Variant report

Variant	esv3354949
Chromosome Location	chr19:56135340-56136538
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:372)
CpG islands
(count:611)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:372 , 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	chr19:56135707-56136348	A549	lung:	n/a	n/a
3	BCL3	chr19:56135762-56136187	GM12878	blood:	n/a	n/a
4	BCL3	chr19:56136008-56136449	A549	lung:	n/a	n/a
5	BCL3	chr19:56135705-56136075	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	chr19:56135848-56136087	K562	blood:	n/a	n/a
12	CEBPB	chr19:56135715-56136079	K562	blood:	n/a	n/a
13	CEBPB	chr19:56135844-56136010	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr19:56135828-56136086	HepG2	liver:	n/a	n/a
15	CEBPB	chr19:56135830-56136094	IMR90	lung:	n/a	n/a
16	CEBPB	chr19:56135414-56135534	A549	lung:	n/a	n/a
17	CEBPB	chr19:56135459-56135596	K562	blood:	n/a	chr19:56135534-56135545 chr19:56135534-56135545 chr19:56135534-56135547
18	CEBPB	chr19:56135816-56136306	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr19:56135831-56136145	A549	lung:	n/a	n/a
20	CEBPD	chr19:56135690-56136061	HepG2	liver:	n/a	n/a
21	CHD2	chr19:56135416-56136318	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr19:56135809-56136141	K562	blood:	n/a	n/a
23	CHD2	chr19:56135754-56136049	HepG2	liver:	n/a	n/a
24	CHD2	chr19:56135734-56136184	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr19:56135727-56136094	GM12878	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	chr19:56136067-56136161	MCF-7	breast:	n/a	n/a
29	CTCF	chr19:56136009-56136189	MCF-7	breast:	n/a	n/a
30	CTCF	chr19:56135690-56136131	K562	blood:	n/a	n/a
31	CTCF	chr19:56136125-56136132	NHEK	skin:	n/a	n/a
32	CTCF	chr19:56136132-56136222	Medullo	brain:	n/a	n/a
33	CTCF	chr19:56136218-56136250	GM13976	blood:	n/a	n/a
34	CTCF	chr19:56136240-56136390	GM12873	blood:	n/a	n/a
35	E2F4	chr19:56135907-56136262	GM12878	blood:	n/a	chr19:56135940-56135949
36	E2F4	chr19:56135795-56136278	MCF10A-Er-Src	breast:	n/a	chr19:56135940-56135949
37	E2F4	chr19:56135448-56136249	K562	blood:	n/a	chr19:56135940-56135949
38	E2F6	chr19:56135761-56136200	K562	blood:	n/a	chr19:56135940-56135949
39	E2F6	chr19:56135901-56136616	H1-hESC	embryonic stem cell:	n/a	chr19:56135940-56135949
40	E2F6	chr19:56135947-56136393	H1-hESC	embryonic stem cell:	n/a	n/a
41	E2F6	chr19:56136267-56136420	K562	blood:	n/a	n/a
42	EBF1	chr19:56135843-56136241	GM12878	blood:	n/a	n/a
43	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
44	EGR1	chr19:56135659-56135905	GM12878	blood:	n/a	chr19:56135783-56135796 chr19:56135754-56135769 chr19:56135752-56135766 chr19:56135755-56135768
45	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
