Variant report

Variant	nsv828554
Chromosome Location	chr19:43268818-43648725
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4926)
CpG islands
(count:2380)
Chromatin interactive
region (count:7)
LncRNA
region (count:49)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4926 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr19:43336336-43336928	A549	lung:	n/a	n/a
2	ATF3	chr19:43355412-43355889	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	chr19:43355048-43355947	A549	lung:	n/a	n/a
7	BATF	chr19:43442962-43443231	GM12878	blood:	n/a	n/a
8	BATF	chr19:43302238-43302533	GM12878	blood:	n/a	chr19:43302344-43302355
9	BATF	chr19:43613006-43613315	GM12878	blood:	n/a	chr19:43613110-43613121
10	BATF	chr19:43552186-43552537	GM12878	blood:	n/a	chr19:43552319-43552330
11	BATF	chr19:43588401-43588710	GM12878	blood:	n/a	n/a
12	BATF	chr19:43271446-43271728	GM12878	blood:	n/a	n/a
13	BATF	chr19:43361555-43361754	GM12878	blood:	n/a	n/a
14	BATF	chr19:43552261-43552460	GM12878	blood:	n/a	chr19:43552319-43552330
15	BATF	chr19:43591924-43592150	GM12878	blood:	n/a	n/a
16	BCL3	chr19:43336292-43336877	A549	lung:	n/a	n/a
17	BCL3	chr19:43335242-43336126	A549	lung:	n/a	chr19:43335602-43335611 chr19:43335603-43335612
18	BCL3	chr19:43297507-43298116	A549	lung:	n/a	n/a
19	BCL3	chr19:43335292-43335990	A549	lung:	n/a	chr19:43335602-43335611 chr19:43335603-43335612
20	BCL3	chr19:43354910-43356058	A549	lung:	n/a	n/a
21	BCL3	chr19:43354946-43356043	A549	lung:	n/a	n/a
22	BCL3	chr19:43336972-43337663	A549	lung:	n/a	n/a
23	BCL3	chr19:43336159-43337656	A549	lung:	n/a	chr19:43336227-43336234
24	BCL3	chr19:43323095-43323355	GM12878	blood:	n/a	n/a
25	BCL3	chr19:43402518-43403428	A549	lung:	n/a	n/a
26	BHLHE40	chr19:43582147-43582203	K562	blood:	n/a	n/a
27	BHLHE40	chr19:43427453-43427512	GM12878	blood:	n/a	n/a
28	BHLHE40	chr19:43385480-43385517	K562	blood:	n/a	n/a
29	BHLHE40	chr19:43355572-43355890	A549	lung:	n/a	n/a
30	BRCA1	chr19:43355288-43355847	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr19:43624776-43624937	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr19:43436723-43436914	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr19:43297623-43297950	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr19:43525934-43526309	Hela-S3	cervix:	n/a	n/a
35	CBX3	chr19:43385505-43385738	K562	blood:	n/a	n/a
36	CBX3	chr19:43385431-43385838	K562	blood:	n/a	n/a
37	CEBPB	chr19:43337225-43337426	IMR90	lung:	n/a	n/a
38	CEBPB	chr19:43510079-43510205	HepG2	liver:	n/a	chr19:43510191-43510202
39	CEBPB	chr19:43496438-43496718	IMR90	lung:	n/a	n/a
40	CEBPB	chr19:43329190-43329511	A549	lung:	n/a	chr19:43329341-43329352
41	CEBPB	chr19:43326599-43326799	A549	lung:	n/a	n/a
42	CEBPB	chr19:43525986-43526150	A549	lung:	n/a	n/a
43	CEBPB	chr19:43496454-43496723	HepG2	liver:	n/a	n/a
44	CEBPB	chr19:43355109-43355962	IMR90	lung:	n/a	n/a
45	CEBPB	chr19:43393825-43394224	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr19:43335434-43335820	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr19:43496486-43496642	K562	blood:	n/a	n/a
48	CEBPB	chr19:43496316-43496617	A549	lung:	n/a	n/a
49	CEBPB	chr19:43562984-43563042	A549	lung:	n/a	n/a
50	CEBPB	chr19:43634604-43634632	HepG2	liver:	n/a	chr19:43634618-43634629 chr19:43634616-43634629 chr19:43634616-43634629 chr19:43634616-43634627

