Variant report

Variant	nsv1038100
Chromosome Location	chr12:59983391-60018745
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:59990012-59990103	HepG2	liver:	n/a	n/a
2	ATF2	chr12:59991078-59991577	GM12878	blood:	n/a	n/a
3	ATF2	chr12:59990321-59991736	GM12878	blood:	n/a	n/a
4	BACH1	chr12:59989925-59990860	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr12:59991262-59991562	GM12878	blood:	n/a	n/a
6	BATF	chr12:59991182-59991631	GM12878	blood:	n/a	n/a
7	BCLAF1	chr12:59991058-59991596	GM12878	blood:	n/a	n/a
8	BCLAF1	chr12:59990577-59991601	GM12878	blood:	n/a	n/a
9	BHLHE40	chr12:59997664-59997902	GM12878	blood:	n/a	n/a
10	BHLHE40	chr12:59989349-59991652	GM12878	blood:	n/a	chr12:59990247-59990263 chr12:59990812-59990825 chr12:59989835-59989851
11	BHLHE40	chr12:59989927-59991031	HepG2	liver:	n/a	chr12:59990247-59990263 chr12:59990812-59990825
12	BRCA1	chr12:59990365-59990437	GM12878	blood:	n/a	n/a
13	BRCA1	chr12:59989213-59989930	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr12:59990143-59990337	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr12:59988732-59988981	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr12:59990664-59990725	GM12878	blood:	n/a	n/a
17	BRCA1	chr12:59990326-59991667	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr12:59991282-59991742	HepG2	liver:	n/a	chr12:59991450-59991461 chr12:59991297-59991309
19	CEBPB	chr12:60012914-60013188	HepG2	liver:	n/a	chr12:60013037-60013048 chr12:60013039-60013048 chr12:60013039-60013050
20	CEBPB	chr12:59988714-59991772	Hela-S3	cervix:	n/a	chr12:59991450-59991461 chr12:59988794-59988811 chr12:59988905-59988916 chr12:59991297-59991309 chr12:59988904-59988915
21	CEBPB	chr12:59988739-59989096	IMR90	lung:	n/a	chr12:59988794-59988811 chr12:59988905-59988916 chr12:59988904-59988915
22	CEBPB	chr12:59991331-59991648	H1-hESC	embryonic stem cell:	n/a	chr12:59991450-59991461
23	CEBPB	chr12:59988780-59988981	H1-hESC	embryonic stem cell:	n/a	chr12:59988794-59988811 chr12:59988905-59988916 chr12:59988904-59988915
24	CEBPB	chr12:59993954-59994284	Hela-S3	cervix:	n/a	chr12:59994188-59994199 chr12:59994100-59994113 chr12:59994102-59994113
25	CEBPB	chr12:59991165-59991683	MCF-7	breast:	n/a	chr12:59991450-59991461 chr12:59991297-59991309
26	CEBPB	chr12:60012900-60013219	IMR90	lung:	n/a	chr12:60013037-60013048 chr12:60013039-60013048 chr12:60013039-60013050
27	CEBPB	chr12:59990609-59991795	IMR90	lung:	n/a	chr12:59991450-59991461 chr12:59991297-59991309
28	CEBPB	chr12:59988728-59989074	A549	lung:	n/a	chr12:59988794-59988811 chr12:59988905-59988916 chr12:59988904-59988915
29	CEBPB	chr12:59988728-59989092	HepG2	liver:	n/a	chr12:59988794-59988811 chr12:59988905-59988916 chr12:59988904-59988915
30	CEBPB	chr12:59994032-59994281	HepG2	liver:	n/a	chr12:59994188-59994199 chr12:59994100-59994113 chr12:59994102-59994113
31	CEBPB	chr12:59994046-59994197	A549	lung:	n/a	chr12:59994100-59994113 chr12:59994102-59994113
32	CEBPB	chr12:59990550-59991546	GM12878	blood:	n/a	chr12:59991450-59991461 chr12:59991297-59991309
33	CEBPB	chr12:59991288-59991748	MCF-7	breast:	n/a	chr12:59991450-59991461 chr12:59991297-59991309
34	CEBPB	chr12:59991311-59991709	A549	lung:	n/a	chr12:59991450-59991461
35	CEBPB	chr12:60012888-60013175	A549	lung:	n/a	chr12:60013037-60013048 chr12:60013039-60013048 chr12:60013039-60013050
36	CHD1	chr12:59990641-59991348	GM12878	blood:	n/a	n/a
37	CHD2	chr12:59989507-59991676	Hela-S3	cervix:	n/a	chr12:59989742-59989752
38	CHD2	chr12:59990104-59990364	HepG2	liver:	n/a	n/a
39	CHD2	chr12:59990239-59990929	GM12878	blood:	n/a	n/a
40	CHD2	chr12:59989937-59991017	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr12:59989745-59990565	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr12:59989775-59991005	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTBP2	chr12:59989838-59990925	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr12:59990555-59990999	GM12878	blood:	n/a	n/a
45	CTCF	chr12:59989760-59989910	GM12867	blood:	n/a	n/a
46	CTCF	chr12:59990459-59990468	MCF-7	breast:	n/a	n/a
47	CTCF	chr12:59990000-59990150	HCM	heart:	n/a	n/a
48	CTCF	chr12:60000850-60000862	GM10248	blood:	n/a	n/a
49	CTCF	chr12:59991340-59991490	AG10803	skin:	n/a	n/a
50	CTCF	chr12:59993978-59994193	GM12878	blood:	n/a	chr12:59994076-59994097 chr12:59994075-59994091 chr12:59994074-59994092

