Variant report

Variant	nsv899022
Chromosome Location	chr12:40014427-40111761
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:571)
CpG islands
(count:552)
Chromatin interactive
region (count:10)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:571 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:40019707-40020121	K562	blood:	n/a	n/a
2	ARID3A	chr12:40067214-40067268	K562	blood:	n/a	n/a
3	ATF1	chr12:40017728-40018001	K562	blood:	n/a	n/a
4	ATF1	chr12:40106808-40106910	K562	blood:	n/a	n/a
5	ATF1	chr12:40107344-40107573	K562	blood:	n/a	n/a
6	ATF2	chr12:40017642-40018058	GM12878	blood:	n/a	n/a
7	ATF2	chr12:40013016-40014468	GM12878	blood:	n/a	n/a
8	ATF2	chr12:40017634-40018151	GM12878	blood:	n/a	n/a
9	ATF2	chr12:40014910-40015547	GM12878	blood:	n/a	n/a
10	ATF2	chr12:40015033-40015558	GM12878	blood:	n/a	n/a
11	BATF	chr12:40015177-40015564	GM12878	blood:	n/a	chr12:40015361-40015369
12	BCL11A	chr12:40015148-40015466	GM12878	blood:	n/a	n/a
13	BCL11A	chr12:40015067-40015497	GM12878	blood:	n/a	n/a
14	BCLAF1	chr12:40015092-40015585	GM12878	blood:	n/a	n/a
15	BCLAF1	chr12:40014878-40015503	GM12878	blood:	n/a	n/a
16	BHLHE40	chr12:40013084-40014481	GM12878	blood:	n/a	n/a
17	BHLHE40	chr12:40019763-40020115	K562	blood:	n/a	n/a
18	CBX3	chr12:40019734-40020137	K562	blood:	n/a	chr12:40019836-40019847
19	CBX3	chr12:40019741-40020095	K562	blood:	n/a	chr12:40019836-40019847
20	CCNT2	chr12:40037078-40037214	K562	blood:	n/a	n/a
21	CCNT2	chr12:40019858-40020181	K562	blood:	n/a	n/a
22	CEBPB	chr12:40040306-40040529	HepG2	liver:	n/a	chr12:40040390-40040403 chr12:40040391-40040402 chr12:40040390-40040403 chr12:40040390-40040401
23	CEBPB	chr12:40032631-40032972	A549	lung:	n/a	chr12:40032834-40032845
24	CEBPB	chr12:40032669-40032993	K562	blood:	n/a	chr12:40032834-40032845
25	CEBPB	chr12:40032657-40033014	HepG2	liver:	n/a	chr12:40032834-40032845
26	CEBPB	chr12:40032653-40033033	Hela-S3	cervix:	n/a	chr12:40032834-40032845
27	CEBPB	chr12:40032511-40033162	K562	blood:	n/a	chr12:40032834-40032845
28	CEBPB	chr12:40032622-40033089	MCF-7	breast:	n/a	chr12:40032834-40032845
29	CEBPB	chr12:40045629-40045769	A549	lung:	n/a	chr12:40045690-40045701
30	CEBPB	chr12:40104177-40104367	A549	lung:	n/a	chr12:40104348-40104361
31	CEBPB	chr12:40032626-40033028	ECC-1	luminal epithelium:	n/a	chr12:40032834-40032845
32	CEBPB	chr12:40013272-40015600	GM12878	blood:	n/a	chr12:40013664-40013672
33	CEBPB	chr12:40032663-40033020	H1-hESC	embryonic stem cell:	n/a	chr12:40032834-40032845
34	CEBPB	chr12:40032695-40032948	K562	blood:	n/a	chr12:40032834-40032845
35	CEBPB	chr12:40032699-40033055	ECC-1	luminal epithelium:	n/a	chr12:40032834-40032845
36	CEBPB	chr12:40032653-40033024	IMR90	lung:	n/a	chr12:40032834-40032845
37	CEBPB	chr12:40040846-40041116	A549	lung:	n/a	chr12:40040993-40041004 chr12:40040994-40041005
38	CEBPB	chr12:40103147-40103392	HepG2	liver:	n/a	chr12:40103250-40103261
39	CEBPB	chr12:40032575-40033116	A549	lung:	n/a	chr12:40032834-40032845
40	CEBPB	chr12:40032661-40033023	A549	lung:	n/a	chr12:40032834-40032845
41	CEBPB	chr12:40045552-40045833	HepG2	liver:	n/a	chr12:40045690-40045701
42	CEBPB	chr12:40020393-40020736	K562	blood:	n/a	n/a
43	CEBPB	chr12:40042634-40042886	HepG2	liver:	n/a	chr12:40042762-40042775 chr12:40042763-40042774
44	CEBPB	chr12:40040823-40041125	HepG2	liver:	n/a	chr12:40040993-40041004 chr12:40040994-40041005
45	CEBPB	chr12:40045625-40045736	K562	blood:	n/a	chr12:40045690-40045701
46	CEBPB	chr12:40042687-40042907	A549	lung:	n/a	chr12:40042762-40042775 chr12:40042763-40042774
47	CHD1	chr12:40012703-40014800	GM12878	blood:	n/a	n/a
48	CHD2	chr12:40020304-40020573	K562	blood:	n/a	n/a
49	CREB1	chr12:40017673-40018269	GM12878	blood:	n/a	n/a
50	CTCF	chr12:40086160-40086310	HPAF	blood vessel:	n/a	n/a

(count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:40019532-40019582	NHBE	bronchial:	n/a
