Variant report

Variant	nsv580046
Chromosome Location	chr19:53485090-53552296
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:663)
CpG islands
(count:1161)
Chromatin interactive
region (count:10)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:663 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr19:53497019-53497409	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr19:53518961-53519336	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr19:53510493-53510782	GM12878	blood:	n/a	n/a
4	BHLHE40	chr19:53510497-53510963	K562	blood:	n/a	n/a
5	BRCA1	chr19:53497048-53497179	H1-hESC	embryonic stem cell:	n/a	n/a
6	BRCA1	chr19:53548078-53548353	H1-hESC	embryonic stem cell:	n/a	n/a
7	CBX3	chr19:53490152-53490462	K562	blood:	n/a	n/a
8	CBX3	chr19:53496785-53497423	K562	blood:	n/a	n/a
9	CBX3	chr19:53487980-53488326	K562	blood:	n/a	n/a
10	CEBPB	chr19:53494404-53494593	H1-hESC	embryonic stem cell:	n/a	chr19:53494449-53494460
11	CEBPB	chr19:53520162-53520365	MCF-7	breast:	n/a	n/a
12	CEBPB	chr19:53499048-53499248	K562	blood:	n/a	n/a
13	CEBPB	chr19:53520045-53520364	IMR90	lung:	n/a	n/a
14	CEBPB	chr19:53514622-53514961	K562	blood:	n/a	chr19:53514790-53514801
15	CEBPB	chr19:53494294-53494605	K562	blood:	n/a	chr19:53494449-53494460
16	CEBPB	chr19:53503242-53503648	K562	blood:	n/a	chr19:53503521-53503534 chr19:53503522-53503533 chr19:53503521-53503532 chr19:53503521-53503534 chr19:53503521-53503534
17	CEBPB	chr19:53514645-53514955	HepG2	liver:	n/a	chr19:53514790-53514801
18	CEBPB	chr19:53494284-53494605	IMR90	lung:	n/a	chr19:53494449-53494460
19	CEBPB	chr19:53514709-53514946	Hela-S3	cervix:	n/a	chr19:53514790-53514801
20	CEBPB	chr19:53494299-53494580	HepG2	liver:	n/a	chr19:53494449-53494460
21	CEBPB	chr19:53494277-53495058	Hela-S3	cervix:	n/a	chr19:53494449-53494460
22	CEBPB	chr19:53520072-53520352	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr19:53503339-53503575	IMR90	lung:	n/a	chr19:53503521-53503534 chr19:53503522-53503533 chr19:53503521-53503532 chr19:53503521-53503534 chr19:53503521-53503534
24	CEBPB	chr19:53514683-53514869	A549	lung:	n/a	chr19:53514790-53514801
25	CEBPB	chr19:53520052-53520352	K562	blood:	n/a	n/a
26	CEBPB	chr19:53503344-53503663	HepG2	liver:	n/a	chr19:53503521-53503534 chr19:53503522-53503533 chr19:53503521-53503532 chr19:53503521-53503534 chr19:53503521-53503534
27	CHD2	chr19:53496660-53497280	K562	blood:	n/a	n/a
28	CHD2	chr19:53496834-53497202	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr19:53531550-53531621	Lung_OC	lung:	n/a	n/a
30	CTCF	chr19:53497143-53497392	T-47D	breast:	n/a	chr19:53497308-53497329 chr19:53497313-53497331 chr19:53497320-53497328
31	CTCF	chr19:53523141-53523173	Spleen_OC	spleen:	n/a	n/a
32	CTCF	chr19:53523080-53523230	RPTEC	kidney:	n/a	n/a
33	CTCF	chr19:53497265-53497376	GM12878	blood:	n/a	chr19:53497308-53497329 chr19:53497313-53497331 chr19:53497320-53497328
34	CTCF	chr19:53523053-53523226	Fibrobl	skin:	n/a	n/a
35	CTCF	chr19:53497200-53497350	HBMEC	blood vessel:	n/a	chr19:53497308-53497329 chr19:53497313-53497331 chr19:53497320-53497328
36	CTCF	chr19:53523073-53523220	MCF-7	breast:	n/a	n/a
37	CTCF	chr19:53497240-53497390	AG09309	skin:	n/a	chr19:53497308-53497329 chr19:53497313-53497331 chr19:53497320-53497328
