Variant report

Variant	nsv911924
Chromosome Location	chr19:43368961-43762327
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5134)
CpG islands
(count:2690)
Chromatin interactive
region (count:5)
LncRNA
region (count:61)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5134 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

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	BATF	chr19:43613006-43613315	GM12878	blood:	n/a	chr19:43613110-43613121
4	BATF	chr19:43591924-43592150	GM12878	blood:	n/a	n/a
5	BATF	chr19:43552186-43552537	GM12878	blood:	n/a	chr19:43552319-43552330
6	BATF	chr19:43738081-43738296	GM12878	blood:	n/a	chr19:43738185-43738196
7	BATF	chr19:43692397-43692675	GM12878	blood:	n/a	n/a
8	BATF	chr19:43711409-43711658	GM12878	blood:	n/a	n/a
9	BATF	chr19:43442962-43443231	GM12878	blood:	n/a	n/a
10	BATF	chr19:43588401-43588710	GM12878	blood:	n/a	n/a
11	BATF	chr19:43552261-43552460	GM12878	blood:	n/a	chr19:43552319-43552330
12	BATF	chr19:43692257-43692526	GM12878	blood:	n/a	n/a
13	BCL3	chr19:43402518-43403428	A549	lung:	n/a	n/a
14	BHLHE40	chr19:43582147-43582203	K562	blood:	n/a	n/a
15	BHLHE40	chr19:43733601-43733620	K562	blood:	n/a	n/a
16	BHLHE40	chr19:43427453-43427512	GM12878	blood:	n/a	n/a
17	BHLHE40	chr19:43709323-43709343	K562	blood:	n/a	n/a
18	BHLHE40	chr19:43385480-43385517	K562	blood:	n/a	n/a
19	BRCA1	chr19:43436723-43436914	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr19:43525934-43526309	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr19:43624776-43624937	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr19:43385505-43385738	K562	blood:	n/a	n/a
23	CBX3	chr19:43385431-43385838	K562	blood:	n/a	n/a
24	CEBPB	chr19:43728619-43728662	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr19:43496438-43496718	IMR90	lung:	n/a	n/a
26	CEBPB	chr19:43496426-43496699	A549	lung:	n/a	n/a
27	CEBPB	chr19:43517268-43517468	HepG2	liver:	n/a	chr19:43517348-43517359
28	CEBPB	chr19:43562984-43563042	A549	lung:	n/a	n/a
29	CEBPB	chr19:43590049-43590324	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr19:43393825-43394224	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr19:43564424-43564703	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr19:43482706-43482918	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr19:43668229-43668245	IMR90	lung:	n/a	n/a
34	CEBPB	chr19:43759754-43759856	K562	blood:	n/a	n/a
35	CEBPB	chr19:43510075-43510341	Hela-S3	cervix:	n/a	chr19:43510191-43510202
36	CEBPB	chr19:43436570-43436856	A549	lung:	n/a	n/a
37	CEBPB	chr19:43500903-43500999	A549	lung:	n/a	n/a
38	CEBPB	chr19:43562943-43563108	MCF-7	breast:	n/a	n/a
39	CEBPB	chr19:43634604-43634632	HepG2	liver:	n/a	chr19:43634618-43634629 chr19:43634616-43634629 chr19:43634616-43634629 chr19:43634616-43634627
40	CEBPB	chr19:43676596-43676779	K562	blood:	n/a	n/a
41	CEBPB	chr19:43709791-43709942	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr19:43379145-43379767	IMR90	lung:	n/a	n/a
43	CEBPB	chr19:43582033-43582419	IMR90	lung:	n/a	n/a
44	CEBPB	chr19:43379142-43379806	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr19:43510146-43510361	IMR90	lung:	n/a	chr19:43510191-43510202
46	CEBPB	chr19:43402907-43403129	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr19:43686010-43686301	A549	lung:	n/a	n/a
48	CEBPB	chr19:43564423-43564649	IMR90	lung:	n/a	n/a
49	CEBPB	chr19:43653804-43654163	IMR90	lung:	n/a	n/a
50	CEBPB	chr19:43685962-43686735	A549	lung:	n/a	n/a

