Variant report

Variant	esv1804937
Chromosome Location	chr1:95051930-95081587
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:462)
CpG islands
(count:305)
Chromatin interactive
region (count:16)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:95068522-95068525	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr1:95063292-95063639	GM12878	blood:	n/a	n/a
3	BHLHE40	chr1:95064269-95064582	K562	blood:	n/a	n/a
4	BRCA1	chr1:95071745-95071785	GM12878	blood:	n/a	n/a
5	CEBPB	chr1:95073106-95073116	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr1:95065084-95065371	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr1:95078287-95078468	HepG2	liver:	n/a	n/a
8	CEBPB	chr1:95063366-95063603	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:95065095-95065304	HepG2	liver:	n/a	n/a
10	CEBPB	chr1:95073784-95074058	HepG2	liver:	n/a	n/a
11	CEBPB	chr1:95063258-95063707	IMR90	lung:	n/a	n/a
12	CEBPB	chr1:95061343-95061661	IMR90	lung:	n/a	n/a
13	CEBPB	chr1:95063164-95063687	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr1:95061275-95061688	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr1:95078300-95078549	K562	blood:	n/a	n/a
16	CEBPB	chr1:95067975-95068859	IMR90	lung:	n/a	chr1:95068159-95068170
17	CEBPB	chr1:95078289-95078574	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr1:95063283-95063615	Hela-S3	cervix:	n/a	n/a
19	CREB1	chr1:95079635-95080202	K562	blood:	n/a	chr1:95079917-95079930 chr1:95079873-95079886
20	CTCF	chr1:95065120-95065270	AG04449	skin:	n/a	n/a
21	CTCF	chr1:95065120-95065270	HCFaa	heart:	n/a	n/a
22	CTCF	chr1:95065125-95065303	K562	blood:	n/a	n/a
23	CTCF	chr1:95076800-95076950	HCT-116	colon:	n/a	n/a
24	CTCF	chr1:95060040-95060190	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr1:95061880-95062030	GM12875	blood:	n/a	n/a
26	CTCF	chr1:95061963-95062018	HepG2	liver:	n/a	n/a
27	CTCF	chr1:95065080-95065230	A549	lung:	n/a	n/a
28	CTCF	chr1:95065082-95065292	A549	lung:	n/a	n/a
29	CTCF	chr1:95065140-95065290	HRE	kidney:	n/a	n/a
30	CTCF	chr1:95065091-95065316	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr1:95061880-95062030	HepG2	liver:	n/a	n/a
32	CTCF	chr1:95065200-95065350	WI-38	lung:	n/a	n/a
33	CTCF	chr1:95065080-95065230	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr1:95065160-95065310	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr1:95065140-95065290	K562	blood:	n/a	n/a
36	CTCF	chr1:95065140-95065290	HPF	lung:	n/a	n/a
37	CTCF	chr1:95074720-95074870	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr1:95065100-95065250	HPF	lung:	n/a	n/a
39	CTCF	chr1:95060060-95060210	NHEK	skin:	n/a	n/a
40	CTCF	chr1:95065120-95065270	NHEK	skin:	n/a	n/a
41	CTCF	chr1:95065220-95065370	AG04450	lung:	n/a	n/a
42	CTCF	chr1:95060078-95060110	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr1:95065140-95065290	AG09319	gingival:	n/a	n/a
44	CTCF	chr1:95071583-95071613	Gliobla	brain:	n/a	n/a
45	CTCF	chr1:95065096-95065308	MCF-7	breast:	n/a	n/a
46	CTCF	chr1:95072417-95072503	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr1:95065080-95065230	BE2_C	brain:	n/a	n/a
48	CTCF	chr1:95065100-95065250	Caco-2	colon:	n/a	n/a
49	CTCF	chr1:95077140-95077290	NB4	blood:	n/a	chr1:95077192-95077210
50	CTCF	chr1:95065180-95065330	HCT-116	colon:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:95080047-95080097	GM12891	blood:	n/a
2	chr1:95074231-95074281	Hela-S3	cervix:	n/a
3	chr1:95074231-95074281	HCF	heart:	n/a
4	chr1:95074231-95074281	GM12892	blood:	n/a
