Variant report

Variant	nsv969946
Chromosome Location	chr5:14867971-14880715
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	chr5:14874566-14874709	K562	blood:	n/a	n/a
2	ARID3A	chr5:14871003-14871218	HepG2	liver:	n/a	n/a
3	ATF1	chr5:14869476-14869665	K562	blood:	n/a	n/a
4	ATF3	chr5:14871995-14872172	K562	blood:	n/a	n/a
5	BACH1	chr5:14872044-14872466	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:14871467-14871605	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr5:14872034-14872193	K562	blood:	n/a	n/a
8	BHLHE40	chr5:14871725-14872235	GM12878	blood:	n/a	n/a
9	BHLHE40	chr5:14871799-14872204	HepG2	liver:	n/a	n/a
10	BRCA1	chr5:14872602-14873086	Hela-S3	cervix:	n/a	n/a
11	CCNT2	chr5:14871835-14872494	K562	blood:	n/a	chr5:14872293-14872302 chr5:14872391-14872400 chr5:14872300-14872309
12	CEBPB	chr5:14880417-14880605	HepG2	liver:	n/a	chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880539 chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880537
13	CEBPB	chr5:14880145-14880333	HepG2	liver:	n/a	n/a
14	CEBPB	chr5:14870576-14870758	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr5:14880249-14880712	H1-hESC	embryonic stem cell:	n/a	chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880539 chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880537
16	CEBPB	chr5:14875565-14875768	A549	lung:	n/a	chr5:14875646-14875659 chr5:14875648-14875659
17	CEBPB	chr5:14880127-14881193	A549	lung:	n/a	chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880539 chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880537
18	CEBPB	chr5:14880147-14880822	HCT-116	colon:	n/a	chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880539 chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880537
19	CEBPB	chr5:14880056-14881209	MCF-7	breast:	n/a	chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880539 chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880537
20	CEBPB	chr5:14880267-14880698	ECC-1	luminal epithelium:	n/a	chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880539 chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880537
21	CEBPB	chr5:14880424-14880576	K562	blood:	n/a	chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880539 chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880537
22	CEBPB	chr5:14880079-14881172	IMR90	lung:	n/a	chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880539 chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880537
23	CEBPB	chr5:14877361-14877535	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr5:14873320-14873352	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr5:14880202-14880784	A549	lung:	n/a	chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880539 chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880537
26	CEBPB	chr5:14880164-14880873	MCF-7	breast:	n/a	chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880539 chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880537
27	CEBPB	chr5:14880202-14880904	K562	blood:	n/a	chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880539 chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880537
28	CEBPB	chr5:14880322-14880708	ECC-1	luminal epithelium:	n/a	chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880539 chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880537
29	CEBPB	chr5:14880115-14880761	HepG2	liver:	n/a	chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880539 chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880537
30	CEBPB	chr5:14879589-14881286	Hela-S3	cervix:	n/a	chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880539 chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880537
31	CEBPB	chr5:14880103-14881139	A549	lung:	n/a	chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880539 chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880537
32	CEBPB	chr5:14870966-14871609	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr5:14880325-14880696	K562	blood:	n/a	chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880539 chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880537
34	CEBPB	chr5:14871936-14873092	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr5:14879942-14881166	HepG2	liver:	n/a	chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880539 chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880537
36	CEBPB	chr5:14880083-14881155	HepG2	liver:	n/a	chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880539 chr5:14880528-14880537 chr5:14880528-14880537 chr5:14880526-14880537
37	CEBPD	chr5:14880110-14880578	HepG2	liver:	n/a	chr5:14880528-14880537 chr5:14880527-14880538
