Variant report

Variant	nsv899476
Chromosome Location	chr12:103568316-103619085
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	ATF2	chr12:103575036-103575649	GM12878	blood:	n/a	n/a
2	ATF2	chr12:103575056-103575875	GM12878	blood:	n/a	n/a
3	BATF	chr12:103575153-103575536	GM12878	blood:	n/a	n/a
4	BATF	chr12:103575105-103575605	GM12878	blood:	n/a	n/a
5	BATF	chr12:103572542-103572768	GM12878	blood:	n/a	n/a
6	BCL11A	chr12:103575155-103575814	GM12878	blood:	n/a	chr12:103575205-103575214
7	BCL11A	chr12:103575242-103575455	GM12878	blood:	n/a	n/a
8	BCL3	chr12:103575150-103575600	GM12878	blood:	n/a	chr12:103575205-103575214
9	BCLAF1	chr12:103575064-103575597	GM12878	blood:	n/a	chr12:103575205-103575214
10	BCLAF1	chr12:103575076-103575710	GM12878	blood:	n/a	chr12:103575205-103575214
11	BHLHE40	chr12:103575141-103576094	GM12878	blood:	n/a	n/a
12	CEBPB	chr12:103590301-103590633	Hela-S3	cervix:	n/a	chr12:103590440-103590451
13	CEBPB	chr12:103569300-103569592	IMR90	lung:	n/a	chr12:103569465-103569476 chr12:103569467-103569476 chr12:103569467-103569478 chr12:103569465-103569478 chr12:103569465-103569478
14	CEBPB	chr12:103590982-103591277	A549	lung:	n/a	chr12:103591147-103591158
15	CEBPB	chr12:103590258-103590636	IMR90	lung:	n/a	chr12:103590440-103590451
16	CEBPB	chr12:103611997-103612283	A549	lung:	n/a	chr12:103612153-103612164 chr12:103612155-103612166 chr12:103612155-103612164
17	CEBPB	chr12:103591014-103591272	HepG2	liver:	n/a	chr12:103591147-103591158
18	CEBPB	chr12:103590122-103590636	H1-hESC	embryonic stem cell:	n/a	chr12:103590440-103590451
19	CEBPB	chr12:103590179-103590632	A549	lung:	n/a	chr12:103590440-103590451
20	CEBPB	chr12:103590255-103590630	HepG2	liver:	n/a	chr12:103590440-103590451
21	CEBPB	chr12:103591772-103592041	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr12:103569282-103569647	HepG2	liver:	n/a	chr12:103569465-103569476 chr12:103569467-103569476 chr12:103569467-103569478 chr12:103569465-103569478 chr12:103569465-103569478
23	CEBPB	chr12:103569313-103569722	MCF-7	breast:	n/a	chr12:103569465-103569476 chr12:103569467-103569476 chr12:103569467-103569478 chr12:103569465-103569478 chr12:103569465-103569478
24	CEBPB	chr12:103611998-103612336	HepG2	liver:	n/a	chr12:103612153-103612164 chr12:103612155-103612166 chr12:103612155-103612164
25	CEBPB	chr12:103590258-103590634	A549	lung:	n/a	chr12:103590440-103590451
26	CEBPB	chr12:103569322-103569621	A549	lung:	n/a	chr12:103569465-103569476 chr12:103569467-103569476 chr12:103569467-103569478 chr12:103569465-103569478 chr12:103569465-103569478
27	CEBPB	chr12:103590255-103590635	K562	blood:	n/a	chr12:103590440-103590451
28	CEBPB	chr12:103592398-103592677	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr12:103569415-103569603	H1-hESC	embryonic stem cell:	n/a	chr12:103569465-103569476 chr12:103569467-103569476 chr12:103569467-103569478 chr12:103569465-103569478 chr12:103569465-103569478
30	CEBPB	chr12:103590210-103590647	A549	lung:	n/a	chr12:103590440-103590451
31	CEBPB	chr12:103611993-103612286	IMR90	lung:	n/a	chr12:103612153-103612164 chr12:103612155-103612166 chr12:103612155-103612164
32	CHD1	chr12:103575198-103575846	GM12878	blood:	n/a	n/a
33	CHD2	chr12:103575140-103575878	GM12878	blood:	n/a	n/a
34	CTCF	chr12:103610663-103610696	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr12:103601688-103601735	GM10248	blood:	n/a	n/a
36	CTCF	chr12:103575450-103575581	GM10266	blood:	n/a	n/a
37	CTCF	chr12:103575430-103575553	GM13977	blood:	n/a	n/a
38	CTCF	chr12:103575258-103575692	GM12878	blood:	n/a	n/a
39	CTCF	chr12:103575556-103575558	GM13977	blood:	n/a	n/a
40	CTCF	chr12:103572540-103572690	GM12878	blood:	n/a	chr12:103572662-103572670
41	CTCF	chr12:103572654-103572714	GM19238	blood:	n/a	chr12:103572662-103572670
42	CTCF	chr12:103575458-103575538	GM10248	blood:	n/a	n/a
43	CTCF	chr12:103572504-103572825	GM12878	blood:	n/a	chr12:103572662-103572670
44	CTCF	chr12:103575441-103575507	GM13976	blood:	n/a	n/a
45	CTCF	chr12:103616303-103616354	Lung_OC	lung:	n/a	n/a
46	CTCF	chr12:103575417-103575585	GM12878	blood:	n/a	n/a
47	CTCF	chr12:103572675-103572709	GM12892	blood:	n/a	n/a
48	CTCF	chr12:103572654-103572725	GM19240	blood:	n/a	chr12:103572662-103572670
49	CTCF	chr12:103575380-103575530	GM12878	blood:	n/a	n/a
50	CTCF	chr12:103575400-103575550	GM12872	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:103591917-103591967	AoSMC	blood vessel:	n/a
