Variant report

Variant	nsv899479
Chromosome Location	chr12:104092996-104138918
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	ATF1	chr12:104112810-104113010	K562	blood:	n/a	n/a
2	BATF	chr12:104125323-104125648	GM12878	blood:	n/a	n/a
3	BATF	chr12:104125409-104125605	GM12878	blood:	n/a	n/a
4	BCL3	chr12:104121485-104121647	GM12878	blood:	n/a	n/a
5	BCL3	chr12:104121397-104121783	GM12878	blood:	n/a	n/a
6	BHLHE40	chr12:104110325-104110467	GM12878	blood:	n/a	n/a
7	BRCA1	chr12:104137577-104137581	HepG2	liver:	n/a	n/a
8	CBX3	chr12:104124942-104125268	K562	blood:	n/a	n/a
9	CBX3	chr12:104099674-104100065	K562	blood:	n/a	n/a
10	CEBPB	chr12:104122189-104122557	HepG2	liver:	n/a	chr12:104122367-104122378
11	CEBPB	chr12:104094211-104094493	IMR90	lung:	n/a	chr12:104094328-104094339 chr12:104094329-104094338
12	CEBPB	chr12:104108541-104108764	A549	lung:	n/a	n/a
13	CEBPB	chr12:104122353-104122441	H1-hESC	embryonic stem cell:	n/a	chr12:104122367-104122378
14	CEBPB	chr12:104137722-104137879	K562	blood:	n/a	n/a
15	CEBPB	chr12:104094198-104094446	K562	blood:	n/a	chr12:104094328-104094339 chr12:104094329-104094338
16	CEBPB	chr12:104094199-104094477	HepG2	liver:	n/a	chr12:104094328-104094339 chr12:104094329-104094338
17	CEBPB	chr12:104094189-104094482	A549	lung:	n/a	chr12:104094328-104094339 chr12:104094329-104094338
18	CEBPB	chr12:104122201-104122469	Hela-S3	cervix:	n/a	chr12:104122367-104122378
19	CEBPB	chr12:104108628-104108640	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr12:104108473-104108719	HepG2	liver:	n/a	n/a
21	CEBPB	chr12:104108612-104108744	K562	blood:	n/a	n/a
22	CEBPB	chr12:104122211-104122516	A549	lung:	n/a	chr12:104122367-104122378
23	CEBPB	chr12:104122191-104122543	IMR90	lung:	n/a	chr12:104122367-104122378
24	CEBPB	chr12:104122247-104122507	K562	blood:	n/a	chr12:104122367-104122378
25	CHD2	chr12:104093254-104093464	K562	blood:	n/a	n/a
26	CTCF	chr12:104096580-104096730	A549	lung:	n/a	n/a
27	CTCF	chr12:104099820-104099970	HCT-116	colon:	n/a	chr12:104099881-104099902 chr12:104099887-104099903
28	CTCF	chr12:104096809-104096811	LNCaP	prostate:	n/a	n/a
29	CTCF	chr12:104099900-104100050	HCM	heart:	n/a	n/a
30	CTCF	chr12:104099222-104100217	A549	lung:	n/a	chr12:104099881-104099902 chr12:104099887-104099903
31	CTCF	chr12:104099880-104100030	AG10803	skin:	n/a	chr12:104099881-104099902 chr12:104099887-104099903
32	CTCF	chr12:104099820-104099970	HEK293	kidney:	n/a	chr12:104099881-104099902 chr12:104099887-104099903
33	CTCF	chr12:104099820-104099970	HUVEC	blood vessel:	n/a	chr12:104099881-104099902 chr12:104099887-104099903
34	CTCF	chr12:104099800-104099950	HCM	heart:	n/a	chr12:104099881-104099902 chr12:104099887-104099903
35	CTCF	chr12:104096620-104096770	NB4	blood:	n/a	n/a
36	CTCF	chr12:104096712-104096761	GM12878	blood:	n/a	n/a
37	CTCF	chr12:104096673-104096797	K562	blood:	n/a	n/a
38	CTCF	chr12:104099860-104100010	GM12867	blood:	n/a	chr12:104099881-104099902 chr12:104099887-104099903
39	CTCF	chr12:104099860-104100010	Hela-S3	cervix:	n/a	chr12:104099881-104099902 chr12:104099887-104099903
40	CTCF	chr12:104099860-104100010	GM06990	blood:	n/a	chr12:104099881-104099902 chr12:104099887-104099903
41	CTCF	chr12:104099840-104099990	SK-N-SH_RA	brain:	n/a	chr12:104099881-104099902 chr12:104099887-104099903
42	CTCF	chr12:104099780-104099930	GM12872	blood:	n/a	chr12:104099881-104099902 chr12:104099887-104099903
43	CTCF	chr12:104099860-104100010	Caco-2	colon:	n/a	chr12:104099881-104099902 chr12:104099887-104099903
44	CTCF	chr12:104107491-104107583	Fibrobl	skin:	n/a	n/a
45	CTCF	chr12:104096700-104096850	GM12864	blood:	n/a	n/a
46	CTCF	chr12:104099860-104100010	GM12874	blood:	n/a	chr12:104099881-104099902 chr12:104099887-104099903
47	CTCF	chr12:104099793-104099980	HepG2	liver:	n/a	chr12:104099881-104099902 chr12:104099887-104099903
48	CTCF	chr12:104099780-104099930	GM12870	blood:	n/a	chr12:104099881-104099902 chr12:104099887-104099903
49	CTCF	chr12:104099840-104099990	A549	lung:	n/a	chr12:104099881-104099902 chr12:104099887-104099903
