Variant report

Variant	nsv898625
Chromosome Location	chr12:4759380-4771682
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:42)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:42 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr12:4759436-4759663	HepG2	liver:	n/a	n/a
2	CEBPB	chr12:4759955-4760222	HepG2	liver:	n/a	chr12:4760126-4760137 chr12:4760126-4760139 chr12:4760127-4760138
3	CEBPB	chr12:4760017-4760288	K562	blood:	n/a	chr12:4760126-4760137 chr12:4760126-4760139 chr12:4760127-4760138
4	CTCF	chr12:4762440-4762590	AG04449	skin:	n/a	n/a
5	CTCF	chr12:4762380-4762530	Caco-2	colon:	n/a	n/a
6	CTCF	chr12:4762380-4762530	HPAF	blood vessel:	n/a	n/a
7	CTCF	chr12:4762500-4762650	AG10803	skin:	n/a	n/a
8	CTCF	chr12:4762380-4762530	HMEC	breast:	n/a	n/a
9	CTCF	chr12:4762460-4762610	HCPEpiC	choroid plexus:	n/a	n/a
10	CTCF	chr12:4762500-4762650	HEK293	kidney:	n/a	n/a
11	CTCF	chr12:4764900-4765050	NHEK	skin:	n/a	n/a
12	CTCF	chr12:4762460-4762610	RPTEC	kidney:	n/a	n/a
13	CTCF	chr12:4762400-4762550	HRPEpiC	eye:	n/a	n/a
14	CTCF	chr12:4762460-4762610	HA-sp	spinal cord:	n/a	n/a
15	CTCF	chr12:4762420-4762570	HRPEpiC	eye:	n/a	n/a
16	CTCF	chr12:4762420-4762570	HVMF	connective:	n/a	n/a
17	CTCF	chr12:4762360-4762510	AG04450	lung:	n/a	n/a
18	ELK1	chr12:4771036-4771111	Hela-S3	cervix:	n/a	n/a
19	GATA3	chr12:4759954-4760238	SH-SY5Y	brain:	n/a	n/a
20	JUN	chr12:4759443-4759617	HepG2	liver:	n/a	n/a
21	JUND	chr12:4763890-4764208	HepG2	liver:	n/a	n/a
22	JUND	chr12:4759421-4759624	HepG2	liver:	n/a	n/a
23	MAFK	chr12:4765883-4765953	HepG2	liver:	n/a	n/a
24	MYC	chr12:4762070-4762179	MCF10A-Er-Src	breast:	n/a	n/a
25	POLR2A	chr12:4767800-4767838	HUVEC	blood vessel:	n/a	n/a
26	POLR2A	chr12:4763504-4763539	MCF-7	breast:	n/a	n/a
27	POLR2A	chr12:4759303-4759386	MCF10A-Er-Src	breast:	n/a	n/a
28	POLR2A	chr12:4763410-4763663	A549	lung:	n/a	n/a
29	POLR2A	chr12:4763543-4763573	MCF-7	breast:	n/a	n/a
30	POLR2A	chr12:4760657-4760691	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr12:4765653-4765744	K562	blood:	n/a	n/a
32	RAD21	chr12:4766037-4766046	A549	lung:	n/a	n/a
33	RAD21	chr12:4762425-4762648	H1-hESC	embryonic stem cell:	n/a	n/a
34	RAD21	chr12:4762377-4762652	H1-hESC	embryonic stem cell:	n/a	n/a
35	REST	chr12:4757476-4759419	H1-neurons	neurons:	n/a	n/a
36	STAT3	chr12:4770649-4770651	MCF10A-Er-Src	breast:	n/a	n/a
37	STAT3	chr12:4769480-4769510	MCF10A-Er-Src	breast:	n/a	n/a
38	STAT3	chr12:4770025-4770032	GM12878	blood:	n/a	n/a
39	STAT3	chr12:4769466-4769686	MCF10A-Er-Src	breast:	n/a	n/a
40	STAT3	chr12:4759542-4759581	MCF10A-Er-Src	breast:	n/a	n/a
41	STAT3	chr12:4762095-4762276	MCF10A-Er-Src	breast:	n/a	n/a
42	ZNF263	chr12:4759676-4760127	HEK293-T-REx	kidney:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:4762206-4762256	SKMC	muscle:	n/a
2	chr12:4762206-4762256	A549	lung:	n/a
3	chr12:4762206-4762256	NB4	blood:	n/a
4	chr12:4762206-4762256	GM12878	blood:	n/a
5	chr12:4762206-4762256	NH-A	brain:	n/a
6	chr12:4762206-4762256	LNCaP	prostate:	n/a
7	chr12:4762206-4762256	HCPEpiC	choroid plexus:	n/a
8	chr12:4762206-4762256	MCF-7	breast:	n/a
9	chr12:4762206-4762256	HRCEpiC	kidney:	n/a
10	chr12:4762206-4762256	HNPCEpiC	eye:	n/a
11	chr12:4762206-4762256	HUVEC	blood vessel:	n/a
12	chr12:4762206-4762256	RPTEC	kidney:	n/a
13	chr12:4762206-4762256	CMK	blood:	n/a
14	chr12:4762206-4762256	AG09319	gingival:	n/a
15	chr12:4762206-4762256	HCM	heart:	n/a
16	chr12:4762206-4762256	Jurkat	blood:	n/a
17	chr12:4762206-4762256	AoSMC	blood vessel:	n/a
18	chr12:4762206-4762256	H1-hESC	embryonic stem cell:	embryo
19	chr12:4762206-4762256	HPAEpiC	pulmonary alveolar:	n/a
20	chr12:4762206-4762256	GM06990	blood:	n/a
21	chr12:4762206-4762256	AG09309	skin:	n/a
22	chr12:4762206-4762256	Hepatocyte	liver:	n/a
