Variant report

Variant	nsv544008
Chromosome Location	chr19:43141984-43741311
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:7646)
CpG islands
(count:4092)
Chromatin interactive
region (count:26)
LncRNA
region (count:84)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:7646 , 50 per page) page: 1 2 3 4 5 6 7 ... 153

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	ATF1	chr19:43733581-43733686	K562	blood:	n/a	n/a
3	ATF3	chr19:43335307-43336092	A549	lung:	n/a	n/a
4	ATF3	chr19:43686016-43686763	A549	lung:	n/a	n/a
5	ATF3	chr19:43336336-43336928	A549	lung:	n/a	n/a
6	ATF3	chr19:43355048-43355947	A549	lung:	n/a	n/a
7	ATF3	chr19:43336349-43336838	A549	lung:	n/a	n/a
8	ATF3	chr19:43355412-43355889	A549	lung:	n/a	n/a
9	ATF3	chr19:43335349-43336094	A549	lung:	n/a	n/a
10	BATF	chr19:43246213-43246502	GM12878	blood:	n/a	n/a
11	BATF	chr19:43692257-43692526	GM12878	blood:	n/a	n/a
12	BATF	chr19:43361555-43361754	GM12878	blood:	n/a	n/a
13	BATF	chr19:43179178-43179402	GM12878	blood:	n/a	n/a
14	BATF	chr19:43552186-43552537	GM12878	blood:	n/a	chr19:43552319-43552330
15	BATF	chr19:43271446-43271728	GM12878	blood:	n/a	n/a
16	BATF	chr19:43588401-43588710	GM12878	blood:	n/a	n/a
17	BATF	chr19:43302238-43302533	GM12878	blood:	n/a	chr19:43302344-43302355
18	BATF	chr19:43552261-43552460	GM12878	blood:	n/a	chr19:43552319-43552330
19	BATF	chr19:43692397-43692675	GM12878	blood:	n/a	n/a
20	BATF	chr19:43738081-43738296	GM12878	blood:	n/a	chr19:43738185-43738196
21	BATF	chr19:43591924-43592150	GM12878	blood:	n/a	n/a
22	BATF	chr19:43613006-43613315	GM12878	blood:	n/a	chr19:43613110-43613121
23	BATF	chr19:43442962-43443231	GM12878	blood:	n/a	n/a
24	BATF	chr19:43711409-43711658	GM12878	blood:	n/a	n/a
25	BCL11A	chr19:43179101-43179287	GM12878	blood:	n/a	n/a
26	BCL3	chr19:43335292-43335990	A549	lung:	n/a	chr19:43335602-43335611 chr19:43335603-43335612
27	BCL3	chr19:43354910-43356058	A549	lung:	n/a	n/a
28	BCL3	chr19:43402518-43403428	A549	lung:	n/a	n/a
29	BCL3	chr19:43323095-43323355	GM12878	blood:	n/a	n/a
30	BCL3	chr19:43336159-43337656	A549	lung:	n/a	chr19:43336227-43336234
31	BCL3	chr19:43335242-43336126	A549	lung:	n/a	chr19:43335602-43335611 chr19:43335603-43335612
32	BCL3	chr19:43354946-43356043	A549	lung:	n/a	n/a
33	BCL3	chr19:43297507-43298116	A549	lung:	n/a	n/a
34	BCL3	chr19:43336292-43336877	A549	lung:	n/a	n/a
35	BCL3	chr19:43336972-43337663	A549	lung:	n/a	n/a
36	BHLHE40	chr19:43733601-43733620	K562	blood:	n/a	n/a
37	BHLHE40	chr19:43709323-43709343	K562	blood:	n/a	n/a
38	BHLHE40	chr19:43427453-43427512	GM12878	blood:	n/a	n/a
39	BHLHE40	chr19:43355572-43355890	A549	lung:	n/a	n/a
40	BHLHE40	chr19:43385480-43385517	K562	blood:	n/a	n/a
41	BHLHE40	chr19:43582147-43582203	K562	blood:	n/a	n/a
42	BRCA1	chr19:43265411-43265577	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr19:43297623-43297950	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr19:43624776-43624937	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr19:43436723-43436914	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr19:43168346-43168356	GM12878	blood:	n/a	n/a
47	BRCA1	chr19:43525934-43526309	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr19:43355288-43355847	Hela-S3	cervix:	n/a	n/a
49	CBX3	chr19:43385505-43385738	K562	blood:	n/a	n/a
50	CBX3	chr19:43190821-43191075	K562	blood:	n/a	n/a

