Variant report

Variant	nsv525329
Chromosome Location	chr19:53336367-53393087
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:558)
CpG islands
(count:733)
Chromatin interactive
region (count:17)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:558 , 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	chr19:53336688-53337003	GM12878	blood:	n/a	chr19:53336917-53336927 chr19:53336913-53336923 chr19:53336723-53336732 chr19:53336898-53336906
3	BATF	chr19:53336721-53337013	GM12878	blood:	n/a	chr19:53336917-53336927 chr19:53336913-53336923 chr19:53336723-53336732 chr19:53336898-53336906
4	BCL11A	chr19:53360679-53360916	GM12878	blood:	n/a	chr19:53360828-53360837
5	BCL11A	chr19:53362420-53362624	GM12878	blood:	n/a	n/a
6	BHLHE40	chr19:53376302-53376339	K562	blood:	n/a	n/a
7	BHLHE40	chr19:53360687-53361035	GM12878	blood:	n/a	chr19:53360820-53360836 chr19:53360998-53361014
8	CBX3	chr19:53376216-53376620	K562	blood:	n/a	n/a
9	CBX3	chr19:53383913-53384365	K562	blood:	n/a	n/a
10	CBX3	chr19:53360595-53361343	K562	blood:	n/a	n/a
11	CCNT2	chr19:53361004-53361276	K562	blood:	n/a	n/a
12	CEBPB	chr19:53363042-53363321	K562	blood:	n/a	n/a
13	CEBPB	chr19:53345865-53346133	HepG2	liver:	n/a	chr19:53346019-53346030
14	CEBPB	chr19:53345961-53346152	A549	lung:	n/a	chr19:53346019-53346030
15	CEBPB	chr19:53345864-53346169	IMR90	lung:	n/a	chr19:53346019-53346030
16	CEBPB	chr19:53363179-53363319	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr19:53363838-53364091	IMR90	lung:	n/a	n/a
18	CEBPD	chr19:53376161-53376655	K562	blood:	n/a	n/a
19	CEBPD	chr19:53360693-53360926	HepG2	liver:	n/a	n/a
20	CHD2	chr19:53360719-53360909	K562	blood:	n/a	n/a
21	CHD2	chr19:53360829-53361263	GM12878	blood:	n/a	n/a
22	CTCF	chr19:53360960-53361110	GM12869	blood:	n/a	chr19:53360990-53361003
23	CTCF	chr19:53361000-53361150	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr19:53360828-53360986	GM19239	blood:	n/a	n/a
25	CTCF	chr19:53360835-53361022	GM19238	blood:	n/a	chr19:53360990-53361003
26	CTCF	chr19:53360746-53361196	K562	blood:	n/a	chr19:53360990-53361003
27	CTCF	chr19:53361060-53361210	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr19:53360907-53360918	GM19240	blood:	n/a	n/a
29	CTCF	chr19:53361000-53361150	GM12870	blood:	n/a	n/a
30	CTCF	chr19:53360909-53361007	LNCaP	prostate:	n/a	chr19:53360990-53361003
31	CTCF	chr19:53361000-53361150	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr19:53361020-53361170	HRE	kidney:	n/a	n/a
33	CTCF	chr19:53360843-53361097	K562	blood:	n/a	chr19:53360990-53361003
34	CTCF	chr19:53361020-53361170	AG09309	skin:	n/a	n/a
35	CTCF	chr19:53360901-53361081	K562	blood:	n/a	chr19:53360990-53361003
36	CTCF	chr19:53361040-53361190	GM12865	blood:	n/a	n/a
37	CTCF	chr19:53360980-53361130	HCM	heart:	n/a	chr19:53360990-53361003
38	CTCF	chr19:53360980-53361130	HMEC	breast:	n/a	chr19:53360990-53361003
39	CTCF	chr19:53361000-53361150	GM12865	blood:	n/a	n/a
40	CTCF	chr19:53361040-53361190	GM12873	blood:	n/a	n/a
41	CTCF	chr19:53391416-53391462	GM20000	blood:	n/a	n/a
42	CTCF	chr19:53360774-53361155	K562	blood:	n/a	chr19:53360990-53361003
43	CTCF	chr19:53360927-53361017	Hela-S3	cervix:	n/a	chr19:53360990-53361003
44	CTCF	chr19:53343023-53343127	GM20000	blood:	n/a	n/a
45	CTCF	chr19:53361020-53361170	K562	blood:	n/a	n/a
46	CTCF	chr19:53361020-53361170	BJ	skin:	n/a	n/a
47	CTCF	chr19:53360859-53361107	Lung_OC	lung:	n/a	chr19:53360990-53361003
48	CTCF	chr19:53360771-53361087	Spleen_OC	spleen:	n/a	chr19:53360990-53361003
49	CTCF	chr19:53361020-53361170	HMF	breast:	n/a	n/a
50	CTCF	chr19:53361020-53361170	HCM	heart:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53359733-53359783	HUVEC	blood vessel:	n/a
2	chr19:53359733-53359783	HUVEC	blood vessel:	n/a
3	chr19:53360213-53360263	HMEC	breast:	n/a
4	chr19:53362925-53362975	HL-60	blood:	n/a
5	chr19:53360728-53360778	MCF10A-Er-Src	breast:	n/a
6	chr19:53360213-53360263	A549	lung:	n/a
7	chr19:53342580-53342630	Caco-2	colon:	n/a
8	chr19:53359733-53359783	Hepatocyte	liver:	n/a
9	chr19:53342580-53342630	HCF	heart:	n/a
10	chr19:53363482-53363532	HCPEpiC	choroid plexus:	n/a
11	chr19:53362925-53362975	NH-A	brain:	n/a
12	chr19:53362925-53362975	HMEC	breast:	n/a
13	chr19:53357134-53357184	Jurkat	blood:	n/a
14	chr19:53360728-53360778	AG04450	lung:	fetal
15	chr19:53361066-53361116	Caco-2	colon:	n/a
