Variant report

Variant	nsv1040
Chromosome Location	chr13:51041591-51090903
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:260)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:260 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:51083366-51083443	HepG2	liver:	n/a	n/a
2	ATF1	chr13:51086067-51086459	K562	blood:	n/a	n/a
3	BACH1	chr13:51068926-51068942	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr13:51058929-51058939	K562	blood:	n/a	n/a
5	BHLHE40	chr13:51086098-51086273	K562	blood:	n/a	n/a
6	CEBPB	chr13:51059624-51060125	A549	lung:	n/a	chr13:51060048-51060061 chr13:51060048-51060059 chr13:51060048-51060061 chr13:51060048-51060061
7	CEBPB	chr13:51084195-51084538	IMR90	lung:	n/a	chr13:51084375-51084386
8	CEBPB	chr13:51059623-51060088	HepG2	liver:	n/a	chr13:51060048-51060061 chr13:51060048-51060059 chr13:51060048-51060061 chr13:51060048-51060061
9	CEBPB	chr13:51084214-51084546	HepG2	liver:	n/a	chr13:51084375-51084386
10	CEBPB	chr13:51059956-51060137	IMR90	lung:	n/a	chr13:51060048-51060061 chr13:51060048-51060059 chr13:51060048-51060061 chr13:51060048-51060061
11	CEBPB	chr13:51086122-51086389	K562	blood:	n/a	n/a
12	CEBPB	chr13:51059998-51060183	K562	blood:	n/a	chr13:51060048-51060061 chr13:51060048-51060059 chr13:51060048-51060061 chr13:51060048-51060061
13	CTCF	chr13:51087113-51087202	K562	blood:	n/a	n/a
14	CTCF	chr13:51065369-51065395	MCF-7	breast:	n/a	n/a
15	CTCF	chr13:51087080-51087230	HPF	lung:	n/a	n/a
16	CTCF	chr13:51087040-51087190	RPTEC	kidney:	n/a	n/a
17	CTCF	chr13:51087160-51087310	GM12871	blood:	n/a	n/a
18	CTCF	chr13:51087099-51087179	GM19240	blood:	n/a	n/a
19	CTCF	chr13:51086970-51087277	IMR90	lung:	n/a	n/a
20	CTCF	chr13:51087260-51087410	HFF	foreskin:	n/a	n/a
21	CTCF	chr13:51051134-51051383	GM12878	blood:	n/a	n/a
22	CTCF	chr13:51087040-51087190	AG09319	gingival:	n/a	n/a
23	CTCF	chr13:51075620-51075770	MCF-7	breast:	n/a	n/a
24	CTCF	chr13:51087020-51087170	GM12872	blood:	n/a	n/a
25	CTCF	chr13:51087080-51087230	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr13:51087060-51087210	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr13:51043108-51043159	K562	blood:	n/a	n/a
28	CTCF	chr13:51087080-51087230	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chr13:51051206-51051339	Spleen_OC	spleen:	n/a	n/a
30	CTCF	chr13:51087060-51087210	HCFaa	heart:	n/a	n/a
31	CTCF	chr13:51087040-51087190	HAc	cerebellar:	n/a	n/a
32	CTCF	chr13:51043841-51043867	GM10266	blood:	n/a	n/a
33	CTCF	chr13:51042960-51043129	K562	blood:	n/a	n/a
34	CTCF	chr13:51087240-51087390	BJ	skin:	n/a	n/a
35	CTCF	chr13:51087060-51087210	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr13:51087040-51087190	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr13:51087060-51087210	NHLF	lung:	n/a	n/a
38	CTCF	chr13:51086976-51087300	K562	blood:	n/a	n/a
39	CTCF	chr13:51087100-51087250	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr13:51087106-51087112	K562	blood:	n/a	n/a
41	CTCF	chr13:51087000-51087150	RPTEC	kidney:	n/a	n/a
42	CTCF	chr13:51087040-51087190	AG10803	skin:	n/a	n/a
43	CTCF	chr13:51087000-51087150	HPF	lung:	n/a	n/a
44	CTCF	chr13:51087115-51087220	Gliobla	brain:	n/a	n/a
45	CTCF	chr13:51087120-51087182	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr13:51051232-51051286	Medullo	brain:	n/a	n/a
47	CTCF	chr13:51087020-51087170	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr13:51047227-51047330	Lung_OC	lung:	n/a	n/a
49	CTCF	chr13:51087080-51087230	AG09319	gingival:	n/a	n/a
50	CTCF	chr13:51087000-51087150	GM12873	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:51060599-51060649	SK-N-SH_RA	brain:	n/a
2	chr13:51086835-51086885	HEK293	kidney:	embryo
3	chr13:51060599-51060649	Hela-S3	cervix:	n/a
4	chr13:51086835-51086885	Hela-S3	cervix:	n/a
5	chr13:51086835-51086885	ovcar-3	ovarian:	n/a
6	chr13:51060599-51060649	MCF10A-Er-Src	breast:	n/a
7	chr13:51086835-51086885	SK-N-MC	brain:	n/a
8	chr13:51060599-51060649	GM06990	blood:	n/a
9	chr13:51060599-51060649	HCPEpiC	choroid plexus:	n/a
10	chr13:51060599-51060649	PANC-1	pancreas:	n/a
11	chr13:51060599-51060649	HAEpiC	amniotic membrane:	n/a
12	chr13:51086835-51086885	SK-N-SH	brain:	n/a
13	chr13:51086835-51086885	MCF-7	breast:	n/a
14	chr13:51086835-51086885	HRCEpiC	kidney:	n/a
15	chr13:51060599-51060649	HUVEC	blood vessel:	n/a
16	chr13:51060599-51060649	ECC-1	luminal epithelium:	n/a
