Variant report

Variant	nsv1065736
Chromosome Location	chr19:43321125-43768182
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5846)
CpG islands
(count:2991)
Chromatin interactive
region (count:5)
LncRNA
region (count:77)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5846 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

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	chr19:43686016-43686763	A549	lung:	n/a	n/a
3	ATF3	chr19:43355048-43355947	A549	lung:	n/a	n/a
4	ATF3	chr19:43335307-43336092	A549	lung:	n/a	n/a
5	ATF3	chr19:43336349-43336838	A549	lung:	n/a	n/a
6	ATF3	chr19:43355412-43355889	A549	lung:	n/a	n/a
7	ATF3	chr19:43335349-43336094	A549	lung:	n/a	n/a
8	ATF3	chr19:43336336-43336928	A549	lung:	n/a	n/a
9	BATF	chr19:43591924-43592150	GM12878	blood:	n/a	n/a
10	BATF	chr19:43442962-43443231	GM12878	blood:	n/a	n/a
11	BATF	chr19:43588401-43588710	GM12878	blood:	n/a	n/a
12	BATF	chr19:43613006-43613315	GM12878	blood:	n/a	chr19:43613110-43613121
13	BATF	chr19:43552186-43552537	GM12878	blood:	n/a	chr19:43552319-43552330
14	BATF	chr19:43738081-43738296	GM12878	blood:	n/a	chr19:43738185-43738196
15	BATF	chr19:43692397-43692675	GM12878	blood:	n/a	n/a
16	BATF	chr19:43361555-43361754	GM12878	blood:	n/a	n/a
17	BATF	chr19:43552261-43552460	GM12878	blood:	n/a	chr19:43552319-43552330
18	BATF	chr19:43692257-43692526	GM12878	blood:	n/a	n/a
19	BATF	chr19:43711409-43711658	GM12878	blood:	n/a	n/a
20	BCL3	chr19:43335242-43336126	A549	lung:	n/a	chr19:43335602-43335611 chr19:43335603-43335612
21	BCL3	chr19:43336159-43337656	A549	lung:	n/a	chr19:43336227-43336234
22	BCL3	chr19:43336292-43336877	A549	lung:	n/a	n/a
23	BCL3	chr19:43335292-43335990	A549	lung:	n/a	chr19:43335602-43335611 chr19:43335603-43335612
24	BCL3	chr19:43402518-43403428	A549	lung:	n/a	n/a
25	BCL3	chr19:43336972-43337663	A549	lung:	n/a	n/a
26	BCL3	chr19:43354946-43356043	A549	lung:	n/a	n/a
27	BCL3	chr19:43323095-43323355	GM12878	blood:	n/a	n/a
28	BCL3	chr19:43354910-43356058	A549	lung:	n/a	n/a
29	BHLHE40	chr19:43709323-43709343	K562	blood:	n/a	n/a
30	BHLHE40	chr19:43355572-43355890	A549	lung:	n/a	n/a
31	BHLHE40	chr19:43385480-43385517	K562	blood:	n/a	n/a
32	BHLHE40	chr19:43733601-43733620	K562	blood:	n/a	n/a
33	BHLHE40	chr19:43427453-43427512	GM12878	blood:	n/a	n/a
34	BHLHE40	chr19:43582147-43582203	K562	blood:	n/a	n/a
35	BRCA1	chr19:43525934-43526309	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr19:43355288-43355847	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr19:43436723-43436914	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr19:43624776-43624937	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr19:43385505-43385738	K562	blood:	n/a	n/a
40	CBX3	chr19:43385431-43385838	K562	blood:	n/a	n/a
41	CEBPB	chr19:43335392-43336031	A549	lung:	n/a	n/a
42	CEBPB	chr19:43500870-43501012	IMR90	lung:	n/a	n/a
43	CEBPB	chr19:43516550-43516678	K562	blood:	n/a	n/a
44	CEBPB	chr19:43564424-43564703	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr19:43403099-43403104	A549	lung:	n/a	n/a
46	CEBPB	chr19:43685985-43686627	IMR90	lung:	n/a	n/a
47	CEBPB	chr19:43517222-43517467	IMR90	lung:	n/a	chr19:43517348-43517359
48	CEBPB	chr19:43500903-43500999	A549	lung:	n/a	n/a
49	CEBPB	chr19:43728619-43728662	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr19:43582033-43582419	IMR90	lung:	n/a	n/a

