Variant report

Variant	nsv544020
Chromosome Location	chr19:43260848-43741311
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6666)
CpG islands
(count:3361)
Chromatin interactive
region (count:9)
LncRNA
region (count:76)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:6666 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:43733581-43733686	K562	blood:	n/a	n/a
2	ATF3	chr19:43336336-43336928	A549	lung:	n/a	n/a
3	ATF3	chr19:43355412-43355889	A549	lung:	n/a	n/a
4	ATF3	chr19:43355048-43355947	A549	lung:	n/a	n/a
5	ATF3	chr19:43335307-43336092	A549	lung:	n/a	n/a
6	ATF3	chr19:43336349-43336838	A549	lung:	n/a	n/a
7	ATF3	chr19:43686016-43686763	A549	lung:	n/a	n/a
8	ATF3	chr19:43335349-43336094	A549	lung:	n/a	n/a
9	BATF	chr19:43442962-43443231	GM12878	blood:	n/a	n/a
10	BATF	chr19:43271446-43271728	GM12878	blood:	n/a	n/a
11	BATF	chr19:43302238-43302533	GM12878	blood:	n/a	chr19:43302344-43302355
12	BATF	chr19:43613006-43613315	GM12878	blood:	n/a	chr19:43613110-43613121
13	BATF	chr19:43552261-43552460	GM12878	blood:	n/a	chr19:43552319-43552330
14	BATF	chr19:43588401-43588710	GM12878	blood:	n/a	n/a
15	BATF	chr19:43552186-43552537	GM12878	blood:	n/a	chr19:43552319-43552330
16	BATF	chr19:43692397-43692675	GM12878	blood:	n/a	n/a
17	BATF	chr19:43692257-43692526	GM12878	blood:	n/a	n/a
18	BATF	chr19:43591924-43592150	GM12878	blood:	n/a	n/a
19	BATF	chr19:43711409-43711658	GM12878	blood:	n/a	n/a
20	BATF	chr19:43738081-43738296	GM12878	blood:	n/a	chr19:43738185-43738196
21	BATF	chr19:43361555-43361754	GM12878	blood:	n/a	n/a
22	BCL3	chr19:43336159-43337656	A549	lung:	n/a	chr19:43336227-43336234
23	BCL3	chr19:43336972-43337663	A549	lung:	n/a	n/a
24	BCL3	chr19:43297507-43298116	A549	lung:	n/a	n/a
25	BCL3	chr19:43354946-43356043	A549	lung:	n/a	n/a
26	BCL3	chr19:43354910-43356058	A549	lung:	n/a	n/a
27	BCL3	chr19:43323095-43323355	GM12878	blood:	n/a	n/a
28	BCL3	chr19:43402518-43403428	A549	lung:	n/a	n/a
29	BCL3	chr19:43336292-43336877	A549	lung:	n/a	n/a
30	BCL3	chr19:43335292-43335990	A549	lung:	n/a	chr19:43335602-43335611 chr19:43335603-43335612
31	BCL3	chr19:43335242-43336126	A549	lung:	n/a	chr19:43335602-43335611 chr19:43335603-43335612
32	BHLHE40	chr19:43733601-43733620	K562	blood:	n/a	n/a
33	BHLHE40	chr19:43427453-43427512	GM12878	blood:	n/a	n/a
34	BHLHE40	chr19:43355572-43355890	A549	lung:	n/a	n/a
35	BHLHE40	chr19:43582147-43582203	K562	blood:	n/a	n/a
36	BHLHE40	chr19:43709323-43709343	K562	blood:	n/a	n/a
37	BHLHE40	chr19:43385480-43385517	K562	blood:	n/a	n/a
38	BRCA1	chr19:43265411-43265577	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr19:43355288-43355847	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr19:43624776-43624937	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr19:43525934-43526309	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr19:43297623-43297950	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr19:43436723-43436914	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr19:43385431-43385838	K562	blood:	n/a	n/a
45	CBX3	chr19:43385505-43385738	K562	blood:	n/a	n/a
46	CEBPB	chr19:43379145-43379767	IMR90	lung:	n/a	n/a
47	CEBPB	chr19:43517258-43517378	A549	lung:	n/a	chr19:43517348-43517359
48	CEBPB	chr19:43496454-43496723	HepG2	liver:	n/a	n/a
49	CEBPB	chr19:43653804-43654163	IMR90	lung:	n/a	n/a
50	CEBPB	chr19:43328208-43328426	Hela-S3	cervix:	n/a	chr19:43328257-43328268

