Variant report

Variant	nsv947111
Chromosome Location	chr1:47277189-47308420
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:89)
CpG islands
(count:122)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:89 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:47298656-47298680	K562	blood:	n/a	n/a
2	CTCF	chr1:47301131-47301466	MCF-7	breast:	n/a	n/a
3	CTCF	chr1:47301240-47301390	HEK293	kidney:	n/a	n/a
4	CTCF	chr1:47301283-47301414	Gliobla	brain:	n/a	n/a
5	CTCF	chr1:47288540-47288690	NHEK	skin:	n/a	n/a
6	CTCF	chr1:47301326-47301394	MCF-7	breast:	n/a	n/a
7	CTCF	chr1:47301280-47301430	HepG2	liver:	n/a	n/a
8	CTCF	chr1:47288040-47288190	WERI-Rb-1	eye:	n/a	n/a
9	CTCF	chr1:47301260-47301410	HCT-116	colon:	n/a	n/a
10	CTCF	chr1:47301274-47301412	MCF-7	breast:	n/a	n/a
11	CTCF	chr1:47278520-47278670	GM12872	blood:	n/a	chr1:47278531-47278540
12	CTCF	chr1:47301145-47301455	K562	blood:	n/a	n/a
13	CTCF	chr1:47301260-47301410	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr1:47301220-47301370	SK-N-SH_RA	brain:	n/a	n/a
15	CTCF	chr1:47301307-47301387	A549	lung:	n/a	n/a
16	CTCF	chr1:47288492-47288561	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr1:47301140-47301290	HCT-116	colon:	n/a	n/a
18	CTCF	chr1:47301323-47301325	MCF-7	breast:	n/a	n/a
19	CTCF	chr1:47301183-47301420	K562	blood:	n/a	n/a
20	CTCF	chr1:47301253-47301414	MCF-7	breast:	n/a	n/a
21	CTCF	chr1:47301244-47301437	K562	blood:	n/a	n/a
22	CTCF	chr1:47301280-47301430	MCF-7	breast:	n/a	n/a
23	CTCF	chr1:47301285-47301408	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr1:47301299-47301399	NHEK	skin:	n/a	n/a
25	CTCF	chr1:47288021-47288125	K562	blood:	n/a	n/a
26	CTCF	chr1:47301249-47301462	K562	blood:	n/a	n/a
27	CTCF	chr1:47301260-47301410	K562	blood:	n/a	n/a
28	CTCF	chr1:47301240-47301390	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr1:47301260-47301410	A549	lung:	n/a	n/a
30	CTCF	chr1:47288047-47288130	K562	blood:	n/a	n/a
31	CTCF	chr1:47301292-47301412	HepG2	liver:	n/a	n/a
32	CTCF	chr1:47288160-47288310	HEK293	kidney:	n/a	n/a
33	CTCF	chr1:47301261-47301411	MCF-7	breast:	n/a	n/a
34	CTCF	chr1:47286580-47286730	HepG2	liver:	n/a	n/a
35	CTCF	chr1:47301297-47301398	Medullo	brain:	n/a	n/a
36	EBF1	chr1:47288635-47288796	GM12878	blood:	n/a	chr1:47288755-47288766 chr1:47288717-47288728
37	EBF1	chr1:47288199-47288413	GM12878	blood:	n/a	n/a
38	EBF1	chr1:47278124-47278273	GM12878	blood:	n/a	chr1:47278159-47278170
39	EBF1	chr1:47288200-47288457	GM12878	blood:	n/a	n/a
40	EGR1	chr1:47301217-47301463	K562	blood:	n/a	n/a
41	EGR1	chr1:47301207-47301439	K562	blood:	n/a	n/a
42	FAM48A	chr1:47308321-47308371	GM12878	blood:	n/a	n/a
43	FAM48A	chr1:47303971-47304146	GM12878	blood:	n/a	n/a
44	FOS	chr1:47283999-47284062	MCF10A-Er-Src	breast:	n/a	n/a
45	FOXA1	chr1:47294284-47294550	HepG2	liver:	n/a	n/a
46	FOXA1	chr1:47296398-47296650	HepG2	liver:	n/a	n/a
47	FOXA1	chr1:47296367-47296755	HepG2	liver:	n/a	n/a
48	FOXA1	chr1:47296373-47296618	HepG2	liver:	n/a	n/a
49	FOXA1	chr1:47296341-47296640	HepG2	liver:	n/a	n/a
50	FOXA2	chr1:47296393-47296637	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:47284627-47284677	ECC-1	luminal epithelium:	n/a
2	chr1:47284627-47284677	NB4	blood:	n/a
3	chr1:47284627-47284677	SK-N-SH	brain:	n/a
4	chr1:47284627-47284677	BJ	skin:	n/a
5	chr1:47279985-47280035	CMK	blood:	n/a
6	chr1:47279985-47280035	HAEpiC	amniotic membrane:	n/a
7	chr1:47284627-47284677	HMEC	breast:	n/a
8	chr1:47284627-47284677	HUVEC	blood vessel:	n/a
9	chr1:47284627-47284677	ovcar-3	ovarian:	n/a
10	chr1:47284627-47284677	AG04450	lung:	fetal
11	chr1:47284627-47284677	NHDF-neo	bronchial:	n/a
12	chr1:47284627-47284677	Hepatocyte	liver:	n/a
13	chr1:47279985-47280035	PFSK-1	brain:	n/a
14	chr1:47279985-47280035	RPTEC	kidney:	n/a
15	chr1:47279985-47280035	SK-N-SH	brain:	n/a
16	chr1:47284627-47284677	HAEpiC	amniotic membrane:	n/a
17	chr1:47279985-47280035	HEK293	kidney:	embryo
18	chr1:47284627-47284677	HNPCEpiC	eye:	n/a
19	chr1:47284627-47284677	HCPEpiC	choroid plexus:	n/a
20	chr1:47279985-47280035	MCF10A-Er-Src	breast:	n/a
21	chr1:47279985-47280035	HCM	heart:	n/a
22	chr1:47284627-47284677	GM12891	blood:	n/a
23	chr1:47284627-47284677	HRPEpiC	eye:	n/a
24	chr1:47279985-47280035	HNPCEpiC	eye:	n/a
25	chr1:47279985-47280035	Jurkat	blood:	n/a
26	chr1:47279985-47280035	SK-N-MC	brain:	n/a
27	chr1:47284627-47284677	T-47D	breast:	n/a
28	chr1:47284627-47284677	CMK	blood:	n/a
29	chr1:47279985-47280035	Hela-S3	cervix:	n/a
30	chr1:47279985-47280035	GM12892	blood:	n/a
31	chr1:47284627-47284677	HEEpiC	esophagus:	n/a
32	chr1:47279985-47280035	GM12878	blood:	n/a
33	chr1:47284627-47284677	AG04449	skin:	fetal
34	chr1:47284627-47284677	MCF10A-Er-Src	breast:	n/a
