Variant report

Variant	esv1845826
Chromosome Location	chr19:43152829-43454902
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4287)
CpG islands
(count:2445)
Chromatin interactive
region (count:19)
LncRNA
region (count:40)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4287 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

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	chr19:43355048-43355947	A549	lung:	n/a	n/a
3	ATF3	chr19:43336349-43336838	A549	lung:	n/a	n/a
4	ATF3	chr19:43335349-43336094	A549	lung:	n/a	n/a
5	ATF3	chr19:43335307-43336092	A549	lung:	n/a	n/a
6	ATF3	chr19:43336336-43336928	A549	lung:	n/a	n/a
7	ATF3	chr19:43355412-43355889	A549	lung:	n/a	n/a
8	BATF	chr19:43361555-43361754	GM12878	blood:	n/a	n/a
9	BATF	chr19:43246213-43246502	GM12878	blood:	n/a	n/a
10	BATF	chr19:43271446-43271728	GM12878	blood:	n/a	n/a
11	BATF	chr19:43179178-43179402	GM12878	blood:	n/a	n/a
12	BATF	chr19:43302238-43302533	GM12878	blood:	n/a	chr19:43302344-43302355
13	BATF	chr19:43442962-43443231	GM12878	blood:	n/a	n/a
14	BCL11A	chr19:43179101-43179287	GM12878	blood:	n/a	n/a
15	BCL3	chr19:43354946-43356043	A549	lung:	n/a	n/a
16	BCL3	chr19:43335242-43336126	A549	lung:	n/a	chr19:43335602-43335611 chr19:43335603-43335612
17	BCL3	chr19:43336292-43336877	A549	lung:	n/a	n/a
18	BCL3	chr19:43335292-43335990	A549	lung:	n/a	chr19:43335602-43335611 chr19:43335603-43335612
19	BCL3	chr19:43323095-43323355	GM12878	blood:	n/a	n/a
20	BCL3	chr19:43336972-43337663	A549	lung:	n/a	n/a
21	BCL3	chr19:43336159-43337656	A549	lung:	n/a	chr19:43336227-43336234
22	BCL3	chr19:43402518-43403428	A549	lung:	n/a	n/a
23	BCL3	chr19:43354910-43356058	A549	lung:	n/a	n/a
24	BCL3	chr19:43297507-43298116	A549	lung:	n/a	n/a
25	BHLHE40	chr19:43355572-43355890	A549	lung:	n/a	n/a
26	BHLHE40	chr19:43427453-43427512	GM12878	blood:	n/a	n/a
27	BHLHE40	chr19:43385480-43385517	K562	blood:	n/a	n/a
28	BRCA1	chr19:43168346-43168356	GM12878	blood:	n/a	n/a
29	BRCA1	chr19:43436723-43436914	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr19:43355288-43355847	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr19:43297623-43297950	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr19:43265411-43265577	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr19:43156238-43156476	K562	blood:	n/a	n/a
34	CBX3	chr19:43188032-43188426	HCT-116	colon:	n/a	n/a
35	CBX3	chr19:43190865-43191064	K562	blood:	n/a	n/a
36	CBX3	chr19:43385505-43385738	K562	blood:	n/a	n/a
37	CBX3	chr19:43190821-43191075	K562	blood:	n/a	n/a
38	CBX3	chr19:43385431-43385838	K562	blood:	n/a	n/a
39	CEBPB	chr19:43329315-43329373	K562	blood:	n/a	chr19:43329341-43329352
40	CEBPB	chr19:43337171-43337381	A549	lung:	n/a	n/a
41	CEBPB	chr19:43329190-43329511	A549	lung:	n/a	chr19:43329341-43329352
42	CEBPB	chr19:43393825-43394224	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr19:43335434-43335820	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr19:43335392-43336031	A549	lung:	n/a	n/a
45	CEBPB	chr19:43328170-43328414	A549	lung:	n/a	chr19:43328257-43328268
46	CEBPB	chr19:43329196-43329407	HepG2	liver:	n/a	chr19:43329341-43329352
47	CEBPB	chr19:43326599-43326799	A549	lung:	n/a	n/a
48	CEBPB	chr19:43156216-43156522	HepG2	liver:	n/a	chr19:43156349-43156360
49	CEBPB	chr19:43379145-43379767	IMR90	lung:	n/a	n/a
50	CEBPB	chr19:43355113-43355853	A549	lung:	n/a	n/a

