Variant report

Variant	nsv1053468
Chromosome Location	chr13:92814581-92893231
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:92839602-92839990	HepG2	liver:	n/a	n/a
2	ATF1	chr13:92827622-92827864	K562	blood:	n/a	n/a
3	ATF2	chr13:92827544-92827875	GM12878	blood:	n/a	n/a
4	ATF2	chr13:92827535-92827932	GM12878	blood:	n/a	n/a
5	BHLHE40	chr13:92839696-92839896	GM12878	blood:	n/a	n/a
6	BRCA1	chr13:92873850-92873902	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr13:92877946-92878005	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr13:92841967-92842314	IMR90	lung:	n/a	chr13:92842126-92842137
9	CEBPB	chr13:92841968-92842220	A549	lung:	n/a	chr13:92842126-92842137
10	CEBPB	chr13:92841955-92842308	HepG2	liver:	n/a	chr13:92842126-92842137
11	CEBPB	chr13:92842007-92842227	Hela-S3	cervix:	n/a	chr13:92842126-92842137
12	CEBPB	chr13:92881690-92881970	HepG2	liver:	n/a	chr13:92881816-92881827
13	CEBPB	chr13:92876786-92877321	IMR90	lung:	n/a	n/a
14	CEBPB	chr13:92877177-92877504	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr13:92881693-92881947	IMR90	lung:	n/a	chr13:92881816-92881827
16	CEBPB	chr13:92842010-92842263	H1-hESC	embryonic stem cell:	n/a	chr13:92842126-92842137
17	CHD2	chr13:92839646-92839864	GM12878	blood:	n/a	n/a
18	CREB1	chr13:92827544-92827932	H1-hESC	embryonic stem cell:	n/a	chr13:92827722-92827735
19	CREB1	chr13:92827507-92827895	GM12878	blood:	n/a	chr13:92827722-92827735
20	CTCF	chr13:92839740-92839890	HepG2	liver:	n/a	chr13:92839827-92839848 chr13:92839825-92839843 chr13:92839826-92839842 chr13:92839828-92839841
21	CTCF	chr13:92839721-92839912	SK-N-SH_RA	brain:	n/a	chr13:92839827-92839848 chr13:92839825-92839843 chr13:92839826-92839842 chr13:92839828-92839841
22	CTCF	chr13:92827720-92827870	NHEK	skin:	n/a	chr13:92827851-92827867 chr13:92827855-92827863 chr13:92827853-92827866
23	CTCF	chr13:92827660-92827810	GM12867	blood:	n/a	n/a
24	CTCF	chr13:92839740-92839890	Hela-S3	cervix:	n/a	chr13:92839827-92839848 chr13:92839825-92839843 chr13:92839826-92839842 chr13:92839828-92839841
25	CTCF	chr13:92839737-92839938	H1-hESC	embryonic stem cell:	n/a	chr13:92839827-92839848 chr13:92839825-92839843 chr13:92839826-92839842 chr13:92839828-92839841
26	CTCF	chr13:92839766-92839932	A549	lung:	n/a	chr13:92839827-92839848 chr13:92839825-92839843 chr13:92839826-92839842 chr13:92839828-92839841
27	CTCF	chr13:92839760-92839910	GM06990	blood:	n/a	chr13:92839827-92839848 chr13:92839825-92839843 chr13:92839826-92839842 chr13:92839828-92839841
28	CTCF	chr13:92839780-92839930	GM12865	blood:	n/a	chr13:92839827-92839848 chr13:92839825-92839843 chr13:92839826-92839842 chr13:92839828-92839841
29	CTCF	chr13:92839704-92839894	A549	lung:	n/a	chr13:92839827-92839848 chr13:92839825-92839843 chr13:92839826-92839842 chr13:92839828-92839841
30	CTCF	chr13:92827818-92827867	Lung_OC	lung:	n/a	chr13:92827851-92827867 chr13:92827855-92827863 chr13:92827853-92827866
31	CTCF	chr13:92827760-92827910	AG10803	skin:	n/a	chr13:92827851-92827867 chr13:92827855-92827863 chr13:92827853-92827866 chr13:92827852-92827873
32	CTCF	chr13:92839733-92839995	MCF-7	breast:	n/a	chr13:92839827-92839848 chr13:92839825-92839843 chr13:92839826-92839842 chr13:92839828-92839841
33	CTCF	chr13:92827744-92827958	LNCaP	prostate:	n/a	chr13:92827851-92827867 chr13:92827855-92827863 chr13:92827853-92827866 chr13:92827852-92827873
34	CTCF	chr13:92827740-92827890	GM12866	blood:	n/a	chr13:92827851-92827867 chr13:92827855-92827863 chr13:92827853-92827866 chr13:92827852-92827873
35	CTCF	chr13:92839760-92839910	Caco-2	colon:	n/a	chr13:92839827-92839848 chr13:92839825-92839843 chr13:92839826-92839842 chr13:92839828-92839841
36	CTCF	chr13:92827750-92827902	SK-N-SH_RA	brain:	n/a	chr13:92827851-92827867 chr13:92827855-92827863 chr13:92827853-92827866 chr13:92827852-92827873
37	CTCF	chr13:92839760-92839910	AG09309	skin:	n/a	chr13:92839827-92839848 chr13:92839825-92839843 chr13:92839826-92839842 chr13:92839828-92839841
38	CTCF	chr13:92839720-92839870	HCM	heart:	n/a	chr13:92839827-92839848 chr13:92839825-92839843 chr13:92839826-92839842 chr13:92839828-92839841
39	CTCF	chr13:92827729-92827955	LNCaP	prostate:	n/a	chr13:92827851-92827867 chr13:92827855-92827863 chr13:92827853-92827866 chr13:92827852-92827873
