Variant report

Variant	esv3416031
Chromosome Location	chr19:56134790-56136988
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:376)
CpG islands
(count:612)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:376 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:56135855-56136222	HepG2	liver:	n/a	n/a
2	BCL3	chr19:56135705-56136075	GM12878	blood:	n/a	n/a
3	BCL3	chr19:56136008-56136449	A549	lung:	n/a	n/a
4	BCL3	chr19:56135707-56136348	A549	lung:	n/a	n/a
5	BCL3	chr19:56135762-56136187	GM12878	blood:	n/a	n/a
6	BCLAF1	chr19:56135666-56136285	GM12878	blood:	n/a	n/a
7	BHLHE40	chr19:56135824-56136305	K562	blood:	n/a	n/a
8	BRCA1	chr19:56135818-56136161	GM12878	blood:	n/a	n/a
9	BRCA1	chr19:56135849-56135975	HepG2	liver:	n/a	n/a
10	CCNT2	chr19:56135393-56136230	K562	blood:	n/a	chr19:56135509-56135518 chr19:56135940-56135949 chr19:56135717-56135726 chr19:56135410-56135419 chr19:56135972-56135981
11	CEBPB	chr19:56135459-56135596	K562	blood:	n/a	chr19:56135534-56135545 chr19:56135534-56135545 chr19:56135534-56135547
12	CEBPB	chr19:56135830-56136094	IMR90	lung:	n/a	n/a
13	CEBPB	chr19:56135828-56136086	HepG2	liver:	n/a	n/a
14	CEBPB	chr19:56135816-56136306	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr19:56135715-56136079	K562	blood:	n/a	n/a
16	CEBPB	chr19:56135848-56136087	K562	blood:	n/a	n/a
17	CEBPB	chr19:56135414-56135534	A549	lung:	n/a	n/a
18	CEBPB	chr19:56135831-56136145	A549	lung:	n/a	n/a
19	CEBPB	chr19:56135844-56136010	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPD	chr19:56135690-56136061	HepG2	liver:	n/a	n/a
21	CHD2	chr19:56135727-56136094	GM12878	blood:	n/a	n/a
22	CHD2	chr19:56135754-56136049	HepG2	liver:	n/a	n/a
23	CHD2	chr19:56135416-56136318	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr19:56135734-56136184	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr19:56135809-56136141	K562	blood:	n/a	n/a
26	CREB1	chr19:56135522-56136184	A549	lung:	n/a	n/a
27	CREB1	chr19:56135442-56136495	HepG2	liver:	n/a	n/a
28	CTCF	chr19:56136009-56136189	MCF-7	breast:	n/a	n/a
29	CTCF	chr19:56136240-56136390	GM12873	blood:	n/a	n/a
30	CTCF	chr19:56136218-56136250	GM13976	blood:	n/a	n/a
31	CTCF	chr19:56135690-56136131	K562	blood:	n/a	n/a
32	CTCF	chr19:56136125-56136132	NHEK	skin:	n/a	n/a
33	CTCF	chr19:56136067-56136161	MCF-7	breast:	n/a	n/a
34	CTCF	chr19:56136132-56136222	Medullo	brain:	n/a	n/a
35	E2F4	chr19:56135448-56136249	K562	blood:	n/a	chr19:56135940-56135949
36	E2F4	chr19:56135907-56136262	GM12878	blood:	n/a	chr19:56135940-56135949
37	E2F4	chr19:56135795-56136278	MCF10A-Er-Src	breast:	n/a	chr19:56135940-56135949
38	E2F4	chr19:56136604-56136854	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F6	chr19:56135761-56136200	K562	blood:	n/a	chr19:56135940-56135949
40	E2F6	chr19:56135901-56136616	H1-hESC	embryonic stem cell:	n/a	chr19:56135940-56135949
41	E2F6	chr19:56136267-56136420	K562	blood:	n/a	n/a
42	E2F6	chr19:56135947-56136393	H1-hESC	embryonic stem cell:	n/a	n/a
43	EBF1	chr19:56135843-56136241	GM12878	blood:	n/a	n/a
44	EGR1	chr19:56135659-56135905	GM12878	blood:	n/a	chr19:56135783-56135796 chr19:56135754-56135769 chr19:56135752-56135766 chr19:56135755-56135768
45	EGR1	chr19:56135426-56136185	K562	blood:	n/a	chr19:56135783-56135796 chr19:56135754-56135769 chr19:56135752-56135766 chr19:56135939-56135949 chr19:56135611-56135624 chr19:56135755-56135768 chr19:56135941-56135954
46	EGR1	chr19:56135429-56136181	K562	blood:	n/a	chr19:56135783-56135796 chr19:56135754-56135769 chr19:56135752-56135766 chr19:56135939-56135949 chr19:56135611-56135624 chr19:56135755-56135768 chr19:56135941-56135954
47	ELF1	chr19:56135681-56136172	GM12878	blood:	n/a	n/a
48	ELF1	chr19:56135708-56136400	GM12878	blood:	n/a	n/a
49	ELF1	chr19:56135737-56136105	K562	blood:	n/a	n/a
50	ELF1	chr19:56135767-56136267	A549	lung:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:56136215-56136265	GM12892	blood:	n/a
2	chr19:56136128-56136178	NHDF-neo	bronchial:	n/a
3	chr19:56136215-56136265	GM12892	blood:	n/a
4	chr19:56136128-56136178	NHDF-neo	bronchial:	n/a
5	chr19:56136067-56136117	K562	blood:	n/a
6	chr19:56136210-56136260	ovcar-3	ovarian:	n/a
7	chr19:56135921-56135971	HL-60	blood:	n/a
8	chr19:56135921-56135971	NHBE	bronchial:	n/a
9	chr19:56136057-56136107	GM12892	blood:	n/a
10	chr19:56136210-56136260	IMR90	lung:	fetal
11	chr19:56135916-56135966	HRCEpiC	kidney:	n/a