2	chr12:40093087-40093137	HEEpiC	esophagus:	n/a
3	chr12:40020000-40020050	HL-60	blood:	n/a
4	chr12:40019532-40019582	NHBE	bronchial:	n/a
5	chr12:40093087-40093137	HEEpiC	esophagus:	n/a
6	chr12:40020000-40020050	HL-60	blood:	n/a
7	chr12:40019768-40019818	GM12891	blood:	n/a
8	chr12:40019883-40019933	H1-hESC	embryonic stem cell:	embryo
9	chr12:40093094-40093144	NT2-D1	testis:	n/a
10	chr12:40020000-40020050	HRCEpiC	kidney:	n/a
11	chr12:40019907-40019957	HMEC	breast:	n/a
12	chr12:40020000-40020050	ECC-1	luminal epithelium:	n/a
13	chr12:40019919-40019969	K562	blood:	n/a
14	chr12:40019919-40019969	HCT-116	colon:	n/a
15	chr12:40020078-40020128	HEEpiC	esophagus:	n/a
16	chr12:40019883-40019933	NH-A	brain:	n/a
17	chr12:40019907-40019957	HRCEpiC	kidney:	n/a
18	chr12:40019907-40019957	ProgFib	skin:	n/a
19	chr12:40020000-40020050	HRPEpiC	eye:	n/a
20	chr12:40019532-40019582	GM19239	blood:	n/a
21	chr12:40093094-40093144	SK-N-MC	brain:	n/a
22	chr12:40019907-40019957	SKMC	muscle:	n/a
23	chr12:40019919-40019969	GM12892	blood:	n/a
24	chr12:40019532-40019582	H1-hESC	embryonic stem cell:	embryo
25	chr12:40019919-40019969	U87	brain:	n/a
26	chr12:40093087-40093137	GM12878	blood:	n/a
27	chr12:40019919-40019969	PANC-1	pancreas:	n/a
28	chr12:40019768-40019818	GM12878	blood:	n/a
29	chr12:40093087-40093137	U87	brain:	n/a
30	chr12:40020078-40020128	SAEC	small airway:	n/a
31	chr12:40020000-40020050	SK-N-MC	brain:	n/a
32	chr12:40019919-40019969	HEEpiC	esophagus:	n/a
33	chr12:40020078-40020128	HCT-116	colon:	n/a
34	chr12:40019532-40019582	HIPEpiC	eye:	n/a
35	chr12:40093094-40093144	GM12878	blood:	n/a
36	chr12:40019919-40019969	SAEC	small airway:	n/a
37	chr12:40019919-40019969	T-47D	breast:	n/a
38	chr12:40019768-40019818	LNCaP	prostate:	n/a
39	chr12:40093094-40093144	GM06990	blood:	n/a
40	chr12:40019532-40019582	SK-N-MC	brain:	n/a
41	chr12:40020000-40020050	SAEC	small airway:	n/a
42	chr12:40019883-40019933	HCF	heart:	n/a
43	chr12:40093087-40093137	AoSMC	blood vessel:	n/a
44	chr12:40020000-40020050	IMR90	lung:	fetal
45	chr12:40019768-40019818	NHDF-neo	bronchial:	n/a
46	chr12:40019532-40019582	PrEC	prostate:	n/a
47	chr12:40020000-40020050	BE2_C	brain:	n/a
48	chr12:40020078-40020128	NT2-D1	testis:	n/a
49	chr12:40019768-40019818	HCT-116	colon:	n/a
50	chr12:40019883-40019933	LNCaP	prostate:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:40010562..40012556-chr12:40014262..40016328,2	K562	blood:
2	chr12:39711735..39712649-chr12:40077357..40078312,2	K562	blood:
3	chr12:40011374..40014177-chr12:40021729..40023684,2	MCF-7	breast:
4	chr12:40065514..40066416-chr12:107873474..107874173,2	MCF-7	breast:
5	chr12:40041383..40044331-chr12:40082931..40085850,2	K562	blood:
6	chr12:40015362..40017426-chr12:40020461..40022505,2	MCF-7	breast:
7	chr12:40012703..40015318-chr12:40031815..40033811,2	K562	blood:
8	chr12:40041383..40044331-chr12:40082931..40085850,2	K562	blood:
9	chr12:40014171..40017168-chr12:40017549..40021409,3	K562	blood:
10	chr12:40015362..40017426-chr12:40020461..40022505,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABCD2-3	chr12:40035446-40035663	uc_337_-
2	lnc-LRRK2-2	chr12:40035446-40035663	uc_337_+

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C12orf40	hsa-miR-1	chr12:40076763-40076785

Variant related genes	Relation type
C12orf40	TF binding region
ABCD2	TF binding region
C12orf40	CpG island
ABCD2	CpG island
ENSG00000173208	chromatin interactions
ENSG00000180116	chromatin interactions

Extended variants
