Variant report

Variant	nsv470487
Chromosome Location	chr2:133811842-133875512
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:218)
CpG islands
(count:183)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:218 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr2:133819747-133820083	IMR90	lung:	n/a	n/a
2	CEBPB	chr2:133833598-133833686	HepG2	liver:	n/a	chr2:133833672-133833683 chr2:133833611-133833622
3	CEBPB	chr2:133821434-133821709	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr2:133819724-133820116	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr2:133862268-133862515	HepG2	liver:	n/a	n/a
6	CEBPB	chr2:133834945-133835142	IMR90	lung:	n/a	chr2:133835029-133835040 chr2:133835029-133835042
7	CEBPB	chr2:133835003-133835062	HepG2	liver:	n/a	chr2:133835029-133835040 chr2:133835029-133835042
8	CEBPB	chr2:133836687-133836898	IMR90	lung:	n/a	n/a
9	CEBPB	chr2:133821472-133821768	MCF-7	breast:	n/a	n/a
10	CEBPB	chr2:133821436-133821710	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr2:133820511-133821222	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr2:133862229-133862527	A549	lung:	n/a	chr2:133862250-133862261 chr2:133862250-133862263
13	CEBPB	chr2:133862217-133862515	IMR90	lung:	n/a	chr2:133862250-133862261 chr2:133862250-133862263
14	CEBPB	chr2:133821440-133821725	IMR90	lung:	n/a	n/a
15	CEBPB	chr2:133867453-133867754	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr2:133836739-133836849	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:133867421-133867772	IMR90	lung:	n/a	n/a
18	CEBPB	chr2:133836703-133836940	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr2:133854739-133854794	MCF-7	breast:	n/a	n/a
20	CTCF	chr2:133847880-133848030	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr2:133854728-133854824	MCF-7	breast:	n/a	n/a
22	CTCF	chr2:133811960-133812110	HRPEpiC	eye:	n/a	n/a
23	CTCF	chr2:133854730-133854822	MCF-7	breast:	n/a	n/a
24	CTCF	chr2:133835200-133835350	HPF	lung:	n/a	chr2:133835226-133835242
25	CTCF	chr2:133835120-133835270	BJ	skin:	n/a	chr2:133835226-133835242
26	CTCF	chr2:133835100-133835250	AG09319	gingival:	n/a	chr2:133835226-133835242
27	CTCF	chr2:133854762-133854803	GM12892	blood:	n/a	n/a
28	CTCF	chr2:133811960-133812110	AG04449	skin:	n/a	n/a
29	CTCF	chr2:133820734-133820803	Medullo	brain:	n/a	n/a
30	CTCF	chr2:133820740-133820890	RPTEC	kidney:	n/a	n/a
31	CTCF	chr2:133820762-133820787	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr2:133854755-133854759	GM12892	blood:	n/a	n/a
33	CTCF	chr2:133854760-133854910	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr2:133835160-133835310	AG10803	skin:	n/a	chr2:133835226-133835242
35	CTCF	chr2:133835200-133835350	HCPEpiC	choroid plexus:	n/a	chr2:133835226-133835242
36	CTCF	chr2:133854738-133854797	A549	lung:	n/a	n/a
37	CTCF	chr2:133854756-133854810	MCF-7	breast:	n/a	n/a
38	CTCF	chr2:133820794-133820799	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr2:133835180-133835330	NHDF-neo	bronchial:	n/a	chr2:133835226-133835242
40	CTCF	chr2:133835120-133835270	AG09319	gingival:	n/a	chr2:133835226-133835242
41	EP300	chr2:133843072-133843763	SK-N-SH	brain:	n/a	n/a
42	EP300	chr2:133847927-133848355	SK-N-SH_RA	brain:	n/a	chr2:133848310-133848320
43	EP300	chr2:133867285-133867761	SK-N-SH_RA	brain:	n/a	chr2:133867574-133867588 chr2:133867730-133867739
44	EP300	chr2:133847937-133848349	SK-N-SH_RA	brain:	n/a	chr2:133848310-133848320
45	EP300	chr2:133847641-133848608	SK-N-SH	brain:	n/a	chr2:133848310-133848320
46	EP300	chr2:133842811-133844086	SK-N-SH	brain:	n/a	n/a
47	EP300	chr2:133819753-133820101	Hela-S3	cervix:	n/a	chr2:133819824-133819833 chr2:133819940-133819949
48	EP300	chr2:133867309-133867793	SK-N-SH_RA	brain:	n/a	chr2:133867574-133867588 chr2:133867730-133867739
49	EP300	chr2:133867196-133867948	SK-N-SH	brain:	n/a	chr2:133867574-133867588 chr2:133867730-133867739
50	EP300	chr2:133843036-133843677	SK-N-SH_RA	brain:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:133855847-133855897	SK-N-SH_RA	brain:	n/a
2	chr2:133868449-133868499	AG04450	lung:	fetal
3	chr2:133855847-133855897	BE2_C	brain:	n/a
4	chr2:133868449-133868499	AG09319	gingival:	n/a
5	chr2:133834998-133835048	GM12878	blood:	n/a
6	chr2:133868449-133868499	ECC-1	luminal epithelium:	n/a
7	chr2:133868449-133868499	T-47D	breast:	n/a
8	chr2:133855847-133855897	LNCaP	prostate:	n/a
9	chr2:133834998-133835048	AG04449	skin:	fetal
10	chr2:133834998-133835048	AG10803	skin:	n/a
11	chr2:133868449-133868499	HAEpiC	amniotic membrane:	n/a
12	chr2:133868449-133868499	LNCaP	prostate:	n/a
13	chr2:133834998-133835048	HRE	kidney:	n/a
14	chr2:133855847-133855897	AG09319	gingival:	n/a
15	chr2:133834998-133835048	PFSK-1	brain:	n/a
16	chr2:133868449-133868499	PFSK-1	brain:	n/a
17	chr2:133855847-133855897	HAEpiC	amniotic membrane:	n/a
18	chr2:133855847-133855897	GM06990	blood:	n/a
19	chr2:133868449-133868499	HepG2	liver:	n/a
20	chr2:133834998-133835048	AG04450	lung:	fetal
21	chr2:133855847-133855897	U87	brain:	n/a
22	chr2:133868449-133868499	HCF	heart:	n/a
23	chr2:133855847-133855897	HCF	heart:	n/a
24	chr2:133855847-133855897	GM19239	blood:	n/a
25	chr2:133834998-133835048	SK-N-SH	brain:	n/a
26	chr2:133868449-133868499	SAEC	small airway:	n/a
27	chr2:133855847-133855897	AG10803	skin:	n/a