38	CTCF	chr19:53497220-53497370	K562	blood:	n/a	chr19:53497308-53497329 chr19:53497313-53497331 chr19:53497320-53497328
39	CTCF	chr19:53496808-53497415	GM12878	blood:	n/a	chr19:53497308-53497329 chr19:53497313-53497331 chr19:53497320-53497328
40	CTCF	chr19:53523000-53523150	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr19:53523000-53523150	HEK293	kidney:	n/a	n/a
42	CTCF	chr19:53496980-53497130	NHEK	skin:	n/a	n/a
43	CTCF	chr19:53523066-53523216	GM12891	blood:	n/a	n/a
44	CTCF	chr19:53497020-53497170	HCM	heart:	n/a	n/a
45	CTCF	chr19:53523020-53523170	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr19:53523113-53523185	ProgFib	skin:	n/a	n/a
47	CTCF	chr19:53496805-53497125	Medullo	brain:	n/a	n/a
48	CTCF	chr19:53523100-53523250	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr19:53496980-53497130	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr19:53497020-53497170	GM12873	blood:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53496094-53496144	HRPEpiC	eye:	n/a
2	chr19:53541186-53541236	NHDF-neo	bronchial:	n/a
3	chr19:53496094-53496144	HRPEpiC	eye:	n/a
4	chr19:53541186-53541236	NHDF-neo	bronchial:	n/a
5	chr19:53496738-53496788	PFSK-1	brain:	n/a
6	chr19:53500997-53501047	HEEpiC	esophagus:	n/a
7	chr19:53497048-53497098	BJ	skin:	n/a
8	chr19:53540845-53540895	Hela-S3	cervix:	n/a
9	chr19:53497027-53497077	CMK	blood:	n/a
10	chr19:53538883-53538933	Jurkat	blood:	n/a
11	chr19:53496738-53496788	HepG2	liver:	n/a
12	chr19:53540902-53540952	HAEpiC	amniotic membrane:	n/a
13	chr19:53496835-53496885	PANC-1	pancreas:	n/a
14	chr19:53500997-53501047	Caco-2	colon:	n/a
15	chr19:53496846-53496896	HRPEpiC	eye:	n/a
16	chr19:53493775-53493825	NT2-D1	testis:	n/a
17	chr19:53496835-53496885	AG10803	skin:	n/a
18	chr19:53540902-53540952	MCF10A-Er-Src	breast:	n/a
19	chr19:53496094-53496144	K562	blood:	n/a
20	chr19:53496835-53496885	NH-A	brain:	n/a
21	chr19:53497027-53497077	NHBE	bronchial:	n/a
22	chr19:53497027-53497077	ovcar-3	ovarian:	n/a
23	chr19:53497027-53497077	AG10803	skin:	n/a
24	chr19:53538687-53538737	MCF10A-Er-Src	breast:	n/a
25	chr19:53496440-53496490	GM12878	blood:	n/a
26	chr19:53496893-53496943	CMK	blood:	n/a
27	chr19:53538883-53538933	LNCaP	prostate:	n/a
28	chr19:53496835-53496885	A549	lung:	n/a
29	chr19:53540902-53540952	PrEC	prostate:	n/a
30	chr19:53496846-53496896	AG09309	skin:	n/a
31	chr19:53496835-53496885	HCM	heart:	n/a
32	chr19:53496738-53496788	MCF10A-Er-Src	breast:	n/a
33	chr19:53496664-53496714	HUVEC	blood vessel:	n/a
34	chr19:53496440-53496490	NB4	blood:	n/a
35	chr19:53496664-53496714	Hela-S3	cervix:	n/a
36	chr19:53496440-53496490	SK-N-MC	brain:	n/a
37	chr19:53496094-53496144	AG09319	gingival:	n/a
38	chr19:53497027-53497077	A549	lung:	n/a
39	chr19:53540845-53540895	HEK293	kidney:	embryo
40	chr19:53540845-53540895	HMEC	breast:	n/a
41	chr19:53496846-53496896	HEK293	kidney:	embryo
42	chr19:53496738-53496788	HNPCEpiC	eye:	n/a
43	chr19:53497027-53497077	AG09319	gingival:	n/a
44	chr19:53540902-53540952	HNPCEpiC	eye:	n/a
45	chr19:53538883-53538933	HEEpiC	esophagus:	n/a
46	chr19:53496893-53496943	HCM	heart:	n/a
47	chr19:53496835-53496885	Hela-S3	cervix:	n/a
48	chr19:53497027-53497077	HNPCEpiC	eye:	n/a
49	chr19:53497281-53497331	HCT-116	colon:	n/a
50	chr19:53541287-53541337	IMR90	lung:	fetal