(count:3361 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43383986-43384036	SK-N-SH	brain:	n/a
2	chr19:43709754-43709804	AG04450	lung:	fetal
3	chr19:43385047-43385097	ovcar-3	ovarian:	n/a
4	chr19:43514144-43514194	HRCEpiC	kidney:	n/a
5	chr19:43697480-43697530	HCF	heart:	n/a
6	chr19:43709832-43709882	NHBE	bronchial:	n/a
7	chr19:43383986-43384036	SK-N-SH	brain:	n/a
8	chr19:43709754-43709804	AG04450	lung:	fetal
9	chr19:43385047-43385097	ovcar-3	ovarian:	n/a
10	chr19:43514144-43514194	HRCEpiC	kidney:	n/a
11	chr19:43697480-43697530	HCF	heart:	n/a
12	chr19:43709832-43709882	NHBE	bronchial:	n/a
13	chr19:43514144-43514194	SK-N-SH	brain:	n/a
14	chr19:43531821-43531871	U87	brain:	n/a
15	chr19:43385047-43385097	HAEpiC	amniotic membrane:	n/a
16	chr19:43383986-43384036	HMEC	breast:	n/a
17	chr19:43383799-43383849	HAEpiC	amniotic membrane:	n/a
18	chr19:43265778-43265828	LNCaP	prostate:	n/a
19	chr19:43442484-43442534	GM06990	blood:	n/a
20	chr19:43697480-43697530	Jurkat	blood:	n/a
21	chr19:43587500-43587550	SK-N-SH_RA	brain:	n/a
22	chr19:43587500-43587550	BE2_C	brain:	n/a
23	chr19:43442484-43442534	Hepatocyte	liver:	n/a
24	chr19:43709654-43709704	HIPEpiC	eye:	n/a
25	chr19:43442804-43442854	HUVEC	blood vessel:	n/a
26	chr19:43588055-43588105	IMR90	lung:	fetal
27	chr19:43690622-43690672	MCF-7	breast:	n/a
28	chr19:43690622-43690672	HCPEpiC	choroid plexus:	n/a
29	chr19:43359870-43359920	CMK	blood:	n/a
30	chr19:43271004-43271054	T-47D	breast:	n/a
31	chr19:43528994-43529044	AG04449	skin:	fetal
32	chr19:43530536-43530586	HL-60	blood:	n/a
33	chr19:43271004-43271054	GM12878	blood:	n/a
34	chr19:43588055-43588105	HCT-116	colon:	n/a
35	chr19:43442693-43442743	HNPCEpiC	eye:	n/a
36	chr19:43421584-43421634	BJ	skin:	n/a
37	chr19:43569592-43569642	RPTEC	kidney:	n/a
38	chr19:43383405-43383455	GM12892	blood:	n/a
39	chr19:43271058-43271108	NH-A	brain:	n/a
40	chr19:43442804-43442854	HIPEpiC	eye:	n/a
41	chr19:43709654-43709704	BE2_C	brain:	n/a
42	chr19:43269877-43269927	AoSMC	blood vessel:	n/a
43	chr19:43680072-43680122	HUVEC	blood vessel:	n/a
44	chr19:43588025-43588075	HPAEpiC	pulmonary alveolar:	n/a
45	chr19:43271004-43271054	ProgFib	skin:	n/a
46	chr19:43588069-43588119	SK-N-MC	brain:	n/a
47	chr19:43360229-43360279	NHDF-neo	bronchial:	n/a
48	chr19:43711064-43711114	HRE	kidney:	n/a
49	chr19:43383405-43383455	RPTEC	kidney:	n/a
50	chr19:43588025-43588075	HAEpiC	amniotic membrane:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:43523469..43524084-chr19:43531918..43532440,2	MCF-7	breast:
2	chr19:43197633..43198568-chr19:43280847..43281639,2	K562	blood:
3	chr19:43197647..43198196-chr19:43280850..43281744,2	MCF-7	breast:
4	chr19:43678340..43681333-chr19:43698109..43700078,2	MCF-7	breast:
5	chr19:43531581..43532101-chr2:1136088..1136613,2	MCF-7	breast:
6	chr19:43297087..43297875-chr19:43423005..43423976,2	MCF-7	breast:
7	chr19:43523469..43524084-chr19:43531918..43532440,2	MCF-7	breast:
8	chr19:43265768..43266290-chr19:43769932..43770473,2	MCF-7	breast:
9	chr19:43608137..43608719-chr19:43820621..43821519,2	MCF-7	breast:

(count:76 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSG6-1	chr19:43433594-43433872	NR_073194
2	lnc-PSG1-1	chr19:43359708-43359870	NONHSAT066571
3	lnc-PSG8-1	chr19:43290505-43290747	NONHSAT066567
4	lnc-PSG1-1	chr19:43359708-43359870	NONHSAT146988
5	lnc-PSG2-3	chr19:43600608-43600855	NONHSAT066582
6	lnc-CD177-1	chr19:43657431-43657763	ENSG00000227606.1
7	lnc-PSG6-1	chr19:43429925-43431729	NONHSAT066573
8	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066592
9	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066591
10	lnc-PSG5-1	chr19:43698107-43698746	NONHSAT066589
11	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066591
12	lnc-PSG9-2	chr19:43727043-43727110	NONHSAT066591
13	lnc-PSG1-1	chr19:43343520-43343530	NONHSAT146988
14	lnc-PSG4-3	chr19:43674207-43674717	NONHSAT066586
15	lnc-CD177-1	chr19:43659324-43659477	ENSG00000227606.1
16	lnc-PSG6-1	chr19:43429925-43430179	NR_073194
17	lnc-PSG11-1	chr19:43544526-43544780	NONHSAT066579
18	lnc-PSG2-5	chr19:43519268-43519426	NONHSAT066577
19	lnc-PSG5-1	chr19:43696890-43697540	NONHSAT066588
20	lnc-PSG5-1	chr19:43698492-43699038	NONHSAT066588
21	lnc-CD177-1	chr19:43665002-43665014	ENSG00000227606.1
22	lnc-PSG4-3	chr19:43671924-43672287	NONHSAT066585
23	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066593
24	lnc-PSG9-2	chr19:43719405-43719531	NONHSAT066591
25	lnc-PSG2-2	chr19:43576503-43576781	NONHSAT066580
26	lnc-PSG8-1	chr19:43285358-43285449	NONHSAT066567
27	lnc-PSG1-1	chr19:43348511-43348765	NONHSAT066571
28	lnc-PSG6-1	chr19:43439556-43439921	NR_073194
29	lnc-PSG4-3	chr19:43672274-43672355	NONHSAT066586
30	lnc-PSG4-2	chr19:43688934-43689087	NONHSAT066587
31	lnc-PSG2-5	chr19:43511982-43512194	NONHSAT066576
32	lnc-PSG1-1	chr19:43349168-43349446	NONHSAT146988
33	lnc-PSG2-2	chr19:43587104-43587197	NONHSAT066580
34	lnc-PSG2-3	chr19:43601248-43601512	NONHSAT066582
35	lnc-PSG6-1	chr19:43441165-43441330	NR_073194
36	lnc-PSG6-2	chr19:43454299-43454539	NONHSAT066575
37	lnc-PSG2-5	chr19:43514110-43514858	NONHSAT066576
38	lnc-PSG1-1	chr19:43570669-43570753	NONHSAT066570
39	lnc-PSG1-1	chr19:43343447-43343530	NONHSAT066571
40	lnc-PSG2-1	chr19:43585939-43586423	NONHSAT066581
41	lnc-PSG11-1	chr19:43545168-43545400	NONHSAT066579
42	lnc-PSG1-1	chr19:43341149-43341534	NONHSAT066571
43	lnc-PSG6-1	chr19:43440309-43440647	NONHSAT066574
44	lnc-PSG8-1	chr19:43289879-43290117	NONHSAT066567
45	lnc-PSG9-2	chr19:43734076-43734177	NONHSAT066591
46	lnc-PSG4-3	chr19:43674207-43674723	NONHSAT066585
47	lnc-PSG2-5	chr19:43514422-43514579	NONHSAT066577
48	lnc-PSG4-1	chr19:43707241-43708403	NONHSAT066590
49	lnc-PSG2-4	chr19:43521383-43521753	NONHSAT066578
50	lnc-PSG6-2	chr19:43453655-43453909	NONHSAT066575

No data

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

Extended variants
information (count: 27169 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:27169 , 50 per page) page: 1 2 3 4 5 6 7 ... 544