(count:2991 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43441294-43441344	HL-60	blood:	n/a
2	chr19:43697480-43697530	NHBE	bronchial:	n/a
3	chr19:43441294-43441344	HL-60	blood:	n/a
4	chr19:43697480-43697530	NHBE	bronchial:	n/a
5	chr19:43709360-43709410	SKMC	muscle:	n/a
6	chr19:43359870-43359920	IMR90	lung:	fetal
7	chr19:43711064-43711114	Jurkat	blood:	n/a
8	chr19:43588055-43588105	NHBE	bronchial:	n/a
9	chr19:43360229-43360279	LNCaP	prostate:	n/a
10	chr19:43691878-43691928	K562	blood:	n/a
11	chr19:43383799-43383849	ECC-1	luminal epithelium:	n/a
12	chr19:43711064-43711114	ovcar-3	ovarian:	n/a
13	chr19:43383405-43383455	GM12892	blood:	n/a
14	chr19:43709654-43709704	NHDF-neo	bronchial:	n/a
15	chr19:43442693-43442743	U87	brain:	n/a
16	chr19:43423265-43423315	T-47D	breast:	n/a
17	chr19:43360229-43360279	HNPCEpiC	eye:	n/a
18	chr19:43709754-43709804	IMR90	lung:	fetal
19	chr19:43383405-43383455	HAEpiC	amniotic membrane:	n/a
20	chr19:43588069-43588119	RPTEC	kidney:	n/a
21	chr19:43442693-43442743	IMR90	lung:	fetal
22	chr19:43360229-43360279	A549	lung:	n/a
23	chr19:43569592-43569642	BE2_C	brain:	n/a
24	chr19:43709654-43709704	SAEC	small airway:	n/a
25	chr19:43385047-43385097	SK-N-SH_RA	brain:	n/a
26	chr19:43423119-43423169	T-47D	breast:	n/a
27	chr19:43441294-43441344	BE2_C	brain:	n/a
28	chr19:43421584-43421634	CMK	blood:	n/a
29	chr19:43385047-43385097	PrEC	prostate:	n/a
30	chr19:43423115-43423165	NT2-D1	testis:	n/a
31	chr19:43442693-43442743	BJ	skin:	n/a
32	chr19:43588069-43588119	AG04449	skin:	fetal
33	chr19:43441294-43441344	SKMC	muscle:	n/a
34	chr19:43680072-43680122	BJ	skin:	n/a
35	chr19:43384780-43384830	HCT-116	colon:	n/a
36	chr19:43360229-43360279	HAEpiC	amniotic membrane:	n/a
37	chr19:43383986-43384036	ovcar-3	ovarian:	n/a
38	chr19:43709654-43709704	Caco-2	colon:	n/a
39	chr19:43711249-43711299	NT2-D1	testis:	n/a
40	chr19:43514144-43514194	U87	brain:	n/a
41	chr19:43383799-43383849	NH-A	brain:	n/a
42	chr19:43423115-43423165	HIPEpiC	eye:	n/a
43	chr19:43711249-43711299	Hela-S3	cervix:	n/a
44	chr19:43442804-43442854	Hepatocyte	liver:	n/a
45	chr19:43530623-43530673	HCM	heart:	n/a
46	chr19:43587500-43587550	HCPEpiC	choroid plexus:	n/a
47	chr19:43588025-43588075	GM12891	blood:	n/a
48	chr19:43710277-43710327	GM12892	blood:	n/a
49	chr19:43423176-43423226	IMR90	lung:	fetal
50	chr19:43680072-43680122	HUVEC	blood vessel:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:43678340..43681333-chr19:43698109..43700078,2	MCF-7	breast:
2	chr19:43531581..43532101-chr2:1136088..1136613,2	MCF-7	breast:
3	chr19:43523469..43524084-chr19:43531918..43532440,2	MCF-7	breast:
4	chr19:43523469..43524084-chr19:43531918..43532440,2	MCF-7	breast:
5	chr19:43608137..43608719-chr19:43820621..43821519,2	MCF-7	breast:

(count:77 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSG5-1	chr19:43698107-43698746	NONHSAT066589
2	lnc-PSG1-1	chr19:43341149-43341534	NONHSAT066571
3	lnc-PSG1-1	chr19:43349168-43349446	NONHSAT066571
4	lnc-PSG5-1	chr19:43698492-43699038	NONHSAT066588
5	lnc-PSG9-2	chr19:43727043-43727110	NONHSAT066591
6	lnc-PSG1-1	chr19:43343447-43343530	NONHSAT066571
7	lnc-PSG5-1	chr19:43696890-43697540	NONHSAT066588
8	lnc-PSG2-5	chr19:43514422-43514579	NONHSAT066577
9	lnc-PSG9-2	chr19:43734076-43734177	NONHSAT066591
10	lnc-PSG6-1	chr19:43440309-43440647	NONHSAT066574
11	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066592
12	lnc-PSG5-1	chr19:43699147-43699301	NONHSAT066589
13	lnc-PSG9-2	chr19:43763009-43764898	NONHSAT066592
14	lnc-PSG6-1	chr19:43428284-43428976	NR_073194
15	lnc-PSG2-2	chr19:43576503-43576781	NONHSAT066580
16	lnc-PSG6-1	chr19:43441165-43441330	NR_073194
17	lnc-PSG6-2	chr19:43454299-43454539	NONHSAT066575
18	lnc-PSG2-2	chr19:43575923-43576106	NONHSAT066580
19	lnc-PSG6-3	chr19:43372253-43372507	NONHSAT066572
20	lnc-PSG9-2	chr19:43752160-43752275	NONHSAT066591
21	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066591
22	lnc-PSG2-4	chr19:43521383-43521753	NONHSAT066578
23	lnc-PSG4-1	chr19:43707241-43708403	NONHSAT066590
24	lnc-PSG2-5	chr19:43519268-43519426	NONHSAT066577
25	lnc-PSG6-1	chr19:43429925-43430179	NR_073194
26	lnc-PSG4-3	chr19:43674207-43674717	NONHSAT066586
27	lnc-PSG6-1	chr19:43441165-43441330	NONHSAT066574
28	lnc-PSG2-3	chr19:43601248-43601512	NONHSAT066582
29	lnc-PSG2-3	chr19:43600608-43600855	NONHSAT066582
30	lnc-PSG4-1	chr19:43710321-43711451	NONHSAT066590
31	lnc-CD177-1	chr19:43665002-43665014	ENSG00000227606.1
32	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066593
33	lnc-PSG9-2	chr19:43719405-43719531	NONHSAT066591
34	lnc-PSG4-3	chr19:43674207-43674723	NONHSAT066585
35	lnc-PSG6-1	chr19:43428286-43428976	NONHSAT066573
36	lnc-CD177-1	chr19:43657665-43657763	ENSG00000227606.1
37	lnc-PSG1-1	chr19:43348511-43348765	NONHSAT146988
38	lnc-PSG2-2	chr19:43587104-43587197	NONHSAT066580
39	lnc-PSG6-3	chr19:43372908-43374797	NONHSAT066572
40	lnc-PSG1-1	chr19:43341149-43341602	NONHSAT066570
41	lnc-PSG9-2	chr19:43737376-43737446	NONHSAT066591
42	lnc-PSG6-1	chr19:43429925-43431729	NONHSAT066573
43	lnc-PSG4-3	chr19:43671924-43672287	NONHSAT066585
44	lnc-CD177-1	chr19:43658863-43659311	ENSG00000227606.1
45	lnc-CD177-1	chr19:43657431-43657763	ENSG00000227606.1
46	lnc-PSG1-1	chr19:43359708-43359870	NONHSAT066571
47	lnc-PSG4-3	chr19:43672274-43672355	NONHSAT066586
48	lnc-PSG1-1	chr19:43343708-43343916	NONHSAT146988
49	lnc-PSG11-1	chr19:43545168-43545400	NONHSAT066579
50	lnc-PSG11-1	chr19:43544526-43544780	NONHSAT066579

No data

Variant related genes	Relation type
CEACAMP7	TF binding region
PSG4	TF binding region
PSG1	TF binding region
PSG7	TF binding region
PSG6	TF binding region
CEACAMP10	TF binding region
PSG11	TF binding region
CEACAMP9	TF binding region
PSG2	TF binding region
ENSG00000225877	TF binding region
ENSG00000227606	TF binding region
PSG5	TF binding region
PSG10P	TF binding region
PSG8	TF binding region
CEACAMP8	TF binding region
PSG9	TF binding region
CEACAMP7	CpG island
PSG4	CpG island
PSG1	CpG island
PSG7	CpG island
PSG6	CpG island
CEACAMP10	CpG island
PSG11	CpG island
CEACAMP9	CpG island
PSG2	CpG island
ENSG00000225877	CpG island
ENSG00000227606	CpG island
PSG5	CpG island
PSG10P	CpG island
PSG8	CpG island
CEACAMP8	CpG island
PSG9	CpG island
ENSG00000243137	chromatin interactions

Extended variants
information (count: 25795 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:25795 , 50 per page) page: 1 2 3 4 5 6 7 ... 516