23	chr12:4762206-4762256	HepG2	liver:	n/a
24	chr12:4762206-4762256	GM19239	blood:	n/a
25	chr12:4762206-4762256	AG04450	lung:	fetal
26	chr12:4762206-4762256	BE2_C	brain:	n/a
27	chr12:4762206-4762256	SK-N-SH	brain:	n/a
28	chr12:4762206-4762256	MCF10A-Er-Src	breast:	n/a
29	chr12:4762206-4762256	HCT-116	colon:	n/a
30	chr12:4762206-4762256	ProgFib	skin:	n/a
31	chr12:4762206-4762256	IMR90	lung:	fetal
32	chr12:4762206-4762256	ECC-1	luminal epithelium:	n/a
33	chr12:4762206-4762256	PrEC	prostate:	n/a
34	chr12:4762206-4762256	SAEC	small airway:	n/a
35	chr12:4762206-4762256	Caco-2	colon:	n/a
36	chr12:4762206-4762256	HL-60	blood:	n/a
37	chr12:4762206-4762256	HCF	heart:	n/a
38	chr12:4762206-4762256	AG04449	skin:	fetal
39	chr12:4762206-4762256	GM12892	blood:	n/a
40	chr12:4762206-4762256	HEK293	kidney:	embryo
41	chr12:4762206-4762256	NHBE	bronchial:	n/a
42	chr12:4762206-4762256	GM12891	blood:	n/a
43	chr12:4762206-4762256	U87	brain:	n/a
44	chr12:4762206-4762256	HIPEpiC	eye:	n/a
45	chr12:4762206-4762256	HMEC	breast:	n/a
46	chr12:4762206-4762256	ovcar-3	ovarian:	n/a
47	chr12:4762206-4762256	HAEpiC	amniotic membrane:	n/a
48	chr12:4762206-4762256	BJ	skin:	n/a
49	chr12:4762206-4762256	NHDF-neo	bronchial:	n/a
50	chr12:4762206-4762256	SK-N-MC	brain:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:4756861..4759668-chr12:4760395..4765208,7	MCF-7	breast:
2	chr12:4757989..4759732-chr12:4759874..4761785,2	MCF-7	breast:
3	chr12:4758240..4760595-chr12:4768074..4769785,2	K562	blood:
4	chr12:4757018..4762059-chr12:4764285..4767290,6	K562	blood:
5	chr12:4754845..4760714-chr12:4761830..4765057,7	MCF-7	breast:
6	chr12:4762857..4765662-chr12:4767685..4769794,2	K562	blood:
7	chr12:4757018..4762059-chr12:4764285..4767290,6	K562	blood:
8	chr12:4762342..4764303-chr12:4764418..4767058,2	K562	blood:
9	chr12:4754845..4760714-chr12:4761830..4765057,7	MCF-7	breast:
10	chr12:4757063..4759938-chr12:4760465..4764038,5	K562	blood:
11	chr12:4762342..4764303-chr12:4764418..4767058,2	K562	blood:
12	chr12:4757063..4759938-chr12:4760465..4764038,5	K562	blood:
13	chr12:4751073..4755821-chr12:4757118..4761577,5	MCF-7	breast:
14	chr12:4758381..4761405-chr12:4778974..4782071,3	K562	blood:
15	chr12:4756861..4759668-chr12:4760395..4765208,7	MCF-7	breast:
16	chr12:4757573..4759938-chr12:4760465..4764276,3	K562	blood:
17	chr12:4757573..4759938-chr12:4760465..4764276,3	K562	blood:
18	chr12:4762857..4765662-chr12:4767685..4769794,2	K562	blood:

No data

Variant related genes	Relation type
NDUFA9	TF binding region
ENSG00000255639	TF binding region
AKAP3	TF binding region
NDUFA9	CpG island
ENSG00000255639	CpG island
AKAP3	CpG island
ENSG00000255639	chromatin interactions
ENSG00000256381	chromatin interactions
ENSG00000139180	chromatin interactions
ENSG00000111254	chromatin interactions

Extended variants
information (count: 486 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:486 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2159352	chr12:4759380-4759381	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs543481177	chr12:4759384-4759385	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs148146378	chr12:4759424-4759425	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs572699388	chr12:4759431-4759432	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs141024838	chr12:4759530-4759531	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs191719250	chr12:4759555-4759556	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs145100393	chr12:4759556-4759557	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs543483363	chr12:4759565-4759566	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs74380742	chr12:4759609-4759610	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs529378192	chr12:4759658-4759659	