Variant report

Variant	esv20968
Chromosome Location	chr19:53322989-53361358
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:703)
CpG islands
(count:979)
Chromatin interactive
region (count:17)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:703 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

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	BACH1	chr19:53324738-53324945	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr19:53336688-53337003	GM12878	blood:	n/a	chr19:53336917-53336927 chr19:53336913-53336923 chr19:53336723-53336732 chr19:53336898-53336906
4	BATF	chr19:53336721-53337013	GM12878	blood:	n/a	chr19:53336917-53336927 chr19:53336913-53336923 chr19:53336723-53336732 chr19:53336898-53336906
5	BCL11A	chr19:53360679-53360916	GM12878	blood:	n/a	chr19:53360828-53360837
6	BHLHE40	chr19:53324867-53324898	K562	blood:	n/a	n/a
7	BHLHE40	chr19:53360687-53361035	GM12878	blood:	n/a	chr19:53360820-53360836 chr19:53360998-53361014
8	CBX3	chr19:53360595-53361343	K562	blood:	n/a	n/a
9	CBX3	chr19:53324640-53325255	K562	blood:	n/a	n/a
10	CCNT2	chr19:53361004-53361276	K562	blood:	n/a	n/a
11	CEBPB	chr19:53345865-53346133	HepG2	liver:	n/a	chr19:53346019-53346030
12	CEBPB	chr19:53329012-53329572	K562	blood:	n/a	n/a
13	CEBPB	chr19:53328995-53329384	K562	blood:	n/a	n/a
14	CEBPB	chr19:53329098-53329325	K562	blood:	n/a	n/a
15	CEBPB	chr19:53329092-53329271	MCF-7	breast:	n/a	n/a
16	CEBPB	chr19:53345961-53346152	A549	lung:	n/a	chr19:53346019-53346030
17	CEBPB	chr19:53345864-53346169	IMR90	lung:	n/a	chr19:53346019-53346030
18	CEBPB	chr19:53329163-53329370	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPD	chr19:53329085-53329417	K562	blood:	n/a	n/a
20	CEBPD	chr19:53360693-53360926	HepG2	liver:	n/a	n/a
21	CHD2	chr19:53360719-53360909	K562	blood:	n/a	n/a
22	CHD2	chr19:53360829-53361263	GM12878	blood:	n/a	n/a
23	CTCF	chr19:53361040-53361190	GM12873	blood:	n/a	n/a
24	CTCF	chr19:53360835-53361022	GM19238	blood:	n/a	chr19:53360990-53361003
25	CTCF	chr19:53361040-53361190	GM12865	blood:	n/a	n/a
26	CTCF	chr19:53360960-53361110	GM12869	blood:	n/a	chr19:53360990-53361003
27	CTCF	chr19:53324940-53325090	AG04449	skin:	n/a	chr19:53325004-53325017
28	CTCF	chr19:53360774-53361155	K562	blood:	n/a	chr19:53360990-53361003
29	CTCF	chr19:53324980-53325130	SK-N-SH_RA	brain:	n/a	chr19:53325004-53325017
30	CTCF	chr19:53325872-53325890	LNCaP	prostate:	n/a	n/a
31	CTCF	chr19:53324459-53324474	GM19238	blood:	n/a	n/a
32	CTCF	chr19:53324938-53325019	MCF-7	breast:	n/a	chr19:53325004-53325017
33	CTCF	chr19:53361000-53361150	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr19:53360980-53361130	HCT-116	colon:	n/a	chr19:53360990-53361003
35	CTCF	chr19:53324761-53325046	K562	blood:	n/a	chr19:53325004-53325017
36	CTCF	chr19:53343023-53343127	GM20000	blood:	n/a	n/a
37	CTCF	chr19:53352092-53352147	GM13976	blood:	n/a	n/a
38	CTCF	chr19:53361000-53361150	GM12870	blood:	n/a	n/a
39	CTCF	chr19:53360887-53361019	GM12891	blood:	n/a	chr19:53360990-53361003
40	CTCF	chr19:53361020-53361170	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr19:53324895-53325063	K562	blood:	n/a	chr19:53325004-53325017
42	CTCF	chr19:53324980-53325130	SAEC	small airway:	n/a	chr19:53325004-53325017
43	CTCF	chr19:53324899-53325011	GM13976	blood:	n/a	n/a
44	CTCF	chr19:53360859-53361107	Lung_OC	lung:	n/a	chr19:53360990-53361003
45	CTCF	chr19:53324779-53325090	Spleen_OC	spleen:	n/a	chr19:53325004-53325017
46	CTCF	chr19:53361020-53361170	GM12871	blood:	n/a	n/a
47	CTCF	chr19:53361020-53361170	K562	blood:	n/a	n/a
48	CTCF	chr19:53360920-53361070	HMEC	breast:	n/a	chr19:53360990-53361003
49	CTCF	chr19:53360980-53361130	HCM	heart:	n/a	chr19:53360990-53361003
50	CTCF	chr19:53360940-53361025	GM12892	blood:	n/a	chr19:53360990-53361003

