Variant report

Variant	nsv900934
Chromosome Location	chr13:96255706-96327574
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:96256406-96256707	HepG2	liver:	n/a	n/a
2	BACH1	chr13:96296108-96296371	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr13:96327371-96329644	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr13:96276318-96276620	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr13:96259660-96260057	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr13:96256419-96257221	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr13:96322132-96322474	K562	blood:	n/a	n/a
8	CEBPB	chr13:96259599-96260058	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr13:96256330-96256841	MCF-7	breast:	n/a	chr13:96256560-96256569 chr13:96256559-96256570 chr13:96256558-96256571 chr13:96256560-96256569 chr13:96256560-96256569
10	CEBPB	chr13:96256482-96256685	K562	blood:	n/a	chr13:96256560-96256569 chr13:96256559-96256570 chr13:96256558-96256571 chr13:96256560-96256569 chr13:96256560-96256569
11	CEBPB	chr13:96256368-96256758	IMR90	lung:	n/a	chr13:96256560-96256569 chr13:96256559-96256570 chr13:96256558-96256571 chr13:96256560-96256569 chr13:96256560-96256569
12	CEBPB	chr13:96256310-96256940	HCT-116	colon:	n/a	chr13:96256560-96256569 chr13:96256559-96256570 chr13:96256558-96256571 chr13:96256560-96256569 chr13:96256560-96256569
13	CEBPB	chr13:96256219-96256769	HepG2	liver:	n/a	chr13:96256560-96256569 chr13:96256559-96256570 chr13:96256558-96256571 chr13:96256560-96256569 chr13:96256560-96256569
14	CEBPB	chr13:96259685-96260016	MCF-7	breast:	n/a	n/a
15	CEBPB	chr13:96256315-96256815	A549	lung:	n/a	chr13:96256560-96256569 chr13:96256559-96256570 chr13:96256558-96256571 chr13:96256560-96256569 chr13:96256560-96256569
16	CEBPB	chr13:96256292-96256770	HepG2	liver:	n/a	chr13:96256560-96256569 chr13:96256559-96256570 chr13:96256558-96256571 chr13:96256560-96256569 chr13:96256560-96256569
17	CEBPB	chr13:96256223-96256941	ECC-1	luminal epithelium:	n/a	chr13:96256560-96256569 chr13:96256559-96256570 chr13:96256558-96256571 chr13:96256560-96256569 chr13:96256560-96256569
18	CEBPB	chr13:96280717-96280917	K562	blood:	n/a	chr13:96280752-96280763
19	CEBPB	chr13:96256378-96256761	H1-hESC	embryonic stem cell:	n/a	chr13:96256560-96256569 chr13:96256559-96256570 chr13:96256558-96256571 chr13:96256560-96256569 chr13:96256560-96256569
20	CEBPB	chr13:96256294-96256846	ECC-1	luminal epithelium:	n/a	chr13:96256560-96256569 chr13:96256559-96256570 chr13:96256558-96256571 chr13:96256560-96256569 chr13:96256560-96256569
21	CEBPB	chr13:96256437-96256675	HepG2	liver:	n/a	chr13:96256560-96256569 chr13:96256559-96256570 chr13:96256558-96256571 chr13:96256560-96256569 chr13:96256560-96256569
22	CEBPB	chr13:96258041-96258236	HepG2	liver:	n/a	chr13:96258127-96258138 chr13:96258126-96258139
23	CEBPB	chr13:96256150-96257052	Hela-S3	cervix:	n/a	chr13:96256560-96256569 chr13:96256559-96256570 chr13:96256558-96256571 chr13:96256560-96256569 chr13:96256560-96256569
24	CEBPB	chr13:96303066-96303187	HepG2	liver:	n/a	n/a
25	CEBPB	chr13:96256157-96256772	HepG2	liver:	n/a	chr13:96256560-96256569 chr13:96256559-96256570 chr13:96256558-96256571 chr13:96256560-96256569 chr13:96256560-96256569
26	CEBPB	chr13:96261305-96261593	IMR90	lung:	n/a	chr13:96261479-96261490
27	CEBPB	chr13:96297114-96297296	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr13:96256358-96256759	A549	lung:	n/a	chr13:96256560-96256569 chr13:96256559-96256570 chr13:96256558-96256571 chr13:96256560-96256569 chr13:96256560-96256569
29	CEBPB	chr13:96277450-96277576	A549	lung:	n/a	chr13:96277506-96277517 chr13:96277507-96277518
30	CEBPB	chr13:96256261-96256872	MCF-7	breast:	n/a	chr13:96256560-96256569 chr13:96256559-96256570 chr13:96256558-96256571 chr13:96256560-96256569 chr13:96256560-96256569