(count:2690 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43680072-43680122	HEEpiC	esophagus:	n/a
2	chr19:43530536-43530586	HRCEpiC	kidney:	n/a
3	chr19:43588025-43588075	HCM	heart:	n/a
4	chr19:43673501-43673551	HRCEpiC	kidney:	n/a
5	chr19:43383986-43384036	NH-A	brain:	n/a
6	chr19:43442693-43442743	MCF10A-Er-Src	breast:	n/a
7	chr19:43680072-43680122	HEEpiC	esophagus:	n/a
8	chr19:43530536-43530586	HRCEpiC	kidney:	n/a
9	chr19:43588025-43588075	HCM	heart:	n/a
10	chr19:43673501-43673551	HRCEpiC	kidney:	n/a
11	chr19:43383986-43384036	NH-A	brain:	n/a
12	chr19:43442693-43442743	MCF10A-Er-Src	breast:	n/a
13	chr19:43587500-43587550	PANC-1	pancreas:	n/a
14	chr19:43683698-43683748	IMR90	lung:	fetal
15	chr19:43697480-43697530	HPAEpiC	pulmonary alveolar:	n/a
16	chr19:43442804-43442854	RPTEC	kidney:	n/a
17	chr19:43421584-43421634	PANC-1	pancreas:	n/a
18	chr19:43423176-43423226	HCF	heart:	n/a
19	chr19:43423119-43423169	HRPEpiC	eye:	n/a
20	chr19:43680072-43680122	AG04450	lung:	fetal
21	chr19:43423265-43423315	HAEpiC	amniotic membrane:	n/a
22	chr19:43697480-43697530	AG09319	gingival:	n/a
23	chr19:43528994-43529044	HMEC	breast:	n/a
24	chr19:43709754-43709804	HNPCEpiC	eye:	n/a
25	chr19:43587500-43587550	HMEC	breast:	n/a
26	chr19:43421584-43421634	IMR90	lung:	fetal
27	chr19:43421584-43421634	HUVEC	blood vessel:	n/a
28	chr19:43709832-43709882	IMR90	lung:	fetal
29	chr19:43383405-43383455	HepG2	liver:	n/a
30	chr19:43569592-43569642	AG10803	skin:	n/a
31	chr19:43691878-43691928	AG09309	skin:	n/a
32	chr19:43690622-43690672	ProgFib	skin:	n/a
33	chr19:43690996-43691046	SK-N-MC	brain:	n/a
34	chr19:43690622-43690672	BE2_C	brain:	n/a
35	chr19:43588055-43588105	HCF	heart:	n/a
36	chr19:43423176-43423226	HNPCEpiC	eye:	n/a
37	chr19:43530536-43530586	HRE	kidney:	n/a
38	chr19:43680072-43680122	HRPEpiC	eye:	n/a
39	chr19:43442693-43442743	AG09309	skin:	n/a
40	chr19:43442804-43442854	SAEC	small airway:	n/a
41	chr19:43442693-43442743	AG10803	skin:	n/a
42	chr19:43383799-43383849	PrEC	prostate:	n/a
43	chr19:43711064-43711114	AG09319	gingival:	n/a
44	chr19:43691878-43691928	AG04450	lung:	fetal
45	chr19:43673501-43673551	HCM	heart:	n/a
46	chr19:43423265-43423315	SAEC	small airway:	n/a
47	chr19:43383799-43383849	RPTEC	kidney:	n/a
48	chr19:43690622-43690672	AG04449	skin:	fetal
49	chr19:43442809-43442859	U87	brain:	n/a
50	chr19:43421584-43421634	SAEC	small airway:	n/a

