Variant report

Variant	nsv254
Chromosome Location	chr1:72734991-72823194
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:733)
CpG islands
(count:1098)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:72750319-72750713	GM12878	blood:	n/a	n/a
2	ATF2	chr1:72750376-72750736	GM12878	blood:	n/a	n/a
3	BACH1	chr1:72748894-72749768	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:72748062-72748227	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr1:72750317-72750778	GM12878	blood:	n/a	n/a
6	BATF	chr1:72750337-72750724	GM12878	blood:	n/a	n/a
7	BRCA1	chr1:72748195-72748394	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr1:72750323-72751066	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr1:72750011-72750992	IMR90	lung:	n/a	chr1:72750584-72750595 chr1:72750585-72750596 chr1:72750147-72750158
10	CEBPB	chr1:72812222-72812489	A549	lung:	n/a	chr1:72812301-72812312 chr1:72812343-72812354
11	CEBPB	chr1:72811065-72811328	IMR90	lung:	n/a	n/a
12	CEBPB	chr1:72814338-72814482	A549	lung:	n/a	n/a
13	CEBPB	chr1:72748554-72748740	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:72812174-72812494	HepG2	liver:	n/a	chr1:72812301-72812312 chr1:72812343-72812354
15	CEBPB	chr1:72755092-72755159	HepG2	liver:	n/a	chr1:72755122-72755131 chr1:72755120-72755131
16	CEBPB	chr1:72812260-72812424	H1-hESC	embryonic stem cell:	n/a	chr1:72812301-72812312 chr1:72812343-72812354
17	CEBPB	chr1:72746375-72746718	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr1:72762099-72762426	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:72749276-72749833	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr1:72748420-72750957	Hela-S3	cervix:	n/a	chr1:72750584-72750595 chr1:72748863-72748876 chr1:72750585-72750596 chr1:72750147-72750158
21	CEBPB	chr1:72748450-72748905	IMR90	lung:	n/a	chr1:72748863-72748876
22	CEBPB	chr1:72823109-72823461	IMR90	lung:	n/a	n/a
23	CEBPB	chr1:72812157-72812489	Hela-S3	cervix:	n/a	chr1:72812301-72812312 chr1:72812343-72812354
24	CEBPB	chr1:72750450-72750705	HepG2	liver:	n/a	chr1:72750584-72750595 chr1:72750585-72750596
25	CEBPB	chr1:72814314-72814570	IMR90	lung:	n/a	n/a
26	CEBPB	chr1:72823103-72823425	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:72818172-72818482	IMR90	lung:	n/a	chr1:72818339-72818350
28	CEBPB	chr1:72748537-72748783	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr1:72746375-72746702	IMR90	lung:	n/a	n/a
30	CEBPB	chr1:72749367-72749678	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr1:72818201-72818500	HepG2	liver:	n/a	chr1:72818339-72818350
32	CHD1	chr1:72748624-72750228	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr1:72748366-72748381	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr1:72748543-72748846	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr1:72748405-72750930	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr1:72749095-72750447	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr1:72748477-72748773	A549	lung:	n/a	n/a
38	CREB1	chr1:72748399-72748786	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr1:72750306-72750765	GM12878	blood:	n/a	n/a
40	CTBP2	chr1:72747565-72750445	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr1:72748471-72748591	GM19239	blood:	n/a	n/a
42	CTCF	chr1:72748380-72748530	AG04450	lung:	n/a	n/a
43	CTCF	chr1:72746560-72746710	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr1:72748420-72748570	GM12873	blood:	n/a	n/a
45	CTCF	chr1:72750120-72750270	NB4	blood:	n/a	n/a
46	CTCF	chr1:72750040-72750190	AG04450	lung:	n/a	n/a
47	CTCF	chr1:72748400-72748550	GM12865	blood:	n/a	n/a
48	CTCF	chr1:72748440-72748590	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr1:72748700-72748850	HA-sp	spinal cord:	n/a	chr1:72748735-72748744
50	CTCF	chr1:72750060-72750210	HPF	lung:	n/a	n/a

