Variant report

Variant	nsv1062793
Chromosome Location	chr17:33944732-33976685
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:97)
CpG islands
(count:61)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:97 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr17:33960293-33960439	A549	lung:	n/a	n/a
2	CEBPB	chr17:33960156-33960446	K562	blood:	n/a	n/a
3	CTCF	chr17:33947317-33947367	GM13976	blood:	n/a	n/a
4	CTCF	chr17:33959280-33959351	Lung_OC	lung:	n/a	n/a
5	CTCF	chr17:33973675-33973725	GM13977	blood:	n/a	n/a
6	CTCF	chr17:33974207-33974229	Lung_OC	lung:	n/a	n/a
7	CTCF	chr17:33953789-33953808	GM10266	blood:	n/a	n/a
8	E2F4	chr17:33963387-33963467	MCF10A-Er-Src	breast:	n/a	n/a
9	ELF1	chr17:33956691-33956949	K562	blood:	n/a	n/a
10	EP300	chr17:33945504-33945519	GM12878	blood:	n/a	n/a
11	ESR1	chr17:33945282-33945598	ECC-1	luminal epithelium:	n/a	n/a
12	FOS	chr17:33957536-33958026	HUVEC	blood vessel:	n/a	chr17:33957689-33957700
13	FOS	chr17:33957502-33957932	MCF10A-Er-Src	breast:	n/a	chr17:33957689-33957700
14	FOS	chr17:33957499-33957985	MCF10A-Er-Src	breast:	n/a	chr17:33957689-33957700
15	FOS	chr17:33957527-33957885	MCF10A-Er-Src	breast:	n/a	chr17:33957689-33957700
16	FOS	chr17:33957558-33957838	MCF10A-Er-Src	breast:	n/a	chr17:33957689-33957700
17	FOSL1	chr17:33957512-33958033	HCT-116	colon:	n/a	n/a
18	FOSL1	chr17:33957465-33958124	HCT-116	colon:	n/a	n/a
19	FOSL2	chr17:33957503-33957999	SK-N-SH	brain:	n/a	n/a
20	FOSL2	chr17:33957399-33958138	SK-N-SH	brain:	n/a	n/a
21	FOXA1	chr17:33954489-33954799	HepG2	liver:	n/a	n/a
22	FOXA1	chr17:33954495-33954799	HepG2	liver:	n/a	n/a
23	FOXA1	chr17:33954524-33954810	HepG2	liver:	n/a	n/a
24	FOXA2	chr17:33954530-33954841	A549	lung:	n/a	n/a
25	FOXA2	chr17:33954447-33955044	HepG2	liver:	n/a	n/a
26	FOXA2	chr17:33954523-33954789	HepG2	liver:	n/a	n/a
27	GATA2	chr17:33957568-33958181	HUVEC	blood vessel:	n/a	chr17:33957857-33957864 chr17:33957857-33957864 chr17:33957857-33957864
28	GATA3	chr17:33958827-33959008	SH-SY5Y	brain:	n/a	n/a
29	GATA3	chr17:33957418-33958180	SK-N-SH	brain:	n/a	chr17:33957857-33957864 chr17:33957857-33957864 chr17:33957857-33957864
30	GATA3	chr17:33957444-33958100	SK-N-SH	brain:	n/a	chr17:33957857-33957864 chr17:33957857-33957864 chr17:33957857-33957864
31	GATA3	chr17:33957823-33958029	SH-SY5Y	brain:	n/a	chr17:33957857-33957864 chr17:33957857-33957864 chr17:33957857-33957864
32	IKZF1	chr17:33945532-33945667	GM12878	blood:	n/a	n/a
33	JUN	chr17:33959700-33959817	K562	blood:	n/a	n/a
34	JUN	chr17:33957559-33957950	HUVEC	blood vessel:	n/a	n/a
35	JUND	chr17:33957452-33958049	SK-N-SH	brain:	n/a	n/a
36	JUND	chr17:33957472-33958042	HCT-116	colon:	n/a	n/a
37	MAZ	chr17:33954017-33954037	HepG2	liver:	n/a	n/a
38	MYC	chr17:33957728-33957957	MCF10A-Er-Src	breast:	n/a	n/a
39	NFYA	chr17:33957600-33957857	Hela-S3	cervix:	n/a	n/a
40	PBX3	chr17:33957537-33958156	SK-N-SH	brain:	n/a	n/a
41	PBX3	chr17:33957488-33958201	SK-N-SH	brain:	n/a	n/a
42	POLR2A	chr17:33957632-33958030	HUVEC	blood vessel:	n/a	n/a
43	POLR2A	chr17:33973211-33973219	K562	blood:	n/a	n/a
44	POLR2A	chr17:33966117-33966120	K562	blood:	n/a	n/a
45	POLR2A	chr17:33956091-33956121	A549	lung:	n/a	n/a
46	POLR2A	chr17:33947002-33949441	K562	blood:	n/a	n/a
47	POLR2A	chr17:33962810-33962827	HepG2	liver:	n/a	n/a
48	POLR2A	chr17:33971193-33971215	GM12878	blood:	n/a	n/a
49	POLR2A	chr17:33956774-33957372	K562	blood:	n/a	n/a
50	POLR2A	chr17:33970253-33970472	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:33957395-33957445	IMR90	lung:	fetal
2	chr17:33957395-33957445	HRPEpiC	eye:	n/a
3	chr17:33957395-33957445	Caco-2	colon:	n/a
4	chr17:33957395-33957445	HIPEpiC	eye:	n/a
5	chr17:33957395-33957445	LNCaP	prostate:	n/a
6	chr17:33957395-33957445	SKMC	muscle:	n/a
7	chr17:33957395-33957445	SK-N-MC	brain:	n/a
8	chr17:33957395-33957445	Hela-S3	cervix:	n/a
9	chr17:33957395-33957445	GM19239	blood:	n/a
10	chr17:33957395-33957445	MCF10A-Er-Src	breast:	n/a
11	chr17:33957395-33957445	SAEC	small airway:	n/a
12	chr17:33957395-33957445	HEEpiC	esophagus:	n/a
13	chr17:33957395-33957445	HRCEpiC	kidney:	n/a
14	chr17:33957395-33957445	NH-A	brain:	n/a
15	chr17:33957395-33957445	AG10803	skin:	n/a
16	chr17:33957395-33957445	CMK	blood:	n/a
17	chr17:33957395-33957445	SK-N-SH_RA	brain:	n/a
18	chr17:33957395-33957445	HRE	kidney:	n/a
19	chr17:33957395-33957445	MCF-7	breast:	n/a
20	chr17:33957395-33957445	HPAEpiC	pulmonary alveolar:	n/a
