Variant report

Variant	nsv432531
Chromosome Location	chr1:98524979-98604179
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	chr1:98552368-98552617	HepG2	liver:	n/a	n/a
2	ATF3	chr1:98552251-98552799	A549	lung:	n/a	n/a
3	ATF3	chr1:98552230-98552787	A549	lung:	n/a	n/a
4	BCL3	chr1:98552152-98552954	A549	lung:	n/a	n/a
5	BCL3	chr1:98552221-98552738	A549	lung:	n/a	n/a
6	CBX3	chr1:98552236-98552869	HCT-116	colon:	n/a	n/a
7	CBX3	chr1:98572786-98573123	HCT-116	colon:	n/a	n/a
8	CCNT2	chr1:98549893-98550241	K562	blood:	n/a	chr1:98550128-98550148
9	CEBPB	chr1:98569910-98570263	IMR90	lung:	n/a	chr1:98570096-98570107
10	CEBPB	chr1:98533630-98534045	Hela-S3	cervix:	n/a	chr1:98533874-98533886 chr1:98533849-98533862 chr1:98533839-98533850 chr1:98533838-98533851
11	CEBPB	chr1:98533666-98534030	A549	lung:	n/a	chr1:98533874-98533886 chr1:98533849-98533862 chr1:98533839-98533850 chr1:98533838-98533851
12	CEBPB	chr1:98552284-98552667	Hela-S3	cervix:	n/a	chr1:98552649-98552661
13	CEBPB	chr1:98541116-98541340	HepG2	liver:	n/a	chr1:98541253-98541264
14	CEBPB	chr1:98533770-98533905	H1-hESC	embryonic stem cell:	n/a	chr1:98533874-98533886 chr1:98533849-98533862 chr1:98533839-98533850 chr1:98533838-98533851
15	CEBPB	chr1:98552357-98552737	A549	lung:	n/a	chr1:98552649-98552661
16	CEBPB	chr1:98536145-98536299	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr1:98569724-98570352	ECC-1	luminal epithelium:	n/a	chr1:98570096-98570107
18	CEBPB	chr1:98552244-98552727	A549	lung:	n/a	chr1:98552649-98552661
19	CEBPB	chr1:98533600-98534062	A549	lung:	n/a	chr1:98533874-98533886 chr1:98533849-98533862 chr1:98533839-98533850 chr1:98533838-98533851
20	CEBPB	chr1:98533743-98534030	ECC-1	luminal epithelium:	n/a	chr1:98533874-98533886 chr1:98533849-98533862 chr1:98533839-98533850 chr1:98533838-98533851
21	CEBPB	chr1:98552202-98552880	A549	lung:	n/a	chr1:98552649-98552661
22	CEBPB	chr1:98533660-98534033	IMR90	lung:	n/a	chr1:98533874-98533886 chr1:98533849-98533862 chr1:98533839-98533850 chr1:98533838-98533851
23	CEBPB	chr1:98552316-98552651	IMR90	lung:	n/a	n/a
24	CEBPB	chr1:98576112-98576265	A549	lung:	n/a	n/a
25	CEBPB	chr1:98544199-98544525	IMR90	lung:	n/a	n/a
26	CEBPB	chr1:98569827-98570283	Hela-S3	cervix:	n/a	chr1:98570096-98570107
27	CEBPB	chr1:98533661-98534033	HepG2	liver:	n/a	chr1:98533874-98533886 chr1:98533849-98533862 chr1:98533839-98533850 chr1:98533838-98533851
28	CEBPB	chr1:98569905-98570278	ECC-1	luminal epithelium:	n/a	chr1:98570096-98570107
29	CHD1	chr1:98552219-98553163	IMR90	lung:	n/a	n/a
30	CTCF	chr1:98569280-98569430	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr1:98569260-98569410	RPTEC	kidney:	n/a	n/a
32	CTCF	chr1:98569360-98569510	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr1:98562062-98562201	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr1:98562082-98562190	NHEK	skin:	n/a	n/a
35	CTCF	chr1:98569280-98569430	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr1:98576350-98576467	NHEK	skin:	n/a	chr1:98576409-98576422
37	CTCF	chr1:98576355-98576432	Fibrobl	skin:	n/a	chr1:98576409-98576422
38	CTCF	chr1:98569300-98569450	HMF	breast:	n/a	n/a
39	CTCF	chr1:98562042-98562220	Gliobla	brain:	n/a	n/a
40	CTCF	chr1:98569360-98569510	RPTEC	kidney:	n/a	n/a
41	CTCF	chr1:98556800-98556950	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr1:98576296-98576503	Gliobla	brain:	n/a	chr1:98576409-98576422
43	CTCF	chr1:98562058-98562187	ProgFib	skin:	n/a	n/a
44	CTCF	chr1:98569314-98569447	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr1:98559400-98559550	GM12869	blood:	n/a	n/a
46	CTCF	chr1:98569260-98569410	AG09319	gingival:	n/a	n/a
47	CTCF	chr1:98569300-98569450	BE2_C	brain:	n/a	n/a
48	CTCF	chr1:98576344-98576480	ProgFib	skin:	n/a	chr1:98576409-98576422
49	CTCF	chr1:98590635-98590710	GM13976	blood:	n/a	n/a
50	CTCF	chr1:98569360-98569510	AG09309	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:98550994-98551044	SK-N-SH	brain:	n/a
2	chr1:98550994-98551044	SK-N-SH	brain:	n/a
3	chr1:98550994-98551044	HCM	heart:	n/a
4	chr1:98569645-98569695	LNCaP	prostate:	n/a
5	chr1:98569645-98569695	HMEC	breast:	n/a
6	chr1:98550994-98551044	AG04449	skin:	fetal
7	chr1:98550994-98551044	NHDF-neo	bronchial:	n/a
8	chr1:98550994-98551044	AG09309	skin:	n/a
9	chr1:98550994-98551044	GM12878	blood:	n/a
10	chr1:98569645-98569695	HPAEpiC	pulmonary alveolar:	n/a
11	chr1:98550994-98551044	A549	lung:	n/a
12	chr1:98550994-98551044	AG10803	skin:	n/a
13	chr1:98569645-98569695	HAEpiC	amniotic membrane:	n/a
14	chr1:98550994-98551044	MCF-7	breast:	n/a
15	chr1:98550994-98551044	Caco-2	colon:	n/a
16	chr1:98569645-98569695	HEEpiC	esophagus:	n/a
17	chr1:98569645-98569695	GM19239	blood:	n/a
18	chr1:98550994-98551044	HAEpiC	amniotic membrane:	n/a
19	chr1:98569645-98569695	HEK293	kidney:	embryo
20	chr1:98550994-98551044	HEK293	kidney:	embryo
21	chr1:98569645-98569695	AG04450	lung:	fetal
22	chr1:98569645-98569695	HCPEpiC	choroid plexus:	n/a
23	chr1:98569645-98569695	PFSK-1	brain:	n/a
24	chr1:98550994-98551044	RPTEC	kidney:	n/a
25	chr1:98569645-98569695	PANC-1	pancreas:	n/a