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:53465058..53468377-chr19:53495533..53497921,4	K562	blood:
2	chr19:53515874..53517968-chr19:53519511..53521544,2	K562	blood:
3	chr19:53541069..53542606-chr19:53543581..53546044,2	K562	blood:
4	chr19:53466473..53468381-chr19:53486482..53488386,2	K562	blood:
5	chr19:53482347..53484833-chr19:53488292..53490832,2	K562	blood:
6	chr10:9353360..9353955-chr19:53525559..53526530,2	MCF-7	breast:
7	chr19:53237008..53239147-chr19:53540786..53542527,2	MCF-7	breast:
8	chr19:53536567..53539141-chr19:53540653..53542425,2	K562	blood:
9	chr14:77866421..77867168-chr19:53501795..53502295,2	MCF-7	breast:
10	chr19:53514929..53517284-chr19:53527300..53529548,2	MCF-7	breast:

(count:27 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF816-2	chr19:53489828-53490099	NONHSAT067609
2	lnc-ZNF816-2	chr19:53493346-53493463	NONHSAT067609
3	lnc-ZNF816-2	chr19:53496733-53496767	NONHSAT067614
4	lnc-ZNF816-2	chr19:53496733-53496779	NONHSAT067618
5	lnc-ZNF816-2	chr19:53489828-53490099	NONHSAT067610
6	lnc-ZNF816-2	chr19:53493346-53493463	NONHSAT067618
7	lnc-ZNF816-2	chr19:53493663-53493785	NONHSAT067619
8	lnc-ZNF816-2	chr19:53496733-53496778	NONHSAT067611
9	lnc-ZNF816-2	chr19:53489705-53490099	NONHSAT067618
10	lnc-ZNF816-2	chr19:53496733-53496779	NONHSAT067610
11	lnc-ZNF816-2	chr19:53489828-53490099	NONHSAT067612
12	lnc-ZNF816-2	chr19:53496733-53496784	NONHSAT067619
13	lnc-ZNF816-2	chr19:53496733-53496784	NONHSAT067612
14	lnc-ZNF816-2	chr19:53493346-53493463	NONHSAT067619
15	lnc-ZNF816-2	chr19:53489828-53490099	NONHSAT067613
16	lnc-ZNF160-1	chr19:53517584-53517806	ENSG00000251255
17	lnc-ZNF816-2	chr19:53540978-53541136	NONHSAT067613
18	lnc-ZNF816-2	chr19:53489828-53490099	NONHSAT067614
19	lnc-ZNF816-2	chr19:53489828-53490099	NONHSAT067611
20	lnc-VN1R2-11	chr19:53485444-53485548	NONHSAT067616
21	lnc-ZNF160-1	chr19:53517843-53519833	ENSG00000251255
22	lnc-ZNF816-2	chr19:53486092-53486512	NONHSAT067617
23	lnc-ZNF816-2	chr19:53496733-53496779	NONHSAT067609
24	lnc-ZNF816-2	chr19:53489819-53490099	NONHSAT067619
25	lnc-VN1R2-11	chr19:53488013-53488207	NONHSAT067616
26	lnc-ZNF816-2	chr19:53489828-53490101	NONHSAT067615
27	lnc-ZNF816-2	chr19:53489828-53489972	NONHSAT067617

No data

Variant related genes	Relation type
ENSG00000268282	TF binding region
ENSG00000267943	TF binding region
ENSG00000269082	TF binding region
ERVV-1	TF binding region
ERVV-2	TF binding region
ZNF702P	TF binding region
ENSG00000268282	CpG island
ENSG00000267943	CpG island
ENSG00000269082	CpG island
ERVV-1	CpG island
ERVV-2	CpG island
ZNF702P	CpG island
ENSG00000269526	chromatin interactions
ENSG00000213020	chromatin interactions
ENSG00000180257	chromatin interactions
ENSG00000242779	chromatin interactions
ENSG00000221874	chromatin interactions
RNF4	miRNA target sites
GPR107	miRNA target sites

