Variant report

Variant	nsv976116
Chromosome Location	chr13:52741751-52768674
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:741)
CpG islands
(count:428)
Chromatin interactive
region (count:9)
LncRNA
region (count:33)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:741 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:52768441-52768762	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:52761418-52761903	K562	blood:	n/a	n/a
3	ARID3A	chr13:52768469-52768764	K562	blood:	n/a	n/a
4	ARID3A	chr13:52761673-52762111	HepG2	liver:	n/a	n/a
5	ATF1	chr13:52761531-52761864	K562	blood:	n/a	n/a
6	ATF2	chr13:52768333-52768885	GM12878	blood:	n/a	n/a
7	ATF2	chr13:52768366-52768847	GM12878	blood:	n/a	n/a
8	ATF2	chr13:52768357-52768861	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr13:52768359-52768829	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr13:52768340-52768838	A549	lung:	n/a	n/a
11	ATF3	chr13:52768417-52768760	A549	lung:	n/a	n/a
12	BACH1	chr13:52768461-52768767	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr13:52755736-52756031	GM12878	blood:	n/a	n/a
14	BATF	chr13:52768413-52768735	GM12878	blood:	n/a	n/a
15	BCL11A	chr13:52761551-52761791	GM12878	blood:	n/a	n/a
16	BCL11A	chr13:52761561-52761785	GM12878	blood:	n/a	n/a
17	BCL3	chr13:52765291-52765615	GM12878	blood:	n/a	n/a
18	BCL3	chr13:52768300-52768869	A549	lung:	n/a	n/a
19	BCL3	chr13:52768317-52768857	A549	lung:	n/a	n/a
20	BCLAF1	chr13:52768310-52768866	K562	blood:	n/a	n/a
21	BCLAF1	chr13:52768287-52768866	GM12878	blood:	n/a	n/a
22	BCLAF1	chr13:52768386-52768935	K562	blood:	n/a	n/a
23	BCLAF1	chr13:52768286-52768892	GM12878	blood:	n/a	n/a
24	BHLHE40	chr13:52768348-52768784	HepG2	liver:	n/a	n/a
25	BHLHE40	chr13:52768336-52768866	K562	blood:	n/a	n/a
26	BHLHE40	chr13:52768325-52769018	GM12878	blood:	n/a	n/a
27	BHLHE40	chr13:52761468-52761785	K562	blood:	n/a	n/a
28	BRCA1	chr13:52768398-52768779	HepG2	liver:	n/a	n/a
29	BRCA1	chr13:52768460-52768830	GM12878	blood:	n/a	n/a
30	BRCA1	chr13:52768343-52768816	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr13:52768329-52768875	K562	blood:	n/a	n/a
32	CBX3	chr13:52761480-52761835	K562	blood:	n/a	n/a
33	CBX3	chr13:52768307-52768888	HCT-116	colon:	n/a	n/a
34	CBX3	chr13:52768407-52768812	K562	blood:	n/a	n/a
35	CBX3	chr13:52768273-52768967	HCT-116	colon:	n/a	n/a
36	CCNT2	chr13:52761474-52761706	K562	blood:	n/a	n/a
37	CEBPB	chr13:52764190-52764257	HepG2	liver:	n/a	chr13:52764220-52764231
38	CEBPB	chr13:52768475-52768732	GM12878	blood:	n/a	n/a
39	CEBPB	chr13:52768507-52768859	K562	blood:	n/a	chr13:52768825-52768838
40	CEBPB	chr13:52745907-52746170	HepG2	liver:	n/a	chr13:52746045-52746054 chr13:52746043-52746054 chr13:52746045-52746056 chr13:52746043-52746056
41	CEBPB	chr13:52768344-52768973	GM12878	blood:	n/a	chr13:52768825-52768838
42	CEBPB	chr13:52745897-52746117	Hela-S3	cervix:	n/a	chr13:52746045-52746054 chr13:52746043-52746054 chr13:52746045-52746056 chr13:52746043-52746056
43	CEBPB	chr13:52745077-52745329	IMR90	lung:	n/a	n/a
44	CEBPB	chr13:52768471-52768555	HepG2	liver:	n/a	n/a
45	CEBPB	chr13:52767738-52767907	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr13:52768442-52768736	HepG2	liver:	n/a	n/a
47	CEBPB	chr13:52768381-52768812	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr13:52745067-52745173	K562	blood:	n/a	n/a
49	CEBPD	chr13:52768319-52768851	HepG2	liver:	n/a	n/a
50	CEBPD	chr13:52761436-52761860	K562	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:52768442-52768492	IMR90	lung:	fetal
2	chr13:52768442-52768492	IMR90	lung:	fetal
3	chr13:52768442-52768492	HRE	kidney:	n/a
4	chr13:52768555-52768605	AG04449	skin:	fetal
5	chr13:52768166-52768216	U87	brain:	n/a
6	chr13:52768166-52768216	NHBE	bronchial:	n/a
7	chr13:52768555-52768605	NB4	blood:	n/a
8	chr13:52768659-52768709	GM12892	blood:	n/a
9	chr13:52766123-52766173	PANC-1	pancreas:	n/a
10	chr13:52768442-52768492	HPAEpiC	pulmonary alveolar:	n/a
11	chr13:52768555-52768605	IMR90	lung:	fetal
12	chr13:52768669-52768719	LNCaP	prostate:	n/a
13	chr13:52768555-52768605	HCPEpiC	choroid plexus:	n/a
14	chr13:52768555-52768605	SKMC	muscle:	n/a
15	chr13:52768442-52768492	RPTEC	kidney:	n/a
16	chr13:52768555-52768605	PFSK-1	brain:	n/a
17	chr13:52766123-52766173	T-47D	breast:	n/a