46	ELF1	chr19:56135681-56136172	GM12878	blood:	n/a	n/a
47	ELF1	chr19:56135737-56136105	K562	blood:	n/a	n/a
48	ELF1	chr19:56135767-56136267	A549	lung:	n/a	n/a
49	ELF1	chr19:56135708-56136400	GM12878	blood:	n/a	n/a
50	ELK1	chr19:56135819-56136012	Hela-S3	cervix:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:56136057-56136107	AG09309	skin:	n/a
2	chr19:56136057-56136107	AG09309	skin:	n/a
3	chr19:56136072-56136122	Jurkat	blood:	n/a
4	chr19:56136210-56136260	BJ	skin:	n/a
5	chr19:56136136-56136186	PANC-1	pancreas:	n/a
6	chr19:56136136-56136186	NHBE	bronchial:	n/a
7	chr19:56135916-56135966	HIPEpiC	eye:	n/a
8	chr19:56136072-56136122	GM19239	blood:	n/a
9	chr19:56136057-56136107	GM12891	blood:	n/a
10	chr19:56136072-56136122	PFSK-1	brain:	n/a
11	chr19:56135916-56135966	MCF-7	breast:	n/a
12	chr19:56135916-56135966	HL-60	blood:	n/a
13	chr19:56136136-56136186	ProgFib	skin:	n/a
14	chr19:56136057-56136107	SAEC	small airway:	n/a
15	chr19:56136128-56136178	CMK	blood:	n/a
16	chr19:56136067-56136117	RPTEC	kidney:	n/a
17	chr19:56135702-56135752	HCT-116	colon:	n/a
18	chr19:56135702-56135752	GM12891	blood:	n/a
19	chr19:56136215-56136265	AG09319	gingival:	n/a
20	chr19:56136072-56136122	LNCaP	prostate:	n/a
21	chr19:56136072-56136122	HAEpiC	amniotic membrane:	n/a
22	chr19:56136057-56136107	HAEpiC	amniotic membrane:	n/a
23	chr19:56136057-56136107	HCF	heart:	n/a
24	chr19:56136136-56136186	Caco-2	colon:	n/a
25	chr19:56136067-56136117	NH-A	brain:	n/a
26	chr19:56136072-56136122	HCT-116	colon:	n/a
27	chr19:56135921-56135971	HMEC	breast:	n/a
28	chr19:56136057-56136107	LNCaP	prostate:	n/a
29	chr19:56135916-56135966	GM12891	blood:	n/a
30	chr19:56135916-56135966	AG09319	gingival:	n/a
31	chr19:56136072-56136122	SK-N-SH_RA	brain:	n/a
32	chr19:56136215-56136265	HRCEpiC	kidney:	n/a
33	chr19:56136210-56136260	HL-60	blood:	n/a
34	chr19:56136072-56136122	GM06990	blood:	n/a
35	chr19:56135916-56135966	HEEpiC	esophagus:	n/a
36	chr19:56136215-56136265	HUVEC	blood vessel:	n/a
37	chr19:56136072-56136122	MCF10A-Er-Src	breast:	n/a
38	chr19:56135921-56135971	AG09319	gingival:	n/a
39	chr19:56136067-56136117	HepG2	liver:	n/a
40	chr19:56135702-56135752	AoSMC	blood vessel:	n/a
41	chr19:56135702-56135752	HAEpiC	amniotic membrane:	n/a
42	chr19:56136072-56136122	SK-N-MC	brain:	n/a
43	chr19:56136136-56136186	SK-N-SH_RA	brain:	n/a
44	chr19:56136136-56136186	ovcar-3	ovarian:	n/a
45	chr19:56136057-56136107	HIPEpiC	eye:	n/a
46	chr19:56136067-56136117	HAEpiC	amniotic membrane:	n/a
47	chr19:56136210-56136260	CMK	blood:	n/a
48	chr19:56136057-56136107	SK-N-SH	brain:	n/a
49	chr19:56136210-56136260	HIPEpiC	eye:	n/a
50	chr19:56136136-56136186	HCF	heart:	n/a