35	chr1:47279985-47280035	IMR90	lung:	fetal
36	chr1:47279985-47280035	ECC-1	luminal epithelium:	n/a
37	chr1:47279985-47280035	ovcar-3	ovarian:	n/a
38	chr1:47284627-47284677	HRE	kidney:	n/a
39	chr1:47284627-47284677	U87	brain:	n/a
40	chr1:47284627-47284677	SK-N-MC	brain:	n/a
41	chr1:47284627-47284677	NT2-D1	testis:	n/a
42	chr1:47279985-47280035	HL-60	blood:	n/a
43	chr1:47284627-47284677	PFSK-1	brain:	n/a
44	chr1:47279985-47280035	AG04449	skin:	fetal
45	chr1:47279985-47280035	HUVEC	blood vessel:	n/a
46	chr1:47284627-47284677	MCF-7	breast:	n/a
47	chr1:47284627-47284677	SKMC	muscle:	n/a
48	chr1:47284627-47284677	HepG2	liver:	n/a
49	chr1:47279985-47280035	GM19239	blood:	n/a
50	chr1:47284627-47284677	BE2_C	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:47282268..47284457-chr1:47286910..47288924,2	K562	blood:
2	chr1:47274872..47277380-chr1:47277423..47279681,2	K562	blood:
3	chr1:47275758..47278616-chr1:47280662..47283634,2	K562	blood:
4	chr1:47272192..47274421-chr1:47282299..47283950,2	K562	blood:
5	chr1:47270918..47272980-chr1:47278589..47280565,2	K562	blood:
6	chr1:47275758..47278616-chr1:47280662..47283634,2	K562	blood:

No data

Variant related genes	Relation type
CYP4B1	TF binding region
CYP4B1	CpG island
ENSG00000142973	chromatin interactions

Extended variants
information (count: 1292 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1292 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189940182	chr1:47277198-47277199	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs34007597	chr1:47277212-47277213	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs4646483	chr1:47277217-47277218	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs369277540	chr1:47277235-47277236	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs45557831	chr1:47277257-47277258	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs547644890	chr1:47277315-47277316	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs550916435	chr1:47277324-47277325	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs566263575	chr1:47277350-47277351	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs533609368	chr1:47277400-47277401	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs551892088	chr1:47277428-47277429	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs570111644	chr1:47277448-47277449	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs537478824	chr1:47277497-47277498	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs375031433	chr1:47277525-47277526	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs45462392	chr1:47277551-47277552	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs368488179	chr1:47277552-47277553	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs183278603	chr1:47277564-47277565	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs567816008	chr1:47277565-47277566	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs11211367	chr1:47277567-47277568	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs61782656	chr1:47277590-47277591	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs35451158	chr1:47277605-47277606	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs553640198	chr1:47277609-47277610	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs572215380	chr1:47277629-47277630	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs527833922	chr1:47277630-47277631	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs530660474	chr1:47277634-47277635	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs545972483	chr1:47277640-47277641	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs371496044	chr1:47277714-47277715	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs564598540	chr1:47277749-47277750	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs139675113	chr1:47277750-47277751	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs576490037	chr1:47277756-47277757	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs149781305	chr1:47277826-47277827	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs11211368	chr1:47277831-47277832	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs529512667	chr1:47277862-47277863	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs144721189	chr1:47277937-47277938	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs559681215	chr1:47277967-47277968	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs533623891	chr1:47277993-47277994	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs551835686	chr1:47278011-47278012	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs570249442	chr1:47278046-47278047	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs531324405	chr1:47278049-47278050	