Variant report

Variant	nsv907730
Chromosome Location	chr17:17358004-17415217
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1552)
CpG islands
(count:2258)
Chromatin interactive
region (count:95)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:1552 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

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	ARID3A	chr17:17399649-17399806	HepG2	liver:	n/a	n/a
3	ATF1	chr17:17380100-17380491	K562	blood:	n/a	n/a
4	ATF1	chr17:17376794-17376993	K562	blood:	n/a	n/a
5	ATF2	chr17:17380050-17380548	GM12878	blood:	n/a	n/a
6	ATF2	chr17:17387871-17388254	GM12878	blood:	n/a	n/a
7	ATF3	chr17:17380110-17380455	HepG2	liver:	n/a	chr17:17380281-17380290 chr17:17380282-17380302
8	ATF3	chr17:17380189-17380407	GM12878	blood:	n/a	chr17:17380281-17380290 chr17:17380282-17380302
9	ATF3	chr17:17380115-17380489	K562	blood:	n/a	chr17:17380281-17380290 chr17:17380282-17380302
10	ATF3	chr17:17380150-17380474	H1-hESC	embryonic stem cell:	n/a	chr17:17380281-17380290 chr17:17380282-17380302
11	ATF3	chr17:17380057-17380511	GM12878	blood:	n/a	chr17:17380281-17380290 chr17:17380282-17380302
12	ATF3	chr17:17380149-17380488	H1-hESC	embryonic stem cell:	n/a	chr17:17380281-17380290 chr17:17380282-17380302
13	ATF3	chr17:17380074-17380550	A549	lung:	n/a	chr17:17380281-17380290 chr17:17380282-17380302
14	ATF3	chr17:17380060-17380556	HepG2	liver:	n/a	chr17:17380281-17380290 chr17:17380282-17380302
15	ATF3	chr17:17380140-17380474	K562	blood:	n/a	chr17:17380281-17380290 chr17:17380282-17380302
16	BACH1	chr17:17397899-17398047	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr17:17400377-17400430	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr17:17397012-17397070	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr17:17398968-17398978	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr17:17398256-17398456	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr17:17387900-17388253	GM12878	blood:	n/a	chr17:17388050-17388059
22	BCL3	chr17:17399191-17400328	A549	lung:	n/a	chr17:17399950-17399963 chr17:17399720-17399733 chr17:17399810-17399823 chr17:17399949-17399962
23	BCL3	chr17:17380075-17380883	A549	lung:	n/a	chr17:17380211-17380220 chr17:17380271-17380284
24	BCLAF1	chr17:17380128-17380568	GM12878	blood:	n/a	chr17:17380211-17380220 chr17:17380271-17380284
25	BHLHE40	chr17:17399896-17399901	K562	blood:	n/a	n/a
26	BHLHE40	chr17:17365437-17365962	HepG2	liver:	n/a	n/a
27	BHLHE40	chr17:17400184-17400385	GM12878	blood:	n/a	chr17:17400331-17400347 chr17:17400309-17400325
28	BHLHE40	chr17:17380168-17380514	GM12878	blood:	n/a	n/a
29	BHLHE40	chr17:17380236-17380590	K562	blood:	n/a	n/a
30	BHLHE40	chr17:17412516-17412612	K562	blood:	n/a	n/a
31	BRCA1	chr17:17380104-17380481	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr17:17380222-17380493	GM12878	blood:	n/a	n/a
33	BRCA1	chr17:17400218-17400383	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr17:17400262-17400288	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr17:17399659-17399849	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr17:17400172-17400311	HepG2	liver:	n/a	n/a
37	BRCA1	chr17:17380149-17380444	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr17:17380179-17380411	HepG2	liver:	n/a	n/a
39	CBX3	chr17:17380179-17380490	K562	blood:	n/a	n/a
40	CCNT2	chr17:17398422-17398517	K562	blood:	n/a	n/a
41	CCNT2	chr17:17399313-17400475	K562	blood:	n/a	chr17:17400175-17400184 chr17:17400169-17400178 chr17:17399874-17399883 chr17:17400444-17400453
42	CCNT2	chr17:17380190-17380570	K562	blood:	n/a	chr17:17380200-17380209 chr17:17380268-17380277
43	CEBPB	chr17:17377524-17377849	K562	blood:	n/a	n/a
44	CEBPB	chr17:17380670-17380749	K562	blood:	n/a	n/a
45	CEBPB	chr17:17400184-17400362	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr17:17399803-17399828	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr17:17367613-17367952	HepG2	liver:	n/a	n/a
48	CEBPB	chr17:17380300-17380312	K562	blood:	n/a	n/a
49	CEBPB	chr17:17400160-17400354	HepG2	liver:	n/a	n/a
50	CEBPB	chr17:17367641-17367866	HepG2	liver:	n/a	n/a