5	chr1:95068029-95068079	MCF10A-Er-Src	breast:	n/a
6	chr1:95080047-95080097	PrEC	prostate:	n/a
7	chr1:95080047-95080097	U87	brain:	n/a
8	chr1:95056619-95056669	AG10803	skin:	n/a
9	chr1:95061616-95061666	ECC-1	luminal epithelium:	n/a
10	chr1:95080047-95080097	Caco-2	colon:	n/a
11	chr1:95080047-95080097	ECC-1	luminal epithelium:	n/a
12	chr1:95080047-95080097	HMEC	breast:	n/a
13	chr1:95061616-95061666	HRE	kidney:	n/a
14	chr1:95074231-95074281	HMEC	breast:	n/a
15	chr1:95056619-95056669	MCF10A-Er-Src	breast:	n/a
16	chr1:95074231-95074281	MCF10A-Er-Src	breast:	n/a
17	chr1:95080047-95080097	HEK293	kidney:	embryo
18	chr1:95074231-95074281	NHBE	bronchial:	n/a
19	chr1:95061616-95061666	HL-60	blood:	n/a
20	chr1:95056619-95056669	HRPEpiC	eye:	n/a
21	chr1:95056619-95056669	Hela-S3	cervix:	n/a
22	chr1:95068029-95068079	AG04450	lung:	fetal
23	chr1:95068029-95068079	HAEpiC	amniotic membrane:	n/a
24	chr1:95080047-95080097	CMK	blood:	n/a
25	chr1:95061616-95061666	NT2-D1	testis:	n/a
26	chr1:95056619-95056669	HCT-116	colon:	n/a
27	chr1:95056619-95056669	AG04450	lung:	fetal
28	chr1:95074231-95074281	AG04449	skin:	fetal
29	chr1:95068029-95068079	NT2-D1	testis:	n/a
30	chr1:95068029-95068079	PFSK-1	brain:	n/a
31	chr1:95061616-95061666	GM12892	blood:	n/a
32	chr1:95068029-95068079	Hepatocyte	liver:	n/a
33	chr1:95056619-95056669	AG09319	gingival:	n/a
34	chr1:95056619-95056669	T-47D	breast:	n/a
35	chr1:95061616-95061666	BJ	skin:	n/a
36	chr1:95056619-95056669	HCPEpiC	choroid plexus:	n/a
37	chr1:95068029-95068079	ovcar-3	ovarian:	n/a
38	chr1:95068029-95068079	NHBE	bronchial:	n/a
39	chr1:95080047-95080097	AG09319	gingival:	n/a
40	chr1:95056619-95056669	PrEC	prostate:	n/a
41	chr1:95068029-95068079	MCF-7	breast:	n/a
42	chr1:95074231-95074281	ovcar-3	ovarian:	n/a
43	chr1:95068029-95068079	GM12892	blood:	n/a
44	chr1:95074231-95074281	HEEpiC	esophagus:	n/a
45	chr1:95080047-95080097	HCF	heart:	n/a
46	chr1:95080047-95080097	GM12892	blood:	n/a
47	chr1:95080047-95080097	Hela-S3	cervix:	n/a
48	chr1:95080047-95080097	AG04450	lung:	fetal
49	chr1:95080047-95080097	SAEC	small airway:	n/a
50	chr1:95080047-95080097	GM12878	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:95044965..95045519-chr1:95065172..95065776,2	MCF-7	breast:
2	chr1:94997172..94998108-chr1:95064305..95065624,5	MCF-7	breast:
3	chr1:94987992..94988549-chr1:95064767..95065433,2	MCF-7	breast:
4	chr1:95079718..95082412-chr1:95085713..95087293,2	MCF-7	breast:
5	chr1:95080479..95082832-chr1:95086788..95088378,2	K562	blood:
6	chr1:95068045..95070486-chr1:95071108..95072675,2	K562	blood:
7	chr1:95067748..95070486-chr1:95070993..95073979,4	K562	blood:
8	chr1:95002334..95004389-chr1:95062847..95065293,3	MCF-7	breast:
9	chr1:95067748..95070486-chr1:95070993..95073979,4	K562	blood:
10	chr1:95054539..95057690-chr1:95058025..95060713,3	K562	blood:
11	chr1:95064700..95065302-chr1:95267166..95268188,3	MCF-7	breast:
12	chr1:94992707..94993493-chr1:95064769..95065395,2	MCF-7	breast:
13	chr1:95075515..95077960-chr1:95084097..95086216,2	K562	blood:
14	chr1:95054539..95057690-chr1:95058025..95060713,3	K562	blood:
15	chr1:95068045..95070486-chr1:95071108..95072675,2	K562	blood:
16	chr1:95007807..95010747-chr1:95056056..95057592,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-F3-3	chr1:95058100-95058233	l_89_chr1:94917575-94970548_76bGuttman_hLF
2	lnc-F3-1	chr1:95051112-95052318	XLOC_000921
3	lnc-F3-1	chr1:95056890-95057853	XLOC_000921

