Variant report

Variant	nsv976745
Chromosome Location	chr12:51203441-51215185
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:34)
CpG islands
(count:62)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:34 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr12:51208925-51208927	Hela-S3	cervix:	n/a	n/a
2	CTCF	chr12:51204735-51204905	MCF-7	breast:	n/a	n/a
3	CTCF	chr12:51204830-51204859	LNCaP	prostate:	n/a	n/a
4	CTCF	chr12:51204786-51204889	MCF-7	breast:	n/a	n/a
5	CTCF	chr12:51204760-51204887	MCF-7	breast:	n/a	n/a
6	CTCF	chr12:51204720-51204870	Hela-S3	cervix:	n/a	n/a
7	CTCF	chr12:51204720-51204870	MCF-7	breast:	n/a	n/a
8	CTCF	chr12:51204814-51204877	Gliobla	brain:	n/a	n/a
9	CTCF	chr12:51204776-51204892	MCF-7	breast:	n/a	n/a
10	E2F4	chr12:51209390-51209547	MCF10A-Er-Src	breast:	n/a	n/a
11	FOXA1	chr12:51215068-51215439	HepG2	liver:	n/a	n/a
12	FOXA1	chr12:51215103-51215431	HepG2	liver:	n/a	n/a
13	FOXA2	chr12:51215140-51215431	HepG2	liver:	n/a	n/a
14	IRF1	chr12:51213930-51214059	K562	blood:	n/a	n/a
15	IRF1	chr12:51206760-51206773	K562	blood:	n/a	n/a
16	MAFK	chr12:51211677-51211781	H1-hESC	embryonic stem cell:	n/a	n/a
17	MYC	chr12:51209991-51209998	MCF-7	breast:	n/a	n/a
18	MYC	chr12:51210007-51210050	MCF-7	breast:	n/a	n/a
19	MYC	chr12:51209974-51209989	MCF-7	breast:	n/a	n/a
20	NRF1	chr12:51213591-51213820	K562	blood:	n/a	n/a
21	POLR2A	chr12:51209868-51210136	K562	blood:	n/a	n/a
22	POLR2A	chr12:51210273-51210351	Hela-S3	cervix:	n/a	n/a
23	POLR2A	chr12:51213013-51213060	MCF-7	breast:	n/a	n/a
24	POLR2A	chr12:51207930-51207973	MCF-7	breast:	n/a	n/a
25	POLR2A	chr12:51213147-51213437	K562	blood:	n/a	n/a
26	POLR2A	chr12:51209937-51210115	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr12:51212137-51212158	MCF-7	breast:	n/a	n/a
28	POLR2A	chr12:51209963-51210086	A549	lung:	n/a	n/a
29	POLR2A	chr12:51212161-51212165	MCF-7	breast:	n/a	n/a
30	POLR2A	chr12:51207454-51207554	HepG2	liver:	n/a	n/a
31	RFX5	chr12:51213922-51214062	K562	blood:	n/a	n/a
32	RFX5	chr12:51211110-51211506	K562	blood:	n/a	n/a
33	SMC3	chr12:51204731-51204907	Hela-S3	cervix:	n/a	n/a
34	ZNF384	chr12:51202992-51203492	K562	blood:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:51213748-51213798	ECC-1	luminal epithelium:	n/a
2	chr12:51213748-51213798	ECC-1	luminal epithelium:	n/a
3	chr12:51213748-51213798	GM12891	blood:	n/a
4	chr12:51213748-51213798	HPAEpiC	pulmonary alveolar:	n/a
5	chr12:51213748-51213798	HCF	heart:	n/a
6	chr12:51213748-51213798	K562	blood:	n/a
7	chr12:51213748-51213798	NHBE	bronchial:	n/a
8	chr12:51213748-51213798	HEK293	kidney:	embryo
9	chr12:51213748-51213798	HNPCEpiC	eye:	n/a
10	chr12:51213748-51213798	AG10803	skin:	n/a
11	chr12:51213748-51213798	GM06990	blood:	n/a
12	chr12:51213748-51213798	SKMC	muscle:	n/a
13	chr12:51213748-51213798	LNCaP	prostate:	n/a
14	chr12:51213748-51213798	GM12892	blood:	n/a
15	chr12:51213748-51213798	Jurkat	blood:	n/a
16	chr12:51213748-51213798	Hela-S3	cervix:	n/a
17	chr12:51213748-51213798	HIPEpiC	eye:	n/a
18	chr12:51213748-51213798	HMEC	breast:	n/a
19	chr12:51213748-51213798	RPTEC	kidney:	n/a
20	chr12:51213748-51213798	PrEC	prostate:	n/a
21	chr12:51213748-51213798	HRE	kidney:	n/a
22	chr12:51213748-51213798	HUVEC	blood vessel:	n/a
23	chr12:51213748-51213798	T-47D	breast:	n/a
24	chr12:51213748-51213798	BJ	skin:	n/a
25	chr12:51213748-51213798	NB4	blood:	n/a
26	chr12:51213748-51213798	HCT-116	colon:	n/a
27	chr12:51213748-51213798	PANC-1	pancreas:	n/a
28	chr12:51213748-51213798	MCF10A-Er-Src	breast:	n/a
29	chr12:51213748-51213798	HCPEpiC	choroid plexus:	n/a
30	chr12:51213748-51213798	ovcar-3	ovarian:	n/a
31	chr12:51213748-51213798	AoSMC	blood vessel:	n/a
32	chr12:51213748-51213798	U87	brain:	n/a
33	chr12:51213748-51213798	SK-N-SH	brain:	n/a
34	chr12:51213748-51213798	PFSK-1	brain:	n/a
35	chr12:51213748-51213798	AG04450	lung:	fetal
36	chr12:51213748-51213798	AG04449	skin:	fetal
37	chr12:51213748-51213798	NT2-D1	testis:	n/a
38	chr12:51213748-51213798	AG09309	skin:	n/a
39	chr12:51213748-51213798	SAEC	small airway:	n/a
40	chr12:51213748-51213798	SK-N-SH_RA	brain:	n/a
41	chr12:51213748-51213798	HL-60	blood:	n/a
42	chr12:51213748-51213798	SK-N-MC	brain:	n/a
43	chr12:51213748-51213798	NHDF-neo	bronchial:	n/a
44	chr12:51213748-51213798	NH-A	brain:	n/a
45	chr12:51213748-51213798	HRPEpiC	eye:	n/a
46	chr12:51213748-51213798	GM19239	blood:	n/a
47	chr12:51213748-51213798	HEEpiC	esophagus:	n/a
48	chr12:51213748-51213798	HepG2	liver:	n/a
49	chr12:51213748-51213798	AG09319	gingival:	n/a
50	chr12:51213748-51213798	MCF-7	breast:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:51203453..51205584-chr12:51379862..51382375,2	MCF-7	breast:
2	chr12:51206635..51209642-chr12:51213405..51216758,3	K562	blood:
3	chr12:51206635..51209642-chr12:51213405..51216758,3	K562	blood:
4	chr12:51213097..51215653-chr12:51224289..51226631,2	K562	blood:
5	chr12:51156903..51159314-chr12:51210199..51212563,2	K562	blood:
6	chr12:51212786..51214358-chr12:51219133..51221117,2	K562	blood:
7	chr12:51211264..51213354-chr12:51419744..51421928,3	K562	blood:
8	chr12:51202962..51206871-chr12:51207911..51210941,4	K562	blood:
9	chr12:51179438..51182295-chr12:51203599..51205649,2	MCF-7	breast:
10	chr12:51207076..51210339-chr12:51211809..51214905,4	K562	blood:
11	chr12:51202962..51206871-chr12:51207911..51210941,4	K562	blood:
12	chr12:51207076..51210339-chr12:51211809..51214905,4	K562	blood:
13	chr12:51156449..51158602-chr12:51202622..51204712,2	K562	blood:
14	chr12:51197517..51200061-chr12:51208152..51209751,2	MCF-7	breast:
15	chr12:51159281..51161379-chr12:51202424..51204535,2	K562	blood:
16	chr12:51212755..51215653-chr12:51225131..51226878,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000271490	TF binding region
ENSG00000271490	CpG island
ENSG00000123268	chromatin interactions
ENSG00000110911	chromatin interactions

Extended variants
information (count: 412 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574020812	chr12:51203453-51203454	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs542900742	chr12:51203473-51203474	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs372561744	chr12:51203483-51203484	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs79399012	chr12:51203506-51203507	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs571398380	chr12:51203541-51203542	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs572963950	chr12:51203567-51203568	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs71443204	chr12:51203602-51203603	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs67271947	chr12:51203603-51203604	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs200464951	chr12:51203634-51203635	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs829115	chr12:51203688-51203689	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs9804973	chr12:51203690-51203691	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs28728041	chr12:51203814-51203815	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs148922575	chr12:51203874-51203875	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs543458786	chr12:51203937-51203938	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs10047618	chr12:51203947-51203948	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs10876096	chr12:51203953-51203954	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs34461103	chr12:51204002-51204003	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs566968790	chr12:51204013-51204014	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs74465543	chr12:51204017-51204018	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs144418653	chr12:51204018-51204019	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs182671405	chr12:51204037-51204038	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs555256165	chr12:51204062-51204063	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs567578716	chr12:51204086-51204087	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs528652195	chr12:51204102-51204103	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs551670378	chr12:51204145-51204146	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs571349298	chr12:51204146-51204147	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs865490	chr12:51204149-51204150	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs556386642	chr12:51204157-51204158	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs61926335	chr12:51204177-51204178	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs536571771	chr12:51204210-51204211	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs148103883	chr12:51204220-51204221	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs374857646	chr12:51204262-51204263	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs553269166	chr12:51204292-51204293	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs829114	chr12:51204295-51204296	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs112819176	chr12:51204311-51204312	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs150337288	chr12:51204315-51204316	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs138124735	chr12:51204381-51204382	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs545215593	chr12:51204394-51204395	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs143670376	chr12:51204432-51204433	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs578079459	chr12:51204445-51204446	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs56994893	chr12:51204460-51204461	