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:59989742-59989792	NT2-D1	testis:	n/a
2	chr12:59986233-59986283	GM19239	blood:	n/a
3	chr12:59989742-59989792	NT2-D1	testis:	n/a
4	chr12:59986233-59986283	GM19239	blood:	n/a
5	chr12:59990894-59990944	Hepatocyte	liver:	n/a
6	chr12:59990794-59990844	AG10803	skin:	n/a
7	chr12:59989652-59989702	AG04450	lung:	fetal
8	chr12:59990675-59990725	SK-N-SH	brain:	n/a
9	chr12:59990794-59990844	HCM	heart:	n/a
10	chr12:59990420-59990470	PANC-1	pancreas:	n/a
11	chr12:59989535-59989585	BE2_C	brain:	n/a
12	chr12:59989742-59989792	GM19239	blood:	n/a
13	chr12:59990420-59990470	HPAEpiC	pulmonary alveolar:	n/a
14	chr12:59993762-59993812	HMEC	breast:	n/a
15	chr12:59990894-59990944	NH-A	brain:	n/a
16	chr12:59986233-59986283	HMEC	breast:	n/a
17	chr12:59993762-59993812	HRE	kidney:	n/a
18	chr12:59990420-59990470	HCM	heart:	n/a
19	chr12:59990420-59990470	HCPEpiC	choroid plexus:	n/a
20	chr12:59989735-59989785	SK-N-SH_RA	brain:	n/a
21	chr12:59986233-59986283	SAEC	small airway:	n/a
22	chr12:59990675-59990725	NH-A	brain:	n/a
23	chr12:59990894-59990944	HIPEpiC	eye:	n/a
24	chr12:59990420-59990470	MCF-7	breast:	n/a
25	chr12:59990120-59990170	HEK293	kidney:	embryo
26	chr12:59990120-59990170	NHDF-neo	bronchial:	n/a
27	chr12:59990894-59990944	HepG2	liver:	n/a
28	chr12:59990794-59990844	MCF-7	breast:	n/a
29	chr12:59989742-59989792	U87	brain:	n/a
30	chr12:59989535-59989585	HCPEpiC	choroid plexus:	n/a
31	chr12:59990894-59990944	IMR90	lung:	fetal
32	chr12:59990120-59990170	HAEpiC	amniotic membrane:	n/a
33	chr12:59990420-59990470	HRCEpiC	kidney:	n/a
34	chr12:59986233-59986283	PFSK-1	brain:	n/a
35	chr12:59990120-59990170	SKMC	muscle:	n/a
36	chr12:59993762-59993812	MCF-7	breast:	n/a
37	chr12:59989742-59989792	HMEC	breast:	n/a
38	chr12:59986233-59986283	GM12891	blood:	n/a
39	chr12:59993762-59993812	IMR90	lung:	fetal
40	chr12:59990794-59990844	HEK293	kidney:	embryo
41	chr12:59986233-59986283	HPAEpiC	pulmonary alveolar:	n/a
42	chr12:59990894-59990944	AG09309	skin:	n/a
43	chr12:59986233-59986283	HepG2	liver:	n/a
44	chr12:59989652-59989702	LNCaP	prostate:	n/a
45	chr12:59989735-59989785	HRE	kidney:	n/a
46	chr12:59989535-59989585	HMEC	breast:	n/a
47	chr12:59990794-59990844	Jurkat	blood:	n/a
48	chr12:59990120-59990170	HL-60	blood:	n/a
49	chr12:59990794-59990844	AG04450	lung:	fetal
50	chr12:59990794-59990844	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:59998248..60000809-chr12:60000863..60003196,2	MCF-7	breast:
2	chr12:59989713..59992381-chr12:60015573..60017703,2	MCF-7	breast:
3	chr12:59993759..59996018-chr12:59997154..59999022,2	MCF-7	breast:
4	chr12:59998248..60000809-chr12:60000863..60003196,2	MCF-7	breast:
5	chr12:59989176..59992374-chr12:59998507..60002701,5	MCF-7	breast:
6	chr12:59983299..59985643-chr12:59988143..59990985,2	K562	blood:
7	chr12:59990837..59991400-chr3:15373811..15374535,2	Hela-S3	cervix:
8	chr12:59993257..59995934-chr12:60002294..60005261,2	MCF-7	breast:
9	chr12:60015509..60017569-chr12:60019579..60022137,3	MCF-7	breast:
10	chr12:59990404..59991079-chr15:65596908..65597443,2	Hela-S3	cervix:
11	chr12:59993257..59995934-chr12:60002294..60005261,2	MCF-7	breast:
12	chr12:59990876..59991528-chr9:32552220..32553126,2	Hela-S3	cervix:
13	chr12:59990711..59992487-chr12:59993395..59995122,2	MCF-7	breast:
14	chr12:60013598..60016258-chr12:60017696..60019251,2	MCF-7	breast:
15	chr12:60017381..60019392-chr12:60100051..60102873,2	MCF-7	breast:
16	chr12:59987463..59989577-chr12:59995845..59998372,2	MCF-7	breast:
17	chr12:59982239..59984090-chr12:59987123..59989672,2	MCF-7	breast:
18	chr12:59990114..59991690-chr12:59995288..59997168,2	MCF-7	breast:
19	chr12:60013598..60016258-chr12:60017696..60019251,2	MCF-7	breast:
20	chr12:59993759..59996018-chr12:59997154..59999022,2	MCF-7	breast:
21	chr12:59987463..59989577-chr12:59995845..59998372,2	MCF-7	breast:
22	chr12:59982239..59984090-chr12:59987123..59989672,2	MCF-7	breast:
23	chr12:59989688..59990375-chr9:133568932..133569541,2	Hela-S3	cervix:
24	chr12:59988960..59991017-chr12:60010230..60012662,2	MCF-7	breast:
25	chr12:59989792..59990315-chr20:388080..388989,2	Hela-S3	cervix:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-362K2.2.1-5	chr12:60011428-60011651	NONHSAT029052

