Variant report

Variant	nsv819146
Chromosome Location	chr19:53325029-53363008
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:596)
CpG islands
(count:916)
Chromatin interactive
region (count:16)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:596 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	BATF	chr19:53336721-53337013	GM12878	blood:	n/a	chr19:53336917-53336927 chr19:53336913-53336923 chr19:53336723-53336732 chr19:53336898-53336906
3	BATF	chr19:53336688-53337003	GM12878	blood:	n/a	chr19:53336917-53336927 chr19:53336913-53336923 chr19:53336723-53336732 chr19:53336898-53336906
4	BCL11A	chr19:53362420-53362624	GM12878	blood:	n/a	n/a
5	BCL11A	chr19:53360679-53360916	GM12878	blood:	n/a	chr19:53360828-53360837
6	BHLHE40	chr19:53360687-53361035	GM12878	blood:	n/a	chr19:53360820-53360836 chr19:53360998-53361014
7	CBX3	chr19:53360595-53361343	K562	blood:	n/a	n/a
8	CBX3	chr19:53324640-53325255	K562	blood:	n/a	n/a
9	CCNT2	chr19:53361004-53361276	K562	blood:	n/a	n/a
10	CEBPB	chr19:53328995-53329384	K562	blood:	n/a	n/a
11	CEBPB	chr19:53329012-53329572	K562	blood:	n/a	n/a
12	CEBPB	chr19:53345865-53346133	HepG2	liver:	n/a	chr19:53346019-53346030
13	CEBPB	chr19:53345961-53346152	A549	lung:	n/a	chr19:53346019-53346030
14	CEBPB	chr19:53329098-53329325	K562	blood:	n/a	n/a
15	CEBPB	chr19:53329163-53329370	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr19:53345864-53346169	IMR90	lung:	n/a	chr19:53346019-53346030
17	CEBPB	chr19:53329092-53329271	MCF-7	breast:	n/a	n/a
18	CEBPD	chr19:53329085-53329417	K562	blood:	n/a	n/a
19	CEBPD	chr19:53360693-53360926	HepG2	liver:	n/a	n/a
20	CHD2	chr19:53360829-53361263	GM12878	blood:	n/a	n/a
21	CHD2	chr19:53360719-53360909	K562	blood:	n/a	n/a
22	CTCF	chr19:53328020-53328170	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr19:53360980-53361130	SK-N-SH_RA	brain:	n/a	chr19:53360990-53361003
24	CTCF	chr19:53343023-53343127	GM20000	blood:	n/a	n/a
25	CTCF	chr19:53324940-53325090	HUVEC	blood vessel:	n/a	chr19:53325004-53325017
26	CTCF	chr19:53325357-53325460	LNCaP	prostate:	n/a	n/a
27	CTCF	chr19:53324785-53325148	K562	blood:	n/a	chr19:53325004-53325017
28	CTCF	chr19:53360774-53361155	K562	blood:	n/a	chr19:53360990-53361003
29	CTCF	chr19:53361000-53361150	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr19:53324761-53325046	K562	blood:	n/a	chr19:53325004-53325017
31	CTCF	chr19:53361040-53361190	GM12873	blood:	n/a	n/a
32	CTCF	chr19:53360980-53361130	HCM	heart:	n/a	chr19:53360990-53361003
33	CTCF	chr19:53360860-53361010	AG04449	skin:	n/a	chr19:53360990-53361003
34	CTCF	chr19:53361000-53361150	GM12870	blood:	n/a	n/a
35	CTCF	chr19:53324891-53325076	GM19238	blood:	n/a	chr19:53325004-53325017
36	CTCF	chr19:53324879-53325039	GM12891	blood:	n/a	chr19:53325004-53325017
37	CTCF	chr19:53360980-53361130	HMEC	breast:	n/a	chr19:53360990-53361003
38	CTCF	chr19:53324960-53325110	HMEC	breast:	n/a	chr19:53325004-53325017
39	CTCF	chr19:53346656-53346707	GM13976	blood:	n/a	n/a
40	CTCF	chr19:53361040-53361190	GM12865	blood:	n/a	n/a
41	CTCF	chr19:53360909-53361007	LNCaP	prostate:	n/a	chr19:53360990-53361003
42	CTCF	chr19:53361020-53361170	K562	blood:	n/a	n/a
43	CTCF	chr19:53360746-53361196	K562	blood:	n/a	chr19:53360990-53361003
44	CTCF	chr19:53361000-53361150	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr19:53324940-53325090	AG04449	skin:	n/a	chr19:53325004-53325017
46	CTCF	chr19:53361060-53361210	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr19:53361020-53361170	AG09309	skin:	n/a	n/a
48	CTCF	chr19:53360887-53361019	GM12891	blood:	n/a	chr19:53360990-53361003
49	CTCF	chr19:53360843-53361069	GM12878	blood:	n/a	chr19:53360990-53361003
50	CTCF	chr19:53361020-53361170	HMF	breast:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53326219-53326269	ProgFib	skin:	n/a
2	chr19:53326219-53326269	ProgFib	skin:	n/a
