Variant report

Variant	nsv870654
Chromosome Location	chr1:74762198-74858724
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:243)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:243 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:74822262-74822579	HepG2	liver:	n/a	n/a
2	BCL3	chr1:74822171-74822614	A549	lung:	n/a	n/a
3	CEBPB	chr1:74783464-74783590	HepG2	liver:	n/a	n/a
4	CEBPB	chr1:74771504-74771688	HepG2	liver:	n/a	chr1:74771612-74771623
5	CEBPB	chr1:74822142-74822758	IMR90	lung:	n/a	chr1:74822623-74822634
6	CEBPB	chr1:74808826-74809251	IMR90	lung:	n/a	chr1:74808957-74808968
7	CEBPB	chr1:74822165-74822718	A549	lung:	n/a	chr1:74822623-74822634
8	CEBPB	chr1:74808794-74809117	H1-hESC	embryonic stem cell:	n/a	chr1:74808957-74808968
9	CEBPB	chr1:74764987-74765324	HepG2	liver:	n/a	chr1:74765155-74765166 chr1:74765142-74765150
10	CEBPB	chr1:74764993-74765325	A549	lung:	n/a	chr1:74765155-74765166 chr1:74765142-74765150
11	CEBPB	chr1:74783362-74783693	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:74780146-74780463	IMR90	lung:	n/a	n/a
13	CEBPB	chr1:74768320-74768669	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr1:74822239-74822574	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:74777395-74777659	HepG2	liver:	n/a	chr1:74777540-74777553 chr1:74777541-74777552
16	CEBPB	chr1:74780245-74780491	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr1:74808794-74809122	HepG2	liver:	n/a	chr1:74808957-74808968
18	CEBPB	chr1:74832214-74832457	HepG2	liver:	n/a	n/a
19	CEBPZ	chr1:74790846-74791124	HepG2	liver:	n/a	n/a
20	CTCF	chr1:74779180-74779330	HAc	cerebellar:	n/a	n/a
21	CTCF	chr1:74817580-74817676	LNCaP	prostate:	n/a	n/a
22	CTCF	chr1:74807840-74807990	GM12868	blood:	n/a	n/a
23	CTCF	chr1:74790800-74790950	HepG2	liver:	n/a	n/a
24	CTCF	chr1:74802103-74802213	Pancreas_OC	pancreas:	n/a	n/a
25	E2F4	chr1:74835256-74835287	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr1:74776700-74776900	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr1:74791612-74791689	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F6	chr1:74781759-74782401	H1-hESC	embryonic stem cell:	n/a	n/a
29	E2F6	chr1:74782034-74782339	H1-hESC	embryonic stem cell:	n/a	n/a
30	EBF1	chr1:74827331-74827339	GM12878	blood:	n/a	n/a
31	EBF1	chr1:74762695-74763155	GM12878	blood:	n/a	chr1:74763014-74763025
32	ELK1	chr1:74801052-74801061	Hela-S3	cervix:	n/a	n/a
33	EP300	chr1:74811735-74812661	SK-N-SH	brain:	n/a	chr1:74812280-74812290
34	EP300	chr1:74808963-74809348	SK-N-SH_RA	brain:	n/a	n/a
35	EP300	chr1:74807269-74810744	SK-N-SH	brain:	n/a	chr1:74809475-74809489 chr1:74809488-74809502 chr1:74809483-74809497 chr1:74808954-74808968
36	EP300	chr1:74822188-74822505	HepG2	liver:	n/a	n/a
37	EP300	chr1:74821969-74822688	A549	lung:	n/a	n/a
38	EP300	chr1:74810115-74810398	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr1:74828474-74829662	SK-N-SH	brain:	n/a	chr1:74829454-74829468 chr1:74828543-74828557 chr1:74828544-74828553
40	EP300	chr1:74841097-74841384	SK-N-SH_RA	brain:	n/a	n/a
41	EP300	chr1:74858490-74858937	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr1:74822063-74822590	HepG2	liver:	n/a	n/a
43	EP300	chr1:74828898-74829216	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr1:74858553-74858926	SK-N-SH_RA	brain:	n/a	n/a
45	EP300	chr1:74857685-74859182	SK-N-SH	brain:	n/a	chr1:74859055-74859069 chr1:74858333-74858342
46	EP300	chr1:74808885-74809399	SK-N-SH_RA	brain:	n/a	chr1:74808954-74808968
47	EP300	chr1:74821973-74822769	A549	lung:	n/a	n/a
48	EP300	chr1:74828892-74829216	SK-N-SH_RA	brain:	n/a	n/a
49	FOS	chr1:74834064-74834331	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr1:74783403-74783707	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:74832752-74832802	U87	brain:	n/a
2	chr1:74832752-74832802	NT2-D1	testis:	n/a
3	chr1:74832752-74832802	GM12891	blood:	n/a
4	chr1:74832752-74832802	HIPEpiC	eye:	n/a
5	chr1:74832752-74832802	IMR90	lung:	fetal
6	chr1:74832752-74832802	SK-N-MC	brain:	n/a
7	chr1:74832752-74832802	GM12892	blood:	n/a
8	chr1:74832752-74832802	HRCEpiC	kidney:	n/a
9	chr1:74832752-74832802	HNPCEpiC	eye:	n/a
10	chr1:74832752-74832802	NHDF-neo	bronchial:	n/a
11	chr1:74832752-74832802	AG10803	skin:	n/a
12	chr1:74832752-74832802	AoSMC	blood vessel:	n/a
13	chr1:74832752-74832802	PFSK-1	brain:	n/a
14	chr1:74832752-74832802	HPAEpiC	pulmonary alveolar:	n/a
15	chr1:74832752-74832802	MCF-7	breast:	n/a
16	chr1:74832752-74832802	CMK	blood:	n/a
17	chr1:74832752-74832802	SAEC	small airway:	n/a
18	chr1:74832752-74832802	RPTEC	kidney:	n/a
19	chr1:74832752-74832802	GM06990	blood:	n/a
20	chr1:74832752-74832802	A549	lung:	n/a
21	chr1:74832752-74832802	AG04450	lung:	fetal
22	chr1:74832752-74832802	PrEC	prostate:	n/a
23	chr1:74832752-74832802	Hepatocyte	liver:	n/a
24	chr1:74832752-74832802	HEK293	kidney:	embryo
25	chr1:74832752-74832802	BE2_C	brain:	n/a
26	chr1:74832752-74832802	AG09319	gingival:	n/a
27	chr1:74832752-74832802	HEEpiC	esophagus:	n/a
28	chr1:74832752-74832802	AG09309	skin:	n/a
29	chr1:74832752-74832802	Jurkat	blood:	n/a
30	chr1:74832752-74832802	HCM	heart:	n/a
31	chr1:74832752-74832802	HCF	heart:	n/a
