Variant report

Variant	nsv1028201
Chromosome Location	chr8:91968527-92009964
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:697)
CpG islands
(count:488)
Chromatin interactive
region (count:79)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:697 , 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	chr8:91997708-91997736	K562	blood:	n/a	n/a
2	ARID3A	chr8:91986489-91987011	K562	blood:	n/a	n/a
3	ARID3A	chr8:92003401-92003701	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:91988694-91988843	K562	blood:	n/a	n/a
5	ARID3A	chr8:91995863-91996770	K562	blood:	n/a	n/a
6	ATF1	chr8:91996240-91996721	K562	blood:	n/a	n/a
7	ATF1	chr8:91986521-91986850	K562	blood:	n/a	n/a
8	ATF2	chr8:91997532-91997979	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr8:91986459-91986845	K562	blood:	n/a	n/a
10	BACH1	chr8:91997054-91997739	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr8:91984909-91985001	K562	blood:	n/a	n/a
12	BCLAF1	chr8:91997507-91997920	K562	blood:	n/a	n/a
13	BCLAF1	chr8:91986436-91986992	K562	blood:	n/a	n/a
14	BHLHE40	chr8:91996617-91996837	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:91986533-91986814	K562	blood:	n/a	n/a
16	BHLHE40	chr8:91997230-91997807	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:91996996-91998092	K562	blood:	n/a	chr8:91997817-91997833
18	BHLHE40	chr8:91996525-91996787	K562	blood:	n/a	n/a
19	CBX3	chr8:91997212-91998058	K562	blood:	n/a	n/a
20	CBX3	chr8:91976306-91976739	K562	blood:	n/a	n/a
21	CBX3	chr8:91976402-91976817	HCT-116	colon:	n/a	n/a
22	CBX3	chr8:91976290-91976652	HCT-116	colon:	n/a	n/a
23	CBX3	chr8:91986249-91986872	K562	blood:	n/a	n/a
24	CCNT2	chr8:92001549-92001773	K562	blood:	n/a	n/a
25	CCNT2	chr8:91997214-91998008	K562	blood:	n/a	n/a
26	CCNT2	chr8:91986611-91986838	K562	blood:	n/a	n/a
27	CEBPB	chr8:92002115-92002324	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr8:91970469-91970579	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr8:91986431-91986926	K562	blood:	n/a	n/a
30	CEBPB	chr8:91986534-91986833	K562	blood:	n/a	n/a
31	CEBPB	chr8:91970418-91970532	K562	blood:	n/a	n/a
32	CEBPB	chr8:92002092-92002300	K562	blood:	n/a	n/a
33	CEBPB	chr8:91981798-91982068	A549	lung:	n/a	chr8:91981944-91981955
34	CEBPB	chr8:91999001-91999338	IMR90	lung:	n/a	n/a
35	CEBPB	chr8:91981777-91982105	IMR90	lung:	n/a	chr8:91981944-91981955
36	CEBPB	chr8:91981837-91982070	HepG2	liver:	n/a	chr8:91981944-91981955
37	CEBPB	chr8:91973331-91973475	K562	blood:	n/a	n/a
38	CEBPB	chr8:91999030-91999292	K562	blood:	n/a	n/a
39	CEBPB	chr8:91981791-91982102	K562	blood:	n/a	chr8:91981944-91981955
40	CEBPB	chr8:91984402-91984516	K562	blood:	n/a	n/a
41	CEBPD	chr8:91986545-91986929	K562	blood:	n/a	n/a
42	CEBPD	chr8:91986459-91986992	K562	blood:	n/a	n/a
43	CHD1	chr8:91988239-91988246	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr8:91996971-91997230	GM12878	blood:	n/a	n/a
45	CHD2	chr8:91997097-91997322	GM12878	blood:	n/a	n/a
46	CHD2	chr8:91997583-91997895	GM12878	blood:	n/a	chr8:91997644-91997654
47	CHD2	chr8:91986420-91986840	K562	blood:	n/a	n/a
48	CHD2	chr8:91997648-91998026	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr8:91997132-91998064	K562	blood:	n/a	chr8:91997555-91997565 chr8:91997644-91997654
50	CREB1	chr8:91997655-91998081	H1-hESC	embryonic stem cell:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:91997985-91998035	MCF10A-Er-Src	breast:	n/a
2	chr8:91997231-91997281	Hela-S3	cervix:	n/a
3	chr8:91993547-91993597	HCPEpiC	choroid plexus:	n/a
4	chr8:91997810-91997860	H1-hESC	embryonic stem cell:	embryo
5	chr8:91997553-91997603	NB4	blood:	n/a
6	chr8:91993547-91993597	Hela-S3	cervix:	n/a
7	chr8:91997553-91997603	NHDF-neo	bronchial:	n/a
8	chr8:91997985-91998035	U87	brain:	n/a
9	chr8:91993547-91993597	HRE	kidney:	n/a
10	chr8:91997810-91997860	NT2-D1	testis:	n/a
11	chr8:91997810-91997860	NHBE	bronchial:	n/a
12	chr8:91997810-91997860	MCF10A-Er-Src	breast:	n/a
13	chr8:91997553-91997603	PANC-1	pancreas:	n/a
14	chr8:91997001-91997051	PrEC	prostate:	n/a
15	chr8:91997001-91997051	HNPCEpiC	eye:	n/a
16	chr8:91997553-91997603	Caco-2	colon:	n/a
17	chr8:91997231-91997281	HIPEpiC	eye:	n/a
18	chr8:91997810-91997860	SKMC	muscle:	n/a
19	chr8:91997810-91997860	AoSMC	blood vessel:	n/a
20	chr8:91997810-91997860	HRE	kidney:	n/a
21	chr8:91993547-91993597	BE2_C	brain:	n/a
22	chr8:91997001-91997051	LNCaP	prostate:	n/a
23	chr8:91997001-91997051	Hepatocyte	liver:	n/a