2	chr12:103591917-103591967	SAEC	small airway:	n/a
3	chr12:103591917-103591967	HepG2	liver:	n/a
4	chr12:103591917-103591967	ovcar-3	ovarian:	n/a
5	chr12:103591917-103591967	HMEC	breast:	n/a
6	chr12:103591917-103591967	HRCEpiC	kidney:	n/a
7	chr12:103591917-103591967	GM12892	blood:	n/a
8	chr12:103591917-103591967	HIPEpiC	eye:	n/a
9	chr12:103591917-103591967	HRE	kidney:	n/a
10	chr12:103591917-103591967	HAEpiC	amniotic membrane:	n/a
11	chr12:103591917-103591967	ECC-1	luminal epithelium:	n/a
12	chr12:103591917-103591967	NH-A	brain:	n/a
13	chr12:103591917-103591967	BJ	skin:	n/a
14	chr12:103591917-103591967	RPTEC	kidney:	n/a
15	chr12:103591917-103591967	SK-N-SH_RA	brain:	n/a
16	chr12:103591917-103591967	AG10803	skin:	n/a
17	chr12:103591917-103591967	GM12891	blood:	n/a
18	chr12:103591917-103591967	AG04450	lung:	fetal
19	chr12:103591917-103591967	HRPEpiC	eye:	n/a
20	chr12:103591917-103591967	U87	brain:	n/a
21	chr12:103591917-103591967	HEEpiC	esophagus:	n/a
22	chr12:103591917-103591967	ProgFib	skin:	n/a
23	chr12:103591917-103591967	HCM	heart:	n/a
24	chr12:103591917-103591967	CMK	blood:	n/a
25	chr12:103591917-103591967	SKMC	muscle:	n/a
26	chr12:103591917-103591967	HL-60	blood:	n/a
27	chr12:103591917-103591967	K562	blood:	n/a
28	chr12:103591917-103591967	GM19239	blood:	n/a
29	chr12:103591917-103591967	HCF	heart:	n/a
30	chr12:103591917-103591967	SK-N-SH	brain:	n/a
31	chr12:103591917-103591967	Hela-S3	cervix:	n/a
32	chr12:103591917-103591967	GM12878	blood:	n/a
33	chr12:103591917-103591967	H1-hESC	embryonic stem cell:	embryo
34	chr12:103591917-103591967	MCF-7	breast:	n/a
35	chr12:103591917-103591967	NHDF-neo	bronchial:	n/a
36	chr12:103591917-103591967	LNCaP	prostate:	n/a
37	chr12:103591917-103591967	HPAEpiC	pulmonary alveolar:	n/a
38	chr12:103591917-103591967	Hepatocyte	liver:	n/a
39	chr12:103591917-103591967	MCF10A-Er-Src	breast:	n/a
40	chr12:103591917-103591967	BE2_C	brain:	n/a
41	chr12:103591917-103591967	HCPEpiC	choroid plexus:	n/a
42	chr12:103591917-103591967	NB4	blood:	n/a
43	chr12:103591917-103591967	NHBE	bronchial:	n/a
44	chr12:103591917-103591967	Caco-2	colon:	n/a
45	chr12:103591917-103591967	HCT-116	colon:	n/a
46	chr12:103591917-103591967	GM06990	blood:	n/a
47	chr12:103591917-103591967	Jurkat	blood:	n/a
48	chr12:103591917-103591967	AG09309	skin:	n/a
49	chr12:103591917-103591967	SK-N-MC	brain:	n/a
50	chr12:103591917-103591967	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:103567485..103570052-chr12:103761974..103764560,2	MCF-7	breast:
2	chr12:103569111..103570024-chr12:103918043..103919091,5	MCF-7	breast:
3	chr12:103345130..103346737-chr12:103603490..103605464,2	MCF-7	breast:
4	chr12:103342479..103343468-chr12:103569109..103570014,11	MCF-7	breast:
5	chr12:103600594..103603379-chr12:103611609..103613668,2	MCF-7	breast:
6	chr12:103569245..103570050-chr12:103639690..103640508,2	MCF-7	breast:
7	chr12:103342538..103343552-chr12:103569117..103569983,3	MCF-7	breast:
8	chr10:97805584..97806458-chr12:103575603..103576420,2	MCF-7	breast:
9	chr12:103600594..103603379-chr12:103611609..103613668,2	MCF-7	breast:
10	chr12:103350008..103351674-chr12:103594791..103596374,2	MCF-7	breast:
11	chr12:103343154..103347521-chr12:103565562..103568893,4	MCF-7	breast:
12	chr12:103344308..103344865-chr12:103569473..103570033,2	MCF-7	breast:
13	chr12:103569173..103569956-chr12:103896987..103897845,3	MCF-7	breast:
14	chr12:103355593..103357176-chr12:103566399..103568963,2	MCF-7	breast:
15	chr12:103567206..103569823-chr12:103663759..103665929,2	MCF-7	breast:
16	chr12:103342479..103343468-chr12:103569109..103570109,23	MCF-7	breast:
17	chr12:103569149..103570117-chr12:103917984..103918759,8	MCF-7	breast:
18	chr12:103569111..103570024-chr12:103918043..103918908,7	MCF-7	breast:
19	chr12:103569035..103569938-chr12:103766846..103767430,3	MCF-7	breast:
20	chr12:103567572..103571382-chr12:103642751..103645285,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C12orf42-2	chr12:103571907-103571976	ENSG00000257703.1
2	lnc-C12orf42-2	chr12:103572357-103572453	ENSG00000257703.1
3	lnc-RP11-552I14.1.1-1	chr12:103571827-103571987	XLOC_009858
4	lnc-RP11-552I14.1.1-1	chr12:103571827-103571987	XLOC_009858
5	lnc-RP11-552I14.1.1-1	chr12:103571826-103571987	NONHSAT030350

Variant related genes	Relation type
ENSG00000257703	TF binding region
ENSG00000257703	CpG island
ENSG00000171759	chromatin interactions
ENSG00000139352	chromatin interactions