(count:2445 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43269877-43269927	Hepatocyte	liver:	n/a
2	chr19:43421584-43421634	LNCaP	prostate:	n/a
3	chr19:43203368-43203418	HCM	heart:	n/a
4	chr19:43423176-43423226	HIPEpiC	eye:	n/a
5	chr19:43202312-43202362	Hepatocyte	liver:	n/a
6	chr19:43269877-43269927	Hepatocyte	liver:	n/a
7	chr19:43421584-43421634	LNCaP	prostate:	n/a
8	chr19:43203368-43203418	HCM	heart:	n/a
9	chr19:43423176-43423226	HIPEpiC	eye:	n/a
10	chr19:43202312-43202362	Hepatocyte	liver:	n/a
11	chr19:43359870-43359920	BE2_C	brain:	n/a
12	chr19:43202122-43202172	Hepatocyte	liver:	n/a
13	chr19:43423119-43423169	U87	brain:	n/a
14	chr19:43202122-43202172	HNPCEpiC	eye:	n/a
15	chr19:43385100-43385150	HPAEpiC	pulmonary alveolar:	n/a
16	chr19:43240516-43240566	GM12892	blood:	n/a
17	chr19:43359870-43359920	HAEpiC	amniotic membrane:	n/a
18	chr19:43383799-43383849	AG04450	lung:	fetal
19	chr19:43203368-43203418	HAEpiC	amniotic membrane:	n/a
20	chr19:43442484-43442534	ProgFib	skin:	n/a
21	chr19:43360229-43360279	HCT-116	colon:	n/a
22	chr19:43271058-43271108	T-47D	breast:	n/a
23	chr19:43383405-43383455	HRE	kidney:	n/a
24	chr19:43442484-43442534	ECC-1	luminal epithelium:	n/a
25	chr19:43360755-43360805	HCF	heart:	n/a
26	chr19:43423265-43423315	HAEpiC	amniotic membrane:	n/a
27	chr19:43423115-43423165	HPAEpiC	pulmonary alveolar:	n/a
28	chr19:43360229-43360279	HL-60	blood:	n/a
29	chr19:43421584-43421634	GM19239	blood:	n/a
30	chr19:43265778-43265828	AG10803	skin:	n/a
31	chr19:43383405-43383455	AG04449	skin:	fetal
32	chr19:43202122-43202172	Jurkat	blood:	n/a
33	chr19:43442484-43442534	CMK	blood:	n/a
34	chr19:43442693-43442743	HepG2	liver:	n/a
35	chr19:43257346-43257396	Caco-2	colon:	n/a
36	chr19:43198154-43198204	AoSMC	blood vessel:	n/a
37	chr19:43442809-43442859	H1-hESC	embryonic stem cell:	embryo
38	chr19:43200890-43200940	T-47D	breast:	n/a
39	chr19:43383986-43384036	MCF-7	breast:	n/a
40	chr19:43269832-43269882	PFSK-1	brain:	n/a
41	chr19:43271058-43271108	A549	lung:	n/a
42	chr19:43423115-43423165	AG09309	skin:	n/a
43	chr19:43198154-43198204	NB4	blood:	n/a
44	chr19:43385047-43385097	PFSK-1	brain:	n/a
45	chr19:43383799-43383849	HRCEpiC	kidney:	n/a
46	chr19:43227392-43227442	ECC-1	luminal epithelium:	n/a
47	chr19:43202122-43202172	GM19239	blood:	n/a
48	chr19:43410455-43410505	HUVEC	blood vessel:	n/a
49	chr19:43383405-43383455	HMEC	breast:	n/a
50	chr19:43361218-43361268	BJ	skin:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:43139154..43139986-chr19:43246322..43246897,2	MCF-7	breast:
2	chr19:43167897..43169449-chr19:43169988..43172834,2	MCF-7	breast:
3	chr19:43138891..43139734-chr19:43166436..43166942,2	MCF-7	breast:
4	chr19:43197633..43198568-chr19:43280847..43281639,2	K562	blood:
5	chr19:43110921..43111495-chr19:43166501..43167328,2	MCF-7	breast:
6	chr19:43196586..43198250-chr19:43213574..43216161,2	MCF-7	breast:
7	chr19:43197619..43198590-chr19:43246174..43246898,3	MCF-7	breast:
8	chr19:43139185..43139985-chr19:43166999..43167914,2	MCF-7	breast:
9	chr19:43197647..43198196-chr19:43280850..43281744,2	MCF-7	breast:
10	chr19:43197626..43198528-chr19:43245881..43246809,2	MCF-7	breast:
11	chr19:43265768..43266290-chr19:43769932..43770473,2	MCF-7	breast:
12	chr19:43197626..43198528-chr19:43245881..43246809,2	MCF-7	breast:
13	chr19:43297087..43297875-chr19:43423005..43423976,2	MCF-7	breast:
14	chr19:43197647..43198196-chr19:43280850..43281744,2	MCF-7	breast:
15	chr19:43197619..43198590-chr19:43246174..43246898,3	MCF-7	breast:
16	chr19:43197633..43198568-chr19:43280847..43281639,2	K562	blood:
17	chr19:43167897..43169449-chr19:43169988..43172834,2	MCF-7	breast:
18	chr19:43196586..43198250-chr19:43213574..43216161,2	MCF-7	breast:
19	chr19:43110594..43111450-chr19:43197610..43198160,2	MCF-7	breast:

