Variant report

Variant	nsv518125
Chromosome Location	chr12:8615809-8671274
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:216)
CpG islands
(count:549)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:216 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:8645592-8646170	GM12878	blood:	n/a	n/a
2	BATF	chr12:8645651-8646023	GM12878	blood:	n/a	n/a
3	BATF	chr12:8645695-8646030	GM12878	blood:	n/a	n/a
4	BCL11A	chr12:8645664-8646072	GM12878	blood:	n/a	n/a
5	BRCA1	chr12:8652165-8652167	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr12:8625361-8625505	K562	blood:	n/a	chr12:8625404-8625415
7	CEBPB	chr12:8618896-8618945	IMR90	lung:	n/a	n/a
8	CEBPB	chr12:8628098-8628488	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr12:8625258-8625572	HepG2	liver:	n/a	chr12:8625404-8625415
10	CEBPB	chr12:8618848-8618887	K562	blood:	n/a	n/a
11	CEBPB	chr12:8625272-8625546	IMR90	lung:	n/a	chr12:8625404-8625415
12	CEBPB	chr12:8618664-8619005	A549	lung:	n/a	chr12:8618759-8618770
13	CEBPB	chr12:8618691-8618961	HepG2	liver:	n/a	chr12:8618759-8618770
14	CEBPB	chr12:8618781-8618905	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr12:8625263-8625538	A549	lung:	n/a	chr12:8625404-8625415
16	CHD2	chr12:8637815-8638033	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr12:8652400-8652550	GM12864	blood:	n/a	n/a
18	CTCF	chr12:8652380-8652530	HCT-116	colon:	n/a	n/a
19	CTCF	chr12:8652300-8652450	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr12:8652340-8652490	GM12867	blood:	n/a	n/a
21	CTCF	chr12:8652380-8652530	GM12871	blood:	n/a	n/a
22	CTCF	chr12:8652360-8652510	GM12873	blood:	n/a	n/a
23	CTCF	chr12:8652400-8652550	RPTEC	kidney:	n/a	n/a
24	CTCF	chr12:8652190-8652665	MCF-7	breast:	n/a	n/a
25	CTCF	chr12:8652320-8652470	HMEC	breast:	n/a	n/a
26	CTCF	chr12:8652340-8652490	Caco-2	colon:	n/a	n/a
27	CTCF	chr12:8652380-8652530	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr12:8652300-8652450	SAEC	small airway:	n/a	n/a
29	CTCF	chr12:8652320-8652470	HEK293	kidney:	n/a	n/a
30	CTCF	chr12:8652360-8652510	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr12:8652300-8652450	HRE	kidney:	n/a	n/a
32	CTCF	chr12:8652340-8652490	GM12873	blood:	n/a	n/a
33	CTCF	chr12:8652300-8652450	GM12869	blood:	n/a	n/a
34	CTCF	chr12:8652300-8652450	GM12866	blood:	n/a	n/a
35	CTCF	chr12:8652386-8652461	GM10266	blood:	n/a	n/a
36	CTCF	chr12:8652359-8652470	NHEK	skin:	n/a	n/a
37	CTCF	chr12:8652300-8652450	GM12873	blood:	n/a	n/a
38	CTCF	chr12:8652325-8652491	MCF-7	breast:	n/a	n/a
39	CTCF	chr12:8652320-8652470	GM12868	blood:	n/a	n/a
40	CTCF	chr12:8652350-8652569	GM12878	blood:	n/a	n/a
41	CTCF	chr12:8652256-8652700	HCT-116	colon:	n/a	n/a
42	CTCF	chr12:8661012-8661118	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr12:8652340-8652490	GM12874	blood:	n/a	n/a
44	CTCF	chr12:8652360-8652510	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr12:8641063-8641127	GM13977	blood:	n/a	n/a
46	CTCF	chr12:8661000-8661150	HepG2	liver:	n/a	n/a
47	CTCF	chr12:8652320-8652470	GM06990	blood:	n/a	n/a
48	CTCF	chr12:8652340-8652490	NHEK	skin:	n/a	n/a
49	CTCF	chr12:8652351-8652492	GM13977	blood:	n/a	n/a
50	CTCF	chr12:8652380-8652530	NHEK	skin:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8665133-8665183	Hela-S3	cervix:	n/a
2	chr12:8661976-8662026	BE2_C	brain:	n/a
3	chr12:8664963-8665013	HRE	kidney:	n/a
4	chr12:8664963-8665013	HRPEpiC	eye:	n/a
5	chr12:8665133-8665183	SKMC	muscle:	n/a
6	chr12:8661336-8661386	AoSMC	blood vessel:	n/a
7	chr12:8665044-8665094	NHBE	bronchial:	n/a
8	chr12:8637618-8637668	GM12878	blood:	n/a
9	chr12:8665373-8665423	Caco-2	colon:	n/a
10	chr12:8637618-8637668	NHDF-neo	bronchial:	n/a
11	chr12:8664963-8665013	HCF	heart:	n/a
12	chr12:8665373-8665423	SK-N-SH_RA	brain:	n/a
13	chr12:8666295-8666345	HCM	heart:	n/a
14	chr12:8661976-8662026	GM12892	blood:	n/a
15	chr12:8661336-8661386	GM12878	blood:	n/a
16	chr12:8665373-8665423	AoSMC	blood vessel:	n/a
17	chr12:8664963-8665013	K562	blood:	n/a
18	chr12:8665092-8665142	GM06990	blood:	n/a
19	chr12:8665133-8665183	A549	lung:	n/a
20	chr12:8665373-8665423	NH-A	brain:	n/a
21	chr12:8665133-8665183	BJ	skin:	n/a
22	chr12:8661976-8662026	ECC-1	luminal epithelium:	n/a
23	chr12:8661336-8661386	SK-N-SH_RA	brain:	n/a
24	chr12:8664963-8665013	PANC-1	pancreas:	n/a
25	chr12:8665092-8665142	HRPEpiC	eye:	n/a
26	chr12:8665373-8665423	NHDF-neo	bronchial:	n/a
27	chr12:8664963-8665013	Jurkat	blood:	n/a
28	chr12:8666295-8666345	HMEC	breast:	n/a
29	chr12:8665092-8665142	ECC-1	luminal epithelium:	n/a
30	chr12:8665133-8665183	HAEpiC	amniotic membrane:	n/a
31	chr12:8661336-8661386	HEK293	kidney:	embryo
32	chr12:8665092-8665142	NT2-D1	testis:	n/a