50	CTCF	chr12:104096701-104096776	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:104105517-104105567	Caco-2	colon:	n/a
2	chr12:104105289-104105339	A549	lung:	n/a
3	chr12:104105289-104105339	GM12891	blood:	n/a
4	chr12:104105289-104105339	Hepatocyte	liver:	n/a
5	chr12:104105517-104105567	HIPEpiC	eye:	n/a
6	chr12:104105517-104105567	HNPCEpiC	eye:	n/a
7	chr12:104105289-104105339	HRPEpiC	eye:	n/a
8	chr12:104105289-104105339	HPAEpiC	pulmonary alveolar:	n/a
9	chr12:104105289-104105339	HCT-116	colon:	n/a
10	chr12:104105517-104105567	HCM	heart:	n/a
11	chr12:104105289-104105339	T-47D	breast:	n/a
12	chr12:104105289-104105339	GM12878	blood:	n/a
13	chr12:104105517-104105567	NHBE	bronchial:	n/a
14	chr12:104105517-104105567	Hela-S3	cervix:	n/a
15	chr12:104105517-104105567	GM06990	blood:	n/a
16	chr12:104105517-104105567	HCF	heart:	n/a
17	chr12:104105289-104105339	NHDF-neo	bronchial:	n/a
18	chr12:104105289-104105339	SKMC	muscle:	n/a
19	chr12:104105289-104105339	H1-hESC	embryonic stem cell:	embryo
20	chr12:104105289-104105339	HCPEpiC	choroid plexus:	n/a
21	chr12:104105517-104105567	A549	lung:	n/a
22	chr12:104105517-104105567	AoSMC	blood vessel:	n/a
23	chr12:104105517-104105567	RPTEC	kidney:	n/a
24	chr12:104105517-104105567	ovcar-3	ovarian:	n/a
25	chr12:104105289-104105339	SK-N-MC	brain:	n/a
26	chr12:104105517-104105567	BJ	skin:	n/a
27	chr12:104105289-104105339	IMR90	lung:	fetal
28	chr12:104105517-104105567	HCPEpiC	choroid plexus:	n/a
29	chr12:104105517-104105567	ProgFib	skin:	n/a
30	chr12:104105289-104105339	BJ	skin:	n/a
31	chr12:104105289-104105339	Jurkat	blood:	n/a
32	chr12:104105517-104105567	SAEC	small airway:	n/a
33	chr12:104105517-104105567	HAEpiC	amniotic membrane:	n/a
34	chr12:104105517-104105567	BE2_C	brain:	n/a
35	chr12:104105289-104105339	ProgFib	skin:	n/a
36	chr12:104105289-104105339	HCF	heart:	n/a
37	chr12:104105517-104105567	Jurkat	blood:	n/a
38	chr12:104105517-104105567	NHDF-neo	bronchial:	n/a
39	chr12:104105517-104105567	AG10803	skin:	n/a
40	chr12:104105289-104105339	AG09319	gingival:	n/a
41	chr12:104105517-104105567	HEK293	kidney:	embryo
42	chr12:104105517-104105567	IMR90	lung:	fetal
43	chr12:104105289-104105339	AG04450	lung:	fetal
44	chr12:104105289-104105339	HAEpiC	amniotic membrane:	n/a
45	chr12:104105517-104105567	SK-N-MC	brain:	n/a
46	chr12:104105289-104105339	PrEC	prostate:	n/a
47	chr12:104105289-104105339	HEEpiC	esophagus:	n/a
48	chr12:104105289-104105339	GM12892	blood:	n/a
49	chr12:104105517-104105567	Hepatocyte	liver:	n/a
50	chr12:104105517-104105567	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:104126083..104127823-chr12:104129253..104131944,2	K562	blood:
2	chr12:104126083..104127823-chr12:104129253..104131944,2	K562	blood:
3	chr12:104109903..104111815-chr12:104233506..104235290,2	MCF-7	breast:
4	chr12:104128241..104130888-chr12:104131454..104134475,3	K562	blood:
5	chr12:104093719..104096610-chr12:104115340..104116948,2	K562	blood:
6	chr12:104093719..104096610-chr12:104115340..104116948,2	K562	blood:
7	chr12:104083504..104086634-chr12:104099409..104102574,3	K562	blood:
8	chr12:104136425..104139178-chr12:104152624..104154639,2	K562	blood:
9	chr12:104112132..104115001-chr12:104117740..104119826,2	K562	blood:
10	chr12:104128241..104130888-chr12:104131454..104134475,3	K562	blood:
11	chr12:104083131..104086634-chr12:104100457..104102574,3	K562	blood:
12	chr12:104131640..104133460-chr12:104142100..104144615,2	K562	blood:
13	chr12:104086671..104088955-chr12:104090916..104093628,2	K562	blood:
14	chr12:104104758..104106401-chr12:104109260..104111411,2	MCF-7	breast:
15	chr12:104102336..104105265-chr12:104119605..104121308,2	MCF-7	breast:
16	chr12:104134942..104137078-chr12:104139812..104142244,2	MCF-7	breast:
17	chr12:104089001..104091974-chr12:104092172..104093862,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000238914	TF binding region
STAB2	TF binding region
ENSG00000238914	CpG island
STAB2	CpG island
ENSG00000257327	chromatin interactions
ENSG00000111696	chromatin interactions
ENSG00000238914	chromatin interactions
ENSG00000136011	chromatin interactions

Extended variants
