Variant report

Variant	nsv912304
Chromosome Location	chr19:53071155-53114267
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1303)
CpG islands
(count:1831)
Chromatin interactive
region (count:38)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1303 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:53073449-53073460	K562	blood:	n/a	n/a
2	ARID3A	chr19:53073479-53073589	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:53104339-53104539	HepG2	liver:	n/a	n/a
4	BACH1	chr19:53073489-53073893	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr19:53104565-53104775	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr19:53103098-53103246	GM12878	blood:	n/a	n/a
7	BHLHE40	chr19:53073465-53074054	GM12878	blood:	n/a	n/a
8	BHLHE40	chr19:53105048-53105160	K562	blood:	n/a	n/a
9	BHLHE40	chr19:53104552-53104837	K562	blood:	n/a	n/a
10	BHLHE40	chr19:53073388-53074192	K562	blood:	n/a	n/a
11	BRCA1	chr19:53073589-53074040	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr19:53073555-53073716	GM12878	blood:	n/a	n/a
13	BRCA1	chr19:53104242-53104408	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr19:53073603-53074083	H1-hESC	embryonic stem cell:	n/a	n/a
15	CBX3	chr19:53104158-53105094	K562	blood:	n/a	n/a
16	CBX3	chr19:53073140-53074166	K562	blood:	n/a	n/a
17	CBX3	chr19:53073512-53073861	K562	blood:	n/a	n/a
18	CCNT2	chr19:53104315-53104658	K562	blood:	n/a	chr19:53104426-53104435
19	CEBPB	chr19:53099901-53100188	A549	lung:	n/a	n/a
20	CEBPB	chr19:53107089-53107422	IMR90	lung:	n/a	chr19:53107272-53107285 chr19:53107272-53107283
21	CEBPB	chr19:53099899-53100273	HepG2	liver:	n/a	n/a
22	CEBPD	chr19:53104439-53104726	HepG2	liver:	n/a	n/a
23	CHD1	chr19:53073518-53074222	GM12878	blood:	n/a	chr19:53074031-53074041
24	CHD1	chr19:53104493-53105133	GM12878	blood:	n/a	chr19:53104872-53104882
25	CHD1	chr19:53073553-53073802	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr19:53073480-53074085	Hela-S3	cervix:	n/a	chr19:53074031-53074041
27	CHD2	chr19:53104533-53104762	K562	blood:	n/a	n/a
28	CHD2	chr19:53110034-53110081	K562	blood:	n/a	n/a
29	CHD2	chr19:53104297-53104823	Hela-S3	cervix:	n/a	chr19:53104469-53104479
30	CHD2	chr19:53104193-53104915	GM12878	blood:	n/a	chr19:53104469-53104479 chr19:53104872-53104882
31	CHD2	chr19:53073339-53074084	GM12878	blood:	n/a	chr19:53074031-53074041
32	CHD2	chr19:53073626-53074145	HepG2	liver:	n/a	chr19:53074031-53074041
33	CHD2	chr19:53073478-53074142	K562	blood:	n/a	chr19:53074031-53074041
34	CHD2	chr19:53073067-53074098	H1-hESC	embryonic stem cell:	n/a	chr19:53074031-53074041
35	CHD2	chr19:53105228-53105277	GM12878	blood:	n/a	n/a
36	CTCF	chr19:53094060-53094210	AG09319	gingival:	n/a	n/a
37	CTCF	chr19:53095580-53095730	HAc	cerebellar:	n/a	n/a
38	CTCF	chr19:53105380-53105530	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr19:53104260-53104410	NHEK	skin:	n/a	n/a
40	CTCF	chr19:53105360-53105510	Caco-2	colon:	n/a	n/a
41	CTCF	chr19:53095660-53095810	GM12873	blood:	n/a	chr19:53095743-53095752
42	CTCF	chr19:53073200-53073350	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr19:53095640-53095790	K562	blood:	n/a	chr19:53095743-53095752
44	CTCF	chr19:53094040-53094190	HEK293	kidney:	n/a	n/a
45	CTCF	chr19:53073240-53073390	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr19:53073340-53073490	AG10803	skin:	n/a	n/a
47	CTCF	chr19:53095660-53095810	HRE	kidney:	n/a	chr19:53095743-53095752
48	CTCF	chr19:53095720-53095870	HCPEpiC	choroid plexus:	n/a	chr19:53095743-53095752
49	CTCF	chr19:53094102-53094191	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr19:53094081-53094229	K562	blood:	n/a	n/a

(count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53086597-53086647	HAEpiC	amniotic membrane:	n/a
2	chr19:53086597-53086647	HAEpiC	amniotic membrane:	n/a
3	chr19:53104398-53104448	HUVEC	blood vessel:	n/a
