Variant report

Variant	nsv891281
Chromosome Location	chr8:110450092-110558622
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1502)
CpG islands
(count:1467)
Chromatin interactive
region (count:143)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1502 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:110552233-110553077	K562	blood:	n/a	n/a
2	ARID3A	chr8:110551476-110551720	K562	blood:	n/a	n/a
3	ARID3A	chr8:110552194-110552864	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:110554116-110554159	HepG2	liver:	n/a	n/a
5	ATF1	chr8:110551609-110552850	K562	blood:	n/a	n/a
6	ATF1	chr8:110473883-110474077	K562	blood:	n/a	n/a
7	ATF2	chr8:110534736-110535369	GM12878	blood:	n/a	n/a
8	ATF2	chr8:110534718-110535360	GM12878	blood:	n/a	n/a
9	ATF2	chr8:110552080-110552998	GM12878	blood:	n/a	n/a
10	ATF2	chr8:110537103-110537934	GM12878	blood:	n/a	n/a
11	ATF2	chr8:110536639-110537915	GM12878	blood:	n/a	n/a
12	ATF2	chr8:110551891-110552996	GM12878	blood:	n/a	n/a
13	ATF3	chr8:110534810-110535151	GM12878	blood:	n/a	n/a
14	ATF3	chr8:110552150-110552546	K562	blood:	n/a	n/a
15	BACH1	chr8:110551041-110551050	K562	blood:	n/a	n/a
16	BACH1	chr8:110552247-110552883	K562	blood:	n/a	n/a
17	BACH1	chr8:110532159-110532187	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr8:110477232-110477389	K562	blood:	n/a	n/a
19	BACH1	chr8:110552031-110552714	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr8:110552580-110552919	GM12878	blood:	n/a	n/a
21	BATF	chr8:110537276-110537612	GM12878	blood:	n/a	n/a
22	BCL11A	chr8:110537252-110537706	GM12878	blood:	n/a	n/a
23	BCL11A	chr8:110552223-110552645	GM12878	blood:	n/a	n/a
24	BCL3	chr8:110461556-110461800	GM12878	blood:	n/a	n/a
25	BCL3	chr8:110551896-110552533	GM12878	blood:	n/a	chr8:110552120-110552133
26	BCL3	chr8:110537205-110537580	GM12878	blood:	n/a	n/a
27	BCL3	chr8:110458697-110459000	GM12878	blood:	n/a	n/a
28	BCL3	chr8:110551900-110552741	A549	lung:	n/a	chr8:110552120-110552133
29	BCL3	chr8:110552172-110552890	A549	lung:	n/a	n/a
30	BCL3	chr8:110461550-110461755	GM12878	blood:	n/a	n/a
31	BCLAF1	chr8:110551951-110553066	GM12878	blood:	n/a	chr8:110552120-110552133
32	BCLAF1	chr8:110534782-110535404	GM12878	blood:	n/a	n/a
33	BCLAF1	chr8:110551358-110551861	GM12878	blood:	n/a	n/a
34	BCLAF1	chr8:110536919-110537947	GM12878	blood:	n/a	n/a
35	BCLAF1	chr8:110551675-110552993	GM12878	blood:	n/a	chr8:110552120-110552133
36	BCLAF1	chr8:110537145-110537870	GM12878	blood:	n/a	n/a
37	BHLHE40	chr8:110534906-110535193	K562	blood:	n/a	n/a
38	BHLHE40	chr8:110551392-110552974	K562	blood:	n/a	chr8:110552091-110552107
39	BHLHE40	chr8:110551556-110552959	GM12878	blood:	n/a	chr8:110552091-110552107
40	BHLHE40	chr8:110477349-110477423	K562	blood:	n/a	n/a
41	BHLHE40	chr8:110534880-110535182	HepG2	liver:	n/a	n/a
42	BHLHE40	chr8:110537286-110537773	GM12878	blood:	n/a	n/a
43	BHLHE40	chr8:110534796-110535336	GM12878	blood:	n/a	n/a
44	BHLHE40	chr8:110463120-110463463	K562	blood:	n/a	n/a
45	BHLHE40	chr8:110551531-110552777	HepG2	liver:	n/a	chr8:110552091-110552107
46	BHLHE40	chr8:110552065-110552744	A549	lung:	n/a	chr8:110552091-110552107
47	BHLHE40	chr8:110555418-110555593	GM12878	blood:	n/a	n/a
48	BHLHE40	chr8:110549436-110549690	K562	blood:	n/a	n/a
49	BHLHE40	chr8:110553208-110553212	GM12878	blood:	n/a	n/a
50	BRCA1	chr8:110553505-110553580	GM12878	blood:	n/a	n/a

(count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:110497696-110497746	HIPEpiC	eye:	n/a
2	chr8:110551708-110551758	HIPEpiC	eye:	n/a
3	chr8:110552613-110552663	HAEpiC	amniotic membrane:	n/a
4	chr8:110497696-110497746	HIPEpiC	eye:	n/a
5	chr8:110551708-110551758	HIPEpiC	eye:	n/a
6	chr8:110552613-110552663	HAEpiC	amniotic membrane:	n/a
7	chr8:110551808-110551858	ECC-1	luminal epithelium:	n/a
8	chr8:110456058-110456108	BJ	skin:	n/a
9	chr8:110543390-110543440	HCM	heart:	n/a
10	chr8:110520471-110520521	ProgFib	skin:	n/a
11	chr8:110551796-110551846	GM06990	blood:	n/a
12	chr8:110552896-110552946	GM19239	blood:	n/a
13	chr8:110552896-110552946	GM12891	blood:	n/a
14	chr8:110551708-110551758	BJ	skin:	n/a
15	chr8:110551578-110551628	A549	lung:	n/a
16	chr8:110552613-110552663	HCPEpiC	choroid plexus:	n/a
17	chr8:110552613-110552663	AG04449	skin:	fetal
18	chr8:110551877-110551927	HEK293	kidney:	embryo
19	chr8:110470148-110470198	HNPCEpiC	eye:	n/a
20	chr8:110551808-110551858	GM12878	blood:	n/a
21	chr8:110456058-110456108	HRPEpiC	eye:	n/a
22	chr8:110552843-110552893	AG09319	gingival:	n/a
23	chr8:110551993-110552043	PANC-1	pancreas:	n/a
24	chr8:110552297-110552347	AG04449	skin:	fetal
25	chr8:110553825-110553875	HCPEpiC	choroid plexus:	n/a
26	chr8:110556472-110556522	Jurkat	blood:	n/a
27	chr8:110470148-110470198	AG09319	gingival:	n/a
