Variant report

Variant	nsv875140
Chromosome Location	chr2:133816484-133904829
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:338)
CpG islands
(count:244)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:338 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr2:133892668-133892866	GM12878	blood:	n/a	n/a
2	BCL11A	chr2:133897445-133897743	H1-hESC	embryonic stem cell:	n/a	chr2:133897635-133897644 chr2:133897634-133897643
3	CEBPB	chr2:133884617-133885020	HepG2	liver:	n/a	chr2:133884879-133884890 chr2:133884881-133884890
4	CEBPB	chr2:133867453-133867754	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr2:133820511-133821222	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr2:133888455-133888729	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr2:133834945-133835142	IMR90	lung:	n/a	chr2:133835029-133835040 chr2:133835029-133835042
8	CEBPB	chr2:133888428-133888781	IMR90	lung:	n/a	n/a
9	CEBPB	chr2:133819747-133820083	IMR90	lung:	n/a	n/a
10	CEBPB	chr2:133821436-133821710	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr2:133884649-133884917	IMR90	lung:	n/a	chr2:133884879-133884890 chr2:133884881-133884890
12	CEBPB	chr2:133897405-133897664	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr2:133835003-133835062	HepG2	liver:	n/a	chr2:133835029-133835040 chr2:133835029-133835042
14	CEBPB	chr2:133862268-133862515	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:133836703-133836940	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr2:133833598-133833686	HepG2	liver:	n/a	chr2:133833672-133833683 chr2:133833611-133833622
17	CEBPB	chr2:133819724-133820116	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr2:133836739-133836849	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:133821434-133821709	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr2:133867421-133867772	IMR90	lung:	n/a	n/a
21	CEBPB	chr2:133862217-133862515	IMR90	lung:	n/a	chr2:133862250-133862261 chr2:133862250-133862263
22	CEBPB	chr2:133836687-133836898	IMR90	lung:	n/a	n/a
23	CEBPB	chr2:133821472-133821768	MCF-7	breast:	n/a	n/a
24	CEBPB	chr2:133862229-133862527	A549	lung:	n/a	chr2:133862250-133862261 chr2:133862250-133862263
25	CEBPB	chr2:133821440-133821725	IMR90	lung:	n/a	n/a
26	CHD2	chr2:133897550-133897741	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr2:133904580-133904730	AG09319	gingival:	n/a	chr2:133904676-133904697
28	CTCF	chr2:133904620-133904770	AG09309	skin:	n/a	chr2:133904676-133904697
29	CTCF	chr2:133835200-133835350	HPF	lung:	n/a	chr2:133835226-133835242
30	CTCF	chr2:133904660-133904810	AG04449	skin:	n/a	chr2:133904676-133904697
31	CTCF	chr2:133904520-133904670	MCF-7	breast:	n/a	n/a
32	CTCF	chr2:133835100-133835250	AG09319	gingival:	n/a	chr2:133835226-133835242
33	CTCF	chr2:133835180-133835330	NHDF-neo	bronchial:	n/a	chr2:133835226-133835242
34	CTCF	chr2:133904612-133904786	MCF-7	breast:	n/a	chr2:133904676-133904697
35	CTCF	chr2:133904615-133904737	Spleen_OC	spleen:	n/a	chr2:133904676-133904697
36	CTCF	chr2:133904542-133904837	GM12878	blood:	n/a	chr2:133904676-133904697
37	CTCF	chr2:133854739-133854794	MCF-7	breast:	n/a	n/a
38	CTCF	chr2:133854756-133854810	MCF-7	breast:	n/a	n/a
39	CTCF	chr2:133904620-133904770	AG04449	skin:	n/a	chr2:133904676-133904697
40	CTCF	chr2:133904556-133904840	IMR90	lung:	n/a	chr2:133904676-133904697
41	CTCF	chr2:133904620-133904770	HPAF	blood vessel:	n/a	chr2:133904676-133904697
42	CTCF	chr2:133904680-133904830	A549	lung:	n/a	n/a
43	CTCF	chr2:133854762-133854803	GM12892	blood:	n/a	n/a
44	CTCF	chr2:133847880-133848030	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr2:133820734-133820803	Medullo	brain:	n/a	n/a
46	CTCF	chr2:133835120-133835270	AG09319	gingival:	n/a	chr2:133835226-133835242
47	CTCF	chr2:133904560-133904710	SK-N-SH_RA	brain:	n/a	chr2:133904676-133904697
48	CTCF	chr2:133904626-133904774	Gliobla	brain:	n/a	chr2:133904676-133904697
49	CTCF	chr2:133820794-133820799	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr2:133904646-133904735	HUVEC	blood vessel:	n/a	chr2:133904676-133904697

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:133868449-133868499	H1-hESC	embryonic stem cell:	embryo
2	chr2:133888263-133888313	SK-N-MC	brain:	n/a
3	chr2:133868449-133868499	Jurkat	blood:	n/a
4	chr2:133868449-133868499	BE2_C	brain:	n/a
5	chr2:133855847-133855897	HMEC	breast:	n/a
6	chr2:133868449-133868499	CMK	blood:	n/a
7	chr2:133855847-133855897	MCF10A-Er-Src	breast:	n/a
8	chr2:133888263-133888313	SK-N-SH	brain:	n/a
9	chr2:133834998-133835048	Caco-2	colon:	n/a
10	chr2:133888263-133888313	HCPEpiC	choroid plexus:	n/a
11	chr2:133868449-133868499	AG04449	skin:	fetal
12	chr2:133868449-133868499	HCF	heart:	n/a
13	chr2:133888263-133888313	CMK	blood:	n/a
14	chr2:133855847-133855897	NT2-D1	testis:	n/a
15	chr2:133834998-133835048	HCF	heart:	n/a
16	chr2:133834998-133835048	HRPEpiC	eye:	n/a
17	chr2:133888263-133888313	MCF-7	breast:	n/a
18	chr2:133855847-133855897	AG04450	lung:	fetal
19	chr2:133855847-133855897	AG10803	skin:	n/a
20	chr2:133868449-133868499	NHDF-neo	bronchial:	n/a
21	chr2:133855847-133855897	NHBE	bronchial:	n/a
22	chr2:133888263-133888313	NHBE	bronchial:	n/a
23	chr2:133868449-133868499	GM12891	blood:	n/a
24	chr2:133888263-133888313	ProgFib	skin:	n/a