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554765774	chr19:43321132-43321133	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs560766970	chr19:43321165-43321166	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs184165930	chr19:43321184-43321185	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs537137782	chr19:43321192-43321193	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs144469659	chr19:43321238-43321239	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs139103002	chr19:43321279-43321280	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs35255783	chr19:43321299-43321300	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs546536147	chr19:43321304-43321305	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs560050652	chr19:43321329-43321330	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs186246670	chr19:43321342-43321343	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs556749402	chr19:43321387-43321388	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs190734081	chr19:43321404-43321405	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs143969605	chr19:43321408-43321409	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs146884744	chr19:43321442-43321443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529833178	chr19:43321460-43321461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549590164	chr19:43321478-43321479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs371513866	chr19:43321480-43321481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529548355	chr19:43321484-43321485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529802278	chr19:43321491-43321492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146868909	chr19:43321567-43321568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs139774856	chr19:43321584-43321585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs559641630	chr19:43321585-43321586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs62113064	chr19:43321586-43321587	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs552062064	chr19:43321627-43321628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs565590743	chr19:43321630-43321631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563550951	chr19:43321658-43321659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182893892	chr19:43321662-43321663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548602833	chr19:43321667-43321668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs59633266	chr19:43321673-43321674	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs551426216	chr19:43321683-43321684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187273881	chr19:43321707-43321708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs192941482	chr19:43321721-43321722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs182916025	chr19:43321722-43321723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs58481580	chr19:43321747-43321748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs57024014	chr19:43321759-43321760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141043267	chr19:43321787-43321788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368071242	chr19:43321788-43321789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs115264738	chr19:43321828-43321829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370178223	chr19:43321843-43321844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs77411853	chr19:43321845-43321846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78299915	chr19:43321854-43321855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs75695176	chr19:43321856-43321857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113514532	chr19:43321889-43321890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112311689	chr19:43321920-43321921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554578967	chr19:43321927-43321928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528167235	chr19:43321944-43321945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548279856	chr19:43321964-43321965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563003100	chr19:43321968-43321969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532178631	chr19:43321994-43321995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545637539	chr19:43321999-43322000	Weak transcription	n/a	n/a	Overlapped CNVs	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:1620 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43317600-43321400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr19:43320600-43321200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr19:43321000-43321400	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr19:43321000-43321400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr19:43321000-43321400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr19:43321000-43321400	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr19:43321000-43321400	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr19:43321000-43321400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr19:43321000-43321400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr19:43321000-43321400	Enhancers	Muscle Satellite Cultured Cells	--
11	chr19:43321000-43321400	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr19:43321000-43321400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr19:43321000-43321400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr19:43321000-43321400	Enhancers	HSMM	muscle
15	chr19:43321000-43321800	Enhancers	A549	lung
16	chr19:43321000-43321800	Enhancers	HMEC	breast
17	chr19:43321000-43321800	Enhancers	NHDF-Ad	bronchial
18	chr19:43321200-43321400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr19:43321200-43321400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr19:43321200-43321400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr19:43321200-43321400	Enhancers	NH-A	brain
22	chr19:43321200-43321400	Enhancers	NHEK	skin
23	chr19:43321200-43321400	Enhancers	NHLF	lung
24	chr19:43321400-43321800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr19:43321400-43322800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr19:43321400-43323000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr19:43321400-43323000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr19:43321400-43323000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr19:43321400-43323000	Weak transcription	NHEK	skin
30	chr19:43321400-43323600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr19:43321400-43323600	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr19:43321400-43324000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr19:43321400-43324200	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr19:43321400-43324800	Weak transcription	HSMM	muscle
35	chr19:43321400-43337400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr19:43321600-43323200	Weak transcription	NHLF	lung
37	chr19:43321800-43323000	Weak transcription	HMEC	breast
38	chr19:43321800-43323000	Weak transcription	NHDF-Ad	bronchial
39	chr19:43321800-43323400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr19:43321800-43323800	Weak transcription	NH-A	brain
41	chr19:43321800-43324000	Weak transcription	Osteobl	bone
42	chr19:43322800-43324200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr19:43323000-43323400	Genic enhancers	NHEK	skin
44	chr19:43323000-43324400	Enhancers	HMEC	breast
45	chr19:43323000-43325200	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr19:43323000-43325200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr19:43323000-43325400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr19:43323000-43326000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr19:43323000-43326200	Enhancers	NHDF-Ad	bronchial
50	chr19:43323200-43325200	Enhancers	NHLF	lung

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