Variant report

Variant	nsv521649
Chromosome Location	chr12:117127540-117136787
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:327)
CpG islands
(count:245)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:327 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:117135223-117135352	K562	blood:	n/a	n/a
2	BHLHE40	chr12:117132904-117133254	GM12878	blood:	n/a	chr12:117133091-117133100
3	BHLHE40	chr12:117135222-117135359	GM12878	blood:	n/a	n/a
4	BHLHE40	chr12:117132941-117133209	K562	blood:	n/a	chr12:117133091-117133100
5	CEBPB	chr12:117127748-117127994	K562	blood:	n/a	chr12:117127894-117127907
6	CEBPB	chr12:117130543-117130753	K562	blood:	n/a	chr12:117130598-117130609
7	CEBPB	chr12:117130470-117130755	HepG2	liver:	n/a	chr12:117130598-117130609
8	CEBPB	chr12:117130534-117130666	HepG2	liver:	n/a	chr12:117130598-117130609
9	CEBPB	chr12:117135860-117136703	MCF-7	breast:	n/a	n/a
10	CTCF	chr12:117135240-117135390	AG04450	lung:	n/a	n/a
11	CTCF	chr12:117135220-117135370	HRE	kidney:	n/a	n/a
12	CTCF	chr12:117131540-117131690	HRE	kidney:	n/a	chr12:117131559-117131572
13	CTCF	chr12:117131550-117131587	GM10248	blood:	n/a	chr12:117131559-117131572
14	CTCF	chr12:117135240-117135390	AG09319	gingival:	n/a	n/a
15	CTCF	chr12:117135163-117135452	HepG2	liver:	n/a	n/a
16	CTCF	chr12:117135220-117135370	HCT-116	colon:	n/a	n/a
17	CTCF	chr12:117135220-117135370	GM06990	blood:	n/a	n/a
18	CTCF	chr12:117131480-117131630	HMEC	breast:	n/a	chr12:117131559-117131572 chr12:117131518-117131539 chr12:117131523-117131541
19	CTCF	chr12:117135267-117135395	Pancreas_OC	pancreas:	n/a	n/a
20	CTCF	chr12:117131460-117131610	AG04449	skin:	n/a	chr12:117131559-117131572 chr12:117131518-117131539 chr12:117131523-117131541
21	CTCF	chr12:117135240-117135390	HCFaa	heart:	n/a	n/a
22	CTCF	chr12:117131600-117131750	HAc	cerebellar:	n/a	n/a
23	CTCF	chr12:117135260-117135410	AG10803	skin:	n/a	n/a
24	CTCF	chr12:117131440-117131590	HPF	lung:	n/a	chr12:117131559-117131572 chr12:117131518-117131539 chr12:117131523-117131541
25	CTCF	chr12:117135240-117135390	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr12:117135219-117135455	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr12:117135223-117135418	GM19239	blood:	n/a	n/a
28	CTCF	chr12:117135140-117135290	HAc	cerebellar:	n/a	n/a
29	CTCF	chr12:117135240-117135390	SAEC	small airway:	n/a	n/a
30	CTCF	chr12:117135205-117135447	A549	lung:	n/a	n/a
31	CTCF	chr12:117131480-117131630	GM12871	blood:	n/a	chr12:117131559-117131572 chr12:117131518-117131539 chr12:117131523-117131541
32	CTCF	chr12:117131514-117131569	GM12892	blood:	n/a	chr12:117131518-117131539 chr12:117131523-117131541
33	CTCF	chr12:117135240-117135390	GM12865	blood:	n/a	n/a
34	CTCF	chr12:117131420-117131570	HCM	heart:	n/a	chr12:117131518-117131539 chr12:117131523-117131541
35	CTCF	chr12:117135200-117135350	GM12872	blood:	n/a	n/a
36	CTCF	chr12:117131460-117131610	BJ	skin:	n/a	chr12:117131559-117131572 chr12:117131518-117131539 chr12:117131523-117131541
37	CTCF	chr12:117135220-117135370	NHLF	lung:	n/a	n/a
38	CTCF	chr12:117135160-117135310	HVMF	connective:	n/a	n/a
39	CTCF	chr12:117135240-117135390	Caco-2	colon:	n/a	n/a
40	CTCF	chr12:117135052-117135485	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr12:117135112-117135474	K562	blood:	n/a	n/a
42	CTCF	chr12:117135200-117135350	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr12:117135280-117135430	HFF	foreskin:	n/a	n/a
44	CTCF	chr12:117131460-117131610	HBMEC	blood vessel:	n/a	chr12:117131559-117131572 chr12:117131518-117131539 chr12:117131523-117131541
45	CTCF	chr12:117135240-117135390	AG09309	skin:	n/a	n/a
46	CTCF	chr12:117135249-117135383	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr12:117135231-117135416	ProgFib	skin:	n/a	n/a
48	CTCF	chr12:117131320-117131470	HRE	kidney:	n/a	n/a
49	CTCF	chr12:117131460-117131610	HepG2	liver:	n/a	chr12:117131559-117131572 chr12:117131518-117131539 chr12:117131523-117131541
50	CTCF	chr12:117135260-117135410	HA-sp	spinal cord:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:117132552-117132602	NHDF-neo	bronchial:	n/a
2	chr12:117132552-117132602	NHDF-neo	bronchial:	n/a