4	chr19:53099757-53099807	AG09319	gingival:	n/a
5	chr19:53107200-53107250	HIPEpiC	eye:	n/a
6	chr19:53073334-53073384	PANC-1	pancreas:	n/a
7	chr19:53073712-53073762	AG10803	skin:	n/a
8	chr19:53104879-53104929	GM06990	blood:	n/a
9	chr19:53073334-53073384	SK-N-SH_RA	brain:	n/a
10	chr19:53092499-53092549	NH-A	brain:	n/a
11	chr19:53073334-53073384	HNPCEpiC	eye:	n/a
12	chr19:53107200-53107250	SAEC	small airway:	n/a
13	chr19:53099757-53099807	SAEC	small airway:	n/a
14	chr19:53088482-53088532	GM12892	blood:	n/a
15	chr19:53073712-53073762	NH-A	brain:	n/a
16	chr19:53073577-53073627	HMEC	breast:	n/a
17	chr19:53085685-53085735	ProgFib	skin:	n/a
18	chr19:53104879-53104929	HepG2	liver:	n/a
19	chr19:53073399-53073449	Jurkat	blood:	n/a
20	chr19:53104398-53104448	ProgFib	skin:	n/a
21	chr19:53075878-53075928	Hela-S3	cervix:	n/a
22	chr19:53092499-53092549	ovcar-3	ovarian:	n/a
23	chr19:53073865-53073915	HRE	kidney:	n/a
24	chr19:53107200-53107250	LNCaP	prostate:	n/a
25	chr19:53088327-53088377	SK-N-SH_RA	brain:	n/a
26	chr19:53074012-53074062	PANC-1	pancreas:	n/a
27	chr19:53074012-53074062	PrEC	prostate:	n/a
28	chr19:53073577-53073627	HepG2	liver:	n/a
29	chr19:53088327-53088377	HIPEpiC	eye:	n/a
30	chr19:53104879-53104929	ProgFib	skin:	n/a
31	chr19:53073285-53073335	HCF	heart:	n/a
32	chr19:53074012-53074062	HEEpiC	esophagus:	n/a
33	chr19:53088482-53088532	HCT-116	colon:	n/a
34	chr19:53073334-53073384	ovcar-3	ovarian:	n/a
35	chr19:53104195-53104245	BJ	skin:	n/a
36	chr19:53088551-53088601	MCF-7	breast:	n/a
37	chr19:53107200-53107250	NHDF-neo	bronchial:	n/a
38	chr19:53073577-53073627	GM12878	blood:	n/a
39	chr19:53074012-53074062	Caco-2	colon:	n/a
40	chr19:53098913-53098963	Hela-S3	cervix:	n/a
41	chr19:53073242-53073292	NHDF-neo	bronchial:	n/a
42	chr19:53073420-53073470	BE2_C	brain:	n/a
43	chr19:53101634-53101684	AG04450	lung:	fetal
44	chr19:53088482-53088532	HepG2	liver:	n/a
45	chr19:53104997-53105047	GM12878	blood:	n/a
46	chr19:53073404-53073454	MCF10A-Er-Src	breast:	n/a
47	chr19:53092499-53092549	AG09309	skin:	n/a
48	chr19:53073309-53073359	GM12891	blood:	n/a
49	chr19:53088327-53088377	HNPCEpiC	eye:	n/a
50	chr19:53098945-53098995	HNPCEpiC	eye:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:53100919..53102551-chr19:53104466..53106179,2	MCF-7	breast:
2	chr19:53073504..53075016-chr19:53086712..53089202,2	MCF-7	breast:
3	chr19:53110675..53112715-chr19:53114135..53115659,2	K562	blood:
4	chr19:53073369..53074894-chr19:53098457..53100751,2	MCF-7	breast:
5	chr19:53098492..53100632-chr19:53102754..53104581,2	K562	blood:
6	chr19:53087080..53089827-chr19:53090383..53092275,2	K562	blood:
7	chr10:79800834..79801581-chr19:53103963..53104926,2	Hela-S3	cervix:
8	chr19:53030382..53031999-chr19:53102744..53106373,4	K562	blood:
9	chr19:53109871..53112715-chr19:53114135..53116216,3	K562	blood:
10	chr19:53109944..53111454-chr19:53116244..53117812,2	K562	blood:
11	chr19:53073369..53074894-chr19:53098457..53100751,2	MCF-7	breast:
12	chr19:52583726..52585349-chr19:53074729..53076869,2	K562	blood:
13	chr19:53029450..53032188-chr19:53072538..53074123,2	K562	blood:
14	chr19:53086321..53088746-chr19:53090945..53093130,2	K562	blood:
15	chr19:53110484..53113305-chr19:53117534..53120246,3	K562	blood:
16	chr19:53103475..53106137-chr19:53106571..53108256,2	K562	blood:
17	chr19:53104394..53106484-chr19:53154672..53157186,2	K562	blood:
18	chr19:53109871..53112715-chr19:53114135..53116216,3	K562	blood:
19	chr19:53105962..53107575-chr19:53107742..53110699,2	MCF-7	breast:
20	chr19:53110675..53112715-chr19:53114135..53115659,2	K562	blood:
21	chr19:53105509..53107487-chr19:53113900..53115997,2	K562	blood:
22	chr19:53105962..53107575-chr19:53107742..53110699,2	MCF-7	breast:
23	chr19:53103475..53106137-chr19:53106571..53108256,2	K562	blood:
24	chr19:53072947..53075360-chr19:53081572..53083842,2	K562	blood:
25	chr19:53109653..53111853-chr19:53175457..53178162,2	K562	blood:
26	chr19:53073504..53075016-chr19:53086712..53089202,2	MCF-7	breast:
27	chr19:53098815..53100632-chr19:53103081..53105260,2	K562	blood:
28	chr19:53105509..53107487-chr19:53113900..53115997,2	K562	blood:
29	chr19:53029127..53032188-chr19:53072538..53075129,3	K562	blood:
30	chr19:53073322..53075540-chr19:53075629..53079478,4	MCF-7	breast:
31	chr19:53030412..53033347-chr19:53075579..53077399,2	K562	blood:
32	chr19:53091479..53093203-chr19:53104357..53107211,2	MCF-7	breast:
33	chr19:53085553..53087688-chr19:53089270..53091312,2	MCF-7	breast:
34	chr19:53085553..53087688-chr19:53089270..53091312,2	MCF-7	breast:
35	chr19:53073084..53075502-chr19:53084084..53086911,2	K562	blood:
36	chr19:52771721..52774334-chr19:53104602..53106334,2	MCF-7	breast:
37	chr19:53100001..53102540-chr19:53104328..53106583,2	MCF-7	breast:
38	chr19:53087080..53089827-chr19:53090383..53092275,2	K562	blood:

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF701-1	chr19:53100006-53100056	NONHSAT067568
2	lnc-ZNF701-1	chr19:53099792-53099841	NONHSAT067568
3	lnc-ZNF701-1	chr19:53098870-53098941	NONHSAT067564
4	lnc-ZNF83-2	chr19:53101902-53102140	ENSG00000268970.1
5	lnc-ZNF701-1	chr19:53099792-53100056	NONHSAT067566
6	lnc-ZNF83-4	chr19:53079136-53079243	ENSG00000268886.1
7	lnc-ZNF701-1	chr19:53099127-53099572	NONHSAT067566
8	lnc-ZNF83-4	chr19:53088283-53088814	ENSG00000268886.1
9	lnc-ZNF701-1	chr19:53100112-53100660	NONHSAT067566
10	lnc-ZNF701-1	chr19:53101468-53102058	NONHSAT067569
11	lnc-ZNF701-1	chr19:53102400-53103405	NONHSAT067569
12	lnc-ZNF701-1	chr19:53099657-53099709	NONHSAT067566
13	lnc-ZNF701-1	chr19:53095291-53095481	NONHSAT067565
14	lnc-ZNF701-1	chr19:53099657-53099709	NONHSAT067568
15	lnc-ZNF701-1	chr19:53100112-53100660	NONHSAT067567
16	lnc-ZNF701-1	chr19:53099127-53099642	NONHSAT067567
17	lnc-ZNF701-1	chr19:53100261-53100564	NONHSAT067568
18	lnc-ZNF701-1	chr19:53095355-53095481	NONHSAT067564
19	lnc-ZNF701-1	chr19:53099890-53100056	NONHSAT067567
20	lnc-ZNF701-1	chr19:53099127-53099572	NONHSAT067568
21	lnc-ZNF701-1	chr19:53099937-53100823	NONHSAT067569
22	lnc-ZNF701-1	chr19:53100112-53100176	NONHSAT067568
23	lnc-ZNF701-1	chr19:53098870-53100598	NONHSAT067565
24	lnc-ZNF701-1	chr19:53091758-53091866	NONHSAT067564
25	lnc-ZNF83-2	chr19:53100952-53101356	ENSG00000268970.1

No data

Variant related genes	Relation type
ZNF137P	TF binding region
ZNF701	TF binding region
ENSG00000268970	TF binding region
ENSG00000268886	TF binding region
ZNF137P	CpG island
ZNF701	CpG island
ENSG00000268970	CpG island
ENSG00000268886	CpG island
ENSG00000268886	chromatin interactions
ENSG00000167562	chromatin interactions
ENSG00000196214	chromatin interactions
ENSG00000268970	chromatin interactions
ENSG00000123870	chromatin interactions
ENSG00000167766	chromatin interactions
ENSG00000198482	chromatin interactions
ENSG00000269825	chromatin interactions

Extended variants
information (count: 2174 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2174 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs329967	chr19:53071155-53071156	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs528501782	chr19:53071170-53071171	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540669672	chr19:53071186-53071187	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs565274880	chr19:53071345-53071346	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs532867577	chr19:53071346-53071347	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs550975527	chr19:53071350-53071351	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs569449304	chr19:53071356-53071357	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530188442	chr19:53071416-53071417	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs111554758	