ENSG00000257415	chromatin interactions
CAB39	miRNA target sites
ZEB2	miRNA target sites

Extended variants
information (count: 1268 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1268 , 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	rs7962035	chr12:103568316-103568317	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566677332	chr12:103568341-103568342	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs187604160	chr12:103568375-103568376	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs544934951	chr12:103568385-103568386	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs571958404	chr12:103568386-103568387	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs77086841	chr12:103568400-103568401	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs531421845	chr12:103568419-103568420	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs145162994	chr12:103568457-103568458	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs7975666	chr12:103568462-103568463	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs147590600	chr12:103568485-103568486	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs575009354	chr12:103568493-103568494	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs192618564	chr12:103568556-103568557	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs564160323	chr12:103568577-103568578	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs112417778	chr12:103568607-103568608	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs544798059	chr12:103568665-103568666	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs546436529	chr12:103568669-103568670	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs140810329	chr12:103568674-103568675	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs576006439	chr12:103568706-103568707	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs7962486	chr12:103568719-103568720	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs184838616	chr12:103568800-103568801	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs189985960	chr12:103568801-103568802	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs546483232	chr12:103568802-103568803	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs563044260	chr12:103568819-103568820	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs150145536	chr12:103568859-103568860	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs145578501	chr12:103568883-103568884	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs568897586	chr12:103568941-103568942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs148898715	chr12:103568977-103568978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548172907	chr12:103568983-103568984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs73383835	chr12:103569020-103569021	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs533836098	chr12:103569067-103569068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554081208	chr12:103569126-103569127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs548824261	chr12:103569136-103569137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs539773139	chr12:103569161-103569162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs556424858	chr12:103569193-103569194	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs576294659	chr12:103569206-103569207	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs115018232	chr12:103569232-103569233	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs145603056	chr12:103569233-103569234	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs541509009	chr12:103569324-103569325	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs560139135	chr12:103569326-103569327	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs532310108	chr12:103569328-103569329	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs138810363	chr12:103569339-103569340	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs562784716	chr12:103569383-103569384	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs531607354	chr12:103569392-103569393	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs377198891	chr12:103569408-103569409	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs548209584	chr12:103569411-103569412	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs568007553	chr12:103569495-103569496	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs141958961	chr12:103569558-103569559	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs75189260	chr12:103569575-103569576	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs570992646	chr12:103569598-103569599	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs539661028	chr12:103569600-103569601	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