38	CHD1	chr5:14871627-14873214	IMR90	lung:	n/a	chr5:14872382-14872392
39	CHD2	chr5:14871121-14873136	Hela-S3	cervix:	n/a	chr5:14872382-14872392
40	CREB1	chr5:14871550-14872537	HepG2	liver:	n/a	n/a
41	CREB1	chr5:14872798-14873191	GM12878	blood:	n/a	n/a
42	CREB1	chr5:14871774-14872629	A549	lung:	n/a	n/a
43	CTCF	chr5:14871948-14872216	GM12891	blood:	n/a	n/a
44	CTCF	chr5:14871980-14872130	GM12867	blood:	n/a	n/a
45	CTCF	chr5:14870680-14870830	RPTEC	kidney:	n/a	n/a
46	CTCF	chr5:14872000-14872150	AG04449	skin:	n/a	n/a
47	CTCF	chr5:14872540-14872690	HCM	heart:	n/a	n/a
48	CTCF	chr5:14871956-14872199	NHEK	skin:	n/a	n/a
49	CTCF	chr5:14871952-14872259	K562	blood:	n/a	n/a
50	CTCF	chr5:14872380-14872530	HCM	heart:	n/a	chr5:14872424-14872437

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:14871910-14871960	NHDF-neo	bronchial:	n/a
2	chr5:14871443-14871493	HMEC	breast:	n/a
3	chr5:14871910-14871960	NHDF-neo	bronchial:	n/a
4	chr5:14871443-14871493	HMEC	breast:	n/a
5	chr5:14870666-14870716	BE2_C	brain:	n/a
6	chr5:14870749-14870799	HCPEpiC	choroid plexus:	n/a
7	chr5:14871469-14871519	HCF	heart:	n/a
8	chr5:14871542-14871592	CMK	blood:	n/a
9	chr5:14871845-14871895	Hepatocyte	liver:	n/a
10	chr5:14871910-14871960	HCPEpiC	choroid plexus:	n/a
11	chr5:14871443-14871493	ProgFib	skin:	n/a
12	chr5:14871469-14871519	HL-60	blood:	n/a
13	chr5:14873039-14873089	BE2_C	brain:	n/a
14	chr5:14871469-14871519	GM06990	blood:	n/a
15	chr5:14870594-14870644	GM19239	blood:	n/a
16	chr5:14871894-14871944	HCT-116	colon:	n/a
17	chr5:14872384-14872434	NHBE	bronchial:	n/a
18	chr5:14872384-14872434	AG09319	gingival:	n/a
19	chr5:14871469-14871519	NHDF-neo	bronchial:	n/a
20	chr5:14870594-14870644	HEK293	kidney:	embryo
21	chr5:14870666-14870716	HRE	kidney:	n/a
22	chr5:14870083-14870133	HCM	heart:	n/a
23	chr5:14872207-14872257	HPAEpiC	pulmonary alveolar:	n/a
24	chr5:14872384-14872434	LNCaP	prostate:	n/a
25	chr5:14871908-14871958	U87	brain:	n/a
26	chr5:14872551-14872601	HEEpiC	esophagus:	n/a
27	chr5:14874832-14874882	AG04450	lung:	fetal
28	chr5:14871845-14871895	SAEC	small airway:	n/a
29	chr5:14870666-14870716	PANC-1	pancreas:	n/a
30	chr5:14871894-14871944	PrEC	prostate:	n/a
31	chr5:14871894-14871944	NB4	blood:	n/a
32	chr5:14874832-14874882	GM12891	blood:	n/a
33	chr5:14872934-14872984	IMR90	lung:	fetal
34	chr5:14870083-14870133	SAEC	small airway:	n/a
35	chr5:14872384-14872434	Hela-S3	cervix:	n/a
36	chr5:14874549-14874599	AG04449	skin:	fetal
37	chr5:14871908-14871958	HAEpiC	amniotic membrane:	n/a
38	chr5:14870749-14870799	SAEC	small airway:	n/a
39	chr5:14872612-14872662	HRCEpiC	kidney:	n/a
40	chr5:14871469-14871519	AG09319	gingival:	n/a
41	chr5:14870666-14870716	PFSK-1	brain:	n/a
42	chr5:14874832-14874882	MCF-7	breast:	n/a
43	chr5:14871894-14871944	HPAEpiC	pulmonary alveolar:	n/a
44	chr5:14870666-14870716	GM12891	blood:	n/a
45	chr5:14871443-14871493	SKMC	muscle:	n/a
46	chr5:14871910-14871960	HNPCEpiC	eye:	n/a
47	chr5:14872207-14872257	SK-N-SH	brain:	n/a
48	chr5:14874549-14874599	HCF	heart:	n/a
49	chr5:14872612-14872662	Hepatocyte	liver:	n/a
50	chr5:14871894-14871944	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:14872363..14873864-chr6:26021710..26023410,2	MCF-7	breast:
2	chr10:93683034..93683876-chr5:14871412..14872027,2	Hela-S3	cervix:
3	chr5:14765139..14767276-chr5:14879416..14882042,3	MCF-7	breast:
4	chr5:14870615..14876771-chr5:14877137..14881397,9	MCF-7	breast:
5	chr5:14870499..14873628-chr5:14876677..14878722,3	MCF-7	breast:
6	chr16:15736896..15737522-chr5:14872268..14872832,2	Hela-S3	cervix:
7	chr12:56511621..56512291-chr5:14872089..14872740,2	Hela-S3	cervix:
8	chr5:14871557..14872468-chr8:128747896..128748761,2	NB4	blood:
9	chr1:11968024..11968902-chr5:14869583..14870398,2	Hela-S3	cervix:
10	chr5:14867615..14869927-chr5:14870237..14872388,4	K562	blood:
11	chr5:14879517..14881326-chr5:14882980..14885197,2	MCF-7	breast:
12	chr5:14727596..14728164-chr5:14870078..14871126,3	K562	blood:
13	chr17:41465783..41466320-chr5:14871948..14872665,2	Hela-S3	cervix:
14	chr5:14871623..14873903-chr5:14874758..14876587,2	K562	blood:
15	chr5:14870499..14873628-chr5:14876677..14878722,3	MCF-7	breast:
16	chr5:14863140..14869148-chr5:14869858..14873392,6	MCF-7	breast:
17	chr5:14864911..14869985-chr5:14870388..14873560,6	K562	blood:
18	chr5:14871623..14873903-chr5:14874758..14876587,2	K562	blood:
19	chr5:14870615..14876771-chr5:14877137..14881397,9	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM105B-8	chr5:14872441-14872822	ENSG00000272057.1
2	lnc-ANKH-5	chr5:14877776-14878028	NONHSAT100570

Variant related genes	Relation type
ENSG00000272057	TF binding region
ANKH	TF binding region
HNRNPKP5	TF binding region