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369933454	chr19:43260865-43260866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs578056361	chr19:43260877-43260878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185024308	chr19:43260887-43260888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534404017	chr19:43260933-43260934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554113961	chr19:43260979-43260980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs202206674	chr19:43261033-43261034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573908411	chr19:43261042-43261043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542868367	chr19:43261063-43261064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370632504	chr19:43261064-43261065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562864657	chr19:43261127-43261128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574860147	chr19:43261150-43261151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543902749	chr19:43261152-43261153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374934782	chr19:43261161-43261162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564187247	chr19:43261177-43261178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532930584	chr19:43261188-43261189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143295508	chr19:43261196-43261197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs74259590	chr19:43261204-43261205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78280164	chr19:43261209-43261210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2107515	chr19:43261222-43261223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547143516	chr19:43261223-43261224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560347583	chr19:43261237-43261238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375100571	chr19:43261246-43261247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549268644	chr19:43261283-43261284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190630756	chr19:43261284-43261285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371887553	chr19:43261340-43261341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569188314	chr19:43261350-43261351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373755790	chr19:43261375-43261376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368541083	chr19:43261383-43261384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192981124	chr19:43261423-43261424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539395118	chr19:43261426-43261427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372259710	chr19:43261440-43261441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185316180	chr19:43261441-43261442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139062966	chr19:43261446-43261447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553853401	chr19:43261454-43261455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs149878057	chr19:43261466-43261467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs375062392	chr19:43261467-43261468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536464971	chr19:43261483-43261484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556424742	chr19:43261491-43261492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576355963	chr19:43261494-43261495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs367879515	chr19:43261532-43261533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544191479	chr19:43261556-43261557	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs563964757	chr19:43261567-43261568	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs577574127	chr19:43261568-43261569	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs539899274	chr19:43261615-43261616	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs560308975	chr19:43261623-43261624	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs529062313	chr19:43261628-43261629	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs369678967	chr19:43261654-43261655	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs562770561	chr19:43261675-43261676	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs58813858	chr19:43261681-43261682	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs10406779	chr19:43261691-43261692	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:88)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1761 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43254000-43261800	Weak transcription	Placenta	Placenta
2	chr19:43261800-43262600	Strong transcription	Placenta	Placenta
3	chr19:43262600-43263200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr19:43262600-43264200	Weak transcription	Placenta	Placenta
5	chr19:43263200-43264600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr19:43263400-43263600	Enhancers	NHLF	lung
7	chr19:43263400-43267600	Enhancers	NHDF-Ad	bronchial
8	chr19:43263600-43264400	Weak transcription	NHLF	lung
9	chr19:43263600-43267600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr19:43264200-43264800	Enhancers	Placenta	Placenta
11	chr19:43264200-43265000	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr19:43264200-43267200	Enhancers	Osteobl	bone
13	chr19:43264400-43265400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr19:43264400-43266200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr19:43264400-43267600	Enhancers	Muscle Satellite Cultured Cells	--
16	chr19:43264400-43267600	Enhancers	NHLF	lung
17	chr19:43264600-43268000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr19:43264800-43265200	Flanking Active TSS	Placenta	Placenta
19	chr19:43264800-43265400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr19:43264800-43265400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr19:43264800-43265800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr19:43264800-43265800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr19:43264800-43265800	Enhancers	HSMM	muscle
24	chr19:43264800-43267400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr19:43264800-43267600	Enhancers	HMEC	breast
26	chr19:43264800-43267600	Enhancers	NH-A	brain
27	chr19:43265000-43265800	Enhancers	A549	lung
28	chr19:43265000-43266000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr19:43265000-43266400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr19:43265000-43267400	Enhancers	NHEK	skin
31	chr19:43265000-43267600	Enhancers	Hela-S3	cervix
32	chr19:43265200-43265400	Enhancers	Esophagus	oesophagus
33	chr19:43265200-43265400	Active TSS	Placenta	Placenta
34	chr19:43265200-43265400	Enhancers	Pancreas	Pancrea
35	chr19:43265200-43267800	Enhancers	HSMMtube	muscle
36	chr19:43265400-43266400	Weak transcription	Esophagus	oesophagus
37	chr19:43265400-43266400	Weak transcription	Pancreas	Pancrea
38	chr19:43265400-43266600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr19:43265400-43266600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr19:43265400-43266600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr19:43265400-43266600	Weak transcription	Placenta	Placenta
42	chr19:43265800-43266200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr19:43265800-43266200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr19:43265800-43266200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr19:43265800-43266200	Weak transcription	HSMM	muscle
46	chr19:43265800-43266400	Weak transcription	A549	lung
47	chr19:43266000-43267000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr19:43266200-43266600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr19:43266200-43266600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr19:43266200-43267600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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