Variant report

Variant	nsv427825
Chromosome Location	chr8:90495139-90653696
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1085)
CpG islands
(count:244)
Chromatin interactive
region (count:44)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1085 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:90629286-90629552	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:90623342-90624520	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:90648425-90649121	HepG2	liver:	n/a	n/a
4	ATF1	chr8:90573557-90573700	K562	blood:	n/a	n/a
5	ATF2	chr8:90573428-90573741	GM12878	blood:	n/a	n/a
6	ATF2	chr8:90573308-90573800	GM12878	blood:	n/a	n/a
7	ATF2	chr8:90555068-90555502	GM12878	blood:	n/a	n/a
8	ATF2	chr8:90555031-90555469	GM12878	blood:	n/a	n/a
9	ATF3	chr8:90623916-90624492	A549	lung:	n/a	n/a
10	ATF3	chr8:90555879-90556517	HCT-116	colon:	n/a	n/a
11	ATF3	chr8:90623655-90624566	HCT-116	colon:	n/a	n/a
12	BACH1	chr8:90546503-90546525	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr8:90623632-90623747	K562	blood:	n/a	n/a
14	BATF	chr8:90558716-90558952	GM12878	blood:	n/a	chr8:90558887-90558897
15	BATF	chr8:90516155-90516592	GM12878	blood:	n/a	n/a
16	BATF	chr8:90598761-90598934	GM12878	blood:	n/a	n/a
17	BATF	chr8:90573358-90573729	GM12878	blood:	n/a	n/a
18	BATF	chr8:90573368-90573648	GM12878	blood:	n/a	n/a
19	BATF	chr8:90555060-90555430	GM12878	blood:	n/a	n/a
20	BATF	chr8:90516113-90516556	GM12878	blood:	n/a	n/a
21	BCL11A	chr8:90516134-90516451	GM12878	blood:	n/a	n/a
22	BCL11A	chr8:90516133-90516491	GM12878	blood:	n/a	n/a
23	BCL11A	chr8:90573431-90573725	GM12878	blood:	n/a	n/a
24	BCL11A	chr8:90591182-90591444	GM12878	blood:	n/a	n/a
25	BCL11A	chr8:90555067-90555483	GM12878	blood:	n/a	n/a
26	BCL11A	chr8:90573395-90573688	GM12878	blood:	n/a	n/a
27	BCL11A	chr8:90555144-90555468	GM12878	blood:	n/a	n/a
28	BCL3	chr8:90555096-90555427	GM12878	blood:	n/a	n/a
29	BCL3	chr8:90623924-90624562	A549	lung:	n/a	chr8:90624090-90624099
30	BCL3	chr8:90624036-90624358	GM12878	blood:	n/a	chr8:90624090-90624099
31	BCL3	chr8:90535421-90535744	GM12878	blood:	n/a	n/a
32	BCL3	chr8:90623906-90624497	A549	lung:	n/a	chr8:90624090-90624099
33	BHLHE40	chr8:90624116-90624389	K562	blood:	n/a	n/a
34	BHLHE40	chr8:90554724-90554739	GM12878	blood:	n/a	n/a
35	BHLHE40	chr8:90623561-90624552	HepG2	liver:	n/a	n/a
36	BHLHE40	chr8:90515959-90516512	GM12878	blood:	n/a	n/a
37	BHLHE40	chr8:90624081-90624473	A549	lung:	n/a	n/a
38	BHLHE40	chr8:90555157-90555502	GM12878	blood:	n/a	n/a
39	BRCA1	chr8:90629299-90629540	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr8:90558744-90558970	Hela-S3	cervix:	n/a	n/a
41	CBX3	chr8:90623739-90624619	HCT-116	colon:	n/a	n/a
42	CBX3	chr8:90554375-90555060	HCT-116	colon:	n/a	n/a
43	CBX3	chr8:90554351-90555342	HCT-116	colon:	n/a	n/a
44	CBX3	chr8:90558457-90559170	HCT-116	colon:	n/a	chr8:90558777-90558788
45	CBX3	chr8:90623486-90624621	HCT-116	colon:	n/a	n/a
46	CBX3	chr8:90629083-90629708	HCT-116	colon:	n/a	n/a
47	CBX3	chr8:90518201-90518630	HCT-116	colon:	n/a	n/a
48	CBX3	chr8:90553503-90554245	HCT-116	colon:	n/a	n/a
49	CBX3	chr8:90558485-90559124	HCT-116	colon:	n/a	chr8:90558777-90558788
50	CEBPB	chr8:90528402-90528739	IMR90	lung:	n/a	chr8:90528579-90528590

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:90556162-90556212	CMK	blood:	n/a
2	chr8:90577545-90577595	HAEpiC	amniotic membrane:	n/a
3	chr8:90624127-90624177	HAEpiC	amniotic membrane:	n/a
4	chr8:90556162-90556212	NH-A	brain:	n/a
5	chr8:90636522-90636572	A549	lung:	n/a
6	chr8:90577545-90577595	RPTEC	kidney:	n/a
7	chr8:90624127-90624177	MCF10A-Er-Src	breast:	n/a
8	chr8:90636522-90636572	ECC-1	luminal epithelium:	n/a
9	chr8:90556162-90556212	HUVEC	blood vessel:	n/a
10	chr8:90577545-90577595	NB4	blood:	n/a
11	chr8:90556162-90556212	K562	blood:	n/a
12	chr8:90624127-90624177	PrEC	prostate:	n/a
13	chr8:90556162-90556212	HPAEpiC	pulmonary alveolar:	n/a
14	chr8:90577545-90577595	GM12878	blood:	n/a
15	chr8:90624127-90624177	NB4	blood:	n/a
16	chr8:90577545-90577595	HCT-116	colon:	n/a
17	chr8:90636522-90636572	HUVEC	blood vessel:	n/a
18	chr8:90636522-90636572	AG10803	skin:	n/a
19	chr8:90577545-90577595	SK-N-SH_RA	brain:	n/a
20	chr8:90636522-90636572	H1-hESC	embryonic stem cell:	embryo
21	chr8:90624127-90624177	HRE	kidney:	n/a
22	chr8:90556162-90556212	AoSMC	blood vessel:	n/a
23	chr8:90577545-90577595	BE2_C	brain:	n/a
24	chr8:90624127-90624177	MCF-7	breast:	n/a
25	chr8:90556162-90556212	NHBE	bronchial:	n/a
26	chr8:90624127-90624177	SK-N-MC	brain:	n/a
27	chr8:90556162-90556212	MCF-7	breast:	n/a
28	chr8:90624127-90624177	NHBE	bronchial:	n/a
