Variant report

Variant	nsv9003
Chromosome Location	chr1:243040557-243188422
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	chr1:243088083-243088303	K562	blood:	n/a	n/a
2	ATF1	chr1:243148543-243148578	K562	blood:	n/a	n/a
3	BACH1	chr1:243122482-243122506	K562	blood:	n/a	n/a
4	BATF	chr1:243178503-243178928	GM12878	blood:	n/a	n/a
5	BATF	chr1:243182370-243182587	GM12878	blood:	n/a	n/a
6	BATF	chr1:243178561-243178941	GM12878	blood:	n/a	n/a
7	BATF	chr1:243186946-243187196	GM12878	blood:	n/a	chr1:243187183-243187192
8	BATF	chr1:243171378-243171664	GM12878	blood:	n/a	n/a
9	BATF	chr1:243186903-243187203	GM12878	blood:	n/a	chr1:243187183-243187192
10	BATF	chr1:243174180-243174389	GM12878	blood:	n/a	n/a
11	BCL11A	chr1:243174177-243174356	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:243178625-243178904	GM12878	blood:	n/a	chr1:243178799-243178808
13	BCL11A	chr1:243169760-243169972	GM12878	blood:	n/a	n/a
14	BCL11A	chr1:243182297-243182573	GM12878	blood:	n/a	chr1:243182520-243182528 chr1:243182526-243182535
15	BCL11A	chr1:243172627-243172798	GM12878	blood:	n/a	n/a
16	BCL11A	chr1:243153505-243153675	GM12878	blood:	n/a	n/a
17	BCL11A	chr1:243178550-243178986	GM12878	blood:	n/a	chr1:243178799-243178808
18	BCL11A	chr1:243186357-243186528	GM12878	blood:	n/a	n/a
19	BCL11A	chr1:243171382-243171573	GM12878	blood:	n/a	n/a
20	BHLHE40	chr1:243087986-243088483	K562	blood:	n/a	n/a
21	BHLHE40	chr1:243186879-243187195	HepG2	liver:	n/a	n/a
22	CBX3	chr1:243100093-243100300	K562	blood:	n/a	n/a
23	CBX3	chr1:243087941-243088379	K562	blood:	n/a	n/a
24	CBX3	chr1:243053418-243053739	K562	blood:	n/a	n/a
25	CBX3	chr1:243130209-243130606	K562	blood:	n/a	n/a
26	CCNT2	chr1:243129321-243129526	K562	blood:	n/a	n/a
27	CCNT2	chr1:243087975-243088306	K562	blood:	n/a	n/a
28	CEBPB	chr1:243118288-243118578	Hela-S3	cervix:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
29	CEBPB	chr1:243072507-243072681	IMR90	lung:	n/a	chr1:243072592-243072603
30	CEBPB	chr1:243088005-243088218	K562	blood:	n/a	n/a
31	CEBPB	chr1:243118303-243118616	K562	blood:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
32	CEBPB	chr1:243072449-243072662	HepG2	liver:	n/a	chr1:243072592-243072603
33	CEBPB	chr1:243118255-243118634	K562	blood:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
34	CEBPB	chr1:243105243-243105313	A549	lung:	n/a	chr1:243105272-243105283
35	CEBPB	chr1:243148513-243148717	K562	blood:	n/a	n/a
36	CEBPB	chr1:243118344-243118540	K562	blood:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
37	CEBPB	chr1:243118268-243118571	HepG2	liver:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
38	CEBPB	chr1:243118300-243118585	A549	lung:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
39	CEBPB	chr1:243072543-243072743	K562	blood:	n/a	chr1:243072592-243072603
40	CEBPB	chr1:243105260-243105310	HepG2	liver:	n/a	chr1:243105272-243105283
41	CEBPB	chr1:243118280-243118602	IMR90	lung:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
42	CHD2	chr1:243080927-243080928	K562	blood:	n/a	n/a
43	CHD2	chr1:243087993-243088116	K562	blood:	n/a	n/a
44	CTCF	chr1:243100162-243100338	GM13977	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
45	CTCF	chr1:243166520-243166670	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr1:243140637-243140652	GM20000	blood:	n/a	n/a
47	CTCF	chr1:243100152-243100343	GM12878	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
48	CTCF	chr1:243048840-243048896	Medullo	brain:	n/a	n/a
49	CTCF	chr1:243186944-243187139	LNCaP	prostate:	n/a	n/a
50	CTCF	chr1:243166420-243166500	Hela-S3	cervix:	n/a	chr1:243166447-243166465 chr1:243166448-243166464