3	chr12:117131820-117131870	ovcar-3	ovarian:	n/a
4	chr12:117132552-117132602	AoSMC	blood vessel:	n/a
5	chr12:117131820-117131870	MCF10A-Er-Src	breast:	n/a
6	chr12:117131719-117131769	HPAEpiC	pulmonary alveolar:	n/a
7	chr12:117131820-117131870	ProgFib	skin:	n/a
8	chr12:117131820-117131870	MCF-7	breast:	n/a
9	chr12:117131820-117131870	HCF	heart:	n/a
10	chr12:117131820-117131870	HRE	kidney:	n/a
11	chr12:117131719-117131769	HMEC	breast:	n/a
12	chr12:117131719-117131769	U87	brain:	n/a
13	chr12:117132552-117132602	NT2-D1	testis:	n/a
14	chr12:117131719-117131769	ECC-1	luminal epithelium:	n/a
15	chr12:117132552-117132602	HL-60	blood:	n/a
16	chr12:117132552-117132602	GM06990	blood:	n/a
17	chr12:117131523-117131573	CMK	blood:	n/a
18	chr12:117132552-117132602	Hepatocyte	liver:	n/a
19	chr12:117131523-117131573	AG04450	lung:	fetal
20	chr12:117131719-117131769	MCF10A-Er-Src	breast:	n/a
21	chr12:117132552-117132602	AG10803	skin:	n/a
22	chr12:117131820-117131870	HEEpiC	esophagus:	n/a
23	chr12:117132552-117132602	ECC-1	luminal epithelium:	n/a
24	chr12:117131820-117131870	SKMC	muscle:	n/a
25	chr12:117131820-117131870	PANC-1	pancreas:	n/a
26	chr12:117131523-117131573	HCM	heart:	n/a
27	chr12:117131523-117131573	AG09309	skin:	n/a
28	chr12:117131719-117131769	SAEC	small airway:	n/a
29	chr12:117131820-117131870	HMEC	breast:	n/a
30	chr12:117131719-117131769	HL-60	blood:	n/a
31	chr12:117131719-117131769	HCM	heart:	n/a
32	chr12:117131820-117131870	SK-N-MC	brain:	n/a
33	chr12:117131820-117131870	NHBE	bronchial:	n/a
34	chr12:117132552-117132602	HCF	heart:	n/a
35	chr12:117132552-117132602	HEEpiC	esophagus:	n/a
36	chr12:117131719-117131769	ProgFib	skin:	n/a
37	chr12:117132552-117132602	SK-N-SH	brain:	n/a
38	chr12:117131820-117131870	GM12892	blood:	n/a
39	chr12:117131523-117131573	PFSK-1	brain:	n/a
40	chr12:117131719-117131769	GM12878	blood:	n/a
41	chr12:117131523-117131573	Hepatocyte	liver:	n/a
42	chr12:117131719-117131769	HRE	kidney:	n/a
43	chr12:117131719-117131769	Hepatocyte	liver:	n/a
44	chr12:117132552-117132602	NHBE	bronchial:	n/a
45	chr12:117131523-117131573	MCF10A-Er-Src	breast:	n/a
46	chr12:117132552-117132602	AG09309	skin:	n/a
47	chr12:117131523-117131573	SK-N-SH	brain:	n/a
48	chr12:117131523-117131573	LNCaP	prostate:	n/a
49	chr12:117131820-117131870	CMK	blood:	n/a
50	chr12:117131523-117131573	Jurkat	blood:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:116862737..116864575-chr12:117134402..117135902,2	MCF-7	breast:
2	chr12:117124906..117127466-chr12:117130857..117133400,3	MCF-7	breast:
3	chr12:117129764..117132726-chr12:117134572..117136682,4	MCF-7	breast:
4	chr12:117126789..117129460-chr12:117131891..117135888,3	MCF-7	breast:
5	chr12:117129402..117130962-chr12:117132498..117134381,2	K562	blood:
6	chr12:116943749..116945743-chr12:117126390..117129079,2	K562	blood:
7	chr12:117124747..117126838-chr12:117131104..117134060,2	K562	blood:
8	chr12:117129402..117130962-chr12:117132498..117134381,2	K562	blood:
9	chr12:117126789..117129460-chr12:117131891..117135888,3	MCF-7	breast:
10	chr12:116827555..116830462-chr12:117125918..117127767,2	MCF-7	breast:
11	chr12:116714346..116716168-chr12:117136403..117139329,2	MCF-7	breast:
12	chr12:117133602..117134470-chr7:99006566..99007107,2	NB4	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNFT2-2	chr12:117136141-117136168	ENSG00000257654

No data

Variant related genes	Relation type
ENSG00000257654	TF binding region
ENSG00000257654	CpG island
ENSG00000257654	chromatin interactions
ENSG00000123066	chromatin interactions
ENSG00000106245	chromatin interactions
EZH2	miRNA target sites

Extended variants