12	chr19:56136072-56136122	BJ	skin:	n/a
13	chr19:56136067-56136117	HRCEpiC	kidney:	n/a
14	chr19:56135702-56135752	ECC-1	luminal epithelium:	n/a
15	chr19:56136057-56136107	HCF	heart:	n/a
16	chr19:56136057-56136107	NHBE	bronchial:	n/a
17	chr19:56135921-56135971	GM12891	blood:	n/a
18	chr19:56136210-56136260	MCF10A-Er-Src	breast:	n/a
19	chr19:56136067-56136117	NHDF-neo	bronchial:	n/a
20	chr19:56136072-56136122	IMR90	lung:	fetal
21	chr19:56136072-56136122	SAEC	small airway:	n/a
22	chr19:56136136-56136186	HCM	heart:	n/a
23	chr19:56135916-56135966	CMK	blood:	n/a
24	chr19:56136136-56136186	ECC-1	luminal epithelium:	n/a
25	chr19:56135702-56135752	HIPEpiC	eye:	n/a
26	chr19:56136072-56136122	A549	lung:	n/a
27	chr19:56135702-56135752	AG04450	lung:	fetal
28	chr19:56136128-56136178	Hela-S3	cervix:	n/a
29	chr19:56136136-56136186	MCF-7	breast:	n/a
30	chr19:56136210-56136260	PANC-1	pancreas:	n/a
31	chr19:56135921-56135971	Caco-2	colon:	n/a
32	chr19:56135916-56135966	PrEC	prostate:	n/a
33	chr19:56136067-56136117	MCF-7	breast:	n/a
34	chr19:56136057-56136107	GM19239	blood:	n/a
35	chr19:56136136-56136186	HRPEpiC	eye:	n/a
36	chr19:56136136-56136186	HL-60	blood:	n/a
37	chr19:56136210-56136260	GM06990	blood:	n/a
38	chr19:56136067-56136117	AG10803	skin:	n/a
39	chr19:56136072-56136122	LNCaP	prostate:	n/a
40	chr19:56136057-56136107	Caco-2	colon:	n/a
41	chr19:56135916-56135966	BJ	skin:	n/a
42	chr19:56135921-56135971	MCF10A-Er-Src	breast:	n/a
43	chr19:56135921-56135971	H1-hESC	embryonic stem cell:	embryo
44	chr19:56136215-56136265	HRPEpiC	eye:	n/a
45	chr19:56136215-56136265	HepG2	liver:	n/a
46	chr19:56136128-56136178	HCPEpiC	choroid plexus:	n/a
47	chr19:56135916-56135966	NT2-D1	testis:	n/a
48	chr19:56136136-56136186	PANC-1	pancreas:	n/a
49	chr19:56136067-56136117	HCPEpiC	choroid plexus:	n/a
50	chr19:56136215-56136265	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:56134460..56137185-chr19:56162633..56166165,3	K562	blood:
2	chr19:56135487..56136284-chr5:172754897..172755890,2	Hela-S3	cervix:
3	chr19:56134733..56137004-chr19:56165358..56168098,3	MCF-7	breast:
4	chr19:55986860..55989470-chr19:56134046..56136997,2	K562	blood:
5	chr19:56134221..56137618-chr19:56162633..56168532,10	K562	blood:
6	chr19:56115235..56119649-chr19:56131831..56136050,11	K562	blood:
7	chr19:55626847..55629043-chr19:56136358..56138081,2	MCF-7	breast:
8	chr19:56109378..56114662-chr19:56134412..56139001,15	K562	blood:
9	chr19:56123945..56128950-chr19:56130054..56135521,12	K562	blood:
10	chr19:56134501..56137412-chr19:56145689..56149345,6	K562	blood:
11	chr19:55950973..55953730-chr19:56134853..56137596,2	K562	blood:
12	chr19:55918880..55921412-chr19:56134337..56137770,3	MCF-7	breast:
13	chr19:56132811..56137423-chr19:56151241..56156557,5	MCF-7	breast:
14	chr19:56116188..56118514-chr19:56134480..56137487,3	MCF-7	breast:
15	chr19:56133602..56135847-chr19:56151330..56154007,2	MCF-7	breast:
16	chr19:56135134..56137131-chr19:56144636..56147133,4	MCF-7	breast:
17	chr19:56110415..56112373-chr19:56134518..56138349,4	MCF-7	breast:
18	chr19:56135761..56137279-chr19:56166087..56167869,2	MCF-7	breast:
19	chr19:55994966..55997371-chr19:56133954..56136992,3	K562	blood:
20	chr19:56133203..56138391-chr19:56150309..56156340,8	K562	blood:
21	chr19:56028711..56031331-chr19:56131776..56135542,3	K562	blood:
22	chr19:56131862..56136924-chr19:56144839..56148352,5	MCF-7	breast:
23	chr19:56125033..56127900-chr19:56132851..56135429,4	MCF-7	breast:
24	chr19:55917750..55919374-chr19:56134333..56135966,2	K562	blood:
25	chr19:56134500..56138557-chr19:56151822..56155582,4	K562	blood:
26	chr19:55969994..55973672-chr19:56134456..56137440,3	MCF-7	breast:

No data

Variant related genes	Relation type
ZNF784	TF binding region
ZNF784	CpG island
ENSG00000187902	chromatin interactions
ENSG00000261221	chromatin interactions
ENSG00000197483	chromatin interactions
ENSG00000213015	chromatin interactions
ENSG00000125503	chromatin interactions
ENSG00000063244	chromatin interactions
ENSG00000090971	chromatin interactions
ENSG00000173581	chromatin interactions
ENSG00000269859	chromatin interactions
ENSG00000171443	chromatin interactions
ENSG00000179943	chromatin interactions
ENSG00000108106	chromatin interactions
ENSG00000113739	chromatin interactions
ENSG00000171425	chromatin interactions
ENSG00000063241	chromatin interactions

