Variant report

Variant	nsv827909
Chromosome Location	chr17:17358945-17394331
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:651)
CpG islands
(count:978)
Chromatin interactive
region (count:36)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:651 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:17380303-17380618	HepG2	liver:	n/a	n/a
2	ATF1	chr17:17380100-17380491	K562	blood:	n/a	n/a
3	ATF1	chr17:17376794-17376993	K562	blood:	n/a	n/a
4	ATF2	chr17:17380050-17380548	GM12878	blood:	n/a	n/a
5	ATF2	chr17:17387871-17388254	GM12878	blood:	n/a	n/a
6	ATF3	chr17:17380140-17380474	K562	blood:	n/a	chr17:17380281-17380290 chr17:17380282-17380302
7	ATF3	chr17:17380115-17380489	K562	blood:	n/a	chr17:17380281-17380290 chr17:17380282-17380302
8	ATF3	chr17:17380149-17380488	H1-hESC	embryonic stem cell:	n/a	chr17:17380281-17380290 chr17:17380282-17380302
9	ATF3	chr17:17380150-17380474	H1-hESC	embryonic stem cell:	n/a	chr17:17380281-17380290 chr17:17380282-17380302
10	ATF3	chr17:17380060-17380556	HepG2	liver:	n/a	chr17:17380281-17380290 chr17:17380282-17380302
11	ATF3	chr17:17380110-17380455	HepG2	liver:	n/a	chr17:17380281-17380290 chr17:17380282-17380302
12	ATF3	chr17:17380074-17380550	A549	lung:	n/a	chr17:17380281-17380290 chr17:17380282-17380302
13	ATF3	chr17:17380189-17380407	GM12878	blood:	n/a	chr17:17380281-17380290 chr17:17380282-17380302
14	ATF3	chr17:17380057-17380511	GM12878	blood:	n/a	chr17:17380281-17380290 chr17:17380282-17380302
15	BATF	chr17:17387900-17388253	GM12878	blood:	n/a	chr17:17388050-17388059
16	BCL3	chr17:17380075-17380883	A549	lung:	n/a	chr17:17380211-17380220 chr17:17380271-17380284
17	BCLAF1	chr17:17380128-17380568	GM12878	blood:	n/a	chr17:17380211-17380220 chr17:17380271-17380284
18	BHLHE40	chr17:17380236-17380590	K562	blood:	n/a	n/a
19	BHLHE40	chr17:17380168-17380514	GM12878	blood:	n/a	n/a
20	BHLHE40	chr17:17365437-17365962	HepG2	liver:	n/a	n/a
21	BRCA1	chr17:17380149-17380444	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr17:17380222-17380493	GM12878	blood:	n/a	n/a
23	BRCA1	chr17:17380179-17380411	HepG2	liver:	n/a	n/a
24	BRCA1	chr17:17380104-17380481	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr17:17380179-17380490	K562	blood:	n/a	n/a
26	CCNT2	chr17:17380190-17380570	K562	blood:	n/a	chr17:17380200-17380209 chr17:17380268-17380277
27	CEBPB	chr17:17380168-17380850	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr17:17364922-17365311	HepG2	liver:	n/a	chr17:17365140-17365153 chr17:17365056-17365067
29	CEBPB	chr17:17382552-17382834	HepG2	liver:	n/a	n/a
30	CEBPB	chr17:17364950-17365125	HepG2	liver:	n/a	chr17:17365056-17365067
31	CEBPB	chr17:17380592-17380865	IMR90	lung:	n/a	n/a
32	CEBPB	chr17:17367748-17367811	K562	blood:	n/a	n/a
33	CEBPB	chr17:17377524-17377849	K562	blood:	n/a	n/a
34	CEBPB	chr17:17367723-17367824	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr17:17380587-17380813	HepG2	liver:	n/a	n/a
36	CEBPB	chr17:17369662-17369872	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr17:17380670-17380749	K562	blood:	n/a	n/a
38	CEBPB	chr17:17364988-17365224	A549	lung:	n/a	chr17:17365140-17365153 chr17:17365056-17365067
39	CEBPB	chr17:17374506-17374657	Hela-S3	cervix:	n/a	chr17:17374572-17374583
40	CEBPB	chr17:17367641-17367866	HepG2	liver:	n/a	n/a
41	CEBPB	chr17:17365047-17365073	K562	blood:	n/a	chr17:17365056-17365067
42	CEBPB	chr17:17367613-17367952	HepG2	liver:	n/a	n/a
43	CEBPB	chr17:17374530-17374600	H1-hESC	embryonic stem cell:	n/a	chr17:17374572-17374583
44	CEBPB	chr17:17367660-17367927	A549	lung:	n/a	n/a
45	CEBPB	chr17:17372692-17372894	HepG2	liver:	n/a	n/a
46	CEBPB	chr17:17380384-17380780	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr17:17380300-17380312	K562	blood:	n/a	n/a
48	CEBPB	chr17:17365034-17365188	IMR90	lung:	n/a	chr17:17365140-17365153 chr17:17365056-17365067
49	CEBPB	chr17:17364905-17365210	HepG2	liver:	n/a	chr17:17365140-17365153 chr17:17365056-17365067
50	CEBPD	chr17:17364936-17365190	HepG2	liver:	n/a	chr17:17365141-17365152