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

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

No data

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

Extended variants
information (count: 61 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:61 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	rs553811097	chr19:56135378-56135379	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
3	rs540856402	chr19:56135413-56135414	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
4	rs576833661	chr19:56135446-56135447	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
5	rs545897942	chr19:56135461-56135462	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
6	rs556295449	chr19:56135501-56135502	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
7	rs565866396	chr19:56135502-56135503	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
8	rs576229604	chr19:56135521-56135522	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
9	rs542112934	chr19:56135532-56135533	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
10	rs562084231	chr19:56135546-56135547	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
11	rs572387941	chr19:56135562-56135563	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
12	rs541093426	chr19:56135570-56135571	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
13	rs111866149	chr19:56135593-56135594	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
14	rs371080406	chr19:56135596-56135597	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
15	rs371093732	chr19:56135599-56135600	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
16	rs564522012	chr19:56135601-56135602	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
17	rs533230441	chr19:56135716-56135717	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
18	rs550301439	chr19:56135732-56135733	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
19	rs562671502	chr19:56135785-56135786	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
20	rs111447614	chr19:56135792-56135793	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
21	rs548490351	chr19:56135833-56135834	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
22	rs141315927	chr19:56135850-56135851	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
23	rs367877730	chr19:56135852-56135853	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
24	rs533088107	chr19:56135871-56135872	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
25	rs57543757	chr19:56135874-56135875	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
26	rs568293968	chr19:56135885-56135886	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
27	rs372115452	chr19:56135897-56135898	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
28	rs149288612	chr19:56135906-56135907	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
29	rs374056984	chr19:56135918-56135919	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
30	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
31	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
32	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
33	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
34	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
35	rs576220028	chr19:56135994-56135995	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
36	rs113532710	chr19:56136016-56136017	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
37	rs535685036	chr19:56136037-56136038	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
38	rs555617143	chr19:56136041-56136042	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
39	rs57314044	chr19:56136059-56136060	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs541720985	chr19:56136060-56136061	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
41	rs564277650	chr19:56136068-56136069	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
42	rs148470225	chr19:56136101-56136102	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
43	rs543926496	chr19:56136138-56136139	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
44	rs563809750	chr19:56136149-56136150	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
45	rs531513263	chr19:56136189-56136190	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
46	rs7248730	chr19:56136194-56136195	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
47	rs548379071	chr19:56136309-56136310	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
48	rs561933312	chr19:56136331-56136332	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
49	rs113236551	chr19:56136345-56136346	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
50	rs547669895	chr19:56136348-56136349	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	14 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:341 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56121600-56135800	Weak transcription	NHDF-Ad	bronchial
2	chr19:56122200-56135800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr19:56128400-56135600	Weak transcription	Small Intestine	intestine
4	chr19:56129200-56135400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr19:56129200-56135400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr19:56129200-56135400	Weak transcription	Colonic Mucosa	Colon
7	chr19:56129200-56135800	Weak transcription	Aorta	Aorta
8	chr19:56129200-56135800	Weak transcription	Brain Substantia Nigra	brain
9	chr19:56132200-56135800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr19:56133600-56135600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr19:56134000-56135400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr19:56134000-56135400	Weak transcription	Esophagus	oesophagus
13	chr19:56134000-56135600	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr19:56134000-56135800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr19:56134000-56135800	Weak transcription	Gastric	stomach
16	chr19:56134000-56135800	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr19:56134200-56135400	Weak transcription	Lung	lung
18	chr19:56134200-56135400	Weak transcription	Ovary	ovary
19	chr19:56134200-56135400	Weak transcription	Thymus	Thymus
20	chr19:56134200-56135600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr19:56134200-56135800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr19:56134200-56136000	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr19:56134400-56135400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr19:56134400-56135400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr19:56134400-56135400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr19:56134400-56135400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr19:56134400-56135600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr19:56134600-56135400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr19:56134600-56135600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
30	chr19:56134800-56135400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr19:56134800-56135400	Enhancers	Fetal Intestine Large	intestine
32	chr19:56134800-56135400	Enhancers	Fetal Stomach	stomach
33	chr19:56134800-56135600	Enhancers	Primary B cells from peripheral blood	blood
34	chr19:56134800-56135600	Enhancers	Fetal Thymus	thymus
35	chr19:56134800-56135600	Flanking Active TSS	K562	blood
36	chr19:56134800-56135600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr19:56134800-56135800	Enhancers	Primary B cells from cord blood	blood
38	chr19:56134800-56135800	Enhancers	Primary hematopoietic stem cells	blood
39	chr19:56134800-56135800	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr19:56134800-56135800	Enhancers	Liver	Liver
41	chr19:56134800-56136600	Active TSS	Right Ventricle	heart
42	chr19:56134800-56136800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr19:56135000-56135400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr19:56135000-56135400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr19:56135000-56135400	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr19:56135000-56135400	Enhancers	Adipose Nuclei	Adipose
47	chr19:56135000-56135400	Enhancers	Stomach Mucosa	stomach
48	chr19:56135000-56135400	Flanking Active TSS	HSMM	muscle
49	chr19:56135000-56135400	Flanking Active TSS	HSMMtube	muscle
50	chr19:56135000-56135400	Flanking Active TSS	NH-A	brain

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