Variant report

Variant	nsv1066098
Chromosome Location	chr19:53357173-53386857
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:476)
CpG islands
(count:610)
Chromatin interactive
region (count:10)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:476 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr19:53360719-53361014	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr19:53362420-53362624	GM12878	blood:	n/a	n/a
3	BCL11A	chr19:53360679-53360916	GM12878	blood:	n/a	chr19:53360828-53360837
4	BHLHE40	chr19:53376302-53376339	K562	blood:	n/a	n/a
5	BHLHE40	chr19:53360687-53361035	GM12878	blood:	n/a	chr19:53360820-53360836 chr19:53360998-53361014
6	CBX3	chr19:53383913-53384365	K562	blood:	n/a	n/a
7	CBX3	chr19:53376216-53376620	K562	blood:	n/a	n/a
8	CBX3	chr19:53360595-53361343	K562	blood:	n/a	n/a
9	CCNT2	chr19:53361004-53361276	K562	blood:	n/a	n/a
10	CEBPB	chr19:53363042-53363321	K562	blood:	n/a	n/a
11	CEBPB	chr19:53363838-53364091	IMR90	lung:	n/a	n/a
12	CEBPB	chr19:53363179-53363319	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPD	chr19:53376161-53376655	K562	blood:	n/a	n/a
14	CEBPD	chr19:53360693-53360926	HepG2	liver:	n/a	n/a
15	CHD2	chr19:53360829-53361263	GM12878	blood:	n/a	n/a
16	CHD2	chr19:53360719-53360909	K562	blood:	n/a	n/a
17	CTCF	chr19:53360960-53361110	GM12869	blood:	n/a	chr19:53360990-53361003
18	CTCF	chr19:53361040-53361190	GM12873	blood:	n/a	n/a
19	CTCF	chr19:53360771-53361087	Spleen_OC	spleen:	n/a	chr19:53360990-53361003
20	CTCF	chr19:53361020-53361170	HMF	breast:	n/a	n/a
21	CTCF	chr19:53361000-53361150	HVMF	connective:	n/a	n/a
22	CTCF	chr19:53360794-53360918	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr19:53360746-53361196	K562	blood:	n/a	chr19:53360990-53361003
24	CTCF	chr19:53360924-53361043	Kidney_OC	kidney:	n/a	chr19:53360990-53361003
25	CTCF	chr19:53361020-53361170	AG10803	skin:	n/a	n/a
26	CTCF	chr19:53360835-53361022	GM19238	blood:	n/a	chr19:53360990-53361003
27	CTCF	chr19:53360843-53361097	K562	blood:	n/a	chr19:53360990-53361003
28	CTCF	chr19:53361000-53361150	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr19:53361000-53361150	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr19:53360887-53361019	GM12891	blood:	n/a	chr19:53360990-53361003
31	CTCF	chr19:53360901-53361081	K562	blood:	n/a	chr19:53360990-53361003
32	CTCF	chr19:53361000-53361150	HRPEpiC	eye:	n/a	n/a
33	CTCF	chr19:53361020-53361170	HRE	kidney:	n/a	n/a
34	CTCF	chr19:53360980-53361130	HMEC	breast:	n/a	chr19:53360990-53361003
35	CTCF	chr19:53360980-53361130	HCT-116	colon:	n/a	chr19:53360990-53361003
36	CTCF	chr19:53360980-53361130	BE2_C	brain:	n/a	chr19:53360990-53361003
37	CTCF	chr19:53360920-53361070	HMEC	breast:	n/a	chr19:53360990-53361003
38	CTCF	chr19:53360855-53360873	NHEK	skin:	n/a	n/a
39	CTCF	chr19:53384676-53384683	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr19:53360940-53361025	GM12892	blood:	n/a	chr19:53360990-53361003
41	CTCF	chr19:53361000-53361150	GM12870	blood:	n/a	n/a
42	CTCF	chr19:53360774-53361155	K562	blood:	n/a	chr19:53360990-53361003
43	CTCF	chr19:53360987-53361008	GM19239	blood:	n/a	chr19:53360990-53361003
44	CTCF	chr19:53361020-53361170	HCM	heart:	n/a	n/a
45	CTCF	chr19:53360980-53361130	SK-N-SH_RA	brain:	n/a	chr19:53360990-53361003
46	CTCF	chr19:53361020-53361170	GM12875	blood:	n/a	n/a
47	CTCF	chr19:53382813-53382847	GM13977	blood:	n/a	n/a
48	CTCF	chr19:53360919-53361045	GM19240	blood:	n/a	chr19:53360990-53361003
49	CTCF	chr19:53360859-53361107	Lung_OC	lung:	n/a	chr19:53360990-53361003
50	CTCF	chr19:53361060-53361210	HCPEpiC	choroid plexus:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53357134-53357184	HCF	heart:	n/a
2	chr19:53357134-53357184	HRCEpiC	kidney:	n/a
3	chr19:53363482-53363532	SK-N-SH_RA	brain:	n/a
4	chr19:53383549-53383599	MCF10A-Er-Src	breast:	n/a
5	chr19:53361164-53361214	PrEC	prostate:	n/a
6	chr19:53360728-53360778	IMR90	lung:	fetal
7	chr19:53361448-53361498	GM12878	blood:	n/a
8	chr19:53362925-53362975	ProgFib	skin:	n/a
9	chr19:53362925-53362975	AG09309	skin:	n/a
10	chr19:53360213-53360263	GM12891	blood:	n/a
11	chr19:53361164-53361214	H1-hESC	embryonic stem cell:	embryo
