Variant report

Variant	nsv832649
Chromosome Location	chr13:76424872-76657891
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2038)
CpG islands
(count:1100)
Chromatin interactive
region (count:30)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2038 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:76537499-76537752	K562	blood:	n/a	n/a
2	ARID3A	chr13:76559284-76559897	K562	blood:	n/a	n/a
3	ARID3A	chr13:76450475-76450923	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:76603056-76603834	K562	blood:	n/a	n/a
5	ARID3A	chr13:76593602-76593887	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:76579598-76579908	K562	blood:	n/a	n/a
7	ARID3A	chr13:76522818-76522965	K562	blood:	n/a	n/a
8	ARID3A	chr13:76602372-76602523	K562	blood:	n/a	n/a
9	ARID3A	chr13:76444552-76444937	HepG2	liver:	n/a	n/a
10	ARID3A	chr13:76450563-76450871	K562	blood:	n/a	n/a
11	ATF2	chr13:76560824-76561287	GM12878	blood:	n/a	n/a
12	ATF2	chr13:76534622-76535151	GM12878	blood:	n/a	n/a
13	ATF2	chr13:76534509-76535156	GM12878	blood:	n/a	n/a
14	BACH1	chr13:76463777-76463874	K562	blood:	n/a	n/a
15	BACH1	chr13:76537470-76537809	K562	blood:	n/a	n/a
16	BACH1	chr13:76537448-76537842	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr13:76463615-76464005	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr13:76560991-76561290	GM12878	blood:	n/a	n/a
19	BATF	chr13:76534633-76534979	GM12878	blood:	n/a	n/a
20	BATF	chr13:76534611-76535247	GM12878	blood:	n/a	n/a
21	BCL11A	chr13:76534761-76534990	GM12878	blood:	n/a	n/a
22	BCL11A	chr13:76534599-76535183	GM12878	blood:	n/a	n/a
23	BCL3	chr13:76583328-76584299	A549	lung:	n/a	n/a
24	BHLHE40	chr13:76559381-76559682	K562	blood:	n/a	n/a
25	BHLHE40	chr13:76444883-76444909	K562	blood:	n/a	n/a
26	BHLHE40	chr13:76579770-76579771	K562	blood:	n/a	n/a
27	BHLHE40	chr13:76570830-76570995	GM12878	blood:	n/a	n/a
28	BHLHE40	chr13:76537516-76537890	K562	blood:	n/a	n/a
29	BHLHE40	chr13:76438943-76439039	HepG2	liver:	n/a	n/a
30	BHLHE40	chr13:76591086-76591286	GM12878	blood:	n/a	n/a
31	BHLHE40	chr13:76536089-76536327	K562	blood:	n/a	n/a
32	BHLHE40	chr13:76591133-76591336	K562	blood:	n/a	n/a
33	BHLHE40	chr13:76450555-76450879	HepG2	liver:	n/a	n/a
34	BRCA1	chr13:76461975-76461988	GM12878	blood:	n/a	n/a
35	BRCA1	chr13:76450604-76450983	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr13:76603174-76603645	K562	blood:	n/a	n/a
37	CBX3	chr13:76590994-76591244	K562	blood:	n/a	n/a
38	CBX3	chr13:76559263-76559793	K562	blood:	n/a	n/a
39	CCNT2	chr13:76577864-76578064	K562	blood:	n/a	n/a
40	CCNT2	chr13:76579693-76579959	K562	blood:	n/a	n/a
41	CCNT2	chr13:76559391-76559719	K562	blood:	n/a	chr13:76559513-76559533
42	CCNT2	chr13:76536196-76536396	K562	blood:	n/a	n/a
43	CCNT2	chr13:76603230-76603534	K562	blood:	n/a	n/a
44	CEBPB	chr13:76444663-76444937	HepG2	liver:	n/a	n/a
45	CEBPB	chr13:76567874-76568379	K562	blood:	n/a	chr13:76568161-76568172
46	CEBPB	chr13:76597815-76598129	IMR90	lung:	n/a	chr13:76597960-76597973
47	CEBPB	chr13:76639577-76639686	HepG2	liver:	n/a	chr13:76639650-76639661
48	CEBPB	chr13:76447678-76448013	IMR90	lung:	n/a	n/a
49	CEBPB	chr13:76438861-76439330	IMR90	lung:	n/a	n/a
50	CEBPB	chr13:76633694-76633985	K562	blood:	n/a	chr13:76633838-76633849

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:76445108-76445158	HCM	heart:	n/a
2	chr13:76508987-76509037	SK-N-MC	brain:	n/a
3	chr13:76445108-76445158	HCM	heart:	n/a
4	chr13:76508987-76509037	SK-N-MC	brain:	n/a
5	chr13:76430089-76430139	BJ	skin:	n/a
6	chr13:76450676-76450726	SAEC	small airway:	n/a
7	chr13:76536939-76536989	HRPEpiC	eye:	n/a
8	chr13:76450676-76450726	AG10803	skin:	n/a
9	chr13:76430665-76430715	HIPEpiC	eye:	n/a
10	chr13:76444831-76444881	HMEC	breast:	n/a
11	chr13:76430089-76430139	LNCaP	prostate:	n/a
12	chr13:76444293-76444343	BJ	skin:	n/a
13	chr13:76430665-76430715	ECC-1	luminal epithelium:	n/a
14	chr13:76444823-76444873	HRE	kidney:	n/a
15	chr13:76445065-76445115	HUVEC	blood vessel:	n/a
16	chr13:76444850-76444900	GM12891	blood:	n/a
17	chr13:76444798-76444848	HEK293	kidney:	embryo
18	chr13:76444823-76444873	Hela-S3	cervix:	n/a
19	chr13:76445108-76445158	NT2-D1	testis:	n/a
20	chr13:76444293-76444343	AG09309	skin:	n/a
21	chr13:76430665-76430715	PrEC	prostate:	n/a
22	chr13:76430722-76430772	H1-hESC	embryonic stem cell:	embryo
23	chr13:76444831-76444881	ECC-1	luminal epithelium:	n/a
