Variant report

Variant	nsv548592
Chromosome Location	chr1:191623693-191936556
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1139)
CpG islands
(count:306)
Chromatin interactive
region (count:73)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1139 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:191857246-191857609	K562	blood:	n/a	n/a
2	ARID3A	chr1:191845875-191846144	K562	blood:	n/a	n/a
3	ARID3A	chr1:191857928-191858619	K562	blood:	n/a	n/a
4	ARID3A	chr1:191792309-191793479	K562	blood:	n/a	n/a
5	ARID3A	chr1:191791882-191792051	K562	blood:	n/a	n/a
6	ARID3A	chr1:191812278-191812435	K562	blood:	n/a	n/a
7	ATF1	chr1:191928315-191928526	K562	blood:	n/a	n/a
8	ATF1	chr1:191845848-191846111	K562	blood:	n/a	n/a
9	ATF1	chr1:191792801-191793314	K562	blood:	n/a	n/a
10	ATF1	chr1:191858055-191858697	K562	blood:	n/a	n/a
11	ATF1	chr1:191637265-191637387	K562	blood:	n/a	n/a
12	ATF1	chr1:191791954-191792148	K562	blood:	n/a	n/a
13	ATF1	chr1:191821456-191821889	K562	blood:	n/a	n/a
14	ATF2	chr1:191838896-191839199	GM12878	blood:	n/a	n/a
15	ATF3	chr1:191858154-191858679	K562	blood:	n/a	n/a
16	ATF3	chr1:191820973-191821210	K562	blood:	n/a	n/a
17	BACH1	chr1:191671302-191671575	K562	blood:	n/a	n/a
18	BACH1	chr1:191671293-191671597	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr1:191838976-191839163	GM12878	blood:	n/a	n/a
20	BATF	chr1:191668480-191668735	GM12878	blood:	n/a	chr1:191668644-191668655
21	BHLHE40	chr1:191858061-191858651	K562	blood:	n/a	n/a
22	BHLHE40	chr1:191857301-191857435	K562	blood:	n/a	n/a
23	BHLHE40	chr1:191853684-191853687	K562	blood:	n/a	n/a
24	BHLHE40	chr1:191792761-191793301	K562	blood:	n/a	n/a
25	BRCA1	chr1:191731156-191731181	GM12878	blood:	n/a	n/a
26	CBX3	chr1:191877847-191878202	K562	blood:	n/a	n/a
27	CBX3	chr1:191782745-191783119	K562	blood:	n/a	n/a
28	CBX3	chr1:191861784-191862212	K562	blood:	n/a	n/a
29	CBX3	chr1:191662926-191663304	K562	blood:	n/a	n/a
30	CBX3	chr1:191861885-191862176	K562	blood:	n/a	n/a
31	CBX3	chr1:191782674-191783126	K562	blood:	n/a	n/a
32	CBX3	chr1:191858024-191858814	K562	blood:	n/a	n/a
33	CBX3	chr1:191728311-191728750	K562	blood:	n/a	n/a
34	CBX3	chr1:191792445-191793273	K562	blood:	n/a	n/a
35	CCNT2	chr1:191896750-191896900	K562	blood:	n/a	n/a
36	CCNT2	chr1:191858179-191858676	K562	blood:	n/a	n/a
37	CCNT2	chr1:191792545-191793400	K562	blood:	n/a	n/a
38	CEBPB	chr1:191936106-191936109	K562	blood:	n/a	n/a
39	CEBPB	chr1:191834758-191834987	A549	lung:	n/a	chr1:191834839-191834850
40	CEBPB	chr1:191858078-191858708	K562	blood:	n/a	n/a
41	CEBPB	chr1:191724410-191724871	K562	blood:	n/a	chr1:191724849-191724860 chr1:191724849-191724862 chr1:191724849-191724862 chr1:191724716-191724729 chr1:191724716-191724729
42	CEBPB	chr1:191738762-191739003	IMR90	lung:	n/a	chr1:191738862-191738875 chr1:191738862-191738873 chr1:191738863-191738874 chr1:191738862-191738875
43	CEBPB	chr1:191922721-191922976	HepG2	liver:	n/a	n/a
44	CEBPB	chr1:191634360-191634664	HepG2	liver:	n/a	chr1:191634503-191634516 chr1:191634504-191634515 chr1:191634503-191634514
45	CEBPB	chr1:191922700-191922938	A549	lung:	n/a	n/a
46	CEBPB	chr1:191670803-191671825	MCF-7	breast:	n/a	n/a
47	CEBPB	chr1:191805286-191805538	A549	lung:	n/a	n/a
48	CEBPB	chr1:191736055-191736395	K562	blood:	n/a	chr1:191736214-191736225 chr1:191736215-191736226 chr1:191736214-191736227
49	CEBPB	chr1:191657782-191658056	HepG2	liver:	n/a	chr1:191657912-191657923
50	CEBPB	chr1:191857259-191857476	HepG2	liver:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:191933198-191933248	HUVEC	blood vessel:	n/a
2	chr1:191933198-191933248	HUVEC	blood vessel:	n/a
3	chr1:191933198-191933248	AG09319	gingival:	n/a
4	chr1:191701782-191701832	HUVEC	blood vessel:	n/a
5	chr1:191740297-191740347	AG04449	skin:	fetal
6	chr1:191701782-191701832	HAEpiC	amniotic membrane:	n/a
7	chr1:191701209-191701259	NB4	blood:	n/a
8	chr1:191701782-191701832	HCM	heart:	n/a
9	chr1:191933198-191933248	HEK293	kidney:	embryo
10	chr1:191933198-191933248	HRCEpiC	kidney:	n/a
11	chr1:191701857-191701907	AG09309	skin:	n/a
12	chr1:191701857-191701907	ProgFib	skin:	n/a
13	chr1:191933198-191933248	AG09309	skin:	n/a
14	chr1:191701857-191701907	HIPEpiC	eye:	n/a
15	chr1:191701209-191701259	HIPEpiC	eye:	n/a
16	chr1:191933198-191933248	T-47D	breast:	n/a
17	chr1:191701209-191701259	HL-60	blood:	n/a
18	chr1:191701209-191701259	HCT-116	colon:	n/a
19	chr1:191740297-191740347	MCF-7	breast:	n/a
20	chr1:191701857-191701907	Hela-S3	cervix:	n/a
21	chr1:191701857-191701907	SK-N-SH	brain:	n/a
22	chr1:191701857-191701907	BE2_C	brain:	n/a
23	chr1:191933198-191933248	AG04450	lung:	fetal
24	chr1:191740297-191740347	ProgFib	skin:	n/a
25	chr1:191701782-191701832	AoSMC	blood vessel:	n/a
26	chr1:191933198-191933248	IMR90	lung:	fetal