information (count: 333 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:333 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7974008	chr12:117127540-117127541	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs57743252	chr12:117127541-117127542	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs533917527	chr12:117127590-117127591	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs557217476	chr12:117127591-117127592	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs16946924	chr12:117127594-117127595	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs149511686	chr12:117127627-117127628	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs183618420	chr12:117127777-117127778	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs189501289	chr12:117127864-117127865	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs541927478	chr12:117127902-117127903	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs556032861	chr12:117127925-117127926	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs35255068	chr12:117127939-117127940	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs181030222	chr12:117127982-117127983	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs34957893	chr12:117127985-117127986	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs143702955	chr12:117127996-117127997	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs544629168	chr12:117128040-117128041	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187369061	chr12:117128121-117128122	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192045834	chr12:117128182-117128183	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs367816942	chr12:117128201-117128202	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs371303709	chr12:117128208-117128209	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs574766482	chr12:117128321-117128322	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs143997615	chr12:117128349-117128350	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73399286	chr12:117128372-117128373	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs139994133	chr12:117128379-117128380	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181477503	chr12:117128397-117128398	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs143458015	chr12:117128423-117128424	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs570692042	chr12:117128488-117128489	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs185925489	chr12:117128511-117128512	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs577064687	chr12:117128588-117128589	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs111692309	chr12:117128692-117128693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs566461061	chr12:117128716-117128717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs113116698	chr12:117128734-117128735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs73399287	chr12:117128737-117128738	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs575755744	chr12:117128749-117128750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs544754533	chr12:117128780-117128781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs113283366	chr12:117128841-117128842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556800689	chr12:117128846-117128847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560154405	chr12:117128878-117128879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs35897401	chr12:117128883-117128884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs189995753	chr12:117128892-117128893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542715143	chr12:117128941-117128942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs34458704	chr12:117128956-117128957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562603102	chr12:117128974-117128975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs374981086	chr12:117128992-117128993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs539642848	chr12:117128993-117128994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs374928306	chr12:117128999-117129000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs550723253	chr12:117129029-117129030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs182532481	chr12:117129039-117129040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs533293770	chr12:117129092-117129093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs546909404	chr12:117129124-117129125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs566522243	chr12:117129157-117129158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	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
