Variant report

Variant	nsv954
Chromosome Location	chr1:57823140-57865799
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:83)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:83 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:57864050-57864128	K562	blood:	n/a	n/a
2	CEBPB	chr1:57850364-57850571	HepG2	liver:	n/a	chr1:57850477-57850488
3	CEBPB	chr1:57850432-57850554	A549	lung:	n/a	chr1:57850477-57850488
4	CEBPB	chr1:57849385-57849579	HepG2	liver:	n/a	n/a
5	CTCF	chr1:57843428-57843788	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr1:57843620-57843770	Caco-2	colon:	n/a	n/a
7	CTCF	chr1:57843621-57843675	K562	blood:	n/a	n/a
8	CTCF	chr1:57833840-57833990	HepG2	liver:	n/a	n/a
9	CTCF	chr1:57833781-57833971	HepG2	liver:	n/a	n/a
10	CTCF	chr1:57843520-57843670	K562	blood:	n/a	n/a
11	CTCF	chr1:57843560-57843710	SK-N-SH_RA	brain:	n/a	n/a
12	CTCF	chr1:57843640-57843790	Caco-2	colon:	n/a	n/a
13	CTCF	chr1:57843680-57843830	NB4	blood:	n/a	n/a
14	CTCF	chr1:57843460-57843610	AG04450	lung:	n/a	n/a
15	CTCF	chr1:57843680-57843830	HepG2	liver:	n/a	n/a
16	CTCF	chr1:57843560-57843710	HEK293	kidney:	n/a	n/a
17	CTCF	chr1:57843520-57843670	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr1:57843580-57843730	GM12867	blood:	n/a	n/a
19	CTCF	chr1:57843550-57843679	K562	blood:	n/a	n/a
20	CTCF	chr1:57843540-57843690	HRPEpiC	eye:	n/a	n/a
21	CTCF	chr1:57843443-57843821	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr1:57843580-57843730	AG10803	skin:	n/a	n/a
23	CTCF	chr1:57833820-57833970	HepG2	liver:	n/a	n/a
24	CTCF	chr1:57832940-57833090	Caco-2	colon:	n/a	n/a
25	CTCF	chr1:57843575-57843798	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr1:57843640-57843790	HFF	foreskin:	n/a	n/a
27	CTCF	chr1:57843600-57843750	NHEK	skin:	n/a	n/a
28	CTCF	chr1:57833931-57833934	Fibrobl	skin:	n/a	n/a
29	CTCF	chr1:57833869-57833923	H1-hESC	embryonic stem cell:	n/a	n/a
30	E2F4	chr1:57849282-57849482	MCF10A-Er-Src	breast:	n/a	n/a
31	EBF1	chr1:57863474-57863589	GM12878	blood:	n/a	n/a
32	EGR1	chr1:57843357-57843510	K562	blood:	n/a	n/a
33	EGR1	chr1:57843349-57843565	K562	blood:	n/a	n/a
34	FOS	chr1:57858909-57859011	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr1:57841925-57841951	MCF10A-Er-Src	breast:	n/a	n/a
36	FOXA1	chr1:57833586-57833908	HepG2	liver:	n/a	n/a
37	FOXA1	chr1:57833620-57833954	HepG2	liver:	n/a	n/a
38	FOXA2	chr1:57833643-57833890	HepG2	liver:	n/a	n/a
39	HNF4A	chr1:57833688-57834003	HepG2	liver:	n/a	chr1:57833831-57833846
40	HNF4A	chr1:57833707-57833935	HepG2	liver:	n/a	chr1:57833831-57833846
41	IRF1	chr1:57857646-57857690	K562	blood:	n/a	n/a
42	IRF3	chr1:57847097-57847177	GM12878	blood:	n/a	n/a
43	KAP1	chr1:57834100-57834574	HEK293	kidney:	n/a	n/a
44	KAP1	chr1:57824903-57825180	K562	blood:	n/a	n/a
45	MAFK	chr1:57855039-57855193	HepG2	liver:	n/a	chr1:57855076-57855091 chr1:57855081-57855092