27	chr1:191740297-191740347	NT2-D1	testis:	n/a
28	chr1:191933198-191933248	K562	blood:	n/a
29	chr1:191740297-191740347	HAEpiC	amniotic membrane:	n/a
30	chr1:191701857-191701907	SK-N-SH_RA	brain:	n/a
31	chr1:191933198-191933248	HL-60	blood:	n/a
32	chr1:191701857-191701907	HRCEpiC	kidney:	n/a
33	chr1:191933198-191933248	AoSMC	blood vessel:	n/a
34	chr1:191701857-191701907	HL-60	blood:	n/a
35	chr1:191701782-191701832	HIPEpiC	eye:	n/a
36	chr1:191933198-191933248	Hepatocyte	liver:	n/a
37	chr1:191701209-191701259	IMR90	lung:	fetal
38	chr1:191701209-191701259	ECC-1	luminal epithelium:	n/a
39	chr1:191701857-191701907	AG04450	lung:	fetal
40	chr1:191701857-191701907	ECC-1	luminal epithelium:	n/a
41	chr1:191740297-191740347	HCF	heart:	n/a
42	chr1:191701857-191701907	GM12892	blood:	n/a
43	chr1:191701782-191701832	ECC-1	luminal epithelium:	n/a
44	chr1:191701209-191701259	HEK293	kidney:	embryo
45	chr1:191701209-191701259	NT2-D1	testis:	n/a
46	chr1:191701782-191701832	K562	blood:	n/a
47	chr1:191933198-191933248	ovcar-3	ovarian:	n/a
48	chr1:191740297-191740347	AoSMC	blood vessel:	n/a
49	chr1:191701857-191701907	AoSMC	blood vessel:	n/a
50	chr1:191933198-191933248	GM12878	blood:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:191815192..191816719-chr1:191819191..191822159,2	K562	blood:
2	chr1:191773972..191778173-chr1:191779534..191782112,5	K562	blood:
3	chr1:191807170..191809175-chr1:191810201..191811757,2	K562	blood:
4	chr1:191708525..191710416-chr1:191713003..191715158,2	K562	blood:
5	chr1:191844983..191847069-chr1:191850769..191852531,2	K562	blood:
6	chr1:191704245..191706560-chr1:191706732..191709677,2	K562	blood:
7	chr1:191850241..191852634-chr1:191855846..191858464,3	K562	blood:
8	chr1:191784628..191787361-chr1:191791989..191794077,2	K562	blood:
9	chr1:191777063..191778903-chr1:191781034..191782929,2	K562	blood:
10	chr1:191658649..191660238-chr1:191662141..191664711,2	K562	blood:
11	chr1:191667560..191670063-chr1:191670444..191673438,2	MCF-7	breast:
12	chr1:191849617..191851741-chr1:191856964..191859134,3	K562	blood:
13	chr1:191788611..191790988-chr1:191796591..191799173,2	MCF-7	breast:
14	chr1:191887988..191890658-chr1:191891458..191893123,2	K562	blood:
15	chr1:191920379..191922752-chr1:191923416..191925124,2	K562	blood:
16	chr1:191864173..191866057-chr1:191874341..191876184,2	K562	blood:
17	chr1:191656150..191658187-chr1:191658870..191661346,2	K562	blood:
18	chr1:191807170..191809175-chr1:191810201..191811757,2	K562	blood:
19	chr1:191849617..191851741-chr1:191856964..191859134,3	K562	blood:
20	chr1:191719906..191721818-chr1:191723940..191725758,2	K562	blood:
21	chr1:191616602..191619321-chr1:191633804..191636058,2	K562	blood:
22	chr1:191788611..191790988-chr1:191796591..191799173,2	MCF-7	breast:
23	chr1:191754947..191757355-chr1:191758290..191760631,2	MCF-7	breast:
24	chr1:191836436..191839226-chr1:191842786..191844832,2	K562	blood:
25	chr1:191722550..191725173-chr1:191726760..191728509,2	K562	blood:
26	chr1:191719906..191721818-chr1:191723940..191725758,2	K562	blood:
27	chr1:191708525..191710416-chr1:191713003..191715158,2	K562	blood:
28	chr1:191666098..191668261-chr1:191671112..191673140,2	MCF-7	breast:
29	chr1:191701608..191705437-chr1:191706302..191708932,3	K562	blood:
30	chr1:191854730..191856594-chr1:191856723..191859160,2	K562	blood:
31	chr1:191754947..191757355-chr1:191758290..191760631,2	MCF-7	breast:
32	chr1:191728187..191729720-chr1:191733696..191735849,2	K562	blood:
33	chr1:191670842..191673088-chr1:191683074..191685461,2	MCF-7	breast:
34	chr1:191666098..191668261-chr1:191671112..191673140,2	MCF-7	breast:
35	chr1:191720033..191721818-chr1:191724258..191727232,2	K562	blood:
36	chr1:191656150..191658187-chr1:191658870..191661346,2	K562	blood:
37	chr1:191764970..191767101-chr1:192222254..192224537,2	K562	blood:
38	chr1:191711996..191714385-chr1:191821887..191824152,2	K562	blood:
39	chr1:191887988..191890658-chr1:191891458..191893123,2	K562	blood:
40	chr1:191701608..191705437-chr1:191706302..191708932,3	K562	blood:
41	chr1:191716548..191718884-chr1:191723444..191727562,3	K562	blood:
42	chr1:191858381..191861097-chr1:191864368..191867185,2	K562	blood:
43	chr1:191670842..191673088-chr1:191683074..191685461,2	MCF-7	breast:
44	chr1:191667560..191670063-chr1:191670444..191673438,2	MCF-7	breast:
45	chr1:191844983..191847069-chr1:191850769..191852531,2	K562	blood:
46	chr1:191931501..191932320-chr18:10905847..10906400,2	MCF-7	breast:
47	chr1:191925492..191927826-chr1:191930519..191932628,2	K562	blood:
48	chr1:191854730..191856594-chr1:191856723..191859160,2	K562	blood:
49	chr1:191858381..191859932-chr1:191864838..191867185,2	K562	blood:
50	chr1:191815192..191816719-chr1:191819191..191822159,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RGS18-1	chr1:191934452-191934543	ENSG00000228215.2
