Variant report

Variant	nsv534005
Chromosome Location	chr3:21387588-22003293
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2611)
CpG islands
(count:1650)
Chromatin interactive
region (count:162)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2611 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:21573683-21573857	K562	blood:	n/a	n/a
2	ARID3A	chr3:21592635-21592859	K562	blood:	n/a	n/a
3	ARID3A	chr3:21581435-21581446	K562	blood:	n/a	n/a
4	ARID3A	chr3:21567931-21568332	K562	blood:	n/a	n/a
5	ARID3A	chr3:21528483-21528486	K562	blood:	n/a	n/a
6	ARID3A	chr3:21663005-21663101	K562	blood:	n/a	n/a
7	ARID3A	chr3:21662923-21663161	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:21573306-21573327	K562	blood:	n/a	n/a
9	ATF1	chr3:21770932-21771044	K562	blood:	n/a	n/a
10	ATF1	chr3:21568030-21568242	K562	blood:	n/a	n/a
11	ATF1	chr3:21573428-21573805	K562	blood:	n/a	n/a
12	ATF1	chr3:21592604-21592903	K562	blood:	n/a	n/a
13	ATF1	chr3:21440459-21440632	K562	blood:	n/a	n/a
14	ATF2	chr3:21487560-21487918	GM12878	blood:	n/a	n/a
15	ATF3	chr3:21447160-21447359	K562	blood:	n/a	n/a
16	BACH1	chr3:21662970-21663192	K562	blood:	n/a	n/a
17	BACH1	chr3:21669239-21669252	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr3:21792431-21793017	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr3:21558769-21558830	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr3:21662660-21663399	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr3:21487397-21487659	GM12878	blood:	n/a	n/a
22	BATF	chr3:21526355-21526594	GM12878	blood:	n/a	chr3:21526456-21526467
23	BCL11A	chr3:21585006-21585200	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL11A	chr3:21487425-21487837	GM12878	blood:	n/a	chr3:21487787-21487796
25	BHLHE40	chr3:21704294-21704295	K562	blood:	n/a	n/a
26	BHLHE40	chr3:21487490-21487873	GM12878	blood:	n/a	n/a
27	BHLHE40	chr3:21584305-21584749	K562	blood:	n/a	n/a
28	BHLHE40	chr3:21589714-21589739	K562	blood:	n/a	n/a
29	BHLHE40	chr3:21592657-21592899	K562	blood:	n/a	n/a
30	BHLHE40	chr3:21573457-21573641	K562	blood:	n/a	n/a
31	BHLHE40	chr3:21825389-21825693	K562	blood:	n/a	n/a
32	BHLHE40	chr3:21906985-21907006	K562	blood:	n/a	n/a
33	BRCA1	chr3:21779878-21779890	GM12878	blood:	n/a	n/a
34	BRCA1	chr3:21526090-21526158	GM12878	blood:	n/a	n/a
35	BRCA1	chr3:21782837-21782869	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr3:21483405-21483415	GM12878	blood:	n/a	n/a
37	BRCA1	chr3:21558865-21558897	HepG2	liver:	n/a	n/a
38	CBX3	chr3:21573374-21573782	K562	blood:	n/a	n/a
39	CBX3	chr3:21583994-21584381	K562	blood:	n/a	n/a
40	CBX3	chr3:21447117-21447403	K562	blood:	n/a	n/a
41	CCNT2	chr3:21953424-21953558	K562	blood:	n/a	n/a
42	CCNT2	chr3:21468599-21468799	K562	blood:	n/a	n/a
43	CCNT2	chr3:21572196-21572328	K562	blood:	n/a	n/a
44	CCNT2	chr3:21773207-21773377	K562	blood:	n/a	n/a
45	CCNT2	chr3:21567997-21568235	K562	blood:	n/a	n/a
46	CEBPB	chr3:21956051-21956262	A549	lung:	n/a	chr3:21956123-21956136 chr3:21956123-21956134
47	CEBPB	chr3:21840231-21840551	IMR90	lung:	n/a	chr3:21840366-21840377
48	CEBPB	chr3:21943011-21943293	MCF-7	breast:	n/a	n/a
49	CEBPB	chr3:21495626-21495863	IMR90	lung:	n/a	chr3:21495766-21495777
50	CEBPB	chr3:21961852-21962386	Hela-S3	cervix:	n/a	n/a