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:17377803-17377853	PrEC	prostate:	n/a
2	chr17:17389863-17389913	HRCEpiC	kidney:	n/a
3	chr17:17377803-17377853	PrEC	prostate:	n/a
4	chr17:17389863-17389913	HRCEpiC	kidney:	n/a
5	chr17:17390793-17390843	HNPCEpiC	eye:	n/a
6	chr17:17380217-17380267	GM12892	blood:	n/a
7	chr17:17359737-17359787	PrEC	prostate:	n/a
8	chr17:17389863-17389913	HepG2	liver:	n/a
9	chr17:17380423-17380473	SK-N-SH_RA	brain:	n/a
10	chr17:17359737-17359787	HNPCEpiC	eye:	n/a
11	chr17:17359737-17359787	K562	blood:	n/a
12	chr17:17380209-17380259	AG04449	skin:	fetal
13	chr17:17380635-17380685	PrEC	prostate:	n/a
14	chr17:17380423-17380473	HCPEpiC	choroid plexus:	n/a
15	chr17:17379109-17379159	HEEpiC	esophagus:	n/a
16	chr17:17389971-17390021	ECC-1	luminal epithelium:	n/a
17	chr17:17359719-17359769	AG10803	skin:	n/a
18	chr17:17359719-17359769	PANC-1	pancreas:	n/a
19	chr17:17379109-17379159	HCPEpiC	choroid plexus:	n/a
20	chr17:17389863-17389913	HPAEpiC	pulmonary alveolar:	n/a
21	chr17:17380209-17380259	HEEpiC	esophagus:	n/a
22	chr17:17380313-17380363	SKMC	muscle:	n/a
23	chr17:17389863-17389913	Caco-2	colon:	n/a
24	chr17:17389971-17390021	HEK293	kidney:	embryo
25	chr17:17380423-17380473	NB4	blood:	n/a
26	chr17:17379358-17379408	AG09319	gingival:	n/a
27	chr17:17383910-17383960	HIPEpiC	eye:	n/a
28	chr17:17359737-17359787	GM12892	blood:	n/a
29	chr17:17380635-17380685	SK-N-SH	brain:	n/a
30	chr17:17389971-17390021	HRE	kidney:	n/a
31	chr17:17389863-17389913	SK-N-MC	brain:	n/a
32	chr17:17379109-17379159	HEK293	kidney:	embryo
33	chr17:17380423-17380473	LNCaP	prostate:	n/a
34	chr17:17380635-17380685	HUVEC	blood vessel:	n/a
35	chr17:17380635-17380685	AG09309	skin:	n/a
36	chr17:17379358-17379408	LNCaP	prostate:	n/a
37	chr17:17380313-17380363	BJ	skin:	n/a
38	chr17:17379358-17379408	BE2_C	brain:	n/a
39	chr17:17380635-17380685	HCF	heart:	n/a
40	chr17:17390793-17390843	HPAEpiC	pulmonary alveolar:	n/a
41	chr17:17359719-17359769	Hepatocyte	liver:	n/a
42	chr17:17380217-17380267	ECC-1	luminal epithelium:	n/a
43	chr17:17359719-17359769	GM12878	blood:	n/a
44	chr17:17359737-17359787	RPTEC	kidney:	n/a
45	chr17:17380209-17380259	HMEC	breast:	n/a
46	chr17:17383910-17383960	HCF	heart:	n/a
47	chr17:17380217-17380267	HCPEpiC	choroid plexus:	n/a
48	chr17:17389971-17390021	HCF	heart:	n/a
49	chr17:17389971-17390021	SK-N-SH	brain:	n/a
50	chr17:17359737-17359787	ProgFib	skin:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:17380272..17389088-chr17:17391260..17395887,13	K562	blood:
2	chr17:17384082..17386692-chr17:17387080..17388772,2	MCF-7	breast:
3	chr17:17389044..17391097-chr17:17393981..17396776,2	MCF-7	breast:
4	chr1:149858995..149859736-chr17:17379941..17380611,2	Hela-S3	cervix:
5	chr17:17349350..17351226-chr17:17382738..17384846,2	K562	blood:
6	chr17:17379236..17381999-chr17:17395224..17401626,6	MCF-7	breast:
7	chr17:17389044..17391097-chr17:17393981..17396776,2	MCF-7	breast:
8	chr17:17377768..17379317-chr17:17494319..17496372,2	K562	blood:
9	chr17:17380262..17386605-chr17:17392311..17397391,9	K562	blood:
10	chr17:17367834..17370645-chr22:35627497..35629414,2	MCF-7	breast:
11	chr17:17389215..17391542-chr17:17392709..17394489,2	K562	blood:
12	chr17:17393460..17395575-chr17:17398622..17401130,3	K562	blood:
13	chr17:17389215..17391542-chr17:17392709..17394489,2	K562	blood:
14	chr17:17382779..17384449-chr17:17466823..17468946,2	MCF-7	breast:
15	chr17:17356389..17359026-chr17:17360679..17363170,2	MCF-7	breast:
16	chr17:17379097..17381966-chr17:17388003..17390791,3	MCF-7	breast:
17	chr17:17356389..17359026-chr17:17360679..17363170,2	MCF-7	breast:
18	chr17:17290560..17292342-chr17:17378041..17380234,2	MCF-7	breast:
19	chr17:17384547..17387384-chr17:17390768..17392757,2	MCF-7	breast:
20	chr17:17394182..17397253-chr17:17397708..17401018,3	K562	blood:
21	chr17:17382327..17386627-chr17:17397610..17400464,6	MCF-7	breast:
22	chr17:17360225..17362152-chr17:17377850..17379702,2	MCF-7	breast:
23	chr17:17360225..17362152-chr17:17377850..17379702,2	MCF-7	breast:
24	chr17:17391754..17393754-chr17:17403950..17406372,2	MCF-7	breast:
25	chr17:17380357..17382707-chr17:17470620..17472293,2	MCF-7	breast:
26	chr17:17367351..17374142-chr17:17375377..17382594,8	MCF-7	breast:
27	chr17:17384082..17386692-chr17:17387080..17388772,2	MCF-7	breast:
28	chr17:17377592..17379713-chr17:17402478..17404778,3	K562	blood:
29	chr17:17379465..17384046-chr17:17386067..17389156,5	MCF-7	breast:
30	chr17:17347895..17349442-chr17:17385421..17387724,2	MCF-7	breast:
31	chr17:17379018..17381864-chr17:17382301..17386049,5	MCF-7	breast:
32	chr17:17391389..17393219-chr17:17395298..17398255,3	K562	blood:
33	chr17:17389683..17393183-chr17:17396173..17400344,4	K562	blood:
34	chr17:17373857..17375758-chr20:56284566..56286236,2	MCF-7	breast:
35	chr17:17380261..17384039-chr17:17397347..17401058,7	MCF-7	breast:
36	chr17:17384547..17387384-chr17:17390768..17392757,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MED9-2	chr17:17359741-17359897	NONHSAT146084
2	lnc-MED9-2	chr17:17360216-17360573	NONHSAT146084

No data

Variant related genes	Relation type
TSEN15P1	TF binding region
MED9	TF binding region
ENSG00000201741	TF binding region
TSEN15P1	CpG island
MED9	CpG island
ENSG00000201741	CpG island
ENSG00000264666	chromatin interactions
ENSG00000133027	chromatin interactions
ENSG00000184270	chromatin interactions
ENSG00000141026	chromatin interactions
ENSG00000108551	chromatin interactions
ENSG00000178096	chromatin interactions
ENSG00000124225	chromatin interactions

Extended variants
information (count: 1356 )
Associated
traits (count: 161 )

Variant overlapped rSNPs/rCNVs (count:1356 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534934913	chr17:17358986-17358987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs563540282	chr17:17359003-17359004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138440442	chr17:17359021-17359022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574575581	chr17:17359036-17359037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144000451	chr17:17359050-17359051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs147309355	chr17:17359066-17359067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576162113	chr17:17359096-17359097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148795755	chr17:17359120-17359121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563943100	chr17:17359134-17359135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564960279	chr17:17359137-17359138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527944659	chr17:17359146-17359147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541720619	chr17:17359169-17359170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs141589258	chr17:17359180-17359181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530307037	chr17:17359190-17359191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150816295	chr17:17359191-17359192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569748044	chr17:17359346-17359347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552180922	chr17:17359458-17359459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552170651	chr17:17359463-17359464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs75431199	chr17:17359464-17359465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534570358	chr17:17359485-17359486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554842659	chr17:17359486-17359487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs139266526	chr17:17359489-17359490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534708129	chr17:17359497-17359498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537233081	chr17:17359515-17359516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556764104	chr17:17359582-17359583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs144245683	