Variant report

Variant	nsv526482
Chromosome Location	chr13:51042258-51065836
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:88)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:88 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr13:51058929-51058939	K562	blood:	n/a	n/a
2	CEBPB	chr13:51059956-51060137	IMR90	lung:	n/a	chr13:51060048-51060061 chr13:51060048-51060059 chr13:51060048-51060061 chr13:51060048-51060061
3	CEBPB	chr13:51059998-51060183	K562	blood:	n/a	chr13:51060048-51060061 chr13:51060048-51060059 chr13:51060048-51060061 chr13:51060048-51060061
4	CEBPB	chr13:51059623-51060088	HepG2	liver:	n/a	chr13:51060048-51060061 chr13:51060048-51060059 chr13:51060048-51060061 chr13:51060048-51060061
5	CEBPB	chr13:51059624-51060125	A549	lung:	n/a	chr13:51060048-51060061 chr13:51060048-51060059 chr13:51060048-51060061 chr13:51060048-51060061
6	CTCF	chr13:51051134-51051383	GM12878	blood:	n/a	n/a
7	CTCF	chr13:51043108-51043159	K562	blood:	n/a	n/a
8	CTCF	chr13:51065369-51065395	MCF-7	breast:	n/a	n/a
9	CTCF	chr13:51061180-51061330	HPF	lung:	n/a	n/a
10	CTCF	chr13:51051206-51051339	Spleen_OC	spleen:	n/a	n/a
11	CTCF	chr13:51051232-51051286	Medullo	brain:	n/a	n/a
12	CTCF	chr13:51047227-51047330	Lung_OC	lung:	n/a	n/a
13	CTCF	chr13:51043841-51043867	GM10266	blood:	n/a	n/a
14	CTCF	chr13:51042960-51043129	K562	blood:	n/a	n/a
15	E2F4	chr13:51065769-51065810	MCF10A-Er-Src	breast:	n/a	n/a
16	EBF1	chr13:51048278-51048503	GM12878	blood:	n/a	chr13:51048391-51048402
17	ELK1	chr13:51058885-51059063	K562	blood:	n/a	n/a
18	EP300	chr13:51059843-51059983	K562	blood:	n/a	n/a
19	EP300	chr13:51060449-51060932	SK-N-SH_RA	brain:	n/a	n/a
20	EP300	chr13:51043088-51043395	K562	blood:	n/a	n/a
21	EP300	chr13:51060390-51060894	SK-N-SH_RA	brain:	n/a	n/a
22	EP300	chr13:51055107-51055238	GM12878	blood:	n/a	n/a
23	EP300	chr13:51060698-51061000	K562	blood:	n/a	chr13:51060983-51060996
24	FOXA1	chr13:51048520-51048773	HepG2	liver:	n/a	n/a
25	FOXA1	chr13:51048472-51048739	T-47D	breast:	n/a	n/a
26	FOXA1	chr13:51048502-51048749	T-47D	breast:	n/a	n/a
27	FOXA1	chr13:51048397-51048785	HepG2	liver:	n/a	n/a
28	FOXA1	chr13:51048457-51048718	A549	lung:	n/a	n/a
29	FOXA1	chr13:51049980-51050135	T-47D	breast:	n/a	n/a
30	FOXA2	chr13:51048510-51048702	HepG2	liver:	n/a	n/a
31	GATA1	chr13:51043004-51043543	PBDE	blood:	n/a	n/a
32	GATA2	chr13:51060631-51061048	SH-SY5Y	brain:	n/a	chr13:51060835-51060847 chr13:51060836-51060845 chr13:51060833-51060849 chr13:51060836-51060846 chr13:51060838-51060845 chr13:51060907-51060916
33	GATA3	chr13:51060408-51060844	SH-SY5Y	brain:	n/a	n/a
34	GATA3	chr13:51050887-51051087	SH-SY5Y	brain:	n/a	n/a
35	IRF1	chr13:51043564-51043705	K562	blood:	n/a	n/a
36	JUND	chr13:51043074-51043258	K562	blood:	n/a	n/a
37	JUND	chr13:51063711-51063809	HepG2	liver:	n/a	n/a
38	JUND	chr13:51051617-51051620	H1-hESC	embryonic stem cell:	n/a	n/a
39	JUND	chr13:51060761-51060953	K562	blood:	n/a	n/a
40	JUND	chr13:51060319-51060364	H1-hESC	embryonic stem cell:	n/a	n/a
41	KAP1	chr13:51060252-51061047	HEK293	kidney:	n/a	n/a
42	MAFF	chr13:51061049-51061357	HepG2	liver:	n/a	chr13:51061190-51061208
43	MAFF	chr13:51051775-51052062	HepG2	liver:	n/a	n/a
44	MAFK	chr13:51051836-51052067	HepG2	liver:	n/a	chr13:51051930-51051945
45	MAFK	chr13:51061040-51061373	HepG2	liver:	n/a	n/a
46	MAFK	chr13:51061044-51061318	IMR90	lung:	n/a	n/a
47	MAFK	chr13:51058854-51059032	K562	blood:	n/a	chr13:51058860-51058871 chr13:51058859-51058870 chr13:51058860-51058871
48	MAFK	chr13:51064019-51064227	HepG2	liver:	n/a	chr13:51064120-51064135
49	MAFK	chr13:51064012-51064278	HepG2	liver:	n/a	chr13:51064120-51064135
50	MAFK	chr13:51051783-51052105	HepG2	liver:	n/a	chr13:51051930-51051945