24	chr8:91993547-91993597	MCF10A-Er-Src	breast:	n/a
25	chr8:91997810-91997860	HepG2	liver:	n/a
26	chr8:91997985-91998035	SK-N-SH_RA	brain:	n/a
27	chr8:91993547-91993597	T-47D	breast:	n/a
28	chr8:91997001-91997051	H1-hESC	embryonic stem cell:	embryo
29	chr8:91997810-91997860	BE2_C	brain:	n/a
30	chr8:91997985-91998035	NB4	blood:	n/a
31	chr8:91997001-91997051	SK-N-SH_RA	brain:	n/a
32	chr8:91986716-91986766	HEEpiC	esophagus:	n/a
33	chr8:91997985-91998035	RPTEC	kidney:	n/a
34	chr8:91997810-91997860	NB4	blood:	n/a
35	chr8:91997553-91997603	HEEpiC	esophagus:	n/a
36	chr8:91997810-91997860	SK-N-SH_RA	brain:	n/a
37	chr8:91997231-91997281	MCF-7	breast:	n/a
38	chr8:91997553-91997603	NT2-D1	testis:	n/a
39	chr8:91997985-91998035	HEEpiC	esophagus:	n/a
40	chr8:91997553-91997603	HRCEpiC	kidney:	n/a
41	chr8:91997985-91998035	Jurkat	blood:	n/a
42	chr8:91986716-91986766	HNPCEpiC	eye:	n/a
43	chr8:91986716-91986766	H1-hESC	embryonic stem cell:	embryo
44	chr8:91997231-91997281	Hepatocyte	liver:	n/a
45	chr8:91997985-91998035	HCM	heart:	n/a
46	chr8:91986716-91986766	ECC-1	luminal epithelium:	n/a
47	chr8:92001646-92001696	ECC-1	luminal epithelium:	n/a
48	chr8:91997001-91997051	RPTEC	kidney:	n/a
49	chr8:91997001-91997051	PANC-1	pancreas:	n/a
50	chr8:91997001-91997051	A549	lung:	n/a

(count:79 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:91983056..91985019-chr8:92051463..92053867,2	K562	blood:
2	chr8:91963528..91965609-chr8:91967085..91969993,2	K562	blood:
3	chr8:91971665..91973537-chr8:91974194..91975735,2	K562	blood:
4	chr8:91999377..92002294-chr8:92003813..92006400,3	K562	blood:
5	chr8:91994788..91999054-chr8:92079277..92083347,7	K562	blood:
6	chr8:91657448..91659157-chr8:91966713..91968601,2	MCF-7	breast:
7	chr8:92002644..92004190-chr8:92081898..92084498,2	K562	blood:
8	chr8:92004322..92007291-chr8:92051053..92053226,2	K562	blood:
9	chr8:91982671..91984562-chr8:92080291..92082134,2	K562	blood:
10	chr8:91989051..91990936-chr8:92080419..92082985,2	K562	blood:
11	chr8:92004303..92007415-chr8:92009979..92012206,3	K562	blood:
12	chr8:91960706..91962552-chr8:91966343..91969048,2	K562	blood:
13	chr8:92000674..92003202-chr8:92089902..92092350,2	K562	blood:
14	chr8:91975435..91977533-chr8:91979660..91982457,2	K562	blood:
15	chr8:91995324..91997173-chr8:92051480..92053172,3	K562	blood:
16	chr8:91996349..91999224-chr8:92056990..92058927,3	K562	blood:
17	chr8:91656414..91658421-chr8:91997770..91999676,2	MCF-7	breast:
18	chr8:91968241..91970029-chr8:91971497..91973539,2	K562	blood:
19	chr8:92002857..92004096-chr8:92088435..92089787,15	MCF-7	breast:
20	chr8:91997724..92001247-chr8:92056707..92058927,3	K562	blood:
21	chr8:91972273..91973917-chr8:91996696..91998329,2	K562	blood:
22	chr8:91658730..91663792-chr8:91996044..91998781,4	K562	blood:
23	chr8:91994028..91996763-chr8:92049752..92051452,2	K562	blood:
24	chr8:91769820..91771750-chr8:91998621..92000554,2	MCF-7	breast:
25	chr8:91977534..91979661-chr8:91982392..91983959,2	K562	blood:
26	chr8:91977444..91979334-chr8:91982814..91985535,2	MCF-7	breast:
27	chr8:91977534..91979661-chr8:91982392..91983959,2	K562	blood:
28	chr8:91977444..91979334-chr8:91982814..91985535,2	MCF-7	breast:
29	chr8:91973901..91977899-chr8:91982620..91986949,4	K562	blood:
30	chr8:91966394..91968978-chr8:91994771..91996720,2	K562	blood:
31	chr8:92001855..92004650-chr8:92090350..92092712,3	MCF-7	breast:
32	chr8:92007845..92010030-chr8:92010499..92013168,3	K562	blood:
33	chr8:90913489..90916241-chr8:91996581..91998462,2	K562	blood:
34	chr8:91992188..91994293-chr8:92084986..92087626,2	K562	blood:
35	chr8:91971665..91973537-chr8:91974194..91975735,2	K562	blood:
36	chr8:91966394..91968978-chr8:91994771..91996720,2	K562	blood:
37	chr8:91997520..92000629-chr8:92050976..92054061,7	K562	blood:
38	chr8:92007098..92008778-chr8:92015883..92017756,2	K562	blood:
39	chr8:91012176..91015175-chr8:91997197..91999133,2	K562	blood:
40	chr8:91737683..91740315-chr8:91995826..91997401,2	K562	blood:
41	chr8:92004208..92005014-chr8:92088692..92089523,2	MCF-7	breast:
42	chr8:92001253..92003816-chr8:92033444..92035272,2	MCF-7	breast:
43	chr8:91996280..91999551-chr8:92008515..92012349,6	K562	blood:
44	chr8:91999536..92001473-chr8:92080470..92083354,2	K562	blood:
45	chr8:92008926..92011654-chr8:92079455..92081464,2	K562	blood:
46	chr8:91978161..91980751-chr8:91981299..91985101,3	K562	blood:
47	chr8:91975064..91976862-chr8:91995756..91998069,2	K562	blood:
48	chr8:91980784..91984297-chr8:91985650..91987857,3	K562	blood:
49	chr8:91982249..91984600-chr8:91984850..91987813,4	K562	blood:
50	chr8:91992188..91994461-chr8:92084904..92087626,3	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	TMEM55A	hsa-miR-375	chr8:92006839-92006860

Variant related genes	Relation type
C8orf88	TF binding region
C8orf88	CpG island
ENSG00000253738	chromatin interactions
ENSG00000180694	chromatin interactions
ENSG00000164823	chromatin interactions
ENSG00000155100	chromatin interactions
ENSG00000155099	chromatin interactions
ENSG00000254219	chromatin interactions
ENSG00000168556	chromatin interactions
ENSG00000104325	chromatin interactions
ENSG00000232648	chromatin interactions
ENSG00000253250	chromatin interactions
ENSG00000246792	chromatin interactions

Extended variants
information (count: 1330 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:1330 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1060583	chr8:91968527-91968528	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs77457754	chr8:91968611-91968612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs146629142	chr8:91968676-91968677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547529899	chr8:91968694-91968695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150656072	chr8:91968697-91968698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114377642	chr8:91968805-91968806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549089110	chr8:91968809-91968810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138899851	chr8:91968850-91968851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375467597	chr8:91968873-91968874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569994418	chr8:91968903-91968904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537312624	chr8:91968934-91968935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558842424	chr8:91968945-91968946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs570661830	chr8:91968983-91968984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs75863427	chr8:91969056-91969057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548151648	chr8:91969077-91969078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552782633	chr8:91969088-91969089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574522179	chr8:91969126-91969127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541438149	chr8:91969165-91969166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557028440	chr8:91969168-91969169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369634999	chr8:91969172-91969173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs398008738	chr8:91969212-91969213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559463817	chr8:91969247-91969248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569959025	chr8:91969256-91969257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556932611	chr8:91969316-91969317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546092845	chr8:91969329-91969330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564375954	chr8:91969332-91969333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528255789	chr8:91969348-91969349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540463445	chr8:91969367-91969368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139777838	chr8:91969393-91969394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536826359	chr8:91969456-91969457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs199652987	chr8:91969485-91969486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs116762348	chr8:91969510-91969511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185436132	chr8:91969517-91969518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113771512	chr8:91969539-91969540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563313379	chr8:91969541-91969542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111304583	chr8:91969555-91969556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs3178490	chr8:91969595-91969596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552438405	chr8:91969614-91969615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373492972	chr8:91969664-91969665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1055146	chr8:91969669-91969670	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs552410759	chr8:91969676-91969677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115714351	