chr17:17359589-17359590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538762643	chr17:17359590-17359591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558482959	chr17:17359600-17359601	Active TSS Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs16961756	chr17:17359619-17359620	Active TSS Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs190558871	chr17:17359622-17359623	Active TSS Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs561611179	chr17:17359717-17359718	Active TSS Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs114977647	chr17:17359719-17359720	Active TSS Weak transcription Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
33	rs181485365	chr17:17359729-17359730	Active TSS Weak transcription Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
34	rs563890434	chr17:17359732-17359733	Active TSS Weak transcription Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
35	rs532207514	chr17:17359750-17359751	Active TSS Weak transcription Enhancers	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs552307225	chr17:17359756-17359757	Active TSS Weak transcription Enhancers	CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs559534208	chr17:17359760-17359761	Active TSS Weak transcription Enhancers	CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs535614035	chr17:17359800-17359801	Active TSS Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs146580606	chr17:17359807-17359808	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs568321335	chr17:17359816-17359817	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs536967255	chr17:17359839-17359840	Weak transcription	CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs186173902	chr17:17359845-17359846	Weak transcription	CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs140099488	chr17:17359875-17359876	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs567807352	chr17:17359941-17359942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538700573	chr17:17359960-17359961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139134709	chr17:17359962-17359963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572482819	chr17:17359972-17359973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112163039	chr17:17359974-17359975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112333000	chr17:17359976-17359977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190048581	chr17:17359984-17359985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:161)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	17237825	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Breast cancer	17603634	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
ovarian endometriomas	16273235	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastric cancer	18160780	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22492990	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Epilepsy	20970697	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Smith-Magenis syndrome	21981782	CNVD
Smith-Magenis syndrome	20188345	CNVD
Smith-Magenis syndrome	16775514	CNVD
Smith-Magenis syndrome	22585170	CNVD
Smith-Magenis syndrome	22241247	CNVD
Autism	20970697	CNVD
Mental retardation	19951919	CNVD
Potocki-Lupski syndrome	21271655	CNVD
Potocki-lupski syndrome	17357070	CNVD
Potocki-lupski syndrome	20110824	CNVD
Potocki-lupski syndrome	18923514	CNVD
Potocki-lupski syndrome	22241247	CNVD
Potocki-lupski syndrome	20188345	CNVD
Schizophrenia	21399695	CNVD
Mental retardation	16773131	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Charcot-marie-tooth disease	22470819	CNVD
Neurofibromatosis	22470819	CNVD
Neuropathy	22470819	CNVD
Smith-Magenis syndrome	18301319	CNVD
Smith-Magenis syndrome	17357070	CNVD
Smith-Magenis syndrome	18469339	CNVD
Smith-Magenis syndrome	22241097	CNVD
Smith-Magenis syndrome	22470819	CNVD
Tourette syndrome	18923514	CNVD
Type 1 diabetes	22470819	CNVD
