Variant report

Variant	nsv874876
Chromosome Location	chr2:113051291-113089267
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:172)
CpG islands
(count:61)
Chromatin interactive
region (count:34)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:172 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:113072097-113072909	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:113074686-113075803	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:113073870-113073910	HepG2	liver:	n/a	n/a
4	CEBPB	chr2:113061081-113061116	HepG2	liver:	n/a	chr2:113061100-113061111
5	CEBPB	chr2:113054273-113054381	H1-hESC	embryonic stem cell:	n/a	chr2:113054295-113054306
6	CEBPB	chr2:113072506-113072647	K562	blood:	n/a	chr2:113072593-113072604
7	CEBPB	chr2:113072435-113072738	A549	lung:	n/a	chr2:113072593-113072604
8	CEBPB	chr2:113072455-113072721	ECC-1	luminal epithelium:	n/a	chr2:113072593-113072604
9	CEBPB	chr2:113072456-113072748	HepG2	liver:	n/a	chr2:113072593-113072604
10	CEBPB	chr2:113061078-113061157	K562	blood:	n/a	chr2:113061100-113061111
11	CEBPB	chr2:113058842-113059151	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr2:113072401-113072796	HepG2	liver:	n/a	chr2:113072593-113072604
13	CEBPB	chr2:113058801-113059089	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:113072469-113072758	IMR90	lung:	n/a	chr2:113072593-113072604
15	CEBPB	chr2:113072403-113072782	Hela-S3	cervix:	n/a	chr2:113072593-113072604
16	CEBPB	chr2:113072448-113072804	HepG2	liver:	n/a	chr2:113072593-113072604
17	CEBPB	chr2:113072439-113072717	MCF-7	breast:	n/a	chr2:113072593-113072604
18	CEBPB	chr2:113054147-113054440	IMR90	lung:	n/a	chr2:113054295-113054306
19	CEBPB	chr2:113072422-113072742	HepG2	liver:	n/a	chr2:113072593-113072604
20	CEBPB	chr2:113054158-113054452	HepG2	liver:	n/a	chr2:113054295-113054306
21	CEBPB	chr2:113054220-113054447	K562	blood:	n/a	chr2:113054295-113054306
22	CEBPB	chr2:113072429-113072784	MCF-7	breast:	n/a	chr2:113072593-113072604
23	CEBPD	chr2:113072419-113072755	HepG2	liver:	n/a	n/a
24	CHD2	chr2:113067341-113067352	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr2:113058763-113058906	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr2:113082975-113083074	GM20000	blood:	n/a	n/a
27	E2F4	chr2:113055716-113055908	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr2:113066781-113066964	MCF10A-Er-Src	breast:	n/a	n/a
29	EBF1	chr2:113058601-113058845	GM12878	blood:	n/a	n/a
30	EP300	chr2:113072442-113072777	HepG2	liver:	n/a	chr2:113072659-113072673 chr2:113072586-113072596 chr2:113072480-113072490
31	EP300	chr2:113072296-113072970	HepG2	liver:	n/a	chr2:113072659-113072673 chr2:113072586-113072596 chr2:113072480-113072490
32	EP300	chr2:113074925-113075213	HepG2	liver:	n/a	n/a
33	EP300	chr2:113075336-113075731	HepG2	liver:	n/a	chr2:113075667-113075677
34	EP300	chr2:113072394-113072885	HepG2	liver:	n/a	chr2:113072659-113072673 chr2:113072586-113072596 chr2:113072480-113072490
35	EP300	chr2:113074772-113075770	HepG2	liver:	n/a	chr2:113075724-113075738 chr2:113075667-113075677
36	EP300	chr2:113075827-113075899	K562	blood:	n/a	n/a
37	EP300	chr2:113058929-113059305	Hela-S3	cervix:	n/a	n/a
38	FOS	chr2:113073958-113074201	MCF10A-Er-Src	breast:	n/a	chr2:113074075-113074086
39	FOS	chr2:113073972-113074250	HUVEC	blood vessel:	n/a	chr2:113074075-113074086
40	FOS	chr2:113074013-113074127	MCF10A-Er-Src	breast:	n/a	chr2:113074075-113074086
41	FOS	chr2:113075420-113075545	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr2:113073992-113074166	MCF10A-Er-Src	breast:	n/a	chr2:113074075-113074086
43	FOS	chr2:113075240-113075628	HUVEC	blood vessel:	n/a	n/a
44	FOS	chr2:113058688-113059298	HUVEC	blood vessel:	n/a	n/a
45	FOXA1	chr2:113074695-113075883	HepG2	liver:	n/a	chr2:113075664-113075676
46	FOXA1	chr2:113072310-113072860	HepG2	liver:	n/a	n/a
47	FOXA1	chr2:113072334-113073002	HepG2	liver:	n/a	n/a
48	FOXA1	chr2:113075374-113075729	HepG2	liver:	n/a	chr2:113075664-113075676
49	FOXA1	chr2:113075426-113075837	HepG2	liver:	n/a	chr2:113075664-113075676
50	FOXA1	chr2:113072363-113072846	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:113058725-113058775	PrEC	prostate:	n/a
2	chr2:113058725-113058775	GM19239	blood:	n/a
3	chr2:113058725-113058775	NT2-D1	testis:	n/a
4	chr2:113058725-113058775	NH-A	brain:	n/a
5	chr2:113058725-113058775	ECC-1	luminal epithelium:	n/a
6	chr2:113058725-113058775	HRPEpiC	eye:	n/a
