Variant report

Variant	nsv1064999
Chromosome Location	chr19:43315599-43811811
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6620)
CpG islands
(count:3361)
Chromatin interactive
region (count:11)
LncRNA
region (count:79)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:6620 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:43779068-43779071	K562	blood:	n/a	n/a
2	ATF1	chr19:43733581-43733686	K562	blood:	n/a	n/a
3	ATF3	chr19:43335349-43336094	A549	lung:	n/a	n/a
4	ATF3	chr19:43335307-43336092	A549	lung:	n/a	n/a
5	ATF3	chr19:43355412-43355889	A549	lung:	n/a	n/a
6	ATF3	chr19:43336336-43336928	A549	lung:	n/a	n/a
7	ATF3	chr19:43355048-43355947	A549	lung:	n/a	n/a
8	ATF3	chr19:43336349-43336838	A549	lung:	n/a	n/a
9	ATF3	chr19:43686016-43686763	A549	lung:	n/a	n/a
10	BATF	chr19:43588401-43588710	GM12878	blood:	n/a	n/a
11	BATF	chr19:43711409-43711658	GM12878	blood:	n/a	n/a
12	BATF	chr19:43442962-43443231	GM12878	blood:	n/a	n/a
13	BATF	chr19:43798559-43798850	GM12878	blood:	n/a	chr19:43798663-43798674
14	BATF	chr19:43552261-43552460	GM12878	blood:	n/a	chr19:43552319-43552330
15	BATF	chr19:43591924-43592150	GM12878	blood:	n/a	n/a
16	BATF	chr19:43361555-43361754	GM12878	blood:	n/a	n/a
17	BATF	chr19:43552186-43552537	GM12878	blood:	n/a	chr19:43552319-43552330
18	BATF	chr19:43692397-43692675	GM12878	blood:	n/a	n/a
19	BATF	chr19:43692257-43692526	GM12878	blood:	n/a	n/a
20	BATF	chr19:43775309-43775522	GM12878	blood:	n/a	n/a
21	BATF	chr19:43738081-43738296	GM12878	blood:	n/a	chr19:43738185-43738196
22	BATF	chr19:43613006-43613315	GM12878	blood:	n/a	chr19:43613110-43613121
23	BCL3	chr19:43336972-43337663	A549	lung:	n/a	n/a
24	BCL3	chr19:43402518-43403428	A549	lung:	n/a	n/a
25	BCL3	chr19:43336292-43336877	A549	lung:	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	chr19:43323095-43323355	GM12878	blood:	n/a	n/a
29	BCL3	chr19:43354946-43356043	A549	lung:	n/a	n/a
30	BCL3	chr19:43335242-43336126	A549	lung:	n/a	chr19:43335602-43335611 chr19:43335603-43335612
31	BCL3	chr19:43336159-43337656	A549	lung:	n/a	chr19:43336227-43336234
32	BHLHE40	chr19:43427453-43427512	GM12878	blood:	n/a	n/a
33	BHLHE40	chr19:43709323-43709343	K562	blood:	n/a	n/a
34	BHLHE40	chr19:43385480-43385517	K562	blood:	n/a	n/a
35	BHLHE40	chr19:43355572-43355890	A549	lung:	n/a	n/a
36	BHLHE40	chr19:43582147-43582203	K562	blood:	n/a	n/a
37	BHLHE40	chr19:43809984-43810194	K562	blood:	n/a	chr19:43810115-43810131
38	BHLHE40	chr19:43733601-43733620	K562	blood:	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	chr19:43769426-43769782	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr19:43436723-43436914	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr19:43809902-43809911	HepG2	liver:	n/a	n/a
44	BRCA1	chr19:43525934-43526309	Hela-S3	cervix:	n/a	n/a
45	CBX3	chr19:43775261-43775711	HCT-116	colon:	n/a	n/a
46	CBX3	chr19:43775276-43775644	K562	blood:	n/a	n/a
47	CBX3	chr19:43385505-43385738	K562	blood:	n/a	n/a
48	CBX3	chr19:43385431-43385838	K562	blood:	n/a	n/a
49	CEBPB	chr19:43496426-43496699	A549	lung:	n/a	n/a
50	CEBPB	chr19:43560474-43560633	A549	lung:	n/a	chr19:43560568-43560581 chr19:43560568-43560579 chr19:43560568-43560581