3	chr19:53359733-53359783	AG09309	skin:	n/a
4	chr19:53342580-53342630	Caco-2	colon:	n/a
5	chr19:53357134-53357184	NH-A	brain:	n/a
6	chr19:53357134-53357184	HRCEpiC	kidney:	n/a
7	chr19:53360213-53360263	BJ	skin:	n/a
8	chr19:53361164-53361214	U87	brain:	n/a
9	chr19:53361448-53361498	AG09309	skin:	n/a
10	chr19:53326091-53326141	PrEC	prostate:	n/a
11	chr19:53325104-53325154	AG09319	gingival:	n/a
12	chr19:53326219-53326269	AG04449	skin:	fetal
13	chr19:53359733-53359783	HCT-116	colon:	n/a
14	chr19:53325104-53325154	BJ	skin:	n/a
15	chr19:53360213-53360263	Hela-S3	cervix:	n/a
16	chr19:53325104-53325154	IMR90	lung:	fetal
17	chr19:53325913-53325963	LNCaP	prostate:	n/a
18	chr19:53325080-53325130	HRCEpiC	kidney:	n/a
19	chr19:53325913-53325963	HAEpiC	amniotic membrane:	n/a
20	chr19:53326091-53326141	HIPEpiC	eye:	n/a
21	chr19:53326091-53326141	NHDF-neo	bronchial:	n/a
22	chr19:53326091-53326141	CMK	blood:	n/a
23	chr19:53325080-53325130	ProgFib	skin:	n/a
24	chr19:53325913-53325963	PFSK-1	brain:	n/a
25	chr19:53326219-53326269	MCF10A-Er-Src	breast:	n/a
26	chr19:53362925-53362975	MCF10A-Er-Src	breast:	n/a
27	chr19:53360728-53360778	HCF	heart:	n/a
28	chr19:53359733-53359783	HEEpiC	esophagus:	n/a
29	chr19:53357134-53357184	HCM	heart:	n/a
30	chr19:53362925-53362975	AG04449	skin:	fetal
31	chr19:53325104-53325154	SK-N-MC	brain:	n/a
32	chr19:53326219-53326269	NHBE	bronchial:	n/a
33	chr19:53360728-53360778	HCM	heart:	n/a
34	chr19:53359733-53359783	SK-N-MC	brain:	n/a
35	chr19:53326219-53326269	HRCEpiC	kidney:	n/a
36	chr19:53325104-53325154	HepG2	liver:	n/a
37	chr19:53357134-53357184	RPTEC	kidney:	n/a
38	chr19:53362925-53362975	U87	brain:	n/a
39	chr19:53360728-53360778	HCT-116	colon:	n/a
40	chr19:53342580-53342630	AoSMC	blood vessel:	n/a
41	chr19:53325104-53325154	A549	lung:	n/a
42	chr19:53326091-53326141	PANC-1	pancreas:	n/a
43	chr19:53361066-53361116	ECC-1	luminal epithelium:	n/a
44	chr19:53326091-53326141	Caco-2	colon:	n/a
45	chr19:53325080-53325130	HPAEpiC	pulmonary alveolar:	n/a
46	chr19:53361164-53361214	NHBE	bronchial:	n/a
47	chr19:53361066-53361116	Jurkat	blood:	n/a
48	chr19:53362925-53362975	T-47D	breast:	n/a
49	chr19:53360213-53360263	H1-hESC	embryonic stem cell:	embryo
50	chr19:53325080-53325130	HNPCEpiC	eye:	n/a

(count:16 , 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	chr19:53339213..53341134-chr20:46203984..46206130,2	MCF-7	breast:
4	chr19:53322321..53326212-chr19:53359240..53361245,4	K562	blood:
5	chr19:53338835..53341536-chr19:53343202..53344870,2	K562	blood:
6	chr19:53357060..53358583-chr19:53400479..53402706,2	MCF-7	breast:
7	chr19:53193532..53195862-chr19:53359115..53361191,3	K562	blood:
8	chr19:53359564..53361265-chr19:53424872..53426783,2	MCF-7	breast:
9	chr19:53324497..53325251-chr19:53360339..53360857,4	MCF-7	breast:
10	chr19:53324497..53325251-chr19:53360339..53360857,4	MCF-7	breast:
11	chr19:53322321..53326212-chr19:53359321..53361245,3	K562	blood:
12	chr19:53335113..53339470-chr19:53340101..53344099,5	K562	blood:
13	chr19:53322321..53326212-chr19:53359321..53361245,3	K562	blood:
14	chr19:53335113..53339470-chr19:53340101..53344099,5	K562	blood:
15	chr19:53359757..53362433-chr19:53464752..53467349,2	MCF-7	breast:
16	chr19:53338835..53341536-chr19:53343202..53344870,2	K562	blood:

(count:18 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 2136 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2136 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372732954	chr19:53325039-53325040	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs183850341	chr19:53325147-53325148	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs201075009	chr19:53325156-53325157	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs28485220	chr19:53325166-53325167	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs575365259	chr19:53325167-53325168	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs28464938	chr19:53325168-53325169	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs541466642	chr19:53325179-53325180	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs112179417	chr19:53325185-53325186	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs72150733	chr19:53325186-53325187	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs560806966	chr19:53325188-53325189	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs74181761	chr19:53325193-53325194	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs398079948	chr19:53325194-53325195	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs113506688	chr19:53325198-53325199	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs540179974	chr19:53325206-53325207	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs34082352	chr19:53325212-53325213	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs564524751	chr19:53325214-53325215	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs527396792	chr19:53325236-53325237	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs532040592	chr19:53325283-53325284	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs550623390	chr19:53325287-53325288	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs552271064	chr19:53325297-53325298	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs145687611	chr19:53325300-53325301	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs560849928	chr19:53325340-53325341	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs386389245	chr19:53325344-53325345	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs58542587	chr19:53325347-53325348	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs148963807	chr19:53325348-53325349	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs12460803	chr19:53325369-53325370	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs531093119	chr19:53325381-53325382	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs113464493	chr19:53325419-53325420	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs145395663	chr19:53325450-53325451	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs532785260	chr19:53325459-53325460	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs534170982	chr19:53325474-53325475	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs567904525	chr19:53325485-53325486	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs59741215	chr19:53325488-53325489	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs535325709	chr19:53325516-53325517	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs369111987	chr19:53325522-53325523	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs553735827	chr19:53325568-53325569	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs571645499	chr19:53325569-53325570	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs144611374	chr19:53325605-53325606	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs557390953	chr19:53325711-53325712	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs4516003	chr19:53325713-53325714	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs373690018	chr19:53325732-53325733	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs77996530	chr19:53325743-53325744	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs562620845	chr19:53325770-53325771	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs147879548	chr19:53325784-53325785	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs187608198	chr19:53325804-53325805	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs192089241	chr19:53325831-53325832	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs184393185	chr19:53325835-53325836	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs117322727	chr19:53325843-53325844	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs569496664	chr19:53325844-53325845	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs75696136	chr19:53325867-53325868	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	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:1165 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53323600-53325200	Active TSS	Primary hematopoietic stem cells short term culture	blood