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:51060599-51060649	HEEpiC	esophagus:	n/a
2	chr13:51060599-51060649	AG10803	skin:	n/a
3	chr13:51060599-51060649	HepG2	liver:	n/a
4	chr13:51060599-51060649	U87	brain:	n/a
5	chr13:51060599-51060649	MCF10A-Er-Src	breast:	n/a
6	chr13:51060599-51060649	HL-60	blood:	n/a
7	chr13:51060599-51060649	BJ	skin:	n/a
8	chr13:51060599-51060649	GM12878	blood:	n/a
9	chr13:51060599-51060649	PFSK-1	brain:	n/a
10	chr13:51060599-51060649	NT2-D1	testis:	n/a
11	chr13:51060599-51060649	HIPEpiC	eye:	n/a
12	chr13:51060599-51060649	IMR90	lung:	fetal
13	chr13:51060599-51060649	SKMC	muscle:	n/a
14	chr13:51060599-51060649	HRCEpiC	kidney:	n/a
15	chr13:51060599-51060649	HAEpiC	amniotic membrane:	n/a
16	chr13:51060599-51060649	A549	lung:	n/a
17	chr13:51060599-51060649	BE2_C	brain:	n/a
18	chr13:51060599-51060649	HEK293	kidney:	embryo
19	chr13:51060599-51060649	HCM	heart:	n/a
20	chr13:51060599-51060649	PrEC	prostate:	n/a
21	chr13:51060599-51060649	GM06990	blood:	n/a
22	chr13:51060599-51060649	ProgFib	skin:	n/a
23	chr13:51060599-51060649	HRPEpiC	eye:	n/a
24	chr13:51060599-51060649	HUVEC	blood vessel:	n/a
25	chr13:51060599-51060649	NHDF-neo	bronchial:	n/a
26	chr13:51060599-51060649	AG09309	skin:	n/a
27	chr13:51060599-51060649	SK-N-SH_RA	brain:	n/a
28	chr13:51060599-51060649	ovcar-3	ovarian:	n/a
29	chr13:51060599-51060649	K562	blood:	n/a
30	chr13:51060599-51060649	HMEC	breast:	n/a
31	chr13:51060599-51060649	GM12892	blood:	n/a
32	chr13:51060599-51060649	AG04449	skin:	fetal
33	chr13:51060599-51060649	SK-N-MC	brain:	n/a
34	chr13:51060599-51060649	RPTEC	kidney:	n/a
35	chr13:51060599-51060649	Hela-S3	cervix:	n/a
36	chr13:51060599-51060649	PANC-1	pancreas:	n/a
37	chr13:51060599-51060649	T-47D	breast:	n/a
38	chr13:51060599-51060649	LNCaP	prostate:	n/a
39	chr13:51060599-51060649	MCF-7	breast:	n/a
40	chr13:51060599-51060649	AG04450	lung:	fetal
41	chr13:51060599-51060649	HCF	heart:	n/a
42	chr13:51060599-51060649	SAEC	small airway:	n/a
43	chr13:51060599-51060649	CMK	blood:	n/a
44	chr13:51060599-51060649	GM19239	blood:	n/a
45	chr13:51060599-51060649	HRE	kidney:	n/a
46	chr13:51060599-51060649	NB4	blood:	n/a
47	chr13:51060599-51060649	NHBE	bronchial:	n/a
48	chr13:51060599-51060649	AoSMC	blood vessel:	n/a
49	chr13:51060599-51060649	HCPEpiC	choroid plexus:	n/a
50	chr13:51060599-51060649	Caco-2	colon:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:51042795..51044976-chr13:51046435..51049054,2	K562	blood:
2	chr13:51042795..51044976-chr13:51046435..51049054,2	K562	blood:
3	chr13:51055961..51057791-chr13:51066613..51068471,2	MCF-7	breast:
4	chr12:132987438..132988105-chr13:51062911..51063480,2	MCF-7	breast:
5	chr13:51057495..51060887-chr13:51065845..51068156,3	K562	blood:
6	chr13:51059299..51061286-chr13:51063138..51065247,2	MCF-7	breast:
7	chr13:51059299..51061286-chr13:51063138..51065247,2	MCF-7	breast:
8	chr13:51040236..51041817-chr13:51041887..51044596,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNASEH2B-3	chr13:51049316-51049702	NONHSAT033859

No data

Variant related genes	Relation type
DLEU1	TF binding region
DLEU1	CpG island
ENSG00000176124	chromatin interactions