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43421584-43421634	ProgFib	skin:	n/a
2	chr19:43769725-43769775	GM06990	blood:	n/a
3	chr19:43423115-43423165	GM12892	blood:	n/a
4	chr19:43441294-43441344	HepG2	liver:	n/a
5	chr19:43423176-43423226	HCM	heart:	n/a
6	chr19:43588055-43588105	HepG2	liver:	n/a
7	chr19:43421584-43421634	ProgFib	skin:	n/a
8	chr19:43769725-43769775	GM06990	blood:	n/a
9	chr19:43423115-43423165	GM12892	blood:	n/a
10	chr19:43441294-43441344	HepG2	liver:	n/a
11	chr19:43423176-43423226	HCM	heart:	n/a
12	chr19:43588055-43588105	HepG2	liver:	n/a
13	chr19:43709754-43709804	SKMC	muscle:	n/a
14	chr19:43423265-43423315	HRCEpiC	kidney:	n/a
15	chr19:43711249-43711299	Caco-2	colon:	n/a
16	chr19:43531821-43531871	HIPEpiC	eye:	n/a
17	chr19:43383405-43383455	HCPEpiC	choroid plexus:	n/a
18	chr19:43423265-43423315	SKMC	muscle:	n/a
19	chr19:43361218-43361268	CMK	blood:	n/a
20	chr19:43680072-43680122	A549	lung:	n/a
21	chr19:43691878-43691928	HRCEpiC	kidney:	n/a
22	chr19:43383405-43383455	HCT-116	colon:	n/a
23	chr19:43361218-43361268	HRPEpiC	eye:	n/a
24	chr19:43588055-43588105	GM12892	blood:	n/a
25	chr19:43580600-43580650	Jurkat	blood:	n/a
26	chr19:43441294-43441344	AG10803	skin:	n/a
27	chr19:43774982-43775032	NH-A	brain:	n/a
28	chr19:43423115-43423165	SAEC	small airway:	n/a
29	chr19:43514144-43514194	HRCEpiC	kidney:	n/a
30	chr19:43697480-43697530	HIPEpiC	eye:	n/a
31	chr19:43360229-43360279	SK-N-MC	brain:	n/a
32	chr19:43709654-43709704	RPTEC	kidney:	n/a
33	chr19:43691878-43691928	AG10803	skin:	n/a
34	chr19:43587500-43587550	SKMC	muscle:	n/a
35	chr19:43441294-43441344	NHDF-neo	bronchial:	n/a
36	chr19:43442804-43442854	GM12892	blood:	n/a
37	chr19:43588025-43588075	IMR90	lung:	fetal
38	chr19:43530623-43530673	K562	blood:	n/a
39	chr19:43361218-43361268	MCF-7	breast:	n/a
40	chr19:43423119-43423169	ovcar-3	ovarian:	n/a
41	chr19:43360755-43360805	PrEC	prostate:	n/a
42	chr19:43709654-43709704	K562	blood:	n/a
43	chr19:43423115-43423165	U87	brain:	n/a
44	chr19:43514144-43514194	LNCaP	prostate:	n/a
45	chr19:43588069-43588119	HCF	heart:	n/a
46	chr19:43514144-43514194	Hela-S3	cervix:	n/a
47	chr19:43690996-43691046	ovcar-3	ovarian:	n/a
48	chr19:43442484-43442534	HepG2	liver:	n/a
49	chr19:43441294-43441344	BJ	skin:	n/a
50	chr19:43442484-43442534	PFSK-1	brain:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:43801843..43804269-chr19:43806143..43807885,2	MCF-7	breast:
2	chr19:43809493..43810365-chr19:43820777..43821441,3	MCF-7	breast:
3	chr19:43523469..43524084-chr19:43531918..43532440,2	MCF-7	breast:
4	chr19:43608137..43608719-chr19:43820621..43821519,2	MCF-7	breast:
5	chr19:43809519..43810435-chr19:43820572..43821543,3	K562	blood:
6	chr19:43523469..43524084-chr19:43531918..43532440,2	MCF-7	breast:
7	chr19:43678340..43681333-chr19:43698109..43700078,2	MCF-7	breast:
8	chr19:43801843..43804269-chr19:43806143..43807885,2	MCF-7	breast:
9	chr19:43531581..43532101-chr2:1136088..1136613,2	MCF-7	breast:
10	chr19:43809862..43810443-chr19:43929397..43930009,2	MCF-7	breast:
11	chr19:43265768..43266290-chr19:43769932..43770473,2	MCF-7	breast:

(count:79 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSG9-2	chr19:43727043-43727110	NONHSAT066591
2	lnc-PSG1-1	chr19:43348511-43348765	NONHSAT066571
3	lnc-PSG2-2	chr19:43587104-43587197	NONHSAT066580
4	lnc-PSG6-1	chr19:43440309-43440647	NONHSAT066574
5	lnc-PSG6-2	chr19:43454299-43454539	NONHSAT066575
6	lnc-PSG1-1	chr19:43343708-43343916	NONHSAT066571
7	lnc-PSG11-1	chr19:43545168-43545400	NONHSAT066579
8	lnc-PSG9-2	chr19:43724783-43725023	NONHSAT066593
9	lnc-PSG6-1	chr19:43429925-43430179	NR_073194
10	lnc-PSG1-1	chr19:43341149-43341602	NONHSAT066570
11	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066591
12	lnc-PSG1-1	chr19:43358101-43358466	NONHSAT066571
13	lnc-PSG9-2	chr19:43762354-43762608	NONHSAT066592
14	lnc-PSG1-1	chr19:43349168-43349446	NONHSAT066571
15	lnc-PSG1-1	chr19:43358101-43358466	NONHSAT146988
16	lnc-PSG6-1	chr19:43428284-43428976	NR_073194
17	lnc-PSG1-1	chr19:43349168-43349446	NONHSAT146988
18	lnc-PSG4-2	chr19:43688934-43689087	NONHSAT066587
19	lnc-PSG2-3	chr19:43600608-43600855	NONHSAT066582
20	lnc-PSG6-1	chr19:43430590-43430868	NR_073194
21	lnc-PSG2-1	chr19:43586658-43586820	NONHSAT066581
22	lnc-PSG11-1	chr19:43544526-43544780	NONHSAT066579
23	lnc-PSG6-1	chr19:43439556-43439921	NR_073194
24	lnc-PSG4-2	chr19:43684499-43684748	NONHSAT066587
25	lnc-PSG5-1	chr19:43698492-43699038	NONHSAT066588
26	lnc-PSG2-5	chr19:43514422-43514579	NONHSAT066577
27	lnc-PSG6-1	chr19:43429925-43431729	NONHSAT066573
28	lnc-PSG1-1	chr19:43343708-43343916	NONHSAT146988
29	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066592
30	lnc-PSG2-1	chr19:43585939-43586423	NONHSAT066581
31	lnc-PSG9-2	chr19:43728324-43728464	NONHSAT066591
32	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066591
33	lnc-PSG6-1	chr19:43433594-43433872	NR_073194
34	lnc-PSG6-1	chr19:43441165-43441330	NR_073194
35	lnc-PSG9-2	chr19:43719405-43719531	NONHSAT066591
36	lnc-CD177-1	chr19:43659324-43659477	ENSG00000227606.1
37	lnc-PSG5-1	chr19:43699147-43699301	NONHSAT066589
38	lnc-PSG5-1	chr19:43698107-43698746	NONHSAT066589
39	lnc-PSG4-1	chr19:43707241-43708403	NONHSAT066590
40	lnc-PSG2-5	chr19:43519268-43519426	NONHSAT066577
41	lnc-PSG9-2	chr19:43734076-43734177	NONHSAT066591
42	lnc-CD177-1	chr19:43657431-43657763	ENSG00000227606.1
43	lnc-PSG1-1	chr19:43348511-43348765	NONHSAT146988
44	lnc-CD177-1	chr19:43665002-43665014	ENSG00000227606.1
45	lnc-PSG9-1	chr19:43807323-43807688	NONHSAT066594
46	lnc-PSG1-1	chr19:43570669-43570753	NONHSAT066570
47	lnc-PSG2-3	chr19:43601248-43601512	NONHSAT066582
48	lnc-CD177-1	chr19:43657665-43657763	ENSG00000227606.1
49	lnc-PSG2-5	chr19:43514110-43514858	NONHSAT066576
50	lnc-PSG9-1	chr19:43808621-43808675	NONHSAT066594

No data

Variant related genes	Relation type
CEACAMP7	TF binding region
CEACAMP9	TF binding region
PSG8	TF binding region
PSG5	TF binding region
CEACAMP4	TF binding region
PSG11	TF binding region
ENSG00000225877	TF binding region
PSG6	TF binding region
CEACAMP10	TF binding region
PSG9	TF binding region
PSG4	TF binding region
CEACAMP8	TF binding region
PSG1	TF binding region
CEACAMP11	TF binding region
PSG2	TF binding region
ENSG00000227606	TF binding region
PSG7	TF binding region
PSG10P	TF binding region
CEACAMP7	CpG island
CEACAMP9	CpG island
PSG8	CpG island
PSG5	CpG island
CEACAMP4	CpG island
PSG11	CpG island
ENSG00000225877	CpG island
PSG6	CpG island
CEACAMP10	CpG island
PSG9	CpG island
PSG4	CpG island
CEACAMP8	CpG island
PSG1	CpG island
CEACAMP11	CpG island
PSG2	CpG island
ENSG00000227606	CpG island
PSG7	CpG island
PSG10P	CpG island
ENSG00000243137	chromatin interactions