Extended variants
information (count: 90 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:90 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs193039216	chr19:56134920-56134921	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
2	rs527731981	chr19:56134979-56134980	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
3	rs547859705	chr19:56134992-56134993	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
4	rs183152967	chr19:56134994-56134995	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
5	rs113139001	chr19:56135004-56135005	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
6	rs76889893	chr19:56135009-56135010	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
7	rs562023938	chr19:56135022-56135023	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
8	rs144621561	chr19:56135045-56135046	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
9	rs113742643	chr19:56135074-56135075	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
10	rs547630338	chr19:56135078-56135079	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
11	rs370039915	chr19:56135211-56135212	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
12	rs538092075	chr19:56135239-56135240	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
13	rs187806054	chr19:56135240-56135241	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
14	rs372673503	chr19:56135300-56135301	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
15	rs192676486	chr19:56135313-56135314	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
16	rs79971808	chr19:56135326-56135327	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
17	rs73934393	chr19:56135341-56135342	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs553811097	chr19:56135378-56135379	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
19	rs540856402	chr19:56135413-56135414	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
20	rs576833661	chr19:56135446-56135447	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
21	rs545897942	chr19:56135461-56135462	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
22	rs556295449	chr19:56135501-56135502	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
23	rs565866396	chr19:56135502-56135503	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
24	rs576229604	chr19:56135521-56135522	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
25	rs542112934	chr19:56135532-56135533	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
26	rs562084231	chr19:56135546-56135547	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
27	rs572387941	chr19:56135562-56135563	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
28	rs541093426	chr19:56135570-56135571	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
29	rs111866149	chr19:56135593-56135594	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
30	rs371080406	chr19:56135596-56135597	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
31	rs371093732	chr19:56135599-56135600	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
32	rs564522012	chr19:56135601-56135602	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
33	rs533230441	chr19:56135716-56135717	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
34	rs550301439	chr19:56135732-56135733	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
35	rs562671502	chr19:56135785-56135786	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
36	rs111447614	chr19:56135792-56135793	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
37	rs548490351	chr19:56135833-56135834	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
38	rs141315927	chr19:56135850-56135851	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
39	rs367877730	chr19:56135852-56135853	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
40	rs533088107	chr19:56135871-56135872	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
41	rs57543757	chr19:56135874-56135875	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
42	rs568293968	chr19:56135885-56135886	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
43	rs372115452	chr19:56135897-56135898	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
44	rs149288612	chr19:56135906-56135907	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
45	rs374056984	chr19:56135918-56135919	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