Potocki-lupski syndrome	18469339	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Neuropathy	17597781	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	17015230	CNVD
Smith-Magenis syndrome	17597781	CNVD
Potocki-lupski syndrome	18059269	CNVD
Potocki-lupski syndrome	17597781	CNVD
Mental retardation	17847001	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21509527	CNVD
Ductal carcinoma	22052326	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	22543975	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1354 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17349600-17363200	Weak transcription	Right Atrium	heart
2	chr17:17350400-17363400	Weak transcription	Gastric	stomach
3	chr17:17354800-17368000	Weak transcription	Fetal Thymus	thymus
4	chr17:17357800-17363200	Weak transcription	Spleen	Spleen
5	chr17:17358800-17359600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr17:17358800-17363200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr17:17359600-17359800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr17:17359600-17359800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr17:17359800-17363200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr17:17359800-17363200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr17:17361200-17361600	Enhancers	Rectal Mucosa Donor 29	rectum
12	chr17:17361400-17363400	Weak transcription	Pancreas	Pancrea
13	chr17:17361600-17365400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr17:17363200-17363400	Genic enhancers	Spleen	Spleen
15	chr17:17363200-17363600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr17:17363200-17363600	ZNF genes & repeats	Fetal Kidney	kidney
17	chr17:17363200-17363600	ZNF genes & repeats	Right Atrium	heart
18	chr17:17363200-17363800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr17:17363200-17363800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr17:17363400-17363600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr17:17363400-17363600	ZNF genes & repeats	Gastric	stomach
22	chr17:17363400-17363600	Enhancers	Lung	lung
23	chr17:17363400-17363600	ZNF genes & repeats	Pancreas	Pancrea
24	chr17:17363400-17363600	Transcr. at gene 5' and 3'	Spleen	Spleen
25	chr17:17363400-17363800	ZNF genes & repeats	Brain Angular Gyrus	brain
26	chr17:17363400-17363800	ZNF genes & repeats	Fetal Lung	lung
27	chr17:17363600-17363800	Active TSS	Spleen	Spleen
28	chr17:17363600-17364800	Weak transcription	Gastric	stomach
29	chr17:17363600-17365000	Enhancers	HepG2	liver
30	chr17:17363600-17365400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr17:17363600-17371000	Weak transcription	Pancreas	Pancrea
32	chr17:17363600-17380000	Weak transcription	Right Atrium	heart
33	chr17:17363800-17365000	Weak transcription	Fetal Lung	lung
34	chr17:17363800-17367400	Weak transcription	Brain Angular Gyrus	brain
35	chr17:17363800-17380200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr17:17365000-17366200	Flanking Active TSS	HepG2	liver
37	chr17:17365200-17365800	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
38	chr17:17365200-17366000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr17:17365200-17366000	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr17:17365200-17367000	Enhancers	Fetal Intestine Small	intestine
41	chr17:17365200-17367600	Enhancers	Fetal Intestine Large	intestine
42	chr17:17365400-17365800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr17:17365400-17365800	Enhancers	Colonic Mucosa	Colon
44	chr17:17365400-17366000	Enhancers	Rectal Mucosa Donor 29	rectum
45	chr17:17365800-17366000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
46	chr17:17365800-17366200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr17:17366000-17370800	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr17:17366000-17371000	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr17:17366200-17367200	Enhancers	HepG2	liver
50	chr17:17366600-17367600	Enhancers	Brain Substantia Nigra	brain

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