(count:2258 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:17399802-17399852	HRE	kidney:	n/a
2	chr17:17399802-17399852	HRE	kidney:	n/a
3	chr17:17389863-17389913	U87	brain:	n/a
4	chr17:17398962-17399012	HCT-116	colon:	n/a
5	chr17:17400111-17400161	GM12892	blood:	n/a
6	chr17:17389971-17390021	AG09319	gingival:	n/a
7	chr17:17399700-17399750	PrEC	prostate:	n/a
8	chr17:17399941-17399991	BE2_C	brain:	n/a
9	chr17:17398962-17399012	AG10803	skin:	n/a
10	chr17:17414998-17415048	HCF	heart:	n/a
11	chr17:17400340-17400390	AG04449	skin:	fetal
12	chr17:17394732-17394782	AG10803	skin:	n/a
13	chr17:17399405-17399455	BE2_C	brain:	n/a
14	chr17:17399795-17399845	GM06990	blood:	n/a
15	chr17:17407880-17407930	Jurkat	blood:	n/a
16	chr17:17359719-17359769	NH-A	brain:	n/a
17	chr17:17407880-17407930	HPAEpiC	pulmonary alveolar:	n/a
18	chr17:17394732-17394782	NH-A	brain:	n/a
19	chr17:17399700-17399750	BJ	skin:	n/a
20	chr17:17407880-17407930	NH-A	brain:	n/a
21	chr17:17399941-17399991	Hela-S3	cervix:	n/a
22	chr17:17399729-17399779	HNPCEpiC	eye:	n/a
23	chr17:17414998-17415048	AG04449	skin:	fetal
24	chr17:17399667-17399717	AG04449	skin:	fetal
25	chr17:17400340-17400390	NB4	blood:	n/a
26	chr17:17383910-17383960	HL-60	blood:	n/a
27	chr17:17380217-17380267	NHBE	bronchial:	n/a
28	chr17:17380209-17380259	SAEC	small airway:	n/a
29	chr17:17399795-17399845	NH-A	brain:	n/a
30	chr17:17414998-17415048	AG09319	gingival:	n/a
31	chr17:17377803-17377853	NT2-D1	testis:	n/a
32	chr17:17399941-17399991	ProgFib	skin:	n/a
33	chr17:17399941-17399991	AG09319	gingival:	n/a
34	chr17:17397972-17398022	NHBE	bronchial:	n/a
35	chr17:17399802-17399852	HCM	heart:	n/a
36	chr17:17399405-17399455	RPTEC	kidney:	n/a
37	chr17:17389971-17390021	SK-N-MC	brain:	n/a
38	chr17:17399700-17399750	Caco-2	colon:	n/a
39	chr17:17379752-17379802	Caco-2	colon:	n/a
40	chr17:17379752-17379802	MCF-7	breast:	n/a
41	chr17:17389971-17390021	U87	brain:	n/a
42	chr17:17407880-17407930	HCT-116	colon:	n/a
43	chr17:17389863-17389913	LNCaP	prostate:	n/a
44	chr17:17400111-17400161	H1-hESC	embryonic stem cell:	embryo
45	chr17:17409003-17409053	CMK	blood:	n/a
46	chr17:17414998-17415048	HL-60	blood:	n/a
47	chr17:17407880-17407930	BJ	skin:	n/a
48	chr17:17403227-17403277	HMEC	breast:	n/a
49	chr17:17399941-17399991	MCF10A-Er-Src	breast:	n/a
50	chr17:17399700-17399750	HEEpiC	esophagus:	n/a