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs563346346	chr12:51204480-51204481	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs529657200	chr12:51204482-51204483	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs553493416	chr12:51204504-51204505	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs529223787	chr12:51204551-51204552	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs117584294	chr12:51204604-51204605	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs111463597	chr12:51204619-51204620	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs560031533	chr12:51204630-51204631	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs540851563	chr12:51204710-51204711	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs143821054	chr12:51204740-51204741	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Seminomas	18059402	CNVD
Wilms tumour	21544195	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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	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
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Cancer	17160897	CNVD
Breast cancer	21858162	CNVD
Urothelial carcinoma	21177765	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:51180800-51204400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr12:51188600-51207800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:51190200-51204000	Weak transcription	Gastric	stomach
4	chr12:51190200-51215200	Weak transcription	Pancreas	Pancrea
5	chr12:51193200-51204400	Weak transcription	Brain Cingulate Gyrus	brain
6	chr12:51193200-51207600	Weak transcription	Fetal Heart	heart
7	chr12:51193200-51207800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr12:51193200-51207800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr12:51193200-51207800	Weak transcription	Esophagus	oesophagus
10	chr12:51193200-51208000	Weak transcription	Small Intestine	intestine
11	chr12:51193200-51211200	Weak transcription	Aorta	Aorta
12	chr12:51193400-51204000	Weak transcription	Psoas Muscle	Psoas
13	chr12:51193400-51207800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr12:51193800-51204200	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr12:51193800-51204400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr12:51193800-51204400	Weak transcription	Fetal Brain Male	brain
17	chr12:51194000-51204200	Weak transcription	NHLF	lung
18	chr12:51194000-51204400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr12:51194000-51204400	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr12:51194000-51204400	Weak transcription	NHEK	skin
21	chr12:51194000-51204600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr12:51194400-51203600	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr12:51194400-51204400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr12:51194400-51204400	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr12:51194400-51204400	Weak transcription	Right Ventricle	heart
26	chr12:51194400-51204400	Weak transcription	HSMMtube	muscle
27	chr12:51194400-51204400	Weak transcription	NH-A	brain
28	chr12:51194400-51204400	Weak transcription	NHDF-Ad	bronchial
29	chr12:51194400-51204600	Weak transcription	Brain Angular Gyrus	brain
30	chr12:51194400-51204600	Weak transcription	Colon Smooth Muscle	Colon
31	chr12:51194400-51207800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr12:51194600-51204200	Weak transcription	HMEC	breast
33	chr12:51194600-51204400	Weak transcription	Brain Germinal Matrix	brain
34	chr12:51194600-51204400	Weak transcription	Ovary	ovary
35	chr12:51194600-51207800	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr12:51194600-51214600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr12:51194800-51204400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr12:51194800-51209200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr12:51195600-51203600	Weak transcription	Liver	Liver
40	chr12:51195600-51204000	Weak transcription	Primary hematopoietic stem cells	blood
41	chr12:51195600-51204400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr12:51195600-51204400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr12:51195600-51204400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr12:51195600-51204400	Weak transcription	Fetal Kidney	kidney
45	chr12:51195800-51204200	Weak transcription	GM12878-XiMat	blood
46	chr12:51197000-51203800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr12:51198600-51215400	Strong transcription	Monocytes-CD14+_RO01746	blood
48	chr12:51199600-51209400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr12:51200400-51203600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr12:51200400-51203600	Weak transcription	Lung	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links