Variant report

Variant	nsv52873
Chromosome Location	chr12:104191266-104193582
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	BCL3	chr12:104193441-104194009	A549	lung:	n/a	n/a
2	BCL3	chr12:104193398-104193993	A549	lung:	n/a	n/a
3	BRCA1	chr12:104193428-104194312	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr12:104193575-104194110	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr12:104193576-104193947	HepG2	liver:	n/a	n/a
6	CEBPB	chr12:104193557-104193979	IMR90	lung:	n/a	n/a
7	CEBPB	chr12:104193558-104193957	A549	lung:	n/a	n/a
8	CEBPB	chr12:104193455-104194064	A549	lung:	n/a	n/a
9	CEBPB	chr12:104193429-104194090	HCT-116	colon:	n/a	n/a
10	CEBPB	chr12:104193532-104193872	HepG2	liver:	n/a	n/a
11	CEBPB	chr12:104193458-104194199	K562	blood:	n/a	n/a
12	CEBPB	chr12:104193262-104194497	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr12:104193356-104193959	HepG2	liver:	n/a	n/a
14	CEBPB	chr12:104193475-104194087	MCF-7	breast:	n/a	n/a
15	CEBPB	chr12:104193379-104194081	HCT-116	colon:	n/a	n/a
16	CEBPB	chr12:104193581-104193896	K562	blood:	n/a	n/a
17	CEBPB	chr12:104193478-104194083	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr12:104193274-104194350	A549	lung:	n/a	n/a
19	CEBPB	chr12:104193407-104194152	MCF-7	breast:	n/a	n/a
20	ELK4	chr12:104193373-104193907	Hela-S3	cervix:	n/a	n/a
21	EP300	chr12:104193524-104194254	Hela-S3	cervix:	n/a	n/a
22	EP300	chr12:104193436-104194082	ECC-1	luminal epithelium:	n/a	n/a
23	ESR1	chr12:104193304-104193902	ECC-1	luminal epithelium:	n/a	n/a
24	FOS	chr12:104191285-104191497	HUVEC	blood vessel:	n/a	n/a
25	FOS	chr12:104193570-104194052	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr12:104193554-104193980	MCF10A-Er-Src	breast:	n/a	n/a
27	FOSL2	chr12:104193529-104194409	A549	lung:	n/a	n/a
28	FOXP2	chr12:104193564-104193914	SK-N-MC	brain:	n/a	n/a
29	GATA1	chr12:104193546-104194666	K562	blood:	n/a	chr12:104194117-104194124 chr12:104194117-104194124 chr12:104194117-104194124 chr12:104193793-104193803
30	GATA2	chr12:104191220-104191458	HUVEC	blood vessel:	n/a	chr12:104191285-104191294 chr12:104191278-104191299
31	GATA3	chr12:104193377-104194533	A549	lung:	n/a	chr12:104194117-104194124 chr12:104194117-104194124 chr12:104194117-104194124 chr12:104193479-104193489 chr12:104193793-104193803
32	GATA3	chr12:104193464-104194436	MCF-7	breast:	n/a	chr12:104194117-104194124 chr12:104194117-104194124 chr12:104194117-104194124 chr12:104193479-104193489 chr12:104193793-104193803
33	GATA3	chr12:104193358-104194457	MCF-7	breast:	n/a	chr12:104194117-104194124 chr12:104194117-104194124 chr12:104194117-104194124 chr12:104193479-104193489 chr12:104193793-104193803
34	GTF2F1	chr12:104193464-104194470	Hela-S3	cervix:	n/a	n/a
35	KAP1	chr12:104193553-104194369	U2OS	brain:	n/a	n/a
36	MAFF	chr12:104192410-104192732	K562	blood:	n/a	n/a
37	MAFK	chr12:104193516-104194222	Hela-S3	cervix:	n/a	n/a
38	MAX	chr12:104193516-104194034	MCF-7	breast:	n/a	chr12:104193879-104193894 chr12:104193883-104193893
39	MAX	chr12:104193479-104193964	ECC-1	luminal epithelium:	n/a	chr12:104193879-104193894 chr12:104193883-104193893
40	MAX	chr12:104193559-104194396	A549	lung:	n/a	chr12:104193879-104193894 chr12:104193883-104193893
41	MAX	chr12:104193532-104194809	A549	lung:	n/a	chr12:104193879-104193894 chr12:104193883-104193893
42	MAX	chr12:104193381-104194251	ECC-1	luminal epithelium:	n/a	chr12:104193879-104193894 chr12:104193433-104193444 chr12:104193883-104193893
43	MAX	chr12:104193387-104194461	Hela-S3	cervix:	n/a	chr12:104193879-104193894 chr12:104193433-104193444 chr12:104193883-104193893
44	MAX	chr12:104193297-104194777	NB4	blood:	n/a	chr12:104193879-104193894 chr12:104193433-104193444 chr12:104193883-104193893
45	MAZ	chr12:104193506-104193902	Hela-S3	cervix:	n/a	chr12:104193879-104193894 chr12:104193883-104193893
46	MXI1	chr12:104193573-104194505	Hela-S3	cervix:	n/a	n/a
47	MYC	chr12:104193312-104194569	NB4	blood:	n/a	chr12:104193879-104193894 chr12:104193433-104193444 chr12:104193883-104193893
48	MYC	chr12:104193559-104194137	MCF10A-Er-Src	breast:	n/a	chr12:104193879-104193894 chr12:104193883-104193893
49	NFIC	chr12:104193467-104194590	ECC-1	luminal epithelium:	n/a	n/a
50	NR2F2	chr12:104193339-104194470	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:104186543..104188821-chr12:104190748..104192615,2	K562	blood:
2	chr12:104192629..104194904-chr12:104224915..104226874,2	MCF-7	breast:
3	chr12:104183990..104193430-chr12:104193641..104204611,16	MCF-7	breast:
4	chr12:104190889..104195812-chr12:104232079..104236624,5	MCF-7	breast:
5	chr12:104192326..104196273-chr12:104235179..104237558,3	K562	blood:
6	chr12:104192165..104193945-chr12:104199242..104201108,2	K562	blood:
7	chr12:104190724..104195360-chr12:104196501..104199658,6	MCF-7	breast:
8	chr12:104183709..104186598-chr12:104189875..104192288,3	K562	blood:
9	chr12:104192525..104200371-chr12:104233987..104238967,10	MCF-7	breast:
10	chr12:104192744..104195300-chr12:104227670..104230455,2	MCF-7	breast:
11	chr12:104192025..104195229-chr12:104233820..104236988,3	K562	blood:
12	chr12:104187183..104188924-chr12:104191126..104192831,2	K562	blood:

Variant related genes	Relation type
NT5DC3	TF binding region
ENSG00000111696	chromatin interactions
ENSG00000257327	chromatin interactions

Extended variants
information (count: 93 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:93 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189857528	chr12:104191282-104191283	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs140978540	chr12:104191304-104191305	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs112626296	chr12:104191341-104191342	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs372359682	chr12:104191349-104191350	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs570761209	chr12:104191368-104191369	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs181270004	chr12:104191386-104191387	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs372815761	chr12:104191483-104191484	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs550087833	chr12:104191501-104191502	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs187147871	chr12:104191507-104191508	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs553545681	chr12:104191517-104191518	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs535616273	chr12:104191531-104191532	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs11111789	chr12:104191540-104191541	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs565733933	chr12:104191611-104191612	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs58513046	chr12:104191663-104191664	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs534343734	chr12:104191674-104191675	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs74524744	chr12:104191696-104191697	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs577926866	chr12:104191707-104191708	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs557076596	chr12:104191778-104191779	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs537389082	chr12:104191783-104191784	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs547589010	chr12:104191785-104191786	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs574183339	chr12:104191837-104191838	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs201545797	chr12:104191854-104191855	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs371487149	chr12:104191870-104191871	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs543193120	chr12:104191925-104191926	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs559609799	chr12:104191953-104191954	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs573262594	chr12:104192032-104192033	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs545080883	chr12:104192035-104192036	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs565318111	chr12:104192040-104192041	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs113757496	chr12:104192041-104192042	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs530921847	chr12:104192042-104192043	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs570954517	chr12:104192067-104192068	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs575221056	chr12:104192171-104192172	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs550124358	chr12:104192208-104192209	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs190449142	chr12:104192299-104192300	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs550683843	chr12:104192303-104192304	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs372490649	chr12:104192348-104192349	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs529093352	chr12:104192354-104192355	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs181977383	chr12:104192360-104192361	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs373393135	chr12:104192401-104192402	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs377569478	chr12:104192412-104192413	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs150924761	chr12:104192416-104192417	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs140726132	chr12:104192437-104192438	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs186364518	chr12:104192438-104192439	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs200110814	chr12:104192465-104192466	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs138821427	chr12:104192470-104192471	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs542641375	chr12:104192478-104192479	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs10082821	chr12:104192506-104192507	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs536630339	chr12:104192531-104192532	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs557268934	chr12:104192534-104192535	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs574243152	chr12:104192542-104192543	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	22032731	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