lymphocytic leukemia	21291569	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Neuroblastoma	20406844	CNVD
Medulloblastoma	16783165	CNVD
mental retardation	16760730	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21045234	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21806811	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:404 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117125000-117130800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr12:117125600-117129000	Enhancers	Primary hematopoietic stem cells	blood
3	chr12:117126000-117131400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:117126000-117133000	Weak transcription	Spleen	Spleen
5	chr12:117126200-117127800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr12:117126200-117128200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr12:117126200-117130800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr12:117126200-117131600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr12:117127000-117128200	Enhancers	Fetal Thymus	thymus
10	chr12:117127000-117128400	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr12:117127200-117127600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
12	chr12:117127200-117128000	Enhancers	Primary B cells from peripheral blood	blood
13	chr12:117127200-117128000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr12:117127200-117128000	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr12:117127200-117128200	Enhancers	Primary B cells from cord blood	blood
16	chr12:117127400-117128400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
17	chr12:117127400-117128400	Enhancers	Brain Germinal Matrix	brain
18	chr12:117127400-117128600	Enhancers	Fetal Brain Female	brain
19	chr12:117127600-117128400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr12:117127600-117128400	Enhancers	Fetal Brain Male	brain
21	chr12:117127600-117128600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr12:117127600-117134800	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr12:117127800-117128000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr12:117127800-117128000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr12:117127800-117128000	Enhancers	Fetal Lung	lung
26	chr12:117127800-117128200	Enhancers	Placenta	Placenta
27	chr12:117127800-117128400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr12:117127800-117128600	Bivalent Enhancer	Fetal Heart	heart
29	chr12:117128000-117129600	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr12:117128000-117130200	Weak transcription	Primary B cells from peripheral blood	blood
31	chr12:117128000-117130400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr12:117128200-117128400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr12:117128200-117128400	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr12:117128200-117130200	Weak transcription	Primary B cells from cord blood	blood
35	chr12:117128400-117129800	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr12:117128400-117130000	Weak transcription	Fetal Brain Male	brain
37	chr12:117128400-117130200	Weak transcription	Brain Germinal Matrix	brain
38	chr12:117128400-117131000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr12:117128600-117130800	Weak transcription	Fetal Brain Female	brain
40	chr12:117129000-117130600	Weak transcription	Primary hematopoietic stem cells	blood
41	chr12:117129600-117129800	Enhancers	Gastric	stomach
42	chr12:117129600-117130200	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr12:117129800-117130600	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr12:117129800-117131400	Weak transcription	Gastric	stomach
45	chr12:117130000-117131200	Enhancers	Fetal Brain Male	brain
46	chr12:117130200-117130400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
47	chr12:117130200-117130600	Enhancers	Liver	Liver
48	chr12:117130200-117130600	Enhancers	Brain Germinal Matrix	brain
49	chr12:117130200-117130600	Enhancers	Duodenum Mucosa	Duodenum
50	chr12:117130200-117131200	Bivalent Enhancer	GM12878-XiMat	blood

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