18	chr13:52766123-52766173	NHBE	bronchial:	n/a
19	chr13:52768442-52768492	HEK293	kidney:	embryo
20	chr13:52768669-52768719	K562	blood:	n/a
21	chr13:52768659-52768709	HRPEpiC	eye:	n/a
22	chr13:52768669-52768719	CMK	blood:	n/a
23	chr13:52768442-52768492	HCPEpiC	choroid plexus:	n/a
24	chr13:52768539-52768589	HIPEpiC	eye:	n/a
25	chr13:52768555-52768605	MCF10A-Er-Src	breast:	n/a
26	chr13:52768669-52768719	HMEC	breast:	n/a
27	chr13:52768659-52768709	HepG2	liver:	n/a
28	chr13:52768166-52768216	AG04450	lung:	fetal
29	chr13:52768669-52768719	Hepatocyte	liver:	n/a
30	chr13:52768659-52768709	Hepatocyte	liver:	n/a
31	chr13:52768555-52768605	NHBE	bronchial:	n/a
32	chr13:52768659-52768709	GM19239	blood:	n/a
33	chr13:52766123-52766173	K562	blood:	n/a
34	chr13:52768555-52768605	NH-A	brain:	n/a
35	chr13:52768669-52768719	PFSK-1	brain:	n/a
36	chr13:52766123-52766173	RPTEC	kidney:	n/a
37	chr13:52768539-52768589	GM12891	blood:	n/a
38	chr13:52768166-52768216	H1-hESC	embryonic stem cell:	embryo
39	chr13:52766123-52766173	BJ	skin:	n/a
40	chr13:52768669-52768719	HCF	heart:	n/a
41	chr13:52768555-52768605	HCF	heart:	n/a
42	chr13:52768442-52768492	ovcar-3	ovarian:	n/a
43	chr13:52766123-52766173	IMR90	lung:	fetal
44	chr13:52766123-52766173	Jurkat	blood:	n/a
45	chr13:52768539-52768589	MCF-7	breast:	n/a
46	chr13:52768555-52768605	HIPEpiC	eye:	n/a
47	chr13:52768669-52768719	HEEpiC	esophagus:	n/a
48	chr13:52768539-52768589	U87	brain:	n/a
49	chr13:52768539-52768589	A549	lung:	n/a
50	chr13:52768539-52768589	Hepatocyte	liver:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:52377651..52379551-chr13:52768569..52770283,3	MCF-7	breast:
2	chr13:52730788..52732496-chr13:52768343..52769860,2	MCF-7	breast:
3	chr13:52377591..52379548-chr13:52768375..52770242,2	K562	blood:
4	chr13:52768239..52768779-chr21:34775626..34776496,2	NB4	blood:
5	chr1:45194788..45196878-chr13:52740302..52742412,2	MCF-7	breast:
6	chr13:52768173..52768983-chr13:53191222..53192131,3	NB4	blood:
7	chr13:52762333..52764289-chr13:52768534..52770234,2	MCF-7	breast:
8	chr13:52701771..52705558-chr13:52767896..52769871,3	MCF-7	breast:
9	chr13:52744500..52746547-chr13:52749671..52752409,2	K562	blood:

(count:33 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NEK3-1	chr13:52760818-52760958	NONHSAT033972
2	lnc-NEK3-1	chr13:52763774-52764049	NONHSAT033972
3	lnc-NEK3-1	chr13:52768394-52768598	NONHSAT033976
4	lnc-NEK3-1	chr13:52760878-52760958	NONHSAT033970
5	lnc-NEK3-1	chr13:52768389-52768582	NONHSAT033972
6	lnc-NEK3-1	chr13:52758138-52758249	NONHSAT033976
7	lnc-NEK3-1	chr13:52768293-52768581	NONHSAT033975
8	lnc-NEK3-1	chr13:52760818-52760958	NONHSAT033975
9	lnc-NEK3-1	chr13:52754717-52754789	NONHSAT033973
10	lnc-NEK3-1	chr13:52743125-52743441	NONHSAT033970
11	lnc-NEK3-1	chr13:52763774-52764049	NONHSAT033975
12	lnc-NEK3-1	chr13:52763774-52764051	NONHSAT033970
13	lnc-NEK3-1	chr13:52758111-52758249	NONHSAT033970
14	lnc-NEK3-1	chr13:52749774-52749911	NONHSAT033970
15	lnc-NEK3-1	chr13:52749774-52749911	NONHSAT033972
16	lnc-NEK3-1	chr13:52745293-52745383	NONHSAT033972
17	lnc-NEK3-1	chr13:52754717-52754789	NONHSAT033970
18	lnc-NEK3-1	chr13:52745293-52745385	NONHSAT033970
19	lnc-NEK3-1	chr13:52758118-52758249	NONHSAT033975
20	lnc-NEK3-1	chr13:52754717-52754789	NONHSAT033972
21	lnc-NEK3-1	chr13:52745293-52745383	NONHSAT033973
22	lnc-NEK3-1	chr13:52768389-52768582	NONHSAT033973
23	lnc-NEK3-1	chr13:52758111-52758249	NONHSAT033972
24	lnc-NEK3-1	chr13:52768389-52768581	NONHSAT033970
25	lnc-NEK3-1	chr13:52744107-52744191	NONHSAT033972
26	lnc-NEK3-1	chr13:52763774-52764049	NONHSAT033976
27	lnc-NEK3-1	chr13:52760818-52760958	NONHSAT033976
28	lnc-NEK3-1	chr13:52744122-52744224	NONHSAT033970
29	lnc-NEK3-1	chr13:52744193-52744234	NONHSAT033973
30	lnc-NEK3-1	chr13:52758111-52758249	NONHSAT033973
31	lnc-NEK3-1	chr13:52766939-52768570	NONHSAT033977
32	lnc-NEK3-1	chr13:52760818-52760958	NONHSAT033973
33	lnc-NEK3-1	chr13:52749774-52749911	NONHSAT033973

No data

Variant related genes	Relation type
MRPS31P5	TF binding region
MRPS31P5	CpG island
ENSG00000136098	chromatin interactions
ENSG00000159128	chromatin interactions
ENSG00000231856	chromatin interactions
ENSG00000102796	chromatin interactions