31	CEBPB	chr13:96260894-96261658	Hela-S3	cervix:	n/a	chr13:96261479-96261490
32	CEBPB	chr13:96257528-96258504	Hela-S3	cervix:	n/a	chr13:96258452-96258465 chr13:96258127-96258138 chr13:96258126-96258139 chr13:96258454-96258465
33	CEBPB	chr13:96277417-96277630	HepG2	liver:	n/a	chr13:96277506-96277517 chr13:96277507-96277518
34	CEBPB	chr13:96256338-96256944	HCT-116	colon:	n/a	chr13:96256560-96256569 chr13:96256559-96256570 chr13:96256558-96256571 chr13:96256560-96256569 chr13:96256560-96256569
35	CEBPB	chr13:96256230-96256948	A549	lung:	n/a	chr13:96256560-96256569 chr13:96256559-96256570 chr13:96256558-96256571 chr13:96256560-96256569 chr13:96256560-96256569
36	CEBPB	chr13:96259708-96259983	IMR90	lung:	n/a	n/a
37	CEBPB	chr13:96256385-96256707	K562	blood:	n/a	chr13:96256560-96256569 chr13:96256559-96256570 chr13:96256558-96256571 chr13:96256560-96256569 chr13:96256560-96256569
38	CEBPB	chr13:96256379-96256750	K562	blood:	n/a	chr13:96256560-96256569 chr13:96256559-96256570 chr13:96256558-96256571 chr13:96256560-96256569 chr13:96256560-96256569
39	CEBPB	chr13:96280591-96280916	HepG2	liver:	n/a	chr13:96280752-96280763
40	CEBPB	chr13:96280583-96280925	IMR90	lung:	n/a	chr13:96280752-96280763
41	CEBPB	chr13:96280632-96280912	A549	lung:	n/a	chr13:96280752-96280763
42	CEBPD	chr13:96308920-96309248	K562	blood:	n/a	n/a
43	CEBPD	chr13:96256383-96256772	HepG2	liver:	n/a	chr13:96256560-96256569
44	CEBPD	chr13:96256397-96256693	HepG2	liver:	n/a	chr13:96256560-96256569
45	CEBPD	chr13:96296812-96297098	HepG2	liver:	n/a	n/a
46	CHD1	chr13:96297013-96297346	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr13:96296008-96296219	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD1	chr13:96295049-96295238	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr13:96313388-96313470	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr13:96256483-96256577	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:96297281-96297331	NHDF-neo	bronchial:	n/a
2	chr13:96297281-96297331	NHDF-neo	bronchial:	n/a
3	chr13:96296997-96297047	PrEC	prostate:	n/a
4	chr13:96297338-96297388	AG09319	gingival:	n/a
5	chr13:96297224-96297274	HRPEpiC	eye:	n/a
6	chr13:96296144-96296194	HEK293	kidney:	embryo
7	chr13:96297058-96297108	H1-hESC	embryonic stem cell:	embryo
8	chr13:96296144-96296194	HUVEC	blood vessel:	n/a
9	chr13:96297058-96297108	K562	blood:	n/a
10	chr13:96297197-96297247	Jurkat	blood:	n/a
11	chr13:96291582-96291632	Caco-2	colon:	n/a
12	chr13:96293882-96293932	K562	blood:	n/a
13	chr13:96256596-96256646	HCM	heart:	n/a
14	chr13:96296979-96297029	A549	lung:	n/a
15	chr13:96294863-96294913	AG04450	lung:	fetal
16	chr13:96297281-96297331	Hela-S3	cervix:	n/a
17	chr13:96294863-96294913	AG09319	gingival:	n/a
18	chr13:96297053-96297103	LNCaP	prostate:	n/a
19	chr13:96296844-96296894	AG04450	lung:	fetal
20	chr13:96296983-96297033	Caco-2	colon:	n/a
21	chr13:96293882-96293932	GM12878	blood:	n/a
22	chr13:96297058-96297108	GM12892	blood:	n/a
23	chr13:96297338-96297388	SK-N-MC	brain:	n/a
24	chr13:96294863-96294913	HCPEpiC	choroid plexus:	n/a
25	chr13:96297338-96297388	HRPEpiC	eye:	n/a
26	chr13:96296983-96297033	HPAEpiC	pulmonary alveolar:	n/a
27	chr13:96296979-96297029	T-47D	breast:	n/a
28	chr13:96297051-96297101	HMEC	breast:	n/a
29	chr13:96293572-96293622	RPTEC	kidney:	n/a
30	chr13:96297058-96297108	ovcar-3	ovarian:	n/a
31	chr13:96297197-96297247	SK-N-MC	brain:	n/a
32	chr13:96294863-96294913	HCT-116	colon:	n/a
33	chr13:96293572-96293622	HL-60	blood:	n/a
34	chr13:96296708-96296758	ECC-1	luminal epithelium:	n/a
35	chr13:96296979-96297029	Jurkat	blood:	n/a
36	chr13:96297281-96297331	ProgFib	skin:	n/a
37	chr13:96297197-96297247	BE2_C	brain:	n/a
38	chr13:96297051-96297101	RPTEC	kidney:	n/a
39	chr13:96291582-96291632	HCPEpiC	choroid plexus:	n/a
40	chr13:96294468-96294518	ECC-1	luminal epithelium:	n/a