Variant related genes	Relation type
RNU4-20P	TF binding region
SLC16A7	TF binding region
RNU4-20P	CpG island
SLC16A7	CpG island
ENSG00000130713	chromatin interactions
ENSG00000131370	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000118596	chromatin interactions
ENSG00000197579	chromatin interactions
ENSG00000235453	chromatin interactions
ENSG00000125826	chromatin interactions

Extended variants
information (count: 1254 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1254 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142250435	chr12:59983421-59983422	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs77555151	chr12:59983431-59983432	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs7966616	chr12:59983472-59983473	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs570264571	chr12:59983480-59983481	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150598992	chr12:59983481-59983482	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs559142601	chr12:59983516-59983517	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs537723322	chr12:59983593-59983594	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs149334521	chr12:59983635-59983636	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs577419263	chr12:59983645-59983646	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs535079460	chr12:59983701-59983702	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs553349759	chr12:59983723-59983724	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs368765449	chr12:59983785-59983786	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs542137881	chr12:59983790-59983791	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs192792049	chr12:59983937-59983938	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs563421621	chr12:59983954-59983955	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs61936293	chr12:59983987-59983988	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs575140957	chr12:59984024-59984025	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs4249321	chr12:59984037-59984038	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs11173092	chr12:59984038-59984039	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs10877319	chr12:59984079-59984080	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs546348592	chr12:59984113-59984114	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs373653737	chr12:59984136-59984137	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs376666913	chr12:59984189-59984190	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs548905773	chr12:59984241-59984242	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs570250809	chr12:59984285-59984286	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs564237708	chr12:59984296-59984297	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs181169334	chr12:59984300-59984301	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs184580802	chr12:59984304-59984305	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs74331368	chr12:59984371-59984372	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs10783992	chr12:59984392-59984393	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs553172876	chr12:59984394-59984395	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs574813541	chr12:59984416-59984417	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs375776575	chr12:59984473-59984474	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs115276686	chr12:59984487-59984488	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs557272664	chr12:59984590-59984591	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs1391130	chr12:59984687-59984688	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs373601791	chr12:59984750-59984751	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs531358704	chr12:59984759-59984760	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs146721095	chr12:59984881-59984882	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs368062533	chr12:59984930-59984931	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs1566164	chr12:59984968-59984969	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs144678134	chr12:59985097-59985098	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs540356975	