UQCRBP3	TF binding region
ENSG00000272057	CpG island
ANKH	CpG island
HNRNPKP5	CpG island
UQCRBP3	CpG island
ENSG00000135482	chromatin interactions
ENSG00000166783	chromatin interactions
ENSG00000139641	chromatin interactions
ENSG00000196176	chromatin interactions
ENSG00000249928	chromatin interactions
ENSG00000272057	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000250662	chromatin interactions
ENSG00000136997	chromatin interactions
ENSG00000154122	chromatin interactions
ENSG00000095564	chromatin interactions
ENSG00000272213	chromatin interactions
ENSG00000072864	chromatin interactions

Extended variants
information (count: 455 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:455 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184868071	chr5:14867978-14867979	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs55779637	chr5:14868057-14868058	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs534794790	chr5:14868072-14868073	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs533513905	chr5:14868086-14868087	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs551791824	chr5:14868124-14868125	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs188480987	chr5:14868138-14868139	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs147107166	chr5:14868284-14868285	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs570075946	chr5:14868328-14868329	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs531065253	chr5:14868360-14868361	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs549672825	chr5:14868368-14868369	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs567724310	chr5:14868380-14868381	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs192922537	chr5:14868385-14868386	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs6868959	chr5:14868397-14868398	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs568116794	chr5:14868405-14868406	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs571004524	chr5:14868407-14868408	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs16903724	chr5:14868459-14868460	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs77266956	chr5:14868506-14868507	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs77825245	chr5:14868507-14868508	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs78281689	chr5:14868509-14868510	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs556495282	chr5:14868543-14868544	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs558367901	chr5:14868544-14868545	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs551019180	chr5:14868554-14868555	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs556951185	chr5:14868634-14868635	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs546505425	chr5:14868699-14868700	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs542525450	chr5:14868725-14868726	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs143951031	chr5:14868743-14868744	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs79750805	chr5:14868765-14868766	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs540426298	chr5:14868779-14868780	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs565117308	chr5:14868815-14868816	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs531865904	chr5:14868817-14868818	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs75811476	chr5:14868829-14868830	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs185651194	chr5:14868839-14868840	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs545521574	chr5:14868870-14868871	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs563505279	chr5:14868910-14868911	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs2921605	chr5:14868921-14868922	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs549142918	chr5:14868965-14868966	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs567924012	chr5:14868966-14868967	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs528805093	chr5:14868988-14868989	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs114903454	chr5:14869006-14869007	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs559269920	chr5:14869034-14869035	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs571514119	chr5:14869085-14869086	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs13181335	chr5:14869153-14869154	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