41	chr13:96293882-96293932	Jurkat	blood:	n/a
42	chr13:96297058-96297108	SKMC	muscle:	n/a
43	chr13:96293572-96293622	AG09309	skin:	n/a
44	chr13:96294131-96294181	GM12878	blood:	n/a
45	chr13:96300257-96300307	H1-hESC	embryonic stem cell:	embryo
46	chr13:96294131-96294181	ProgFib	skin:	n/a
47	chr13:96296708-96296758	MCF-7	breast:	n/a
48	chr13:96300257-96300307	HIPEpiC	eye:	n/a
49	chr13:96297058-96297108	Hela-S3	cervix:	n/a
50	chr13:96297338-96297388	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:96315925..96317996-chr13:96327867..96330110,2	K562	blood:
2	chr13:96275761..96276878-chr13:96313133..96314021,4	MCF-7	breast:
3	chr13:96305271..96306913-chr13:96309464..96311893,2	K562	blood:
4	chr13:96266664..96268802-chr13:96328604..96330482,2	MCF-7	breast:
5	chr13:96305861..96308688-chr13:96312615..96314888,2	K562	blood:
6	chr13:96189087..96189713-chr13:96275598..96276486,2	MCF-7	breast:
7	chr13:96319017..96320779-chr13:96328614..96330642,2	K562	blood:
8	chr13:96324907..96328412-chr13:96405169..96408703,4	K562	blood:
9	chr13:96275895..96276755-chr13:96486107..96487061,4	MCF-7	breast:
10	chr13:96256070..96258661-chr13:96261703..96264658,2	K562	blood:
11	chr13:96305271..96306913-chr13:96309464..96311893,2	K562	blood:
12	chr13:96307904..96310179-chr13:96327912..96330273,2	MCF-7	breast:
13	chr13:96184927..96187757-chr13:96272226..96274633,2	K562	blood:
14	chr13:96323652..96326335-chr13:96327203..96330421,3	K562	blood:
15	chr13:96256829..96259595-chr13:96329198..96332002,2	MCF-7	breast:
16	chr13:96256070..96258661-chr13:96261703..96264658,2	K562	blood:
17	chr13:96275761..96276878-chr13:96313133..96314021,4	MCF-7	breast:
18	chr13:96305861..96308688-chr13:96312615..96314888,2	K562	blood:
19	chr13:96119619..96122365-chr13:96309013..96311626,2	MCF-7	breast:
20	chr13:96321544..96324613-chr13:96328623..96330410,3	MCF-7	breast:
21	chr13:96275906..96276854-chr13:96486114..96486980,5	K562	blood:
22	chr13:96276047..96276870-chr13:96313091..96313781,2	MCF-7	breast:
23	chr13:96255180..96257718-chr13:96261326..96264048,2	MCF-7	breast:
24	chr13:96276047..96276870-chr13:96313091..96313781,2	MCF-7	breast:
25	chr13:96316222..96317996-chr13:96327067..96329367,2	K562	blood:
26	chr13:96277245..96279112-chr13:96327226..96329266,2	MCF-7	breast:
27	chr13:96275890..96276432-chr13:96486160..96486773,2	MCF-7	breast:
28	chr13:96320722..96323080-chr13:96327579..96329585,2	MCF-7	breast:
29	chr13:96255180..96257718-chr13:96261326..96264048,2	MCF-7	breast:
30	chr13:96323460..96326525-chr13:96328286..96330704,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DZIP1-1	chr13:96325097-96326922	XLOC_010698
2	lnc-DZIP1-1	chr13:96325124-96329183	NONHSAT034769
3	lnc-DZIP1-1	chr13:96300987-96301088	ENSG00000247400.3

Variant related genes	Relation type
DNAJC3	TF binding region
DZIP1	TF binding region
DNAJC3	CpG island
DZIP1	CpG island
ENSG00000223392	chromatin interactions
ENSG00000102580	chromatin interactions
ENSG00000247400	chromatin interactions
NT5C3	miRNA target sites

Extended variants
information (count: 2355 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2355 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9590305	chr13:96255706-96255707	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572405598	chr13:96255720-96255721	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534955517	chr13:96255736-96255737	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558043949	chr13:96255746-96255747	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs186768998	chr13:96255762-96255763	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139513773	chr13:96255765-96255766	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543635928	chr13:96255799-96255800	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189051055	chr13:96255800-96255801	