2	chr19:53323600-53325200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr19:53323600-53325400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr19:53323600-53325400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr19:53323800-53325200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr19:53323800-53325200	Active TSS	Cortex derived primary cultured neurospheres	brain
7	chr19:53323800-53325200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr19:53323800-53325200	Active TSS	Hela-S3	cervix
9	chr19:53323800-53325200	Active TSS	NHEK	skin
10	chr19:53323800-53325400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr19:53323800-53325400	Active TSS	Fetal Intestine Large	intestine
12	chr19:53323800-53325400	Active TSS	GM12878-XiMat	blood
13	chr19:53323800-53325600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr19:53323800-53325600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr19:53323800-53325600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr19:53324000-53325200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr19:53324000-53325200	Active TSS	HUES64 Cell Line	embryonic stem cell
18	chr19:53324000-53325200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr19:53324000-53325200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr19:53324000-53325200	Active TSS	Brain Angular Gyrus	brain
21	chr19:53324000-53325200	Active TSS	Brain Anterior Caudate	brain
22	chr19:53324000-53325200	Active TSS	Brain Germinal Matrix	brain
23	chr19:53324000-53325200	Active TSS	Esophagus	oesophagus
24	chr19:53324000-53325200	Active TSS	Fetal Intestine Small	intestine
25	chr19:53324000-53325200	Active TSS	Pancreas	Pancrea
26	chr19:53324000-53325200	Active TSS	Psoas Muscle	Psoas
27	chr19:53324000-53325200	Active TSS	Rectal Mucosa Donor 29	rectum
28	chr19:53324000-53325200	Active TSS	Rectal Smooth Muscle	rectum
29	chr19:53324000-53325200	Active TSS	Right Ventricle	heart
30	chr19:53324000-53325200	Active TSS	HSMM	muscle
31	chr19:53324000-53325200	Active TSS	HSMMtube	muscle
32	chr19:53324000-53325200	Active TSS	NHLF	lung
33	chr19:53324000-53325400	Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr19:53324000-53325400	Active TSS	Breast Myoepithelial Primary Cells	Breast
35	chr19:53324000-53325400	Active TSS	Primary T cells from cord blood	blood
36	chr19:53324000-53325400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr19:53324000-53325400	Active TSS	Duodenum Mucosa	Duodenum
38	chr19:53324000-53325400	Active TSS	Fetal Brain Female	brain
39	chr19:53324000-53325400	Active TSS	Fetal Kidney	kidney
40	chr19:53324000-53325400	Active TSS	Pancreatic Islets	Pancreatic Islet
41	chr19:53324000-53325400	Active TSS	Ovary	ovary
42	chr19:53324000-53325400	Active TSS	HMEC	breast
43	chr19:53324200-53325200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr19:53324200-53325200	Active TSS	Primary hematopoietic stem cells	blood
45	chr19:53324200-53325200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
46	chr19:53324200-53325200	Active TSS	Primary T helper cells PMA-I stimulated	--
47	chr19:53324200-53325200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
48	chr19:53324200-53325200	Active TSS	Muscle Satellite Cultured Cells	--
49	chr19:53324200-53325200	Active TSS	Aorta	Aorta
50	chr19:53324200-53325200	Active TSS	Duodenum Smooth Muscle	Duodenum

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