Variant report

Variant	nsv517916
Chromosome Location	chr12:30454845-30485611
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	CEBPB	chr12:30463057-30463220	K562	blood:	n/a	chr12:30463102-30463113
2	CEBPB	chr12:30462983-30463258	A549	lung:	n/a	chr12:30463102-30463113
3	CEBPB	chr12:30461079-30461749	ECC-1	luminal epithelium:	n/a	n/a
4	CEBPB	chr12:30463025-30463240	IMR90	lung:	n/a	chr12:30463102-30463113
5	CEBPB	chr12:30462995-30463269	HepG2	liver:	n/a	chr12:30463102-30463113
6	CEBPB	chr12:30461222-30461696	ECC-1	luminal epithelium:	n/a	n/a
7	CTCF	chr12:30457660-30457810	Caco-2	colon:	n/a	n/a
8	CTCF	chr12:30476040-30476190	HVMF	connective:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
9	CTCF	chr12:30455833-30455900	MCF-7	breast:	n/a	n/a
10	CTCF	chr12:30476000-30476150	Caco-2	colon:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
11	CTCF	chr12:30455652-30455654	LNCaP	prostate:	n/a	n/a
12	CTCF	chr12:30476040-30476190	AG09309	skin:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
13	CTCF	chr12:30476040-30476190	GM12875	blood:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
14	CTCF	chr12:30476100-30476250	BE2_C	brain:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476234-30476242 chr12:30476129-30476147
15	CTCF	chr12:30455852-30455911	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr12:30476067-30476221	MCF-7	breast:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
17	CTCF	chr12:30476040-30476190	HCM	heart:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
18	CTCF	chr12:30475997-30476388	HCT-116	colon:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476234-30476242 chr12:30476129-30476147
19	CTCF	chr12:30476100-30476250	Hela-S3	cervix:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476234-30476242 chr12:30476129-30476147
20	CTCF	chr12:30476040-30476211	Hela-S3	cervix:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
21	CTCF	chr12:30476100-30476250	HepG2	liver:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476234-30476242 chr12:30476129-30476147
22	CTCF	chr12:30476060-30476210	AG10803	skin:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
23	CTCF	chr12:30468280-30468430	Caco-2	colon:	n/a	n/a
24	CTCF	chr12:30457600-30457750	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr12:30476077-30476223	HepG2	liver:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
26	CTCF	chr12:30476020-30476170	MCF-7	breast:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
27	CTCF	chr12:30457640-30457790	HMF	breast:	n/a	n/a
28	CTCF	chr12:30476084-30476211	A549	lung:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
29	CTCF	chr12:30476020-30476170	HFF	foreskin:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
30	CTCF	chr12:30476008-30476319	MCF-7	breast:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476234-30476242 chr12:30476129-30476147
31	CTCF	chr12:30455740-30455777	GM13976	blood:	n/a	n/a
32	CTCF	chr12:30476120-30476270	NHEK	skin:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476234-30476242 chr12:30476129-30476147
33	CTCF	chr12:30476060-30476210	HCFaa	heart:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
34	CTCF	chr12:30476048-30476211	HUVEC	blood vessel:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
35	CTCF	chr12:30455609-30455704	HepG2	liver:	n/a	n/a
36	CTCF	chr12:30476156-30476168	GM12878	blood:	n/a	n/a
37	CTCF	chr12:30476056-30476226	MCF-7	breast:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
38	CTCF	chr12:30476020-30476170	HFF-Myc	foreskin:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
39	CTCF	chr12:30476102-30476178	H1-hESC	embryonic stem cell:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
40	CTCF	chr12:30476093-30476205	GM12878	blood:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
41	CTCF	chr12:30476060-30476210	HVMF	connective:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
42	CTCF	chr12:30455580-30455730	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr12:30455579-30455650	LNCaP	prostate:	n/a	n/a
44	CTCF	chr12:30476020-30476170	SK-N-SH_RA	brain:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
45	CTCF	chr12:30457640-30457790	HEK293	kidney:	n/a	n/a
46	CTCF	chr12:30476100-30476250	MCF-7	breast:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476234-30476242 chr12:30476129-30476147
47	CTCF	chr12:30476045-30476240	MCF-7	breast:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476129-30476147
48	CTCF	chr12:30476100-30476250	HCPEpiC	choroid plexus:	n/a	chr12:30476130-30476146 chr12:30476132-30476145 chr12:30476234-30476242 chr12:30476129-30476147
49	CTCF	chr12:30457580-30457730	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr12:30475980-30476130	HMEC	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:30484029-30484079	HAEpiC	amniotic membrane:	n/a
2	chr12:30484029-30484079	HIPEpiC	eye:	n/a
3	chr12:30484029-30484079	BE2_C	brain:	n/a
4	chr12:30484029-30484079	SK-N-SH_RA	brain:	n/a
5	chr12:30484029-30484079	HPAEpiC	pulmonary alveolar:	n/a