25	chr2:133834998-133835048	SAEC	small airway:	n/a
26	chr2:133834998-133835048	Hela-S3	cervix:	n/a
27	chr2:133868449-133868499	RPTEC	kidney:	n/a
28	chr2:133855847-133855897	HCM	heart:	n/a
29	chr2:133855847-133855897	HCF	heart:	n/a
30	chr2:133834998-133835048	A549	lung:	n/a
31	chr2:133868449-133868499	ECC-1	luminal epithelium:	n/a
32	chr2:133868449-133868499	SKMC	muscle:	n/a
33	chr2:133834998-133835048	HPAEpiC	pulmonary alveolar:	n/a
34	chr2:133888263-133888313	NHDF-neo	bronchial:	n/a
35	chr2:133888263-133888313	HNPCEpiC	eye:	n/a
36	chr2:133855847-133855897	AG04449	skin:	fetal
37	chr2:133868449-133868499	SK-N-SH	brain:	n/a
38	chr2:133868449-133868499	HCM	heart:	n/a
39	chr2:133888263-133888313	HEEpiC	esophagus:	n/a
40	chr2:133868449-133868499	HepG2	liver:	n/a
41	chr2:133868449-133868499	A549	lung:	n/a
42	chr2:133834998-133835048	PFSK-1	brain:	n/a
43	chr2:133855847-133855897	NB4	blood:	n/a
44	chr2:133834998-133835048	CMK	blood:	n/a
45	chr2:133834998-133835048	AG04449	skin:	fetal
46	chr2:133888263-133888313	HRE	kidney:	n/a
47	chr2:133855847-133855897	IMR90	lung:	fetal
48	chr2:133834998-133835048	K562	blood:	n/a
49	chr2:133868449-133868499	NT2-D1	testis:	n/a
50	chr2:133888263-133888313	PANC-1	pancreas:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:133811077..133813218-chr2:133838444..133841047,2	MCF-7	breast:
2	chr2:133826353..133828506-chr2:133839741..133842653,2	MCF-7	breast:
3	chr2:133836968..133839255-chr2:133840150..133841905,2	K562	blood:
4	chr2:133831745..133832436-chr8:97637034..97637925,2	MCF-7	breast:
5	chr2:133427195..133430167-chr2:133854644..133856509,2	MCF-7	breast:
6	chr2:133865556..133868534-chr2:133870878..133873548,2	K562	blood:
7	chr2:133850084..133851752-chr2:133851774..133853791,2	MCF-7	breast:
8	chr2:133850171..133852489-chr2:133854080..133856768,2	MCF-7	breast:
9	chr2:133828442..133830137-chr2:133831672..133833496,2	MCF-7	breast:
10	chr2:133865556..133868534-chr2:133870878..133873548,2	K562	blood:
11	chr2:133836968..133839255-chr2:133840150..133841905,2	K562	blood:
12	chr2:133850171..133852489-chr2:133854080..133856768,2	MCF-7	breast:
13	chr2:133826353..133828506-chr2:133839741..133842653,2	MCF-7	breast:
14	chr2:133850084..133851752-chr2:133851774..133853791,2	MCF-7	breast:
15	chr2:133828442..133830137-chr2:133831672..133833496,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000269686	TF binding region
ENSG00000269686	CpG island
ENSG00000150551	chromatin interactions

Extended variants
information (count: 3345 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:3345 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1595416	chr2:133816484-133816485	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372333751	chr2:133816498-133816499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536008077	chr2:133816526-133816527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548260152	chr2:133816533-133816534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569875018	chr2:133816535-133816536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537209513	chr2:133816561-133816562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs111831913	chr2:133816595-133816596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142764081	chr2:133816632-133816633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534903704	chr2:133816704-133816705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553921330	chr2:133816724-133816725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191043565	chr2:133816798-133816799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542719104	chr2:133816803-133816804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375389633	chr2:133816860-133816861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561009565	chr2:133816880-133816881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs151013919	chr2:133816891-133816892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543634168	chr2:133816911-133816912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs72842435	chr2:133816914-133816915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs139613155	chr2:133816977-133816978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113543145	chr2:133816984-133816985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559089459	chr2:133816992-133816993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529651409	chr2:133817086-133817087	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369074155	chr2:133817106-133817107	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs75942781	chr2:133817109-133817110	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569741761	chr2:133817142-133817143	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6736952	chr2:133817216-133817217	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs75560454	chr2:133817246-133817247	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79871838	chr2:133817247-133817248	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552438329	chr2:133817268-133817269	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369532002	chr2:133817285-133817286	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147823128	chr2:133817341-133817342	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372385478	chr2:133817342-133817343	