7	chr2:113058725-113058775	HPAEpiC	pulmonary alveolar:	n/a
8	chr2:113058725-113058775	NHDF-neo	bronchial:	n/a
9	chr2:113058725-113058775	Caco-2	colon:	n/a
10	chr2:113058725-113058775	HEK293	kidney:	embryo
11	chr2:113058725-113058775	SK-N-MC	brain:	n/a
12	chr2:113058725-113058775	NB4	blood:	n/a
13	chr2:113058725-113058775	HepG2	liver:	n/a
14	chr2:113058725-113058775	HRE	kidney:	n/a
15	chr2:113058725-113058775	HCM	heart:	n/a
16	chr2:113058725-113058775	AG04450	lung:	fetal
17	chr2:113058725-113058775	HRCEpiC	kidney:	n/a
18	chr2:113058725-113058775	A549	lung:	n/a
19	chr2:113058725-113058775	GM12892	blood:	n/a
20	chr2:113058725-113058775	LNCaP	prostate:	n/a
21	chr2:113058725-113058775	HMEC	breast:	n/a
22	chr2:113058725-113058775	SK-N-SH_RA	brain:	n/a
23	chr2:113058725-113058775	HCT-116	colon:	n/a
24	chr2:113058725-113058775	PANC-1	pancreas:	n/a
25	chr2:113058725-113058775	Hela-S3	cervix:	n/a
26	chr2:113058725-113058775	GM12878	blood:	n/a
27	chr2:113058725-113058775	GM12891	blood:	n/a
28	chr2:113058725-113058775	AoSMC	blood vessel:	n/a
29	chr2:113058725-113058775	SAEC	small airway:	n/a
30	chr2:113058725-113058775	AG09309	skin:	n/a
31	chr2:113058725-113058775	H1-hESC	embryonic stem cell:	embryo
32	chr2:113058725-113058775	HNPCEpiC	eye:	n/a
33	chr2:113058725-113058775	T-47D	breast:	n/a
34	chr2:113058725-113058775	RPTEC	kidney:	n/a
35	chr2:113058725-113058775	HUVEC	blood vessel:	n/a
36	chr2:113058725-113058775	ovcar-3	ovarian:	n/a
37	chr2:113058725-113058775	HIPEpiC	eye:	n/a
38	chr2:113058725-113058775	MCF-7	breast:	n/a
39	chr2:113058725-113058775	CMK	blood:	n/a
40	chr2:113058725-113058775	ProgFib	skin:	n/a
41	chr2:113058725-113058775	BE2_C	brain:	n/a
42	chr2:113058725-113058775	AG10803	skin:	n/a
43	chr2:113058725-113058775	HEEpiC	esophagus:	n/a
44	chr2:113058725-113058775	HCF	heart:	n/a
45	chr2:113058725-113058775	AG09319	gingival:	n/a
46	chr2:113058725-113058775	HAEpiC	amniotic membrane:	n/a
47	chr2:113058725-113058775	SK-N-SH	brain:	n/a
48	chr2:113058725-113058775	MCF10A-Er-Src	breast:	n/a
49	chr2:113058725-113058775	IMR90	lung:	fetal
50	chr2:113058725-113058775	HCPEpiC	choroid plexus:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:113059563..113061506-chr2:113099982..113102313,2	K562	blood:
2	chr2:113067314..113070627-chr2:113070650..113073571,3	MCF-7	breast:
3	chr2:113032119..113034119-chr2:113066343..113068200,2	MCF-7	breast:
4	chr2:113059113..113060618-chr2:113068906..113071132,2	K562	blood:
5	chr2:113033709..113035506-chr2:113052735..113055582,2	K562	blood:
6	chr2:113054203..113055924-chr2:113078046..113079641,2	K562	blood:
7	chr2:113032800..113035291-chr2:113079698..113082235,2	K562	blood:
8	chr2:113032271..113034005-chr2:113074454..113077183,2	K562	blood:
9	chr2:113052733..113055599-chr2:113064270..113066173,2	MCF-7	breast:
10	chr2:113011178..113013626-chr2:113087133..113089227,2	K562	blood:
11	chr2:113058676..113061409-chr2:113063002..113065958,2	K562	blood:
12	chr2:113059113..113060618-chr2:113068906..113071132,2	K562	blood:
13	chr2:113070301..113072407-chr2:113075065..113076958,2	K562	blood:
14	chr2:113073679..113075576-chr2:113078954..113082131,3	K562	blood:
15	chr2:113031293..113035273-chr2:113059413..113062262,3	MCF-7	breast:
16	chr2:113070638..113072405-chr2:113074120..113076541,2	MCF-7	breast:
17	chr2:113080011..113082440-chr2:113099330..113101627,2	K562	blood:
18	chr2:113059113..113060824-chr2:113069400..113071132,2	K562	blood:
19	chr2:113052733..113055599-chr2:113064270..113066173,2	MCF-7	breast:
20	chr2:113054203..113055924-chr2:113078046..113079641,2	K562	blood:
21	chr2:113065168..113067342-chr2:113068406..113071056,2	K562	blood:
22	chr2:113031311..113033993-chr2:113061525..113063078,2	K562	blood:
23	chr2:113065168..113067342-chr2:113068406..113071056,2	K562	blood:
24	chr2:113059113..113060824-chr2:113069400..113071132,2	K562	blood:
25	chr2:113032164..113034154-chr2:113058503..113060205,2	K562	blood:
26	chr2:113070301..113072407-chr2:113075065..113076958,2	K562	blood:
27	chr2:113033771..113036191-chr2:113057480..113059266,2	K562	blood:
28	chr2:113070638..113072405-chr2:113074120..113076541,2	MCF-7	breast:
29	chr2:113032266..113035570-chr2:113088065..113092560,6	MCF-7	breast:
30	chr2:113067314..113070627-chr2:113070650..113073571,3	MCF-7	breast:
31	chr2:113073679..113075576-chr2:113078954..113082131,3	K562	blood:
32	chr2:113058676..113061409-chr2:113063002..113065958,2	K562	blood:
33	chr2:112973461..112975614-chr2:113086983..113088947,2	K562	blood:
34	chr2:113033406..113035209-chr2:113052659..113055582,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBLN7-4	chr2:113065544-113065987	NONHSAT073690
2	lnc-FBLN7-4	chr2:113064844-113064928	NONHSAT073690

No data

Variant related genes	Relation type
ZC3H6	TF binding region
ENSG00000248341	TF binding region
ZC3H6	CpG island
ENSG00000248341	CpG island
ENSG00000188177	chromatin interactions
ENSG00000144161	chromatin interactions

Extended variants
information (count: 1223 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10203614	chr2:113051291-113051292	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs367574655	chr2:113051357-113051358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183378555	chr2:113051360-113051361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554570456	chr2:113051389-113051390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188364389	chr2:113051402-113051403	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs536158434	chr2:113051409-113051410	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs556284235	chr2:113051420-113051421	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs114348088	chr2:113051460-113051461	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs10203843	chr2:113051511-113051512	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs564822248	chr2:113051535-113051536	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572141801	chr2:113051673-113051674	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
12	rs541008187	chr2:113051694-113051695	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs544487597	chr2:113051701-113051702	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs4539797	chr2:113051746-113051747	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs550496582	chr2:113051747-113051748	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
16	rs554798402	chr2:113051753-113051754	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs532587333	chr2:113051774-113051775	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs192041113	chr2:113051775-113051776	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs566018303	chr2:113051782-113051783	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
20	rs574864969	chr2:113051800-113051801	Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs534811735	chr2:113051815-113051816	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs555277515	chr2:113051816-113051817	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs548146372	chr2:113051833-113051834	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs115414732	chr2:113051883-113051884	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs536095650	chr2:113051905-113051906	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs572919847	chr2:113051928-113051929	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs540227911	chr2:113051993-113051994	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs540323196	chr2:113051998-113051999	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs556180766	chr2:113052004-113052005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs576328918	chr2:113052006-113052007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs74908122	chr2:113052025-113052026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs558747114	chr2:113052047-113052048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs183668536	chr2:113052073-113052074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554147672	chr2:113052078-113052079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560817066	chr2:113052149-113052150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs574479132	chr2:113052176-113052177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs35415720	chr2:113052202-113052203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs577130906	chr2:113052216-113052217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs564984243	chr2:113052219-113052220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563812458	chr2:113052309-113052310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs546110751	chr2:113052354-113052355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532867740	chr2:113052362-113052363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs142141328	chr2:113052389-113052390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187898546	