43	rs113877053	chr5:14869160-14869161	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs568896077	chr5:14869297-14869298	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs150665005	chr5:14869317-14869318	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs554316335	chr5:14869417-14869418	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs573083641	chr5:14869587-14869588	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs10513191	chr5:14869666-14869667	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs558738648	chr5:14869668-14869669	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs577133369	chr5:14869673-14869674	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Autism	22495311	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
Breast cancer	21364760	CNVD
Non-small cell lung cancer	17643093	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	18940311	CNVD
Central neurocytomas	17123091	CNVD
Mental retardation	17847001	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	19546859	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Williams Syndrome	20824207	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Gastric cancer	17229543	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:701 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:14824800-14869600	Weak transcription	Stomach Smooth Muscle	stomach
2	chr5:14831000-14870400	Weak transcription	Spleen	Spleen
3	chr5:14835600-14869000	Weak transcription	NHDF-Ad	bronchial
4	chr5:14837400-14869400	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr5:14844800-14869200	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr5:14848800-14870000	Weak transcription	Thymus	Thymus
7	chr5:14849200-14869800	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr5:14850800-14869000	Weak transcription	Brain Germinal Matrix	brain
9	chr5:14851600-14869800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr5:14853200-14869000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr5:14855400-14868800	Weak transcription	Hela-S3	cervix
12	chr5:14855400-14870000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr5:14855400-14870000	Weak transcription	Placenta	Placenta
14	chr5:14856600-14869000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr5:14857400-14869000	Weak transcription	Primary T cells from cord blood	blood
16	chr5:14860400-14868800	Weak transcription	Dnd41	blood
17	chr5:14860800-14869200	Weak transcription	HMEC	breast
18	chr5:14860800-14869400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr5:14861800-14869400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr5:14861800-14870400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr5:14862000-14869200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr5:14862000-14869400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr5:14862200-14868800	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr5:14862400-14868800	Weak transcription	Adipose Nuclei	Adipose
25	chr5:14863000-14868000	Weak transcription	Fetal Intestine Large	intestine
26	chr5:14863000-14868000	Weak transcription	Osteobl	bone
27	chr5:14863200-14868200	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr5:14863200-14868800	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr5:14863400-14868400	Weak transcription	Fetal Intestine Small	intestine
30	chr5:14863600-14868600	Weak transcription	Liver	Liver
31	chr5:14863600-14868800	Weak transcription	Right Atrium	heart
32	chr5:14863600-14869000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr5:14863800-14868600	Weak transcription	Stomach Mucosa	stomach
34	chr5:14863800-14868800	Weak transcription	Fetal Brain Female	brain
35	chr5:14863800-14868800	Weak transcription	Right Ventricle	heart
36	chr5:14864000-14868400	Weak transcription	Duodenum Mucosa	Duodenum
37	chr5:14864000-14868600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr5:14864000-14868600	Weak transcription	HepG2	liver
39	chr5:14864200-14869200	Weak transcription	Aorta	Aorta
40	chr5:14864200-14870000	Weak transcription	Pancreas	Pancrea
41	chr5:14864800-14868000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr5:14864800-14869000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr5:14864800-14869000	Weak transcription	Brain Angular Gyrus	brain
44	chr5:14864800-14869000	Weak transcription	Brain Cingulate Gyrus	brain
45	chr5:14865000-14868600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr5:14865000-14868600	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr5:14865000-14869000	Weak transcription	Brain Anterior Caudate	brain
48	chr5:14865200-14868200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr5:14865200-14868600	Weak transcription	Left Ventricle	heart
50	chr5:14865200-14870200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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