(count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53360728-53360778	IMR90	lung:	fetal
2	chr19:53360213-53360263	Hela-S3	cervix:	n/a
3	chr19:53359733-53359783	HEEpiC	esophagus:	n/a
4	chr19:53360728-53360778	IMR90	lung:	fetal
5	chr19:53360213-53360263	Hela-S3	cervix:	n/a
6	chr19:53359733-53359783	HEEpiC	esophagus:	n/a
7	chr19:53361164-53361214	ovcar-3	ovarian:	n/a
8	chr19:53325080-53325130	GM12878	blood:	n/a
9	chr19:53360728-53360778	MCF10A-Er-Src	breast:	n/a
10	chr19:53325080-53325130	NB4	blood:	n/a
11	chr19:53324198-53324248	GM12891	blood:	n/a
12	chr19:53324732-53324782	PFSK-1	brain:	n/a
13	chr19:53359733-53359783	NHDF-neo	bronchial:	n/a
14	chr19:53361066-53361116	RPTEC	kidney:	n/a
15	chr19:53326091-53326141	AG10803	skin:	n/a
16	chr19:53326091-53326141	AG04449	skin:	fetal
17	chr19:53344366-53344416	MCF-7	breast:	n/a
18	chr19:53324198-53324248	HL-60	blood:	n/a
19	chr19:53325080-53325130	RPTEC	kidney:	n/a
20	chr19:53325104-53325154	RPTEC	kidney:	n/a
21	chr19:53361066-53361116	PFSK-1	brain:	n/a
22	chr19:53360728-53360778	PFSK-1	brain:	n/a
23	chr19:53325913-53325963	ECC-1	luminal epithelium:	n/a
24	chr19:53324278-53324328	NHBE	bronchial:	n/a
25	chr19:53344366-53344416	CMK	blood:	n/a
26	chr19:53361164-53361214	SK-N-SH_RA	brain:	n/a
27	chr19:53359733-53359783	GM12892	blood:	n/a
28	chr19:53324198-53324248	SK-N-MC	brain:	n/a
29	chr19:53361164-53361214	AG09319	gingival:	n/a
30	chr19:53326091-53326141	GM12891	blood:	n/a
31	chr19:53324278-53324328	BE2_C	brain:	n/a
32	chr19:53357134-53357184	ProgFib	skin:	n/a
33	chr19:53360213-53360263	GM06990	blood:	n/a
34	chr19:53359733-53359783	GM12878	blood:	n/a
35	chr19:53361164-53361214	ProgFib	skin:	n/a
36	chr19:53357134-53357184	AG04449	skin:	fetal
37	chr19:53325080-53325130	K562	blood:	n/a
38	chr19:53360213-53360263	IMR90	lung:	fetal
39	chr19:53326091-53326141	HepG2	liver:	n/a
40	chr19:53325913-53325963	CMK	blood:	n/a
41	chr19:53344366-53344416	U87	brain:	n/a
42	chr19:53324732-53324782	HCF	heart:	n/a
43	chr19:53359733-53359783	U87	brain:	n/a
44	chr19:53361164-53361214	PANC-1	pancreas:	n/a
45	chr19:53326219-53326269	MCF10A-Er-Src	breast:	n/a
46	chr19:53325080-53325130	HNPCEpiC	eye:	n/a
47	chr19:53360213-53360263	BE2_C	brain:	n/a
48	chr19:53361164-53361214	HEEpiC	esophagus:	n/a