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
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	22032731	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
lymphocytic leukemia	21291569	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Neurocytoma	17123091	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:103565400-103570400	Enhancers	Liver	Liver
2	chr12:103571000-103571400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr12:103571000-103571600	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr12:103571400-103571600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr12:103571400-103571600	Enhancers	Brain Germinal Matrix	brain
6	chr12:103571400-103571600	Enhancers	Brain Hippocampus Middle	brain
7	chr12:103571400-103571600	Enhancers	Fetal Brain Male	brain
8	chr12:103571400-103571800	Enhancers	Brain Anterior Caudate	brain
9	chr12:103571400-103572400	Active TSS	Brain Substantia Nigra	brain
10	chr12:103571600-103571800	Bivalent Enhancer	Fetal Brain Male	brain
11	chr12:103571600-103572200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr12:103571600-103572200	Active TSS	Fetal Brain Female	brain
13	chr12:103571600-103572400	Flanking Active TSS	Brain Germinal Matrix	brain
14	chr12:103571600-103572400	Active TSS	Brain Hippocampus Middle	brain
15	chr12:103571600-103572600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
16	chr12:103571800-103572200	Active TSS	Brain Anterior Caudate	brain
17	chr12:103572000-103572400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr12:103572200-103572400	Bivalent/Poised TSS	Brain Anterior Caudate	brain
19	chr12:103572200-103572600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr12:103572200-103573400	Enhancers	GM12878-XiMat	blood
21	chr12:103572400-103572600	Enhancers	Brain Germinal Matrix	brain
22	chr12:103572600-103573200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr12:103572600-103573800	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr12:103573400-103573600	Weak transcription	GM12878-XiMat	blood
25	chr12:103573600-103574200	ZNF genes & repeats	GM12878-XiMat	blood
26	chr12:103574200-103574800	Weak transcription	GM12878-XiMat	blood
27	chr12:103574800-103575200	Enhancers	GM12878-XiMat	blood
28	chr12:103575200-103576000	Flanking Active TSS	GM12878-XiMat	blood
29	chr12:103575400-103575800	Enhancers	Primary B cells from peripheral blood	blood
30	chr12:103576000-103576200	Enhancers	GM12878-XiMat	blood
31	chr12:103576000-103576400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr12:103578800-103579000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr12:103583400-103583600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr12:103583600-103584600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr12:103584000-103584400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
36	chr12:103591000-103592400	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr12:103591200-103592000	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr12:103591400-103592000	Enhancers	H9 Cell Line	embryonic stem cell
39	chr12:103591400-103592400	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr12:103591600-103592000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr12:103591600-103592200	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr12:103591600-103592200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr12:103591600-103592400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr12:103591600-103592400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr12:103591800-103592400	Enhancers	H1 Cell Line	embryonic stem cell
46	chr12:103591800-103592400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr12:103600200-103602600	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr12:103601600-103602600	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr12:103602200-103602400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr12:103602200-103602800	Enhancers	Brain Germinal Matrix	brain

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