12	chr19:53362925-53362975	AG10803	skin:	n/a
13	chr19:53361066-53361116	NH-A	brain:	n/a
14	chr19:53360728-53360778	HepG2	liver:	n/a
15	chr19:53361066-53361116	AG04450	lung:	fetal
16	chr19:53360728-53360778	CMK	blood:	n/a
17	chr19:53361164-53361214	BJ	skin:	n/a
18	chr19:53363482-53363532	PrEC	prostate:	n/a
19	chr19:53357134-53357184	HEEpiC	esophagus:	n/a
20	chr19:53362925-53362975	Hela-S3	cervix:	n/a
21	chr19:53360213-53360263	GM06990	blood:	n/a
22	chr19:53361066-53361116	CMK	blood:	n/a
23	chr19:53357134-53357184	HMEC	breast:	n/a
24	chr19:53359733-53359783	HRE	kidney:	n/a
25	chr19:53383549-53383599	AG04449	skin:	fetal
26	chr19:53360728-53360778	AoSMC	blood vessel:	n/a
27	chr19:53357134-53357184	AG09319	gingival:	n/a
28	chr19:53361066-53361116	ovcar-3	ovarian:	n/a
29	chr19:53359733-53359783	ProgFib	skin:	n/a
30	chr19:53361066-53361116	HMEC	breast:	n/a
31	chr19:53361164-53361214	NHDF-neo	bronchial:	n/a
32	chr19:53362925-53362975	HEEpiC	esophagus:	n/a
33	chr19:53363482-53363532	HIPEpiC	eye:	n/a
34	chr19:53361448-53361498	GM12891	blood:	n/a
35	chr19:53361448-53361498	BE2_C	brain:	n/a
36	chr19:53361164-53361214	MCF-7	breast:	n/a
37	chr19:53361448-53361498	NH-A	brain:	n/a
38	chr19:53361164-53361214	HCPEpiC	choroid plexus:	n/a
39	chr19:53383549-53383599	BE2_C	brain:	n/a
40	chr19:53361448-53361498	IMR90	lung:	fetal
41	chr19:53361448-53361498	AG09319	gingival:	n/a
42	chr19:53362925-53362975	SKMC	muscle:	n/a
43	chr19:53363482-53363532	HEEpiC	esophagus:	n/a
44	chr19:53361448-53361498	HCPEpiC	choroid plexus:	n/a
45	chr19:53363482-53363532	AG04449	skin:	fetal
46	chr19:53357134-53357184	SK-N-SH_RA	brain:	n/a
47	chr19:53361448-53361498	NB4	blood:	n/a
48	chr19:53361448-53361498	NT2-D1	testis:	n/a
49	chr19:53383549-53383599	HPAEpiC	pulmonary alveolar:	n/a
50	chr19:53359733-53359783	HUVEC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:53324563..53325122-chr19:53360322..53360852,2	NB4	blood:
2	chr19:53322321..53326212-chr19:53359240..53361245,4	K562	blood:
3	chr19:53322321..53326212-chr19:53359321..53361245,3	K562	blood:
4	chr19:53380234..53382987-chr19:53399088..53400987,2	K562	blood:
5	chr19:53359757..53362433-chr19:53464752..53467349,2	MCF-7	breast:
6	chr19:53193532..53195862-chr19:53359115..53361191,3	K562	blood:
7	chr19:53359564..53361265-chr19:53424872..53426783,2	MCF-7	breast:
8	chr19:53377771..53379611-chr19:53399736..53401870,2	K562	blood:
9	chr19:53324497..53325251-chr19:53360339..53360857,4	MCF-7	breast:
10	chr19:53357060..53358583-chr19:53400479..53402706,2	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF468-1	chr19:53357125-53357379	NR_102299
2	lnc-ZNF468-1	chr19:53360825-53360902	NR_102300
3	lnc-ZNF468-1	chr19:53357511-53357598	NR_102300
4	lnc-ZNF468-2	chr19:53365060-53366119	NONHSAT067590
5	lnc-ZNF468-1	chr19:53357125-53357379	NR_102301
6	lnc-ZNF320-3	chr19:53382704-53382886	NONHSAT067592
7	lnc-ZNF320-3	chr19:53377245-53377325	NONHSAT067591
8	lnc-ZNF468-1	chr19:53357125-53357360	NR_102300
9	lnc-ZNF320-3	chr19:53367175-53367412	NONHSAT067592
10	lnc-ZNF320-3	chr19:53377411-53377490	NONHSAT067591
11	lnc-ZNF468-1	chr19:53357511-53357598	NR_102299
12	lnc-ZNF320-3	chr19:53377245-53377325	NONHSAT067592
13	lnc-ZNF320-1	chr19:53379431-53379838	NONHSAT067593
14	lnc-ZNF320-3	chr19:53367043-53367412	NONHSAT067591
15	lnc-ZNF468-1	chr19:53360825-53360902	NR_102301
16	lnc-ZNF468-1	chr19:53357511-53357598	NR_102301
17	lnc-ZNF468-1	chr19:53360825-53360902	NR_102299

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ZNF320	hsa-miR-192-5p	chr19:53381440-53381461

Variant related genes	Relation type
ENSG00000268225	TF binding region
ZNF320	TF binding region
ZNF28	TF binding region
ZNF468	TF binding region
ENSG00000268225	CpG island
ZNF320	CpG island
ZNF28	CpG island
ZNF468	CpG island
ENSG00000269646	chromatin interactions
ENSG00000221874	chromatin interactions
ENSG00000213793	chromatin interactions
ENSG00000182986	chromatin interactions
ENSG00000198538	chromatin interactions
ENSG00000180257	chromatin interactions
ENSG00000167766	chromatin interactions

Extended variants
