Variant report

Variant	nsv1002958
Chromosome Location	chr1:56278696-56295112
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	BHLHE40	chr1:56282179-56282491	GM12878	blood:	n/a	n/a
2	CEBPB	chr1:56287091-56287158	H1-hESC	embryonic stem cell:	n/a	chr1:56287104-56287117
3	CEBPB	chr1:56279281-56279644	A549	lung:	n/a	chr1:56279458-56279469
4	CEBPB	chr1:56279338-56279553	HepG2	liver:	n/a	chr1:56279458-56279469
5	CEBPB	chr1:56292980-56293358	IMR90	lung:	n/a	n/a
6	CEBPB	chr1:56279223-56279616	HepG2	liver:	n/a	chr1:56279458-56279469
7	CEBPB	chr1:56279246-56279897	Hela-S3	cervix:	n/a	chr1:56279458-56279469
8	CEBPB	chr1:56279236-56279765	A549	lung:	n/a	chr1:56279458-56279469
9	CEBPB	chr1:56279273-56279658	IMR90	lung:	n/a	chr1:56279458-56279469
10	CEBPB	chr1:56292980-56293367	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr1:56279282-56279648	HepG2	liver:	n/a	chr1:56279458-56279469
12	CEBPB	chr1:56293144-56293300	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:56279334-56279586	H1-hESC	embryonic stem cell:	n/a	chr1:56279458-56279469
14	CEBPB	chr1:56279326-56279603	K562	blood:	n/a	chr1:56279458-56279469
15	CEBPB	chr1:56293607-56294272	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr1:56286956-56287260	IMR90	lung:	n/a	chr1:56287104-56287117
17	CEBPB	chr1:56279380-56279554	ECC-1	luminal epithelium:	n/a	chr1:56279458-56279469
18	CEBPB	chr1:56279284-56279651	A549	lung:	n/a	chr1:56279458-56279469
19	CEBPB	chr1:56279269-56279649	HepG2	liver:	n/a	chr1:56279458-56279469
20	CEBPB	chr1:56279269-56279626	MCF-7	breast:	n/a	chr1:56279458-56279469
21	CEBPB	chr1:56287050-56287246	Hela-S3	cervix:	n/a	chr1:56287104-56287117
22	CEBPD	chr1:56279380-56279542	HepG2	liver:	n/a	n/a
23	CTCF	chr1:56289355-56289421	LNCaP	prostate:	n/a	n/a
24	CTCF	chr1:56289341-56289448	LNCaP	prostate:	n/a	n/a
25	E2F4	chr1:56289695-56289970	MCF10A-Er-Src	breast:	n/a	n/a
26	EBF1	chr1:56282180-56282683	GM12878	blood:	n/a	n/a
27	EP300	chr1:56292966-56293401	SK-N-SH_RA	brain:	n/a	chr1:56293245-56293254 chr1:56293244-56293253
28	EP300	chr1:56282198-56282492	GM12878	blood:	n/a	n/a
29	EP300	chr1:56292917-56293429	SK-N-SH_RA	brain:	n/a	chr1:56293245-56293254 chr1:56293244-56293253
30	EP300	chr1:56279180-56279681	Hela-S3	cervix:	n/a	chr1:56279209-56279218 chr1:56279220-56279229
31	EP300	chr1:56282259-56282467	GM12878	blood:	n/a	n/a
32	EP300	chr1:56291119-56291565	SK-N-SH_RA	brain:	n/a	n/a
33	EP300	chr1:56293634-56294164	Hela-S3	cervix:	n/a	n/a
34	EP300	chr1:56279247-56279953	SK-N-SH_RA	brain:	n/a	n/a
35	EP300	chr1:56292027-56292598	SK-N-SH_RA	brain:	n/a	n/a
36	EP300	chr1:56291785-56294498	SK-N-SH	brain:	n/a	chr1:56293245-56293254 chr1:56293244-56293253
37	EP300	chr1:56279225-56279551	HepG2	liver:	n/a	n/a
38	EP300	chr1:56291146-56291508	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr1:56292045-56292564	SK-N-SH_RA	brain:	n/a	n/a
40	EP300	chr1:56279238-56279856	SK-N-SH	brain:	n/a	n/a
41	EP300	chr1:56293051-56293390	Hela-S3	cervix:	n/a	chr1:56293245-56293254 chr1:56293244-56293253
42	EP300	chr1:56279239-56279791	SK-N-SH_RA	brain:	n/a	n/a