29	chr8:90577545-90577595	K562	blood:	n/a
30	chr8:90636522-90636572	MCF10A-Er-Src	breast:	n/a
31	chr8:90556162-90556212	GM12891	blood:	n/a
32	chr8:90636522-90636572	AG04450	lung:	fetal
33	chr8:90577545-90577595	HRPEpiC	eye:	n/a
34	chr8:90624127-90624177	Hela-S3	cervix:	n/a
35	chr8:90636522-90636572	HEEpiC	esophagus:	n/a
36	chr8:90577545-90577595	ECC-1	luminal epithelium:	n/a
37	chr8:90636522-90636572	GM12891	blood:	n/a
38	chr8:90636522-90636572	CMK	blood:	n/a
39	chr8:90624127-90624177	ovcar-3	ovarian:	n/a
40	chr8:90556162-90556212	LNCaP	prostate:	n/a
41	chr8:90624127-90624177	HL-60	blood:	n/a
42	chr8:90577545-90577595	HUVEC	blood vessel:	n/a
43	chr8:90556162-90556212	ovcar-3	ovarian:	n/a
44	chr8:90577545-90577595	A549	lung:	n/a
45	chr8:90577545-90577595	HepG2	liver:	n/a
46	chr8:90624127-90624177	GM12892	blood:	n/a
47	chr8:90556162-90556212	GM12892	blood:	n/a
48	chr8:90556162-90556212	Caco-2	colon:	n/a
49	chr8:90636522-90636572	RPTEC	kidney:	n/a
50	chr8:90624127-90624177	HRCEpiC	kidney:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:90539182..90543934-chr8:90545577..90548881,5	MCF-7	breast:
2	chr8:90627324..90629190-chr8:90732562..90735490,2	MCF-7	breast:
3	chr8:90576363..90578196-chr8:90582814..90584387,2	MCF-7	breast:
4	chr8:90270487..90271274-chr8:90627944..90628605,2	MCF-7	breast:
5	chr8:90573142..90574734-chr8:90574796..90577742,2	MCF-7	breast:
6	chr8:90355900..90357965-chr8:90616064..90618024,2	MCF-7	breast:
7	chr8:90570319..90572702-chr8:90573054..90574779,2	MCF-7	breast:
8	chr8:90580330..90583016-chr8:90584267..90585810,2	MCF-7	breast:
9	chr8:90639321..90642147-chr8:90642418..90643951,2	K562	blood:
10	chr15:42762017..42764640-chr8:90562337..90564364,2	MCF-7	breast:
11	chr8:90579098..90579926-chr8:90624854..90625740,2	MCF-7	breast:
12	chr8:90630071..90632374-chr8:90637298..90640018,2	K562	blood:
13	chr8:90531252..90532820-chr8:90536073..90538212,2	MCF-7	breast:
14	chr8:90508884..90510843-chr8:90512576..90514659,2	K562	blood:
15	chr8:90531252..90532820-chr8:90536073..90538212,2	MCF-7	breast:
16	chr8:90639321..90642147-chr8:90642418..90643951,2	K562	blood:
17	chr8:90580330..90583016-chr8:90584267..90585810,2	MCF-7	breast:
18	chr8:90539182..90543934-chr8:90545577..90548881,5	MCF-7	breast:
19	chr8:90617470..90619221-chr8:90620152..90623030,2	K562	blood:
20	chr8:90515684..90517302-chr8:90531815..90534034,2	MCF-7	breast:
21	chr8:90531780..90534462-chr8:90543332..90544920,2	MCF-7	breast:
22	chr8:90573142..90574734-chr8:90574796..90577742,2	MCF-7	breast:
23	chr8:87713968..87715831-chr8:90615267..90617535,2	K562	blood:
24	chr1:11967266..11970144-chr8:90594461..90596817,2	K562	blood:
25	chr8:90570319..90572702-chr8:90573054..90574779,2	MCF-7	breast:
26	chr8:90633001..90635193-chr8:90639788..90641553,2	MCF-7	breast:
27	chr8:90613823..90615408-chr8:90662744..90664750,2	MCF-7	breast:
28	chr8:90638748..90641688-chr8:90643639..90646193,2	K562	blood:
29	chr8:90509802..90512432-chr8:90513213..90514927,2	MCF-7	breast:
30	chr8:90531640..90533471-chr8:90537181..90540329,3	MCF-7	breast:
31	chr8:90531640..90533471-chr8:90537181..90540329,3	MCF-7	breast:
32	chr8:90630071..90632374-chr8:90637298..90640018,2	K562	blood:
33	chr8:90531780..90534462-chr8:90543332..90544920,2	MCF-7	breast:
34	chr8:90508884..90510843-chr8:90512576..90514659,2	K562	blood:
35	chr8:90638748..90641688-chr8:90643639..90646193,2	K562	blood:
36	chr8:90497830..90499463-chr8:90622312..90625050,2	MCF-7	breast:
37	chr8:90576363..90578196-chr8:90582814..90584387,2	MCF-7	breast:
38	chr8:90634966..90637202-chr8:90644245..90646181,2	MCF-7	breast:
39	chr8:90497830..90499463-chr8:90622312..90625050,2	MCF-7	breast:
40	chr8:90515684..90517302-chr8:90531815..90534034,2	MCF-7	breast:
41	chr8:90617470..90619221-chr8:90620152..90623030,2	K562	blood:
42	chr8:90509802..90512432-chr8:90513213..90514927,2	MCF-7	breast:
43	chr8:90545613..90547386-chr8:90627990..90630572,2	MCF-7	breast:
44	chr8:90579098..90579926-chr8:90624854..90625740,2	MCF-7	breast:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NBN-1	chr8:90623663-90623699	ENSG00000251136
2	lnc-NBN-1	chr8:90627412-90627534	ENSG00000251136
3	lnc-NBN-1	chr8:90635314-90635433	ENSG00000251136
4	lnc-NBN-1	chr8:90627412-90627534	ENSG00000251136
5	lnc-NBN-1	chr8:90623663-90623699	ENSG00000251136.4
6	lnc-NBN-1	chr8:90623585-90624218	ENSG00000251136
7	lnc-NBN-1	chr8:90641382-90641499	ENSG00000251136.4
8	lnc-NBN-1	chr8:90608315-90608741	NONHSAT127610
9	lnc-NBN-1	chr8:90629222-90629385	ENSG00000251136
10	lnc-NBN-1	chr8:90627412-90627568	NONHSAT127613
11	lnc-NBN-1	chr8:90621638-90621723	ENSG00000251136.4