(count:95 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr17:17400013..17403525-chr17:17411408..17414122,3	MCF-7	breast:
2	chr17:17384547..17387384-chr17:17390768..17392757,2	MCF-7	breast:
3	chr17:17389044..17391097-chr17:17393981..17396776,2	MCF-7	breast:
4	chr17:17349350..17351226-chr17:17382738..17384846,2	K562	blood:
5	chr17:17356865..17358826-chr17:17575976..17578412,2	MCF-7	breast:
6	chr17:17389044..17391097-chr17:17393981..17396776,2	MCF-7	breast:
7	chr17:17391754..17393754-chr17:17403950..17406372,2	MCF-7	breast:
8	chr17:17384547..17387384-chr17:17390768..17392757,2	MCF-7	breast:
9	chr17:17356389..17359026-chr17:17360679..17363170,2	MCF-7	breast:
10	chr17:17398240..17400896-chr17:17493826..17497836,5	MCF-7	breast:
11	chr17:17400222..17400791-chr17:17471763..17472291,2	K562	blood:
12	chr1:149858995..149859736-chr17:17379941..17380611,2	Hela-S3	cervix:
13	chr17:17396995..17404908-chr17:17406815..17414609,13	MCF-7	breast:
14	chr17:17389683..17393183-chr17:17396173..17400344,4	K562	blood:
15	chr17:17398634..17401491-chr17:17403383..17405495,2	K562	blood:
16	chr17:17291335..17291987-chr17:17399782..17400706,3	MCF-7	breast:
17	chr17:17384082..17386692-chr17:17387080..17388772,2	MCF-7	breast:
18	chr17:17367834..17370645-chr22:35627497..35629414,2	MCF-7	breast:
19	chr17:17399866..17402763-chr17:17404179..17406127,2	MCF-7	breast:
20	chr17:17400013..17403525-chr17:17411408..17414122,3	MCF-7	breast:
21	chr17:17394585..17397525-chr17:17493940..17496244,2	K562	blood:
22	chr17:17377592..17379713-chr17:17402478..17404778,3	K562	blood:
23	chr17:17396999..17399572-chr17:17585740..17587599,2	MCF-7	breast:
24	chr17:17290560..17292342-chr17:17378041..17380234,2	MCF-7	breast:
25	chr17:17380272..17389088-chr17:17391260..17395887,13	K562	blood:
26	chr17:17379236..17381999-chr17:17395224..17401626,6	MCF-7	breast:
27	chr17:17282517..17284843-chr17:17397818..17399697,2	MCF-7	breast:
28	chr17:17398348..17401153-chr17:17494060..17496594,3	MCF-7	breast:
29	chr17:17291141..17292010-chr17:17399819..17400387,2	MCF-7	breast:
30	chr17:17379236..17381999-chr17:17395224..17401626,6	MCF-7	breast:
31	chr17:17399769..17400801-chr17:17471936..17472657,4	MCF-7	breast:
32	chr17:17259223..17259968-chr17:17404096..17405018,2	MCF-7	breast:
33	chr17:17405820..17407609-chr17:17411201..17413921,2	MCF-7	breast:
34	chr17:17290815..17292388-chr17:17395387..17396915,2	MCF-7	breast:
35	chr17:17360225..17362152-chr17:17377850..17379702,2	MCF-7	breast:
36	chr17:17373857..17375758-chr20:56284566..56286236,2	MCF-7	breast:
37	chr17:17400144..17400698-chr17:17545089..17545735,2	MCF-7	breast:
38	chr17:17400239..17400807-chr17:17472787..17473779,2	K562	blood:
39	chr17:17349182..17349868-chr17:17399782..17400771,2	MCF-7	breast:
40	chr17:17398131..17401509-chr17:17403115..17406009,4	MCF-7	breast:
41	chr17:17402799..17405333-chr17:17413416..17415879,2	K562	blood:
42	chr17:17380357..17382707-chr17:17470620..17472293,2	MCF-7	breast:
43	chr17:17379097..17381966-chr17:17388003..17390791,3	MCF-7	breast:
44	chr17:17379155..17381711-chr17:17395124..17397164,2	MCF-7	breast:
45	chr17:17384082..17386692-chr17:17387080..17388772,2	MCF-7	breast:
46	chr17:17404753..17406377-chr17:17407243..17409547,3	K562	blood:
47	chr17:17412469..17415269-chr17:17430447..17432803,2	MCF-7	breast:
48	chr17:17394182..17397253-chr17:17397708..17401018,3	K562	blood:
49	chr17:17377768..17379317-chr17:17494319..17496372,2	K562	blood:
50	chr17:17404753..17406377-chr17:17407243..17409547,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MED9-1	chr17:17411095-17411622	ENSG00000265511.1
2	lnc-MED9-2	chr17:17359741-17359897	NONHSAT146084
3	lnc-MED9-2	chr17:17360216-17360573	NONHSAT146084
4	lnc-MED9-1	chr17:17410665-17410931	ENSG00000265511.1

