Variant report

Variant	nsv1221
Chromosome Location	chr1:67047908-67092696
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	chr1:67058001-67058099	HepG2	liver:	n/a	n/a
2	CEBPB	chr1:67048835-67048953	K562	blood:	n/a	chr1:67048900-67048917 chr1:67048901-67048912 chr1:67048902-67048913 chr1:67048901-67048914 chr1:67048901-67048914
3	CEBPB	chr1:67064396-67064738	IMR90	lung:	n/a	n/a
4	CEBPB	chr1:67053250-67053363	K562	blood:	n/a	chr1:67053287-67053298
5	CEBPB	chr1:67071320-67071648	HepG2	liver:	n/a	chr1:67071470-67071483 chr1:67071470-67071481
6	CEBPB	chr1:67048827-67049057	HepG2	liver:	n/a	chr1:67048900-67048917 chr1:67048901-67048912 chr1:67048902-67048913 chr1:67048901-67048914 chr1:67048901-67048914
7	CEBPB	chr1:67071282-67071655	IMR90	lung:	n/a	chr1:67071470-67071483 chr1:67071470-67071481
8	CEBPB	chr1:67076531-67076739	IMR90	lung:	n/a	n/a
9	CEBPB	chr1:67071371-67071610	H1-hESC	embryonic stem cell:	n/a	chr1:67071470-67071483 chr1:67071470-67071481
10	CEBPB	chr1:67084002-67084488	IMR90	lung:	n/a	n/a
11	CEBPB	chr1:67053147-67053405	IMR90	lung:	n/a	chr1:67053287-67053298
12	CEBPB	chr1:67060800-67061067	IMR90	lung:	n/a	chr1:67060851-67060859 chr1:67060921-67060934
13	CEBPB	chr1:67060819-67061021	HepG2	liver:	n/a	chr1:67060851-67060859 chr1:67060921-67060934
14	CEBPB	chr1:67071322-67071550	K562	blood:	n/a	chr1:67071470-67071483 chr1:67071470-67071481
15	CEBPB	chr1:67053159-67053435	HepG2	liver:	n/a	chr1:67053287-67053298
16	CEBPB	chr1:67048720-67049090	IMR90	lung:	n/a	chr1:67048900-67048917 chr1:67048901-67048912 chr1:67048902-67048913 chr1:67048901-67048914 chr1:67048901-67048914
17	CEBPB	chr1:67071305-67071646	K562	blood:	n/a	chr1:67071470-67071483 chr1:67071470-67071481
18	CEBPB	chr1:67064427-67064710	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:67071306-67071664	A549	lung:	n/a	chr1:67071470-67071483 chr1:67071470-67071481
20	CEBPB	chr1:67078905-67079239	IMR90	lung:	n/a	n/a
21	CTCF	chr1:67073320-67073470	GM12865	blood:	n/a	chr1:67073355-67073376 chr1:67073353-67073371 chr1:67073356-67073365
22	CTCF	chr1:67052140-67052290	HCFaa	heart:	n/a	n/a
23	CTCF	chr1:67073180-67073492	H1-hESC	embryonic stem cell:	n/a	chr1:67073355-67073376 chr1:67073353-67073371 chr1:67073356-67073365
24	CTCF	chr1:67079000-67079150	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr1:67086173-67086198	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr1:67073188-67073520	GM12878	blood:	n/a	chr1:67073355-67073376 chr1:67073353-67073371 chr1:67073356-67073365
27	CTCF	chr1:67073240-67073390	SAEC	small airway:	n/a	chr1:67073355-67073376 chr1:67073353-67073371 chr1:67073356-67073365
28	CTCF	chr1:67073216-67073513	K562	blood:	n/a	chr1:67073355-67073376 chr1:67073353-67073371 chr1:67073356-67073365
29	CTCF	chr1:67073260-67073410	GM12865	blood:	n/a	chr1:67073355-67073376 chr1:67073353-67073371 chr1:67073356-67073365
30	CTCF	chr1:67073240-67073390	GM12872	blood:	n/a	chr1:67073355-67073376 chr1:67073353-67073371 chr1:67073356-67073365
31	CTCF	chr1:67073200-67073350	A549	lung:	n/a	n/a
32	CTCF	chr1:67073280-67073430	HCPEpiC	choroid plexus:	n/a	chr1:67073355-67073376 chr1:67073353-67073371 chr1:67073356-67073365
33	CTCF	chr1:67073080-67073230	NHDF-neo	bronchial:	n/a	n/a
34	CTCF	chr1:67073240-67073390	AG04450	lung:	n/a	chr1:67073355-67073376 chr1:67073353-67073371 chr1:67073356-67073365
35	CTCF	chr1:67073298-67073419	HepG2	liver:	n/a	chr1:67073355-67073376 chr1:67073353-67073371 chr1:67073356-67073365
36	CTCF	chr1:67089720-67089870	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr1:67073220-67073370	AoAF	blood vessel:	n/a	chr1:67073356-67073365
38	CTCF	chr1:67073260-67073410	GM12868	blood:	n/a	chr1:67073355-67073376 chr1:67073353-67073371 chr1:67073356-67073365
39	CTCF	chr1:67073260-67073410	Caco-2	colon:	n/a	chr1:67073355-67073376 chr1:67073353-67073371 chr1:67073356-67073365
40	CTCF	chr1:67073341-67073386	LNCaP	prostate:	n/a	chr1:67073355-67073376 chr1:67073353-67073371 chr1:67073356-67073365
41	CTCF	chr1:67077820-67077970	GM12872	blood:	n/a	n/a