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs56011427	chr1:47278081-47278082	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs186729867	chr1:47278095-47278096	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs45500401	chr1:47278169-47278170	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs377363512	chr1:47278173-47278174	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs148753850	chr1:47278174-47278175	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs372658454	chr1:47278181-47278182	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs376850847	chr1:47278188-47278189	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs370962235	chr1:47278201-47278202	Genic enhancers Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs200388090	chr1:47278202-47278203	Genic enhancers Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs151255408	chr1:47278226-47278227	Genic enhancers Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs144157811	chr1:47278243-47278244	Genic enhancers Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs539678720	chr1:47278257-47278258	Genic enhancers Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Neuroblastoma	21899760	CNVD
Uveal melanoma	20484589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Glioblastoma	20031968	CNVD
Leukemia	18688285	CNVD
Rett syndrome	21593744	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47265600-47279200	Weak transcription	Gastric	stomach
2	chr1:47273400-47285600	Weak transcription	Spleen	Spleen
3	chr1:47275600-47278200	Enhancers	Left Ventricle	heart
4	chr1:47275800-47277800	Weak transcription	Psoas Muscle	Psoas
5	chr1:47276000-47277600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr1:47276000-47278000	Enhancers	Adipose Nuclei	Adipose
7	chr1:47276000-47278000	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr1:47276200-47278600	Enhancers	Right Ventricle	heart
9	chr1:47276400-47278400	Genic enhancers	Lung	lung
10	chr1:47276400-47278400	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr1:47277000-47278000	Weak transcription	Right Atrium	heart
12	chr1:47277000-47286800	Strong transcription	Esophagus	oesophagus
13	chr1:47277600-47278000	Enhancers	Stomach Smooth Muscle	stomach
14	chr1:47277800-47278000	Enhancers	Psoas Muscle	Psoas
15	chr1:47278000-47278200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
16	chr1:47278000-47278600	Enhancers	Right Atrium	heart
17	chr1:47278000-47278800	Genic enhancers	Adipose Nuclei	Adipose
18	chr1:47278200-47278800	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr1:47278200-47279400	Genic enhancers	Left Ventricle	heart
20	chr1:47278400-47279200	Weak transcription	Lung	lung
21	chr1:47278600-47279400	Weak transcription	Right Ventricle	heart
22	chr1:47278800-47279000	Genic enhancers	Skeletal Muscle Male	skeletal muscle
23	chr1:47278800-47285000	Strong transcription	Adipose Nuclei	Adipose
24	chr1:47279000-47281000	Strong transcription	Skeletal Muscle Male	skeletal muscle
25	chr1:47279200-47284400	Strong transcription	Lung	lung
26	chr1:47279400-47279600	Enhancers	Gastric	stomach
27	chr1:47279400-47280400	Strong transcription	Left Ventricle	heart
28	chr1:47279400-47281200	Strong transcription	Right Ventricle	heart
29	chr1:47280400-47281000	Genic enhancers	Left Ventricle	heart
30	chr1:47281000-47283200	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr1:47281000-47284600	Strong transcription	Left Ventricle	heart
32	chr1:47281200-47285800	Weak transcription	Right Ventricle	heart
33	chr1:47283200-47285400	Strong transcription	Skeletal Muscle Male	skeletal muscle
34	chr1:47284400-47285600	Weak transcription	Lung	lung
35	chr1:47284600-47285400	Weak transcription	Left Ventricle	heart
36	chr1:47285000-47285400	Weak transcription	Adipose Nuclei	Adipose
37	chr1:47285400-47286600	Enhancers	Adipose Nuclei	Adipose
38	chr1:47285400-47286600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
39	chr1:47285400-47286800	Enhancers	Left Ventricle	heart
40	chr1:47285600-47285800	Enhancers	Lung	lung
41	chr1:47285600-47286600	Enhancers	Spleen	Spleen
42	chr1:47285600-47286800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr1:47285800-47286000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr1:47285800-47286000	Genic enhancers	Lung	lung
45	chr1:47285800-47286600	Enhancers	Fetal Muscle Trunk	muscle
46	chr1:47285800-47286600	Enhancers	Right Atrium	heart
47	chr1:47285800-47286600	Enhancers	Right Ventricle	heart
48	chr1:47286000-47286600	Enhancers	Lung	lung
49	chr1:47286000-47288400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:47286200-47286600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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