Variant report

Variant	esv3436439
Chromosome Location	chr12:120616469-120620667
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	ARID3A	chr12:120619852-120620358	HepG2	liver:	n/a	n/a
2	BATF	chr12:120620122-120620444	GM12878	blood:	n/a	n/a
3	BRCA1	chr12:120619926-120620436	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr12:120619685-120620120	MCF-7	breast:	n/a	chr12:120619902-120619913 chr12:120620001-120620009
5	CEBPB	chr12:120619729-120620470	Hela-S3	cervix:	n/a	chr12:120619902-120619913 chr12:120620001-120620009
6	CEBPB	chr12:120619824-120620008	K562	blood:	n/a	chr12:120619902-120619913
7	CEBPB	chr12:120619795-120620124	HepG2	liver:	n/a	chr12:120619902-120619913 chr12:120620001-120620009
8	CEBPB	chr12:120619798-120620017	HepG2	liver:	n/a	chr12:120619902-120619913 chr12:120620001-120620009
9	CEBPB	chr12:120619743-120620251	HepG2	liver:	n/a	chr12:120619902-120619913 chr12:120620001-120620009
10	CEBPB	chr12:120619686-120620181	MCF-7	breast:	n/a	chr12:120619902-120619913 chr12:120620001-120620009
11	CEBPB	chr12:120619742-120620521	IMR90	lung:	n/a	chr12:120619902-120619913 chr12:120620001-120620009
12	CEBPB	chr12:120619782-120620181	ECC-1	luminal epithelium:	n/a	chr12:120619902-120619913 chr12:120620001-120620009
13	CEBPB	chr12:120619793-120620151	A549	lung:	n/a	chr12:120619902-120619913 chr12:120620001-120620009
14	CEBPB	chr12:120619769-120620158	ECC-1	luminal epithelium:	n/a	chr12:120619902-120619913 chr12:120620001-120620009
15	CEBPB	chr12:120619731-120620287	HepG2	liver:	n/a	chr12:120619902-120619913 chr12:120620001-120620009
16	CEBPD	chr12:120619798-120619961	HepG2	liver:	n/a	n/a
17	CHD2	chr12:120619932-120620326	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr12:120620180-120620330	HPAF	blood vessel:	n/a	n/a
19	CTCF	chr12:120620120-120620270	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr12:120620060-120620210	BJ	skin:	n/a	n/a
21	CTCF	chr12:120620120-120620270	HMEC	breast:	n/a	n/a
22	CTCF	chr12:120620080-120620230	HCT-116	colon:	n/a	n/a
23	CTCF	chr12:120620120-120620270	HMF	breast:	n/a	n/a
24	CTCF	chr12:120620180-120620330	HepG2	liver:	n/a	n/a
25	CTCF	chr12:120620220-120620370	HEEpiC	esophagus:	n/a	n/a
26	CTCF	chr12:120620200-120620350	AG10803	skin:	n/a	n/a
27	CTCF	chr12:120619940-120620090	GM12875	blood:	n/a	n/a
28	CTCF	chr12:120620180-120620330	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr12:120620100-120620250	AG04449	skin:	n/a	n/a
30	CTCF	chr12:120620080-120620230	MCF-7	breast:	n/a	n/a
31	CTCF	chr12:120620100-120620250	HCFaa	heart:	n/a	n/a
32	CTCF	chr12:120620120-120620270	HAc	cerebellar:	n/a	n/a
33	CTCF	chr12:120620180-120620330	GM12873	blood:	n/a	n/a
34	CTCF	chr12:120620100-120620250	RPTEC	kidney:	n/a	n/a
35	CTCF	chr12:120620120-120620270	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr12:120620120-120620270	NHEK	skin:	n/a	n/a
37	CTCF	chr12:120620240-120620390	HCM	heart:	n/a	n/a
38	CTCF	chr12:120620160-120620310	HMEC	breast:	n/a	n/a
39	CTCF	chr12:120620149-120620293	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr12:120620200-120620350	A549	lung:	n/a	n/a
41	CTCF	chr12:120620160-120620310	SAEC	small airway:	n/a	n/a
42	CTCF	chr12:120620080-120620230	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr12:120620060-120620210	HVMF	connective:	n/a	n/a
44	CTCF	chr12:120620100-120620250	HEK293	kidney:	n/a	n/a
45	CTCF	chr12:120620140-120620290	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr12:120620140-120620290	Caco-2	colon:	n/a	n/a
47	CTCF	chr12:120620140-120620290	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr12:120620120-120620270	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr12:120620223-120620271	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr12:120620100-120620250	HPAF	blood vessel:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:120612920..120617279-chr12:120727207..120731965,7	MCF-7	breast:
2	chr12:120618523..120621724-chr12:120727766..120729932,3	MCF-7	breast:
3	chr12:120619424..120625759-chr12:120727314..120731443,12	MCF-7	breast:
4	chr12:120593461..120596062-chr12:120615949..120618513,2	MCF-7	breast:
5	chr12:120609971..120612239-chr12:120618473..120621270,2	K562	blood:
6	chr12:120561767..120563673-chr12:120616678..120618274,2	K562	blood:
7	chr12:120554783..120557550-chr12:120616110..120617995,2	MCF-7	breast:
8	chr12:120616088..120618170-chr12:120622990..120624902,2	MCF-7	breast:
9	chr12:120614885..120617842-chr12:120729498..120731481,2	K562	blood:
10	chr12:120614418..120617057-chr12:120617332..120619128,2	K562	blood:
11	chr12:120589085..120591419-chr12:120620211..120622247,2	K562	blood:
12	chr12:120609425..120611927-chr12:120614187..120616646,3	K562	blood:
13	chr12:120615329..120617657-chr12:120728352..120730114,2	MCF-7	breast:
14	chr12:120619924..120622463-chr12:120623831..120626792,4	MCF-7	breast:

Variant related genes	Relation type
GCN1L1	TF binding region
ENSG00000200795	chromatin interactions
ENSG00000111737	chromatin interactions
ENSG00000089154	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000263913	chromatin interactions

Extended variants
information (count: 176 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:176 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370555428	chr12:120616494-120616495	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs577485899	chr12:120616496-120616497	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs373394524	chr12:120616524-120616525	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs546463497	chr12:120616557-120616558	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs377430139	chr12:120616602-120616603	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs191351073	chr12:120616612-120616613	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs572601640	chr12:120616624-120616625	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs371103125	chr12:120616627-120616628	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs553135919	chr12:120616651-120616652	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs201776262	chr12:120616661-120616662	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs368315746	chr12:120616671-120616672	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs200979023	chr12:120616697-120616698	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs375349958	chr12:120616707-120616708	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs201362488	chr12:120616718-120616719	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs182105738	chr12:120616768-120616769	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs139597413	chr12:120616780-120616781	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs374976302	chr12:120616803-120616804	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs115260960	chr12:120616818-120616819	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs71454628	chr12:120616865-120616866	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs533109131	chr12:120616877-120616878	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs546862950	chr12:120616895-120616896	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs186575063	chr12:120616896-120616897	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs193284432	chr12:120616921-120616922	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs75141654	chr12:120617042-120617043	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs185508542	chr12:120617058-120617059	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs149992212	chr12:120617066-120617067	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs190420216	chr12:120617074-120617075	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs550918476	chr12:120617111-120617112	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs571018103	chr12:120617126-120617127	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs539794289	chr12:120617127-120617128	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs534890303	chr12:120617139-120617140	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs553256311	chr12:120617174-120617175	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs573161665	chr12:120617194-120617195	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs112033924	chr12:120617231-120617232	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs145167709	chr12:120617264-120617265	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs542132532	chr12:120617266-120617267	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs35405952	chr12:120617289-120617290	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs575678158	chr12:120617295-120617296	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs370382216	chr12:120617328-120617329	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs559999243	chr12:120617439-120617440	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs577764931	chr12:120617454-120617455	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs540004569	chr12:120617502-120617503	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs376587787	chr12:120617544-120617545	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs192809746	chr12:120617573-120617574	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs529165484	chr12:120617581-120617582	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs549019216	chr12:120617653-120617654	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs562443243	chr12:120617760-120617761	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs531349551	chr12:120617783-120617784	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs528834641	chr12:120617786-120617787	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs551456168	chr12:120617797-120617798	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD

Chromatin state (count:256 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:120563000-120629800	Strong transcription	Fetal Stomach	stomach
2	chr12:120563000-120630200	Strong transcription	Fetal Muscle Leg	muscle
3	chr12:120563200-120630400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr12:120563400-120629200	Strong transcription	Fetal Intestine Small	intestine
5	chr12:120563400-120630200	Strong transcription	Fetal Thymus	thymus
6	chr12:120563600-120626000	Strong transcription	Brain Cingulate Gyrus	brain
7	chr12:120563600-120626200	Strong transcription	Placenta Amnion	Placenta Amnion
8	chr12:120563600-120629000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr12:120563600-120630200	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr12:120563600-120630200	Strong transcription	HUES6 Cell Line	embryonic stem cell
11	chr12:120563600-120630200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr12:120563600-120630200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr12:120563600-120630200	Strong transcription	Fetal Muscle Trunk	muscle
14	chr12:120563800-120629800	Strong transcription	H1 Cell Line	embryonic stem cell
15	chr12:120563800-120630000	Strong transcription	Rectal Mucosa Donor 29	rectum
16	chr12:120563800-120630200	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr12:120564200-120624400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr12:120564200-120629600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr12:120564400-120628600	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr12:120564400-120631800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr12:120564800-120618000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr12:120565000-120628800	Strong transcription	Primary T helper cells PMA-I stimulated	--
23	chr12:120565000-120630200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr12:120565000-120630800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr12:120565200-120630200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr12:120565400-120618000	Strong transcription	Primary neutrophils fromperipheralblood	blood
27	chr12:120565400-120628400	Strong transcription	Adipose Nuclei	Adipose
28	chr12:120565800-120625200	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr12:120565800-120629400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr12:120565800-120630200	Strong transcription	Monocytes-CD14+_RO01746	blood
31	chr12:120565800-120630400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
32	chr12:120571000-120621200	Weak transcription	Right Atrium	heart
33	chr12:120571200-120617800	Strong transcription	Skeletal Muscle Female	skeletal muscle
34	chr12:120571200-120628200	Strong transcription	Fetal Intestine Large	intestine
35	chr12:120580400-120619600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr12:120594200-120631600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr12:120594600-120630200	Strong transcription	Primary T cells fromperipheralblood	blood
38	chr12:120597800-120618800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr12:120601400-120628400	Strong transcription	Liver	Liver
40	chr12:120604400-120619000	Strong transcription	A549	lung
41	chr12:120604600-120619000	Strong transcription	Osteobl	bone
42	chr12:120604600-120630200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr12:120604600-120630200	Strong transcription	Stomach Smooth Muscle	stomach
44	chr12:120604800-120628200	Strong transcription	Duodenum Mucosa	Duodenum
45	chr12:120605000-120617200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr12:120605000-120618400	Strong transcription	Lung	lung
47	chr12:120605000-120628200	Strong transcription	Duodenum Smooth Muscle	Duodenum
48	chr12:120605000-120628400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr12:120605000-120628400	Strong transcription	Brain Hippocampus Middle	brain
50	chr12:120605000-120628600	Strong transcription	Dnd41	blood

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