Variant report

Variant	nsv544010
Chromosome Location	chr19:43173814-43584478
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5160)
CpG islands
(count:2932)
Chromatin interactive
region (count:17)
LncRNA
region (count:46)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5160 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:43208643-43208644	K562	blood:	n/a	n/a
2	ATF3	chr19:43335307-43336092	A549	lung:	n/a	n/a
3	ATF3	chr19:43355048-43355947	A549	lung:	n/a	n/a
4	ATF3	chr19:43336349-43336838	A549	lung:	n/a	n/a
5	ATF3	chr19:43355412-43355889	A549	lung:	n/a	n/a
6	ATF3	chr19:43335349-43336094	A549	lung:	n/a	n/a
7	ATF3	chr19:43336336-43336928	A549	lung:	n/a	n/a
8	BATF	chr19:43246213-43246502	GM12878	blood:	n/a	n/a
9	BATF	chr19:43179178-43179402	GM12878	blood:	n/a	n/a
10	BATF	chr19:43302238-43302533	GM12878	blood:	n/a	chr19:43302344-43302355
11	BATF	chr19:43552261-43552460	GM12878	blood:	n/a	chr19:43552319-43552330
12	BATF	chr19:43552186-43552537	GM12878	blood:	n/a	chr19:43552319-43552330
13	BATF	chr19:43361555-43361754	GM12878	blood:	n/a	n/a
14	BATF	chr19:43442962-43443231	GM12878	blood:	n/a	n/a
15	BATF	chr19:43271446-43271728	GM12878	blood:	n/a	n/a
16	BCL11A	chr19:43179101-43179287	GM12878	blood:	n/a	n/a
17	BCL3	chr19:43335242-43336126	A549	lung:	n/a	chr19:43335602-43335611 chr19:43335603-43335612
18	BCL3	chr19:43336972-43337663	A549	lung:	n/a	n/a
19	BCL3	chr19:43402518-43403428	A549	lung:	n/a	n/a
20	BCL3	chr19:43354910-43356058	A549	lung:	n/a	n/a
21	BCL3	chr19:43336292-43336877	A549	lung:	n/a	n/a
22	BCL3	chr19:43336159-43337656	A549	lung:	n/a	chr19:43336227-43336234
23	BCL3	chr19:43354946-43356043	A549	lung:	n/a	n/a
24	BCL3	chr19:43335292-43335990	A549	lung:	n/a	chr19:43335602-43335611 chr19:43335603-43335612
25	BCL3	chr19:43323095-43323355	GM12878	blood:	n/a	n/a
26	BCL3	chr19:43297507-43298116	A549	lung:	n/a	n/a
27	BHLHE40	chr19:43385480-43385517	K562	blood:	n/a	n/a
28	BHLHE40	chr19:43427453-43427512	GM12878	blood:	n/a	n/a
29	BHLHE40	chr19:43355572-43355890	A549	lung:	n/a	n/a
30	BHLHE40	chr19:43582147-43582203	K562	blood:	n/a	n/a
31	BRCA1	chr19:43436723-43436914	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr19:43297623-43297950	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr19:43355288-43355847	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr19:43525934-43526309	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr19:43265411-43265577	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr19:43190821-43191075	K562	blood:	n/a	n/a
37	CBX3	chr19:43190865-43191064	K562	blood:	n/a	n/a
38	CBX3	chr19:43385431-43385838	K562	blood:	n/a	n/a
39	CBX3	chr19:43385505-43385738	K562	blood:	n/a	n/a
40	CBX3	chr19:43188032-43188426	HCT-116	colon:	n/a	n/a
41	CEBPB	chr19:43562867-43563067	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr19:43345870-43346046	IMR90	lung:	n/a	n/a
43	CEBPB	chr19:43328208-43328426	Hela-S3	cervix:	n/a	chr19:43328257-43328268
44	CEBPB	chr19:43336488-43336863	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr19:43496486-43496642	K562	blood:	n/a	n/a
46	CEBPB	chr19:43562943-43563108	MCF-7	breast:	n/a	n/a
47	CEBPB	chr19:43337158-43337425	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr19:43496316-43496617	A549	lung:	n/a	n/a
49	CEBPB	chr19:43516550-43516678	K562	blood:	n/a	n/a
50	CEBPB	chr19:43355051-43355897	A549	lung:	n/a	n/a