42	CTCF	chr1:67073288-67073430	Gliobla	brain:	n/a	chr1:67073355-67073376 chr1:67073353-67073371 chr1:67073356-67073365
43	CTCF	chr1:67073280-67073430	GM12867	blood:	n/a	chr1:67073355-67073376 chr1:67073353-67073371 chr1:67073356-67073365
44	CTCF	chr1:67073300-67073450	HFF	foreskin:	n/a	chr1:67073355-67073376 chr1:67073353-67073371 chr1:67073356-67073365
45	CTCF	chr1:67073240-67073390	HMEC	breast:	n/a	chr1:67073355-67073376 chr1:67073353-67073371 chr1:67073356-67073365
46	CTCF	chr1:67073240-67073390	GM12871	blood:	n/a	chr1:67073355-67073376 chr1:67073353-67073371 chr1:67073356-67073365
47	CTCF	chr1:67073300-67073450	BE2_C	brain:	n/a	chr1:67073355-67073376 chr1:67073353-67073371 chr1:67073356-67073365
48	CTCF	chr1:67073260-67073410	HCFaa	heart:	n/a	chr1:67073355-67073376 chr1:67073353-67073371 chr1:67073356-67073365
49	CTCF	chr1:67073220-67073370	HBMEC	blood vessel:	n/a	chr1:67073356-67073365
50	CTCF	chr1:67073200-67073350	HFF-Myc	foreskin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:67084672-67084722	AoSMC	blood vessel:	n/a
2	chr1:67084672-67084722	AoSMC	blood vessel:	n/a
3	chr1:67064359-67064409	Caco-2	colon:	n/a
4	chr1:67064359-67064409	Hepatocyte	liver:	n/a
5	chr1:67072952-67073002	GM06990	blood:	n/a
6	chr1:67064359-67064409	HNPCEpiC	eye:	n/a
7	chr1:67072952-67073002	PFSK-1	brain:	n/a
8	chr1:67084672-67084722	SK-N-SH_RA	brain:	n/a
9	chr1:67072952-67073002	PANC-1	pancreas:	n/a
10	chr1:67072952-67073002	BJ	skin:	n/a
11	chr1:67084672-67084722	HRE	kidney:	n/a
12	chr1:67064359-67064409	U87	brain:	n/a
13	chr1:67072952-67073002	HL-60	blood:	n/a
14	chr1:67072952-67073002	RPTEC	kidney:	n/a
15	chr1:67064359-67064409	HCM	heart:	n/a
16	chr1:67064359-67064409	SK-N-SH	brain:	n/a
17	chr1:67072952-67073002	AG04450	lung:	fetal
18	chr1:67072952-67073002	NT2-D1	testis:	n/a
19	chr1:67072952-67073002	LNCaP	prostate:	n/a
20	chr1:67064359-67064409	MCF10A-Er-Src	breast:	n/a
21	chr1:67064359-67064409	BE2_C	brain:	n/a
22	chr1:67084672-67084722	NB4	blood:	n/a
23	chr1:67084672-67084722	GM12892	blood:	n/a
24	chr1:67064359-67064409	PrEC	prostate:	n/a
25	chr1:67064359-67064409	GM06990	blood:	n/a
26	chr1:67072952-67073002	Jurkat	blood:	n/a
27	chr1:67072952-67073002	AG09309	skin:	n/a
28	chr1:67084672-67084722	ovcar-3	ovarian:	n/a
29	chr1:67084672-67084722	HCPEpiC	choroid plexus:	n/a
30	chr1:67064359-67064409	SK-N-SH_RA	brain:	n/a
31	chr1:67072952-67073002	HCF	heart:	n/a
32	chr1:67072952-67073002	Hepatocyte	liver:	n/a
33	chr1:67084672-67084722	PANC-1	pancreas:	n/a
34	chr1:67084672-67084722	HepG2	liver:	n/a
35	chr1:67072952-67073002	ECC-1	luminal epithelium:	n/a
36	chr1:67072952-67073002	PrEC	prostate:	n/a
37	chr1:67084672-67084722	HCT-116	colon:	n/a
38	chr1:67084672-67084722	AG09309	skin:	n/a
39	chr1:67084672-67084722	BJ	skin:	n/a
40	chr1:67084672-67084722	RPTEC	kidney:	n/a
41	chr1:67064359-67064409	ProgFib	skin:	n/a
42	chr1:67064359-67064409	RPTEC	kidney:	n/a
43	chr1:67084672-67084722	HIPEpiC	eye:	n/a
44	chr1:67064359-67064409	AoSMC	blood vessel:	n/a
45	chr1:67072952-67073002	AG10803	skin:	n/a
46	chr1:67072952-67073002	IMR90	lung:	fetal
47	chr1:67064359-67064409	GM12878	blood:	n/a
48	chr1:67064359-67064409	NB4	blood:	n/a
49	chr1:67064359-67064409	HRCEpiC	kidney:	n/a
50	chr1:67072952-67073002	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:67048310..67050858-chr1:67148438..67150245,2	K562	blood:
2	chr1:67064848..67066944-chr1:67071232..67073081,2	K562	blood:
3	chr1:67088339..67090517-chr1:67091923..67094068,2	K562	blood:
4	chr1:67072874..67073739-chr1:67191676..67192371,2	K562	blood:
5	chr1:67064848..67066944-chr1:67071232..67073081,2	K562	blood:
6	chr1:67047745..67048246-chr6:116563756..116564256,2	NB4	blood:
7	chr1:67088339..67090517-chr1:67091923..67094068,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TCTEX1D1-5	chr1:67091530-67091743	NONHSAT003757

Variant related genes	Relation type
SGIP1	TF binding region
MIR3117	TF binding region
SGIP1	CpG island
MIR3117	CpG island

Extended variants