24	chr13:76444293-76444343	NT2-D1	testis:	n/a
25	chr13:76445055-76445105	BE2_C	brain:	n/a
26	chr13:76464782-76464832	HCF	heart:	n/a
27	chr13:76444823-76444873	MCF10A-Er-Src	breast:	n/a
28	chr13:76430722-76430772	HMEC	breast:	n/a
29	chr13:76444850-76444900	SK-N-MC	brain:	n/a
30	chr13:76508987-76509037	SK-N-SH_RA	brain:	n/a
31	chr13:76464782-76464832	Caco-2	colon:	n/a
32	chr13:76462678-76462728	HRCEpiC	kidney:	n/a
33	chr13:76430665-76430715	MCF10A-Er-Src	breast:	n/a
34	chr13:76444293-76444343	LNCaP	prostate:	n/a
35	chr13:76508987-76509037	AG09309	skin:	n/a
36	chr13:76430722-76430772	Caco-2	colon:	n/a
37	chr13:76445108-76445158	RPTEC	kidney:	n/a
38	chr13:76464782-76464832	A549	lung:	n/a
39	chr13:76430089-76430139	HUVEC	blood vessel:	n/a
40	chr13:76430188-76430238	U87	brain:	n/a
41	chr13:76432094-76432144	HepG2	liver:	n/a
42	chr13:76445108-76445158	CMK	blood:	n/a
43	chr13:76464782-76464832	ProgFib	skin:	n/a
44	chr13:76445108-76445158	AG10803	skin:	n/a
45	chr13:76430089-76430139	CMK	blood:	n/a
46	chr13:76444850-76444900	NT2-D1	testis:	n/a
47	chr13:76432094-76432144	Caco-2	colon:	n/a
48	chr13:76432094-76432144	NT2-D1	testis:	n/a
49	chr13:76430089-76430139	NH-A	brain:	n/a
50	chr13:76444823-76444873	BJ	skin:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:76569777..76571605-chr13:76572909..76574640,2	K562	blood:
2	chr13:76450119..76450751-chr13:76590749..76591620,4	MCF-7	breast:
3	chr13:76450119..76450751-chr13:76590749..76591620,4	MCF-7	breast:
4	chr13:76269693..76270610-chr13:76444514..76445100,2	MCF-7	breast:
5	chr13:76547458..76549080-chr13:76550616..76553437,2	K562	blood:
6	chr13:76450221..76451145-chr13:76590691..76591575,2	K562	blood:
7	chr13:76613524..76614133-chr13:77047364..77048499,5	MCF-7	breast:
8	chr13:76613162..76614105-chr13:77047335..77048422,4	MCF-7	breast:
9	chr13:76515246..76517813-chr7:2394882..2397172,2	MCF-7	breast:
10	chr13:76450136..76450986-chr13:77047347..77048254,3	K562	blood:
11	chr13:76425109..76426616-chr13:76428342..76430833,2	K562	blood:
12	chr13:76505508..76507844-chr13:76509844..76512114,2	K562	blood:
13	chr13:76438174..76440869-chr13:76485798..76487391,2	K562	blood:
14	chr13:76450462..76451207-chr13:76591002..76591569,2	MCF-7	breast:
15	chr13:76444326..76445057-chr13:77047425..77048326,2	K562	blood:
16	chr13:76438174..76440869-chr13:76485798..76487391,2	K562	blood:
17	chr13:76569777..76571605-chr13:76572909..76574640,2	K562	blood:
18	chr13:76540838..76542386-chr13:76542518..76545047,2	MCF-7	breast:
19	chr13:76450221..76451145-chr13:76590691..76591575,2	K562	blood:
20	chr13:76450462..76451207-chr13:76591002..76591569,2	MCF-7	breast:
21	chr13:76596252..76598622-chr13:76601248..76603382,2	K562	blood:
22	chr13:76444133..76445077-chr13:77047746..77048410,4	MCF-7	breast:
23	chr13:76596252..76598622-chr13:76601248..76603382,2	K562	blood:
24	chr13:76444149..76445101-chr13:76593232..76594146,4	MCF-7	breast:
25	chr13:76444149..76445101-chr13:76593232..76594146,4	MCF-7	breast:
26	chr13:76386406..76389041-chr13:76432929..76434756,2	MCF-7	breast:
27	chr13:76547458..76549080-chr13:76550616..76553437,2	K562	blood:
28	chr13:76450288..76451169-chr13:77047376..77048381,7	MCF-7	breast:
29	chr13:76540838..76542386-chr13:76542518..76545047,2	MCF-7	breast:
30	chr13:76505508..76507844-chr13:76509844..76512114,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL359392.1-1	chr13:76447793-76447870	XLOC_010433
2	lnc-COMMD6-3	chr13:76506531-76509268	ENSG00000261206.1
3	lnc-AL359392.1-2	chr13:76588495-76588637	XLOC_010435
4	lnc-AL359392.1-2	chr13:76587159-76587292	XLOC_010435
5	lnc-COMMD6-11	chr13:76587159-76587292	ENSG00000224933.2
6	lnc-AL359392.1-1	chr13:76457186-76457947	XLOC_010433
7	lnc-COMMD6-11	chr13:76588495-76588637	ENSG00000224933.2
8	lnc-AL359392.1-1	chr13:76445174-76445379	XLOC_010433
9	lnc-AL359392.1-1	chr13:76447988-76448108	XLOC_010433
10	lnc-COMMD6-10	chr13:76434594-76435511	NONHSAT034374

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	LMO7	hsa-miR-16-5p	chr13:76432682-76432703
2	LMO7	hsa-miR-16-5p	chr13:76432114-76432135

Variant related genes	Relation type
C13orf45	TF binding region
LINC01034	TF binding region
ENSG00000223458	TF binding region
LINC00561	TF binding region
LMO7	TF binding region
C13orf45	CpG island
LINC01034	CpG island
ENSG00000223458	CpG island
LINC00561	CpG island
LMO7	CpG island