information (count: 1520 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1520 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376546196	chr19:53357188-53357189	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs58476100	chr19:53357192-53357193	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs557229689	chr19:53357194-53357195	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs191190481	chr19:53357200-53357201	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs10426239	chr19:53357211-53357212	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs539225979	chr19:53357215-53357216	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs150181302	chr19:53357219-53357220	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs10425068	chr19:53357239-53357240	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs530144638	chr19:53357254-53357255	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs570242226	chr19:53357279-53357280	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs183357663	chr19:53357300-53357301	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs201787090	chr19:53357306-53357307	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs371900076	chr19:53357307-53357308	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs556023879	chr19:53357329-53357330	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs567907549	chr19:53357337-53357338	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs377509244	chr19:53357348-53357349	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs534685832	chr19:53357349-53357350	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs187609598	chr19:53357355-53357356	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs577679588	chr19:53357357-53357358	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs545105782	chr19:53357364-53357365	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs556830852	chr19:53357366-53357367	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs190563992	chr19:53357382-53357383	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs572001721	chr19:53357396-53357397	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs183508346	chr19:53357403-53357404	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs561219246	chr19:53357439-53357440	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs115993467	chr19:53357478-53357479	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs200166570	chr19:53357481-53357482	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs376068805	chr19:53357486-53357487	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs564889711	chr19:53357490-53357491	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs201728832	chr19:53357498-53357499	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs201215683	chr19:53357499-53357500	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs371645428	chr19:53357502-53357503	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs376389706	chr19:53357526-53357527	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs550655954	chr19:53357537-53357538	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs201700471	chr19:53357567-53357568	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs188060532	chr19:53357572-53357573	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs142006371	chr19:53357580-53357581	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs146326376	chr19:53357582-53357583	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs567588556	chr19:53357601-53357602	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs534998710	chr19:53357625-53357626	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs552906594	chr19:53357626-53357627	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs192816485	chr19:53357640-53357641	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs184391955	chr19:53357695-53357696	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs112282343	chr19:53357709-53357710	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs186631978	chr19:53357710-53357711	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs575678134	chr19:53357737-53357738	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs73069445	chr19:53357748-53357749	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs138367230	chr19:53357760-53357761	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs8113354	chr19:53357764-53357765	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs573146640	chr19:53357769-53357770	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:924 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53339000-53357600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr19:53339000-53357800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
