Variant report

Variant	nsv544074
Chromosome Location	chr19:54325041-54366732
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:878)
CpG islands
(count:368)
Chromatin interactive
region (count:69)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:878 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:54345326-54345759	K562	blood:	n/a	n/a
2	ARID3A	chr19:54345335-54345883	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:54362290-54362337	HepG2	liver:	n/a	n/a
4	ATF1	chr19:54345402-54345741	K562	blood:	n/a	n/a
5	ATF2	chr19:54345267-54345680	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr19:54345369-54345722	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr19:54345388-54345705	K562	blood:	n/a	n/a
8	ATF3	chr19:54345257-54346029	A549	lung:	n/a	n/a
9	ATF3	chr19:54345236-54345912	A549	lung:	n/a	n/a
10	ATF3	chr19:54345373-54345824	K562	blood:	n/a	n/a
11	BACH1	chr19:54345375-54345723	H1-hESC	embryonic stem cell:	n/a	chr19:54345603-54345617
12	BCL3	chr19:54345247-54346022	A549	lung:	n/a	chr19:54345605-54345614
13	BCL3	chr19:54345267-54346077	A549	lung:	n/a	chr19:54345605-54345614
14	BHLHE40	chr19:54347211-54347542	HepG2	liver:	n/a	n/a
15	BHLHE40	chr19:54345501-54345746	K562	blood:	n/a	n/a
16	BHLHE40	chr19:54351575-54351598	HepG2	liver:	n/a	n/a
17	BHLHE40	chr19:54327373-54327676	K562	blood:	n/a	n/a
18	BHLHE40	chr19:54347333-54347401	K562	blood:	n/a	n/a
19	BHLHE40	chr19:54347380-54347407	A549	lung:	n/a	n/a
20	BHLHE40	chr19:54356189-54356389	K562	blood:	n/a	n/a
21	CBX3	chr19:54345238-54346098	HCT-116	colon:	n/a	n/a
22	CBX3	chr19:54345223-54346048	HCT-116	colon:	n/a	n/a
23	CEBPB	chr19:54348127-54348412	K562	blood:	n/a	n/a
24	CEBPB	chr19:54354997-54355311	IMR90	lung:	n/a	n/a
25	CEBPB	chr19:54327393-54327651	HepG2	liver:	n/a	chr19:54327513-54327524
26	CEBPB	chr19:54327395-54327614	K562	blood:	n/a	chr19:54327513-54327524
27	CEBPB	chr19:54348095-54348427	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr19:54333321-54333547	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr19:54348101-54348452	A549	lung:	n/a	n/a
30	CEBPB	chr19:54352575-54352682	A549	lung:	n/a	n/a
31	CEBPB	chr19:54362160-54362500	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr19:54345385-54346127	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr19:54327363-54327732	K562	blood:	n/a	chr19:54327513-54327524
34	CEBPB	chr19:54348041-54348482	A549	lung:	n/a	n/a
35	CEBPB	chr19:54355071-54355344	HepG2	liver:	n/a	n/a
36	CEBPB	chr19:54333392-54333527	HepG2	liver:	n/a	n/a
37	CEBPB	chr19:54347974-54348482	A549	lung:	n/a	n/a
38	CEBPB	chr19:54344184-54344468	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr19:54348094-54348451	HepG2	liver:	n/a	n/a
40	CEBPB	chr19:54345337-54346105	A549	lung:	n/a	n/a
41	CEBPB	chr19:54344199-54344456	A549	lung:	n/a	n/a
42	CEBPB	chr19:54348094-54348445	IMR90	lung:	n/a	n/a
43	CEBPB	chr19:54344178-54344548	IMR90	lung:	n/a	n/a
44	CEBPB	chr19:54344162-54344639	A549	lung:	n/a	n/a
45	CHD2	chr19:54345309-54345724	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr19:54345533-54345700	K562	blood:	n/a	n/a
47	CREB1	chr19:54345315-54345645	A549	lung:	n/a	n/a
48	CREB1	chr19:54356018-54356471	A549	lung:	n/a	n/a
49	CTCF	chr19:54345389-54345672	Spleen_OC	spleen:	n/a	chr19:54345513-54345529 chr19:54345515-54345528 chr19:54345512-54345530 chr19:54345514-54345535 chr19:54345515-54345528
50	CTCF	chr19:54345423-54345620	ProgFib	skin:	n/a	chr19:54345513-54345529 chr19:54345515-54345528 chr19:54345512-54345530 chr19:54345514-54345535 chr19:54345515-54345528

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:54327847-54327897	HRPEpiC	eye:	n/a
2	chr19:54327404-54327454	U87	brain:	n/a
3	chr19:54327847-54327897	HRPEpiC	eye:	n/a
4	chr19:54327404-54327454	U87	brain:	n/a
5	chr19:54327404-54327454	ProgFib	skin:	n/a
6	chr19:54327437-54327487	ProgFib	skin:	n/a
7	chr19:54328302-54328352	SKMC	muscle:	n/a
8	chr19:54327437-54327487	MCF-7	breast:	n/a
9	chr19:54327780-54327830	CMK	blood:	n/a
10	chr19:54327847-54327897	HCF	heart:	n/a