49	chr19:53325913-53325963	HRPEpiC	eye:	n/a
50	chr19:53361164-53361214	U87	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:53322321..53326212-chr19:53359321..53361245,3	K562	blood:
2	chr19:53338835..53341536-chr19:53343202..53344870,2	K562	blood:
3	chr19:53322321..53326212-chr19:53359240..53361245,4	K562	blood:
4	chr19:53324392..53324894-chr19:53934932..53935516,2	MCF-7	breast:
5	chr19:53193532..53195862-chr19:53359115..53361191,3	K562	blood:
6	chr19:53324497..53325251-chr19:53360339..53360857,4	MCF-7	breast:
7	chr19:53359564..53361265-chr19:53424872..53426783,2	MCF-7	breast:
8	chr19:53335113..53339470-chr19:53340101..53344099,5	K562	blood:
9	chr19:53359757..53362433-chr19:53464752..53467349,2	MCF-7	breast:
10	chr19:53357060..53358583-chr19:53400479..53402706,2	MCF-7	breast:
11	chr19:53324497..53325251-chr19:53360339..53360857,4	MCF-7	breast:
12	chr19:53338835..53341536-chr19:53343202..53344870,2	K562	blood:
13	chr19:53339213..53341134-chr20:46203984..46206130,2	MCF-7	breast:
14	chr19:53322321..53326212-chr19:53359321..53361245,3	K562	blood:
15	chr19:53322321..53326212-chr19:53359240..53361245,4	K562	blood:
16	chr19:53335113..53339470-chr19:53340101..53344099,5	K562	blood:
17	chr19:53324563..53325122-chr19:53360322..53360852,2	NB4	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF468-1	chr19:53357511-53357598	NR_102301
2	lnc-ZNF468-1	chr19:53360825-53360902	NR_102301
3	lnc-ZNF468-1	chr19:53360825-53360902	NR_102300
4	lnc-ZNF468-1	chr19:53357125-53357379	NR_102301
5	lnc-ZNF468-1	chr19:53352340-53352466	NR_102300
6	lnc-ZNF468-1	chr19:53352340-53352466	NR_102301
7	lnc-ZNF468-1	chr19:53357511-53357598	NR_102300
8	lnc-ZNF468-1	chr19:53357511-53357598	NR_102299
9	lnc-ZNF468-3	chr19:53324839-53324886	NONHSAT067588
10	lnc-ZNF468-1	chr19:53360825-53360902	NR_102299
11	lnc-ZNF468-1	chr19:53341785-53345404	NR_102301
12	lnc-ZNF468-1	chr19:53357125-53357360	NR_102300
13	lnc-ZNF468-1	chr19:53348432-53348549	NR_102299
14	lnc-ZNF468-1	chr19:53352340-53352466	NR_102299
15	lnc-ZNF468-1	chr19:53348432-53348549	NR_102300
16	lnc-ZNF468-1	chr19:53341785-53345404	NR_102300
17	lnc-ZNF468-1	chr19:53341785-53345404	NR_102299
18	lnc-ZNF701-2	chr19:53342913-53343520	NONHSAT067585
19	lnc-ZNF468-1	chr19:53357125-53357379	NR_102299