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	RASD1	hsa-miR-375	chr17:17397855-17397848
2	PEMT	hsa-miR-124-3p	chr17:17408980-17408974
3	PEMT	hsa-miR-124-3p	chr17:17408974-17408994
4	RASD1	hsa-miR-375	chr17:17398413-17398435
5	RASD1	hsa-miR-375	chr17:17397849-17397871

Variant related genes	Relation type
MED9	TF binding region
PEMT	TF binding region
ENSG00000265511	TF binding region
ENSG00000201741	TF binding region
TSEN15P1	TF binding region
RASD1	TF binding region
MED9	CpG island
PEMT	CpG island
ENSG00000265511	CpG island
ENSG00000201741	CpG island
TSEN15P1	CpG island
RASD1	CpG island
ENSG00000187954	chromatin interactions
ENSG00000133027	chromatin interactions
ENSG00000234006	chromatin interactions
ENSG00000264187	chromatin interactions
ENSG00000198563	chromatin interactions
ENSG00000264666	chromatin interactions
ENSG00000154803	chromatin interactions
ENSG00000108551	chromatin interactions
ENSG00000167702	chromatin interactions
ENSG00000184270	chromatin interactions
ENSG00000178096	chromatin interactions
ENSG00000265511	chromatin interactions
ENSG00000254578	chromatin interactions
ENSG00000108557	chromatin interactions
ENSG00000141026	chromatin interactions
ENSG00000124225	chromatin interactions

Extended variants
information (count: 2340 )
Associated
traits (count: 162 )

Variant overlapped rSNPs/rCNVs (count:2340 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55710209	chr17:17358004-17358005	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs556151125	chr17:17358012-17358013	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs576229882	chr17:17358013-17358014	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs189219133	chr17:17358015-17358016	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs565026897	chr17:17358025-17358026	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs572268185	chr17:17358118-17358119	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs541269945	chr17:17358165-17358166	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs374992651	chr17:17358205-17358206	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs73978919	chr17:17358206-17358207	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs376398786	chr17:17358216-17358217	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs549081902	chr17:17358230-17358231	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs562919950	chr17:17358241-17358242	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs115204193	chr17:17358250-17358251	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs551659509	chr17:17358255-17358256	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs571652977	chr17:17358256-17358257	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs534115147	chr17:17358260-17358261	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs562140533	chr17:17358396-17358397	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs548002894	chr17:17358403-17358404	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs1242477	chr17:17358442-17358443	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs182369996	chr17:17358466-17358467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555851563	chr17:17358479-17358480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114295046	chr17:17358506-17358507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs114612039	chr17:17358508-17358509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs558883529	chr17:17358587-17358588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs572404939	chr17:17358610-17358611	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541206895	chr17:17358631-17358632	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201982806	chr17:17358659-17358660	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554773266	chr17:17358694-17358695	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574018889	chr17:17358744-17358745	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs71364025	chr17:17358753-17358754	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs562690990	chr17:17358754-17358755	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373701158	chr17:17358763-17358764	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570395393	chr17:17358768-17358769	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565221600	chr17:17358780-17358781	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528005920	chr17:17358785-17358786	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564279952	chr17:17358801-17358802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187416500	chr17:17358840-17358841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150082235	chr17:17358851-17358852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529709542	chr17:17358854-17358855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138408321	chr17:17358902-17358903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149262091	chr17:17358906-17358907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs147384045	chr17:17358907-17358908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558615970	chr17:17358928-17358929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565954027	chr17:17358944-17358945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534934913	chr17:17358986-17358987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563540282	chr17:17359003-17359004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138440442	chr17:17359021-17359022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574575581	chr17:17359036-17359037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144000451	chr17:17359050-17359051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs147309355	chr17:17359066-17359067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:162)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2552 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