information (count: 1958 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1958 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs697210	chr12:104092996-104092997	Active TSS Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
2	rs374683198	chr12:104093009-104093010	Active TSS Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs545722368	chr12:104093010-104093011	Active TSS Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs145142182	chr12:104093187-104093188	Active TSS Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531086883	chr12:104093188-104093189	Active TSS Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs12578430	chr12:104093212-104093213	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561330642	chr12:104093228-104093229	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs530238903	chr12:104093239-104093240	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs546995955	chr12:104093240-104093241	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs147612655	chr12:104093242-104093243	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs10778278	chr12:104093247-104093248	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs572998323	chr12:104093274-104093275	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs551702894	chr12:104093276-104093277	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs571456475	chr12:104093280-104093281	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs565473974	chr12:104093323-104093324	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs148442812	chr12:104093334-104093335	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs373296879	chr12:104093339-104093340	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs113376623	chr12:104093352-104093353	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
19	rs190459746	chr12:104093401-104093402	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs566998036	chr12:104093423-104093424	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs371477772	chr12:104093453-104093454	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs146110900	chr12:104093457-104093458	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs562812773	chr12:104093504-104093505	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs375042398	chr12:104093505-104093506	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs184182406	chr12:104093648-104093649	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs145660088	chr12:104093666-104093667	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs530139809	chr12:104093704-104093705	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs148906414	chr12:104093724-104093725	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs377668511	chr12:104093764-104093765	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200900964	chr12:104093767-104093768	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576021782	chr12:104093777-104093778	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12422614	chr12:104093790-104093791	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs561495930	chr12:104093803-104093804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530203691	chr12:104093864-104093865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12426734	chr12:104093868-104093869	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs187104100	chr12:104093919-104093920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12426747	chr12:104093940-104093941	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs549640658	chr12:104094008-104094009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552340861	chr12:104094062-104094063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78608317	chr12:104094130-104094131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571486471	chr12:104094131-104094132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7309088	chr12:104094133-104094134	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs547195956	chr12:104094157-104094158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192164211	chr12:104094159-104094160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537611775	chr12:104094169-104094170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368734158	chr12:104094246-104094247	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs542631461	chr12:104094256-104094257	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs567162828	chr12:104094259-104094260	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs182623832	chr12:104094293-104094294	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs372336935	chr12:104094366-104094367	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Breast cancer	22522925	CNVD