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72748139-72748189	HEEpiC	esophagus:	n/a
2	chr1:72753076-72753126	NH-A	brain:	n/a
3	chr1:72753076-72753126	Hepatocyte	liver:	n/a
4	chr1:72748610-72748660	GM19239	blood:	n/a
5	chr1:72749015-72749065	GM06990	blood:	n/a
6	chr1:72750241-72750291	HCT-116	colon:	n/a
7	chr1:72750671-72750721	Jurkat	blood:	n/a
8	chr1:72748389-72748439	SK-N-SH	brain:	n/a
9	chr1:72748607-72748657	HMEC	breast:	n/a
10	chr1:72748610-72748660	BE2_C	brain:	n/a
11	chr1:72750502-72750552	PFSK-1	brain:	n/a
12	chr1:72748610-72748660	Hepatocyte	liver:	n/a
13	chr1:72750671-72750721	SKMC	muscle:	n/a
14	chr1:72748610-72748660	GM12891	blood:	n/a
15	chr1:72749275-72749325	K562	blood:	n/a
16	chr1:72749880-72749930	NH-A	brain:	n/a
17	chr1:72748607-72748657	HepG2	liver:	n/a
18	chr1:72748610-72748660	U87	brain:	n/a
19	chr1:72749735-72749785	U87	brain:	n/a
20	chr1:72750671-72750721	MCF-7	breast:	n/a
21	chr1:72750502-72750552	AG10803	skin:	n/a
22	chr1:72753076-72753126	HCPEpiC	choroid plexus:	n/a
23	chr1:72753076-72753126	ovcar-3	ovarian:	n/a
24	chr1:72749735-72749785	SKMC	muscle:	n/a
25	chr1:72749275-72749325	MCF-7	breast:	n/a
26	chr1:72749735-72749785	CMK	blood:	n/a
27	chr1:72748610-72748660	HAEpiC	amniotic membrane:	n/a
28	chr1:72749275-72749325	HCM	heart:	n/a
29	chr1:72749015-72749065	HAEpiC	amniotic membrane:	n/a
30	chr1:72748124-72748174	HPAEpiC	pulmonary alveolar:	n/a
31	chr1:72747802-72747852	LNCaP	prostate:	n/a
32	chr1:72748389-72748439	NT2-D1	testis:	n/a
33	chr1:72747802-72747852	AoSMC	blood vessel:	n/a
34	chr1:72748139-72748189	HRE	kidney:	n/a
35	chr1:72749581-72749631	NH-A	brain:	n/a
36	chr1:72748610-72748660	HEK293	kidney:	embryo
37	chr1:72748389-72748439	LNCaP	prostate:	n/a
38	chr1:72748610-72748660	Jurkat	blood:	n/a
39	chr1:72747802-72747852	IMR90	lung:	fetal
40	chr1:72748601-72748651	NB4	blood:	n/a
41	chr1:72747802-72747852	K562	blood:	n/a
42	chr1:72748124-72748174	SK-N-SH	brain:	n/a
43	chr1:72748124-72748174	NHBE	bronchial:	n/a
44	chr1:72748389-72748439	SK-N-SH_RA	brain:	n/a
45	chr1:72748389-72748439	AG09309	skin:	n/a
46	chr1:72748610-72748660	NHDF-neo	bronchial:	n/a
47	chr1:72749581-72749631	BJ	skin:	n/a
48	chr1:72748601-72748651	HepG2	liver:	n/a
49	chr1:72749275-72749325	PFSK-1	brain:	n/a
50	chr1:72748610-72748660	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr1:72752065..72752600-chr8:87527466..87528155,2	MCF-7	breast:
2	chr1:72748974..72749649-chr17:56420933..56421808,2	NB4	blood:
3	chr1:72748841..72749750-chr13:47370740..47371446,2	NB4	blood:

No data

Variant related genes	Relation type
RPL31P12	TF binding region
NEGR1	TF binding region
GDI2P2	TF binding region
RPL31P12	CpG island
NEGR1	CpG island
GDI2P2	CpG island
ENSG00000139684	chromatin interactions