11	chr19:54327404-54327454	GM12892	blood:	n/a
12	chr19:54327847-54327897	AoSMC	blood vessel:	n/a
13	chr19:54327995-54328045	HCF	heart:	n/a
14	chr19:54327847-54327897	NB4	blood:	n/a
15	chr19:54327847-54327897	AG09319	gingival:	n/a
16	chr19:54327847-54327897	GM12878	blood:	n/a
17	chr19:54327847-54327897	SK-N-SH_RA	brain:	n/a
18	chr19:54327995-54328045	AG04449	skin:	fetal
19	chr19:54327995-54328045	U87	brain:	n/a
20	chr19:54327437-54327487	IMR90	lung:	fetal
21	chr19:54328302-54328352	ECC-1	luminal epithelium:	n/a
22	chr19:54327995-54328045	HRE	kidney:	n/a
23	chr19:54327780-54327830	Caco-2	colon:	n/a
24	chr19:54327404-54327454	MCF-7	breast:	n/a
25	chr19:54327995-54328045	SK-N-SH	brain:	n/a
26	chr19:54327437-54327487	A549	lung:	n/a
27	chr19:54327847-54327897	AG04450	lung:	fetal
28	chr19:54327780-54327830	IMR90	lung:	fetal
29	chr19:54327437-54327487	LNCaP	prostate:	n/a
30	chr19:54327437-54327487	CMK	blood:	n/a
31	chr19:54327780-54327830	Jurkat	blood:	n/a
32	chr19:54327437-54327487	NHBE	bronchial:	n/a
33	chr19:54327995-54328045	GM12891	blood:	n/a
34	chr19:54327404-54327454	T-47D	breast:	n/a
35	chr19:54327780-54327830	T-47D	breast:	n/a
36	chr19:54327780-54327830	AG04450	lung:	fetal
37	chr19:54327847-54327897	GM12891	blood:	n/a
38	chr19:54327780-54327830	NT2-D1	testis:	n/a
39	chr19:54327437-54327487	AG04450	lung:	fetal
40	chr19:54327404-54327454	NHBE	bronchial:	n/a
41	chr19:54327780-54327830	HMEC	breast:	n/a
42	chr19:54327404-54327454	HMEC	breast:	n/a
43	chr19:54327437-54327487	HEEpiC	esophagus:	n/a
44	chr19:54327404-54327454	HRE	kidney:	n/a
45	chr19:54327437-54327487	RPTEC	kidney:	n/a
46	chr19:54327404-54327454	SK-N-SH_RA	brain:	n/a
47	chr19:54327404-54327454	BJ	skin:	n/a
48	chr19:54327437-54327487	Jurkat	blood:	n/a
49	chr19:54327780-54327830	U87	brain:	n/a
50	chr19:54327437-54327487	NHDF-neo	bronchial:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type	Cell Stage
1	19:54331773-54346301..19:54663039-54664754	K562	blood:
2	19:54357838-54358893..19:54677284-54691409	Hela-S3	cervix:
3	chr19:54345610..54348540-chr19:54371943..54373506,2	MCF-7	breast:
4	chr19:54345130..54345698-chr19:54450636..54451237,2	MCF-7	breast:
5	19:54359237-54361186..19:54600850-54620705	H1-hESC	embryonic stem cell:	embryo
6	19:54359237-54361186..19:54927412-54932667	K562	blood:
7	chr19:54345232..54345814-chr19:54415826..54416493,2	K562	blood:
8	19:54331773-54346301..19:54361186-54373774	Hela-S3	cervix:
9	chr19:54343985..54346791-chr19:54661785..54663833,2	K562	blood:
10	chr19:54366577..54369792-chr19:54370978..54372974,4	K562	blood:
11	chr19:54355884..54356820-chr19:54526546..54527779,4	MCF-7	breast:
12	19:54349211-54357838..19:54552819-54563729	Hela-S3	cervix:
13	19:54331773-54346301..19:54552819-54563729	K562	blood:
14	19:54358893-54359237..19:54600850-54620705	Hela-S3	cervix:
15	chr19:54364687..54367587-chr19:54369431..54371067,2	MCF-7	breast:
16	chr19:54366710..54368264-chr19:54369239..54370782,2	K562	blood:
17	chr19:54345141..54346284-chr19:54526826..54527910,9	MCF-7	breast:
18	chr19:54366092..54368264-chr19:54369282..54370803,2	K562	blood:
19	19:54331773-54346301..19:54677284-54691409	Hela-S3	cervix:
20	chr19:54344996..54345979-chr19:54526590..54528026,5	K562	blood:
21	19:54359237-54361186..19:54643159-54647787	K562	blood:
22	19:54359237-54361186..19:54667671-54677284	K562	blood:
23	19:54359237-54361186..19:54620705-54622004	Hela-S3	cervix:
24	chr19:54361458..54364085-chr19:54370964..54373954,2	K562	blood:
25	19:54331773-54346301..19:54647787-54653912	Hela-S3	cervix:
26	19:54349211-54357838..19:54738658-54764091	K562	blood:
27	19:54331773-54346301..19:54935996-54949475	Hela-S3	cervix:
28	chr19:54361458..54364085-chr19:54370964..54374077,3	K562	blood:
29	19:54349211-54357838..19:54471705-54498373	H1-hESC	embryonic stem cell:	embryo
30	19:54331773-54346301..19:54600850-54620705	GM12878	blood:
31	19:54359237-54361186..19:54677284-54691409	Hela-S3	cervix:
32	19:54331773-54346301..19:55010971-55030075	K562	blood:
33	chr19:54351110..54352913-chr19:54359613..54361419,2	MCF-7	breast:
34	19:54359237-54361186..19:54471705-54498373	GM12878	blood:
35	19:54331773-54346301..19:54664754-54667583	Hela-S3	cervix:
36	19:54331773-54346301..19:54667671-54677284	Hela-S3	cervix:
37	19:54331773-54346301..19:54964441-54971082	Hela-S3	cervix:
38	chr19:54354857..54357181-chr19:54372188..54373892,2	MCF-7	breast:
39	19:54349211-54357838..19:54882151-54893239	Hela-S3	cervix:
40	chr19:54351863..54353862-chr19:54356246..54357875,2	MCF-7	breast:
41	19:54331773-54346301..19:54882151-54893239	Hela-S3	cervix:
42	19:54349211-54357838..19:54837886-54859497	K562	blood:
43	19:54331773-54346301..19:54622004-54643159	Hela-S3	cervix:
44	19:54349211-54357838..19:54677284-54691409	K562	blood:
45	19:54331773-54346301..19:54772822-54786052	GM12878	blood:
46	chr19:54351863..54353862-chr19:54356246..54357875,2	MCF-7	breast:
47	19:54349211-54357838..19:54463218-54469094	Hela-S3	cervix:
48	19:54331773-54346301..19:54837886-54859497	K562	blood:
49	19:54359237-54361186..19:54622004-54643159	Hela-S3	cervix:
50	19:54359237-54361186..19:54882151-54893239	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NLRP12-1	chr19:54357835-54357889	ENSG00000228323.2
2	lnc-NLRP12-1	chr19:54366334-54366431	ENSG00000228323.2
3	lnc-NLRP12-1	chr19:54361132-54361218	ENSG00000228323.2
4	lnc-MYADM-3	chr19:54361112-54361397	NONHSAT067845
5	lnc-MYADM-2	chr19:54362212-54362592	NONHSAT067846
6	lnc-NLRP12-1	chr19:54361797-54361894	ENSG00000228323.1
7	lnc-NLRP12-1	chr19:54357835-54357889	ENSG00000228323.1
8	lnc-NLRP12-1	chr19:54361132-54361218	ENSG00000228323.1
9	lnc-NLRP12-1	chr19:54361132-54361218	NONHSAT067842
10	lnc-NLRP12-1	chr19:54357327-54357889	NONHSAT067842

No data

Variant related genes	Relation type
ENSG00000232324	TF binding region
NLRP12	TF binding region
MYADM	TF binding region
ENSG00000232324	CpG island
NLRP12	CpG island
MYADM	CpG island
ENSG00000142408	chromatin interactions
ENSG00000170906	chromatin interactions
ENSG00000250507	chromatin interactions
ENSG00000189068	chromatin interactions
ENSG00000264703	chromatin interactions
ENSG00000268164	chromatin interactions
ENSG00000105617	chromatin interactions
ENSG00000244482	chromatin interactions
ENSG00000167615	chromatin interactions
ENSG00000105609	chromatin interactions
ENSG00000088038	chromatin interactions
ENSG00000239961	chromatin interactions
ENSG00000167618	chromatin interactions
ENSG00000131042	chromatin interactions
ENSG00000237955	chromatin interactions
ENSG00000105605	chromatin interactions
ENSG00000232324	chromatin interactions
ENSG00000126583	chromatin interactions
ENSG00000170909	chromatin interactions
ENSG00000237017	chromatin interactions
ENSG00000104972	chromatin interactions
ENSG00000268496	chromatin interactions
ENSG00000238094	chromatin interactions
ENSG00000105619	chromatin interactions
ENSG00000227407	chromatin interactions
ENSG00000179820	chromatin interactions
ENSG00000167614	chromatin interactions
ENSG00000223660	chromatin interactions
ENSG00000167608	chromatin interactions
ENSG00000249189	chromatin interactions
ENSG00000228323	chromatin interactions
ENSG00000130433	chromatin interactions
ENSG00000125505	chromatin interactions
ENSG00000170889	chromatin interactions
ENSG00000167613	chromatin interactions
ENSG00000215998	chromatin interactions
ENSG00000105618	chromatin interactions
ENSG00000248166	chromatin interactions

Extended variants