(count:40 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSG6-3	chr19:43372253-43372507	NONHSAT066572
2	lnc-PSG6-2	chr19:43453655-43453909	NONHSAT066575
3	lnc-AC011497.1-2	chr19:43155869-43156816	NONHSAT066564
4	lnc-PSG8-1	chr19:43290505-43290747	NONHSAT066567
5	lnc-PSG1-1	chr19:43343708-43343916	NONHSAT066571
6	lnc-PSG8-1	chr19:43289879-43290117	NONHSAT066567
7	lnc-PSG3-1	chr19:43258485-43260276	NONHSAT066566
8	lnc-PSG1-1	chr19:43341149-43341534	NONHSAT066571
9	lnc-PSG6-1	chr19:43441165-43441330	NONHSAT066574
10	lnc-PSG1-1	chr19:43358101-43358466	NONHSAT066571
11	lnc-PSG6-1	chr19:43428286-43428976	NONHSAT066573
12	lnc-PSG1-1	chr19:43349168-43349446	NONHSAT066571
13	lnc-PSG6-1	chr19:43430590-43430868	NR_073194
14	lnc-PSG1-1	chr19:43359708-43359870	NONHSAT066571
15	lnc-PSG6-2	chr19:43454299-43454539	NONHSAT066575
16	lnc-PSG1-1	chr19:43358101-43358466	NONHSAT146988
17	lnc-PSG1-1	chr19:43343708-43343916	NONHSAT146988
18	lnc-AC011497.1-2	chr19:43155239-43156507	NONHSAT066548
19	lnc-PSG8-1	chr19:43285358-43285449	NONHSAT066567
20	lnc-PSG6-1	chr19:43428284-43428976	NR_073194
21	lnc-PSG6-1	chr19:43441165-43441330	NR_073194
22	lnc-AC011497.1-2	chr19:43155388-43155602	NONHSAT066564
23	lnc-PSG1-1	chr19:43348511-43348765	NONHSAT146988
24	lnc-PSG1-1	chr19:43343447-43343530	NONHSAT066571
25	lnc-PSG6-3	chr19:43372908-43374797	NONHSAT066572
26	lnc-PSG1-1	chr19:43348511-43348765	NONHSAT066571
27	lnc-PSG6-3	chr19:43370618-43371302	NONHSAT066572
28	lnc-PSG6-1	chr19:43429925-43430179	NR_073194
29	lnc-AC011497.1-2	chr19:43155239-43156507	NONHSAT066551
30	lnc-PSG6-1	chr19:43429925-43431729	NONHSAT066573
31	lnc-AC011497.1-2	chr19:43155239-43156507	ENSG00000213904.4
32	lnc-PSG1-1	chr19:43349168-43349446	NONHSAT146988
33	lnc-PSG1-1	chr19:43359708-43359870	NONHSAT146988
34	lnc-AC011497.1-2	chr19:43155239-43156171	ENSG00000213904.4
35	lnc-PSG6-1	chr19:43433594-43433872	NR_073194
36	lnc-PSG3-1	chr19:43256843-43257528	NONHSAT066566
37	lnc-PSG1-1	chr19:43343520-43343530	NONHSAT146988
38	lnc-PSG1-1	chr19:43341149-43341602	NONHSAT066570
39	lnc-PSG6-1	chr19:43439556-43439921	NR_073194
40	lnc-PSG6-1	chr19:43440309-43440647	NONHSAT066574

No data

Variant related genes	Relation type
CEACAMP7	TF binding region
PSG8	TF binding region
RPS10P28	TF binding region
ENSG00000225877	TF binding region
PSG6	TF binding region
CEACAMP6	TF binding region
PSG1	TF binding region
PSG7	TF binding region
CEACAMP5	TF binding region
PSG3	TF binding region
PSG10P	TF binding region
CEACAMP7	CpG island
PSG8	CpG island
RPS10P28	CpG island
ENSG00000225877	CpG island
PSG6	CpG island
CEACAMP6	CpG island
PSG1	CpG island
PSG7	CpG island
CEACAMP5	CpG island
PSG3	CpG island
PSG10P	CpG island
ENSG00000170848	chromatin interactions

