr7:11120505..11122093-chr7:11122139..11123895,2	K562	blood:
16	chr7:11128812..11130687-chr7:11131248..11133734,2	MCF-7	breast:
17	chr7:11034938..11037740-chr7:11039775..11043561,3	K562	blood:
18	chr7:11130768..11133331-chr7:11134322..11136010,2	K562	blood:
19	chr7:11104144..11105857-chr7:11109203..11110826,2	K562	blood:
20	chr7:10978536..10980200-chr7:11047753..11049829,2	MCF-7	breast:
21	chr7:11050410..11053088-chr7:11054274..11057224,2	K562	blood:
22	chr7:11086741..11089284-chr7:11093452..11095479,2	MCF-7	breast:
23	chr7:11088216..11090960-chr7:11126210..11129188,2	K562	blood:
24	chr7:11070822..11073698-chr7:11080421..11082466,2	MCF-7	breast:
25	chr7:10978342..10981036-chr7:11051873..11053394,2	K562	blood:
26	chr7:11088216..11090960-chr7:11126210..11129188,2	K562	blood:
27	chr7:11075307..11077062-chr7:11087663..11089190,2	K562	blood:
28	chr7:11035549..11039203-chr7:11040306..11043561,4	K562	blood:
29	chr7:11121943..11123973-chr7:11130475..11132999,2	K562	blood:
30	chr7:11113760..11116450-chr7:11117895..11120001,2	MCF-7	breast:
31	chr7:11118440..11120387-chr7:11122259..11124478,2	K562	blood:
32	chr7:11102318..11104655-chr7:11104749..11107010,2	K562	blood:
33	chr7:11130768..11133783-chr7:11134322..11137393,4	K562	blood:
34	chr7:11086741..11089284-chr7:11093452..11095479,2	MCF-7	breast:
35	chr7:11075307..11077062-chr7:11087663..11089190,2	K562	blood:
36	chr7:11102318..11104655-chr7:11104749..11107010,2	K562	blood:
37	chr7:11059468..11061173-chr7:11066901..11068645,2	K562	blood:
38	chr7:11011539..11015300-chr7:11077351..11081429,5	MCF-7	breast:
39	chr7:11113760..11116450-chr7:11117895..11120001,2	MCF-7	breast:
40	chr7:11076840..11078456-chr7:11079311..11081268,2	MCF-7	breast:
41	chr7:11130768..11133331-chr7:11134322..11136010,2	K562	blood:
42	chr7:11121943..11123973-chr7:11130475..11132999,2	K562	blood:
43	chr7:11126725..11129133-chr7:11132639..11135110,2	MCF-7	breast:
44	chr7:11121527..11123973-chr7:11131499..11134132,2	K562	blood:
45	chr7:11140028..11142682-chr7:11145035..11146787,2	K562	blood:
46	chr7:11049695..11051561-chr7:11052440..11055377,3	K562	blood:
47	chr16:28565167..28565701-chr7:11071813..11072350,2	Hela-S3	cervix:
48	chr7:11059468..11061173-chr7:11066901..11068645,2	K562	blood:
49	chr7:11126725..11129133-chr7:11132639..11135110,2	MCF-7	breast:
50	chr7:11012451..11014446-chr7:11075009..11077346,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDUFA4-3	chr7:11046026-11046503	NONHSAT119197

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PHF14	hsa-miR-155-5p	chr7:11142799-11142820
2	PHF14	hsa-miR-155-5p	chr7:11142813-11142835

Variant related genes	Relation type
PHF14	TF binding region
ENSG00000230370	TF binding region
PHF14	CpG island
ENSG00000230370	CpG island
ENSG00000106443	chromatin interactions
ENSG00000271185	chromatin interactions
ENSG00000176476	chromatin interactions
ENSG00000189043	chromatin interactions