information (count: 2046 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2046 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545397726	chr19:54325051-54325052	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs563971058	chr19:54325187-54325188	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs575442987	chr19:54325216-54325217	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs187667966	chr19:54325217-54325218	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs542766100	chr19:54325283-54325284	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs62143205	chr19:54325353-54325354	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs528602421	chr19:54325357-54325358	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs142922110	chr19:54325358-54325359	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs73056711	chr19:54325418-54325419	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs376854407	chr19:54325477-54325478	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs192484388	chr19:54325527-54325528	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs185036007	chr19:54325528-54325529	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs530014839	chr19:54325600-54325601	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs189359077	chr19:54325624-54325625	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs566654310	chr19:54325651-54325652	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs146129305	chr19:54325679-54325680	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs558590829	chr19:54325708-54325709	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs555579726	chr19:54325728-54325729	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs371270224	chr19:54325729-54325730	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs537807116	chr19:54325742-54325743	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs549716795	chr19:54325760-54325761	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs557234400	chr19:54325768-54325769	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs192403083	chr19:54325814-54325815	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs369791507	chr19:54325938-54325939	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs554770906	chr19:54325947-54325948	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs140170012	chr19:54325972-54325973	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs35709423	chr19:54325990-54325991	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs377595007	chr19:54326010-54326011	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs184745069	chr19:54326023-54326024	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs565340295	chr19:54326049-54326050	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs532406995	chr19:54326089-54326090	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs544644139	chr19:54326101-54326102	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs142475020	chr19:54326124-54326125	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs530052319	chr19:54326125-54326126	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs548480621	chr19:54326166-54326167	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs189605067	chr19:54326211-54326212	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs62143206	chr19:54326212-54326213	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs527444059	chr19:54326239-54326240	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs181371842	chr19:54326245-54326246	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs185857379	chr19:54326249-54326250	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs189095445	chr19:54326266-54326267	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs555779055	chr19:54326269-54326270	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs567701198	chr19:54326296-54326297	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs62143207	chr19:54326346-54326347	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs77284763	chr19:54326352-54326353	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs74394542	chr19:54326354-54326355	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs137959316	chr19:54326358-54326359	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs532442453	chr19:54326375-54326376	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs554809480	chr19:54326384-54326385	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs78215353	chr19:54326387-54326388	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20459607	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Alzheimer''s disease	22166940	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Glioblastoma multiforme	21922591	CNVD