Extended variants
information (count: 27977 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:27977 , 50 per page) page: 1 2 3 4 5 6 7 ... 560

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527316547	chr19:43317004-43317005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs145709394	chr19:43317007-43317008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs372010321	chr19:43317008-43317009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567414226	chr19:43317014-43317015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs367871123	chr19:43317018-43317019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200246183	chr19:43317024-43317025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547560781	chr19:43317032-43317033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs114303407	chr19:43317034-43317035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532819422	chr19:43317035-43317036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538584739	chr19:43317037-43317038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs181989666	chr19:43317040-43317041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187281062	chr19:43317043-43317044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540985478	chr19:43317056-43317057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554645884	chr19:43317067-43317068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574637776	chr19:43317078-43317079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543887475	chr19:43317079-43317080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191751705	chr19:43317096-43317097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560045867	chr19:43317099-43317100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs527308972	chr19:43317103-43317104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546197769	chr19:43317105-43317106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs560050602	chr19:43317118-43317119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs182012773	chr19:43317122-43317123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186549763	chr19:43317127-43317128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149551911	chr19:43317136-43317137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191514914	chr19:43317152-43317153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs144160215	chr19:43317153-43317154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs371464042	chr19:43317165-43317166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs569773176	chr19:43317167-43317168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568570956	chr19:43317171-43317172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182557598	chr19:43317180-43317181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs565590628	chr19:43317198-43317199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534599590	chr19:43317205-43317206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs535898415	chr19:43317208-43317209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs186934360	chr19:43317210-43317211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543578225	chr19:43317215-43317216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs114152177	chr19:43317221-43317222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577379164	chr19:43317228-43317229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs144494294	chr19:43317229-43317230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539437655	chr19:43317234-43317235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs371795263	chr19:43317244-43317245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147414281	chr19:43317253-43317254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs139655637	chr19:43317256-43317257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs560897360	chr19:43317269-43317270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs10401982	chr19:43317280-43317281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs145182942	chr19:43317286-43317287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs375914373	chr19:43317302-43317303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs532209789	chr19:43317312-43317313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs189770404	chr19:43317320-43317321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183549354	chr19:43317326-43317327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs534633727	chr19:43317332-43317333	Enhancers	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:1712 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43317000-43317600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr19:43317400-43317600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr19:43317600-43321400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr19:43320600-43321200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr19:43321000-43321400	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr19:43321000-43321400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr19:43321000-43321400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr19:43321000-43321400	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr19:43321000-43321400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr19:43321000-43321400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr19:43321000-43321400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr19:43321000-43321400	Enhancers	Muscle Satellite Cultured Cells	--
13	chr19:43321000-43321400	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr19:43321000-43321400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr19:43321000-43321400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr19:43321000-43321400	Enhancers	HSMM	muscle
17	chr19:43321000-43321800	Enhancers	A549	lung
18	chr19:43321000-43321800	Enhancers	HMEC	breast
19	chr19:43321000-43321800	Enhancers	NHDF-Ad	bronchial
20	chr19:43321200-43321400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr19:43321200-43321400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr19:43321200-43321400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr19:43321200-43321400	Enhancers	NH-A	brain
24	chr19:43321200-43321400	Enhancers	NHEK	skin
25	chr19:43321200-43321400	Enhancers	NHLF	lung
26	chr19:43321400-43321800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr19:43321400-43322800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr19:43321400-43323000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr19:43321400-43323000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr19:43321400-43323000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr19:43321400-43323000	Weak transcription	NHEK	skin
32	chr19:43321400-43323600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr19:43321400-43323600	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr19:43321400-43324000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr19:43321400-43324200	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr19:43321400-43324800	Weak transcription	HSMM	muscle
37	chr19:43321400-43337400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr19:43321600-43323200	Weak transcription	NHLF	lung
39	chr19:43321800-43323000	Weak transcription	HMEC	breast
40	chr19:43321800-43323000	Weak transcription	NHDF-Ad	bronchial
41	chr19:43321800-43323400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr19:43321800-43323800	Weak transcription	NH-A	brain
43	chr19:43321800-43324000	Weak transcription	Osteobl	bone
44	chr19:43322800-43324200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr19:43323000-43323400	Genic enhancers	NHEK	skin
46	chr19:43323000-43324400	Enhancers	HMEC	breast
47	chr19:43323000-43325200	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr19:43323000-43325200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr19:43323000-43325400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr19:43323000-43326000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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