33	chr12:8665044-8665094	MCF10A-Er-Src	breast:	n/a
34	chr12:8664963-8665013	HEK293	kidney:	embryo
35	chr12:8665373-8665423	HRPEpiC	eye:	n/a
36	chr12:8637618-8637668	PFSK-1	brain:	n/a
37	chr12:8664963-8665013	HRCEpiC	kidney:	n/a
38	chr12:8665373-8665423	K562	blood:	n/a
39	chr12:8665373-8665423	GM12878	blood:	n/a
40	chr12:8665092-8665142	U87	brain:	n/a
41	chr12:8665044-8665094	HRE	kidney:	n/a
42	chr12:8664963-8665013	ECC-1	luminal epithelium:	n/a
43	chr12:8665092-8665142	SKMC	muscle:	n/a
44	chr12:8665373-8665423	HIPEpiC	eye:	n/a
45	chr12:8664963-8665013	AoSMC	blood vessel:	n/a
46	chr12:8665133-8665183	IMR90	lung:	fetal
47	chr12:8665133-8665183	HEK293	kidney:	embryo
48	chr12:8666295-8666345	Hepatocyte	liver:	n/a
49	chr12:8661976-8662026	HPAEpiC	pulmonary alveolar:	n/a
50	chr12:8664963-8665013	AG10803	skin:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:8625872..8627990-chr12:8629712..8631446,2	K562	blood:
2	chr12:8625872..8627990-chr12:8629712..8631446,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC4E-3	chr12:8664970-8665322	NONHSAT026344

No data

Variant related genes	Relation type
RNU6-275P	TF binding region
CLEC4D	TF binding region
ENSG00000246115	TF binding region
RNU6-275P	CpG island
CLEC4D	CpG island
ENSG00000246115	CpG island

Extended variants
information (count: 1274 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1274 , 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	rs4242889	chr12:8615809-8615810	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs73243430	chr12:8615902-8615903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183941528	chr12:8615911-8615912	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs74750864	chr12:8615926-8615927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs56372453	chr12:8615927-8615928	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374650794	chr12:8615949-8615950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34569377	chr12:8616037-8616038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189406258	chr12:8616089-8616090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553178277	chr12:8616141-8616142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4883154	chr12:8616149-8616150	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs541019564	chr12:8616259-8616260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs386760101	chr12:8616392-8616393	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192606462	chr12:8616394-8616395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs4242891	chr12:8616402-8616403	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs4242892	chr12:8616436-8616437	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs185644038	chr12:8616444-8616445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139259085	chr12:8616453-8616454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114194490	chr12:8616509-8616510	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563574783	chr12:8616550-8616551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147578494	chr12:8616608-8616609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371625636	chr12:8616755-8616756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190110898	chr12:8616830-8616831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529235258	chr12:8616846-8616847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141965572	chr12:8616895-8616896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145817485	chr12:8616919-8616920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200090850	chr12:8616930-8616931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148767383	chr12:8616931-8616932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs56131540	chr12:8616932-8616933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12810595	chr12:8616933-8616934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200064976	chr12:8616944-8616945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528231720	chr12:8616945-8616946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4301855	chr12:8616957-8616958	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs181761205	chr12:8616960-8616961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571694852	chr12:8616961-8616962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs370290009	chr12:8616964-8616965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4301856	chr12:8617018-8617019	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs374205852	chr12:8617026-8617027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs4303299	chr12:8617071-8617072	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs186321447	