ENSG00000250299	chromatin interactions
ENSG00000243406	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000139675	chromatin interactions
ENSG00000197168	chromatin interactions

Extended variants
information (count: 888 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:888 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376526168	chr13:52741753-52741754	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs578013981	chr13:52741760-52741761	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs201293251	chr13:52741827-52741828	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs184746079	chr13:52741841-52741842	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs1052737	chr13:52741877-52741878	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs1052733	chr13:52741895-52741896	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs397774592	chr13:52741958-52741959	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs553941644	chr13:52742003-52742004	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs540732332	chr13:52742006-52742007	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs147906082	chr13:52742042-52742043	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs141510213	chr13:52742045-52742046	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs1052719	chr13:52742067-52742068	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs562918558	chr13:52742091-52742092	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs576800584	chr13:52742200-52742201	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs200873752	chr13:52742209-52742210	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs545676855	chr13:52742231-52742232	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs565580981	chr13:52742236-52742237	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs1052710	chr13:52742315-52742316	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs527855531	chr13:52742340-52742341	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs574297193	chr13:52742352-52742353	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs145368651	chr13:52742366-52742367	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs190395718	chr13:52742369-52742370	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs529013980	chr13:52742421-52742422	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs548558456	chr13:52742445-52742446	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs568472927	chr13:52742447-52742448	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181671052	chr13:52742472-52742473	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs7491829	chr13:52742497-52742498	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs551231886	chr13:52742521-52742522	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs543277728	chr13:52742566-52742567	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs151110197	chr13:52742629-52742630	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187568293	chr13:52742651-52742652	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs9535890	chr13:52742660-52742661	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs574045694	chr13:52742719-52742720	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs536795537	chr13:52742738-52742739	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs189334674	chr13:52742825-52742826	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs180912017	chr13:52742837-52742838	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs545441725	chr13:52742861-52742862	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559262106	chr13:52742862-52742863	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs572735569	chr13:52742880-52742881	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541246413	chr13:52742894-52742895	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs113321441	chr13:52742899-52742900	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs561577715	chr13:52742915-52742916	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530238259	chr13:52742924-52742925	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538720059	chr13:52742970-52742971	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185127340	chr13:52743005-52743006	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189846243	chr13:52743022-52743023	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531957586	chr13:52743027-52743028	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs55901035	chr13:52743047-52743048	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs550996311	chr13:52743054-52743055	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs11620261	chr13:52743056-52743057	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	18852474	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD

Chromatin state (count:1280 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52733800-52743000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr13:52733800-52757000	Weak transcription	Spleen	Spleen
3	chr13:52734000-52760000	Weak transcription	Gastric	stomach
4	chr13:52734200-52742200	Weak transcription	Fetal Lung	lung
5	chr13:52734200-52742400	Weak transcription	Brain Germinal Matrix	brain
6	chr13:52734200-52742400	Weak transcription	Fetal Brain Female	brain
7	chr13:52734200-52742600	Weak transcription	Esophagus	oesophagus
8	chr13:52734200-52743000	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr13:52734200-52747800	Weak transcription	Fetal Brain Male	brain
10	chr13:52734200-52751800	Weak transcription	Psoas Muscle	Psoas
11	chr13:52734200-52752400	Weak transcription	GM12878-XiMat	blood
12	chr13:52734200-52754000	Weak transcription	Right Ventricle	heart
13	chr13:52734200-52754000	Weak transcription	Hela-S3	cervix
14	chr13:52734400-52741800	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr13:52734400-52742400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr13:52734400-52742400	Weak transcription	Pancreas	Pancrea
17	chr13:52734400-52746000	Weak transcription	Primary B cells from cord blood	blood
18	chr13:52734400-52746200	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr13:52734400-52751200	Weak transcription	Colon Smooth Muscle	Colon
20	chr13:52734400-52753400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr13:52734400-52753600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr13:52734400-52754000	Weak transcription	NHEK	skin
23	chr13:52734400-52761000	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr13:52734400-52768000	Weak transcription	Aorta	Aorta
25	chr13:52734600-52742800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr13:52734600-52766000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr13:52734800-52742400	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr13:52734800-52742400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr13:52735000-52741800	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr13:52735000-52743000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr13:52735000-52744200	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr13:52735000-52746200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr13:52735200-52747400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr13:52735400-52742400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr13:52735400-52744000	Weak transcription	Fetal Kidney	kidney
36	chr13:52735600-52754000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr13:52736400-52754000	Weak transcription	Colonic Mucosa	Colon
38	chr13:52736400-52767200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr13:52736600-52742400	Weak transcription	Small Intestine	intestine
40	chr13:52736600-52742600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr13:52736600-52754200	Weak transcription	Fetal Heart	heart
42	chr13:52736800-52742200	Weak transcription	Adipose Nuclei	Adipose
43	chr13:52736800-52765600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr13:52737200-52742400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr13:52737200-52747600	Weak transcription	HSMMtube	muscle
46	chr13:52737200-52748800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
47	chr13:52737200-52767400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr13:52737400-52751400	Weak transcription	A549	lung
49	chr13:52737400-52754000	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr13:52737600-52743000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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