information (count: 1731 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1731 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149951228	chr1:67047946-67047947	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs527539982	chr1:67047950-67047951	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs10128053	chr1:67047957-67047958	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs145124896	chr1:67047990-67047991	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs549845672	chr1:67047995-67047996	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185104231	chr1:67048025-67048026	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs190002060	chr1:67048026-67048027	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552707626	chr1:67048131-67048132	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566153853	chr1:67048137-67048138	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535290478	chr1:67048188-67048189	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs117082924	chr1:67048208-67048209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs142322920	chr1:67048220-67048221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs34654467	chr1:67048223-67048224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs536288775	chr1:67048246-67048247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs111878557	chr1:67048269-67048270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546061401	chr1:67048354-67048355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181264547	chr1:67048368-67048369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs11208911	chr1:67048489-67048490	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs200322294	chr1:67048490-67048491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs12027701	chr1:67048496-67048497	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs11208912	chr1:67048499-67048500	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs540915885	chr1:67048503-67048504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535121389	chr1:67048519-67048520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs72676184	chr1:67048562-67048563	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs534764123	chr1:67048576-67048577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs553095802	chr1:67048623-67048624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530012243	chr1:67048706-67048707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs4147266	chr1:67048743-67048744	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs369681852	chr1:67048759-67048760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535411417	chr1:67048809-67048810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563551567	chr1:67048824-67048825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146372390	chr1:67048839-67048840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532600447	chr1:67048856-67048857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111696510	chr1:67048875-67048876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557306215	chr1:67048909-67048910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11208913	chr1:67048924-67048925	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs12066541	chr1:67048928-67048929	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs12072937	chr1:67048995-67048996	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs186295816	chr1:67049008-67049009	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188312879	chr1:67049016-67049017	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572793949	chr1:67049032-67049033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564351163	chr1:67049039-67049040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74803103	chr1:67049106-67049107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558408212	chr1:67049110-67049111	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370445080	chr1:67049113-67049114	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139101995	chr1:67049119-67049120	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540854391	chr1:67049138-67049139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375588294	chr1:67049211-67049212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554361960	chr1:67049244-67049245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574353704	chr1:67049258-67049259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal cancer	21851588	CNVD