chr12:59985118-59985119	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs375274756	chr12:59985119-59985120	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs568101487	chr12:59985139-59985140	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs140322878	chr12:59985148-59985149	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs144053066	chr12:59985158-59985159	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs188897671	chr12:59985185-59985186	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs533168881	chr12:59985207-59985208	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs371030765	chr12:59985208-59985209	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:899 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:59981400-59989400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:59981600-59984400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr12:59981800-59988200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr12:59984400-59984600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr12:59984600-59988600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr12:59985400-59986400	Enhancers	Thymus	Thymus
7	chr12:59986400-59988800	Weak transcription	Thymus	Thymus
8	chr12:59987000-59988800	Weak transcription	Stomach Mucosa	stomach
9	chr12:59987600-59988800	Enhancers	Dnd41	blood
10	chr12:59987800-59988800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr12:59987800-59989000	Enhancers	Primary T cells from cord blood	blood
12	chr12:59988200-59988800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr12:59988200-59989000	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr12:59988200-59989000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr12:59988200-59989000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
16	chr12:59988200-59989000	Enhancers	NHDF-Ad	bronchial
17	chr12:59988200-59989200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr12:59988200-59989200	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr12:59988200-59989200	Enhancers	Fetal Lung	lung
20	chr12:59988400-59988800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr12:59988400-59988800	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr12:59988400-59988800	Enhancers	Fetal Kidney	kidney
23	chr12:59988400-59988800	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr12:59988400-59988800	Enhancers	NHLF	lung
25	chr12:59988400-59989000	Enhancers	Brain Substantia Nigra	brain
26	chr12:59988600-59988800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr12:59988600-59988800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr12:59988600-59988800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr12:59988600-59988800	Enhancers	GM12878-XiMat	blood
30	chr12:59988600-59989000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr12:59988600-59989000	Enhancers	Primary B cells from cord blood	blood
32	chr12:59988600-59989000	Enhancers	Primary hematopoietic stem cells	blood
33	chr12:59988600-59989000	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr12:59988600-59989000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr12:59988600-59989000	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr12:59988600-59989000	Enhancers	Hela-S3	cervix
37	chr12:59988600-59989000	Enhancers	NHEK	skin
38	chr12:59988600-59989200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr12:59988800-59989000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
40	chr12:59988800-59989000	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr12:59988800-59989000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr12:59988800-59989000	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr12:59988800-59989000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr12:59988800-59989000	Enhancers	Muscle Satellite Cultured Cells	--
45	chr12:59988800-59989000	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr12:59988800-59989000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr12:59988800-59989000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr12:59988800-59989000	Enhancers	Liver	Liver
49	chr12:59988800-59989000	Enhancers	Brain Anterior Caudate	brain
50	chr12:59988800-59989000	Enhancers	Brain Hippocampus Middle	brain

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