Variant report

Variant	nsv899173
Chromosome Location	chr12:63931879-64051877
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:173)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:173 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr12:64000417-64000676	GM12878	blood:	n/a	n/a
2	BATF	chr12:64000419-64000618	GM12878	blood:	n/a	n/a
3	BHLHE40	chr12:63945192-63945476	K562	blood:	n/a	n/a
4	BRCA1	chr12:63978333-63978494	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr12:63978276-63978475	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr12:64020552-64020778	MCF-7	breast:	n/a	n/a
7	CEBPB	chr12:63951128-63951259	IMR90	lung:	n/a	n/a
8	CEBPB	chr12:64037188-64037554	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:64037247-64037445	IMR90	lung:	n/a	n/a
10	CEBPD	chr12:64037519-64037921	K562	blood:	n/a	n/a
11	CHD2	chr12:63945273-63945559	K562	blood:	n/a	n/a
12	CTCF	chr12:63995175-63995200	LNCaP	prostate:	n/a	n/a
13	CTCF	chr12:63950545-63950604	Kidney_OC	kidney:	n/a	n/a
14	CTCF	chr12:63998896-63998962	ProgFib	skin:	n/a	n/a
15	CTCF	chr12:63966265-63966385	MCF-7	breast:	n/a	n/a
16	CTCF	chr12:64004776-64004863	Lung_OC	lung:	n/a	n/a
17	CTCF	chr12:63988384-63988423	A549	lung:	n/a	n/a
18	CTCF	chr12:63988399-63988434	MCF-7	breast:	n/a	n/a
19	CTCF	chr12:63966286-63966362	MCF-7	breast:	n/a	n/a
20	CTCF	chr12:63966610-63966687	Medullo	brain:	n/a	n/a
21	CTCF	chr12:63954921-63954975	GM20000	blood:	n/a	n/a
22	CTCF	chr12:64037457-64037530	GM13977	blood:	n/a	n/a
23	CTCF	chr12:63998269-63998323	Pancreas_OC	pancreas:	n/a	n/a
24	CTCF	chr12:63958476-63958518	GM13977	blood:	n/a	n/a
25	CTCF	chr12:63998913-63998941	LNCaP	prostate:	n/a	n/a
26	CTCF	chr12:63989475-63989500	GM13977	blood:	n/a	n/a
27	CTCF	chr12:64041876-64041933	Medullo	brain:	n/a	n/a
28	CTCF	chr12:63966661-63966684	MCF-7	breast:	n/a	n/a
29	CTCF	chr12:63966622-63966719	A549	lung:	n/a	n/a
30	CTCF	chr12:63976578-63976616	GM20000	blood:	n/a	n/a
31	CTCF	chr12:63958519-63958521	GM13977	blood:	n/a	n/a
32	CTCF	chr12:63941726-63941828	Fibrobl	skin:	n/a	n/a
33	CTCF	chr12:63988418-63988424	MCF-7	breast:	n/a	n/a
34	CTCF	chr12:64049268-64049334	GM13976	blood:	n/a	n/a
35	CTCF	chr12:63966280-63966367	MCF-7	breast:	n/a	n/a
36	CTCF	chr12:63998966-63998969	ProgFib	skin:	n/a	n/a
37	CTCF	chr12:63966634-63966685	HepG2	liver:	n/a	n/a
38	CTCF	chr12:63966275-63966370	MCF-7	breast:	n/a	n/a
39	CTCF	chr12:63996819-63996903	GM10248	blood:	n/a	n/a
40	CTCF	chr12:63939556-63939591	GM10248	blood:	n/a	n/a
41	CTCF	chr12:63988425-63988451	MCF-7	breast:	n/a	n/a
42	CTCF	chr12:63978674-63978707	GM20000	blood:	n/a	n/a
43	CTCF	chr12:64000127-64000151	GM10248	blood:	n/a	n/a
44	EBF1	chr12:63965117-63965439	GM12878	blood:	n/a	n/a
45	EP300	chr12:63978314-63978495	Hela-S3	cervix:	n/a	n/a
46	EP300	chr12:63988849-63988862	Hela-S3	cervix:	n/a	n/a
47	EP300	chr12:64037229-64037553	Hela-S3	cervix:	n/a	n/a
48	FOS	chr12:63978185-63978534	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr12:63978185-63978549	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr12:64043434-64043634	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:63998373-63998423	PrEC	prostate:	n/a
2	chr12:63998373-63998423	HRE	kidney:	n/a
3	chr12:63998373-63998423	Hepatocyte	liver:	n/a
4	chr12:63998373-63998423	NB4	blood:	n/a
5	chr12:63998373-63998423	GM12891	blood:	n/a
6	chr12:63998373-63998423	HCPEpiC	choroid plexus:	n/a
7	chr12:63998373-63998423	HCT-116	colon:	n/a
8	chr12:63998373-63998423	GM06990	blood:	n/a
9	chr12:63998373-63998423	RPTEC	kidney:	n/a
10	chr12:63998373-63998423	GM12892	blood:	n/a
11	chr12:63998373-63998423	PFSK-1	brain:	n/a
12	chr12:63998373-63998423	HCF	heart:	n/a
13	chr12:63998373-63998423	Jurkat	blood:	n/a
14	chr12:63998373-63998423	H1-hESC	embryonic stem cell:	embryo
15	chr12:63998373-63998423	K562	blood:	n/a
16	chr12:63998373-63998423	AG04449	skin:	fetal
17	chr12:63998373-63998423	GM19239	blood:	n/a
18	chr12:63998373-63998423	HPAEpiC	pulmonary alveolar:	n/a
19	chr12:63998373-63998423	AG09309	skin:	n/a
20	chr12:63998373-63998423	HepG2	liver:	n/a
21	chr12:63998373-63998423	PANC-1	pancreas:	n/a
22	chr12:63998373-63998423	NT2-D1	testis:	n/a
23	chr12:63998373-63998423	NHBE	bronchial:	n/a
24	chr12:63998373-63998423	HNPCEpiC	eye:	n/a
25	chr12:63998373-63998423	HUVEC	blood vessel:	n/a
26	chr12:63998373-63998423	ECC-1	luminal epithelium:	n/a
27	chr12:63998373-63998423	SKMC	muscle:	n/a
28	chr12:63998373-63998423	NHDF-neo	bronchial:	n/a
29	chr12:63998373-63998423	IMR90	lung:	fetal
30	chr12:63998373-63998423	T-47D	breast:	n/a
31	chr12:63998373-63998423	AoSMC	blood vessel:	n/a
32	chr12:63998373-63998423	HIPEpiC	eye:	n/a
33	chr12:63998373-63998423	U87	brain:	n/a