26	chr1:98569645-98569695	AG10803	skin:	n/a
27	chr1:98569645-98569695	AG09319	gingival:	n/a
28	chr1:98569645-98569695	HCF	heart:	n/a
29	chr1:98569645-98569695	A549	lung:	n/a
30	chr1:98569645-98569695	SK-N-MC	brain:	n/a
31	chr1:98550994-98551044	NT2-D1	testis:	n/a
32	chr1:98569645-98569695	SK-N-SH_RA	brain:	n/a
33	chr1:98550994-98551044	U87	brain:	n/a
34	chr1:98569645-98569695	SK-N-SH	brain:	n/a
35	chr1:98569645-98569695	HUVEC	blood vessel:	n/a
36	chr1:98550994-98551044	ECC-1	luminal epithelium:	n/a
37	chr1:98569645-98569695	HIPEpiC	eye:	n/a
38	chr1:98550994-98551044	AG04450	lung:	fetal
39	chr1:98569645-98569695	NT2-D1	testis:	n/a
40	chr1:98569645-98569695	H1-hESC	embryonic stem cell:	embryo
41	chr1:98550994-98551044	BE2_C	brain:	n/a
42	chr1:98550994-98551044	HPAEpiC	pulmonary alveolar:	n/a
43	chr1:98569645-98569695	NHBE	bronchial:	n/a
44	chr1:98569645-98569695	GM06990	blood:	n/a
45	chr1:98550994-98551044	PrEC	prostate:	n/a
46	chr1:98569645-98569695	HRPEpiC	eye:	n/a
47	chr1:98569645-98569695	CMK	blood:	n/a
48	chr1:98550994-98551044	HCPEpiC	choroid plexus:	n/a
49	chr1:98550994-98551044	HCT-116	colon:	n/a
50	chr1:98550994-98551044	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:98569136..98572043-chr1:98573208..98575634,2	K562	blood:
2	chr1:98543496..98545967-chr1:98546001..98547800,2	MCF-7	breast:
3	chr1:98515802..98518516-chr1:98526110..98527932,2	MCF-7	breast:
4	chr1:98569136..98572043-chr1:98573208..98575634,2	K562	blood:
5	chr1:98543496..98545967-chr1:98546001..98547800,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNX7-5	chr1:98596254-98596350	NONHSAT004742
2	lnc-SNX7-6	chr1:98542556-98543024	NONHSAT004741
3	lnc-SNX7-5	chr1:98552543-98553146	NONHSAT004742
4	lnc-SNX7-5	chr1:98596970-98597419	NONHSAT004742

Variant related genes	Relation type
NFU1P2	TF binding region
NFU1P2	CpG island

Extended variants
information (count: 2779 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:2779 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75269296	chr1:98525009-98525010	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs574431956	chr1:98525108-98525109	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192015547	chr1:98525109-98525110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs1782818	chr1:98525221-98525222	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs532184280	chr1:98525270-98525271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184140114	chr1:98525368-98525369	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532328068	chr1:98525370-98525371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559650247	chr1:98525375-98525376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562408407	chr1:98525405-98525406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs527706887	chr1:98525459-98525460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554288454	chr1:98525495-98525496	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144601766	chr1:98525521-98525522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148282917	chr1:98525547-98525548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530769636	chr1:98525552-98525553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549985327	chr1:98525555-98525556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570264857	chr1:98525581-98525582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141335206	chr1:98525606-98525607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs72735986	chr1:98525641-98525642	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs544846751	chr1:98525673-98525674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565985535	chr1:98525681-98525682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534325118	chr1:98525686-98525687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189567376	chr1:98525718-98525719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs115670170	chr1:98525765-98525766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574346770	chr1:98525771-98525772	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181107750	chr1:98525774-98525775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs150779839	chr1:98525784-98525785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577125354	chr1:98525797-98525798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564553829	chr1:98525806-98525807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545991009	chr1:98525818-98525819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559696844	chr1:98525843-98525844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528438623	chr1:98525908-98525909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542144509	chr1:98525926-98525927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs184390449	chr1:98525987-98525988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78576334	chr1:98526015-98526016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550264659	chr1:98526018-98526019	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570025117	