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs114477218	chr12:4759677-4759678	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs183814685	chr12:4759699-4759700	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs187012422	chr12:4759769-4759770	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs547599147	chr12:4759822-4759823	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs367600327	chr12:4759944-4759945	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs117919566	chr12:4759968-4759969	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs78398398	chr12:4759984-4759985	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs372250984	chr12:4760045-4760046	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs569693711	chr12:4760082-4760083	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs112133437	chr12:4760094-4760095	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs551917543	chr12:4760108-4760109	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs11063279	chr12:4760135-4760136	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs566020758	chr12:4760148-4760149	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs534951674	chr12:4760195-4760196	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs11063280	chr12:4760229-4760230	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs574646187	chr12:4760255-4760256	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs528735094	chr12:4760274-4760275	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs192267539	chr12:4760296-4760297	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs35167443	chr12:4760317-4760318	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs577312971	chr12:4760383-4760384	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs546157134	chr12:4760412-4760413	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs372110415	chr12:4760436-4760437	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs116593611	chr12:4760437-4760438	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs573287678	chr12:4760444-4760445	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs541301912	chr12:4760465-4760466	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs561168682	chr12:4760467-4760468	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs185115878	chr12:4760530-4760531	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs543300867	chr12:4760542-4760543	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs563377769	chr12:4760543-4760544	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs532145513	chr12:4760545-4760546	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs144624993	chr12:4760566-4760567	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs565309065	chr12:4760571-4760572	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs80178477	chr12:4760585-4760586	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs11615364	chr12:4760662-4760663	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs201830079	chr12:4760674-4760675	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs568456804	chr12:4760683-4760684	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs369643340	chr12:4760685-4760686	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs2159351	chr12:4760725-4760726	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs190757684	chr12:4760748-4760749	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs10744657	chr12:4760790-4760791	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Ovarian cancer	20844748	CNVD
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
low-grade B-cell lymphoma tumor	18367492	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