chr8:91969844-91969845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534902955	chr8:91969900-91969901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs77747755	chr8:91969912-91969913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113115541	chr8:91969925-91969926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200125253	chr8:91969932-91969933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138936315	chr8:91969957-91969958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547199260	chr8:91970004-91970005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567147726	chr8:91970009-91970010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551782970	chr8:91970010-91970011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:910 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91951800-91986400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr8:91953400-91972000	Weak transcription	NHDF-Ad	bronchial
3	chr8:91953400-91981400	Weak transcription	HSMM	muscle
4	chr8:91953400-91984600	Weak transcription	NH-A	brain
5	chr8:91953600-91970000	Weak transcription	Brain Anterior Caudate	brain
6	chr8:91953600-91974800	Weak transcription	Brain Cingulate Gyrus	brain
7	chr8:91953600-91976000	Weak transcription	Brain Substantia Nigra	brain
8	chr8:91953600-91977600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr8:91954000-91970600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr8:91954000-91974400	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr8:91955000-91974800	Weak transcription	Fetal Muscle Leg	muscle
12	chr8:91955600-91972000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr8:91955600-91975000	Weak transcription	Adipose Nuclei	Adipose
14	chr8:91955800-91972000	Weak transcription	Fetal Lung	lung
15	chr8:91956600-91974400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr8:91957200-91976200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr8:91957400-91974400	Weak transcription	Primary hematopoietic stem cells	blood
18	chr8:91958000-91976200	Weak transcription	K562	blood
19	chr8:91958200-91996000	Weak transcription	Fetal Stomach	stomach
20	chr8:91958800-91972000	Weak transcription	Brain Angular Gyrus	brain
21	chr8:91959200-91969800	Weak transcription	Aorta	Aorta
22	chr8:91959200-91974600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr8:91960600-91974800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr8:91960600-91975200	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr8:91960600-91976000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr8:91960800-91972000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr8:91961200-91972200	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr8:91961200-91975400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr8:91961200-91976000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr8:91961600-91975000	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr8:91963000-91975000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr8:91963600-91975800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr8:91963600-91979000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr8:91964600-91972000	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr8:91964600-91989800	Weak transcription	Left Ventricle	heart
36	chr8:91964800-91996600	Weak transcription	Ovary	ovary
37	chr8:91965600-91979200	Weak transcription	Stomach Smooth Muscle	stomach
38	chr8:91966200-91974800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr8:91966200-91976200	Weak transcription	Colon Smooth Muscle	Colon
40	chr8:91970400-91976200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr8:91970600-91970800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr8:91970800-91971000	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr8:91971000-91971200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr8:91971200-91972000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr8:91971800-91976400	Weak transcription	Brain Hippocampus Middle	brain
46	chr8:91971800-91996600	Weak transcription	Thymus	Thymus
47	chr8:91972000-91972400	ZNF genes & repeats	Brain Angular Gyrus	brain
48	chr8:91972000-91972600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr8:91972000-91972600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr8:91972000-91972600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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