6	chr12:30484029-30484079	Jurkat	blood:	n/a
7	chr12:30484029-30484079	NB4	blood:	n/a
8	chr12:30484029-30484079	GM12878	blood:	n/a
9	chr12:30484029-30484079	GM19239	blood:	n/a
10	chr12:30484029-30484079	ovcar-3	ovarian:	n/a
11	chr12:30484029-30484079	HL-60	blood:	n/a
12	chr12:30484029-30484079	GM06990	blood:	n/a
13	chr12:30484029-30484079	SKMC	muscle:	n/a
14	chr12:30484029-30484079	PANC-1	pancreas:	n/a
15	chr12:30484029-30484079	CMK	blood:	n/a
16	chr12:30484029-30484079	HCPEpiC	choroid plexus:	n/a
17	chr12:30484029-30484079	PFSK-1	brain:	n/a
18	chr12:30484029-30484079	HNPCEpiC	eye:	n/a
19	chr12:30484029-30484079	RPTEC	kidney:	n/a
20	chr12:30484029-30484079	HCM	heart:	n/a
21	chr12:30484029-30484079	ECC-1	luminal epithelium:	n/a
22	chr12:30484029-30484079	U87	brain:	n/a
23	chr12:30484029-30484079	HEK293	kidney:	embryo
24	chr12:30484029-30484079	SAEC	small airway:	n/a
25	chr12:30484029-30484079	HUVEC	blood vessel:	n/a
26	chr12:30484029-30484079	H1-hESC	embryonic stem cell:	embryo
27	chr12:30484029-30484079	AG04450	lung:	fetal
28	chr12:30484029-30484079	NT2-D1	testis:	n/a
29	chr12:30484029-30484079	Hela-S3	cervix:	n/a
30	chr12:30484029-30484079	AG10803	skin:	n/a
31	chr12:30484029-30484079	AG09319	gingival:	n/a
32	chr12:30484029-30484079	HRCEpiC	kidney:	n/a
33	chr12:30484029-30484079	HEEpiC	esophagus:	n/a
34	chr12:30484029-30484079	HepG2	liver:	n/a
35	chr12:30484029-30484079	K562	blood:	n/a
36	chr12:30484029-30484079	BJ	skin:	n/a
37	chr12:30484029-30484079	NHDF-neo	bronchial:	n/a
38	chr12:30484029-30484079	HCT-116	colon:	n/a
39	chr12:30484029-30484079	GM12892	blood:	n/a
40	chr12:30484029-30484079	AoSMC	blood vessel:	n/a
41	chr12:30484029-30484079	NH-A	brain:	n/a
42	chr12:30484029-30484079	NHBE	bronchial:	n/a
43	chr12:30484029-30484079	MCF10A-Er-Src	breast:	n/a
44	chr12:30484029-30484079	SK-N-MC	brain:	n/a
45	chr12:30484029-30484079	HRE	kidney:	n/a
46	chr12:30484029-30484079	GM12891	blood:	n/a
47	chr12:30484029-30484079	MCF-7	breast:	n/a
48	chr12:30484029-30484079	HCF	heart:	n/a
49	chr12:30484029-30484079	Caco-2	colon:	n/a
50	chr12:30484029-30484079	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:30457702..30459650-chr12:30461692..30463708,2	K562	blood:
2	chr12:30448261..30450995-chr12:30458439..30460562,2	K562	blood:
3	chr12:30130967..30132688-chr12:30459870..30462012,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSPAN11-4	chr12:30473767-30473831	ENSG00000257932
2	lnc-TSPAN11-4	chr12:30474054-30474550	ENSG00000257932

Variant related genes	Relation type
ENSG00000257932	TF binding region
RNA5SP356	TF binding region
ENSG00000257932	CpG island
RNA5SP356	CpG island
ENSG00000257756	chromatin interactions
ENSG00000251781	chromatin interactions
MOBP	miRNA target sites
USP33	miRNA target sites

Extended variants
information (count: 854 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571097999	chr12:30455603-30455604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs2564527	chr12:30455639-30455640	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs553565111	chr12:30455642-30455643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575088911	chr12:30455663-30455664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536100967	chr12:30455707-30455708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs144908226	chr12:30455723-30455724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs368081121	chr12:30455726-30455727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs80332676	chr12:30455729-30455730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs184788067	chr12:30455771-30455772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs187557433	chr12:30455790-30455791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs112354887	chr12:30455855-30455856	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538758315	chr12:30455870-30455871	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540143914	chr12:30455885-30455886	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184887571	chr12:30455904-30455905	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2703363	chr12:30455907-30455908	Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs374258298	chr12:30455915-30455916	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544115755	chr12:30455916-30455917	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs111791624	chr12:30455956-30455957	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs532908408	chr12:30455967-30455968	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189766575	chr12:30455975-30455976	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs566355922	chr12:30455989-30455990	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs11614412	chr12:30456029-30456030	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs10466816	chr12:30456043-30456044	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs2564526	chr12:30456075-30456076	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs1731503	chr12:30456102-30456103	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs386761623	