43	FOS	chr1:56289248-56289545	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr1:56293098-56293409	HUVEC	blood vessel:	n/a	chr1:56293245-56293254 chr1:56293245-56293253 chr1:56293243-56293254 chr1:56293246-56293253
45	FOS	chr1:56293821-56294083	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr1:56285085-56285488	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr1:56279289-56279542	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr1:56289264-56289581	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr1:56293911-56294156	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr1:56285112-56285446	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:56293135-56293185	HPAEpiC	pulmonary alveolar:	n/a
2	chr1:56293135-56293185	MCF10A-Er-Src	breast:	n/a
3	chr1:56293135-56293185	GM19239	blood:	n/a
4	chr1:56293135-56293185	Caco-2	colon:	n/a
5	chr1:56293135-56293185	AG09319	gingival:	n/a
6	chr1:56293135-56293185	SK-N-SH	brain:	n/a
7	chr1:56293135-56293185	HCF	heart:	n/a
8	chr1:56293135-56293185	SAEC	small airway:	n/a
9	chr1:56293135-56293185	SKMC	muscle:	n/a
10	chr1:56293135-56293185	K562	blood:	n/a
11	chr1:56293135-56293185	HEEpiC	esophagus:	n/a
12	chr1:56293135-56293185	AG04450	lung:	fetal
13	chr1:56293135-56293185	BE2_C	brain:	n/a
14	chr1:56293135-56293185	BJ	skin:	n/a
15	chr1:56293135-56293185	HCT-116	colon:	n/a
16	chr1:56293135-56293185	ovcar-3	ovarian:	n/a
17	chr1:56293135-56293185	GM12878	blood:	n/a
18	chr1:56293135-56293185	SK-N-MC	brain:	n/a
19	chr1:56293135-56293185	AG09309	skin:	n/a
20	chr1:56293135-56293185	HCPEpiC	choroid plexus:	n/a
21	chr1:56293135-56293185	HCM	heart:	n/a
22	chr1:56293135-56293185	ECC-1	luminal epithelium:	n/a
23	chr1:56293135-56293185	LNCaP	prostate:	n/a
24	chr1:56293135-56293185	HRE	kidney:	n/a
25	chr1:56293135-56293185	IMR90	lung:	fetal
26	chr1:56293135-56293185	RPTEC	kidney:	n/a
27	chr1:56293135-56293185	HNPCEpiC	eye:	n/a
28	chr1:56293135-56293185	NHDF-neo	bronchial:	n/a
29	chr1:56293135-56293185	ProgFib	skin:	n/a
30	chr1:56293135-56293185	AG04449	skin:	fetal
31	chr1:56293135-56293185	HUVEC	blood vessel:	n/a
32	chr1:56293135-56293185	MCF-7	breast:	n/a
33	chr1:56293135-56293185	HRCEpiC	kidney:	n/a
34	chr1:56293135-56293185	AG10803	skin:	n/a
35	chr1:56293135-56293185	NT2-D1	testis:	n/a
36	chr1:56293135-56293185	HMEC	breast:	n/a
37	chr1:56293135-56293185	NB4	blood:	n/a
38	chr1:56293135-56293185	NHBE	bronchial:	n/a
39	chr1:56293135-56293185	PANC-1	pancreas:	n/a
40	chr1:56293135-56293185	A549	lung:	n/a
41	chr1:56293135-56293185	HL-60	blood:	n/a
42	chr1:56293135-56293185	HepG2	liver:	n/a
43	chr1:56293135-56293185	CMK	blood:	n/a
44	chr1:56293135-56293185	GM06990	blood:	n/a
45	chr1:56293135-56293185	GM12892	blood:	n/a
46	chr1:56293135-56293185	U87	brain:	n/a
47	chr1:56293135-56293185	PrEC	prostate:	n/a
48	chr1:56293135-56293185	T-47D	breast:	n/a
49	chr1:56293135-56293185	HRPEpiC	eye:	n/a
50	chr1:56293135-56293185	HAEpiC	amniotic membrane:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCSK9-4	chr1:56289431-56289574	NONHSAT003421
2	lnc-PCSK9-4	chr1:56289480-56289574	XLOC_000207
3	lnc-PCSK9-4	chr1:56289421-56289574	NONHSAT003420
4	lnc-PCSK9-4	chr1:56289440-56289574	XLOC_000207
5	lnc-PCSK9-4	chr1:56289505-56289574	XLOC_000207