(count:4092 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43355659-43355709	Jurkat	blood:	n/a
2	chr19:43709360-43709410	SK-N-MC	brain:	n/a
3	chr19:43203368-43203418	HIPEpiC	eye:	n/a
4	chr19:43673501-43673551	NHBE	bronchial:	n/a
5	chr19:43531821-43531871	ECC-1	luminal epithelium:	n/a
6	chr19:43355659-43355709	Jurkat	blood:	n/a
7	chr19:43709360-43709410	SK-N-MC	brain:	n/a
8	chr19:43203368-43203418	HIPEpiC	eye:	n/a
9	chr19:43673501-43673551	NHBE	bronchial:	n/a
10	chr19:43531821-43531871	ECC-1	luminal epithelium:	n/a
11	chr19:43442693-43442743	BJ	skin:	n/a
12	chr19:43673501-43673551	HEEpiC	esophagus:	n/a
13	chr19:43442809-43442859	ovcar-3	ovarian:	n/a
14	chr19:43709832-43709882	AG10803	skin:	n/a
15	chr19:43691930-43691980	H1-hESC	embryonic stem cell:	embryo
16	chr19:43383986-43384036	AG09309	skin:	n/a
17	chr19:43245921-43245971	Caco-2	colon:	n/a
18	chr19:43710277-43710327	ECC-1	luminal epithelium:	n/a
19	chr19:43690622-43690672	HUVEC	blood vessel:	n/a
20	chr19:43198154-43198204	HepG2	liver:	n/a
21	chr19:43359870-43359920	AG04450	lung:	fetal
22	chr19:43244680-43244730	HRPEpiC	eye:	n/a
23	chr19:43361218-43361268	Caco-2	colon:	n/a
24	chr19:43423176-43423226	BJ	skin:	n/a
25	chr19:43385100-43385150	HCT-116	colon:	n/a
26	chr19:43244680-43244730	LNCaP	prostate:	n/a
27	chr19:43383986-43384036	HPAEpiC	pulmonary alveolar:	n/a
28	chr19:43442484-43442534	GM19239	blood:	n/a
29	chr19:43691878-43691928	MCF10A-Er-Src	breast:	n/a
30	chr19:43410455-43410505	HRCEpiC	kidney:	n/a
31	chr19:43384780-43384830	Hela-S3	cervix:	n/a
32	chr19:43385047-43385097	IMR90	lung:	fetal
33	chr19:43269832-43269882	NH-A	brain:	n/a
34	chr19:43710277-43710327	HUVEC	blood vessel:	n/a
35	chr19:43711064-43711114	PANC-1	pancreas:	n/a
36	chr19:43360229-43360279	GM12891	blood:	n/a
37	chr19:43257346-43257396	HepG2	liver:	n/a
38	chr19:43580600-43580650	HPAEpiC	pulmonary alveolar:	n/a
39	chr19:43423119-43423169	GM19239	blood:	n/a
40	chr19:43530623-43530673	T-47D	breast:	n/a
41	chr19:43245921-43245971	GM12892	blood:	n/a
42	chr19:43709754-43709804	HepG2	liver:	n/a
43	chr19:43588055-43588105	MCF-7	breast:	n/a
44	chr19:43410455-43410505	HRPEpiC	eye:	n/a
45	chr19:43423176-43423226	NHBE	bronchial:	n/a
46	chr19:43588069-43588119	Caco-2	colon:	n/a
47	chr19:43709754-43709804	AG04450	lung:	fetal
48	chr19:43360229-43360279	GM12878	blood:	n/a
49	chr19:43580600-43580650	MCF-7	breast:	n/a
50	chr19:43587500-43587550	U87	brain:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:43167897..43169449-chr19:43169988..43172834,2	MCF-7	breast:
2	chr19:43197647..43198196-chr19:43280850..43281744,2	MCF-7	breast:
3	chr19:43197619..43198590-chr19:43246174..43246898,3	MCF-7	breast:
4	chr19:43110921..43111495-chr19:43166501..43167328,2	MCF-7	breast:
5	chr19:43149390..43151656-chr19:43158079..43159963,2	MCF-7	breast:
6	chr19:43197647..43198196-chr19:43280850..43281744,2	MCF-7	breast:
7	chr19:43197619..43198590-chr19:43246174..43246898,3	MCF-7	breast:
8	chr19:43265768..43266290-chr19:43769932..43770473,2	MCF-7	breast:
9	chr19:43197633..43198568-chr19:43280847..43281639,2	K562	blood:
10	chr19:43531581..43532101-chr2:1136088..1136613,2	MCF-7	breast:
11	chr19:43167897..43169449-chr19:43169988..43172834,2	MCF-7	breast:
12	chr19:43139185..43139985-chr19:43166999..43167914,2	MCF-7	breast:
13	chr19:43196586..43198250-chr19:43213574..43216161,2	MCF-7	breast:
14	chr19:43196586..43198250-chr19:43213574..43216161,2	MCF-7	breast:
15	chr19:43197626..43198528-chr19:43245881..43246809,2	MCF-7	breast:
16	chr19:43197626..43198528-chr19:43245881..43246809,2	MCF-7	breast:
17	chr19:43523469..43524084-chr19:43531918..43532440,2	MCF-7	breast:
18	chr19:43523469..43524084-chr19:43531918..43532440,2	MCF-7	breast:
19	chr19:43148558..43149434-chr20:53015100..53015659,2	MCF-7	breast:
20	chr19:43678340..43681333-chr19:43698109..43700078,2	MCF-7	breast:
21	chr19:43138891..43139734-chr19:43166436..43166942,2	MCF-7	breast:
22	chr19:43139154..43139986-chr19:43246322..43246897,2	MCF-7	breast:
23	chr19:43110594..43111450-chr19:43197610..43198160,2	MCF-7	breast:
24	chr19:43197633..43198568-chr19:43280847..43281639,2	K562	blood:
25	chr19:43297087..43297875-chr19:43423005..43423976,2	MCF-7	breast:
26	chr19:43608137..43608719-chr19:43820621..43821519,2	MCF-7	breast:

(count:84 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSG2-3	chr19:43600608-43600855	NONHSAT066582
2	lnc-PSG9-2	chr19:43728324-43728464	NONHSAT066591
3	lnc-PSG6-1	chr19:43440309-43440647	NONHSAT066574
4	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066593
5	lnc-PSG1-1	chr19:43348511-43348765	NONHSAT146988
6	lnc-PSG6-1	chr19:43441165-43441330	NR_073194
7	lnc-PSG1-1	chr19:43349168-43349446	NONHSAT066571
8	lnc-PSG9-2	chr19:43724783-43725023	NONHSAT066593
9	lnc-PSG2-2	chr19:43576503-43576781	NONHSAT066580
10	lnc-PSG5-1	chr19:43699147-43699301	NONHSAT066589
11	lnc-PSG1-1	chr19:43359708-43359870	NONHSAT066571
12	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066591
13	lnc-PSG6-3	chr19:43370618-43371302	NONHSAT066572
14	lnc-PSG2-1	chr19:43585939-43586423	NONHSAT066581
15	lnc-PSG9-2	chr19:43737376-43737446	NONHSAT066591
16	lnc-PSG9-2	chr19:43719405-43719531	NONHSAT066591
17	lnc-PSG5-1	chr19:43696890-43697540	NONHSAT066588
18	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066591
19	lnc-PSG6-3	chr19:43372908-43374797	NONHSAT066572
20	lnc-PSG1-1	chr19:43349168-43349446	NONHSAT146988
21	lnc-PSG9-2	chr19:43727043-43727110	NONHSAT066591
22	lnc-PSG1-1	chr19:43358101-43358466	NONHSAT146988
23	lnc-AC011497.1-2	chr19:43155239-43156171	ENSG00000213904.4
24	lnc-PSG4-3	chr19:43674207-43674723	NONHSAT066585
25	lnc-PSG6-1	chr19:43430590-43430868	NR_073194
26	lnc-CD177-1	chr19:43665002-43665014	ENSG00000227606.1
27	lnc-PSG6-1	chr19:43429925-43430179	NR_073194
28	lnc-PSG5-1	chr19:43698492-43699038	NONHSAT066588
29	lnc-PSG4-1	chr19:43710321-43711451	NONHSAT066590
30	lnc-PSG5-1	chr19:43698107-43698746	NONHSAT066589
31	lnc-CD177-1	chr19:43657431-43657763	ENSG00000227606.1
32	lnc-AC011497.1-2	chr19:43155388-43155602	NONHSAT066564
33	lnc-PSG1-1	chr19:43358101-43358466	NONHSAT066571
34	lnc-PSG6-2	chr19:43453655-43453909	NONHSAT066575
35	lnc-CD177-1	chr19:43658863-43659311	ENSG00000227606.1
36	lnc-PSG9-2	chr19:43734076-43734177	NONHSAT066591
37	lnc-PSG6-1	chr19:43439556-43439921	NR_073194
38	lnc-PSG6-3	chr19:43372253-43372507	NONHSAT066572
39	lnc-PSG6-1	chr19:43433594-43433872	NR_073194
40	lnc-PSG4-1	chr19:43707241-43708403	NONHSAT066590
41	lnc-PSG8-1	chr19:43289879-43290117	NONHSAT066567
42	lnc-PSG8-1	chr19:43285358-43285449	NONHSAT066567
43	lnc-PSG2-5	chr19:43514422-43514579	NONHSAT066577
44	lnc-PSG4-3	chr19:43671924-43672287	NONHSAT066585
45	lnc-PSG4-3	chr19:43674207-43674717	NONHSAT066586
46	lnc-PSG1-1	chr19:43343520-43343530	NONHSAT146988
47	lnc-PSG11-1	chr19:43540021-43540112	NONHSAT066579
48	lnc-PSG6-2	chr19:43454299-43454539	NONHSAT066575
49	lnc-PSG2-5	chr19:43511982-43512194	NONHSAT066576
50	lnc-PSG4-2	chr19:43688934-43689087	NONHSAT066587