(count:2932 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43423119-43423169	Hepatocyte	liver:	n/a
2	chr19:43423176-43423226	ProgFib	skin:	n/a
3	chr19:43410455-43410505	GM12891	blood:	n/a
4	chr19:43384780-43384830	HEK293	kidney:	embryo
5	chr19:43423119-43423169	Hepatocyte	liver:	n/a
6	chr19:43423176-43423226	ProgFib	skin:	n/a
7	chr19:43410455-43410505	GM12891	blood:	n/a
8	chr19:43384780-43384830	HEK293	kidney:	embryo
9	chr19:43245860-43245910	LNCaP	prostate:	n/a
10	chr19:43442804-43442854	GM12891	blood:	n/a
11	chr19:43244635-43244685	HEK293	kidney:	embryo
12	chr19:43421584-43421634	HCT-116	colon:	n/a
13	chr19:43441294-43441344	MCF10A-Er-Src	breast:	n/a
14	chr19:43530536-43530586	HL-60	blood:	n/a
15	chr19:43257346-43257396	SAEC	small airway:	n/a
16	chr19:43202122-43202172	HMEC	breast:	n/a
17	chr19:43265778-43265828	HUVEC	blood vessel:	n/a
18	chr19:43528994-43529044	ProgFib	skin:	n/a
19	chr19:43442804-43442854	HCPEpiC	choroid plexus:	n/a
20	chr19:43423119-43423169	SK-N-SH_RA	brain:	n/a
21	chr19:43202312-43202362	PANC-1	pancreas:	n/a
22	chr19:43423119-43423169	NH-A	brain:	n/a
23	chr19:43530623-43530673	BE2_C	brain:	n/a
24	chr19:43361218-43361268	GM12878	blood:	n/a
25	chr19:43385047-43385097	RPTEC	kidney:	n/a
26	chr19:43531821-43531871	AG04449	skin:	fetal
27	chr19:43531821-43531871	T-47D	breast:	n/a
28	chr19:43202312-43202362	NHBE	bronchial:	n/a
29	chr19:43244680-43244730	AG04450	lung:	fetal
30	chr19:43383799-43383849	GM12892	blood:	n/a
31	chr19:43385047-43385097	ProgFib	skin:	n/a
32	chr19:43530623-43530673	LNCaP	prostate:	n/a
33	chr19:43244635-43244685	AG04449	skin:	fetal
34	chr19:43383405-43383455	AG09309	skin:	n/a
35	chr19:43202312-43202362	HUVEC	blood vessel:	n/a
36	chr19:43383799-43383849	HIPEpiC	eye:	n/a
37	chr19:43410455-43410505	PFSK-1	brain:	n/a
38	chr19:43385100-43385150	AG04450	lung:	fetal
39	chr19:43421584-43421634	Hepatocyte	liver:	n/a
40	chr19:43198154-43198204	A549	lung:	n/a
41	chr19:43360229-43360279	GM12891	blood:	n/a
42	chr19:43383986-43384036	RPTEC	kidney:	n/a
43	chr19:43383799-43383849	BJ	skin:	n/a
44	chr19:43271112-43271162	SK-N-MC	brain:	n/a
45	chr19:43245921-43245971	HepG2	liver:	n/a
46	chr19:43361218-43361268	GM06990	blood:	n/a
47	chr19:43355659-43355709	H1-hESC	embryonic stem cell:	embryo
48	chr19:43271004-43271054	GM12891	blood:	n/a
49	chr19:43269877-43269927	A549	lung:	n/a
50	chr19:43580600-43580650	AG04449	skin:	fetal