28	chr8:110520471-110520521	BE2_C	brain:	n/a
29	chr8:110497696-110497746	HRCEpiC	kidney:	n/a
30	chr8:110552794-110552844	SAEC	small airway:	n/a
31	chr8:110552416-110552466	AG09319	gingival:	n/a
32	chr8:110556472-110556522	PFSK-1	brain:	n/a
33	chr8:110551808-110551858	HL-60	blood:	n/a
34	chr8:110551708-110551758	ECC-1	luminal epithelium:	n/a
35	chr8:110470148-110470198	Caco-2	colon:	n/a
36	chr8:110551799-110551849	GM12878	blood:	n/a
37	chr8:110543390-110543440	SK-N-SH	brain:	n/a
38	chr8:110551884-110551934	MCF10A-Er-Src	breast:	n/a
39	chr8:110551808-110551858	HEEpiC	esophagus:	n/a
40	chr8:110520471-110520521	HCM	heart:	n/a
41	chr8:110552297-110552347	NH-A	brain:	n/a
42	chr8:110556472-110556522	NH-A	brain:	n/a
43	chr8:110497696-110497746	NHBE	bronchial:	n/a
44	chr8:110497696-110497746	GM12891	blood:	n/a
45	chr8:110551808-110551858	HIPEpiC	eye:	n/a
46	chr8:110497696-110497746	K562	blood:	n/a
47	chr8:110551976-110552026	HL-60	blood:	n/a
48	chr8:110552297-110552347	Hepatocyte	liver:	n/a
49	chr8:110551799-110551849	HUVEC	blood vessel:	n/a
50	chr8:110551796-110551846	Caco-2	colon:	n/a

(count:143 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:110443668..110447226-chr8:110448028..110451170,4	K562	blood:
2	chr8:110345326..110347078-chr8:110455442..110456980,2	K562	blood:
3	chr8:110462548..110464182-chr8:110467144..110470132,2	MCF-7	breast:
4	chr8:110514077..110516433-chr8:110518182..110521221,3	K562	blood:
5	chr8:110487318..110489249-chr8:110492747..110497686,4	MCF-7	breast:
6	chr8:110462782..110463819-chr8:110664356..110665380,8	MCF-7	breast:
7	chr8:110525800..110528090-chr8:110551913..110554000,2	MCF-7	breast:
8	chr8:110546124..110548249-chr8:110656124..110658861,2	MCF-7	breast:
9	chr8:110526872..110528592-chr8:110535005..110537105,2	K562	blood:
10	chr8:110500097..110503001-chr8:110504877..110506686,2	MCF-7	breast:
11	chr8:110551479..110553406-chr8:110554109..110556947,2	MCF-7	breast:
12	chr8:110459151..110460064-chr8:110664745..110665328,2	MCF-7	breast:
13	chr8:110520565..110523239-chr8:110549875..110552142,3	MCF-7	breast:
14	chr8:110492411..110494617-chr8:110510142..110512481,2	MCF-7	breast:
15	chr8:110462548..110464182-chr8:110467144..110470132,2	MCF-7	breast:
16	chr8:110500097..110503001-chr8:110504877..110506686,2	MCF-7	breast:
17	chr8:110485934..110489021-chr8:110489156..110492335,3	MCF-7	breast:
18	chr12:49658713..49659445-chr8:110552398..110552940,2	Hela-S3	cervix:
19	chr8:110344871..110348245-chr8:110549404..110554651,7	MCF-7	breast:
20	chr8:110480733..110484366-chr8:110549857..110553138,3	MCF-7	breast:
21	chr8:110450010..110452519-chr8:110455545..110457090,2	K562	blood:
22	chr8:110525756..110528832-chr8:110532009..110534427,3	K562	blood:
23	chr8:110550857..110553602-chr8:110653501..110657228,5	K562	blood:
24	chr8:110462528..110463405-chr8:110651980..110652480,2	MCF-7	breast:
25	chr8:110510174..110512174-chr8:110514390..110516726,2	K562	blood:
26	chr8:110535396..110538672-chr8:110538896..110541782,3	MCF-7	breast:
27	chr8:110528786..110530891-chr8:110547707..110549539,2	MCF-7	breast:
28	chr8:110550854..110555574-chr8:110655521..110658971,8	MCF-7	breast:
29	chr8:110492889..110495153-chr8:110496090..110498329,2	MCF-7	breast:
30	chr8:110506183..110508052-chr8:110509587..110512256,2	MCF-7	breast:
31	chr8:110539789..110542278-chr8:110544776..110546854,2	K562	blood:
32	chr8:110550694..110556278-chr8:110557032..110565525,15	MCF-7	breast:
33	chr8:110536248..110538918-chr8:110543681..110545993,2	K562	blood:
34	chr8:110472022..110474272-chr8:110550110..110552856,2	MCF-7	breast:
35	chr8:110550942..110554132-chr8:110556577..110560924,6	K562	blood:
36	chr8:110532017..110535509-chr8:110550359..110553902,4	K562	blood:
37	chr8:110463060..110463781-chr8:110664134..110664918,2	MCF-7	breast:
38	chr8:110514077..110516433-chr8:110518182..110521221,3	K562	blood:
39	chr8:110476428..110479434-chr8:110485234..110488569,3	MCF-7	breast:
40	chr8:110536248..110538918-chr8:110543681..110545993,2	K562	blood:
41	chr11:797687..798265-chr8:110552821..110553365,2	HCT-116	colon:
42	chr8:110486322..110490229-chr8:110490493..110494144,5	MCF-7	breast:
43	chr8:110491337..110493958-chr8:110550109..110551629,2	MCF-7	breast:
44	chr8:110351472..110353589-chr8:110551719..110554657,2	K562	blood:
45	chr8:110462866..110463874-chr8:110563606..110564958,17	MCF-7	breast:
46	chr8:110483309..110485365-chr8:110487237..110489170,2	MCF-7	breast:
47	chr8:110461291..110465454-chr8:110550197..110554392,6	MCF-7	breast:
48	chr8:110490813..110493110-chr8:110549363..110552380,3	MCF-7	breast:
49	chr8:110547547..110552585-chr8:110554404..110556574,4	K562	blood:
50	chr8:110375572..110377365-chr8:110452939..110455019,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000254185	TF binding region