No data

Variant related genes	Relation type
CEACAMP7	TF binding region
PSG4	TF binding region
CEACAMP1	TF binding region
CEACAMP9	TF binding region
PSG8	TF binding region
CEACAMP8	TF binding region
PSG1	TF binding region
PSG2	TF binding region
ENSG00000227606	TF binding region
RPS10P28	TF binding region
PSG5	TF binding region
PSG7	TF binding region
PSG11	TF binding region
ENSG00000225877	TF binding region
CEACAMP5	TF binding region
PSG6	TF binding region
CEACAMP10	TF binding region
CEACAMP6	TF binding region
PSG3	TF binding region
PSG10P	TF binding region
CEACAMP7	CpG island
PSG4	CpG island
CEACAMP1	CpG island
CEACAMP9	CpG island
PSG8	CpG island
CEACAMP8	CpG island
PSG1	CpG island
PSG2	CpG island
ENSG00000227606	CpG island
RPS10P28	CpG island
PSG5	CpG island
PSG7	CpG island
PSG11	CpG island
ENSG00000225877	CpG island
CEACAMP5	CpG island
PSG6	CpG island
CEACAMP10	CpG island
CEACAMP6	CpG island
PSG3	CpG island
PSG10P	CpG island
ENSG00000170848	chromatin interactions
ENSG00000231561	chromatin interactions
ENSG00000243137	chromatin interactions

Extended variants
information (count: 31026 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:31026 , 50 per page) page: 1 2 3 4 5 6 7 ... 621