information (count: 2465 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2465 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4072006	chr12:40014427-40014428	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs549014133	chr12:40014446-40014447	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs374109676	chr12:40014460-40014461	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs190598303	chr12:40014498-40014499	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs563817967	chr12:40014543-40014544	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs148086755	chr12:40014546-40014547	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs564750594	chr12:40014568-40014569	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs4072005	chr12:40014581-40014582	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs549557956	chr12:40014613-40014614	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs567873957	chr12:40014642-40014643	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs141817407	chr12:40014643-40014644	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs150591474	chr12:40014790-40014791	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs565521704	chr12:40014809-40014810	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs371559982	chr12:40014828-40014829	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs182883994	chr12:40014869-40014870	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs34112970	chr12:40014889-40014890	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs79169990	chr12:40014911-40014912	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs111871190	chr12:40014932-40014933	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs368231066	chr12:40014975-40014976	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs569367786	chr12:40014984-40014985	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs74818159	chr12:40014988-40014989	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs141771382	chr12:40014989-40014990	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs529491821	chr12:40015032-40015033	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs187902509	chr12:40015080-40015081	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs540946276	chr12:40015097-40015098	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs553267894	chr12:40015108-40015109	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs369037469	chr12:40015112-40015113	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs545338632	chr12:40015128-40015129	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs563682285	chr12:40015138-40015139	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs530991477	chr12:40015145-40015146	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs190927652	chr12:40015166-40015167	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs146236970	chr12:40015244-40015245	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs554090015	chr12:40015261-40015262	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs528715950	chr12:40015263-40015264	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs546967488	chr12:40015269-40015270	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs6581228	chr12:40015286-40015287	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs377717053	chr12:40015323-40015324	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs532699675	chr12:40015397-40015398	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs550924713	chr12:40015454-40015455	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs569329854	chr12:40015462-40015463	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs536723236	chr12:40015519-40015520	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs11172886	chr12:40015535-40015536	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs145077716	chr12:40015597-40015598	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs555073713	chr12:40015655-40015656	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs139234933	chr12:40015691-40015692	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs534861377	chr12:40015692-40015693	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs557757556	chr12:40015776-40015777	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs377643368	chr12:40015829-40015830	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs577826313	chr12:40015830-40015831	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs144036632	chr12:40015832-40015833	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:502 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40006800-40015000	Active TSS	GM12878-XiMat	blood