abnormal development	18461090	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD

Chromatin state (count:365 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:67041600-67062400	Weak transcription	Stomach Smooth Muscle	stomach
2	chr1:67043200-67052000	Weak transcription	Brain Angular Gyrus	brain
3	chr1:67043200-67056800	Weak transcription	Brain Anterior Caudate	brain
4	chr1:67043200-67064400	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr1:67043400-67056200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr1:67043600-67050600	Weak transcription	Brain Hippocampus Middle	brain
7	chr1:67043600-67066600	Weak transcription	Fetal Brain Male	brain
8	chr1:67044000-67057200	Weak transcription	Aorta	Aorta
9	chr1:67044200-67064000	Weak transcription	NH-A	brain
10	chr1:67044800-67050600	Weak transcription	NHDF-Ad	bronchial
11	chr1:67044800-67064000	Weak transcription	Osteobl	bone
12	chr1:67045000-67050400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr1:67045000-67050600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr1:67045000-67050600	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr1:67045600-67056000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr1:67046000-67049400	Weak transcription	Psoas Muscle	Psoas
17	chr1:67046400-67060400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr1:67047600-67048200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr1:67047600-67048600	Enhancers	Fetal Lung	lung
20	chr1:67048200-67049000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr1:67049000-67049600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr1:67049400-67049600	Enhancers	Psoas Muscle	Psoas
23	chr1:67049600-67051000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr1:67049600-67062600	Weak transcription	Psoas Muscle	Psoas
25	chr1:67050000-67050800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr1:67050200-67051200	Enhancers	HepG2	liver
27	chr1:67050200-67052200	Enhancers	Fetal Heart	heart
28	chr1:67050400-67051000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr1:67050400-67051200	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr1:67050400-67051200	Enhancers	Brain Substantia Nigra	brain
31	chr1:67050600-67050800	Weak transcription	Brain Cingulate Gyrus	brain
32	chr1:67050600-67051000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr1:67050600-67051000	Enhancers	Brain Hippocampus Middle	brain
34	chr1:67050600-67051200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:67050600-67051200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr1:67050600-67051200	Enhancers	Muscle Satellite Cultured Cells	--
37	chr1:67050600-67051200	Enhancers	NHDF-Ad	bronchial
38	chr1:67050600-67051200	Enhancers	NHLF	lung
39	chr1:67050800-67051000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr1:67050800-67051000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr1:67050800-67051000	Enhancers	Brain Cingulate Gyrus	brain
42	chr1:67050800-67051200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
43	chr1:67051000-67051600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr1:67051000-67056200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr1:67051000-67060400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr1:67051000-67061600	Weak transcription	Brain Hippocampus Middle	brain
47	chr1:67051000-67064200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr1:67051000-67064400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr1:67051000-67065000	Weak transcription	Brain Cingulate Gyrus	brain
50	chr1:67051200-67055200	Weak transcription	HepG2	liver

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