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	chr17:17354200-17358200	Weak transcription	Fetal Muscle Trunk	muscle
4	chr17:17354800-17368000	Weak transcription	Fetal Thymus	thymus
5	chr17:17355800-17358600	Enhancers	Brain Germinal Matrix	brain
6	chr17:17357400-17358600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr17:17357800-17363200	Weak transcription	Spleen	Spleen
8	chr17:17358000-17358800	Enhancers	Fetal Muscle Leg	muscle
9	chr17:17358400-17358600	Enhancers	Fetal Muscle Trunk	muscle
10	chr17:17358600-17358800	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr17:17358600-17358800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr17:17358600-17358800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
13	chr17:17358800-17359600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr17:17358800-17363200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr17:17359600-17359800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr17:17359600-17359800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr17:17359800-17363200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr17:17359800-17363200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr17:17361200-17361600	Enhancers	Rectal Mucosa Donor 29	rectum
20	chr17:17361400-17363400	Weak transcription	Pancreas	Pancrea
21	chr17:17361600-17365400	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr17:17363200-17363400	Genic enhancers	Spleen	Spleen
23	chr17:17363200-17363600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr17:17363200-17363600	ZNF genes & repeats	Fetal Kidney	kidney
25	chr17:17363200-17363600	ZNF genes & repeats	Right Atrium	heart
26	chr17:17363200-17363800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr17:17363200-17363800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr17:17363400-17363600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr17:17363400-17363600	ZNF genes & repeats	Gastric	stomach
30	chr17:17363400-17363600	Enhancers	Lung	lung
31	chr17:17363400-17363600	ZNF genes & repeats	Pancreas	Pancrea
32	chr17:17363400-17363600	Transcr. at gene 5' and 3'	Spleen	Spleen
33	chr17:17363400-17363800	ZNF genes & repeats	Brain Angular Gyrus	brain
34	chr17:17363400-17363800	ZNF genes & repeats	Fetal Lung	lung
35	chr17:17363600-17363800	Active TSS	Spleen	Spleen
36	chr17:17363600-17364800	Weak transcription	Gastric	stomach
37	chr17:17363600-17365000	Enhancers	HepG2	liver
38	chr17:17363600-17365400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr17:17363600-17371000	Weak transcription	Pancreas	Pancrea
40	chr17:17363600-17380000	Weak transcription	Right Atrium	heart
41	chr17:17363800-17365000	Weak transcription	Fetal Lung	lung
42	chr17:17363800-17367400	Weak transcription	Brain Angular Gyrus	brain
43	chr17:17363800-17380200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr17:17365000-17366200	Flanking Active TSS	HepG2	liver
45	chr17:17365200-17365800	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
46	chr17:17365200-17366000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr17:17365200-17366000	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr17:17365200-17367000	Enhancers	Fetal Intestine Small	intestine
49	chr17:17365200-17367600	Enhancers	Fetal Intestine Large	intestine
50	chr17:17365400-17365800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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