Chromatin state (count:167 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104089800-104093800	Strong transcription	Spleen	Spleen
2	chr12:104090200-104097000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr12:104091400-104093600	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr12:104091800-104093800	Enhancers	GM12878-XiMat	blood
5	chr12:104092400-104093200	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr12:104092800-104093200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr12:104092800-104093200	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr12:104092800-104093200	Weak transcription	Right Atrium	heart
9	chr12:104093200-104093400	Enhancers	Right Atrium	heart
10	chr12:104093200-104093600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
11	chr12:104093400-104105400	Weak transcription	Right Atrium	heart
12	chr12:104093600-104093800	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr12:104093800-104099400	Weak transcription	Spleen	Spleen
14	chr12:104098600-104099400	Enhancers	Liver	Liver
15	chr12:104098600-104099600	Enhancers	Duodenum Mucosa	Duodenum
16	chr12:104099400-104101400	Strong transcription	Spleen	Spleen
17	chr12:104099800-104102600	Enhancers	Fetal Muscle Leg	muscle
18	chr12:104100400-104101000	Enhancers	Fetal Muscle Trunk	muscle
19	chr12:104101400-104103800	Weak transcription	Spleen	Spleen
20	chr12:104102600-104103000	Weak transcription	Fetal Muscle Leg	muscle
21	chr12:104103000-104103200	Enhancers	Fetal Muscle Leg	muscle
22	chr12:104103200-104105200	Weak transcription	Fetal Muscle Leg	muscle
23	chr12:104103400-104104400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr12:104103800-104104400	Enhancers	Spleen	Spleen
25	chr12:104104000-104104400	Enhancers	Duodenum Smooth Muscle	Duodenum
26	chr12:104104400-104104600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr12:104104400-104105800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr12:104104400-104111000	Weak transcription	Spleen	Spleen
29	chr12:104104600-104105600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr12:104105200-104106800	Enhancers	Fetal Heart	heart
31	chr12:104105200-104106800	Enhancers	Fetal Muscle Leg	muscle
32	chr12:104105400-104106000	Enhancers	HSMMtube	muscle
33	chr12:104105400-104106400	Enhancers	Left Ventricle	heart
34	chr12:104105400-104106400	Enhancers	Right Atrium	heart
35	chr12:104105400-104106800	Enhancers	HSMM	muscle
36	chr12:104105600-104107200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr12:104105800-104106400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr12:104105800-104106800	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr12:104106000-104106200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr12:104106000-104106800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr12:104106000-104108800	Weak transcription	HSMMtube	muscle
42	chr12:104106400-104109600	Weak transcription	Left Ventricle	heart
43	chr12:104106800-104108800	Weak transcription	HSMM	muscle
44	chr12:104107400-104107600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr12:104108800-104109000	Enhancers	HSMMtube	muscle
46	chr12:104108800-104109800	Enhancers	HSMM	muscle
47	chr12:104109000-104109400	Weak transcription	HSMMtube	muscle
48	chr12:104109400-104109800	Enhancers	HSMMtube	muscle
49	chr12:104109600-104110200	Enhancers	Left Ventricle	heart
50	chr12:104109800-104110200	Flanking Active TSS	HSMMtube	muscle

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