(count:1650 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:21792543-21792593	HCT-116	colon:	n/a
2	chr3:21792248-21792298	ovcar-3	ovarian:	n/a
3	chr3:21706663-21706713	PFSK-1	brain:	n/a
4	chr3:21792543-21792593	HCT-116	colon:	n/a
5	chr3:21792248-21792298	ovcar-3	ovarian:	n/a
6	chr3:21706663-21706713	PFSK-1	brain:	n/a
7	chr3:21426059-21426109	HEK293	kidney:	embryo
8	chr3:21558209-21558259	HEK293	kidney:	embryo
9	chr3:21558209-21558259	HRE	kidney:	n/a
10	chr3:21448012-21448062	GM12891	blood:	n/a
11	chr3:21790232-21790282	HRCEpiC	kidney:	n/a
12	chr3:21792434-21792484	HUVEC	blood vessel:	n/a
13	chr3:21832523-21832573	NH-A	brain:	n/a
14	chr3:21792543-21792593	NT2-D1	testis:	n/a
15	chr3:21448012-21448062	SK-N-SH_RA	brain:	n/a
16	chr3:21792938-21792988	GM06990	blood:	n/a
17	chr3:21792248-21792298	SK-N-SH_RA	brain:	n/a
18	chr3:21446874-21446924	HMEC	breast:	n/a
19	chr3:21792857-21792907	GM12891	blood:	n/a
20	chr3:21445979-21446029	PrEC	prostate:	n/a
21	chr3:21792991-21793041	Caco-2	colon:	n/a
22	chr3:21792684-21792734	CMK	blood:	n/a
23	chr3:21790232-21790282	GM12878	blood:	n/a
24	chr3:21792543-21792593	IMR90	lung:	fetal
25	chr3:21792684-21792734	PANC-1	pancreas:	n/a
26	chr3:21447501-21447551	HepG2	liver:	n/a
27	chr3:21720400-21720450	Hepatocyte	liver:	n/a
28	chr3:21447391-21447441	U87	brain:	n/a
29	chr3:21792684-21792734	HCM	heart:	n/a
30	chr3:21584249-21584299	HRPEpiC	eye:	n/a
31	chr3:21447667-21447717	HRCEpiC	kidney:	n/a
32	chr3:21426059-21426109	SK-N-SH	brain:	n/a
33	chr3:21960904-21960954	AG09319	gingival:	n/a
34	chr3:21448012-21448062	HCM	heart:	n/a
35	chr3:21792543-21792593	SK-N-SH_RA	brain:	n/a
36	chr3:21792543-21792593	HepG2	liver:	n/a
37	chr3:21960904-21960954	SK-N-SH_RA	brain:	n/a
38	chr3:21790232-21790282	HPAEpiC	pulmonary alveolar:	n/a
39	chr3:21790232-21790282	ECC-1	luminal epithelium:	n/a
40	chr3:21558209-21558259	NT2-D1	testis:	n/a
41	chr3:21448049-21448099	GM12891	blood:	n/a
42	chr3:21706663-21706713	NHBE	bronchial:	n/a
43	chr3:21793557-21793607	GM19239	blood:	n/a
44	chr3:21714788-21714838	H1-hESC	embryonic stem cell:	embryo
45	chr3:21792543-21792593	HCPEpiC	choroid plexus:	n/a
46	chr3:21761217-21761267	HCM	heart:	n/a
47	chr3:21447501-21447551	ProgFib	skin:	n/a
48	chr3:21447667-21447717	AG10803	skin:	n/a
49	chr3:21792991-21793041	Jurkat	blood:	n/a
50	chr3:21792938-21792988	HCM	heart:	n/a