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573695341	chr13:96255867-96255868	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs562375195	chr13:96255942-96255943	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542711424	chr13:96255953-96255954	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559058859	chr13:96256016-96256017	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs34234397	chr13:96256041-96256042	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531421308	chr13:96256076-96256077	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs149676415	chr13:96256084-96256085	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs144431926	chr13:96256102-96256103	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181722631	chr13:96256110-96256111	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530723984	chr13:96256173-96256174	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185636319	chr13:96256196-96256197	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs190363129	chr13:96256258-96256259	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs182713754	chr13:96256348-96256349	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs369570245	chr13:96256362-96256363	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs186027646	chr13:96256371-96256372	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs565898837	chr13:96256378-96256379	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs534729677	chr13:96256389-96256390	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs558007179	chr13:96256419-96256420	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs571653185	chr13:96256457-96256458	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs192135564	chr13:96256461-96256462	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs148488705	chr13:96256462-96256463	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs541601568	chr13:96256544-96256545	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs145307206	chr13:96256597-96256598	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs183891582	chr13:96256630-96256631	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs562305535	chr13:96256631-96256632	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs373117461	chr13:96256664-96256665	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs377412892	chr13:96256668-96256669	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs527833854	chr13:96256672-96256673	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs58692855	chr13:96256692-96256693	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs545072131	chr13:96256707-96256708	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs187944547	chr13:96256732-96256733	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs530787961	chr13:96256739-96256740	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs544524025	chr13:96256783-96256784	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs147631221	chr13:96256792-96256793	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs34574131	chr13:96256806-96256807	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs74109012	chr13:96256819-96256820	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs142173898	chr13:96256855-96256856	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs144410069	chr13:96256864-96256865	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs370759502	chr13:96256869-96256870	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs528463809	chr13:96256964-96256965	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs551401736	chr13:96256988-96256989	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs151285543	chr13:96256994-96256995	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Rhabdomyosarcoma	17210683	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Burkitt''s lymphoma	20823134	CNVD