No data

Variant related genes	Relation type
ZNF28	TF binding region
ZNF468	TF binding region
ZNF28	CpG island
ZNF468	CpG island
ENSG00000198538	chromatin interactions
ENSG00000213793	chromatin interactions
ENSG00000241015	chromatin interactions
ENSG00000180257	chromatin interactions
ENSG00000167766	chromatin interactions
ENSG00000182986	chromatin interactions
ENSG00000221874	chromatin interactions
ENSG00000269646	chromatin interactions
ENSG00000160336	chromatin interactions
ENSG00000204604	chromatin interactions

Extended variants
information (count: 2175 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2175 , 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	rs112181154	chr19:53322992-53322993	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs13343698	chr19:53323004-53323005	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs199560504	chr19:53323043-53323044	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs568687929	chr19:53323131-53323132	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs535276767	chr19:53323145-53323146	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs139879581	chr19:53323153-53323154	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs74200825	chr19:53323191-53323192	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs547619315	chr19:53323212-53323213	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs184085081	chr19:53323227-53323228	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs539737898	chr19:53323244-53323245	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs188425094	chr19:53323262-53323263	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs71183842	chr19:53323381-53323382	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs376079009	chr19:53323398-53323399	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs537072363	chr19:53323434-53323435	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs555135590	chr19:53323518-53323519	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs573690212	chr19:53323578-53323579	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs541971752	chr19:53323650-53323651	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs553941425	chr19:53323652-53323653	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs572343683	chr19:53323666-53323667	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs74176185	chr19:53323683-53323684	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs115008835	chr19:53323688-53323689	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs12978148	chr19:53323689-53323690	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs180935523	chr19:53323713-53323714	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs374936490	chr19:53323738-53323739	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs558660801	chr19:53323787-53323788	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs543810962	chr19:53323797-53323798	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs2910627	chr19:53323802-53323803	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs185851903	chr19:53323808-53323809	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs148996465	chr19:53323834-53323835	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs529387008	chr19:53323836-53323837	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs12983993	chr19:53323888-53323889	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs12984218	chr19:53323891-53323892	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs12984004	chr19:53323898-53323899	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs551673221	chr19:53323899-53323900	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs12984230	chr19:53323904-53323905	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs376442331	chr19:53323916-53323917	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs112750257	chr19:53323921-53323922	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs192317519	chr19:53323927-53323928	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs536602956	chr19:53323942-53323943	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs370570365	chr19:53323961-53323962	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs548965404	chr19:53323976-53323977	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs375140342	chr19:53324076-53324077	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs2910626	chr19:53324152-53324153	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs181936280	chr19:53324189-53324190	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs2910625	chr19:53324198-53324199	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs552681933	chr19:53324201-53324202	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs12985019	chr19:53324217-53324218	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs562780928	chr19:53324218-53324219	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs12985688	chr19:53324236-53324237	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs12985295	chr19:53324256-53324257	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:68)

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
Adrenocortical carcinoma	18281524	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1386 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53296200-53324000	Weak transcription	Fetal Brain Male	brain
2	chr19:53306000-53324000	Weak transcription	Colon Smooth Muscle	Colon
3	chr19:53306600-53324000	Weak transcription	Psoas Muscle	Psoas
4	chr19:53308200-53324000	Weak transcription	Fetal Kidney	kidney
5	chr19:53311000-53323600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr19:53311400-53323600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr19:53311400-53324000	Weak transcription	NHDF-Ad	bronchial
8	chr19:53313600-53324000	Weak transcription	Fetal Lung	lung
9	chr19:53313600-53324000	Weak transcription	Right Ventricle	heart
10	chr19:53313600-53324200	Weak transcription	Brain Substantia Nigra	brain
11	chr19:53313800-53323600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr19:53313800-53323800	Weak transcription	Stomach Mucosa	stomach
13	chr19:53313800-53324000	Weak transcription	Brain Angular Gyrus	brain
14	chr19:53313800-53324000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr19:53313800-53324000	Weak transcription	HSMM	muscle
16	chr19:53313800-53324000	Weak transcription	NHLF	lung
17	chr19:53313800-53324200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr19:53314000-53323600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr19:53314000-53323600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr19:53314000-53323600	Weak transcription	K562	blood
21	chr19:53314000-53323800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr19:53314000-53323800	Weak transcription	Brain Germinal Matrix	brain
23	chr19:53314000-53323800	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr19:53314000-53323800	Weak transcription	Small Intestine	intestine
25	chr19:53314000-53324000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr19:53314000-53324000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr19:53314000-53324000	Weak transcription	Fetal Brain Female	brain
28	chr19:53314000-53324200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr19:53314000-53324200	Weak transcription	Aorta	Aorta
30	chr19:53319200-53324000	Weak transcription	Osteobl	bone
31	chr19:53319600-53323600	Weak transcription	Gastric	stomach
32	chr19:53319600-53324200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr19:53320400-53323800	Weak transcription	HUVEC	blood vessel
34	chr19:53320600-53323800	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr19:53321000-53323600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr19:53321000-53323800	Weak transcription	Primary B cells from peripheral blood	blood
37	chr19:53321200-53323600	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr19:53321200-53323600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr19:53321200-53323600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr19:53321200-53323600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr19:53321200-53323600	Weak transcription	Primary hematopoietic stem cells	blood
42	chr19:53321200-53323600	Weak transcription	Placenta	Placenta
43	chr19:53321200-53323600	Weak transcription	Thymus	Thymus
44	chr19:53321200-53323800	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr19:53321200-53323800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr19:53321200-53323800	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr19:53321200-53323800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr19:53321200-53323800	Weak transcription	Adipose Nuclei	Adipose
49	chr19:53321200-53323800	Weak transcription	Brain Hippocampus Middle	brain
50	chr19:53321200-53323800	Weak transcription	Rectal Mucosa Donor 31	rectum

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