chr1:98526118-98526119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532571425	chr1:98526124-98526125	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1702291	chr1:98526167-98526168	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs189324013	chr1:98526193-98526194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535032109	chr1:98526212-98526213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566808494	chr1:98526354-98526355	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139159708	chr1:98526364-98526365	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs374485146	chr1:98526384-98526385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs143595548	chr1:98526422-98526423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529313254	chr1:98526438-98526439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566347871	chr1:98526444-98526445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536606944	chr1:98526453-98526454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557039178	chr1:98526456-98526457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576964280	chr1:98526457-98526458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs114927657	chr1:98526481-98526482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
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
Papillary thyroid carcinoma	21436994	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
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
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Gastric cancer	16891809	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:98520400-98530000	Weak transcription	NHDF-Ad	bronchial
2	chr1:98520800-98525000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr1:98521400-98525200	Weak transcription	HUVEC	blood vessel
4	chr1:98522600-98526000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr1:98523000-98526000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr1:98524400-98525000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr1:98524400-98525200	Enhancers	A549	lung
8	chr1:98524400-98525600	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr1:98524400-98526000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr1:98524600-98525600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr1:98524800-98525200	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr1:98524800-98525800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:98525000-98526000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr1:98525200-98525600	Enhancers	HUVEC	blood vessel
15	chr1:98525200-98526400	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr1:98525200-98526800	Weak transcription	A549	lung
17	chr1:98525600-98537400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr1:98526000-98526200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr1:98527800-98544200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr1:98529600-98532400	Weak transcription	A549	lung
21	chr1:98530000-98530400	Enhancers	NHDF-Ad	bronchial
22	chr1:98530400-98533600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr1:98530400-98542600	Weak transcription	NHDF-Ad	bronchial
24	chr1:98532200-98532600	Enhancers	Dnd41	blood
25	chr1:98532200-98532800	Enhancers	Muscle Satellite Cultured Cells	--
26	chr1:98532200-98532800	Enhancers	HUVEC	blood vessel
27	chr1:98532400-98532600	Enhancers	A549	lung
28	chr1:98532600-98539600	Weak transcription	A549	lung
29	chr1:98532800-98533800	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr1:98532800-98537400	Weak transcription	HUVEC	blood vessel
31	chr1:98533000-98533600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr1:98533600-98533800	Enhancers	H9 Cell Line	embryonic stem cell
33	chr1:98533600-98533800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr1:98533600-98533800	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr1:98533600-98534000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr1:98533600-98534000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:98533600-98534000	Enhancers	Hela-S3	cervix
38	chr1:98533800-98534000	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr1:98533800-98534000	Enhancers	Muscle Satellite Cultured Cells	--
40	chr1:98533800-98535000	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr1:98533800-98535200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr1:98534000-98535000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr1:98534800-98535000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr1:98534800-98535400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr1:98534800-98535800	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr1:98535000-98535800	Enhancers	H9 Cell Line	embryonic stem cell
47	chr1:98535000-98535800	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr1:98535000-98535800	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr1:98535000-98536200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr1:98535000-98540200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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