2	lnc-UCHL5-3	chr1:191827837-191828310	XLOC_001132
3	lnc-UCHL5-3	chr1:191835950-191836090	XLOC_001132
4	lnc-UCHL5-7	chr1:191921333-191921542	NONHSAT008526
5	lnc-UCHL5-7	chr1:191924009-191924182	NONHSAT008526
6	lnc-RGS18-8	chr1:191914647-191914758	NONHSAT008525
7	lnc-FAM5C-3	chr1:191686588-191686611	XLOC_001131
8	lnc-RGS18-1	chr1:191844625-191844830	ENSG00000228215.2
9	lnc-RGS18-1	chr1:191934452-191934543	XLOC_000507
10	lnc-UCHL5-7	chr1:191919999-191920464	NONHSAT008526
11	lnc-UCHL5-3	chr1:191827893-191828310	XLOC_001132
12	lnc-FAM5C-3	chr1:191685359-191685577	XLOC_001131
13	lnc-RGS18-1	chr1:191933524-191933619	XLOC_000507
14	lnc-UCHL5-3	chr1:191859195-191859359	XLOC_001132
15	lnc-RGS18-1	chr1:191933524-191933619	ENSG00000228215.2
16	lnc-RGS18-1	chr1:191844625-191844830	XLOC_000507

No data

Variant related genes	Relation type
ENSG00000228215	TF binding region
ENSG00000223344	TF binding region
ENSG00000228215	CpG island
ENSG00000223344	CpG island
ENSG00000228215	chromatin interactions
ENSG00000223344	chromatin interactions
PLAG1	miRNA target sites
CCNT2	miRNA target sites
ARSB	miRNA target sites
G6PC3	miRNA target sites

Extended variants
information (count: 4676 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4676 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11804493	chr1:191630028-191630029	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs540947441	chr1:191630038-191630039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187282858	chr1:191630058-191630059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs71639139	chr1:191630102-191630103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545490306	chr1:191630122-191630123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562245165	chr1:191630138-191630139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs191844531	chr1:191630198-191630199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs368397233	chr1:191630245-191630246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150672811	chr1:191630257-191630258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs370307430	chr1:191630258-191630259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs1336866	chr1:191630277-191630278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs527569711	chr1:191630289-191630290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138848401	chr1:191630342-191630343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs77731770	chr1:191630345-191630346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533210796	chr1:191630373-191630374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs371301202	chr1:191630396-191630397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs552658321	chr1:191630426-191630427	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569385988	chr1:191630443-191630444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs10590530	chr1:191630463-191630464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538206713	chr1:191630482-191630483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554642721	chr1:191630516-191630517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs118037702	chr1:191630536-191630537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs16833655	chr1:191630540-191630541	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs182232119	chr1:191630541-191630542	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs114506831	chr1:191630579-191630580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574810880	chr1:191630582-191630583	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376795377	chr1:191630585-191630586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186466059	chr1:191630618-191630619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs55897399	chr1:191630637-191630638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs7517393	chr1:191630653-191630654	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs146340805	chr1:191630660-191630661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs76827713	chr1:191630685-191630686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548483035	chr1:191630688-191630689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541937353	chr1:191630763-191630764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12025778	chr1:191630788-191630789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557530568	chr1:191630799-191630800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs115054431	chr1:191630864-191630865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540964714	chr1:191630902-191630903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564377893	chr1:191630904-191630905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533122717	