2	chr12:40009400-40015400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr12:40009600-40014800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
4	chr12:40009600-40015000	Active TSS	Primary T killer memory cells from peripheral blood	blood
5	chr12:40009800-40014800	Active TSS	Brain Angular Gyrus	brain
6	chr12:40009800-40015000	Active TSS	Primary T cells fromperipheralblood	blood
7	chr12:40009800-40015000	Active TSS	Primary T helper naive cells from peripheral blood	blood
8	chr12:40009800-40015200	Active TSS	Brain Inferior Temporal Lobe	brain
9	chr12:40009800-40015200	Active TSS	Right Atrium	heart
10	chr12:40010200-40014600	Active TSS	Brain Germinal Matrix	brain
11	chr12:40010800-40015000	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
12	chr12:40011800-40015200	Active TSS	Brain Cingulate Gyrus	brain
13	chr12:40012000-40014600	Active TSS	Brain Substantia Nigra	brain
14	chr12:40012200-40014600	Active TSS	Colon Smooth Muscle	Colon
15	chr12:40012400-40014600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr12:40012600-40014600	Active TSS	Right Ventricle	heart
17	chr12:40012600-40014800	Active TSS	Psoas Muscle	Psoas
18	chr12:40012600-40015000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr12:40012600-40015200	Active TSS	Colonic Mucosa	Colon
20	chr12:40012800-40014600	Active TSS	Fetal Brain Female	brain
21	chr12:40012800-40014600	Active TSS	Thymus	Thymus
22	chr12:40012800-40014800	Active TSS	Muscle Satellite Cultured Cells	--
23	chr12:40012800-40014800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr12:40012800-40014800	Active TSS	Brain Hippocampus Middle	brain
25	chr12:40012800-40014800	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr12:40012800-40015000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr12:40012800-40015200	Active TSS	Primary T killer naive cells fromperipheralblood	blood
28	chr12:40013000-40014600	Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr12:40013000-40014600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr12:40013000-40014600	Active TSS	Ovary	ovary
31	chr12:40013000-40014800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr12:40013000-40014800	Active TSS	Duodenum Smooth Muscle	Duodenum
33	chr12:40013000-40014800	Active TSS	Fetal Brain Male	brain
34	chr12:40013000-40014800	Active TSS	HSMMtube	muscle
35	chr12:40013000-40015000	Active TSS	Rectal Mucosa Donor 29	rectum
36	chr12:40013000-40015200	Active TSS	Rectal Smooth Muscle	rectum
37	chr12:40013200-40014600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
38	chr12:40013200-40014600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
39	chr12:40013200-40014600	Active TSS	Brain Anterior Caudate	brain
40	chr12:40013200-40014600	Active TSS	Fetal Thymus	thymus
41	chr12:40013200-40014800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr12:40013200-40014800	Active TSS	Aorta	Aorta
43	chr12:40013200-40014800	Active TSS	Stomach Smooth Muscle	stomach
44	chr12:40013200-40015000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr12:40013200-40015200	Active TSS	Duodenum Mucosa	Duodenum
46	chr12:40013400-40014600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr12:40013400-40014600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr12:40013400-40014600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr12:40013400-40014600	Flanking Active TSS	Liver	Liver
50	chr12:40013400-40014600	Active TSS	Fetal Intestine Small	intestine

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