ENSG00000136153	chromatin interactions
LBR	miRNA target sites
LCLAT1	miRNA target sites

Extended variants
information (count: 6279 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:6279 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7996791	chr13:76424935-76424936	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs555828876	chr13:76424945-76424946	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs576850289	chr13:76424951-76424952	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs74736274	chr13:76424981-76424982	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs151169317	chr13:76425004-76425005	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs558518460	chr13:76425092-76425093	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs182506542	chr13:76425107-76425108	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs559058769	chr13:76425114-76425115	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs530030997	chr13:76425140-76425141	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs9593134	chr13:76425153-76425154	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs563473217	chr13:76425159-76425160	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs568440822	chr13:76425162-76425163	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs186757273	chr13:76425203-76425204	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs140150288	chr13:76425229-76425230	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs71434811	chr13:76425240-76425241	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs150297385	chr13:76425256-76425257	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs547789155	chr13:76425284-76425285	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs554316054	chr13:76425351-76425352	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs565698758	chr13:76425369-76425370	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs536552064	chr13:76425382-76425383	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs79148070	chr13:76425386-76425387	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs137874412	chr13:76425419-76425420	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs537686108	chr13:76425450-76425451	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs558862627	chr13:76425587-76425588	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs576894196	chr13:76425595-76425596	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs372664734	chr13:76425607-76425608	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs574168473	chr13:76425643-76425644	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs79869458	chr13:76425676-76425677	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs574436612	chr13:76425695-76425696	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs144864752	chr13:76425696-76425697	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs563612144	chr13:76425816-76425817	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs575591946	chr13:76425817-76425818	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs139232592	chr13:76425838-76425839	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs201246666	chr13:76425839-76425840	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs376131235	chr13:76425843-76425844	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs546003869	chr13:76425885-76425886	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs564095782	chr13:76425980-76425981	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs138700674	chr13:76426009-76426010	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs4885353	chr13:76426048-76426049	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs192058232	chr13:76426064-76426065	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs533046652	chr13:76426084-76426085	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs146006200	chr13:76426098-76426099	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs530077221	chr13:76426136-76426137	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs548161944	chr13:76426250-76426251	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs564721734	chr13:76426262-76426263	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs182536924	chr13:76426339-76426340	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs537316697	chr13:76426342-76426343	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs187189115	chr13:76426349-76426350	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs570915119	chr13:76426392-76426393	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs534718342	chr13:76426403-76426404	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	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