(count:2380 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43587500-43587550	Jurkat	blood:	n/a
2	chr19:43587500-43587550	Jurkat	blood:	n/a
3	chr19:43442809-43442859	GM12892	blood:	n/a
4	chr19:43530536-43530586	SKMC	muscle:	n/a
5	chr19:43359870-43359920	ECC-1	luminal epithelium:	n/a
6	chr19:43383799-43383849	SKMC	muscle:	n/a
7	chr19:43423176-43423226	ECC-1	luminal epithelium:	n/a
8	chr19:43360229-43360279	SKMC	muscle:	n/a
9	chr19:43442804-43442854	Jurkat	blood:	n/a
10	chr19:43442809-43442859	HCT-116	colon:	n/a
11	chr19:43355659-43355709	SK-N-SH	brain:	n/a
12	chr19:43588055-43588105	H1-hESC	embryonic stem cell:	embryo
13	chr19:43269877-43269927	HCM	heart:	n/a
14	chr19:43530536-43530586	HPAEpiC	pulmonary alveolar:	n/a
15	chr19:43385100-43385150	HCPEpiC	choroid plexus:	n/a
16	chr19:43588069-43588119	NH-A	brain:	n/a
17	chr19:43360229-43360279	LNCaP	prostate:	n/a
18	chr19:43269832-43269882	HIPEpiC	eye:	n/a
19	chr19:43384780-43384830	MCF-7	breast:	n/a
20	chr19:43587500-43587550	HepG2	liver:	n/a
21	chr19:43410455-43410505	IMR90	lung:	fetal
22	chr19:43588055-43588105	AG04450	lung:	fetal
23	chr19:43588025-43588075	HRCEpiC	kidney:	n/a
24	chr19:43528994-43529044	SK-N-SH_RA	brain:	n/a
25	chr19:43587500-43587550	AG09309	skin:	n/a
26	chr19:43271058-43271108	LNCaP	prostate:	n/a
27	chr19:43359870-43359920	PrEC	prostate:	n/a
28	chr19:43271004-43271054	GM12892	blood:	n/a
29	chr19:43359870-43359920	HUVEC	blood vessel:	n/a
30	chr19:43271058-43271108	U87	brain:	n/a
31	chr19:43385047-43385097	AG04450	lung:	fetal
32	chr19:43269877-43269927	HNPCEpiC	eye:	n/a
33	chr19:43442484-43442534	GM12891	blood:	n/a
34	chr19:43588069-43588119	HRPEpiC	eye:	n/a
35	chr19:43359870-43359920	HepG2	liver:	n/a
36	chr19:43360755-43360805	HPAEpiC	pulmonary alveolar:	n/a
37	chr19:43383799-43383849	PFSK-1	brain:	n/a
38	chr19:43442693-43442743	PFSK-1	brain:	n/a
39	chr19:43441294-43441344	HepG2	liver:	n/a
40	chr19:43441294-43441344	AG10803	skin:	n/a
41	chr19:43423115-43423165	HRCEpiC	kidney:	n/a
42	chr19:43588069-43588119	ProgFib	skin:	n/a
43	chr19:43269877-43269927	HEEpiC	esophagus:	n/a
44	chr19:43383799-43383849	GM12892	blood:	n/a
45	chr19:43530536-43530586	NHDF-neo	bronchial:	n/a
46	chr19:43360755-43360805	HIPEpiC	eye:	n/a
47	chr19:43569592-43569642	U87	brain:	n/a
48	chr19:43587500-43587550	MCF-7	breast:	n/a
49	chr19:43588069-43588119	T-47D	breast:	n/a
50	chr19:43423176-43423226	GM12892	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:43523469..43524084-chr19:43531918..43532440,2	MCF-7	breast:
2	chr19:43523469..43524084-chr19:43531918..43532440,2	MCF-7	breast:
3	chr19:43531581..43532101-chr2:1136088..1136613,2	MCF-7	breast:
4	chr19:43608137..43608719-chr19:43820621..43821519,2	MCF-7	breast:
5	chr19:43197633..43198568-chr19:43280847..43281639,2	K562	blood:
6	chr19:43197647..43198196-chr19:43280850..43281744,2	MCF-7	breast:
7	chr19:43297087..43297875-chr19:43423005..43423976,2	MCF-7	breast:

(count:49 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSG11-1	chr19:43544526-43544780	NONHSAT066579
2	lnc-PSG6-1	chr19:43440309-43440647	NONHSAT066574
3	lnc-PSG2-3	chr19:43601248-43601512	NONHSAT066582
4	lnc-PSG1-1	chr19:43343708-43343916	NONHSAT146988
5	lnc-PSG2-5	chr19:43511982-43512194	NONHSAT066576
6	lnc-PSG1-1	chr19:43343520-43343530	NONHSAT146988
7	lnc-PSG6-1	chr19:43433594-43433872	NR_073194
8	lnc-PSG1-1	chr19:43359708-43359870	NONHSAT146988
9	lnc-PSG6-1	chr19:43429925-43430179	NR_073194
10	lnc-PSG1-1	chr19:43570669-43570753	NONHSAT066570
11	lnc-PSG6-3	chr19:43370618-43371302	NONHSAT066572
12	lnc-PSG1-1	chr19:43359708-43359870	NONHSAT066571
13	lnc-PSG2-5	chr19:43519268-43519426	NONHSAT066577
14	lnc-PSG1-1	chr19:43341149-43341602	NONHSAT066570
15	lnc-PSG6-1	chr19:43428284-43428976	NR_073194
16	lnc-PSG2-2	chr19:43587104-43587197	NONHSAT066580
17	lnc-PSG6-1	chr19:43441165-43441330	NR_073194
18	lnc-PSG2-1	chr19:43586658-43586820	NONHSAT066581
19	lnc-PSG2-4	chr19:43522922-43523199	NONHSAT066578
20	lnc-PSG6-2	chr19:43453655-43453909	NONHSAT066575
21	lnc-PSG8-1	chr19:43290505-43290747	NONHSAT066567
22	lnc-PSG1-1	chr19:43358101-43358466	NONHSAT146988
23	lnc-PSG1-1	chr19:43348511-43348765	NONHSAT066571
24	lnc-PSG2-2	chr19:43576503-43576781	NONHSAT066580
25	lnc-PSG1-1	chr19:43349168-43349446	NONHSAT066571
26	lnc-PSG1-1	chr19:43343447-43343530	NONHSAT066571
27	lnc-PSG1-1	chr19:43349168-43349446	NONHSAT146988
28	lnc-PSG8-1	chr19:43289879-43290117	NONHSAT066567
29	lnc-PSG2-5	chr19:43514422-43514579	NONHSAT066577
30	lnc-PSG8-1	chr19:43285358-43285449	NONHSAT066567
31	lnc-PSG1-1	chr19:43358101-43358466	NONHSAT066571
32	lnc-PSG1-1	chr19:43341149-43341534	NONHSAT066571
33	lnc-PSG2-2	chr19:43575923-43576106	NONHSAT066580
34	lnc-PSG6-1	chr19:43441165-43441330	NONHSAT066574
35	lnc-PSG2-1	chr19:43585939-43586423	NONHSAT066581
36	lnc-PSG6-3	chr19:43372908-43374797	NONHSAT066572
37	lnc-PSG6-2	chr19:43454299-43454539	NONHSAT066575
38	lnc-PSG2-4	chr19:43521383-43521753	NONHSAT066578
39	lnc-PSG6-3	chr19:43372253-43372507	NONHSAT066572
40	lnc-PSG2-5	chr19:43514110-43514858	NONHSAT066576
41	lnc-PSG6-1	chr19:43428286-43428976	NONHSAT066573
42	lnc-PSG11-1	chr19:43540021-43540112	NONHSAT066579
43	lnc-PSG6-1	chr19:43429925-43431729	NONHSAT066573
44	lnc-PSG1-1	chr19:43348511-43348765	NONHSAT146988
45	lnc-PSG11-1	chr19:43545168-43545400	NONHSAT066579
46	lnc-PSG6-1	chr19:43430590-43430868	NR_073194
47	lnc-PSG1-1	chr19:43343708-43343916	NONHSAT066571
48	lnc-PSG2-3	chr19:43600608-43600855	NONHSAT066582
49	lnc-PSG6-1	chr19:43439556-43439921	NR_073194

No data

Variant related genes	Relation type
CEACAMP7	TF binding region
CEACAMP9	TF binding region
PSG8	TF binding region
PSG11	TF binding region
ENSG00000225877	TF binding region
PSG6	TF binding region
CEACAMP6	TF binding region
CEACAMP8	TF binding region
PSG1	TF binding region
PSG2	TF binding region
PSG7	TF binding region
PSG10P	TF binding region
CEACAMP7	CpG island
CEACAMP9	CpG island
PSG8	CpG island
PSG11	CpG island
ENSG00000225877	CpG island
PSG6	CpG island
CEACAMP6	CpG island
CEACAMP8	CpG island
PSG1	CpG island
PSG2	CpG island
PSG7	CpG island
PSG10P	CpG island
ENSG00000170848	chromatin interactions

Extended variants
information (count: 21731 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:21731 , 50 per page) page: 1 2 3 4 5 6 7 ... 435

