Variant report

Variant	nsv1035270
Chromosome Location	chr12:8619562-8674062
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:213)
CpG islands
(count:610)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:213 , 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	chr12:8625272-8625546	IMR90	lung:	n/a	chr12:8625404-8625415
8	CEBPB	chr12:8625263-8625538	A549	lung:	n/a	chr12:8625404-8625415
9	CEBPB	chr12:8628098-8628488	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr12:8625258-8625572	HepG2	liver:	n/a	chr12:8625404-8625415
11	CHD2	chr12:8637815-8638033	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr12:8661012-8661118	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr12:8652383-8652409	LNCaP	prostate:	n/a	n/a
14	CTCF	chr12:8652340-8652490	GM12867	blood:	n/a	n/a
15	CTCF	chr12:8652386-8652461	GM10266	blood:	n/a	n/a
16	CTCF	chr12:8652340-8652490	GM12873	blood:	n/a	n/a
17	CTCF	chr12:8652380-8652530	NHEK	skin:	n/a	n/a
18	CTCF	chr12:8652234-8652517	MCF-7	breast:	n/a	n/a
19	CTCF	chr12:8652300-8652450	GM12869	blood:	n/a	n/a
20	CTCF	chr12:8652280-8652430	GM12872	blood:	n/a	n/a
21	CTCF	chr12:8661000-8661150	HepG2	liver:	n/a	n/a
22	CTCF	chr12:8652320-8652470	GM12872	blood:	n/a	n/a
23	CTCF	chr12:8652418-8652427	LNCaP	prostate:	n/a	n/a
24	CTCF	chr12:8652320-8652470	HMEC	breast:	n/a	n/a
25	CTCF	chr12:8652380-8652530	GM12864	blood:	n/a	n/a
26	CTCF	chr12:8652280-8652430	GM12868	blood:	n/a	n/a
27	CTCF	chr12:8635079-8635145	GM20000	blood:	n/a	n/a
28	CTCF	chr12:8652420-8652570	GM12801	blood:	n/a	n/a
29	CTCF	chr12:8652396-8652422	K562	blood:	n/a	n/a
30	CTCF	chr12:8652320-8652470	HEK293	kidney:	n/a	n/a
31	CTCF	chr12:8652020-8652170	GM06990	blood:	n/a	n/a
32	CTCF	chr12:8652300-8652450	SAEC	small airway:	n/a	n/a
33	CTCF	chr12:8652385-8652437	HepG2	liver:	n/a	n/a
34	CTCF	chr12:8652320-8652470	GM12870	blood:	n/a	n/a
35	CTCF	chr12:8652380-8652530	GM12871	blood:	n/a	n/a
36	CTCF	chr12:8652340-8652490	Caco-2	colon:	n/a	n/a
37	CTCF	chr12:8652400-8652550	GM12864	blood:	n/a	n/a
38	CTCF	chr12:8660900-8661050	GM12872	blood:	n/a	n/a
39	CTCF	chr12:8652400-8652550	HL-60	blood:	n/a	n/a
40	CTCF	chr12:8641063-8641127	GM13977	blood:	n/a	n/a
41	CTCF	chr12:8652340-8652490	GM12875	blood:	n/a	n/a
42	CTCF	chr12:8652360-8652510	GM12865	blood:	n/a	n/a
43	CTCF	chr12:8652340-8652490	NB4	blood:	n/a	n/a
44	CTCF	chr12:8652340-8652490	SAEC	small airway:	n/a	n/a
45	CTCF	chr12:8652340-8652490	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr12:8652360-8652510	GM12873	blood:	n/a	n/a
47	CTCF	chr12:8652400-8652550	RPTEC	kidney:	n/a	n/a
48	CTCF	chr12:8652362-8652481	GM12878	blood:	n/a	n/a
49	CTCF	chr12:8652380-8652530	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr12:8652080-8652230	HMEC	breast:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8664963-8665013	HNPCEpiC	eye:	n/a
2	chr12:8665133-8665183	HCPEpiC	choroid plexus:	n/a
3	chr12:8661976-8662026	HRPEpiC	eye:	n/a
4	chr12:8665092-8665142	HUVEC	blood vessel:	n/a
5	chr12:8672038-8672088	MCF10A-Er-Src	breast:	n/a
6	chr12:8637618-8637668	IMR90	lung:	fetal
7	chr12:8665092-8665142	Hepatocyte	liver:	n/a
8	chr12:8665133-8665183	NT2-D1	testis:	n/a
9	chr12:8661336-8661386	LNCaP	prostate:	n/a
10	chr12:8666295-8666345	Jurkat	blood:	n/a
11	chr12:8664963-8665013	HPAEpiC	pulmonary alveolar:	n/a
12	chr12:8665044-8665094	ProgFib	skin:	n/a
13	chr12:8664963-8665013	NHDF-neo	bronchial:	n/a
14	chr12:8666295-8666345	NHBE	bronchial:	n/a
15	chr12:8665133-8665183	SAEC	small airway:	n/a
16	chr12:8665133-8665183	HCT-116	colon:	n/a
17	chr12:8661336-8661386	Hepatocyte	liver:	n/a
18	chr12:8672038-8672088	HEK293	kidney:	embryo
19	chr12:8661336-8661386	H1-hESC	embryonic stem cell:	embryo
20	chr12:8665092-8665142	GM19239	blood:	n/a
21	chr12:8665092-8665142	HL-60	blood:	n/a
22	chr12:8664963-8665013	HL-60	blood:	n/a
23	chr12:8665044-8665094	HEEpiC	esophagus:	n/a
24	chr12:8665044-8665094	RPTEC	kidney:	n/a
25	chr12:8665133-8665183	SK-N-SH_RA	brain:	n/a
26	chr12:8665044-8665094	HIPEpiC	eye:	n/a
27	chr12:8665133-8665183	HAEpiC	amniotic membrane:	n/a
28	chr12:8661336-8661386	GM19239	blood:	n/a
29	chr12:8661976-8662026	PrEC	prostate:	n/a
30	chr12:8665044-8665094	SKMC	muscle:	n/a
31	chr12:8666295-8666345	Caco-2	colon:	n/a
32	chr12:8637618-8637668	GM19239	blood:	n/a
33	chr12:8665373-8665423	HAEpiC	amniotic membrane:	n/a
34	chr12:8665044-8665094	NH-A	brain:	n/a
35	chr12:8665373-8665423	AG04450	lung:	fetal
36	chr12:8637618-8637668	HIPEpiC	eye:	n/a
37	chr12:8672038-8672088	AG10803	skin:	n/a
38	chr12:8661976-8662026	MCF10A-Er-Src	breast:	n/a
39	chr12:8637618-8637668	ovcar-3	ovarian:	n/a
40	chr12:8665044-8665094	MCF10A-Er-Src	breast:	n/a
41	chr12:8661976-8662026	GM06990	blood:	n/a
42	chr12:8665092-8665142	HCM	heart:	n/a
43	chr12:8665373-8665423	HRE	kidney:	n/a
44	chr12:8661336-8661386	NHBE	bronchial:	n/a
45	chr12:8665373-8665423	NH-A	brain:	n/a
46	chr12:8661976-8662026	K562	blood:	n/a
47	chr12:8664963-8665013	SAEC	small airway:	n/a
48	chr12:8637618-8637668	HEEpiC	esophagus:	n/a
49	chr12:8665092-8665142	HAEpiC	amniotic membrane:	n/a
50	chr12:8666295-8666345	HepG2	liver:	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: 1252 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1252 , 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	rs4447245	chr12:8619562-8619563	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569408245	chr12:8619617-8619618	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs71447503	chr12:8619653-8619654	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs77545239	chr12:8619700-8619701	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs143320702	chr12:8619737-8619738	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs537161204	chr12:8619749-8619750	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs4427631	chr12:8619792-8619793	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs141108958	chr12:8619852-8619853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs78055995	chr12:8619858-8619859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188794395	chr12:8619871-8619872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs144818726	chr12:8619923-8619924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs75220987	chr12:8619968-8619969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs117876331	chr12:8619973-8619974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs7978179	chr12:8620065-8620066	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs34324812	chr12:8620134-8620135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs397740921	chr12:8620135-8620136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs7962791	