Variant report

Variant	nsv557274
Chromosome Location	chr12:7826305-7864976
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	chr12:7829849-7830314	K562	blood:	n/a	n/a
2	ATF1	chr12:7830074-7830292	K562	blood:	n/a	n/a
3	BCL11A	chr12:7847177-7847525	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr12:7830115-7830384	K562	blood:	n/a	n/a
5	CCNT2	chr12:7830037-7830516	K562	blood:	n/a	n/a
6	CEBPB	chr12:7831378-7831569	HepG2	liver:	n/a	chr12:7831481-7831492
7	CEBPB	chr12:7830048-7830266	K562	blood:	n/a	n/a
8	CEBPB	chr12:7829994-7830410	K562	blood:	n/a	n/a
9	CEBPB	chr12:7831347-7831597	A549	lung:	n/a	chr12:7831481-7831492
10	CEBPB	chr12:7831409-7831572	H1-hESC	embryonic stem cell:	n/a	chr12:7831481-7831492
11	CEBPB	chr12:7831324-7831596	K562	blood:	n/a	chr12:7831481-7831492
12	CEBPB	chr12:7858008-7858310	MCF-7	breast:	n/a	n/a
13	CEBPB	chr12:7831271-7831764	A549	lung:	n/a	chr12:7831481-7831492
14	CEBPB	chr12:7831324-7831648	MCF-7	breast:	n/a	chr12:7831481-7831492
15	CEBPB	chr12:7862941-7863193	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr12:7830001-7830305	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr12:7862936-7863185	K562	blood:	n/a	n/a
18	CEBPB	chr12:7830082-7830313	MCF-7	breast:	n/a	n/a
19	CEBPB	chr12:7831340-7831533	Hela-S3	cervix:	n/a	chr12:7831481-7831492
20	CEBPB	chr12:7830093-7830216	HepG2	liver:	n/a	n/a
21	CEBPB	chr12:7829991-7830371	K562	blood:	n/a	n/a
22	CEBPD	chr12:7829922-7830476	K562	blood:	n/a	n/a
23	CEBPD	chr12:7829937-7830385	K562	blood:	n/a	n/a
24	CTCF	chr12:7830040-7830190	HPF	lung:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
25	CTCF	chr12:7830075-7830263	Lung_OC	lung:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
26	CTCF	chr12:7830060-7830210	HEEpiC	esophagus:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
27	CTCF	chr12:7829709-7830320	SK-N-SH	brain:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
28	CTCF	chr12:7829757-7830368	HCT-116	colon:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
29	CTCF	chr12:7830020-7830170	GM06990	blood:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
30	CTCF	chr12:7829620-7829770	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr12:7830019-7830208	Pancreas_OC	pancreas:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
32	CTCF	chr12:7830020-7830170	GM12868	blood:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
33	CTCF	chr12:7830020-7830170	AG10803	skin:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
34	CTCF	chr12:7830060-7830210	NHEK	skin:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
35	CTCF	chr12:7829929-7830310	GM12878	blood:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
36	CTCF	chr12:7830000-7830150	HAc	cerebellar:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
37	CTCF	chr12:7830060-7830210	HMF	breast:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
38	CTCF	chr12:7829853-7830290	HCT-116	colon:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
39	CTCF	chr12:7830030-7830231	LNCaP	prostate:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
40	CTCF	chr12:7864095-7864203	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr12:7830020-7830170	AG04450	lung:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
42	CTCF	chr12:7830004-7830245	Gliobla	brain:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
43	CTCF	chr12:7830014-7830188	A549	lung:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
44	CTCF	chr12:7829969-7830240	IMR90	lung:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
45	CTCF	chr12:7830060-7830210	MCF-7	breast:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
46	CTCF	chr12:7858580-7858730	Caco-2	colon:	n/a	n/a
47	CTCF	chr12:7830020-7830170	GM12871	blood:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
48	CTCF	chr12:7830080-7830230	GM12873	blood:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
49	CTCF	chr12:7830080-7830230	AG04449	skin:	n/a	chr12:7830113-7830131 chr12:7830115-7830136
50	CTCF	chr12:7829977-7830201	SK-N-SH_RA	brain:	n/a	chr12:7830113-7830131 chr12:7830115-7830136