17	chr13:51060599-51060649	SK-N-SH	brain:	n/a
18	chr13:51060599-51060649	NH-A	brain:	n/a
19	chr13:51060599-51060649	HL-60	blood:	n/a
20	chr13:51086835-51086885	NHDF-neo	bronchial:	n/a
21	chr13:51086835-51086885	HIPEpiC	eye:	n/a
22	chr13:51086835-51086885	NH-A	brain:	n/a
23	chr13:51086835-51086885	H1-hESC	embryonic stem cell:	embryo
24	chr13:51060599-51060649	Hepatocyte	liver:	n/a
25	chr13:51086835-51086885	AG04450	lung:	fetal
26	chr13:51060599-51060649	BE2_C	brain:	n/a
27	chr13:51086835-51086885	GM12878	blood:	n/a
28	chr13:51060599-51060649	MCF-7	breast:	n/a
29	chr13:51086835-51086885	AoSMC	blood vessel:	n/a
30	chr13:51086835-51086885	PrEC	prostate:	n/a
31	chr13:51060599-51060649	HEK293	kidney:	embryo
32	chr13:51086835-51086885	HNPCEpiC	eye:	n/a
33	chr13:51060599-51060649	HepG2	liver:	n/a
34	chr13:51060599-51060649	GM12878	blood:	n/a
35	chr13:51060599-51060649	AG04450	lung:	fetal
36	chr13:51060599-51060649	IMR90	lung:	fetal
37	chr13:51086835-51086885	NB4	blood:	n/a
38	chr13:51060599-51060649	GM12891	blood:	n/a
39	chr13:51086835-51086885	HUVEC	blood vessel:	n/a
40	chr13:51086835-51086885	T-47D	breast:	n/a
41	chr13:51086835-51086885	GM12892	blood:	n/a
42	chr13:51086835-51086885	PANC-1	pancreas:	n/a
43	chr13:51086835-51086885	Hepatocyte	liver:	n/a
44	chr13:51086835-51086885	SAEC	small airway:	n/a
45	chr13:51060599-51060649	NHDF-neo	bronchial:	n/a
46	chr13:51086835-51086885	HCPEpiC	choroid plexus:	n/a
47	chr13:51086835-51086885	IMR90	lung:	fetal
48	chr13:51060599-51060649	GM12892	blood:	n/a
49	chr13:51060599-51060649	T-47D	breast:	n/a
50	chr13:51086835-51086885	ProgFib	skin:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:51059299..51061286-chr13:51063138..51065247,2	MCF-7	breast:
2	chr13:51057495..51060887-chr13:51065845..51068156,3	K562	blood:
3	chr13:51042795..51044976-chr13:51046435..51049054,2	K562	blood:
4	chr13:50655760..50657850-chr13:51088498..51090922,2	K562	blood:
5	chr13:51085819..51089100-chr13:51090794..51093089,4	K562	blood:
6	chr12:132987438..132988105-chr13:51062911..51063480,2	MCF-7	breast:
7	chr13:50569721..50571547-chr13:51085881..51088680,2	MCF-7	breast:
8	chr13:51065916..51068221-chr13:51075145..51077143,2	K562	blood:
9	chr13:51040236..51041817-chr13:51041887..51044596,2	MCF-7	breast:
10	chr13:51059299..51061286-chr13:51063138..51065247,2	MCF-7	breast:
11	chr13:50698955..50699740-chr13:51085777..51086281,2	NB4	blood:
12	chr13:51066276..51068266-chr13:51086109..51088000,2	K562	blood:
13	chr13:51085819..51089100-chr13:51090794..51093089,4	K562	blood:
14	chr13:51087212..51089990-chr13:51483181..51484978,2	K562	blood:
15	chr13:51042795..51044976-chr13:51046435..51049054,2	K562	blood:
16	chr13:51040236..51041817-chr13:51041887..51044596,2	MCF-7	breast:
17	chr13:51055961..51057791-chr13:51066613..51068471,2	MCF-7	breast:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT140131
2	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033815
3	lnc-RNASEH2B-3	chr13:51066787-51066897	XLOC_010390
4	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033821
5	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033846
6	lnc-RNASEH2B-3	chr13:51066787-51067189	NONHSAT033842
7	lnc-RNASEH2B-3	chr13:51066780-51066897	NONHSAT033861
8	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033819
9	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033855
10	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033850
11	lnc-RNASEH2B-3	chr13:51049316-51049702	NONHSAT033859
12	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033825
13	lnc-RNASEH2B-3	chr13:51066787-51066897	NR_109974
14	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033817
15	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033856
16	lnc-RNASEH2B-3	chr13:51067608-51067670	NONHSAT033856
17	lnc-RNASEH2B-3	chr13:51066787-51066897	XLOC_010390
18	lnc-RNASEH2B-3	chr13:51069312-51069605	NONHSAT033856
19	lnc-RNASEH2B-3	chr13:51086748-51087029	NONHSAT033861
20	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033827
21	lnc-RNASEH2B-3	chr13:51066787-51066897	XLOC_010390
22	lnc-RNASEH2B-3	chr13:51076948-51077016	XLOC_010390
23	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033812

No data

Variant related genes	Relation type
DLEU1	TF binding region
DLEU1	CpG island
ENSG00000231607	chromatin interactions
ENSG00000204977	chromatin interactions
ENSG00000233672	chromatin interactions