12	lnc-NBN-1	chr8:90627412-90627534	ENSG00000251136.4
13	lnc-NBN-1	chr8:90641382-90641499	ENSG00000251136
14	lnc-RIPK2-2	chr8:90627189-90627723	NONHSAT127614
15	lnc-NBN-1	chr8:90640384-90640528	ENSG00000251136.4
16	lnc-NBN-1	chr8:90640384-90640528	ENSG00000251136
17	lnc-NBN-1	chr8:90629158-90629385	ENSG00000251136
18	lnc-NBN-1	chr8:90623631-90624218	NONHSAT127613
19	lnc-NBN-1	chr8:90621629-90621723	ENSG00000251136
20	lnc-NBN-1	chr8:90624013-90624218	ENSG00000251136.4
21	lnc-NBN-1	chr8:90629308-90629386	ENSG00000251136
22	lnc-NBN-1	chr8:90632912-90633104	ENSG00000251136
23	lnc-NBN-1	chr8:90624013-90624218	ENSG00000251136

No data

Variant related genes	Relation type
ENSG00000251136	TF binding region
ENSG00000251136	CpG island
ENSG00000199347	chromatin interactions
ENSG00000251136	chromatin interactions
ENSG00000201801	chromatin interactions
MFHAS1	miRNA target sites
MORF4L2	miRNA target sites
EIF2C1	miRNA target sites
EIF4G3	miRNA target sites
HNF4A	miRNA target sites
HIPK3	miRNA target sites
HNRNPD	miRNA target sites
CLN6	miRNA target sites
NCOA3	miRNA target sites
NAPEPLD	miRNA target sites

Extended variants
information (count: 5289 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:5289 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113942549	chr8:90495182-90495183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566652550	chr8:90495185-90495186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548818675	chr8:90495211-90495212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183917816	chr8:90495216-90495217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567210800	chr8:90495222-90495223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs372796928	chr8:90495230-90495231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376052423	chr8:90495247-90495248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190000375	chr8:90495259-90495260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs145008056	chr8:90495334-90495335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557267298	chr8:90495347-90495348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569155839	chr8:90495355-90495356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539670194	chr8:90495533-90495534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557977904	chr8:90495648-90495649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573012756	chr8:90495690-90495691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181292796	chr8:90495698-90495699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs77654995	chr8:90495699-90495700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573527612	chr8:90495787-90495788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544903827	chr8:90495800-90495801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs115713802	chr8:90495875-90495876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563842575	chr8:90495974-90495975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533424741	chr8:90495987-90495988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs34059260	chr8:90496053-90496054	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs530498952	chr8:90496108-90496109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549411925	chr8:90496120-90496121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141379650	chr8:90496138-90496139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549163607	chr8:90496151-90496152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569198312	chr8:90496153-90496154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73303847	chr8:90496208-90496209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531642069	chr8:90496226-90496227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186816721	chr8:90496238-90496239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138058161	chr8:90496245-90496246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191651676	chr8:90496314-90496315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539776895	chr8:90496318-90496319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539732115	chr8:90496320-90496321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557992280	chr8:90496333-90496334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs28601654	chr8:90496380-90496381	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs75343790	chr8:90496401-90496402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34316942	chr8:90496442-90496443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113802635	