Extended variants
information (count: 1012 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1012 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540259170	chr1:72735022-72735023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs375832426	chr1:72735030-72735031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577544004	chr1:72735077-72735078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572578743	chr1:72735102-72735103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539814536	chr1:72735118-72735119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553464653	chr1:72735153-72735154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573360269	chr1:72735158-72735159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542020496	chr1:72735247-72735248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562136992	chr1:72735261-72735262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192595935	chr1:72735319-72735320	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs544560018	chr1:72735393-72735394	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs544736995	chr1:72735408-72735409	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs116244409	chr1:72735434-72735435	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs575156087	chr1:72735444-72735445	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs533389378	chr1:72735455-72735456	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs12137231	chr1:72735458-72735459	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs566982854	chr1:72735470-72735471	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs71762127	chr1:72735493-72735494	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs184390261	chr1:72735517-72735518	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs575440501	chr1:72735551-72735552	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs188878549	chr1:72735552-72735553	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs192514508	chr1:72735564-72735565	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs115374642	chr1:72735584-72735585	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs185087809	chr1:72735591-72735592	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs571484239	chr1:72735661-72735662	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533551924	chr1:72735668-72735669	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553303093	chr1:72735670-72735671	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573447632	chr1:72735712-72735713	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143942415	chr1:72735718-72735719	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75171439	chr1:72735734-72735735	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555958482	chr1:72735745-72735746	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146846336	chr1:72735791-72735792	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139720462	chr1:72735795-72735796	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564643977	chr1:72735801-72735802	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552383885	chr1:72735831-72735832	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74088557	chr1:72735890-72735891	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs143254244	chr1:72735902-72735903	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537192753	chr1:72735911-72735912	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564630136	chr1:72735931-72735932	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549194238	chr1:72735968-72735969	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs12138135	chr1:72735996-72735997	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs145522513	chr1:72736029-72736030	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs531421959	chr1:72736039-72736040	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs13376275	chr1:72736069-72736070	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs35026260	chr1:72736085-72736086	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571454075	chr1:72736109-72736110	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533830794	chr1:72736117-72736118	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547028153	chr1:72736131-72736132	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561199001	chr1:72736158-72736159	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188737191	chr1:72736287-72736288	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:683 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72713800-72735600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr1:72728400-72738600	Weak transcription	Colon Smooth Muscle	Colon
3	chr1:72735600-72737600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr1:72737600-72744200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr1:72738000-72744200	Weak transcription	Stomach Smooth Muscle	stomach
6	chr1:72738000-72745800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr1:72738200-72739000	Enhancers	Rectal Smooth Muscle	rectum
8	chr1:72738400-72738800	Enhancers	Brain Germinal Matrix	brain
9	chr1:72738400-72739000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr1:72738600-72739200	Enhancers	Colon Smooth Muscle	Colon
11	chr1:72739000-72744400	Weak transcription	Rectal Smooth Muscle	rectum
12	chr1:72739200-72741600	Weak transcription	Colon Smooth Muscle	Colon
13	chr1:72741600-72741800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr1:72741600-72741800	Enhancers	Brain Angular Gyrus	brain
15	chr1:72741600-72741800	Enhancers	Colon Smooth Muscle	Colon
16	chr1:72741800-72742000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr1:72741800-72742200	Weak transcription	Colon Smooth Muscle	Colon
18	chr1:72741800-72742800	Weak transcription	Brain Angular Gyrus	brain
19	chr1:72742200-72744000	Enhancers	Colon Smooth Muscle	Colon
20	chr1:72742400-72742600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
21	chr1:72742600-72742800	Weak transcription	Brain Cingulate Gyrus	brain
22	chr1:72742600-72742800	Enhancers	Brain Substantia Nigra	brain
23	chr1:72742600-72743000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
24	chr1:72742800-72743000	Enhancers	Brain Angular Gyrus	brain
25	chr1:72742800-72743000	Enhancers	Brain Cingulate Gyrus	brain
26	chr1:72742800-72743200	Enhancers	Dnd41	blood
27	chr1:72742800-72744000	Weak transcription	Brain Substantia Nigra	brain
28	chr1:72742800-72745800	Weak transcription	Brain Anterior Caudate	brain
29	chr1:72743000-72745000	Weak transcription	Brain Angular Gyrus	brain
30	chr1:72743000-72745000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr1:72743000-72745800	Weak transcription	Brain Cingulate Gyrus	brain
32	chr1:72743200-72743600	Weak transcription	Dnd41	blood
33	chr1:72743600-72745800	Enhancers	Dnd41	blood
34	chr1:72743800-72744200	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr1:72743800-72751600	Active TSS	Brain Inferior Temporal Lobe	brain
36	chr1:72744000-72744200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr1:72744000-72745000	Weak transcription	Colon Smooth Muscle	Colon
38	chr1:72744000-72745200	Enhancers	Brain Substantia Nigra	brain
39	chr1:72744200-72744400	Enhancers	NHDF-Ad	bronchial
40	chr1:72744200-72744600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
41	chr1:72744200-72744800	Active TSS	Stomach Smooth Muscle	stomach
42	chr1:72744200-72744800	Enhancers	HUVEC	blood vessel
43	chr1:72744200-72745400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr1:72744200-72745800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr1:72744200-72746000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr1:72744400-72744600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:72744400-72745000	Enhancers	Muscle Satellite Cultured Cells	--
48	chr1:72744400-72745800	Weak transcription	NHDF-Ad	bronchial
49	chr1:72744400-72746400	Enhancers	Rectal Smooth Muscle	rectum
50	chr1:72744600-72744800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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