No data

Variant related genes	Relation type
ENSG00000223675	TF binding region
ENSG00000223675	CpG island

Extended variants
information (count: 1268 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1268 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1041042	chr1:95051930-95051931	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573283724	chr1:95051970-95051971	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs189100927	chr1:95051999-95052000	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs181001691	chr1:95052009-95052010	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs2022030	chr1:95052032-95052033	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs1041041	chr1:95052051-95052052	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs41292687	chr1:95052054-95052055	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs572543254	chr1:95052127-95052128	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs35808762	chr1:95052135-95052136	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs550542044	chr1:95052204-95052205	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs535101246	chr1:95052227-95052228	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs1778205	chr1:95052228-95052229	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs373046956	chr1:95052231-95052232	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs539475839	chr1:95052235-95052236	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs12758064	chr1:95052267-95052268	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs544409876	chr1:95052283-95052284	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs564227396	chr1:95052290-95052291	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs578007270	chr1:95052303-95052304	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs540574466	chr1:95052307-95052308	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs6675255	chr1:95052322-95052323	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs1772905	chr1:95052325-95052326	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs148300855	chr1:95052338-95052339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs577786286	chr1:95052391-95052392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542642798	chr1:95052400-95052401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs563017036	chr1:95052410-95052411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189181202	chr1:95052412-95052413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs78006331	chr1:95052417-95052418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs112584866	chr1:95052435-95052436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs181902444	chr1:95052446-95052447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2022309	chr1:95052476-95052477	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
31	rs142197886	chr1:95052483-95052484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs1408340	chr1:95052503-95052504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs185681514	chr1:95052519-95052520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs555028553	chr1:95052525-95052526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146400338	chr1:95052574-95052575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs537504130	chr1:95052577-95052578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574781016	chr1:95052590-95052591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs192068727	chr1:95052615-95052616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181238692	chr1:95052629-95052630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs841676	chr1:95052668-95052669	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs554146090	chr1:95052709-95052710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs139661894	chr1:95052759-95052760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs543032365	chr1:95052779-95052780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs370367052	chr1:95052805-95052806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs114404559	chr1:95052806-95052807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531840261	chr1:95052846-95052847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186709224	chr1:95052873-95052874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190699808	chr1:95052886-95052887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs527908701	chr1:95052900-95052901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs1778206	chr1:95052909-95052910	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:104)

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
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	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
Acute lymphoblastic leukemia	22237106	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
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:659 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:95046000-95065400	Weak transcription	Fetal Intestine Large	intestine
2	chr1:95046400-95055200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:95047000-95055800	Weak transcription	NHLF	lung
4	chr1:95051000-95052000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr1:95051600-95052200	Enhancers	HSMMtube	muscle
6	chr1:95051600-95052600	Enhancers	Dnd41	blood
7	chr1:95051800-95052400	Enhancers	HSMM	muscle
8	chr1:95052000-95052200	Enhancers	Fetal Lung	lung
9	chr1:95052000-95052400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr1:95052200-95052400	Enhancers	Brain Germinal Matrix	brain
11	chr1:95052200-95053000	Weak transcription	Fetal Lung	lung
12	chr1:95052400-95053800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr1:95052400-95054200	Weak transcription	Brain Germinal Matrix	brain
14	chr1:95052400-95055000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr1:95052400-95056000	Weak transcription	HSMM	muscle
16	chr1:95052600-95053000	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr1:95052600-95053600	Enhancers	Duodenum Smooth Muscle	Duodenum
18	chr1:95053000-95053200	Enhancers	Brain Cingulate Gyrus	brain
19	chr1:95053000-95053200	Enhancers	Fetal Stomach	stomach
20	chr1:95053000-95053600	Enhancers	Fetal Lung	lung
21	chr1:95053000-95053800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr1:95053000-95055400	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr1:95053200-95053600	Enhancers	Brain Hippocampus Middle	brain
24	chr1:95053200-95055000	Weak transcription	Fetal Stomach	stomach
25	chr1:95053400-95053600	Enhancers	Brain Substantia Nigra	brain
26	chr1:95053600-95055000	Weak transcription	Brain Hippocampus Middle	brain
27	chr1:95053600-95055200	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr1:95053600-95055800	Weak transcription	Fetal Lung	lung
29	chr1:95053800-95055000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr1:95053800-95055000	Weak transcription	Brain Substantia Nigra	brain
31	chr1:95053800-95057800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr1:95054200-95054400	Enhancers	Brain Germinal Matrix	brain
33	chr1:95054400-95055200	Weak transcription	Brain Germinal Matrix	brain
34	chr1:95055000-95056000	Enhancers	Brain Hippocampus Middle	brain
35	chr1:95055000-95056200	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr1:95055000-95056200	Enhancers	Brain Substantia Nigra	brain
37	chr1:95055000-95056600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr1:95055000-95056600	Enhancers	Fetal Stomach	stomach
39	chr1:95055000-95059200	Enhancers	Brain Cingulate Gyrus	brain
40	chr1:95055000-95061400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr1:95055000-95061600	Enhancers	Brain Anterior Caudate	brain
42	chr1:95055000-95062000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr1:95055200-95055400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr1:95055200-95055400	Enhancers	Duodenum Smooth Muscle	Duodenum
45	chr1:95055200-95055600	Bivalent Enhancer	HepG2	liver
46	chr1:95055200-95055800	Enhancers	Brain Germinal Matrix	brain
47	chr1:95055200-95056000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr1:95055200-95056200	Enhancers	Right Atrium	heart
49	chr1:95055200-95057600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:95055200-95057600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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