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:7864122-7864172	HCM	heart:	n/a
2	chr12:7864122-7864172	HCM	heart:	n/a
3	chr12:7863853-7863903	AG04449	skin:	fetal
4	chr12:7858664-7858714	AG09319	gingival:	n/a
5	chr12:7857833-7857883	HepG2	liver:	n/a
6	chr12:7864058-7864108	K562	blood:	n/a
7	chr12:7849439-7849489	ovcar-3	ovarian:	n/a
8	chr12:7848348-7848398	HUVEC	blood vessel:	n/a
9	chr12:7858763-7858813	SK-N-SH	brain:	n/a
10	chr12:7858598-7858648	ovcar-3	ovarian:	n/a
11	chr12:7847919-7847969	Caco-2	colon:	n/a
12	chr12:7864013-7864063	HPAEpiC	pulmonary alveolar:	n/a
13	chr12:7854553-7854603	HPAEpiC	pulmonary alveolar:	n/a
14	chr12:7848093-7848143	HL-60	blood:	n/a
15	chr12:7863229-7863279	HRCEpiC	kidney:	n/a
16	chr12:7864013-7864063	HCPEpiC	choroid plexus:	n/a
17	chr12:7858668-7858718	HEEpiC	esophagus:	n/a
18	chr12:7848348-7848398	GM19239	blood:	n/a
19	chr12:7863229-7863279	AG04449	skin:	fetal
20	chr12:7864013-7864063	HIPEpiC	eye:	n/a
21	chr12:7847919-7847969	HRCEpiC	kidney:	n/a
22	chr12:7858592-7858642	Hela-S3	cervix:	n/a
23	chr12:7862691-7862741	Caco-2	colon:	n/a
24	chr12:7857833-7857883	CMK	blood:	n/a
25	chr12:7848647-7848697	NH-A	brain:	n/a
26	chr12:7864076-7864126	HCM	heart:	n/a
27	chr12:7864013-7864063	Hela-S3	cervix:	n/a
28	chr12:7864047-7864097	HUVEC	blood vessel:	n/a
29	chr12:7862691-7862741	A549	lung:	n/a
30	chr12:7864058-7864108	GM12878	blood:	n/a
31	chr12:7864047-7864097	RPTEC	kidney:	n/a
32	chr12:7848647-7848697	K562	blood:	n/a
33	chr12:7858848-7858898	HCPEpiC	choroid plexus:	n/a
34	chr12:7858668-7858718	AG09319	gingival:	n/a
35	chr12:7849439-7849489	NT2-D1	testis:	n/a
36	chr12:7864013-7864063	NHDF-neo	bronchial:	n/a
37	chr12:7863229-7863279	H1-hESC	embryonic stem cell:	embryo
38	chr12:7858592-7858642	HRCEpiC	kidney:	n/a
39	chr12:7858598-7858648	PFSK-1	brain:	n/a
40	chr12:7864122-7864172	Hela-S3	cervix:	n/a
41	chr12:7848093-7848143	HCF	heart:	n/a
42	chr12:7848647-7848697	HCM	heart:	n/a
43	chr12:7858598-7858648	ECC-1	luminal epithelium:	n/a
44	chr12:7858668-7858718	MCF-7	breast:	n/a
45	chr12:7858763-7858813	PANC-1	pancreas:	n/a
46	chr12:7858763-7858813	Jurkat	blood:	n/a
47	chr12:7848093-7848143	GM12892	blood:	n/a
48	chr12:7858848-7858898	AG04450	lung:	fetal
49	chr12:7849439-7849489	HEEpiC	esophagus:	n/a
50	chr12:7858598-7858648	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:7830039..7830628-chr12:7959515..7960112,3	K562	blood:
2	chr12:7829622..7830601-chr12:7959144..7960112,6	MCF-7	breast:

Variant related genes	Relation type
GDF3	TF binding region
DPPA3	TF binding region
GDF3	CpG island
DPPA3	CpG island