16	chr19:53361066-53361116	GM12878	blood:	n/a
17	chr19:53361066-53361116	HRCEpiC	kidney:	n/a
18	chr19:53361164-53361214	SKMC	muscle:	n/a
19	chr19:53360213-53360263	PFSK-1	brain:	n/a
20	chr19:53363482-53363532	H1-hESC	embryonic stem cell:	embryo
21	chr19:53360728-53360778	AoSMC	blood vessel:	n/a
22	chr19:53383549-53383599	Caco-2	colon:	n/a
23	chr19:53359733-53359783	SAEC	small airway:	n/a
24	chr19:53383549-53383599	HPAEpiC	pulmonary alveolar:	n/a
25	chr19:53361164-53361214	PFSK-1	brain:	n/a
26	chr19:53363482-53363532	ProgFib	skin:	n/a
27	chr19:53363482-53363532	ovcar-3	ovarian:	n/a
28	chr19:53361164-53361214	GM12878	blood:	n/a
29	chr19:53363482-53363532	Caco-2	colon:	n/a
30	chr19:53360213-53360263	NHDF-neo	bronchial:	n/a
31	chr19:53361448-53361498	ovcar-3	ovarian:	n/a
32	chr19:53363482-53363532	HCF	heart:	n/a
33	chr19:53363482-53363532	SAEC	small airway:	n/a
34	chr19:53344366-53344416	Caco-2	colon:	n/a
35	chr19:53361164-53361214	HCM	heart:	n/a
36	chr19:53344366-53344416	GM12891	blood:	n/a
37	chr19:53383549-53383599	SAEC	small airway:	n/a
38	chr19:53361448-53361498	GM19239	blood:	n/a
39	chr19:53363482-53363532	HRPEpiC	eye:	n/a
40	chr19:53383549-53383599	LNCaP	prostate:	n/a
41	chr19:53359733-53359783	HCPEpiC	choroid plexus:	n/a
42	chr19:53361448-53361498	Hepatocyte	liver:	n/a
43	chr19:53361164-53361214	RPTEC	kidney:	n/a
44	chr19:53362925-53362975	HIPEpiC	eye:	n/a
45	chr19:53360213-53360263	GM06990	blood:	n/a
46	chr19:53362925-53362975	SKMC	muscle:	n/a
47	chr19:53359733-53359783	HAEpiC	amniotic membrane:	n/a
48	chr19:53357134-53357184	HCPEpiC	choroid plexus:	n/a
49	chr19:53357134-53357184	HCM	heart:	n/a
50	chr19:53361164-53361214	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:53338835..53341536-chr19:53343202..53344870,2	K562	blood:
2	chr19:53391514..53397028-chr19:53398889..53402751,6	K562	blood:
3	chr19:53193532..53195862-chr19:53359115..53361191,3	K562	blood:
4	chr19:53359757..53362433-chr19:53464752..53467349,2	MCF-7	breast:
5	chr19:53322321..53326212-chr19:53359321..53361245,3	K562	blood:
6	chr19:53324497..53325251-chr19:53360339..53360857,4	MCF-7	breast:
7	chr19:53339213..53341134-chr20:46203984..46206130,2	MCF-7	breast:
8	chr19:53335113..53339470-chr19:53340101..53344099,5	K562	blood:
9	chr19:53335113..53339470-chr19:53340101..53344099,5	K562	blood:
10	chr19:53377771..53379611-chr19:53399736..53401870,2	K562	blood:
11	chr19:53322321..53326212-chr19:53359240..53361245,4	K562	blood:
12	chr19:53357060..53358583-chr19:53400479..53402706,2	MCF-7	breast:
13	chr19:53390480..53393412-chr19:53415932..53418277,2	K562	blood:
14	chr19:53324563..53325122-chr19:53360322..53360852,2	NB4	blood:
15	chr19:53338835..53341536-chr19:53343202..53344870,2	K562	blood:
16	chr19:53380234..53382987-chr19:53399088..53400987,2	K562	blood:
17	chr19:53359564..53361265-chr19:53424872..53426783,2	MCF-7	breast:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF468-1	chr19:53341785-53345404	NR_102299
2	lnc-ZNF468-1	chr19:53352340-53352466	NR_102299
3	lnc-ZNF468-1	chr19:53348432-53348549	NR_102300
4	lnc-ZNF320-3	chr19:53377245-53377325	NONHSAT067591
5	lnc-ZNF320-3	chr19:53367175-53367412	NONHSAT067592
6	lnc-ZNF320-3	chr19:53367043-53367412	NONHSAT067591
7	lnc-ZNF468-1	chr19:53352340-53352466	NR_102300
8	lnc-ZNF320-3	chr19:53377411-53377490	NONHSAT067591
9	lnc-ZNF468-1	chr19:53341785-53345404	NR_102301
10	lnc-ZNF468-1	chr19:53357125-53357379	NR_102301
11	lnc-ZNF468-1	chr19:53348432-53348549	NR_102299
12	lnc-ZNF468-2	chr19:53365060-53366119	NONHSAT067590
13	lnc-ZNF468-1	chr19:53357125-53357360	NR_102300
14	lnc-ZNF468-1	chr19:53357511-53357598	NR_102299
15	lnc-ZNF468-1	chr19:53352340-53352466	NR_102301
16	lnc-ZNF468-1	chr19:53360825-53360902	NR_102301
17	lnc-ZNF320-1	chr19:53379431-53379838	NONHSAT067593
18	lnc-ZNF468-1	chr19:53360825-53360902	NR_102299
19	lnc-ZNF468-1	chr19:53360825-53360902	NR_102300
20	lnc-ZNF320-3	chr19:53382704-53382886	NONHSAT067592
21	lnc-ZNF701-2	chr19:53342913-53343520	NONHSAT067585
22	lnc-ZNF468-1	chr19:53357511-53357598	NR_102300
23	lnc-ZNF468-1	chr19:53357125-53357379	NR_102299
24	lnc-ZNF468-1	chr19:53357511-53357598	NR_102301
25	lnc-ZNF468-1	chr19:53341785-53345404	NR_102300
26	lnc-ZNF320-3	chr19:53377245-53377325	NONHSAT067592

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