Extended variants
information (count: 770 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:770 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10492410	chr13:51042258-51042259	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs544924400	chr13:51042311-51042312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs34097267	chr13:51042354-51042355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564604798	chr13:51042395-51042396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs112968137	chr13:51042411-51042412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187963508	chr13:51042455-51042456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs577298491	chr13:51042459-51042460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs9568418	chr13:51042466-51042467	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs143963645	chr13:51042468-51042469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146424828	chr13:51042485-51042486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs541732568	chr13:51042486-51042487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563197325	chr13:51042487-51042488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs530833426	chr13:51042508-51042509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs17074391	chr13:51042509-51042510	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs190901236	chr13:51042537-51042538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528204467	chr13:51042583-51042584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs183219116	chr13:51042612-51042613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs75903984	chr13:51042625-51042626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535391996	chr13:51042630-51042631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560225115	chr13:51042666-51042667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556991345	chr13:51042672-51042673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188146719	chr13:51042688-51042689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs529305263	chr13:51042794-51042795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537731311	chr13:51042809-51042810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs558913399	chr13:51042811-51042812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546266822	chr13:51042864-51042865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs577339870	chr13:51042891-51042892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149750321	chr13:51042935-51042936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs553008534	chr13:51042944-51042945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs193148756	chr13:51042948-51042949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs145662478	chr13:51042969-51042970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563333954	chr13:51042994-51042995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs575483623	chr13:51042999-51043000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs377178992	chr13:51043030-51043031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546059250	chr13:51043060-51043061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs79048926	chr13:51043062-51043063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs114722022	chr13:51043084-51043085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs182901691	chr13:51043132-51043133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs531583375	chr13:51043179-51043180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs9568419	chr13:51043194-51043195	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs570748900	chr13:51043235-51043236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560710178	chr13:51043247-51043248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs187567287	chr13:51043290-51043291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192567726	chr13:51043365-51043366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs529832699	chr13:51043423-51043424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs568813871	chr13:51043430-51043431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs184798842	chr13:51043436-51043437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs148870275	chr13:51043446-51043447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs570964429	chr13:51043502-51043503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535175675	chr13:51043504-51043505	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:185 , 50 per page) page: 1 2 3 4

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	chr13:51041200-51043800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr13:51041200-51043800	Enhancers	Fetal Heart	heart
5	chr13:51041400-51043000	Enhancers	Fetal Kidney	kidney
6	chr13:51041800-51060600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr13:51042200-51042400	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr13:51042400-51043800	Enhancers	K562	blood
9	chr13:51042600-51043600	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr13:51043000-51043400	Enhancers	Brain Cingulate Gyrus	brain
11	chr13:51043000-51043800	Enhancers	Brain Hippocampus Middle	brain
12	chr13:51043000-51043800	Enhancers	HUVEC	blood vessel
13	chr13:51043200-51043600	Enhancers	Adipose Nuclei	Adipose
14	chr13:51043200-51044000	Enhancers	Brain Substantia Nigra	brain
15	chr13:51043400-51044400	Weak transcription	Brain Cingulate Gyrus	brain
16	chr13:51043600-51044000	Active TSS	Brain Inferior Temporal Lobe	brain
17	chr13:51043800-51044000	Weak transcription	Fetal Heart	heart
18	chr13:51044400-51044600	Enhancers	Brain Cingulate Gyrus	brain
19	chr13:51048000-51048800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr13:51048000-51049000	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr13:51048200-51048600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr13:51048200-51048600	Weak transcription	Right Ventricle	heart
23	chr13:51048200-51048800	Enhancers	NHDF-Ad	bronchial
24	chr13:51048400-51048800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr13:51048600-51048800	Enhancers	Right Ventricle	heart
26	chr13:51048800-51050400	Weak transcription	NHDF-Ad	bronchial
27	chr13:51048800-51050600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr13:51048800-51050600	Weak transcription	Right Ventricle	heart
29	chr13:51048800-51051400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr13:51049000-51051600	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr13:51050000-51051000	Enhancers	Fetal Lung	lung
32	chr13:51050400-51050800	Enhancers	Left Ventricle	heart
33	chr13:51050400-51050800	Enhancers	Psoas Muscle	Psoas
34	chr13:51050400-51051000	Enhancers	Fetal Muscle Leg	muscle
35	chr13:51050400-51052000	Enhancers	NHDF-Ad	bronchial
36	chr13:51050600-51051000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr13:51050600-51051000	Enhancers	Right Ventricle	heart
38	chr13:51050600-51051000	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr13:51050600-51051800	Enhancers	Fetal Heart	heart
40	chr13:51051200-51052000	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr13:51051400-51051800	Enhancers	Primary B cells from cord blood	blood
42	chr13:51051400-51051800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr13:51051400-51052000	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr13:51051400-51052000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr13:51051400-51052200	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr13:51051600-51052000	Enhancers	Primary B cells from peripheral blood	blood
47	chr13:51051600-51052400	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr13:51051600-51053000	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr13:51051800-51057200	Weak transcription	Fetal Heart	heart
50	chr13:51052200-51057400	Weak transcription	Primary neutrophils fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links