Extended variants
information (count: 2700 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2700 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8102939	chr19:53485090-53485091	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs329725	chr19:53485091-53485092	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs532176489	chr19:53485164-53485165	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544014260	chr19:53485165-53485166	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562398852	chr19:53485204-53485205	Strong transcription Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs529985884	chr19:53485219-53485220	Strong transcription Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs142678350	chr19:53485237-53485238	Strong transcription Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs566380808	chr19:53485326-53485327	Strong transcription Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs397954395	chr19:53485363-53485364	Strong transcription Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs577793873	chr19:53485377-53485378	Strong transcription Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs113502621	chr19:53485389-53485390	Strong transcription Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs551958537	chr19:53485407-53485408	Strong transcription Weak transcription ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs11280039	chr19:53485427-53485428	Strong transcription Weak transcription ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs111348659	chr19:53485477-53485478	Strong transcription Weak transcription ZNF genes & repeats	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs28409939	chr19:53485487-53485488	Strong transcription Weak transcription ZNF genes & repeats	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs570543637	chr19:53485518-53485519	Strong transcription Weak transcription ZNF genes & repeats	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs1837922	chr19:53485519-53485520	Strong transcription Weak transcription ZNF genes & repeats	TF binding region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs191244425	chr19:53485535-53485536	Strong transcription Weak transcription ZNF genes & repeats	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs575458490	chr19:53485537-53485538	Strong transcription Weak transcription ZNF genes & repeats	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs569567096	chr19:53485544-53485545	Strong transcription Weak transcription ZNF genes & repeats	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs28493524	chr19:53485547-53485548	Strong transcription Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
22	rs536985284	chr19:53485561-53485562	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs533094058	chr19:53485618-53485619	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542941386	chr19:53485630-53485631	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184995879	chr19:53485632-53485633	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573182670	chr19:53485643-53485644	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs368083484	chr19:53485660-53485661	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs4627482	chr19:53485690-53485691	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs73068730	chr19:53485693-53485694	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374791067	chr19:53485746-53485747	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7249605	chr19:53485771-53485772	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs544002262	chr19:53485789-53485790	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562384785	chr19:53485795-53485796	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374376579	chr19:53485808-53485809	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs143972542	chr19:53485809-53485810	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs329723	chr19:53485814-53485815	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs560420203	chr19:53485816-53485817	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs189325329	chr19:53485840-53485841	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs148769079	chr19:53485843-53485844	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs1867054	chr19:53485851-53485852	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs329722	chr19:53485861-53485862	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs181707590	chr19:53485866-53485867	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs116420532	chr19:53485867-53485868	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs536922009	chr19:53485902-53485903	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs375319151	chr19:53485907-53485908	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs548571175	chr19:53486004-53486005	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs567166118	chr19:53486058-53486059	Strong transcription Weak transcription ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs1867055	chr19:53486060-53486061	Strong transcription Weak transcription ZNF genes & repeats	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs532853415	chr19:53486092-53486093	Strong transcription Weak transcription ZNF genes & repeats	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
50	rs558959820	chr19:53486110-53486111	Strong transcription Weak transcription ZNF genes & repeats	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	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
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:967 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53467000-53489000	Weak transcription	Right Ventricle	heart
2	chr19:53467000-53494600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr19:53467200-53488600	Weak transcription	Rectal Smooth Muscle	rectum
4	chr19:53467200-53489200	Weak transcription	Colon Smooth Muscle	Colon
5	chr19:53467200-53495400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr19:53471600-53487600	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr19:53472600-53489000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr19:53472800-53487800	Weak transcription	Adipose Nuclei	Adipose
9	chr19:53472800-53495800	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr19:53473000-53488000	Weak transcription	K562	blood
11	chr19:53473000-53488600	Weak transcription	Colonic Mucosa	Colon
12	chr19:53473000-53489400	Weak transcription	Brain Anterior Caudate	brain
13	chr19:53473600-53488600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr19:53473600-53495800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr19:53473800-53487800	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr19:53474000-53488200	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr19:53474000-53488800	Weak transcription	Fetal Kidney	kidney
18	chr19:53474000-53495800	Weak transcription	Fetal Lung	lung
19	chr19:53474200-53488000	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr19:53474200-53488000	Weak transcription	HUVEC	blood vessel
21	chr19:53480200-53487800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr19:53480400-53488200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr19:53481200-53495400	Weak transcription	Fetal Muscle Trunk	muscle
24	chr19:53481800-53487600	Weak transcription	Aorta	Aorta
25	chr19:53482000-53487600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr19:53482000-53487600	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr19:53482000-53487800	Weak transcription	Gastric	stomach
28	chr19:53482000-53489800	Weak transcription	NHLF	lung
29	chr19:53482000-53491200	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr19:53482200-53485200	Weak transcription	Pancreas	Pancrea
31	chr19:53482200-53485400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr19:53482200-53485800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr19:53482200-53487600	Weak transcription	Left Ventricle	heart
34	chr19:53482200-53487600	Weak transcription	Spleen	Spleen
35	chr19:53482400-53487400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr19:53482400-53487600	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr19:53482400-53487600	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr19:53482600-53487200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr19:53482600-53487200	Weak transcription	Fetal Intestine Small	intestine
40	chr19:53482600-53487600	Weak transcription	Ovary	ovary
41	chr19:53482600-53487800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr19:53482600-53488600	Weak transcription	Fetal Stomach	stomach
43	chr19:53483200-53487400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr19:53483200-53487600	Weak transcription	Placenta	Placenta
45	chr19:53484000-53487600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr19:53484000-53487800	Weak transcription	Stomach Smooth Muscle	stomach
47	chr19:53484200-53487600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr19:53484800-53487600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr19:53485000-53487800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr19:53485400-53485600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived

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