Acute lymphoblastic leukemia	21339820	CNVD
lymphocytic leukemia	21291569	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Neurocytoma	17123091	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:208 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104163600-104204200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr12:104165800-104193400	Weak transcription	Fetal Lung	lung
3	chr12:104167200-104199800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:104169000-104197800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr12:104171200-104193600	Weak transcription	Primary hematopoietic stem cells	blood
6	chr12:104171600-104194000	Weak transcription	Brain Substantia Nigra	brain
7	chr12:104171800-104216000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr12:104172400-104191400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr12:104173800-104208800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr12:104174000-104194200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr12:104177800-104207600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr12:104178600-104193400	Weak transcription	Left Ventricle	heart
13	chr12:104178800-104194000	Weak transcription	Brain Angular Gyrus	brain
14	chr12:104178800-104194200	Weak transcription	Esophagus	oesophagus
15	chr12:104179000-104193200	Weak transcription	Spleen	Spleen
16	chr12:104179000-104193600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr12:104179400-104191400	Weak transcription	Hela-S3	cervix
18	chr12:104179400-104193800	Weak transcription	Fetal Kidney	kidney
19	chr12:104179800-104192800	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr12:104179800-104193800	Weak transcription	NHDF-Ad	bronchial
21	chr12:104183600-104192800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr12:104183800-104193600	Weak transcription	Stomach Mucosa	stomach
23	chr12:104184800-104192600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr12:104184800-104193400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr12:104185200-104192000	Strong transcription	A549	lung
26	chr12:104185200-104192400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr12:104185200-104192600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr12:104185400-104192800	Strong transcription	HSMM	muscle
29	chr12:104185400-104193600	Strong transcription	Primary T cells from cord blood	blood
30	chr12:104185400-104193800	Strong transcription	K562	blood
31	chr12:104185800-104192800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr12:104185800-104198800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr12:104186000-104191600	Genic enhancers	Colon Smooth Muscle	Colon
34	chr12:104186000-104192800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr12:104186200-104192000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr12:104186400-104192800	Strong transcription	HMEC	breast
37	chr12:104186600-104192600	Weak transcription	Duodenum Mucosa	Duodenum
38	chr12:104186600-104194400	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr12:104187400-104206800	Weak transcription	Primary T helper cells fromperipheralblood	blood
40	chr12:104187600-104191800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr12:104187600-104193200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr12:104187600-104193200	Weak transcription	Pancreas	Pancrea
43	chr12:104187600-104193600	Weak transcription	Brain Hippocampus Middle	brain
44	chr12:104187600-104193600	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr12:104187800-104191600	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr12:104187800-104193600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr12:104187800-104193800	Weak transcription	Brain Cingulate Gyrus	brain
48	chr12:104187800-104198200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr12:104187800-104212600	Weak transcription	GM12878-XiMat	blood
50	chr12:104188200-104193200	Weak transcription	Sigmoid Colon	Sigmoid Colon

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