3	chr19:53339000-53359200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
4	chr19:53340800-53357400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr19:53340800-53357800	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
6	chr19:53342200-53357600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr19:53342400-53357800	ZNF genes & repeats	Liver	Liver
8	chr19:53343200-53359200	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
9	chr19:53344000-53358000	ZNF genes & repeats	Lung	lung
10	chr19:53345400-53360200	Weak transcription	Fetal Heart	heart
11	chr19:53345400-53360200	Weak transcription	Hela-S3	cervix
12	chr19:53345800-53360400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr19:53346200-53357800	Strong transcription	HUES48 Cell Line	embryonic stem cell
14	chr19:53346200-53357800	Strong transcription	Fetal Stomach	stomach
15	chr19:53346400-53357800	Strong transcription	Fetal Muscle Leg	muscle
16	chr19:53346400-53360400	Weak transcription	Fetal Brain Male	brain
17	chr19:53347600-53357600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
18	chr19:53347600-53360000	Weak transcription	HMEC	breast
19	chr19:53347800-53357600	Strong transcription	Stomach Smooth Muscle	stomach
20	chr19:53348000-53359200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr19:53348000-53359200	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr19:53348000-53360200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr19:53348200-53357600	Strong transcription	Adipose Nuclei	Adipose
24	chr19:53348200-53358200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr19:53348600-53357600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr19:53348600-53358800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr19:53348600-53360200	Weak transcription	Stomach Mucosa	stomach
28	chr19:53349200-53360200	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr19:53349600-53357600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr19:53349800-53360000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr19:53349800-53360000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr19:53350000-53357800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
33	chr19:53350200-53359200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr19:53350600-53357400	Strong transcription	Small Intestine	intestine
35	chr19:53350800-53358000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr19:53351000-53357400	Strong transcription	Muscle Satellite Cultured Cells	--
37	chr19:53351000-53357800	ZNF genes & repeats	Fetal Intestine Small	intestine
38	chr19:53351200-53358400	Strong transcription	Dnd41	blood
39	chr19:53351600-53357600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr19:53351600-53357600	Strong transcription	Primary T helper cells PMA-I stimulated	--
41	chr19:53351600-53357800	Strong transcription	Duodenum Smooth Muscle	Duodenum
42	chr19:53351600-53358000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr19:53351600-53360200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr19:53351800-53357600	Strong transcription	Primary B cells from peripheral blood	blood
45	chr19:53351800-53357800	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr19:53352000-53357600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr19:53352000-53357600	Strong transcription	Primary T helper cells fromperipheralblood	blood
48	chr19:53352000-53357800	Strong transcription	Primary T cells fromperipheralblood	blood
49	chr19:53352000-53359200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr19:53352000-53360200	Weak transcription	Brain Substantia Nigra	brain

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