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:43110594..43111450-chr19:43197610..43198160,2	MCF-7	breast:
2	chr19:43197633..43198568-chr19:43280847..43281639,2	K562	blood:
3	chr19:43531581..43532101-chr2:1136088..1136613,2	MCF-7	breast:
4	chr19:43265768..43266290-chr19:43769932..43770473,2	MCF-7	breast:
5	chr19:43197619..43198590-chr19:43246174..43246898,3	MCF-7	breast:
6	chr19:43523469..43524084-chr19:43531918..43532440,2	MCF-7	breast:
7	chr19:43197626..43198528-chr19:43245881..43246809,2	MCF-7	breast:
8	chr19:43196586..43198250-chr19:43213574..43216161,2	MCF-7	breast:
9	chr19:43197647..43198196-chr19:43280850..43281744,2	MCF-7	breast:
10	chr19:43197619..43198590-chr19:43246174..43246898,3	MCF-7	breast:
11	chr19:43197647..43198196-chr19:43280850..43281744,2	MCF-7	breast:
12	chr19:43197633..43198568-chr19:43280847..43281639,2	K562	blood:
13	chr19:43196586..43198250-chr19:43213574..43216161,2	MCF-7	breast:
14	chr19:43523469..43524084-chr19:43531918..43532440,2	MCF-7	breast:
15	chr19:43197626..43198528-chr19:43245881..43246809,2	MCF-7	breast:
16	chr19:43297087..43297875-chr19:43423005..43423976,2	MCF-7	breast:
17	chr19:43139154..43139986-chr19:43246322..43246897,2	MCF-7	breast:

(count:46 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSG1-1	chr19:43359708-43359870	NONHSAT066571
2	lnc-PSG1-1	chr19:43358101-43358466	NONHSAT066571
3	lnc-PSG6-3	chr19:43372908-43374797	NONHSAT066572
4	lnc-PSG8-1	chr19:43285358-43285449	NONHSAT066567
5	lnc-PSG6-1	chr19:43439556-43439921	NR_073194
6	lnc-PSG6-3	chr19:43370618-43371302	NONHSAT066572
7	lnc-PSG6-3	chr19:43372253-43372507	NONHSAT066572
8	lnc-PSG8-1	chr19:43289879-43290117	NONHSAT066567
9	lnc-PSG6-2	chr19:43453655-43453909	NONHSAT066575
10	lnc-PSG6-1	chr19:43429925-43431729	NONHSAT066573
11	lnc-PSG1-1	chr19:43343708-43343916	NONHSAT066571
12	lnc-PSG2-4	chr19:43521383-43521753	NONHSAT066578
13	lnc-PSG1-1	chr19:43343520-43343530	NONHSAT146988
14	lnc-PSG1-1	chr19:43343708-43343916	NONHSAT146988
15	lnc-PSG6-1	chr19:43441165-43441330	NONHSAT066574
16	lnc-PSG1-1	chr19:43570669-43570753	NONHSAT066570
17	lnc-PSG2-2	chr19:43575923-43576106	NONHSAT066580
18	lnc-PSG2-5	chr19:43514422-43514579	NONHSAT066577
19	lnc-PSG3-1	chr19:43258485-43260276	NONHSAT066566
20	lnc-PSG2-2	chr19:43576503-43576781	NONHSAT066580
21	lnc-PSG3-1	chr19:43256843-43257528	NONHSAT066566
22	lnc-PSG11-1	chr19:43540021-43540112	NONHSAT066579
23	lnc-PSG6-1	chr19:43441165-43441330	NR_073194
24	lnc-PSG6-1	chr19:43429925-43430179	NR_073194
25	lnc-PSG2-5	chr19:43519268-43519426	NONHSAT066577
26	lnc-PSG8-1	chr19:43290505-43290747	NONHSAT066567
27	lnc-PSG2-4	chr19:43522922-43523199	NONHSAT066578
28	lnc-PSG6-1	chr19:43428284-43428976	NR_073194
29	lnc-PSG1-1	chr19:43349168-43349446	NONHSAT146988
30	lnc-PSG11-1	chr19:43545168-43545400	NONHSAT066579
31	lnc-PSG1-1	chr19:43343447-43343530	NONHSAT066571
32	lnc-PSG6-1	chr19:43440309-43440647	NONHSAT066574
33	lnc-PSG1-1	chr19:43341149-43341534	NONHSAT066571
34	lnc-PSG6-2	chr19:43454299-43454539	NONHSAT066575
35	lnc-PSG1-1	chr19:43348511-43348765	NONHSAT146988
36	lnc-PSG6-1	chr19:43433594-43433872	NR_073194
37	lnc-PSG1-1	chr19:43341149-43341602	NONHSAT066570
38	lnc-PSG6-1	chr19:43430590-43430868	NR_073194
39	lnc-PSG2-5	chr19:43514110-43514858	NONHSAT066576
40	lnc-PSG2-5	chr19:43511982-43512194	NONHSAT066576
41	lnc-PSG1-1	chr19:43359708-43359870	NONHSAT146988
42	lnc-PSG1-1	chr19:43358101-43358466	NONHSAT146988
43	lnc-PSG1-1	chr19:43349168-43349446	NONHSAT066571
44	lnc-PSG11-1	chr19:43544526-43544780	NONHSAT066579
45	lnc-PSG1-1	chr19:43348511-43348765	NONHSAT066571
46	lnc-PSG6-1	chr19:43428286-43428976	NONHSAT066573