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	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
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Intracranial aneurysm	16715129	CNVD
Non-small cell lung cancer	19010865	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1288 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76387800-76427200	Weak transcription	Ovary	ovary
2	chr13:76391200-76431600	Strong transcription	Hela-S3	cervix
3	chr13:76394400-76435800	Weak transcription	Colon Smooth Muscle	Colon
4	chr13:76396400-76432000	Weak transcription	Brain Substantia Nigra	brain
5	chr13:76396400-76436800	Weak transcription	Fetal Brain Male	brain
6	chr13:76399000-76433200	Weak transcription	Small Intestine	intestine
7	chr13:76399800-76433000	Weak transcription	Rectal Smooth Muscle	rectum
8	chr13:76400800-76428400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr13:76406000-76428600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr13:76406000-76429600	Weak transcription	Primary hematopoietic stem cells	blood
11	chr13:76406000-76430600	Strong transcription	Osteobl	bone
12	chr13:76406000-76436800	Strong transcription	Muscle Satellite Cultured Cells	--
13	chr13:76406600-76435000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr13:76406800-76427800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr13:76408400-76435000	Strong transcription	HSMMtube	muscle
16	chr13:76408400-76435200	Strong transcription	NH-A	brain
17	chr13:76413200-76436800	Strong transcription	NHDF-Ad	bronchial
18	chr13:76413800-76437600	Strong transcription	HSMM	muscle
19	chr13:76414000-76433000	Strong transcription	Liver	Liver
20	chr13:76414200-76433400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr13:76414400-76426200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr13:76414400-76435200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr13:76414800-76425400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr13:76415400-76429200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr13:76416000-76426800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr13:76416400-76425000	Weak transcription	Esophagus	oesophagus
27	chr13:76416400-76425200	Weak transcription	Lung	lung
28	chr13:76416400-76434600	Weak transcription	Spleen	Spleen
29	chr13:76416600-76426400	Weak transcription	HUVEC	blood vessel
30	chr13:76416600-76429800	Weak transcription	Stomach Mucosa	stomach
31	chr13:76417200-76427200	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr13:76417200-76427200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr13:76417400-76427400	Weak transcription	Stomach Smooth Muscle	stomach
34	chr13:76417400-76429200	Weak transcription	Adipose Nuclei	Adipose
35	chr13:76417400-76431000	Weak transcription	Brain Cingulate Gyrus	brain
36	chr13:76417400-76433000	Weak transcription	Primary B cells from peripheral blood	blood
37	chr13:76417400-76434600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr13:76417400-76443800	Weak transcription	Fetal Brain Female	brain
39	chr13:76417600-76425000	Weak transcription	Gastric	stomach
40	chr13:76417600-76427000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr13:76417600-76427200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr13:76417600-76427200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr13:76417600-76427200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr13:76417600-76427200	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr13:76417600-76427200	Weak transcription	Fetal Stomach	stomach
46	chr13:76417600-76427400	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr13:76417600-76427400	Weak transcription	Fetal Muscle Trunk	muscle
48	chr13:76417600-76431400	Weak transcription	Brain Angular Gyrus	brain
49	chr13:76417600-76432600	Weak transcription	Brain Hippocampus Middle	brain
50	chr13:76417600-76434200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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