chr19:53071440-53071441	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs373133674	chr19:53071454-53071455	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547891571	chr19:53071483-53071484	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566272268	chr19:53071486-53071487	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535774556	chr19:53071496-53071497	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142463862	chr19:53071542-53071543	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs113032876	chr19:53071625-53071626	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576473983	chr19:53071626-53071627	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs537368966	chr19:53071630-53071631	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs151337374	chr19:53071644-53071645	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs71335658	chr19:53071650-53071651	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs141543423	chr19:53071651-53071652	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538161060	chr19:53071678-53071679	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116702567	chr19:53071696-53071697	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574575539	chr19:53071711-53071712	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs62117203	chr19:53071731-53071732	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541616251	chr19:53071744-53071745	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs143510397	chr19:53071745-53071746	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs185016210	chr19:53071766-53071767	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs145376201	chr19:53071781-53071782	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs540708334	chr19:53071821-53071822	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs9639	chr19:53071837-53071838	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs565312272	chr19:53071874-53071875	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs9676610	chr19:53071899-53071900	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs112701127	chr19:53072024-53072025	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571327344	chr19:53072034-53072035	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs371289449	chr19:53072081-53072082	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530413182	chr19:53072118-53072119	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548421685	chr19:53072162-53072163	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs35888888	chr19:53072177-53072178	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs60617297	chr19:53072205-53072206	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs374655182	chr19:53072206-53072207	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs570452177	chr19:53072322-53072323	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs113349468	chr19:53072426-53072427	Weak transcription Active TSS ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs190995331	chr19:53072451-53072452	Weak transcription Active TSS ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs146976286	chr19:53072466-53072467	Weak transcription Active TSS ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535743226	chr19:53072496-53072497	Weak transcription Active TSS ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558781249	chr19:53072547-53072548	Weak transcription Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs371308739	chr19:53072551-53072552	Weak transcription Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs572253794	chr19:53072572-53072573	Weak transcription Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs183962895	chr19:53072611-53072612	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs138036792	chr19:53072619-53072620	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Cancer	20164920	CNVD