46	rs367641134	chr19:56135932-56135933	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
47	rs570433837	chr19:56135944-56135945	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
48	rs377357707	chr19:56135958-56135959	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
49	rs117034576	chr19:56135983-56135984	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
50	rs555887120	chr19:56135986-56135987	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20459607	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Alzheimer''s disease	22166940	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Glioblastoma multiforme	21922591	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:534 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56118200-56135000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr19:56118400-56135200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr19:56118400-56135200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr19:56118400-56135200	Weak transcription	HUVEC	blood vessel
5	chr19:56118600-56134800	Strong transcription	Fetal Intestine Small	intestine
6	chr19:56118600-56134800	Weak transcription	K562	blood
7	chr19:56118600-56135200	Weak transcription	Fetal Brain Male	brain
8	chr19:56119600-56134800	Weak transcription	Hela-S3	cervix
9	chr19:56121200-56135000	Weak transcription	NH-A	brain
10	chr19:56121600-56135800	Weak transcription	NHDF-Ad	bronchial
11	chr19:56122200-56135800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr19:56122800-56135000	Weak transcription	HSMM	muscle
13	chr19:56128400-56135600	Weak transcription	Small Intestine	intestine
14	chr19:56129000-56135000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr19:56129000-56135200	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr19:56129200-56134800	Weak transcription	Primary B cells from peripheral blood	blood
17	chr19:56129200-56134800	Weak transcription	Colon Smooth Muscle	Colon
18	chr19:56129200-56134800	Weak transcription	NHEK	skin
19	chr19:56129200-56135000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr19:56129200-56135000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr19:56129200-56135000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr19:56129200-56135000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr19:56129200-56135000	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr19:56129200-56135000	Weak transcription	Stomach Mucosa	stomach
25	chr19:56129200-56135400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr19:56129200-56135400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr19:56129200-56135400	Weak transcription	Colonic Mucosa	Colon
28	chr19:56129200-56135800	Weak transcription	Aorta	Aorta
29	chr19:56129200-56135800	Weak transcription	Brain Substantia Nigra	brain
30	chr19:56129400-56135000	Weak transcription	Osteobl	bone
31	chr19:56130600-56135200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr19:56131400-56135000	Weak transcription	Adipose Nuclei	Adipose
33	chr19:56132200-56135800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr19:56132400-56134800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr19:56132400-56134800	Weak transcription	Fetal Heart	heart
36	chr19:56132400-56135000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr19:56132400-56135200	Weak transcription	Right Atrium	heart
38	chr19:56132600-56134800	Weak transcription	Dnd41	blood
39	chr19:56132600-56135000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr19:56132800-56134800	Weak transcription	Primary hematopoietic stem cells	blood
41	chr19:56132800-56134800	Weak transcription	Brain Angular Gyrus	brain
42	chr19:56132800-56135000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr19:56132800-56135000	Weak transcription	Brain Anterior Caudate	brain
44	chr19:56132800-56135200	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr19:56132800-56135200	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr19:56132800-56135200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr19:56132800-56135200	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr19:56132800-56135200	Weak transcription	Psoas Muscle	Psoas
49	chr19:56133000-56134800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr19:56133000-56134800	Weak transcription	Fetal Lung	lung

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