Variant report

Variant	nsv1045275
Chromosome Location	chr12:63950663-64135427
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	BATF	chr12:64000419-64000618	GM12878	blood:	n/a	n/a
2	BATF	chr12:64000417-64000676	GM12878	blood:	n/a	n/a
3	BATF	chr12:64106394-64106647	GM12878	blood:	n/a	n/a
4	BATF	chr12:64106436-64106667	GM12878	blood:	n/a	n/a
5	BHLHE40	chr12:64062203-64062590	GM12878	blood:	n/a	chr12:64062378-64062391
6	BHLHE40	chr12:64062231-64062577	A549	lung:	n/a	chr12:64062378-64062391
7	BRCA1	chr12:63978333-63978494	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr12:64020552-64020778	MCF-7	breast:	n/a	n/a
9	CEBPB	chr12:64112080-64112114	Hela-S3	cervix:	n/a	chr12:64112093-64112106
10	CEBPB	chr12:64037247-64037445	IMR90	lung:	n/a	n/a
11	CEBPB	chr12:64056902-64057024	K562	blood:	n/a	chr12:64056989-64057000
12	CEBPB	chr12:64056829-64057077	IMR90	lung:	n/a	chr12:64056989-64057000
13	CEBPB	chr12:64056829-64057086	A549	lung:	n/a	chr12:64056989-64057000
14	CEBPB	chr12:63978276-63978475	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr12:64074503-64074713	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:64056832-64057070	HepG2	liver:	n/a	chr12:64056989-64057000
17	CEBPB	chr12:63951128-63951259	IMR90	lung:	n/a	n/a
18	CEBPB	chr12:64056822-64057106	K562	blood:	n/a	chr12:64056989-64057000
19	CEBPB	chr12:64056875-64057025	Hela-S3	cervix:	n/a	chr12:64056989-64057000
20	CEBPB	chr12:64037188-64037554	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr12:64056827-64057142	K562	blood:	n/a	chr12:64056989-64057000
22	CEBPB	chr12:64056841-64057129	H1-hESC	embryonic stem cell:	n/a	chr12:64056989-64057000
23	CEBPD	chr12:64037519-64037921	K562	blood:	n/a	n/a
24	CHD2	chr12:64062070-64062344	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr12:64062224-64062592	A549	lung:	n/a	n/a
26	CTCF	chr12:64069142-64069249	GM10248	blood:	n/a	n/a
27	CTCF	chr12:63988425-63988451	MCF-7	breast:	n/a	n/a
28	CTCF	chr12:63988418-63988424	MCF-7	breast:	n/a	n/a
29	CTCF	chr12:64061980-64062130	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr12:64066540-64066690	AG10803	skin:	n/a	n/a
31	CTCF	chr12:64068059-64068087	GM10248	blood:	n/a	n/a
32	CTCF	chr12:63989475-63989500	GM13977	blood:	n/a	n/a
33	CTCF	chr12:64041876-64041933	Medullo	brain:	n/a	n/a
34	CTCF	chr12:64062780-64062930	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr12:63998269-63998323	Pancreas_OC	pancreas:	n/a	n/a
36	CTCF	chr12:64066320-64066570	BJ	skin:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
37	CTCF	chr12:64068528-64068580	GM10248	blood:	n/a	n/a
38	CTCF	chr12:64090705-64090726	GM13977	blood:	n/a	n/a
39	CTCF	chr12:63988384-63988423	A549	lung:	n/a	n/a
40	CTCF	chr12:64066462-64066580	HUVEC	blood vessel:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
41	CTCF	chr12:63966634-63966685	HepG2	liver:	n/a	n/a
42	CTCF	chr12:64066246-64066780	A549	lung:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
43	CTCF	chr12:63958476-63958518	GM13977	blood:	n/a	n/a
44	CTCF	chr12:64066414-64066647	Medullo	brain:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
45	CTCF	chr12:64066450-64066601	LNCaP	prostate:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
46	CTCF	chr12:64066420-64066570	Caco-2	colon:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
47	CTCF	chr12:64066440-64066590	GM12873	blood:	n/a	chr12:64066529-64066550 chr12:64066528-64066544 chr12:64066527-64066545
48	CTCF	chr12:64066220-64066370	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr12:64066164-64066278	GM10248	blood:	n/a	n/a
50	CTCF	chr12:64066182-64066269	GM13977	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:64062724-64062774	PANC-1	pancreas:	n/a
2	chr12:64062724-64062774	PANC-1	pancreas:	n/a
3	chr12:64062526-64062576	HRPEpiC	eye:	n/a
4	chr12:64062544-64062594	ECC-1	luminal epithelium:	n/a
5	chr12:64062505-64062555	K562	blood:	n/a
6	chr12:64062526-64062576	K562	blood:	n/a
7	chr12:64062542-64062592	A549	lung:	n/a
8	chr12:64062221-64062271	SKMC	muscle:	n/a
9	chr12:63998373-63998423	HRCEpiC	kidney:	n/a
10	chr12:64063071-64063121	HRPEpiC	eye:	n/a
11	chr12:63998373-63998423	HCM	heart:	n/a
12	chr12:64080144-64080194	HRE	kidney:	n/a
13	chr12:64062564-64062614	U87	brain:	n/a
14	chr12:64080622-64080672	ECC-1	luminal epithelium:	n/a
15	chr12:64062384-64062434	HUVEC	blood vessel:	n/a
16	chr12:64062724-64062774	NHBE	bronchial:	n/a
17	chr12:64062526-64062576	BJ	skin:	n/a
18	chr12:64062221-64062271	HL-60	blood:	n/a
19	chr12:64062498-64062548	MCF10A-Er-Src	breast:	n/a
20	chr12:64062384-64062434	HCPEpiC	choroid plexus:	n/a
21	chr12:64062564-64062614	H1-hESC	embryonic stem cell:	embryo
22	chr12:63998373-63998423	HEK293	kidney:	embryo
23	chr12:64080144-64080194	AG09309	skin:	n/a
24	chr12:64062221-64062271	MCF10A-Er-Src	breast:	n/a
25	chr12:64062498-64062548	NT2-D1	testis:	n/a
26	chr12:64062526-64062576	GM06990	blood:	n/a
27	chr12:64062564-64062614	NB4	blood:	n/a
28	chr12:64062526-64062576	HCM	heart:	n/a