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:243057080-243057130	ECC-1	luminal epithelium:	n/a
2	chr1:243053934-243053984	Jurkat	blood:	n/a
3	chr1:243139525-243139575	NHDF-neo	bronchial:	n/a
4	chr1:243053673-243053723	GM06990	blood:	n/a
5	chr1:243053673-243053723	GM12892	blood:	n/a
6	chr1:243138527-243138577	HRPEpiC	eye:	n/a
7	chr1:243054071-243054121	RPTEC	kidney:	n/a
8	chr1:243050875-243050925	SK-N-SH_RA	brain:	n/a
9	chr1:243057080-243057130	SAEC	small airway:	n/a
10	chr1:243053425-243053475	IMR90	lung:	fetal
11	chr1:243138527-243138577	ProgFib	skin:	n/a
12	chr1:243053673-243053723	NHBE	bronchial:	n/a
13	chr1:243054071-243054121	Hela-S3	cervix:	n/a
14	chr1:243138527-243138577	HCM	heart:	n/a
15	chr1:243053673-243053723	GM12878	blood:	n/a
16	chr1:243139525-243139575	ProgFib	skin:	n/a
17	chr1:243057080-243057130	BJ	skin:	n/a
18	chr1:243053865-243053915	T-47D	breast:	n/a
19	chr1:243057080-243057130	RPTEC	kidney:	n/a
20	chr1:243138527-243138577	AG04450	lung:	fetal
21	chr1:243139525-243139575	K562	blood:	n/a
22	chr1:243050875-243050925	Hela-S3	cervix:	n/a
23	chr1:243053934-243053984	HepG2	liver:	n/a
24	chr1:243053865-243053915	GM06990	blood:	n/a
25	chr1:243053425-243053475	PANC-1	pancreas:	n/a
26	chr1:243053865-243053915	NH-A	brain:	n/a
27	chr1:243053865-243053915	Hepatocyte	liver:	n/a
28	chr1:243050875-243050925	HAEpiC	amniotic membrane:	n/a
29	chr1:243053934-243053984	ovcar-3	ovarian:	n/a
30	chr1:243138527-243138577	PFSK-1	brain:	n/a
31	chr1:243054071-243054121	Hepatocyte	liver:	n/a
32	chr1:243053425-243053475	HCF	heart:	n/a
33	chr1:243053425-243053475	Caco-2	colon:	n/a
34	chr1:243054071-243054121	CMK	blood:	n/a
35	chr1:243053673-243053723	ovcar-3	ovarian:	n/a
36	chr1:243054071-243054121	IMR90	lung:	fetal
37	chr1:243057080-243057130	PrEC	prostate:	n/a
38	chr1:243050875-243050925	CMK	blood:	n/a
39	chr1:243053934-243053984	T-47D	breast:	n/a
40	chr1:243053934-243053984	HEEpiC	esophagus:	n/a
41	chr1:243053865-243053915	HIPEpiC	eye:	n/a
42	chr1:243139525-243139575	HUVEC	blood vessel:	n/a
43	chr1:243057080-243057130	NHBE	bronchial:	n/a
44	chr1:243053425-243053475	PFSK-1	brain:	n/a
45	chr1:243053425-243053475	RPTEC	kidney:	n/a
46	chr1:243053425-243053475	AG09319	gingival:	n/a
47	chr1:243053865-243053915	HL-60	blood:	n/a
48	chr1:243050875-243050925	HIPEpiC	eye:	n/a
49	chr1:243057080-243057130	HL-60	blood:	n/a
50	chr1:243057080-243057130	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:242991254..242992220-chr1:243099841..243100636,3	MCF-7	breast:
2	chr1:243174257..243175773-chr22:20004723..20006804,2	K562	blood:
3	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:
4	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEP170-9	chr1:243070564-243075269	refGeneNc_994_NR_026778
2	lnc-CEP170-9	chr1:243076529-243076866	refGeneNc_994_NR_026778
3	lnc-CEP170-8	chr1:243077153-243077520	expReg_chr1_22679_-
4	lnc-CEP170-3	chr1:243169714-243169980	XLOC_001282
5	lnc-CEP170-9	chr1:243076807-243077141	expReg_chr1_22678_-
6	lnc-CEP170-3	chr1:243170676-243170770	XLOC_001282
7	lnc-CEP170-3	chr1:243169147-243169576	XLOC_001282
8	lnc-CEP170-7	chr1:243078426-243078834	expReg_chr1_22680_-

Variant related genes	Relation type
ENSG00000234116	TF binding region
ENSG00000230199	TF binding region
ENSG00000270818	TF binding region
ENSG00000264972	TF binding region
ENSG00000234116	CpG island
ENSG00000230199	CpG island
ENSG00000270818	CpG island
ENSG00000264972	CpG island
LEPREL4	miRNA target sites
LEFTY2	miRNA target sites