chr12:8617074-8617075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs112974505	chr12:8617175-8617176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs188739108	chr12:8617179-8617180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs371953454	chr12:8617205-8617206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs142518109	chr12:8617219-8617220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs369154938	chr12:8617221-8617222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536564809	chr12:8617223-8617224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs201517684	chr12:8617233-8617234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs180817093	chr12:8617259-8617260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs145055661	chr12:8617331-8617332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550376812	chr12:8617342-8617343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs201235229	chr12:8617382-8617383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8613600-8617400	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr12:8613800-8616600	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr12:8615200-8616400	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr12:8615200-8616600	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr12:8615200-8616600	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr12:8615200-8616800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr12:8615600-8616600	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr12:8615800-8616200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr12:8615800-8616600	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr12:8616200-8617000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr12:8616600-8618600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr12:8617000-8617200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr12:8617200-8617400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr12:8617200-8620200	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr12:8617400-8617600	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr12:8617400-8618800	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr12:8617600-8618400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
18	chr12:8618400-8619400	Active TSS	Monocytes-CD14+_RO01746	blood
19	chr12:8618800-8619000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr12:8618800-8619200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
21	chr12:8619200-8620400	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr12:8619400-8619800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
23	chr12:8619800-8620400	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr12:8624600-8625200	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr12:8624600-8625200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr12:8624800-8625000	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr12:8624800-8625200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr12:8624800-8625200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr12:8624800-8625200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr12:8625000-8625600	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr12:8625000-8627800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr12:8625200-8625600	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr12:8625200-8627600	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr12:8625200-8627800	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr12:8625200-8628000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr12:8625200-8628000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr12:8625200-8628000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr12:8626200-8627800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr12:8626600-8628000	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr12:8627600-8628800	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr12:8627600-8628800	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr12:8627600-8628800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr12:8627800-8628000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr12:8627800-8628000	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr12:8627800-8629000	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr12:8628000-8628200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr12:8628000-8628400	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr12:8628000-8628400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr12:8628000-8628400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr12:8628000-8628400	Enhancers	Fetal Intestine Large	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links