21	chr17:33957395-33957445	SK-N-SH	brain:	n/a
22	chr17:33957395-33957445	HL-60	blood:	n/a
23	chr17:33957395-33957445	HCM	heart:	n/a
24	chr17:33957395-33957445	AG04450	lung:	fetal
25	chr17:33957395-33957445	RPTEC	kidney:	n/a
26	chr17:33957395-33957445	PrEC	prostate:	n/a
27	chr17:33957395-33957445	HUVEC	blood vessel:	n/a
28	chr17:33957395-33957445	HEK293	kidney:	embryo
29	chr17:33957395-33957445	GM06990	blood:	n/a
30	chr17:33957395-33957445	PFSK-1	brain:	n/a
31	chr17:33957395-33957445	AG09309	skin:	n/a
32	chr17:33957395-33957445	NB4	blood:	n/a
33	chr17:33957395-33957445	A549	lung:	n/a
34	chr17:33957395-33957445	BE2_C	brain:	n/a
35	chr17:33957395-33957445	PANC-1	pancreas:	n/a
36	chr17:33957395-33957445	NT2-D1	testis:	n/a
37	chr17:33957395-33957445	AG09319	gingival:	n/a
38	chr17:33957395-33957445	HAEpiC	amniotic membrane:	n/a
39	chr17:33957395-33957445	Jurkat	blood:	n/a
40	chr17:33957395-33957445	HCT-116	colon:	n/a
41	chr17:33957395-33957445	BJ	skin:	n/a
42	chr17:33957395-33957445	GM12891	blood:	n/a
43	chr17:33957395-33957445	U87	brain:	n/a
44	chr17:33957395-33957445	GM12878	blood:	n/a
45	chr17:33957395-33957445	ovcar-3	ovarian:	n/a
46	chr17:33957395-33957445	NHDF-neo	bronchial:	n/a
47	chr17:33957395-33957445	K562	blood:	n/a
48	chr17:33957395-33957445	T-47D	breast:	n/a
49	chr17:33957395-33957445	GM12892	blood:	n/a
50	chr17:33957395-33957445	HepG2	liver:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:33948219..33950290-chr17:33951562..33953635,2	K562	blood:
2	chr17:33958136..33960077-chr17:33969151..33971266,2	K562	blood:
3	chr17:33958136..33960077-chr17:33969151..33971266,2	K562	blood:
4	chr17:33959378..33962063-chr17:33964670..33966856,2	K562	blood:
5	chr17:33949132..33951570-chr17:33954798..33957288,2	K562	blood:
6	chr17:33948790..33950739-chr17:33951562..33953109,2	K562	blood:
7	chr17:33951186..33955408-chr17:33958518..33961561,4	K562	blood:
8	chr17:33959378..33962063-chr17:33964670..33966856,2	K562	blood:
9	chr17:33945134..33947432-chr17:33947574..33949899,2	MCF-7	breast:
10	chr17:33903102..33905242-chr17:33943673..33945209,2	MCF-7	breast:
11	chr17:33952642..33955408-chr17:33957507..33960024,3	K562	blood:
12	chr17:33946407..33948892-chr17:33953816..33956714,3	K562	blood:
13	chr17:33940042..33942067-chr17:33943790..33945473,2	K562	blood:
14	chr17:33954511..33957116-chr17:33962502..33964057,2	K562	blood:
15	chr17:33954511..33957116-chr17:33962502..33964057,2	K562	blood:
16	chr17:33948219..33950290-chr17:33951562..33953635,2	K562	blood:
17	chr17:33949132..33951570-chr17:33954798..33957288,2	K562	blood:
18	chr17:33902749..33905169-chr17:33948992..33950595,2	K562	blood:
19	chr17:33921434..33923649-chr17:33954336..33955867,2	K562	blood:
20	chr17:33952642..33955408-chr17:33957507..33960024,3	K562	blood:
21	chr17:33950625..33954392-chr17:33964410..33966864,3	K562	blood:
22	chr17:33942997..33945980-chr17:33946523..33950492,3	K562	blood:
23	chr17:33942629..33946842-chr17:33950583..33953394,3	K562	blood:
24	chr17:33936111..33938621-chr17:33942127..33945092,2	K562	blood:

No data

Variant related genes	Relation type
AP2B1	TF binding region
AP2B1	CpG island
ENSG00000006125	chromatin interactions

Extended variants
information (count: 1173 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:1173 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs225246	chr17:33944773-33944774	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369136818	chr17:33944783-33944784	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs372880074	chr17:33944798-33944799	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs113749999	chr17:33944829-33944830	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs181503561	chr17:33944832-33944833	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs565795777	chr17:33944862-33944863	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs534238354	chr17:33944907-33944908	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs201409533	chr17:33945011-33945012	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs201675823	chr17:33945013-33945014	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs200869321	chr17:33945018-33945019	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs148945769	chr17:33945028-33945029	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs115982414	chr17:33945119-33945120	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs539955458	