ENSG00000198538	chromatin interactions
ENSG00000213793	chromatin interactions
ENSG00000182986	chromatin interactions
ENSG00000180257	chromatin interactions
ENSG00000167766	chromatin interactions
ENSG00000221874	chromatin interactions
ENSG00000269646	chromatin interactions

Extended variants
information (count: 2957 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2957 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10401828	chr19:53336367-53336368	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs538061929	chr19:53336388-53336389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs550404891	chr19:53336416-53336417	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs115066085	chr19:53336438-53336439	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs116909877	chr19:53336451-53336452	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs566296823	chr19:53336459-53336460	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs553863117	chr19:53336464-53336465	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs572498445	chr19:53336472-53336473	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs10426640	chr19:53336491-53336492	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs10402232	chr19:53336513-53336514	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs576263894	chr19:53336519-53336520	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs180935702	chr19:53336528-53336529	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs561959125	chr19:53336557-53336558	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs573838238	chr19:53336562-53336563	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs576780233	chr19:53336591-53336592	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs373061054	chr19:53336603-53336604	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs140798130	chr19:53336612-53336613	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs559059160	chr19:53336647-53336648	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs532782349	chr19:53336654-53336655	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs561337492	chr19:53336697-53336698	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs111594138	chr19:53336700-53336701	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs78110800	chr19:53336731-53336732	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs149814161	chr19:53336734-53336735	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs530568361	chr19:53336735-53336736	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs550095809	chr19:53336746-53336747	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs185979101	chr19:53336747-53336748	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs190404682	chr19:53336765-53336766	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs145814793	chr19:53336772-53336773	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs545734156	chr19:53336780-53336781	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs140701868	chr19:53336807-53336808	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs564814771	chr19:53336824-53336825	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs377648836	chr19:53336865-53336866	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs558236023	chr19:53336878-53336879	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs576602171	chr19:53336886-53336887	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs532044653	chr19:53336889-53336890	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs557073973	chr19:53336896-53336897	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs550540222	chr19:53336910-53336911	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs565614344	chr19:53336913-53336914	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs368261932	chr19:53336948-53336949	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs570235657	chr19:53336953-53336954	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs555250225	chr19:53337001-53337002	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs573803033	chr19:53337017-53337018	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs182230676	chr19:53337027-53337028	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs117423592	chr19:53337033-53337034	