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs79744286	chr2:133817358-133817359	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182855817	chr2:133817403-133817404	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188335060	chr2:133817436-133817437	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536214433	chr2:133817477-133817478	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543304483	chr2:133817507-133817508	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200566473	chr2:133817508-133817509	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs397827036	chr2:133817518-133817519	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs114639740	chr2:133817527-133817528	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375290222	chr2:133817582-133817583	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs75358968	chr2:133817589-133817590	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558931378	chr2:133817607-133817608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141291670	chr2:133817729-133817730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376637979	chr2:133817838-133817839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541370573	chr2:133817847-133817848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559963241	chr2:133817908-133817909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146958154	chr2:133817943-133817944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs75740299	chr2:133817992-133817993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147581634	chr2:133818014-133818015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192105275	chr2:133818015-133818016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133811000-133823600	Weak transcription	Fetal Brain Male	brain
2	chr2:133816400-133817000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:133817000-133817600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:133817600-133825600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:133819200-133819600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr2:133819200-133820600	Enhancers	Hela-S3	cervix
7	chr2:133819400-133820800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr2:133819600-133830800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr2:133819800-133820600	Enhancers	NHDF-Ad	bronchial
10	chr2:133820200-133820800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr2:133820600-133820800	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr2:133820600-133830800	Weak transcription	Hela-S3	cervix
13	chr2:133820800-133821200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr2:133820800-133825800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr2:133821800-133823600	Weak transcription	Fetal Brain Female	brain
16	chr2:133823600-133824400	Enhancers	Fetal Brain Male	brain
17	chr2:133824400-133828800	Weak transcription	Fetal Brain Male	brain
18	chr2:133825600-133825800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:133825800-133826600	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr2:133825800-133826600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr2:133826600-133830600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr2:133829000-133830000	Weak transcription	Fetal Brain Male	brain
23	chr2:133830000-133830600	Enhancers	NHEK	skin
24	chr2:133830000-133831400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr2:133830400-133831600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr2:133830600-133831200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr2:133830600-133831400	Flanking Active TSS	NHEK	skin
28	chr2:133830600-133831600	Enhancers	HMEC	breast
29	chr2:133830800-133831200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr2:133830800-133831200	Enhancers	Brain Angular Gyrus	brain
31	chr2:133830800-133831400	Enhancers	Hela-S3	cervix
32	chr2:133830800-133831600	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr2:133830800-133831600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr2:133831000-133831800	Enhancers	Brain Hippocampus Middle	brain
35	chr2:133831000-133831800	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr2:133831200-133834000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr2:133831200-133834200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr2:133831400-133831600	Enhancers	Brain Cingulate Gyrus	brain
39	chr2:133831400-133831600	Enhancers	NHEK	skin
40	chr2:133831400-133835800	Weak transcription	Right Ventricle	heart
41	chr2:133831600-133855200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr2:133832800-133834200	Weak transcription	Fetal Brain Male	brain
43	chr2:133833400-133834000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr2:133834000-133834800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr2:133834000-133837800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr2:133834200-133834400	Weak transcription	Brain Cingulate Gyrus	brain
47	chr2:133834200-133834600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr2:133834200-133835200	Enhancers	Fetal Lung	lung
49	chr2:133834200-133836400	Enhancers	Fetal Brain Male	brain
50	chr2:133834400-133834600	Enhancers	Brain Cingulate Gyrus	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links