46	MAFK	chr1:57839661-57839903	HepG2	liver:	n/a	chr1:57839744-57839755 chr1:57839744-57839760 chr1:57839747-57839764 chr1:57839745-57839756 chr1:57839743-57839757
47	MAFK	chr1:57829694-57829729	HepG2	liver:	n/a	chr1:57829710-57829721 chr1:57829711-57829722 chr1:57829710-57829721 chr1:57829711-57829722
48	MAFK	chr1:57855021-57855143	HepG2	liver:	n/a	chr1:57855076-57855091 chr1:57855081-57855092
49	MAX	chr1:57823398-57823628	H1-hESC	embryonic stem cell:	n/a	n/a
50	MAX	chr1:57843407-57843600	NB4	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:57836927-57836977	Hela-S3	cervix:	n/a
2	chr1:57836927-57836977	SKMC	muscle:	n/a
3	chr1:57836927-57836977	A549	lung:	n/a
4	chr1:57836927-57836977	PANC-1	pancreas:	n/a
5	chr1:57836927-57836977	SK-N-MC	brain:	n/a
6	chr1:57836927-57836977	ProgFib	skin:	n/a
7	chr1:57836927-57836977	GM12891	blood:	n/a
8	chr1:57836927-57836977	HRCEpiC	kidney:	n/a
9	chr1:57836927-57836977	HCM	heart:	n/a
10	chr1:57836927-57836977	AG04450	lung:	fetal
11	chr1:57836927-57836977	PFSK-1	brain:	n/a
12	chr1:57836927-57836977	PrEC	prostate:	n/a
13	chr1:57836927-57836977	MCF10A-Er-Src	breast:	n/a
14	chr1:57836927-57836977	BE2_C	brain:	n/a
15	chr1:57836927-57836977	T-47D	breast:	n/a
16	chr1:57836927-57836977	HCPEpiC	choroid plexus:	n/a
17	chr1:57836927-57836977	HNPCEpiC	eye:	n/a
18	chr1:57836927-57836977	NHBE	bronchial:	n/a
19	chr1:57836927-57836977	MCF-7	breast:	n/a
20	chr1:57836927-57836977	Hepatocyte	liver:	n/a
21	chr1:57836927-57836977	AoSMC	blood vessel:	n/a
22	chr1:57836927-57836977	CMK	blood:	n/a
23	chr1:57836927-57836977	HepG2	liver:	n/a
24	chr1:57836927-57836977	HAEpiC	amniotic membrane:	n/a
25	chr1:57836927-57836977	NT2-D1	testis:	n/a
26	chr1:57836927-57836977	U87	brain:	n/a
27	chr1:57836927-57836977	AG09309	skin:	n/a
28	chr1:57836927-57836977	HRPEpiC	eye:	n/a
29	chr1:57836927-57836977	GM19239	blood:	n/a
30	chr1:57836927-57836977	HL-60	blood:	n/a
31	chr1:57836927-57836977	ovcar-3	ovarian:	n/a
32	chr1:57836927-57836977	IMR90	lung:	fetal
33	chr1:57836927-57836977	HRE	kidney:	n/a
34	chr1:57836927-57836977	ECC-1	luminal epithelium:	n/a
35	chr1:57836927-57836977	AG09319	gingival:	n/a
36	chr1:57836927-57836977	HEK293	kidney:	embryo
37	chr1:57836927-57836977	NHDF-neo	bronchial:	n/a
38	chr1:57836927-57836977	NH-A	brain:	n/a
39	chr1:57836927-57836977	Jurkat	blood:	n/a
40	chr1:57836927-57836977	HUVEC	blood vessel:	n/a
41	chr1:57836927-57836977	NB4	blood:	n/a
42	chr1:57836927-57836977	SK-N-SH_RA	brain:	n/a
43	chr1:57836927-57836977	Caco-2	colon:	n/a
44	chr1:57836927-57836977	GM12878	blood:	n/a
45	chr1:57836927-57836977	SAEC	small airway:	n/a
46	chr1:57836927-57836977	SK-N-SH	brain:	n/a
47	chr1:57836927-57836977	HIPEpiC	eye:	n/a
48	chr1:57836927-57836977	HEEpiC	esophagus:	n/a
49	chr1:57836927-57836977	GM06990	blood:	n/a
50	chr1:57836927-57836977	HCT-116	colon:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8A-3	chr1:57852562-57853122	ENSG00000227935
2	lnc-C8A-3	chr1:57852248-57852394	ENSG00000227935