chr12:30456128-30456129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs111831791	chr12:30456129-30456130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1652195	chr12:30456130-30456131	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs539563051	chr12:30456145-30456146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs571361156	chr12:30456176-30456177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs532991390	chr12:30456276-30456277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs149029297	chr12:30456316-30456317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1429636	chr12:30456327-30456328	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs1429635	chr12:30456355-30456356	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs35779884	chr12:30456357-30456358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573629976	chr12:30456393-30456394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183729694	chr12:30456395-30456396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1652193	chr12:30456439-30456440	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs1731500	chr12:30456451-30456452	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs11050810	chr12:30456472-30456473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs142242047	chr12:30456496-30456497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560335346	chr12:30456497-30456498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527268098	chr12:30456523-30456524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs77378546	chr12:30456560-30456561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568748153	chr12:30456588-30456589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34689193	chr12:30456594-30456595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188048741	chr12:30456664-30456665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551117866	chr12:30456670-30456671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569358319	chr12:30456675-30456676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371690359	chr12:30456742-30456743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
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
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	17133270	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:30455600-30456200	Enhancers	Fetal Muscle Leg	muscle
2	chr12:30455800-30456000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
3	chr12:30456200-30456800	Weak transcription	Fetal Muscle Leg	muscle
4	chr12:30456800-30457000	Enhancers	Fetal Muscle Leg	muscle
5	chr12:30458400-30460800	Enhancers	Placenta	Placenta
6	chr12:30459200-30461600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr12:30460600-30461400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr12:30460600-30461800	Enhancers	NHEK	skin
9	chr12:30460800-30461200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr12:30461000-30461400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr12:30461000-30461400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr12:30461600-30461800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr12:30463000-30463800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr12:30467200-30468400	Enhancers	HepG2	liver
15	chr12:30467600-30468000	Enhancers	Liver	Liver
16	chr12:30469800-30470200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
17	chr12:30471400-30476000	Weak transcription	Gastric	stomach
18	chr12:30480600-30482800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr12:30481000-30482400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
20	chr12:30482000-30482400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr12:30482000-30482800	Enhancers	Muscle Satellite Cultured Cells	--
22	chr12:30482000-30483000	Enhancers	Hela-S3	cervix
23	chr12:30482400-30483000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:30482400-30483800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr12:30482800-30484600	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr12:30483000-30483800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr12:30483000-30484400	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr12:30483000-30484600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr12:30483000-30485800	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr12:30483200-30483600	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr12:30483800-30484400	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr12:30483800-30485200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr12:30484200-30484400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr12:30484400-30485400	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr12:30484600-30490400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr12:30485200-30486000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr12:30485400-30485600	Enhancers	HUES64 Cell Line	embryonic stem cell

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