32	chr1:74832752-74832802	MCF10A-Er-Src	breast:	n/a
33	chr1:74832752-74832802	HepG2	liver:	n/a
34	chr1:74832752-74832802	K562	blood:	n/a
35	chr1:74832752-74832802	HUVEC	blood vessel:	n/a
36	chr1:74832752-74832802	GM19239	blood:	n/a
37	chr1:74832752-74832802	HRE	kidney:	n/a
38	chr1:74832752-74832802	SKMC	muscle:	n/a
39	chr1:74832752-74832802	HAEpiC	amniotic membrane:	n/a
40	chr1:74832752-74832802	T-47D	breast:	n/a
41	chr1:74832752-74832802	BJ	skin:	n/a
42	chr1:74832752-74832802	Caco-2	colon:	n/a
43	chr1:74832752-74832802	SK-N-SH	brain:	n/a
44	chr1:74832752-74832802	AG04449	skin:	fetal
45	chr1:74832752-74832802	ovcar-3	ovarian:	n/a
46	chr1:74832752-74832802	HCT-116	colon:	n/a
47	chr1:74832752-74832802	HL-60	blood:	n/a
48	chr1:74832752-74832802	PANC-1	pancreas:	n/a
49	chr1:74832752-74832802	SK-N-SH_RA	brain:	n/a
50	chr1:74832752-74832802	LNCaP	prostate:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:74835693..74838448-chr1:74838770..74840805,3	K562	blood:
2	chr1:74847175..74848707-chr1:74848769..74850609,2	MCF-7	breast:
3	chr1:74835693..74838448-chr1:74838770..74840795,2	K562	blood:
4	chr1:74701198..74703916-chr1:74780316..74782785,2	K562	blood:
5	chr1:74847175..74848707-chr1:74848769..74850609,2	MCF-7	breast:
6	chr1:74799781..74801961-chr1:74805527..74808251,2	MCF-7	breast:
7	chr1:74789903..74792042-chr1:74796412..74799113,2	MCF-7	breast:
8	chr1:74789903..74792042-chr1:74796412..74799113,2	MCF-7	breast:
9	chr1:74641537..74643099-chr1:74809509..74811733,2	K562	blood:
10	chr1:74835693..74838448-chr1:74838770..74840795,2	K562	blood:
11	chr1:74622416..74625063-chr1:74764779..74767346,2	K562	blood:
12	chr1:74835693..74838448-chr1:74838770..74840805,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC53-1	chr1:74844380-74844486	ENSG00000237324.2
2	lnc-FPGT-7	chr1:74815702-74815781	ucscGeneNc_uc001dgh_2
3	lnc-LRRC53-1	chr1:74832267-74832410	ENSG00000237324.2
4	lnc-LRRC53-1	chr1:74807263-74807671	ENSG00000237324.2
5	lnc-FPGT-7	chr1:74853478-74853568	ucscGeneNc_uc001dgh_2
6	lnc-LRRC53-1	chr1:74834673-74834803	ENSG00000237324.2

No data

Variant related genes	Relation type
TNNI3K	TF binding region
ENSG00000237324	TF binding region
TNNI3K	CpG island
ENSG00000237324	CpG island
ENSG00000116783	chromatin interactions

Extended variants
information (count: 3553 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:3553 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6684409	chr1:74762198-74762199	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs186484764	chr1:74762201-74762202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555834660	chr1:74762214-74762215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143766376	chr1:74762340-74762341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs578042899	chr1:74762355-74762356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191029176	chr1:74762431-74762432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182739610	chr1:74762483-74762484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs75181773	chr1:74762524-74762525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542880847	chr1:74762533-74762534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs79404037	chr1:74762546-74762547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186657854	chr1:74762551-74762552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs151309910	chr1:74762561-74762562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565376224	chr1:74762594-74762595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192373094	chr1:74762642-74762643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551504003	chr1:74762717-74762718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563245748	chr1:74762730-74762731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553032227	chr1:74762812-74762813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs57828371	chr1:74762852-74762853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183286338	chr1:74762996-74762997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534652200	chr1:74763014-74763015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12060389	chr1:74763034-74763035	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs187308627	chr1:74763056-74763057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538721385	chr1:74763117-74763118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557053129	chr1:74763175-74763176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575370132	chr1:74763183-74763184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs77912894	chr1:74763206-74763207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs61776174	chr1:74763207-74763208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs139218783	chr1:74763208-74763209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192956177	chr1:74763233-74763234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10670747	chr1:74763238-74763239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs61776175	chr1:74763239-74763240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs77746395	chr1:74763242-74763243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76469409	