34	chr12:63998373-63998423	HCM	heart:	n/a
35	chr12:63998373-63998423	ovcar-3	ovarian:	n/a
36	chr12:63998373-63998423	HL-60	blood:	n/a
37	chr12:63998373-63998423	HEEpiC	esophagus:	n/a
38	chr12:63998373-63998423	Hela-S3	cervix:	n/a
39	chr12:63998373-63998423	SAEC	small airway:	n/a
40	chr12:63998373-63998423	LNCaP	prostate:	n/a
41	chr12:63998373-63998423	SK-N-SH_RA	brain:	n/a
42	chr12:63998373-63998423	HEK293	kidney:	embryo
43	chr12:63998373-63998423	BE2_C	brain:	n/a
44	chr12:63998373-63998423	HAEpiC	amniotic membrane:	n/a
45	chr12:63998373-63998423	MCF10A-Er-Src	breast:	n/a
46	chr12:63998373-63998423	Caco-2	colon:	n/a
47	chr12:63998373-63998423	AG10803	skin:	n/a
48	chr12:63998373-63998423	A549	lung:	n/a
49	chr12:63998373-63998423	SK-N-SH	brain:	n/a
50	chr12:63998373-63998423	HMEC	breast:	n/a

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No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:63978668..63979594-chr20:52240028..52240873,2	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
DPY19L2	TF binding region
ENSG00000257005	TF binding region
DPY19L2	CpG island
ENSG00000257005	CpG island

Extended variants
information (count: 4969 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4969 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55692287	chr12:63931879-63931880	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566064004	chr12:63931945-63931946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs12319490	chr12:63931951-63931952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs573024439	chr12:63932008-63932009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537854336	chr12:63932036-63932037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs56218370	chr12:63932044-63932045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541040637	chr12:63932051-63932052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs117418434	chr12:63932062-63932063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574765762	chr12:63932066-63932067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs543509918	chr12:63932079-63932080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545193586	chr12:63932099-63932100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563583070	chr12:63932100-63932101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532725680	chr12:63932126-63932127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552624973	chr12:63932130-63932131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543561892	chr12:63932141-63932142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187424575	chr12:63932171-63932172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs145237356	chr12:63932198-63932199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs548217576	chr12:63932202-63932203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568014102	chr12:63932242-63932243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368561414	chr12:63932278-63932279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs2257662	chr12:63932323-63932324	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs2647728	chr12:63932344-63932345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145105701	chr12:63932355-63932356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs576173490	chr12:63932362-63932363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs552855958	chr12:63932385-63932386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565087322	chr12:63932390-63932391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs3863368	chr12:63932392-63932393	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs545259331	chr12:63932393-63932394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs4044441	chr12:63932399-63932400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs535316241	chr12:63932436-63932437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs2659936	chr12:63932448-63932449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554588620	chr12:63932449-63932450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574486394	chr12:63932450-63932451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2814421	chr12:63932461-63932462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs3863369	chr12:63932482-63932483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs2659935	chr12:63932483-63932484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs543548402	chr12:63932488-63932489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191811894	chr12:63932532-63932533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs577241229	chr12:63932546-63932547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546393876	