chr1:191630923-191630924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550018568	chr1:191630949-191630950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10920987	chr1:191631003-191631004	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs190287814	chr1:191631042-191631043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548702468	chr1:191631107-191631108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7528072	chr1:191631131-191631132	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs66478619	chr1:191631139-191631140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs71742038	chr1:191631141-191631142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs74130249	chr1:191631152-191631153	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs188507857	chr1:191631164-191631165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs144228092	chr1:191631183-191631184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	17086460	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	17086460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:191630000-191630600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr1:191630200-191630400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:191630200-191630600	Enhancers	H9 Cell Line	embryonic stem cell
4	chr1:191630400-191631200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:191631200-191631400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:191631400-191632200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr1:191632200-191633200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:191633200-191634400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr1:191634400-191635800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr1:191635800-191637400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr1:191637800-191638000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr1:191638200-191639400	Enhancers	Muscle Satellite Cultured Cells	--
13	chr1:191638200-191641000	Enhancers	NH-A	brain
14	chr1:191639200-191639400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr1:191639400-191640600	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr1:191639600-191640600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr1:191640600-191641000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr1:191640600-191641000	Enhancers	Muscle Satellite Cultured Cells	--
19	chr1:191640600-191641000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr1:191641000-191641200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr1:191641200-191643600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:191643400-191645200	Enhancers	Colon Smooth Muscle	Colon
23	chr1:191643400-191645600	Enhancers	Rectal Smooth Muscle	rectum
24	chr1:191643600-191643800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr1:191643600-191644200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr1:191643600-191644200	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr1:191643600-191644200	Enhancers	Fetal Muscle Leg	muscle
28	chr1:191643600-191644400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr1:191643600-191644400	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr1:191643600-191644400	Enhancers	Fetal Stomach	stomach
31	chr1:191643600-191645400	Enhancers	Adipose Nuclei	Adipose
32	chr1:191643800-191644200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr1:191643800-191644200	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr1:191643800-191644200	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr1:191643800-191644400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr1:191643800-191644400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr1:191643800-191644400	Enhancers	Fetal Heart	heart
38	chr1:191643800-191644600	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr1:191643800-191645200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr1:191644000-191644400	Enhancers	Ovary	ovary
41	chr1:191644600-191645200	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr1:191645200-191645400	Enhancers	Duodenum Smooth Muscle	Duodenum
43	chr1:191645200-191646000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr1:191646000-191646200	Enhancers	Ovary	ovary
45	chr1:191648800-191650000	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr1:191649000-191649800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr1:191649200-191649600	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr1:191650400-191651600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr1:191651600-191652000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr1:191652000-191654000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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