Extended variants
information (count: 4155 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:4155 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73063417	chr7:11042943-11042944	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564821961	chr7:11042946-11042947	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530529643	chr7:11042969-11042970	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs550155774	chr7:11042993-11042994	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs372726769	chr7:11043001-11043002	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs73063418	chr7:11043039-11043040	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs75764265	chr7:11043053-11043054	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs75890304	chr7:11043054-11043055	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538417519	chr7:11043085-11043086	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539069393	chr7:11043141-11043142	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559013670	chr7:11043156-11043157	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185731254	chr7:11043163-11043164	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538278854	chr7:11043165-11043166	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs376617625	chr7:11043171-11043172	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs111861141	chr7:11043254-11043255	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs117491489	chr7:11043330-11043331	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs540949187	chr7:11043341-11043342	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs4720927	chr7:11043368-11043369	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs79000237	chr7:11043375-11043376	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546033403	chr7:11043382-11043383	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs193178916	chr7:11043386-11043387	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565036307	chr7:11043413-11043414	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs567464165	chr7:11043418-11043419	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs530510042	chr7:11043447-11043448	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs114870424	chr7:11043489-11043490	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs560575093	chr7:11043506-11043507	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs529610988	chr7:11043507-11043508	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs77801652	chr7:11043550-11043551	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs376013618	chr7:11043552-11043553	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs566604507	chr7:11043569-11043570	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs113572603	chr7:11043573-11043574	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139983233	chr7:11043599-11043600	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569369312	chr7:11043600-11043601	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs537930900	chr7:11043613-11043614	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575027458	chr7:11043673-11043674	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs145410191	chr7:11043680-11043681	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534142024	chr7:11043687-11043688	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs184447084	chr7:11043706-11043707	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs117665999	chr7:11043709-11043710	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs220092	chr7:11043718-11043719	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs556461837	chr7:11043725-11043726	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs567174918	chr7:11043729-11043730	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs575323057	chr7:11043746-11043747	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188450343	chr7:11043820-11043821	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs13241669	chr7:11043838-11043839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs11976137	chr7:11043852-11043853	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs13241568	chr7:11043854-11043855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs13241581	chr7:11043880-11043881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs55917513	chr7:11043895-11043896	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369355330	chr7:11043897-11043898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Gastric cancer	22014070	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	22495309	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1448 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:11014600-11045400	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr7:11014600-11092000	Weak transcription	Colonic Mucosa	Colon
3	chr7:11014800-11054200	Weak transcription	NHLF	lung
4	chr7:11014800-11075200	Weak transcription	Stomach Smooth Muscle	stomach
5	chr7:11014800-11117400	Weak transcription	HSMMtube	muscle
6	chr7:11015000-11064000	Weak transcription	Colon Smooth Muscle	Colon
7	chr7:11015200-11108200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr7:11016800-11057200	Weak transcription	Fetal Brain Male	brain
9	chr7:11017200-11076000	Weak transcription	HUVEC	blood vessel
10	chr7:11018600-11063800	Weak transcription	Brain Angular Gyrus	brain
11	chr7:11022800-11044800	Weak transcription	Hela-S3	cervix
12	chr7:11022800-11071000	Weak transcription	Right Ventricle	heart
13	chr7:11023000-11053600	Weak transcription	Primary B cells from peripheral blood	blood
14	chr7:11023200-11076200	Weak transcription	NH-A	brain
15	chr7:11023600-11053600	Weak transcription	Fetal Kidney	kidney
16	chr7:11031600-11103800	Weak transcription	Brain Cingulate Gyrus	brain
17	chr7:11033200-11053600	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr7:11033400-11053600	Weak transcription	HSMM	muscle
19	chr7:11033800-11045600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr7:11033800-11053600	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr7:11034400-11053400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr7:11034800-11064200	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr7:11035000-11047000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr7:11035200-11053600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr7:11035400-11046000	Weak transcription	Fetal Brain Female	brain
26	chr7:11035400-11054200	Weak transcription	Pancreas	Pancrea
27	chr7:11035400-11064000	Weak transcription	Brain Germinal Matrix	brain
28	chr7:11035600-11043400	Weak transcription	Fetal Thymus	thymus
29	chr7:11035600-11048000	Weak transcription	Gastric	stomach
30	chr7:11035800-11046000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr7:11035800-11046000	Weak transcription	Aorta	Aorta
32	chr7:11035800-11046000	Weak transcription	Fetal Muscle Leg	muscle
33	chr7:11035800-11047800	Weak transcription	Ovary	ovary
34	chr7:11035800-11053400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr7:11035800-11053400	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr7:11035800-11053600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr7:11035800-11054000	Weak transcription	Fetal Muscle Trunk	muscle
38	chr7:11035800-11054200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr7:11035800-11057200	Weak transcription	Spleen	Spleen
40	chr7:11035800-11063000	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr7:11035800-11063800	Weak transcription	Brain Hippocampus Middle	brain
42	chr7:11035800-11076000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr7:11035800-11092600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr7:11035800-11113000	Weak transcription	Esophagus	oesophagus
45	chr7:11035800-11113200	Weak transcription	Lung	lung
46	chr7:11035800-11123000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr7:11036000-11044800	Weak transcription	A549	lung
48	chr7:11036000-11053600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr7:11036000-11101600	Weak transcription	Placenta	Placenta
50	chr7:11036200-11046000	Weak transcription	Thymus	Thymus

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