(count:162 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr3:21434215..21436621-chr3:21438277..21440578,2	MCF-7	breast:
2	chr3:21793963..21794585-chr3:21876272..21877179,2	MCF-7	breast:
3	chr3:21948578..21950299-chr3:21951052..21953875,2	MCF-7	breast:
4	chr3:21593555..21596291-chr3:21602038..21604298,2	K562	blood:
5	chr3:21533469..21535837-chr3:21555368..21557096,2	K562	blood:
6	chr3:21508162..21510011-chr3:21513396..21515534,2	K562	blood:
7	chr3:21547308..21549346-chr3:21549742..21551685,2	K562	blood:
8	chr3:20267223..20267887-chr3:21592292..21593221,2	MCF-7	breast:
9	chr3:21721634..21724337-chr3:21728946..21730736,2	K562	blood:
10	chr3:21942258..21944994-chr3:21945829..21948153,2	K562	blood:
11	chr3:21874988..21876733-chr3:21878025..21880087,4	K562	blood:
12	chr3:21820384..21822203-chr3:21834742..21836819,2	K562	blood:
13	chr3:21892806..21894849-chr3:21897852..21900833,2	K562	blood:
14	chr3:20378280..20380658-chr3:21571258..21574044,2	K562	blood:
15	chr3:21700043..21701909-chr3:21703783..21705920,2	K562	blood:
16	chr3:21622806..21624810-chr3:21626312..21628211,2	K562	blood:
17	chr3:21439366..21441034-chr3:21442770..21445274,2	K562	blood:
18	chr3:21793981..21794891-chr3:21935742..21936689,4	MCF-7	breast:
19	chr3:21603848..21605723-chr3:21608841..21613038,5	K562	blood:
20	chr3:21647916..21649691-chr3:21651335..21653463,2	K562	blood:
21	chr3:19926567..19927530-chr3:21592329..21593167,2	MCF-7	breast:
22	chr3:21388598..21390467-chr3:21391576..21393925,2	K562	blood:
23	chr3:21434090..21435912-chr3:21501028..21503829,2	K562	blood:
24	chr3:21927265..21931115-chr3:21931720..21934482,3	K562	blood:
25	chr3:21604223..21605998-chr3:21608773..21611314,2	K562	blood:
26	chr3:21565324..21568095-chr3:21579893..21581736,2	K562	blood:
27	chr3:21547308..21549346-chr3:21549742..21551685,2	K562	blood:
28	chr3:21942258..21944994-chr3:21945829..21948153,2	K562	blood:
29	chr3:21827028..21830015-chr3:21877815..21880748,2	K562	blood:
30	chr3:21622806..21624810-chr3:21626312..21628211,2	K562	blood:
31	chr3:21565324..21568095-chr3:21579893..21581736,2	K562	blood:
32	chr3:21551694..21553640-chr3:21557602..21559224,2	K562	blood:
33	chr3:21593555..21596291-chr3:21602038..21604298,2	K562	blood:
34	chr3:21508162..21510011-chr3:21513396..21515534,2	K562	blood:
35	chr3:21793981..21794891-chr3:21935742..21936689,4	MCF-7	breast:
36	chr3:21565741..21568055-chr3:21571417..21573750,2	K562	blood:
37	chr3:21731209..21733494-chr3:21734239..21737036,2	K562	blood:
38	chr3:21794398..21795153-chr3:22159350..22159975,2	MCF-7	breast:
39	chr3:21386176..21388301-chr3:21404995..21407589,2	K562	blood:
40	chr3:21829102..21831903-chr3:21833288..21835106,2	MCF-7	breast:
41	chr3:21647916..21649691-chr3:21651335..21653463,2	K562	blood:
42	chr3:21058395..21059158-chr3:21525879..21526450,3	MCF-7	breast:
43	chr3:21919005..21921576-chr3:21924260..21925811,2	K562	blood:
44	chr3:21386176..21388301-chr3:21404995..21407589,2	K562	blood:
45	chr3:21834699..21836749-chr3:21841872..21843616,2	K562	blood:
46	chr3:21567837..21569821-chr3:21573520..21576475,3	K562	blood:
47	chr3:21534337..21537084-chr3:21554573..21557096,2	K562	blood:
48	chr3:21835216..21837652-chr3:21840366..21842817,3	K562	blood:
49	chr3:21927265..21931115-chr3:21931720..21934482,3	K562	blood:
50	chr3:21902249..21903949-chr3:21904642..21906995,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SGOL1-3	chr3:21603411-21603587	NONHSAT088646
2	lnc-UBE2E2-2	chr3:21998628-21998684	ENSG00000223351
3	lnc-ZNF385D-1	chr3:21453714-21455436	ENSG00000272511.1
4	lnc-KAT2B-4	chr3:21620681-21620873	ENSG00000225542.1
5	lnc-KAT2B-4	chr3:21584308-21584487	ENSG00000225542.1
6	lnc-UBE2E2-2	chr3:21984058-21984156	ENSG00000223351
7	lnc-UBE2E2-2	chr3:22000324-22000415	ENSG00000223351
8	lnc-UBE2E2-7	chr3:21975327-21975419	l_2330_chr3:21975326-21982219_testes
9	lnc-UBE2E2-7	chr3:21982020-21982219	l_2330_chr3:21975326-21982219_testes
10	lnc-SGOL1-3	chr3:21606066-21606178	NONHSAT088646
11	lnc-UBE2E2-2	chr3:22000324-22000415	ENSG00000223351
12	lnc-UBE2E2-2	chr3:22002908-22003032	ENSG00000223351
13	lnc-SGOL1-3	chr3:21919332-21919650	NONHSAT088650
14	lnc-KAT2B-4	chr3:21621120-21621451	ENSG00000225542.1
15	lnc-UBE2E2-2	chr3:21998631-21998684	ENSG00000223351

No data

Variant related genes	Relation type
ENSG00000221384	TF binding region
ZNF385D-AS2	TF binding region
VENTXP7	TF binding region
ZNF385D	TF binding region
ZNF385D-AS1	TF binding region
ENSG00000252306	TF binding region
ENSG00000272511	TF binding region
ENSG00000221384	CpG island
ZNF385D-AS2	CpG island
VENTXP7	CpG island
ZNF385D	CpG island
ZNF385D-AS1	CpG island
ENSG00000252306	CpG island
ENSG00000272511	CpG island
ENSG00000151789	chromatin interactions
ENSG00000272511	chromatin interactions
ENSG00000110074	chromatin interactions
ENSG00000225542	chromatin interactions
ENSG00000236380	chromatin interactions