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs115188868	chr19:53337034-53337035	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs544604405	chr19:53337047-53337048	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs145902960	chr19:53337049-53337050	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs571986926	chr19:53337055-53337056	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs138494872	chr19:53337062-53337063	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs186943764	chr19:53337063-53337064	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	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:1663 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53333600-53345000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:53333800-53339000	Weak transcription	Placenta	Placenta
3	chr19:53335000-53338000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr19:53335000-53342800	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr19:53336400-53337400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr19:53336400-53337400	Enhancers	Dnd41	blood
7	chr19:53336600-53336800	Enhancers	K562	blood
8	chr19:53336800-53339000	Weak transcription	K562	blood
9	chr19:53337000-53337200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr19:53337000-53340800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr19:53337000-53340800	Weak transcription	Ovary	ovary
12	chr19:53337200-53337800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr19:53337200-53338200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr19:53337400-53338000	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr19:53337400-53340600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr19:53337400-53340600	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr19:53337400-53340600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr19:53337400-53340800	Weak transcription	Brain Hippocampus Middle	brain
19	chr19:53337400-53340800	Weak transcription	Fetal Brain Female	brain
20	chr19:53337400-53340800	Weak transcription	Dnd41	blood
21	chr19:53337600-53337800	Enhancers	H9 Cell Line	embryonic stem cell
22	chr19:53337600-53338000	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
23	chr19:53337600-53342200	Weak transcription	Brain Germinal Matrix	brain
24	chr19:53337600-53342200	Weak transcription	Fetal Stomach	stomach
25	chr19:53337800-53338000	Enhancers	H1 Cell Line	embryonic stem cell
26	chr19:53337800-53338000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr19:53337800-53338000	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr19:53337800-53338000	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr19:53337800-53338800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr19:53337800-53341400	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr19:53337800-53342200	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr19:53337800-53342400	Weak transcription	Right Ventricle	heart
33	chr19:53338000-53338200	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr19:53338000-53340800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr19:53338000-53341400	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr19:53338000-53342400	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr19:53338000-53342600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr19:53338000-53343400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr19:53338200-53339000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr19:53338200-53340600	Weak transcription	Rectal Smooth Muscle	rectum
41	chr19:53338200-53341400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr19:53338200-53342600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr19:53338600-53339200	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr19:53338800-53342200	Weak transcription	Fetal Muscle Trunk	muscle
45	chr19:53338800-53342600	Weak transcription	Brain Substantia Nigra	brain
46	chr19:53338800-53349200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr19:53338800-53352000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr19:53338800-53355000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr19:53339000-53339800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr19:53339000-53339800	Enhancers	K562	blood

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