Chromatin state (count:1727 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:96229000-96256200	Weak transcription	Gastric	stomach
2	chr13:96229600-96256000	Weak transcription	Right Ventricle	heart
3	chr13:96230200-96258200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr13:96231600-96260000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr13:96231800-96256800	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr13:96232200-96272800	Weak transcription	Brain Substantia Nigra	brain
7	chr13:96235600-96284200	Weak transcription	Rectal Smooth Muscle	rectum
8	chr13:96238000-96256400	Weak transcription	Placenta	Placenta
9	chr13:96238200-96261000	Weak transcription	Spleen	Spleen
10	chr13:96239800-96259800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr13:96240000-96261200	Weak transcription	Colon Smooth Muscle	Colon
12	chr13:96240000-96272800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr13:96240000-96273000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr13:96240200-96255800	Weak transcription	Fetal Intestine Large	intestine
15	chr13:96240200-96256000	Weak transcription	Fetal Intestine Small	intestine
16	chr13:96240200-96256200	Weak transcription	Aorta	Aorta
17	chr13:96241200-96260800	Weak transcription	Fetal Heart	heart
18	chr13:96242200-96272600	Weak transcription	Brain Angular Gyrus	brain
19	chr13:96243200-96256200	Weak transcription	Fetal Brain Male	brain
20	chr13:96246400-96278600	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr13:96247200-96259600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr13:96247200-96267000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr13:96247800-96256000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr13:96247800-96261200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr13:96247800-96293600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr13:96248000-96256200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr13:96248000-96276600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr13:96248200-96256000	Weak transcription	Esophagus	oesophagus
29	chr13:96249000-96264800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
30	chr13:96249400-96272200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr13:96251400-96294400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr13:96251600-96255800	Strong transcription	Osteobl	bone
33	chr13:96252000-96258000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr13:96252000-96259000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr13:96252200-96256000	Strong transcription	Fetal Brain Female	brain
36	chr13:96252200-96256200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr13:96252200-96256600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr13:96252200-96257000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr13:96252200-96258400	Strong transcription	Fetal Stomach	stomach
40	chr13:96252800-96260000	Strong transcription	HUES6 Cell Line	embryonic stem cell
41	chr13:96253400-96259000	Strong transcription	NHLF	lung
42	chr13:96253400-96264800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
43	chr13:96253600-96256000	Strong transcription	A549	lung
44	chr13:96253600-96257000	Strong transcription	H9 Cell Line	embryonic stem cell
45	chr13:96253600-96263200	Weak transcription	Brain Cingulate Gyrus	brain
46	chr13:96254000-96261000	Weak transcription	Right Atrium	heart
47	chr13:96254200-96256200	Strong transcription	NHDF-Ad	bronchial
48	chr13:96254200-96256600	Strong transcription	Fetal Lung	lung
49	chr13:96254200-96265000	Strong transcription	HUES64 Cell Line	embryonic stem cell
50	chr13:96254400-96256000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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