chr12:8620185-8620186	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs545266538	chr12:8620298-8620299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs564953993	chr12:8620306-8620307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs7963053	chr12:8620339-8620340	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs138656121	chr12:8620358-8620359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140624407	chr12:8620361-8620362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs190549342	chr12:8624667-8624668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs144336501	chr12:8624714-8624715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs574261337	chr12:8624724-8624725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs75353866	chr12:8624743-8624744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs376662565	chr12:8624804-8624805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs7976958	chr12:8624890-8624891	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs148439770	chr12:8624902-8624903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142553353	chr12:8624943-8624944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537910650	chr12:8624949-8624950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554188720	chr12:8625081-8625082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577259990	chr12:8625082-8625083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546217891	chr12:8625133-8625134	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376546666	chr12:8625204-8625205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs370123765	chr12:8625247-8625248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562853426	chr12:8625294-8625295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs202070610	chr12:8625593-8625594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs532071854	chr12:8625869-8625870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12321576	chr12:8625870-8625871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200064030	chr12:8625887-8625888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201215747	chr12:8625888-8625889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201702280	chr12:8625889-8625890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376226774	chr12:8625993-8625994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs72621031	chr12:8626008-8626009	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs114070724	chr12:8626040-8626041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114623774	chr12:8626080-8626081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115368803	chr12:8626091-8626092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146744618	chr12:8626098-8626099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373625839	chr12:8626137-8626138	Weak transcription	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:295 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8617200-8620200	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr12:8619200-8620400	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr12:8619400-8619800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr12:8619800-8620400	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr12:8624600-8625200	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr12:8624600-8625200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr12:8624800-8625000	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr12:8624800-8625200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr12:8624800-8625200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr12:8624800-8625200	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr12:8625000-8625600	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr12:8625000-8627800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr12:8625200-8625600	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr12:8625200-8627600	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr12:8625200-8627800	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr12:8625200-8628000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr12:8625200-8628000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr12:8625200-8628000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr12:8626200-8627800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr12:8626600-8628000	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr12:8627600-8628800	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr12:8627600-8628800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr12:8627600-8628800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr12:8627800-8628000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr12:8627800-8628000	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr12:8627800-8629000	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr12:8628000-8628200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr12:8628000-8628400	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr12:8628000-8628400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr12:8628000-8628400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr12:8628000-8628400	Enhancers	Fetal Intestine Large	intestine
32	chr12:8628000-8628400	Enhancers	Fetal Intestine Small	intestine
33	chr12:8628000-8628800	Enhancers	H9 Cell Line	embryonic stem cell
34	chr12:8628000-8628800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr12:8628000-8628800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
36	chr12:8628000-8628800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr12:8628000-8629000	Enhancers	H1 Cell Line	embryonic stem cell
38	chr12:8628000-8629600	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr12:8628000-8638200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr12:8628200-8628400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
41	chr12:8628400-8628600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr12:8628400-8630000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr12:8628400-8637400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr12:8628600-8628800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr12:8628800-8629800	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr12:8628800-8630200	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr12:8628800-8630200	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr12:8629800-8630000	Enhancers	H9 Cell Line	embryonic stem cell
49	chr12:8630000-8630600	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr12:8634400-8636200	Enhancers	Fetal Thymus	thymus

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