29	chr12:64062544-64062594	ovcar-3	ovarian:	n/a
30	chr12:64062542-64062592	HEK293	kidney:	embryo
31	chr12:64062384-64062434	HAEpiC	amniotic membrane:	n/a
32	chr12:64080622-64080672	AG10803	skin:	n/a
33	chr12:64062564-64062614	MCF-7	breast:	n/a
34	chr12:64062221-64062271	HCF	heart:	n/a
35	chr12:64062724-64062774	HIPEpiC	eye:	n/a
36	chr12:64062544-64062594	PFSK-1	brain:	n/a
37	chr12:64062564-64062614	AG09319	gingival:	n/a
38	chr12:64062544-64062594	AG10803	skin:	n/a
39	chr12:64080144-64080194	SK-N-SH_RA	brain:	n/a
40	chr12:63998373-63998423	HUVEC	blood vessel:	n/a
41	chr12:64062505-64062555	SAEC	small airway:	n/a
42	chr12:64062724-64062774	NHDF-neo	bronchial:	n/a
43	chr12:64062505-64062555	MCF10A-Er-Src	breast:	n/a
44	chr12:64063071-64063121	AG09319	gingival:	n/a
45	chr12:64080622-64080672	Hela-S3	cervix:	n/a
46	chr12:64062724-64062774	Jurkat	blood:	n/a
47	chr12:64080622-64080672	HL-60	blood:	n/a
48	chr12:64062505-64062555	IMR90	lung:	fetal
49	chr12:64062505-64062555	SK-N-SH_RA	brain:	n/a
50	chr12:64062505-64062555	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:64105781..64108214-chr12:64111007..64113844,2	K562	blood:
2	chr12:64116942..64118463-chr7:35277697..35279270,2	MCF-7	breast:
3	chr12:63978668..63979594-chr20:52240028..52240873,2	MCF-7	breast:
4	chr12:64088585..64090481-chr12:64171623..64173907,2	MCF-7	breast:
5	chr12:64130174..64132619-chr12:64170875..64173477,2	MCF-7	breast:
6	chr12:64105781..64108214-chr12:64111007..64113844,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DPY19L2-1	chr12:64017568-64017604	ENSG00000249753.2

Variant related genes	Relation type
ENSG00000257005	TF binding region
ENSG00000255583	TF binding region
DPY19L2	TF binding region
ENSG00000257005	CpG island
ENSG00000255583	CpG island
DPY19L2	CpG island
ENSG00000118600	chromatin interactions

Extended variants
information (count: 5309 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:5309 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78940398	chr12:63950663-63950664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs190521432	chr12:63950664-63950665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs78719361	chr12:63950666-63950667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs2814397	chr12:63950767-63950768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182177759	chr12:63950806-63950807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs526969	chr12:63950838-63950839	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs111634674	chr12:63950856-63950857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539935328	chr12:63950873-63950874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201526321	chr12:63950912-63950913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575449532	chr12:63950921-63950922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564702130	chr12:63951006-63951007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs527414636	chr12:63951023-63951024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547188436	chr12:63951030-63951031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567338819	chr12:63951032-63951033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368179385	chr12:63951037-63951038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536462217	chr12:63951045-63951046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549994086	chr12:63951060-63951061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs570014652	chr12:63951072-63951073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189991113	chr12:63951115-63951116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113598672	chr12:63951147-63951148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558167780	chr12:63951210-63951211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs181182789	chr12:63951242-63951243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs201754170	chr12:63951254-63951255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs397834787	chr12:63951314-63951315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534168842	chr12:63951316-63951317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553978498	chr12:63951326-63951327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573755577	chr12:63951358-63951359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185619426	chr12:63951365-63951366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562737839	chr12:63951383-63951384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189643884	chr12:63951427-63951428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545358772	chr12:63951465-63951466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372441810	chr12:63951482-63951483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs79587950	chr12:63951497-63951498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs398055635	chr12:63951507-63951508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs398019889	