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138111763	chr19:43149434-43149435	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs386809437	chr19:43149435-43149436	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs78857130	chr19:43149436-43149437	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs545088133	chr19:43149437-43149438	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs375538841	chr19:43149462-43149463	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs372189545	chr19:43149494-43149495	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs575299822	chr19:43149593-43149594	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs370622175	chr19:43149604-43149605	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs116359333	chr19:43149613-43149614	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs551222560	chr19:43149616-43149617	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs565080588	chr19:43149621-43149622	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs527528823	chr19:43149726-43149727	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs542690231	chr19:43149761-43149762	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs143719983	chr19:43149775-43149776	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs536621440	chr19:43149843-43149844	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs186338383	chr19:43149859-43149860	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs550127690	chr19:43149878-43149879	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs569984360	chr19:43149923-43149924	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs114970392	chr19:43149944-43149945	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs558833799	chr19:43149986-43149987	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs572555599	chr19:43150006-43150007	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs566248622	chr19:43150056-43150057	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs8108816	chr19:43150071-43150072	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs548336772	chr19:43150078-43150079	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs554805642	chr19:43150127-43150128	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs574812623	chr19:43150132-43150133	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs74413120	chr19:43150155-43150156	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs56978333	chr19:43150164-43150165	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs191598398	chr19:43150209-43150210	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs118025601	chr19:43150214-43150215	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs183500580	chr19:43150251-43150252	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs201624433	chr19:43150362-43150363	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs8109269	chr19:43150440-43150441	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs188141870	chr19:43150444-43150445	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs573270375	chr19:43150448-43150449	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs561094883	chr19:43150493-43150494	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs377451256	chr19:43150526-43150527	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs557514043	chr19:43150572-43150573	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs570896245	chr19:43150581-43150582	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs532461111	chr19:43150737-43150738	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs530000582	chr19:43150764-43150765	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs145972780	chr19:43150807-43150808	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs191410901	chr19:43150835-43150836	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs532406958	chr19:43150883-43150884	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs182695459	chr19:43150899-43150900	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs544902549	chr19:43150904-43150905	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs375383379	chr19:43151019-43151020	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs368922404	chr19:43151113-43151114	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs551046264	chr19:43151115-43151116	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs138777675	chr19:43151132-43151133	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
early-passage human iPS cells	21368824	CNVD
Primary Severe Spermatogenic Failure	20378930	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1900 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43150400-43150600	ZNF genes & repeats	Brain Hippocampus Middle	brain
2	chr19:43150600-43159800	Weak transcription	Brain Hippocampus Middle	brain
3	chr19:43153200-43158000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr19:43154000-43154200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr19:43154400-43156000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr19:43154800-43159800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr19:43155200-43155400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr19:43155400-43156000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr19:43155400-43157600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr19:43155800-43157800	Weak transcription	Adipose Nuclei	Adipose
11	chr19:43156000-43156600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr19:43156000-43156600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr19:43156000-43162000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr19:43156400-43156800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr19:43156600-43159800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr19:43156800-43157800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr19:43157200-43158000	Enhancers	Esophagus	oesophagus
18	chr19:43157400-43157800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr19:43157400-43158600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr19:43157600-43160000	Weak transcription	Brain Angular Gyrus	brain
21	chr19:43157600-43160200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr19:43157800-43158000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr19:43157800-43158000	Enhancers	Pancreas	Pancrea
24	chr19:43157800-43158600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr19:43157800-43163000	Enhancers	Adipose Nuclei	Adipose
26	chr19:43158000-43158600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr19:43158200-43159800	Weak transcription	Pancreas	Pancrea
28	chr19:43158600-43162400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr19:43159200-43163000	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr19:43159400-43162000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr19:43159600-43159800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr19:43159800-43160000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr19:43159800-43160600	Enhancers	Pancreas	Pancrea
34	chr19:43159800-43161800	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr19:43159800-43161800	Enhancers	Brain Substantia Nigra	brain
36	chr19:43159800-43162000	Enhancers	Brain Hippocampus Middle	brain
37	chr19:43160000-43160400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr19:43160000-43160600	Enhancers	Gastric	stomach
39	chr19:43160000-43161400	Enhancers	Brain Anterior Caudate	brain
40	chr19:43160000-43161600	Enhancers	Brain Cingulate Gyrus	brain
41	chr19:43160000-43162000	Enhancers	Brain Angular Gyrus	brain
42	chr19:43160200-43161800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr19:43160200-43174800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr19:43160400-43161200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
45	chr19:43160800-43161000	Enhancers	Left Ventricle	heart
46	chr19:43161000-43161400	Enhancers	Colon Smooth Muscle	Colon
47	chr19:43161400-43161800	Weak transcription	Colon Smooth Muscle	Colon
48	chr19:43161400-43163000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr19:43161800-43162600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr19:43161800-43162600	Enhancers	Colon Smooth Muscle	Colon

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