PKHD1L1	TF binding region
EBAG9	TF binding region
ENSG00000254185	CpG island
PKHD1L1	CpG island
EBAG9	CpG island
ENSG00000147642	chromatin interactions
ENSG00000120526	chromatin interactions
ENSG00000263809	chromatin interactions
ENSG00000235010	chromatin interactions
ENSG00000205038	chromatin interactions
ENSG00000177542	chromatin interactions
ENSG00000126903	chromatin interactions
ENSG00000147654	chromatin interactions
ENSG00000161970	chromatin interactions
ENSG00000266967	chromatin interactions
ENSG00000120533	chromatin interactions
ENSG00000254185	chromatin interactions
ENSG00000242110	chromatin interactions
ENSG00000167553	chromatin interactions
ENSG00000248050	chromatin interactions

Extended variants
information (count: 3737 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:3737 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7816624	chr8:110450092-110450093	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs111807727	chr8:110450103-110450104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532413592	chr8:110450105-110450106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553518012	chr8:110450109-110450110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552139049	chr8:110450126-110450127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145864854	chr8:110450137-110450138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529514232	chr8:110450155-110450156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537918054	chr8:110450156-110450157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146641985	chr8:110450169-110450170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186499837	chr8:110450219-110450220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372199472	chr8:110450221-110450222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536157318	chr8:110450250-110450251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191484254	chr8:110450255-110450256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573148510	chr8:110450284-110450285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573165185	chr8:110450301-110450302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545055868	chr8:110450321-110450322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558559868	chr8:110450345-110450346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs199986337	chr8:110450368-110450369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183237208	chr8:110450442-110450443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543141651	chr8:110450533-110450534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs141337729	chr8:110450543-110450544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200694836	chr8:110450571-110450572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs117037399	chr8:110450593-110450594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201538871	chr8:110450605-110450606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369696441	chr8:110450623-110450624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540463740	chr8:110450649-110450650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560449366	chr8:110450674-110450675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35624217	chr8:110450676-110450677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs199965963	chr8:110450687-110450688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10088783	chr8:110450775-110450776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552173574	chr8:110450818-110450819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562507564	chr8:110450852-110450853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531718050	chr8:110450864-110450865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548614943	chr8:110450882-110450883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568457524	chr8:110450898-110450899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536487520	chr8:110450899-110450900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72687010	chr8:110450908-110450909	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs202123815	chr8:110451008-110451009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576331484	chr8:110451027-110451028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566799656	chr8:110451038-110451039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533886106	chr8:110451043-110451044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538901783	chr8:110451078-110451079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547372654	chr8:110451103-110451104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187002780	chr8:110451125-110451126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs190992304	chr8:110451127-110451128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs202179223	chr8:110451186-110451187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201067450	chr8:110451187-110451188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200212277	chr8:110451189-110451190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200525842	chr8:110451198-110451199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs61741363	chr8:110451271-110451272	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:100)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	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