40	CTCF	chr13:92827800-92827950	HRE	kidney:	n/a	chr13:92827851-92827867 chr13:92827855-92827863 chr13:92827853-92827866 chr13:92827852-92827873
41	CTCF	chr13:92827761-92827867	Fibrobl	skin:	n/a	chr13:92827851-92827867 chr13:92827855-92827863 chr13:92827853-92827866
42	CTCF	chr13:92827740-92827890	HMEC	breast:	n/a	chr13:92827851-92827867 chr13:92827855-92827863 chr13:92827853-92827866 chr13:92827852-92827873
43	CTCF	chr13:92839680-92839830	GM12869	blood:	n/a	n/a
44	CTCF	chr13:92827840-92827990	BE2_C	brain:	n/a	chr13:92827851-92827867 chr13:92827855-92827863 chr13:92827853-92827866 chr13:92827852-92827873
45	CTCF	chr13:92827700-92827850	GM12872	blood:	n/a	n/a
46	CTCF	chr13:92827775-92827884	MCF-7	breast:	n/a	chr13:92827851-92827867 chr13:92827855-92827863 chr13:92827853-92827866 chr13:92827852-92827873
47	CTCF	chr13:92827760-92827910	AG04450	lung:	n/a	chr13:92827851-92827867 chr13:92827855-92827863 chr13:92827853-92827866 chr13:92827852-92827873
48	CTCF	chr13:92839820-92839970	HA-sp	spinal cord:	n/a	chr13:92839827-92839848 chr13:92839825-92839843 chr13:92839826-92839842 chr13:92839828-92839841
49	CTCF	chr13:92839712-92839970	Pancreas_OC	pancreas:	n/a	chr13:92839827-92839848 chr13:92839825-92839843 chr13:92839826-92839842 chr13:92839828-92839841
50	CTCF	chr13:92839713-92839946	MCF-7	breast:	n/a	chr13:92839827-92839848 chr13:92839825-92839843 chr13:92839826-92839842 chr13:92839828-92839841

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:92863315-92863365	HCF	heart:	n/a
2	chr13:92863315-92863365	ECC-1	luminal epithelium:	n/a
3	chr13:92863315-92863365	Hepatocyte	liver:	n/a
4	chr13:92863315-92863365	AG04450	lung:	fetal
5	chr13:92863315-92863365	HRE	kidney:	n/a
6	chr13:92863315-92863365	SK-N-MC	brain:	n/a
7	chr13:92863315-92863365	HUVEC	blood vessel:	n/a
8	chr13:92863315-92863365	SK-N-SH_RA	brain:	n/a
9	chr13:92863315-92863365	Jurkat	blood:	n/a
10	chr13:92863315-92863365	ProgFib	skin:	n/a
11	chr13:92863315-92863365	AoSMC	blood vessel:	n/a
12	chr13:92863315-92863365	PANC-1	pancreas:	n/a
13	chr13:92863315-92863365	HCPEpiC	choroid plexus:	n/a
14	chr13:92863315-92863365	A549	lung:	n/a
15	chr13:92863315-92863365	Hela-S3	cervix:	n/a
16	chr13:92863315-92863365	AG10803	skin:	n/a
17	chr13:92863315-92863365	PFSK-1	brain:	n/a
18	chr13:92863315-92863365	HCM	heart:	n/a
19	chr13:92863315-92863365	NH-A	brain:	n/a
20	chr13:92863315-92863365	BE2_C	brain:	n/a
21	chr13:92863315-92863365	RPTEC	kidney:	n/a
22	chr13:92863315-92863365	MCF-7	breast:	n/a
23	chr13:92863315-92863365	PrEC	prostate:	n/a
24	chr13:92863315-92863365	T-47D	breast:	n/a
25	chr13:92863315-92863365	K562	blood:	n/a
26	chr13:92863315-92863365	NT2-D1	testis:	n/a
27	chr13:92863315-92863365	GM06990	blood:	n/a
28	chr13:92863315-92863365	HRCEpiC	kidney:	n/a
29	chr13:92863315-92863365	HNPCEpiC	eye:	n/a
30	chr13:92863315-92863365	GM12891	blood:	n/a
31	chr13:92863315-92863365	MCF10A-Er-Src	breast:	n/a
32	chr13:92863315-92863365	AG04449	skin:	fetal
33	chr13:92863315-92863365	SK-N-SH	brain:	n/a
34	chr13:92863315-92863365	H1-hESC	embryonic stem cell:	embryo
35	chr13:92863315-92863365	GM12878	blood:	n/a
36	chr13:92863315-92863365	U87	brain:	n/a
37	chr13:92863315-92863365	LNCaP	prostate:	n/a
38	chr13:92863315-92863365	SAEC	small airway:	n/a
39	chr13:92863315-92863365	Caco-2	colon:	n/a
40	chr13:92863315-92863365	IMR90	lung:	fetal
41	chr13:92863315-92863365	CMK	blood:	n/a
42	chr13:92863315-92863365	GM19239	blood:	n/a
43	chr13:92863315-92863365	AG09319	gingival:	n/a
44	chr13:92863315-92863365	HCT-116	colon:	n/a
45	chr13:92863315-92863365	HL-60	blood:	n/a
46	chr13:92863315-92863365	SKMC	muscle:	n/a
47	chr13:92863315-92863365	GM12892	blood:	n/a
48	chr13:92863315-92863365	NHDF-neo	bronchial:	n/a
49	chr13:92863315-92863365	HEK293	kidney:	embryo
50	chr13:92863315-92863365	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:92839355..92840221-chr13:93007230..93007787,2	MCF-7	breast:
2	chr13:92598450..92599301-chr13:92827714..92828302,2	MCF-7	breast:
3	chr13:91998776..92000555-chr13:92831916..92834550,2	K562	blood:
4	chr13:92839375..92840322-chr13:93182374..93183100,3	MCF-7	breast:
5	chr13:92841987..92842813-chr13:93007626..93008163,2	MCF-7	breast:

Variant related genes	Relation type
FABP5P4	TF binding region
FABP5P4	CpG island
ENSG00000215417	chromatin interactions

Extended variants
information (count: 1415 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1415 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138191937	chr13:92824023-92824024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs533556629	chr13:92824067-92824068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149594850	chr13:92824133-92824134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs77979530	chr13:92824154-92824155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs77679671	chr13:92824159-92824160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs73622759	chr13:92824185-92824186	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs567943146	chr13:92824220-92824221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs533579818	chr13:92824272-92824273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs115660211	chr13:92824293-92824294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576777721	chr13:92824354-92824355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545549692	chr13:92824379-92824380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556092438	chr13:92824417-92824418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs79694530	chr13:92824445-92824446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148720024	chr13:92824483-92824484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs562236849	chr13:92824497-92824498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527670228	chr13:92824499-92824500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs541477377	chr13:92824520-92824521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192751364	chr13:92824528-92824529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533677155	chr13:92824581-92824582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs7993836	chr13:92824598-92824599	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs141437367	chr13:92824610-92824611	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs368960430	chr13:92824626-92824627	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs529519732	chr13:92824674-92824675	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs185138235	chr13:92824707-92824708	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs567856606	chr13:92824735-92824736	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs533544072	chr13:92824738-92824739	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs553358099	chr13:92824759-92824760	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs552691251	chr13:92824770-92824771	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs147535591	chr13:92824772-92824773	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs115205977	chr13:92824827-92824828	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs536053940	chr13:92824872-92824873	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs80259981	chr13:92824874-92824875	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs78030048	chr13:92824885-92824886	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs140220722	chr13:92824911-92824912	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs142647135	chr13:92824990-92824991	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs555570148	chr13:92824992-92824993	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs572619164	chr13:92824999-92825000	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs17188425	chr13:92825010-92825011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs73622761	chr13:92825026-92825027	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs73622763	chr13:92825150-92825151	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs145536746	chr13:92825154-92825155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564044931	chr13:92825186-92825187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs377091889	chr13:92825212-92825213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs73622767	chr13:92825213-92825214	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs200594094	chr13:92825226-92825227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549603211	chr13:92825233-92825234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147723297	chr13:92825305-92825306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs73622769	chr13:92825314-92825315	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs545471035	chr13:92825322-92825323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs546951777	chr13:92825330-92825331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD
Developmental delay	21147756	CNVD
Melanoma	20877625	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Osteosarcoma	21215367	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:92824000-92824600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr13:92824400-92825200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr13:92824600-92825000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr13:92825000-92825600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr13:92825200-92827400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr13:92825600-92827400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr13:92827400-92827600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr13:92827400-92827800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr13:92827600-92827800	Enhancers	Brain Anterior Caudate	brain
10	chr13:92827600-92828200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr13:92830200-92830600	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr13:92839600-92839800	Enhancers	Fetal Heart	heart
13	chr13:92846400-92847000	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr13:92847000-92848800	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr13:92848800-92849000	Active TSS	Ovary	ovary
16	chr13:92848800-92849000	Active TSS	Right Atrium	heart
17	chr13:92848800-92849200	Enhancers	Brain Hippocampus Middle	brain
18	chr13:92848800-92849200	Active TSS	Fetal Lung	lung
19	chr13:92848800-92849200	Active TSS	NH-A	brain
20	chr13:92848800-92849400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr13:92848800-92849400	Active TSS	Fetal Adrenal Gland	Adrenal Gland
22	chr13:92848800-92849400	Active TSS	Fetal Kidney	kidney
23	chr13:92848800-92849400	Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr13:92848800-92850200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr13:92849000-92849200	Flanking Active TSS	Right Atrium	heart
26	chr13:92849000-92849400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr13:92849000-92849400	Flanking Active TSS	Ovary	ovary
28	chr13:92849200-92849400	Flanking Active TSS	NH-A	brain
29	chr13:92849200-92849600	Enhancers	Fetal Lung	lung
30	chr13:92849600-92854600	Weak transcription	Fetal Lung	lung
31	chr13:92854600-92855000	Enhancers	Fetal Lung	lung
32	chr13:92856600-92857000	Enhancers	Liver	Liver
33	chr13:92862800-92863000	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr13:92863000-92863400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr13:92863000-92863800	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr13:92863000-92864000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr13:92863000-92864400	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr13:92863200-92864000	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr13:92863400-92864000	Enhancers	H1 Cell Line	embryonic stem cell
40	chr13:92863600-92863800	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr13:92863600-92864000	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr13:92863800-92864000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr13:92863800-92870800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr13:92864000-92870600	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr13:92864000-92871200	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr13:92865000-92865200	Enhancers	Ovary	ovary
47	chr13:92865000-92865800	Enhancers	Fetal Intestine Small	intestine
48	chr13:92865000-92866000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr13:92865200-92865800	Enhancers	Fetal Intestine Large	intestine
50	chr13:92865200-92867200	Enhancers	Fetal Lung	lung

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