lymphocytic leukemia	21291569	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Epilepsy	21858020	CNVD
Colorectal cancer	19359472	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:586 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:4757200-4759400	Flanking Active TSS	Primary B cells from cord blood	blood
2	chr12:4757200-4759400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr12:4757200-4759400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr12:4757200-4759400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr12:4757200-4759400	Active TSS	K562	blood
6	chr12:4757200-4759400	Active TSS	NHDF-Ad	bronchial
7	chr12:4757200-4760200	Active TSS	Right Atrium	heart
8	chr12:4757400-4759400	Active TSS	Fetal Intestine Small	intestine
9	chr12:4757400-4759600	Active TSS	H1 Cell Line	embryonic stem cell
10	chr12:4757400-4759600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr12:4757400-4759800	Active TSS	Psoas Muscle	Psoas
12	chr12:4757400-4759800	Active TSS	Right Ventricle	heart
13	chr12:4757600-4759400	Active TSS	HUES48 Cell Line	embryonic stem cell
14	chr12:4757600-4759400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr12:4757600-4759400	Active TSS	Skeletal Muscle Male	skeletal muscle
16	chr12:4757600-4759400	Active TSS	HSMM	muscle
17	chr12:4757600-4759600	Active TSS	HUES6 Cell Line	embryonic stem cell
18	chr12:4757600-4759600	Active TSS	Left Ventricle	heart
19	chr12:4757600-4760000	Active TSS	iPS-20b Cell Line	embryonic stem cell
20	chr12:4757600-4760200	Active TSS	HUES64 Cell Line	embryonic stem cell
21	chr12:4758000-4759400	Active TSS	Fetal Muscle Leg	muscle
22	chr12:4758600-4759400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
23	chr12:4758600-4759400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
24	chr12:4758600-4759400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
25	chr12:4758600-4759600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
26	chr12:4758600-4759600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr12:4758600-4759600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr12:4758600-4759600	Flanking Active TSS	Adipose Nuclei	Adipose
29	chr12:4758800-4759400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
30	chr12:4758800-4759400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
31	chr12:4758800-4759400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
32	chr12:4758800-4759400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr12:4758800-4759400	Flanking Active TSS	Liver	Liver
34	chr12:4758800-4759400	Flanking Active TSS	Brain Cingulate Gyrus	brain
35	chr12:4758800-4759400	Flanking Active TSS	Colonic Mucosa	Colon
36	chr12:4758800-4759400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
37	chr12:4758800-4759400	Active TSS	HepG2	liver
38	chr12:4758800-4759600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr12:4758800-4759600	Flanking Active TSS	Brain Anterior Caudate	brain
40	chr12:4758800-4759600	Flanking Active TSS	Brain Hippocampus Middle	brain
41	chr12:4758800-4759600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
42	chr12:4758800-4759600	Flanking Active TSS	Fetal Brain Male	brain
43	chr12:4758800-4759800	Flanking Active TSS	Primary T cells from cord blood	blood
44	chr12:4758800-4759800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
45	chr12:4758800-4759800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
46	chr12:4758800-4759800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr12:4758800-4759800	Flanking Active TSS	HUVEC	blood vessel
48	chr12:4758800-4760000	Flanking Active TSS	Brain Angular Gyrus	brain
49	chr12:4758800-4760000	Flanking Active TSS	Brain Germinal Matrix	brain
50	chr12:4758800-4760000	Flanking Active TSS	Duodenum Mucosa	Duodenum

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