chr2:113052417-113052418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs528526288	chr2:113052419-113052420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs548279616	chr2:113052424-113052425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs568262053	chr2:113052432-113052433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562823140	chr2:113052445-113052446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537040728	chr2:113052519-113052520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs550989464	chr2:113052528-113052529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	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
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Lung cancer	18438408	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:875 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113034200-113058200	Weak transcription	Ovary	ovary
2	chr2:113034400-113051400	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr2:113034400-113097000	Weak transcription	Psoas Muscle	Psoas
4	chr2:113035000-113057800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr2:113035000-113057800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr2:113035000-113057800	Weak transcription	Fetal Intestine Small	intestine
7	chr2:113035600-113058200	Weak transcription	Primary B cells from cord blood	blood
8	chr2:113035800-113058000	Weak transcription	Primary T cells from cord blood	blood
9	chr2:113035800-113060400	Weak transcription	Fetal Thymus	thymus
10	chr2:113035800-113067400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr2:113036600-113058000	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr2:113037000-113054200	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr2:113040000-113081800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr2:113040600-113054400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr2:113041200-113058600	Weak transcription	Fetal Heart	heart
16	chr2:113041400-113058600	Weak transcription	K562	blood
17	chr2:113042400-113051600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr2:113045600-113051400	Weak transcription	Aorta	Aorta
19	chr2:113046000-113052600	Weak transcription	Fetal Lung	lung
20	chr2:113046200-113057800	Weak transcription	Thymus	Thymus
21	chr2:113046600-113079800	Weak transcription	Fetal Stomach	stomach
22	chr2:113046800-113065000	Weak transcription	HSMMtube	muscle
23	chr2:113047200-113058200	Weak transcription	Primary B cells from peripheral blood	blood
24	chr2:113047600-113058400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr2:113048000-113052200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr2:113048000-113084400	Weak transcription	Fetal Kidney	kidney
27	chr2:113048200-113051400	Weak transcription	Osteobl	bone
28	chr2:113048200-113051600	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr2:113048200-113064200	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr2:113048400-113051400	Weak transcription	Spleen	Spleen
31	chr2:113048400-113061000	Weak transcription	Brain Hippocampus Middle	brain
32	chr2:113048600-113051800	Weak transcription	Brain Cingulate Gyrus	brain
33	chr2:113048600-113060800	Weak transcription	Brain Substantia Nigra	brain
34	chr2:113048600-113081600	Weak transcription	Brain Anterior Caudate	brain
35	chr2:113048600-113081800	Weak transcription	Duodenum Mucosa	Duodenum
36	chr2:113049000-113054200	Weak transcription	Liver	Liver
37	chr2:113050400-113057800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr2:113050600-113090600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr2:113051000-113053000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr2:113051000-113088600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr2:113051400-113051600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr2:113051400-113051600	Genic enhancers	Aorta	Aorta
43	chr2:113051400-113051600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr2:113051400-113051600	Enhancers	Esophagus	oesophagus
45	chr2:113051400-113051600	Enhancers	Spleen	Spleen
46	chr2:113051400-113051800	Enhancers	Gastric	stomach
47	chr2:113051400-113051800	Enhancers	Left Ventricle	heart
48	chr2:113051400-113051800	Enhancers	Lung	lung
49	chr2:113051400-113051800	Enhancers	Pancreas	Pancrea
50	chr2:113051400-113051800	Enhancers	Right Atrium	heart

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