chr12:63932578-63932579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs559649888	chr12:63932593-63932594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs528787114	chr12:63932610-63932611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs2659934	chr12:63932661-63932662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs61934996	chr12:63932662-63932663	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs560733969	chr12:63932690-63932691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs143457488	chr12:63932696-63932697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs549629134	chr12:63932707-63932708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs142634006	chr12:63932716-63932717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs147377970	chr12:63932755-63932756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs532844369	chr12:63932787-63932788	Weak transcription Enhancers	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
Breast cancer	21364760	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	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:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63931800-63932000	Enhancers	Fetal Brain Male	brain
2	chr12:63931800-63932400	Enhancers	HSMMtube	muscle
3	chr12:63931800-63933200	Enhancers	Fetal Heart	heart
4	chr12:63932000-63938800	Weak transcription	Fetal Brain Male	brain
5	chr12:63938800-63939200	Enhancers	Fetal Brain Male	brain
6	chr12:63942400-63943800	Enhancers	Fetal Heart	heart
7	chr12:63943800-63969400	Weak transcription	Fetal Heart	heart
8	chr12:63959200-63960800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr12:63960000-63969200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr12:63960200-63964200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr12:63960200-63971200	Weak transcription	Primary hematopoietic stem cells	blood
12	chr12:63960800-63967200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr12:63962000-64027800	Weak transcription	Ovary	ovary
14	chr12:63962600-63964200	Weak transcription	Left Ventricle	heart
15	chr12:63964200-63964600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr12:63964200-63965400	Strong transcription	Left Ventricle	heart
17	chr12:63964600-63965200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr12:63964800-63967200	Weak transcription	Pancreas	Pancrea
19	chr12:63965200-63971200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr12:63965400-63998800	Weak transcription	Left Ventricle	heart
21	chr12:63967200-63967800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr12:63967800-63971200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr12:63968600-63969000	Enhancers	Dnd41	blood
24	chr12:63971200-63971600	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr12:63971200-63971800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr12:63971200-63972000	Enhancers	Primary hematopoietic stem cells	blood
27	chr12:63971200-63972000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr12:63971800-63989200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr12:63972000-63988400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr12:63986200-63999200	Weak transcription	Fetal Heart	heart
31	chr12:63988200-63988600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr12:63988400-63989600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr12:63989600-63990400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr12:63990400-63990800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr12:63990800-63997200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr12:63997200-63997800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr12:63997800-64012400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr12:63998800-63999200	Enhancers	Left Ventricle	heart
39	chr12:63999000-63999200	Enhancers	Colon Smooth Muscle	Colon
40	chr12:63999200-63999400	Enhancers	Fetal Heart	heart
41	chr12:63999200-64008600	Weak transcription	Left Ventricle	heart
42	chr12:63999400-63999600	Weak transcription	Fetal Heart	heart
43	chr12:64008200-64009000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr12:64008600-64008800	Enhancers	Left Ventricle	heart
45	chr12:64008600-64009000	Enhancers	NHDF-Ad	bronchial
46	chr12:64008800-64009400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr12:64009000-64009800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr12:64009800-64010000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr12:64012400-64012800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr12:64012800-64027400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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