chr17:33945163-33945164	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs556668835	chr17:33945212-33945213	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs143701062	chr17:33945232-33945233	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs575611700	chr17:33945298-33945299	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs542403515	chr17:33945419-33945420	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs185645694	chr17:33945424-33945425	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs190011838	chr17:33945425-33945426	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs3785759	chr17:33945432-33945433	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs563907492	chr17:33945444-33945445	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs532904852	chr17:33945452-33945453	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs148126351	chr17:33945483-33945484	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs562996649	chr17:33945490-33945491	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs115436900	chr17:33945516-33945517	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs548756975	chr17:33945550-33945551	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs180966829	chr17:33945665-33945666	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs575260283	chr17:33945688-33945689	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs528360542	chr17:33945735-33945736	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs34156177	chr17:33945743-33945744	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs551619864	chr17:33945765-33945766	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs570780298	chr17:33945774-33945775	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs140931500	chr17:33945807-33945808	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs185816984	chr17:33945811-33945812	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs370356035	chr17:33945831-33945832	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs146376865	chr17:33945898-33945899	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs143340415	chr17:33945945-33945946	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs72828065	chr17:33945969-33945970	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs572731140	chr17:33945971-33945972	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs552274230	chr17:33945979-33945980	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs562412024	chr17:33946070-33946071	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs147501183	chr17:33946072-33946073	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs225245	chr17:33946107-33946108	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs116310939	chr17:33946114-33946115	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs117395866	chr17:33946120-33946121	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs56227129	chr17:33946182-33946183	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs573398603	chr17:33946255-33946256	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs34055513	chr17:33946278-33946279	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs567716019	chr17:33946287-33946288	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs542448693	chr17:33946379-33946380	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Melanoma	18172304	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	17603634	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
Breast cancer	16397240	CNVD
Myxofibrosarcoma	16751306	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17157792	CNVD
Bladder cancer	19088036	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Meningioma	19431122	CNVD
Neurocytoma	17123091	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Cervical cancer	21062161	CNVD
Colorectal cancer	22860045	CNVD
Ductal carcinoma	18381933	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16417655	CNVD
Renal cysts	20603712	CNVD
Epilepsy	21858020	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Autism	20587423	CNVD
Renal cysts	20587423	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Mayer-Rokitansky-Kuster-Hauser syndrome	19889212	CNVD
Endometrial cancer	23636398	CNVD
Urothelial cell carcinoma	18451213	CNVD
Gastric cancer	24379144	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	17850661	CNVD