chr1:74763252-74763253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536225191	chr1:74763259-74763260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200474395	chr1:74763269-74763270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554710563	chr1:74763286-74763287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541659123	chr1:74763344-74763345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573471171	chr1:74763345-74763346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540552685	chr1:74763346-74763347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540577520	chr1:74763352-74763353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369707696	chr1:74763382-74763383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565427681	chr1:74763441-74763442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs115944098	chr1:74763484-74763485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545089879	chr1:74763537-74763538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555254477	chr1:74763582-74763583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563355880	chr1:74763583-74763584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543669637	chr1:74763676-74763677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184867840	chr1:74763679-74763680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376704838	chr1:74763759-74763760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548990884	chr1:74763771-74763772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
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
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
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
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:330 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:74748000-74769200	Weak transcription	Fetal Heart	heart
2	chr1:74764000-74771000	Weak transcription	Left Ventricle	heart
3	chr1:74766000-74771000	Weak transcription	Brain Hippocampus Middle	brain
4	chr1:74768000-74768800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr1:74768000-74769200	Weak transcription	Adipose Nuclei	Adipose
6	chr1:74768200-74768600	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr1:74769200-74769400	ZNF genes & repeats	Adipose Nuclei	Adipose
8	chr1:74769200-74773200	Strong transcription	Fetal Heart	heart
9	chr1:74769400-74771000	Weak transcription	Adipose Nuclei	Adipose
10	chr1:74769400-74772000	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr1:74771000-74771400	Enhancers	Adipose Nuclei	Adipose
12	chr1:74771000-74771400	Enhancers	Left Ventricle	heart
13	chr1:74771400-74778600	Weak transcription	Left Ventricle	heart
14	chr1:74773200-74776800	Weak transcription	Fetal Heart	heart
15	chr1:74776800-74779400	Enhancers	Fetal Heart	heart
16	chr1:74777200-74777600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr1:74777600-74781800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr1:74778600-74779400	Enhancers	Left Ventricle	heart
19	chr1:74778600-74779400	Enhancers	Right Atrium	heart
20	chr1:74778800-74779200	Enhancers	Brain Germinal Matrix	brain
21	chr1:74779400-74781400	Weak transcription	Fetal Heart	heart
22	chr1:74779400-74784800	Weak transcription	Left Ventricle	heart
23	chr1:74779400-74784800	Weak transcription	Right Atrium	heart
24	chr1:74781400-74781600	Enhancers	Fetal Heart	heart
25	chr1:74781400-74783000	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr1:74781600-74782000	Weak transcription	Fetal Heart	heart
27	chr1:74781800-74782200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:74781800-74782200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr1:74781800-74782200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr1:74781800-74782200	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr1:74781800-74782200	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr1:74781800-74782400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr1:74782000-74782200	Enhancers	Fetal Heart	heart
34	chr1:74782200-74784400	Weak transcription	Fetal Heart	heart
35	chr1:74782200-74786400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr1:74782400-74786600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr1:74784400-74786800	Enhancers	Fetal Heart	heart
38	chr1:74784800-74785000	ZNF genes & repeats	Aorta	Aorta
39	chr1:74784800-74785000	Enhancers	Left Ventricle	heart
40	chr1:74784800-74785000	Enhancers	Right Atrium	heart
41	chr1:74785000-74785400	Weak transcription	Left Ventricle	heart
42	chr1:74785000-74789200	Weak transcription	Aorta	Aorta
43	chr1:74785400-74785600	Genic enhancers	Left Ventricle	heart
44	chr1:74785600-74808800	Weak transcription	Left Ventricle	heart
45	chr1:74786400-74787200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr1:74786600-74787000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr1:74786800-74787200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr1:74786800-74787200	Weak transcription	Fetal Heart	heart
49	chr1:74787200-74789000	Enhancers	Fetal Heart	heart
50	chr1:74787200-74790600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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