Extended variants
information (count: 24725 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:24725 , 50 per page) page: 1 2 3 4 5 6 7 ... 495

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189724096	chr3:21397436-21397437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs549166432	chr3:21397481-21397482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181183148	chr3:21397498-21397499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs530944459	chr3:21397553-21397554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552577636	chr3:21397577-21397578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564598564	chr3:21397651-21397652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369922787	chr3:21397653-21397654	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547315428	chr3:21397655-21397656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552925389	chr3:21397738-21397739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565863586	chr3:21397742-21397743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs13095327	chr3:21397755-21397756	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs548085441	chr3:21397791-21397792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186159423	chr3:21397862-21397863	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs538083949	chr3:21397873-21397874	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs551691546	chr3:21397894-21397895	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs376997409	chr3:21397900-21397901	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs576573480	chr3:21397916-21397917	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs534716292	chr3:21397944-21397945	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs145512020	chr3:21397972-21397973	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs116451180	chr3:21397985-21397986	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs542024420	chr3:21397991-21397992	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs563995289	chr3:21398011-21398012	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs33998065	chr3:21398020-21398021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575984961	chr3:21398104-21398105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188913663	chr3:21398105-21398106	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181932186	chr3:21398139-21398140	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528625122	chr3:21398155-21398156	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201107189	chr3:21398173-21398174	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540720874	chr3:21398174-21398175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561997818	chr3:21398183-21398184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529913914	chr3:21398190-21398191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547952682	chr3:21398232-21398233	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs569650700	chr3:21398267-21398268	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs530707782	chr3:21398276-21398277	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs151091032	chr3:21398298-21398299	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs570433694	chr3:21398309-21398310	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs534282570	chr3:21398350-21398351	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs553048982	chr3:21398497-21398498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs186596771	chr3:21398519-21398520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs116136299	chr3:21398569-21398570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs375823559	chr3:21398585-21398586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372651650	chr3:21398703-21398704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs75094266	chr3:21398711-21398712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs369923707	chr3:21398745-21398746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs576046337	chr3:21398834-21398835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs546515566	chr3:21398882-21398883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs985976	chr3:21398894-21398895	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs573197146	chr3:21398896-21398897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540225691	chr3:21398903-21398904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs562231184	chr3:21398919-21398920	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Melanoma	20688739	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2100 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21397400-21397600	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr3:21397400-21397800	Enhancers	NHDF-Ad	bronchial
3	chr3:21397600-21398400	Enhancers	Muscle Satellite Cultured Cells	--
4	chr3:21397600-21398400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr3:21397600-21398600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr3:21397800-21398000	Flanking Active TSS	NHDF-Ad	bronchial
7	chr3:21398000-21398200	Enhancers	NHDF-Ad	bronchial
8	chr3:21398200-21398400	Flanking Active TSS	NHDF-Ad	bronchial
9	chr3:21398400-21399000	Enhancers	NHDF-Ad	bronchial
10	chr3:21398600-21399400	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr3:21398800-21399200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr3:21398800-21399200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr3:21413400-21413800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:21413800-21414200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:21413800-21414400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr3:21413800-21414600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr3:21414000-21414600	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr3:21414200-21414400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:21414400-21414600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr3:21414600-21414800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:21414600-21418200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr3:21414800-21418000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:21418000-21419200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:21418200-21418800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr3:21418600-21420000	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr3:21418800-21420200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr3:21420200-21420400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr3:21424000-21424200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr3:21424200-21432800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr3:21425400-21426400	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr3:21426200-21426800	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr3:21426800-21427800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
33	chr3:21428800-21429200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
34	chr3:21429200-21431800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr3:21430400-21431800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr3:21431000-21431600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr3:21431200-21432000	Enhancers	Rectal Smooth Muscle	rectum
38	chr3:21431200-21432200	Enhancers	Muscle Satellite Cultured Cells	--
39	chr3:21431200-21432200	Enhancers	NHDF-Ad	bronchial
40	chr3:21431200-21432800	Enhancers	NH-A	brain
41	chr3:21431200-21435400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr3:21431600-21432000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr3:21431800-21432000	Enhancers	Aorta	Aorta
44	chr3:21431800-21432200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr3:21431800-21432600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr3:21431800-21433600	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr3:21432000-21435200	Weak transcription	Aorta	Aorta
48	chr3:21432200-21433800	Weak transcription	NHDF-Ad	bronchial
49	chr3:21432200-21435400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr3:21432800-21433000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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