28	chr2:133855847-133855897	HCPEpiC	choroid plexus:	n/a
29	chr2:133855847-133855897	RPTEC	kidney:	n/a
30	chr2:133868449-133868499	MCF10A-Er-Src	breast:	n/a
31	chr2:133834998-133835048	PANC-1	pancreas:	n/a
32	chr2:133834998-133835048	HRPEpiC	eye:	n/a
33	chr2:133834998-133835048	MCF-7	breast:	n/a
34	chr2:133855847-133855897	HCT-116	colon:	n/a
35	chr2:133855847-133855897	HL-60	blood:	n/a
36	chr2:133834998-133835048	BJ	skin:	n/a
37	chr2:133868449-133868499	CMK	blood:	n/a
38	chr2:133868449-133868499	A549	lung:	n/a
39	chr2:133855847-133855897	HRCEpiC	kidney:	n/a
40	chr2:133834998-133835048	HL-60	blood:	n/a
41	chr2:133868449-133868499	Jurkat	blood:	n/a
42	chr2:133868449-133868499	HEK293	kidney:	embryo
43	chr2:133855847-133855897	ProgFib	skin:	n/a
44	chr2:133868449-133868499	ovcar-3	ovarian:	n/a
45	chr2:133834998-133835048	Jurkat	blood:	n/a
46	chr2:133868449-133868499	AG04449	skin:	fetal
47	chr2:133855847-133855897	Hela-S3	cervix:	n/a
48	chr2:133855847-133855897	HIPEpiC	eye:	n/a
49	chr2:133834998-133835048	NB4	blood:	n/a
50	chr2:133868449-133868499	HEEpiC	esophagus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:133836968..133839255-chr2:133840150..133841905,2	K562	blood:
2	chr2:133811077..133813218-chr2:133838444..133841047,2	MCF-7	breast:
3	chr2:133850084..133851752-chr2:133851774..133853791,2	MCF-7	breast:
4	chr2:133826353..133828506-chr2:133839741..133842653,2	MCF-7	breast:
5	chr2:133828442..133830137-chr2:133831672..133833496,2	MCF-7	breast:
6	chr2:133850171..133852489-chr2:133854080..133856768,2	MCF-7	breast:
7	chr2:133836968..133839255-chr2:133840150..133841905,2	K562	blood:
8	chr2:133865556..133868534-chr2:133870878..133873548,2	K562	blood:
9	chr2:133831745..133832436-chr8:97637034..97637925,2	MCF-7	breast:
10	chr2:133850171..133852489-chr2:133854080..133856768,2	MCF-7	breast:
11	chr2:133811077..133813218-chr2:133838444..133841047,2	MCF-7	breast:
12	chr2:133427195..133430167-chr2:133854644..133856509,2	MCF-7	breast:
13	chr2:133865556..133868534-chr2:133870878..133873548,2	K562	blood:
14	chr2:133850084..133851752-chr2:133851774..133853791,2	MCF-7	breast:
15	chr2:133826353..133828506-chr2:133839741..133842653,2	MCF-7	breast:
16	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: 2417 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2417 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1550243	chr2:133811842-133811843	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs563933595	chr2:133811875-133811876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530537611	chr2:133811881-133811882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546785564	chr2:133811938-133811939	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545789474	chr2:133811941-133811942	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547381160	chr2:133812012-133812013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564053821	chr2:133812056-133812057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568602782	chr2:133812070-133812071	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187840590	chr2:133812106-133812107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535688892	chr2:133812161-133812162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369747730	chr2:133812183-133812184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539863567	chr2:133812193-133812194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143113006	chr2:133812204-133812205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546669580	chr2:133812259-133812260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs4954025	chr2:133812306-133812307	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs529043038	chr2:133812319-133812320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs16846451	chr2:133812333-133812334	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs369991865	chr2:133812343-133812344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs372586746	chr2:133812351-133812352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs537026655	chr2:133812354-133812355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs539325703	chr2:133812366-133812367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs375536474	chr2:133812369-133812370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189576126	chr2:133812382-133812383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570504869	chr2:133812383-133812384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534852986	chr2:133812394-133812395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs112111541	chr2:133812444-133812445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553386312	chr2:133812537-133812538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs558624127	chr2:133812540-133812541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182307682	chr2:133812559-133812560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs576859156	chr2:133812614-133812615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537368539	chr2:133812642-133812643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs188257973	chr2:133812674-133812675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557710149	chr2:133812723-133812724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375758076	