chr8:90496477-90496478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555133612	chr8:90496483-90496484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573666015	chr8:90496488-90496489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111651788	chr8:90496565-90496566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537477063	chr8:90496585-90496586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555737906	chr8:90496613-90496614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577958043	chr8:90496670-90496671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149510559	chr8:90496673-90496674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs77544647	chr8:90496680-90496681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572521834	chr8:90496699-90496700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147184069	chr8:90496713-90496714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561251362	chr8:90496765-90496766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:522 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90487200-90517600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:90495800-90503400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:90497800-90498200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr8:90498800-90499200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr8:90498800-90499400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr8:90498800-90499600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr8:90498800-90499600	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr8:90498800-90499600	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr8:90498800-90499600	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr8:90499200-90499800	Enhancers	H9 Cell Line	embryonic stem cell
11	chr8:90499200-90501800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr8:90499400-90503000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr8:90506200-90506400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr8:90506400-90506600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr8:90506600-90511200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr8:90516000-90516800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr8:90517600-90517800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr8:90517800-90518600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr8:90529400-90529800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr8:90532800-90533000	Enhancers	HSMMtube	muscle
21	chr8:90533000-90534200	Weak transcription	HSMMtube	muscle
22	chr8:90533400-90534200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr8:90533400-90534200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr8:90534200-90534800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr8:90534200-90535200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr8:90534200-90535600	Enhancers	HSMMtube	muscle
27	chr8:90534800-90536400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr8:90535200-90535600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr8:90536400-90541400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr8:90540800-90542600	Enhancers	Hela-S3	cervix
31	chr8:90541400-90541800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr8:90541400-90542400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr8:90541600-90542000	Enhancers	Adipose Nuclei	Adipose
34	chr8:90542600-90546400	Weak transcription	Hela-S3	cervix
35	chr8:90545200-90545600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr8:90545600-90546200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr8:90546000-90546200	Enhancers	A549	lung
38	chr8:90546200-90546400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr8:90546200-90546400	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr8:90546200-90546800	Flanking Active TSS	A549	lung
41	chr8:90546400-90546600	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr8:90546400-90546600	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr8:90546400-90546600	Enhancers	Hela-S3	cervix
44	chr8:90546400-90546800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
45	chr8:90546400-90547000	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr8:90546400-90547800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr8:90546600-90546800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr8:90546600-90546800	Flanking Active TSS	Hela-S3	cervix
49	chr8:90546600-90547000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
50	chr8:90546600-90547000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell

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