ENSG00000176124	chromatin interactions
ENSG00000264864	chromatin interactions
ENSG00000136104	chromatin interactions
NAGK	miRNA target sites

Extended variants
information (count: 1558 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:1558 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532636022	chr13:51041641-51041642	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs541107493	chr13:51041692-51041693	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs559303750	chr13:51041703-51041704	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs146044611	chr13:51041737-51041738	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs529964018	chr13:51041796-51041797	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs548050188	chr13:51041827-51041828	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs569528854	chr13:51041833-51041834	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs9316496	chr13:51041880-51041881	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs56329261	chr13:51041980-51041981	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs570502524	chr13:51041983-51041984	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs534710207	chr13:51041984-51041985	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs550508318	chr13:51042007-51042008	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs568040826	chr13:51042066-51042067	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs555313827	chr13:51042079-51042080	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs563310138	chr13:51042119-51042120	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs555269283	chr13:51042138-51042139	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs201792172	chr13:51042152-51042153	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs182134912	chr13:51042243-51042244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs10492410	chr13:51042258-51042259	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs544924400	chr13:51042311-51042312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34097267	chr13:51042354-51042355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564604798	chr13:51042395-51042396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112968137	chr13:51042411-51042412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs187963508	chr13:51042455-51042456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs577298491	chr13:51042459-51042460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs9568418	chr13:51042466-51042467	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs143963645	chr13:51042468-51042469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs146424828	chr13:51042485-51042486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs541732568	chr13:51042486-51042487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563197325	chr13:51042487-51042488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs530833426	chr13:51042508-51042509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs17074391	chr13:51042509-51042510	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs190901236	chr13:51042537-51042538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528204467	chr13:51042583-51042584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs183219116	chr13:51042612-51042613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs75903984	chr13:51042625-51042626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs535391996	chr13:51042630-51042631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560225115	chr13:51042666-51042667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556991345	chr13:51042672-51042673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188146719	chr13:51042688-51042689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529305263	chr13:51042794-51042795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs537731311	chr13:51042809-51042810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs558913399	chr13:51042811-51042812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546266822	chr13:51042864-51042865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577339870	chr13:51042891-51042892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs149750321	chr13:51042935-51042936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553008534	chr13:51042944-51042945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs193148756	chr13:51042948-51042949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145662478	chr13:51042969-51042970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563333954	chr13:51042994-51042995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:124)