Primary lung adenocarcinoma	16799635	CNVD
HIV/AIDS	18848619	CNVD
Rheumatoid arthritis	19220326	CNVD
Rheumatoid arthritis	18848619	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	18848619	CNVD
Type 1 diabetes	19220326	CNVD
HIV/AIDS	17330138	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Acute monocytic leukemia	16498392	CNVD
Breast cancer	20409316	CNVD
Myelodysplastic syndrome	18663149	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	19153074	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Adrenocortical carcinoma	18281524	CNVD
Lung cancer	21569311	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Gastric cancer	21811585	CNVD

Chromatin state (count:927 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:33915600-33954600	Weak transcription	Small Intestine	intestine
2	chr17:33916400-33944800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr17:33916800-33945400	Weak transcription	Stomach Mucosa	stomach
4	chr17:33916800-34001200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr17:33920600-33969800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr17:33920800-33975800	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr17:33921000-33946200	Strong transcription	HUES48 Cell Line	embryonic stem cell
8	chr17:33921000-33946600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr17:33921000-34024400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr17:33926000-33955200	Weak transcription	Pancreas	Pancrea
11	chr17:33926800-33952600	Weak transcription	Fetal Brain Male	brain
12	chr17:33931000-34040200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr17:33933000-33967400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr17:33933000-33997800	Weak transcription	Esophagus	oesophagus
15	chr17:33933600-33952800	Weak transcription	Brain Substantia Nigra	brain
16	chr17:33933600-33967400	Weak transcription	Gastric	stomach
17	chr17:33934200-33945600	Strong transcription	K562	blood
18	chr17:33935000-33951400	Weak transcription	Brain Angular Gyrus	brain
19	chr17:33935600-33953000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr17:33935600-33953400	Weak transcription	HSMMtube	muscle
21	chr17:33936000-33953800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr17:33936800-33956800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr17:33937000-33951000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr17:33937000-33951400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr17:33937000-33951400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr17:33937000-33951800	Weak transcription	HepG2	liver
27	chr17:33937200-33947000	Weak transcription	Placenta	Placenta
28	chr17:33937200-33951200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr17:33937200-33951400	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr17:33937400-33951400	Weak transcription	Ovary	ovary
31	chr17:33937400-33965000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr17:33938200-33953200	Weak transcription	Colonic Mucosa	Colon
33	chr17:33938400-33951400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr17:33938600-33945400	Weak transcription	Colon Smooth Muscle	Colon
35	chr17:33938600-33946800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr17:33938600-33950600	Weak transcription	Stomach Smooth Muscle	stomach
37	chr17:33938600-33951000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr17:33938600-33951000	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr17:33938600-33951200	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr17:33938600-33951400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr17:33938600-33951400	Weak transcription	Primary T helper cells PMA-I stimulated	--
42	chr17:33938600-33951400	Weak transcription	Brain Cingulate Gyrus	brain
43	chr17:33938600-33952000	Weak transcription	Fetal Brain Female	brain
44	chr17:33938600-33952800	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr17:33938600-33953400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr17:33938600-33953600	Weak transcription	Spleen	Spleen
47	chr17:33938600-33954600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr17:33938800-33945200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr17:33938800-33951600	Weak transcription	Brain Germinal Matrix	brain
50	chr17:33939000-33953800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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