chr2:133812738-133812739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs576038002	chr2:133812739-133812740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546509116	chr2:133812835-133812836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs564115404	chr2:133812842-133812843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs199726620	chr2:133812867-133812868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs386650738	chr2:133812868-133812869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375864692	chr2:133812869-133812870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs138757762	chr2:133812895-133812896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113300761	chr2:133812908-133812909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141207624	chr2:133813002-133813003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10545459	chr2:133813046-133813047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528200778	chr2:133813048-133813049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200319958	chr2:133813057-133813058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148965237	chr2:133813060-133813061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374651584	chr2:133813061-133813062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs5834343	chr2:133813062-133813063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs367965984	chr2:133813063-133813064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Oral cancer	21386901	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:194 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133802600-133813600	Weak transcription	Ovary	ovary
2	chr2:133807600-133812000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr2:133810400-133812000	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr2:133810600-133812000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr2:133810800-133812000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr2:133810800-133812000	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr2:133810800-133812000	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr2:133810800-133812000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr2:133810800-133813000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr2:133811000-133812000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr2:133811000-133812400	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr2:133811000-133823600	Weak transcription	Fetal Brain Male	brain
13	chr2:133811200-133812000	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr2:133811200-133812200	Enhancers	Brain Hippocampus Middle	brain
15	chr2:133811200-133812400	Enhancers	Duodenum Smooth Muscle	Duodenum
16	chr2:133811600-133812200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr2:133811600-133812200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr2:133811600-133812200	Enhancers	Stomach Smooth Muscle	stomach
19	chr2:133811800-133812000	Enhancers	Brain Anterior Caudate	brain
20	chr2:133811800-133812000	Enhancers	Brain Substantia Nigra	brain
21	chr2:133811800-133812200	Enhancers	Rectal Smooth Muscle	rectum
22	chr2:133812000-133812200	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr2:133812000-133812400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr2:133812000-133815400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr2:133812200-133812400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:133812200-133815400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr2:133812400-133813400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr2:133813400-133813600	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr2:133813600-133813800	Enhancers	Ovary	ovary
30	chr2:133815200-133815400	Weak transcription	Fetal Brain Female	brain
31	chr2:133815400-133815600	ZNF genes & repeats	Fetal Brain Female	brain
32	chr2:133815400-133815800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr2:133815400-133816200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr2:133815800-133816200	Weak transcription	Fetal Brain Female	brain
35	chr2:133816200-133816400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr2:133816400-133817000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr2:133817000-133817600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr2:133817600-133825600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr2:133819200-133819600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr2:133819200-133820600	Enhancers	Hela-S3	cervix
41	chr2:133819400-133820800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr2:133819600-133830800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr2:133819800-133820600	Enhancers	NHDF-Ad	bronchial
44	chr2:133820200-133820800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr2:133820600-133820800	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr2:133820600-133830800	Weak transcription	Hela-S3	cervix
47	chr2:133820800-133821200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr2:133820800-133825800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr2:133821800-133823600	Weak transcription	Fetal Brain Female	brain
50	chr2:133823600-133824400	Enhancers	Fetal Brain Male	brain

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