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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Multiple myeloma	16461302	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Gastric cancer	22539939	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	22341455	CNVD
Colorectal cancer	21645411	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:883 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:110448800-110454200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr8:110454200-110455200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:110454200-110455400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:110455000-110455400	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr8:110455000-110456400	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr8:110455200-110455600	Enhancers	H9 Cell Line	embryonic stem cell
7	chr8:110455200-110455600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr8:110455200-110455600	Enhancers	K562	blood
9	chr8:110455200-110456000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:110455200-110456000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr8:110455200-110456200	Enhancers	H1 Cell Line	embryonic stem cell
12	chr8:110455200-110456800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr8:110455400-110455600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr8:110455400-110455800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:110455400-110455800	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr8:110455400-110456200	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr8:110455400-110456400	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr8:110455400-110456400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr8:110455600-110456000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr8:110455600-110456000	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr8:110455600-110463000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr8:110455800-110456200	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr8:110455800-110457800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr8:110456000-110456400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr8:110456000-110457800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr8:110456400-110457200	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr8:110457800-110462800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr8:110457800-110462800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr8:110459400-110462800	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr8:110462600-110462800	Enhancers	K562	blood
31	chr8:110462800-110463000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr8:110462800-110463000	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr8:110462800-110463200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr8:110462800-110463600	Flanking Active TSS	K562	blood
35	chr8:110463000-110463200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr8:110463000-110463400	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr8:110463000-110463400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr8:110463000-110463400	Enhancers	Liver	Liver
39	chr8:110463000-110463800	Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr8:110463000-110464000	Enhancers	HepG2	liver
41	chr8:110463200-110463400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr8:110463200-110463400	Enhancers	Gastric	stomach
43	chr8:110463200-110463400	ZNF genes & repeats	Pancreas	Pancrea
44	chr8:110463200-110463600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr8:110463200-110492400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr8:110463400-110463600	Enhancers	GM12878-XiMat	blood
47	chr8:110463400-110463800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr8:110463600-110463800	Active TSS	K562	blood
49	chr8:110463800-110464000	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr8:110467000-110467200	Active TSS	Gastric	stomach

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