No data

Variant related genes	Relation type
CEACAMP7	TF binding region
PSG8	TF binding region
CEACAMP8	TF binding region
PSG1	TF binding region
PSG2	TF binding region
RPS10P28	TF binding region
PSG7	TF binding region
PSG11	TF binding region
ENSG00000225877	TF binding region
PSG6	TF binding region
CEACAMP6	TF binding region
PSG3	TF binding region
PSG10P	TF binding region
CEACAMP7	CpG island
PSG8	CpG island
CEACAMP8	CpG island
PSG1	CpG island
PSG2	CpG island
RPS10P28	CpG island
PSG7	CpG island
PSG11	CpG island
ENSG00000225877	CpG island
PSG6	CpG island
CEACAMP6	CpG island
PSG3	CpG island
PSG10P	CpG island
ENSG00000170848	chromatin interactions

Extended variants
information (count: 21523 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:21523 , 50 per page) page: 1 2 3 4 5 6 7 ... 431

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546365147	chr19:43173821-43173822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs34775251	chr19:43173833-43173834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs139394456	chr19:43173836-43173837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149941880	chr19:43173855-43173856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543242326	chr19:43173897-43173898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182081171	chr19:43173911-43173912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555154134	chr19:43173974-43173975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570133160	chr19:43173990-43173991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs73562346	chr19:43174038-43174039	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs554166278	chr19:43174069-43174070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs73562347	chr19:43174103-43174104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111296495	chr19:43174147-43174148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs75780037	chr19:43174156-43174157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540642668	chr19:43174169-43174170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538394658	chr19:43174176-43174177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577711982	chr19:43174178-43174179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552344502	chr19:43174184-43174185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs397859452	chr19:43174197-43174198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148638719	chr19:43174251-43174252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559305402	chr19:43174288-43174289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113532833	chr19:43174292-43174293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554456040	chr19:43174350-43174351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542579078	chr19:43174358-43174359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545709543	chr19:43174362-43174363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186680875	chr19:43174363-43174364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560104291	chr19:43174373-43174374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537024197	chr19:43174440-43174441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557108677	chr19:43174478-43174479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577260903	chr19:43174497-43174498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs546029584	chr19:43174505-43174506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559854930	chr19:43174631-43174632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573369513	chr19:43174720-43174721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542507650	chr19:43174762-43174763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549985995	chr19:43186863-43186864	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
35	rs115437551	chr19:43186887-43186888	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
36	rs190796930	chr19:43186895-43186896	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
37	rs540056450	chr19:43186912-43186913	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
38	rs180721832	chr19:43186969-43186970	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
39	rs187395390	chr19:43186970-43186971	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
40	rs4141247	chr19:43198010-43198011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs111932096	chr19:43198015-43198016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs10421714	chr19:43198035-43198036	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs532726348	chr19:43198044-43198045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs535667847	chr19:43198063-43198064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs76758542	chr19:43198108-43198109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555665363	chr19:43198120-43198121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs150278901	chr19:43198126-43198127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs544569010	chr19:43198134-43198135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs182182299	chr19:43198154-43198155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs566226059	chr19:43198158-43198159	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD
Autism	19492091	CNVD
Ovarian cancer	20800559	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21240255	CNVD
early-passage human iPS cells	21368824	CNVD
Primary Severe Spermatogenic Failure	20378930	CNVD