No data

Variant related genes	Relation type
ENSG00000227935	TF binding region
ENSG00000227935	CpG island

Extended variants
information (count: 1654 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1654 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570621071	chr1:57823142-57823143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs547989278	chr1:57823146-57823147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200298171	chr1:57823187-57823188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373171626	chr1:57823191-57823192	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs61769671	chr1:57823208-57823209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371034164	chr1:57823209-57823210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs79254000	chr1:57823210-57823211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141002213	chr1:57823224-57823225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533735116	chr1:57823279-57823280	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553457922	chr1:57823280-57823281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185158289	chr1:57823291-57823292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539036579	chr1:57823292-57823293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145842402	chr1:57823339-57823340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs189085112	chr1:57823364-57823365	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544964041	chr1:57823382-57823383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181818650	chr1:57823398-57823399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184997978	chr1:57823401-57823402	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568193976	chr1:57823423-57823424	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375166040	chr1:57823452-57823453	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189570199	chr1:57823511-57823512	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532081875	chr1:57823525-57823526	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545787927	chr1:57823530-57823531	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11207017	chr1:57823563-57823564	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs535593376	chr1:57823585-57823586	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553734668	chr1:57823615-57823616	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs531197108	chr1:57823618-57823619	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs548124247	chr1:57823627-57823628	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs572130315	chr1:57823630-57823631	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs180802190	chr1:57823637-57823638	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs370094873	chr1:57823679-57823680	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs527515091	chr1:57823690-57823691	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs116227488	chr1:57823702-57823703	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs186238160	chr1:57823709-57823710	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs375564659	chr1:57823755-57823756	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs542595124	chr1:57823756-57823757	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs374412661	chr1:57823779-57823780	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs191162179	chr1:57823804-57823805	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569323459	chr1:57823808-57823809	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538224022	chr1:57823895-57823896	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12565446	chr1:57823915-57823916	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs575151996	chr1:57823933-57823934	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138465025	chr1:57823941-57823942	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12565636	chr1:57823951-57823952	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs77129304	chr1:57823952-57823953	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143094943	chr1:57824023-57824024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573441186	chr1:57824033-57824034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs540670729	chr1:57824132-57824133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs368290045	chr1:57824193-57824194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs12025486	chr1:57824276-57824277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201712256	chr1:57824289-57824290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	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
Breast cancer	17603634	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
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
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Meckel-Gruber syndrome	21572526	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	16616336	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	19490664	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Developmental delay	21147756	CNVD

Chromatin state (count:222 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57800000-57826600	Weak transcription	Left Ventricle	heart
2	chr1:57817600-57826600	Weak transcription	Fetal Brain Male	brain
3	chr1:57819400-57826600	Weak transcription	Fetal Stomach	stomach
4	chr1:57819400-57832000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr1:57821400-57826000	Weak transcription	Fetal Heart	heart
6	chr1:57821800-57823600	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr1:57822000-57824000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr1:57822200-57823200	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr1:57822400-57823200	Enhancers	Fetal Brain Female	brain
10	chr1:57822400-57823400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr1:57822400-57823600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr1:57822400-57823800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr1:57822400-57824000	Enhancers	H1 Cell Line	embryonic stem cell
14	chr1:57822400-57824200	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr1:57822600-57823600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr1:57822600-57823800	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr1:57822600-57824200	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr1:57823000-57823200	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr1:57823200-57826000	Weak transcription	Fetal Brain Female	brain
20	chr1:57823400-57823600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr1:57823600-57823800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr1:57823600-57824000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr1:57823800-57824000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr1:57823800-57833200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr1:57824000-57824200	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr1:57824000-57826400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr1:57826000-57827000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr1:57826000-57827400	Enhancers	Fetal Brain Female	brain
29	chr1:57826000-57829600	Enhancers	Fetal Heart	heart
30	chr1:57826400-57827000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr1:57826400-57827600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr1:57826600-57826800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr1:57826600-57826800	Enhancers	Left Ventricle	heart
34	chr1:57826600-57827000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr1:57826600-57827400	Enhancers	Fetal Brain Male	brain
36	chr1:57826600-57827400	Enhancers	Fetal Stomach	stomach
37	chr1:57826800-57827400	Weak transcription	Left Ventricle	heart
38	chr1:57826800-57828400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr1:57827400-57827600	Enhancers	Left Ventricle	heart
40	chr1:57827400-57829800	Weak transcription	Fetal Brain Male	brain
41	chr1:57827400-57833800	Weak transcription	Fetal Brain Female	brain
42	chr1:57827600-57828000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr1:57827600-57828200	Weak transcription	Left Ventricle	heart
44	chr1:57828000-57828600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr1:57828200-57829600	Enhancers	Left Ventricle	heart
46	chr1:57828400-57829200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr1:57828600-57836800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr1:57829200-57833000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr1:57829600-57843400	Weak transcription	Fetal Heart	heart
50	chr1:57829800-57830200	Enhancers	Fetal Brain Male	brain

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