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD

Chromatin state (count:2423 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53051600-53073200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr19:53058400-53072600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr19:53058600-53072800	Weak transcription	Fetal Brain Male	brain
4	chr19:53059200-53073000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr19:53060800-53072800	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr19:53061000-53072600	Weak transcription	Fetal Brain Female	brain
7	chr19:53061000-53072800	Weak transcription	Brain Angular Gyrus	brain
8	chr19:53061200-53072600	Weak transcription	Fetal Heart	heart
9	chr19:53061200-53072800	Weak transcription	Brain Anterior Caudate	brain
10	chr19:53061400-53072600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr19:53062000-53077800	ZNF genes & repeats	Liver	Liver
12	chr19:53062200-53072800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr19:53062400-53072800	Weak transcription	Fetal Kidney	kidney
14	chr19:53062400-53073000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr19:53063000-53072800	Weak transcription	Right Ventricle	heart
16	chr19:53063600-53073000	Weak transcription	HUVEC	blood vessel
17	chr19:53064000-53072800	Weak transcription	Brain Germinal Matrix	brain
18	chr19:53064200-53072200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr19:53064200-53073000	Weak transcription	Psoas Muscle	Psoas
20	chr19:53064400-53072400	Weak transcription	Osteobl	bone
21	chr19:53065400-53072800	Weak transcription	Brain Hippocampus Middle	brain
22	chr19:53065400-53073000	Weak transcription	Brain Substantia Nigra	brain
23	chr19:53066400-53072800	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr19:53067400-53072600	Weak transcription	Fetal Lung	lung
25	chr19:53067600-53072600	Weak transcription	Fetal Muscle Leg	muscle
26	chr19:53067600-53072800	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr19:53067800-53072800	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr19:53067800-53072800	Weak transcription	HSMM	muscle
29	chr19:53068000-53072000	Weak transcription	Dnd41	blood
30	chr19:53068000-53072600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr19:53068000-53072600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr19:53068000-53072800	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr19:53068000-53072800	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr19:53068000-53073000	Weak transcription	Ovary	ovary
35	chr19:53068200-53072600	Weak transcription	Fetal Stomach	stomach
36	chr19:53068200-53072600	Weak transcription	Stomach Smooth Muscle	stomach
37	chr19:53068600-53072400	Weak transcription	Fetal Muscle Trunk	muscle
38	chr19:53068600-53072800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr19:53068600-53072800	Weak transcription	Left Ventricle	heart
40	chr19:53068800-53072800	Enhancers	Placenta	Placenta
41	chr19:53069000-53073000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr19:53069200-53071200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr19:53069200-53073000	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr19:53069400-53072800	Weak transcription	Adipose Nuclei	Adipose
45	chr19:53070000-53071800	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr19:53070000-53072800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr19:53070200-53072600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr19:53070200-53072800	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr19:53070200-53072800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr19:53070400-53072600	Weak transcription	H1 Cell Line	embryonic stem cell

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