Lung cancer	19153074	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:54302000-54327200	Weak transcription	Lung	lung
2	chr19:54313800-54327000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr19:54314000-54327400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr19:54314400-54327000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr19:54314600-54327000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr19:54314600-54327000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr19:54318400-54327000	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr19:54318400-54327000	Weak transcription	Spleen	Spleen
9	chr19:54318400-54327200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr19:54318400-54327200	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr19:54318800-54327200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr19:54321200-54327200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr19:54322400-54326800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr19:54323600-54327000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr19:54324200-54326400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
16	chr19:54324400-54325800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr19:54324800-54326200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
18	chr19:54325000-54325400	Flanking Active TSS	Primary B cells from cord blood	blood
19	chr19:54325000-54326000	Active TSS	Primary hematopoietic stem cells	blood
20	chr19:54325400-54327800	Active TSS	Primary B cells from cord blood	blood
21	chr19:54325800-54326000	Active TSS	Monocytes-CD14+_RO01746	blood
22	chr19:54326000-54326200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
23	chr19:54326000-54327000	Weak transcription	Primary hematopoietic stem cells	blood
24	chr19:54326200-54327800	Active TSS	Primary monocytes fromperipheralblood	blood
25	chr19:54326200-54327800	Active TSS	Monocytes-CD14+_RO01746	blood
26	chr19:54326400-54326800	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr19:54326800-54327000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr19:54326800-54327000	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
29	chr19:54326800-54328600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
30	chr19:54327000-54327200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr19:54327000-54327400	Enhancers	Primary hematopoietic stem cells	blood
32	chr19:54327000-54327400	Active TSS	Adipose Nuclei	Adipose
33	chr19:54327000-54327400	Bivalent Enhancer	Placenta	Placenta
34	chr19:54327000-54327600	Enhancers	H1 Cell Line	embryonic stem cell
35	chr19:54327000-54327600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr19:54327000-54327600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr19:54327000-54327600	Bivalent/Poised TSS	Primary mononuclear cells fromperipheralblood	Blood
38	chr19:54327000-54327600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
39	chr19:54327000-54327600	Active TSS	Right Atrium	heart
40	chr19:54327000-54327600	ZNF genes & repeats	Spleen	Spleen
41	chr19:54327000-54327800	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr19:54327000-54327800	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr19:54327000-54327800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr19:54327000-54328000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
45	chr19:54327000-54328400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr19:54327200-54327400	Flanking Active TSS	Liver	Liver
47	chr19:54327200-54327400	Flanking Bivalent TSS/Enh	Lung	lung
48	chr19:54327200-54327400	Active TSS	Skeletal Muscle Female	skeletal muscle
49	chr19:54327200-54327400	Flanking Active TSS	HepG2	liver
50	chr19:54327200-54327600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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