Chromatin state (count:1291 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43160200-43174800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr19:43186800-43187000	Flanking Bivalent TSS/Enh	A549	lung
3	chr19:43198000-43199400	Enhancers	Placenta	Placenta
4	chr19:43199400-43200600	Weak transcription	Placenta	Placenta
5	chr19:43200000-43200400	Bivalent Enhancer	A549	lung
6	chr19:43200400-43201000	Enhancers	A549	lung
7	chr19:43200600-43200800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr19:43200600-43201000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
9	chr19:43200600-43203000	Enhancers	Placenta	Placenta
10	chr19:43202200-43202400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr19:43203000-43204600	Weak transcription	Placenta	Placenta
12	chr19:43204000-43204200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr19:43204600-43204800	Enhancers	Placenta	Placenta
14	chr19:43213600-43215000	Enhancers	Placenta	Placenta
15	chr19:43214400-43214800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr19:43215000-43215600	Enhancers	A549	lung
17	chr19:43215000-43216600	Weak transcription	Placenta	Placenta
18	chr19:43216600-43217400	Enhancers	Placenta	Placenta
19	chr19:43217400-43217800	Weak transcription	Placenta	Placenta
20	chr19:43217800-43218000	Enhancers	Placenta	Placenta
21	chr19:43218000-43227200	Weak transcription	Placenta	Placenta
22	chr19:43227200-43229200	Strong transcription	Placenta	Placenta
23	chr19:43229200-43233600	Weak transcription	Placenta	Placenta
24	chr19:43232400-43233600	Enhancers	Brain Hippocampus Middle	brain
25	chr19:43232600-43233200	Enhancers	Brain Cingulate Gyrus	brain
26	chr19:43232800-43233200	Enhancers	Brain Substantia Nigra	brain
27	chr19:43233200-43236800	Weak transcription	Brain Substantia Nigra	brain
28	chr19:43233600-43233800	Genic enhancers	Placenta	Placenta
29	chr19:43233800-43234200	Weak transcription	Placenta	Placenta
30	chr19:43234200-43235000	Genic enhancers	Placenta	Placenta
31	chr19:43235000-43236600	Weak transcription	Placenta	Placenta
32	chr19:43236600-43237600	Genic enhancers	Placenta	Placenta
33	chr19:43236800-43237200	Active TSS	Brain Substantia Nigra	brain
34	chr19:43237600-43238400	Weak transcription	Placenta	Placenta
35	chr19:43238400-43241600	Active TSS	Placenta	Placenta
36	chr19:43239000-43240400	Enhancers	NHDF-Ad	bronchial
37	chr19:43239000-43242200	Enhancers	Osteobl	bone
38	chr19:43239000-43242800	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr19:43239200-43242000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr19:43239400-43240400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr19:43239400-43242000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr19:43239400-43242200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr19:43239400-43242400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr19:43239400-43242400	Enhancers	HMEC	breast
45	chr19:43239400-43242800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr19:43239800-43240400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr19:43239800-43242000	Enhancers	NH-A	brain
48	chr19:43239800-43242600	Enhancers	NHEK	skin
49	chr19:43240000-43240200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr19:43240000-43240200	Enhancers	HSMM	muscle

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