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
Trisomy	24170809	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
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	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
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	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
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Sezary syndrome	18413736	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21990379	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:680 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51030600-51050000	Weak transcription	Fetal Lung	lung
2	chr13:51035000-51042400	Weak transcription	K562	blood
3	chr13:51040600-51042200	Enhancers	Fetal Muscle Leg	muscle
4	chr13:51040800-51041600	Weak transcription	Fetal Stomach	stomach
5	chr13:51041000-51042000	Enhancers	Brain Germinal Matrix	brain
6	chr13:51041200-51041600	Enhancers	Right Ventricle	heart
7	chr13:51041200-51041600	Bivalent Enhancer	NHDF-Ad	bronchial
8	chr13:51041200-51041800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr13:51041200-51042000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr13:51041200-51043800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr13:51041200-51043800	Enhancers	Fetal Heart	heart
12	chr13:51041400-51041600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
13	chr13:51041400-51041800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr13:51041400-51041800	Enhancers	Psoas Muscle	Psoas
15	chr13:51041400-51042000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
16	chr13:51041400-51043000	Enhancers	Fetal Kidney	kidney
17	chr13:51041600-51041800	Enhancers	Fetal Stomach	stomach
18	chr13:51041600-51042000	Active TSS	Skeletal Muscle Female	skeletal muscle
19	chr13:51041800-51042200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr13:51041800-51060600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr13:51042000-51042200	Active TSS	Skeletal Muscle Male	skeletal muscle
22	chr13:51042000-51042200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
23	chr13:51042200-51042400	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr13:51042400-51043800	Enhancers	K562	blood
25	chr13:51042600-51043600	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr13:51043000-51043400	Enhancers	Brain Cingulate Gyrus	brain
27	chr13:51043000-51043800	Enhancers	Brain Hippocampus Middle	brain
28	chr13:51043000-51043800	Enhancers	HUVEC	blood vessel
29	chr13:51043200-51043600	Enhancers	Adipose Nuclei	Adipose
30	chr13:51043200-51044000	Enhancers	Brain Substantia Nigra	brain
31	chr13:51043400-51044400	Weak transcription	Brain Cingulate Gyrus	brain
32	chr13:51043600-51044000	Active TSS	Brain Inferior Temporal Lobe	brain
33	chr13:51043800-51044000	Weak transcription	Fetal Heart	heart
34	chr13:51044400-51044600	Enhancers	Brain Cingulate Gyrus	brain
35	chr13:51048000-51048800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr13:51048000-51049000	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr13:51048200-51048600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr13:51048200-51048600	Weak transcription	Right Ventricle	heart
39	chr13:51048200-51048800	Enhancers	NHDF-Ad	bronchial
40	chr13:51048400-51048800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr13:51048600-51048800	Enhancers	Right Ventricle	heart
42	chr13:51048800-51050400	Weak transcription	NHDF-Ad	bronchial
43	chr13:51048800-51050600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr13:51048800-51050600	Weak transcription	Right Ventricle	heart
45	chr13:51048800-51051400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr13:51049000-51051600	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr13:51050000-51051000	Enhancers	Fetal Lung	lung
48	chr13:51050400-51050800	Enhancers	Left Ventricle	heart
49	chr13:51050400-51050800	Enhancers	Psoas Muscle	Psoas
50	chr13:51050400-51051000	Enhancers	Fetal Muscle Leg	muscle

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