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

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

(count:61 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSG6-1	chr19:43433594-43433872	NR_073194
2	lnc-PSG2-1	chr19:43586658-43586820	NONHSAT066581
3	lnc-PSG4-3	chr19:43671924-43672287	NONHSAT066585
4	lnc-PSG9-2	chr19:43737376-43737446	NONHSAT066591
5	lnc-PSG4-3	chr19:43672274-43672355	NONHSAT066586
6	lnc-PSG4-3	chr19:43674207-43674723	NONHSAT066585
7	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066591
8	lnc-PSG1-1	chr19:43570669-43570753	NONHSAT066570
9	lnc-PSG9-2	chr19:43734076-43734177	NONHSAT066591
10	lnc-PSG6-1	chr19:43428286-43428976	NONHSAT066573
11	lnc-PSG5-1	chr19:43696890-43697540	NONHSAT066588
12	lnc-PSG9-2	chr19:43728324-43728464	NONHSAT066591
13	lnc-PSG4-2	chr19:43688934-43689087	NONHSAT066587
14	lnc-PSG6-1	chr19:43429925-43431729	NONHSAT066573
15	lnc-CD177-1	chr19:43658863-43659311	ENSG00000227606.1
16	lnc-PSG9-2	chr19:43752160-43752275	NONHSAT066591
17	lnc-PSG2-2	chr19:43587104-43587197	NONHSAT066580
18	lnc-PSG5-1	chr19:43698107-43698746	NONHSAT066589
19	lnc-PSG5-1	chr19:43698492-43699038	NONHSAT066588
20	lnc-PSG11-1	chr19:43540021-43540112	NONHSAT066579
21	lnc-CD177-1	chr19:43665002-43665014	ENSG00000227606.1
22	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066592
23	lnc-PSG4-1	chr19:43707241-43708403	NONHSAT066590
24	lnc-CD177-1	chr19:43657665-43657763	ENSG00000227606.1
25	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066591
26	lnc-PSG9-2	chr19:43752643-43752798	NONHSAT066591
27	lnc-PSG4-2	chr19:43684499-43684748	NONHSAT066587
28	lnc-PSG2-5	chr19:43511982-43512194	NONHSAT066576
29	lnc-PSG6-1	chr19:43441165-43441330	NONHSAT066574
30	lnc-PSG9-2	chr19:43727043-43727110	NONHSAT066591
31	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066593
32	lnc-PSG6-3	chr19:43370618-43371302	NONHSAT066572
33	lnc-PSG2-5	chr19:43514422-43514579	NONHSAT066577
34	lnc-PSG2-1	chr19:43585939-43586423	NONHSAT066581
35	lnc-PSG5-1	chr19:43699147-43699301	NONHSAT066589
36	lnc-PSG2-5	chr19:43519268-43519426	NONHSAT066577
37	lnc-PSG6-1	chr19:43440309-43440647	NONHSAT066574
38	lnc-PSG2-4	chr19:43521383-43521753	NONHSAT066578
39	lnc-PSG6-3	chr19:43372253-43372507	NONHSAT066572
40	lnc-CD177-1	chr19:43659324-43659477	ENSG00000227606.1
41	lnc-PSG4-3	chr19:43674207-43674717	NONHSAT066586
42	lnc-PSG2-3	chr19:43601248-43601512	NONHSAT066582
43	lnc-PSG2-2	chr19:43576503-43576781	NONHSAT066580
44	lnc-PSG2-3	chr19:43600608-43600855	NONHSAT066582
45	lnc-CD177-1	chr19:43657431-43657763	ENSG00000227606.1
46	lnc-PSG4-1	chr19:43710321-43711451	NONHSAT066590
47	lnc-PSG9-2	chr19:43724783-43725023	NONHSAT066593
48	lnc-PSG6-2	chr19:43454299-43454539	NONHSAT066575
49	lnc-PSG6-1	chr19:43429925-43430179	NR_073194
50	lnc-PSG11-1	chr19:43544526-43544780	NONHSAT066579

No data

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

Extended variants
information (count: 22017 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:22017 , 50 per page) page: 1 2 3 4 5 6 7 ... 441