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146967288	chr19:43268818-43268819	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs138006883	chr19:43268850-43268851	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs181983943	chr19:43268851-43268852	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs546538023	chr19:43268857-43268858	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs367699171	chr19:43268862-43268863	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs546468399	chr19:43268903-43268904	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs559986812	chr19:43268907-43268908	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs573418496	chr19:43268909-43268910	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs570120186	chr19:43268914-43268915	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs542515074	chr19:43268916-43268917	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs560062337	chr19:43268918-43268919	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs529658976	chr19:43268927-43268928	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs184771045	chr19:43268934-43268935	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs149034646	chr19:43268940-43268941	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs189206090	chr19:43268958-43268959	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs181623078	chr19:43268971-43268972	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs539972051	chr19:43268975-43268976	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs143007584	chr19:43269003-43269004	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs528327915	chr19:43269014-43269015	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs576475291	chr19:43269020-43269021	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs148171623	chr19:43269021-43269022	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs371845563	chr19:43269022-43269023	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs200981263	chr19:43269031-43269032	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs76435895	chr19:43269038-43269039	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs557489534	chr19:43269039-43269040	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs570998102	chr19:43269083-43269084	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs539949239	chr19:43269087-43269088	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs76688983	chr19:43269105-43269106	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs369089716	chr19:43269107-43269108	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs186740033	chr19:43269116-43269117	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs191134744	chr19:43269119-43269120	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs181115583	chr19:43269135-43269136	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs574071448	chr19:43269167-43269168	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs186048311	chr19:43269202-43269203	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs530290104	chr19:43269208-43269209	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs534073266	chr19:43269209-43269210	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs113131452	chr19:43269214-43269215	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs371886244	chr19:43269215-43269216	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs375483870	chr19:43269220-43269221	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs545885869	chr19:43269221-43269222	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs559252882	chr19:43269259-43269260	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs372970245	chr19:43269260-43269261	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs553763507	chr19:43269309-43269310	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs542075541	chr19:43269311-43269312	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs548172451	chr19:43269318-43269319	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs568411427	chr19:43269320-43269321	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs530919544	chr19:43269325-43269326	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs189589309	chr19:43269348-43269349	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs570863026	chr19:43269356-43269357	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs539915308	chr19:43269361-43269362	Enhancers Weak transcription Active TSS	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:1338 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43266600-43269800	Active TSS	Placenta	Placenta
2	chr19:43267200-43269600	Weak transcription	Esophagus	oesophagus
3	chr19:43267200-43271000	Weak transcription	Pancreas	Pancrea
4	chr19:43267800-43269000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr19:43268400-43269800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr19:43268400-43269800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr19:43268600-43269200	Enhancers	NHDF-Ad	bronchial
8	chr19:43268800-43269000	Enhancers	Hela-S3	cervix
9	chr19:43268800-43269000	Enhancers	HSMM	muscle
10	chr19:43268800-43269000	Enhancers	NHLF	lung
11	chr19:43268800-43269400	Enhancers	Muscle Satellite Cultured Cells	--
12	chr19:43269000-43269400	Weak transcription	Hela-S3	cervix
13	chr19:43269000-43269800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr19:43269200-43269400	Enhancers	Osteobl	bone
15	chr19:43269400-43269800	Enhancers	Hela-S3	cervix
16	chr19:43269600-43269800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr19:43269600-43269800	Enhancers	Esophagus	oesophagus
18	chr19:43269800-43270800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr19:43269800-43271000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr19:43269800-43278800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr19:43270800-43271200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr19:43271000-43271400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr19:43271000-43271400	Enhancers	Placenta	Placenta
24	chr19:43271000-43271400	ZNF genes & repeats	Pancreas	Pancrea
25	chr19:43271000-43271400	Active TSS	Spleen	Spleen
26	chr19:43271400-43278800	Weak transcription	Pancreas	Pancrea
27	chr19:43278400-43279200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr19:43278600-43278800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr19:43278800-43279000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
30	chr19:43278800-43279000	Active TSS	iPS-18 Cell Line	embryonic stem cell
31	chr19:43278800-43279000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr19:43278800-43279000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr19:43278800-43279200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
34	chr19:43278800-43279200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
35	chr19:43278800-43279200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
36	chr19:43278800-43279200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr19:43278800-43279200	Enhancers	Pancreas	Pancrea
38	chr19:43278800-43279400	Active TSS	ES-I3 Cell Line	embryonic stem cell
39	chr19:43278800-43279400	Active TSS	iPS-15b Cell Line	embryonic stem cell
40	chr19:43279000-43279200	Flanking Active TSS	ES-WA7 Cell Line	embryonic stem cell
41	chr19:43279000-43279200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr19:43279000-43279200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
43	chr19:43279000-43279200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
44	chr19:43279000-43279200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr19:43279000-43279200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
46	chr19:43279000-43279200	Bivalent Enhancer	Left Ventricle	heart
47	chr19:43279000-43281000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr19:43279200-43281000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr19:43279200-43281800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr19:43281000-43281200	Enhancers	Brain Substantia Nigra	brain

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