chr12:63951508-63951509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113429316	chr12:63951558-63951559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565537020	chr12:63951561-63951562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527307539	chr12:63951602-63951603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182299053	chr12:63951611-63951612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs199508916	chr12:63951673-63951674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186053992	chr12:63951688-63951689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192156366	chr12:63951693-63951694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146085185	chr12:63951722-63951723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140155530	chr12:63951745-63951746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538794242	chr12:63951752-63951753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552210129	chr12:63951783-63951784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565920177	chr12:63951793-63951794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs1986097	chr12:63951811-63951812	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs553740932	chr12:63951815-63951816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573842576	chr12:63951848-63951849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:452 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63943800-63969400	Weak transcription	Fetal Heart	heart
2	chr12:63959200-63960800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr12:63960000-63969200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr12:63960200-63964200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr12:63960200-63971200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr12:63960800-63967200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr12:63962000-64027800	Weak transcription	Ovary	ovary
8	chr12:63962600-63964200	Weak transcription	Left Ventricle	heart
9	chr12:63964200-63964600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr12:63964200-63965400	Strong transcription	Left Ventricle	heart
11	chr12:63964600-63965200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr12:63964800-63967200	Weak transcription	Pancreas	Pancrea
13	chr12:63965200-63971200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr12:63965400-63998800	Weak transcription	Left Ventricle	heart
15	chr12:63967200-63967800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr12:63967800-63971200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr12:63968600-63969000	Enhancers	Dnd41	blood
18	chr12:63971200-63971600	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr12:63971200-63971800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr12:63971200-63972000	Enhancers	Primary hematopoietic stem cells	blood
21	chr12:63971200-63972000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr12:63971800-63989200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr12:63972000-63988400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr12:63986200-63999200	Weak transcription	Fetal Heart	heart
25	chr12:63988200-63988600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr12:63988400-63989600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr12:63989600-63990400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr12:63990400-63990800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr12:63990800-63997200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr12:63997200-63997800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr12:63997800-64012400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr12:63998800-63999200	Enhancers	Left Ventricle	heart
33	chr12:63999000-63999200	Enhancers	Colon Smooth Muscle	Colon
34	chr12:63999200-63999400	Enhancers	Fetal Heart	heart
35	chr12:63999200-64008600	Weak transcription	Left Ventricle	heart
36	chr12:63999400-63999600	Weak transcription	Fetal Heart	heart
37	chr12:64008200-64009000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr12:64008600-64008800	Enhancers	Left Ventricle	heart
39	chr12:64008600-64009000	Enhancers	NHDF-Ad	bronchial
40	chr12:64008800-64009400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr12:64009000-64009800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr12:64009800-64010000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr12:64012400-64012800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr12:64012800-64027400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr12:64019400-64059000	Weak transcription	Left Ventricle	heart
46	chr12:64020200-64022600	Weak transcription	Right Ventricle	heart
47	chr12:64021800-64022400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
48	chr12:64022400-64027800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr12:64027400-64031000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr12:64027600-64037400	Weak transcription	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links