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10422635	chr19:43368961-43368962	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551003736	chr19:43368975-43368976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563041417	chr19:43368984-43368985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575038061	chr19:43368987-43368988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs542219162	chr19:43368992-43368993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553600025	chr19:43369029-43369030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567198378	chr19:43369030-43369031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs139763773	chr19:43369032-43369033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554283781	chr19:43369046-43369047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs574347593	chr19:43369065-43369066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185854048	chr19:43369071-43369072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs190708614	chr19:43369093-43369094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs372217185	chr19:43369097-43369098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs115525753	chr19:43369100-43369101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs368582892	chr19:43369120-43369121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs182041730	chr19:43369125-43369126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559102896	chr19:43369169-43369170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572814116	chr19:43369173-43369174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs71350629	chr19:43369181-43369182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185983714	chr19:43369215-43369216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs78898608	chr19:43369233-43369234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs149628684	chr19:43369241-43369242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530891899	chr19:43369251-43369252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs190453317	chr19:43369253-43369254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560945104	chr19:43369254-43369255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs144362385	chr19:43369282-43369283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547248951	chr19:43369283-43369284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs148768124	chr19:43369290-43369291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs536178403	chr19:43369291-43369292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs373063481	chr19:43369304-43369305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs549607492	chr19:43369339-43369340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182736459	chr19:43369343-43369344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs537092447	chr19:43369345-43369346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547253988	chr19:43369346-43369347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs142370081	chr19:43369350-43369351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539134102	chr19:43369362-43369363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185471027	chr19:43369386-43369387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs572652622	chr19:43369390-43369391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs147898413	chr19:43369408-43369409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201595051	chr19:43369412-43369413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369427851	chr19:43369431-43369432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562054378	chr19:43369500-43369501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs575444404	chr19:43369525-43369526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs1987627	chr19:43369556-43369557	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs111630542	chr19:43369560-43369561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191057995	chr19:43369593-43369594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs182910627	chr19:43369601-43369602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560672097	chr19:43369622-43369623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529470082	chr19:43369629-43369630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549302715	chr19:43369640-43369641	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:1277 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43357600-43378800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr19:43362400-43369200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr19:43369000-43369400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr19:43369200-43369600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr19:43370000-43374000	Weak transcription	Placenta	Placenta
6	chr19:43374000-43375400	Strong transcription	Placenta	Placenta
7	chr19:43374600-43378000	Weak transcription	NHDF-Ad	bronchial
8	chr19:43375400-43376800	Genic enhancers	Placenta	Placenta
9	chr19:43376200-43376800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr19:43376800-43377000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr19:43376800-43377000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr19:43376800-43378000	Strong transcription	Placenta	Placenta
13	chr19:43376800-43380200	Enhancers	HMEC	breast
14	chr19:43377000-43378400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr19:43377200-43378400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr19:43378000-43378200	Transcr. at gene 5' and 3'	Placenta	Placenta
17	chr19:43378000-43380600	Enhancers	NHDF-Ad	bronchial
18	chr19:43378200-43380000	Active TSS	Placenta	Placenta
19	chr19:43378200-43380000	Enhancers	NHEK	skin
20	chr19:43378400-43381600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr19:43378400-43381600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr19:43378400-43382200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr19:43378600-43378800	Enhancers	Muscle Satellite Cultured Cells	--
24	chr19:43378600-43379000	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr19:43378600-43381600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr19:43378600-43382200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr19:43378800-43379200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
28	chr19:43378800-43379600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr19:43378800-43380200	Enhancers	A549	lung
30	chr19:43378800-43380600	Enhancers	Hela-S3	cervix
31	chr19:43378800-43381000	Enhancers	NH-A	brain
32	chr19:43378800-43381400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr19:43378800-43381400	Enhancers	Osteobl	bone
34	chr19:43378800-43381600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr19:43378800-43381600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr19:43378800-43381600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr19:43378800-43381600	Enhancers	HSMM	muscle
38	chr19:43378800-43382200	Enhancers	NHLF	lung
39	chr19:43379000-43379200	Enhancers	Colon Smooth Muscle	Colon
40	chr19:43379000-43379200	Enhancers	Rectal Smooth Muscle	rectum
41	chr19:43379000-43380000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr19:43379200-43380200	Weak transcription	Rectal Smooth Muscle	rectum
43	chr19:43379200-43381600	Enhancers	Muscle Satellite Cultured Cells	--
44	chr19:43379200-43381600	Enhancers	HSMMtube	muscle
45	chr19:43379400-43380200	Weak transcription	Colon Smooth Muscle	Colon
46	chr19:43379400-43381400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr19:43379600-43380200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr19:43379800-43380400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr19:43380000-43380200	Flanking Active TSS	Placenta	Placenta
50	chr19:43380000-43380400	Flanking Active TSS	NHEK	skin

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