Extended variants
information (count: 16328 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:16328 , 50 per page) page: 1 2 3 4 5 6 7 ... 327

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550875174	chr19:43152932-43152933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs78976737	chr19:43152941-43152942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571061203	chr19:43152946-43152947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539735634	chr19:43152966-43152967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112308224	chr19:43152992-43152993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112062871	chr19:43153015-43153016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534612991	chr19:43153030-43153031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113666759	chr19:43153089-43153090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112055262	chr19:43153167-43153168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537176828	chr19:43153175-43153176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140116710	chr19:43153176-43153177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372968129	chr19:43153204-43153205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs111605849	chr19:43153210-43153211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547705389	chr19:43153213-43153214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs145774917	chr19:43153223-43153224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554620392	chr19:43153273-43153274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369081628	chr19:43153274-43153275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs71361025	chr19:43153284-43153285	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs73562329	chr19:43153301-43153302	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs148953684	chr19:43153310-43153311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565481465	chr19:43153330-43153331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530894687	chr19:43153336-43153337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113345863	chr19:43153415-43153416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577366541	chr19:43153422-43153423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189686349	chr19:43153431-43153432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368146458	chr19:43153490-43153491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533578453	chr19:43153496-43153497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547277219	chr19:43153500-43153501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192881476	chr19:43153561-43153562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534574871	chr19:43153639-43153640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570959259	chr19:43153655-43153656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112195588	chr19:43153659-43153660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568080236	chr19:43153661-43153662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536736261	chr19:43153685-43153686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs370087579	chr19:43153747-43153748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544432804	chr19:43153785-43153786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562627560	chr19:43153819-43153820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543927602	chr19:43153845-43153846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs76740535	chr19:43153873-43153874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539259092	chr19:43153923-43153924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs142834153	chr19:43153930-43153931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530151951	chr19:43153933-43153934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539918033	chr19:43153985-43153986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548152834	chr19:43154000-43154001	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558512044	chr19:43154038-43154039	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565851822	chr19:43154040-43154041	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560540159	chr19:43154084-43154085	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373657833	chr19:43154088-43154089	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528331904	chr19:43154105-43154106	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575640667	chr19:43154106-43154107	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Non-syndromic sensorineural hearing loss	22037309	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

Chromatin state (count:1029 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43150600-43159800	Weak transcription	Brain Hippocampus Middle	brain
2	chr19:43153200-43158000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr19:43154000-43154200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr19:43154400-43156000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr19:43154800-43159800	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr19:43155200-43155400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr19:43155400-43156000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr19:43155400-43157600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr19:43155800-43157800	Weak transcription	Adipose Nuclei	Adipose
10	chr19:43156000-43156600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr19:43156000-43156600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr19:43156000-43162000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr19:43156400-43156800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr19:43156600-43159800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr19:43156800-43157800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr19:43157200-43158000	Enhancers	Esophagus	oesophagus
17	chr19:43157400-43157800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr19:43157400-43158600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr19:43157600-43160000	Weak transcription	Brain Angular Gyrus	brain
20	chr19:43157600-43160200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr19:43157800-43158000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr19:43157800-43158000	Enhancers	Pancreas	Pancrea
23	chr19:43157800-43158600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr19:43157800-43163000	Enhancers	Adipose Nuclei	Adipose
25	chr19:43158000-43158600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr19:43158200-43159800	Weak transcription	Pancreas	Pancrea
27	chr19:43158600-43162400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr19:43159200-43163000	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr19:43159400-43162000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr19:43159600-43159800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr19:43159800-43160000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr19:43159800-43160600	Enhancers	Pancreas	Pancrea
33	chr19:43159800-43161800	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr19:43159800-43161800	Enhancers	Brain Substantia Nigra	brain
35	chr19:43159800-43162000	Enhancers	Brain Hippocampus Middle	brain
36	chr19:43160000-43160400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr19:43160000-43160600	Enhancers	Gastric	stomach
38	chr19:43160000-43161400	Enhancers	Brain Anterior Caudate	brain
39	chr19:43160000-43161600	Enhancers	Brain Cingulate Gyrus	brain
40	chr19:43160000-43162000	Enhancers	Brain Angular Gyrus	brain
41	chr19:43160200-43161800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr19:43160200-43174800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr19:43160400-43161200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr19:43160800-43161000	Enhancers	Left Ventricle	heart
45	chr19:43161000-43161400	Enhancers	Colon Smooth Muscle	Colon
46	chr19:43161400-43161800	Weak transcription	Colon Smooth Muscle	Colon
47	chr19:43161400-43163000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr19:43161800-43162600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr19:43161800-43162600	Enhancers	Colon Smooth Muscle	Colon
50	chr19:43162000-43162200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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