Extended variants
information (count: 1924 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1924 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540266824	chr1:243040584-243040585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs553475930	chr1:243040613-243040614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576559011	chr1:243040615-243040616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115457617	chr1:243040629-243040630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12097996	chr1:243040659-243040660	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs531751367	chr1:243040670-243040671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542014606	chr1:243040726-243040727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562444458	chr1:243040765-243040766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs4658370	chr1:243040780-243040781	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs185360877	chr1:243040821-243040822	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs570725377	chr1:243040829-243040830	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs542216525	chr1:243040839-243040840	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs533478776	chr1:243040860-243040861	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs188997791	chr1:243040895-243040896	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs144281822	chr1:243040905-243040906	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs538086223	chr1:243040909-243040910	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs554459686	chr1:243040916-243040917	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs180845933	chr1:243040923-243040924	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs12032023	chr1:243040970-243040971	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs76531328	chr1:243040997-243040998	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs186488559	chr1:243041025-243041026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs4658504	chr1:243041047-243041048	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs111610464	chr1:243041064-243041065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79725943	chr1:243041066-243041067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535376760	chr1:243041112-243041113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs35389501	chr1:243041115-243041116	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542443199	chr1:243041121-243041122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191328084	chr1:243041159-243041160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556173118	chr1:243041209-243041210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572720883	chr1:243041253-243041254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541325708	chr1:243041279-243041280	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564478748	chr1:243041281-243041282	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562122547	chr1:243041309-243041310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564959611	chr1:243041465-243041466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554960138	chr1:243041510-243041511	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550197752	chr1:243041545-243041546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563815739	chr1:243041596-243041597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529393374	chr1:243041646-243041647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs377024817	chr1:243041663-243041664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548395960	chr1:243041729-243041730	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182952493	chr1:243041813-243041814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185724173	chr1:243041826-243041827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12059612	chr1:243041828-243041829	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs142393529	chr1:243041931-243041932	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs190923226	chr1:243041952-243041953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575759512	chr1:243041964-243041965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535173316	chr1:243042012-243042013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115723888	chr1:243042036-243042037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534312721	chr1:243042130-243042131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183069923	chr1:243042131-243042132	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:243033200-243042200	Enhancers	Fetal Heart	heart
2	chr1:243039200-243042200	Enhancers	Left Ventricle	heart
3	chr1:243039600-243040600	Weak transcription	Right Atrium	heart
4	chr1:243040000-243041400	Enhancers	A549	lung
5	chr1:243040200-243041000	Enhancers	Pancreas	Pancrea
6	chr1:243040200-243041400	Enhancers	K562	blood
7	chr1:243040600-243041000	Enhancers	Right Atrium	heart
8	chr1:243040600-243041000	Enhancers	Right Ventricle	heart
9	chr1:243040800-243041000	Bivalent Enhancer	Hela-S3	cervix
10	chr1:243040800-243042200	Enhancers	Liver	Liver
11	chr1:243041000-243043800	Weak transcription	Right Atrium	heart
12	chr1:243041000-243046600	Weak transcription	Pancreas	Pancrea
13	chr1:243041800-243042200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr1:243042000-243042600	Enhancers	H9 Cell Line	embryonic stem cell
15	chr1:243042200-243044400	Weak transcription	Fetal Heart	heart
16	chr1:243044400-243045400	Enhancers	Fetal Heart	heart
17	chr1:243046600-243046800	Enhancers	Pancreas	Pancrea
18	chr1:243046800-243053600	Weak transcription	Pancreas	Pancrea
19	chr1:243047200-243049000	Weak transcription	A549	lung
20	chr1:243049000-243049200	Enhancers	A549	lung
21	chr1:243049200-243049800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr1:243049200-243049800	Enhancers	Liver	Liver
23	chr1:243049200-243049800	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr1:243049200-243049800	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr1:243049200-243049800	Flanking Active TSS	A549	lung
26	chr1:243049200-243049800	Enhancers	HepG2	liver
27	chr1:243049600-243049800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr1:243049800-243050600	Enhancers	A549	lung
29	chr1:243049800-243053600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr1:243049800-243053600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr1:243050600-243051800	Weak transcription	A549	lung
32	chr1:243053400-243053600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr1:243053600-243053800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr1:243053600-243054000	Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chr1:243053600-243054000	Active TSS	H1 Cell Line	embryonic stem cell
36	chr1:243053600-243054000	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr1:243053600-243054000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr1:243053600-243054000	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr1:243053600-243054000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr1:243053600-243054000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr1:243053600-243054000	Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr1:243053600-243054000	Active TSS	iPS-18 Cell Line	embryonic stem cell
43	chr1:243053600-243054000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr1:243053600-243054000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr1:243053600-243054000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
46	chr1:243053600-243054000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr1:243053600-243054000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr1:243053600-243054000	Bivalent Enhancer	Brain Hippocampus Middle	brain
49	chr1:243053600-243054000	Enhancers	Fetal Brain Male	brain
50	chr1:243053600-243054000	Bivalent/Poised TSS	Fetal Brain Female	brain

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