Variant related genes	Relation type
ENSG00000233147	TF binding region
ENSG00000233147	CpG island
BLCAP	miRNA target sites
SOX2	miRNA target sites

Extended variants
information (count: 660 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:660 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536659738	chr1:56278717-56278718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs35979802	chr1:56278723-56278724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573388808	chr1:56278743-56278744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547052892	chr1:56278798-56278799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186747116	chr1:56278821-56278822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189680608	chr1:56278832-56278833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs577951336	chr1:56278839-56278840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs557758641	chr1:56278986-56278987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs183374494	chr1:56278996-56278997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560472232	chr1:56279032-56279033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs536802278	chr1:56279092-56279093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs527261300	chr1:56279141-56279142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188671349	chr1:56279161-56279162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs141683637	chr1:56279168-56279169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs150548002	chr1:56279170-56279171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552595274	chr1:56279197-56279198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs138405584	chr1:56279249-56279250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559106669	chr1:56279254-56279255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545303659	chr1:56279256-56279257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs193172323	chr1:56279275-56279276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs112966140	chr1:56279291-56279292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs185110234	chr1:56279321-56279322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188375954	chr1:56279444-56279445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs544443416	chr1:56279457-56279458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191678547	chr1:56279465-56279466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs560963523	chr1:56279487-56279488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs142991281	chr1:56279488-56279489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567068238	chr1:56279492-56279493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs117115434	chr1:56279497-56279498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs532509396	chr1:56279498-56279499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75039847	chr1:56279508-56279509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs146144636	chr1:56279529-56279530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531265088	chr1:56279543-56279544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs574768903	chr1:56279544-56279545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs571425570	chr1:56279550-56279551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183770623	chr1:56279563-56279564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556902764	chr1:56279623-56279624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs549477101	chr1:56279631-56279632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs567118727	chr1:56279638-56279639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs11583637	chr1:56279652-56279653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs56353261	chr1:56279661-56279662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs138222546	chr1:56279668-56279669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs12564526	chr1:56279686-56279687	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs188200979	chr1:56279716-56279717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532615710	chr1:56279717-56279718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs544650020	chr1:56279750-56279751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559217401	chr1:56279791-56279792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs180688706	chr1:56279835-56279836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185742147	chr1:56279854-56279855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs561370503	chr1:56279863-56279864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Prostate cancer	18632612	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
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	19490664	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD

Chromatin state (count:207 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:56276600-56280200	Enhancers	Hela-S3	cervix
2	chr1:56277400-56280000	Enhancers	NHDF-Ad	bronchial
3	chr1:56277400-56280200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:56277600-56279000	Enhancers	Ovary	ovary
5	chr1:56277600-56279800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr1:56277600-56279800	Enhancers	Osteobl	bone
7	chr1:56277600-56280000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr1:56277600-56280000	Enhancers	NHLF	lung
9	chr1:56277800-56281000	Weak transcription	Fetal Intestine Large	intestine
10	chr1:56278000-56279000	Enhancers	Placenta	Placenta
11	chr1:56278000-56280000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr1:56278000-56280000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr1:56278200-56279800	Enhancers	Adipose Nuclei	Adipose
14	chr1:56278200-56280400	Enhancers	Colon Smooth Muscle	Colon
15	chr1:56278400-56278800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr1:56278400-56279400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr1:56278400-56280400	Weak transcription	Aorta	Aorta
18	chr1:56278400-56282600	Weak transcription	Fetal Intestine Small	intestine
19	chr1:56278600-56278800	Enhancers	Right Atrium	heart
20	chr1:56278600-56279000	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr1:56278600-56279000	Enhancers	Lung	lung
22	chr1:56278600-56279800	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr1:56278600-56281600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr1:56278600-56282200	Weak transcription	Pancreas	Pancrea
25	chr1:56278800-56279400	Weak transcription	Right Atrium	heart
26	chr1:56278800-56280800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr1:56279000-56279400	Weak transcription	Placenta	Placenta
28	chr1:56279000-56279400	Weak transcription	Lung	lung
29	chr1:56279000-56279400	Weak transcription	Ovary	ovary
30	chr1:56279000-56279600	Enhancers	Muscle Satellite Cultured Cells	--
31	chr1:56279200-56280200	Enhancers	Rectal Smooth Muscle	rectum
32	chr1:56279200-56282600	Enhancers	Liver	Liver
33	chr1:56279400-56279600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr1:56279400-56279600	Enhancers	Placenta	Placenta
35	chr1:56279400-56279600	Enhancers	Fetal Stomach	stomach
36	chr1:56279400-56279600	Enhancers	Left Ventricle	heart
37	chr1:56279400-56279600	Enhancers	Lung	lung
38	chr1:56279400-56279600	Enhancers	Ovary	ovary
39	chr1:56279400-56279600	Enhancers	Right Atrium	heart
40	chr1:56279400-56279800	Enhancers	HepG2	liver
41	chr1:56279600-56280800	Weak transcription	Lung	lung
42	chr1:56279600-56281400	Weak transcription	Placenta	Placenta
43	chr1:56279600-56281400	Weak transcription	Ovary	ovary
44	chr1:56279600-56282000	Weak transcription	Fetal Stomach	stomach
45	chr1:56279600-56282800	Weak transcription	Right Atrium	heart
46	chr1:56279800-56280800	Weak transcription	HepG2	liver
47	chr1:56279800-56281000	Weak transcription	Left Ventricle	heart
48	chr1:56279800-56281000	Enhancers	Placenta Amnion	Placenta Amnion
49	chr1:56279800-56281600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr1:56279800-56282000	Weak transcription	Adipose Nuclei	Adipose

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