Extended variants
information (count: 1209 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1209 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10845677	chr12:7826305-7826306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186138865	chr12:7826347-7826348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148845960	chr12:7826371-7826372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190810530	chr12:7826398-7826399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574494721	chr12:7826490-7826491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs113932820	chr12:7826516-7826517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs147181872	chr12:7826523-7826524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs67415580	chr12:7826590-7826591	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs188107016	chr12:7826620-7826621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546354792	chr12:7826644-7826645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs10845679	chr12:7826657-7826658	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs370103904	chr12:7826685-7826686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs10845680	chr12:7826705-7826706	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs377709137	chr12:7826718-7826719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371170921	chr12:7826746-7826747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs111810423	chr12:7826814-7826815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201012974	chr12:7826817-7826818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567226745	chr12:7826859-7826860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs61937022	chr12:7826887-7826888	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs546883055	chr12:7826920-7826921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567717143	chr12:7826942-7826943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192576660	chr12:7827059-7827060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182648995	chr12:7827070-7827071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs11055171	chr12:7827072-7827073	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs375032852	chr12:7827095-7827096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs538584818	chr12:7827205-7827206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144870551	chr12:7827274-7827275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs558708246	chr12:7827297-7827298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556548622	chr12:7827449-7827450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs67346847	chr12:7827510-7827511	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs372663359	chr12:7827543-7827544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs538289125	chr12:7827559-7827560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs35247626	chr12:7827722-7827723	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs111365263	chr12:7827728-7827729	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs539364333	chr12:7827744-7827745	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs117266200	chr12:7827767-7827768	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs10845681	chr12:7827807-7827808	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs147838403	chr12:7827878-7827879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573020206	chr12:7827887-7827888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs540251290	chr12:7827946-7827947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs188861438	chr12:7827957-7827958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192530460	chr12:7828060-7828061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141490132	chr12:7828151-7828152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7955948	chr12:7828221-7828222	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs7978728	chr12:7828231-7828232	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs543195972	chr12:7828275-7828276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs184844737	chr12:7828336-7828337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188922489	chr12:7828404-7828405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs7967641	chr12:7828425-7828426	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs138053584	chr12:7828494-7828495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	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
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Nasopharyngeal cancer	20548289	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Type 2 diabetes	21526130	CNVD

Chromatin state (count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:7824200-7846000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:7827000-7828800	Enhancers	Primary B cells from cord blood	blood
3	chr12:7827000-7828800	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr12:7827000-7831200	Enhancers	Primary hematopoietic stem cells	blood
5	chr12:7827000-7832600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr12:7827200-7829600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr12:7827200-7830400	Enhancers	Primary B cells from peripheral blood	blood
8	chr12:7827200-7832600	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr12:7827400-7828200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr12:7827400-7829000	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr12:7827600-7827800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
12	chr12:7827600-7828200	Enhancers	Rectal Mucosa Donor 29	rectum
13	chr12:7828800-7829600	Weak transcription	Primary B cells from cord blood	blood
14	chr12:7828800-7830000	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr12:7829000-7830200	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr12:7829400-7830400	Enhancers	A549	lung
17	chr12:7829600-7830000	Enhancers	Primary B cells from cord blood	blood
18	chr12:7829600-7830000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr12:7829600-7830200	Enhancers	Duodenum Mucosa	Duodenum
20	chr12:7829600-7830200	Enhancers	HepG2	liver
21	chr12:7829600-7830400	Enhancers	GM12878-XiMat	blood
22	chr12:7829800-7830000	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr12:7829800-7830000	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr12:7829800-7830200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr12:7829800-7830400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr12:7829800-7830600	Enhancers	K562	blood
27	chr12:7829800-7830800	Enhancers	HUVEC	blood vessel
28	chr12:7829800-7831400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr12:7830000-7830400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr12:7830000-7830400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr12:7830000-7830400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
32	chr12:7830000-7832000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr12:7830000-7846400	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr12:7830200-7830600	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr12:7830200-7830600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
36	chr12:7830200-7830600	Weak transcription	Duodenum Mucosa	Duodenum
37	chr12:7830200-7830600	Enhancers	Fetal Brain Male	brain
38	chr12:7830200-7832200	Enhancers	Adipose Nuclei	Adipose
39	chr12:7830200-7832200	Weak transcription	HepG2	liver
40	chr12:7830400-7830600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr12:7830400-7830600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr12:7830400-7832000	Enhancers	Placenta	Placenta
43	chr12:7830400-7832200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr12:7830400-7832200	Weak transcription	A549	lung
45	chr12:7830600-7831200	Enhancers	Duodenum Mucosa	Duodenum
46	chr12:7830600-7831800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr12:7830600-7832400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr12:7831200-7831600	Weak transcription	Primary hematopoietic stem cells	blood
49	chr12:7831600-7832600	Enhancers	Primary hematopoietic stem cells	blood
50	chr12:7831800-7832600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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