Variant report

Variant	nsv818915
Chromosome Location	chr12:41784997-41811063
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	CEBPB	chr12:41804428-41804688	A549	lung:	n/a	n/a
2	CEBPB	chr12:41793677-41794018	A549	lung:	n/a	chr12:41793843-41793852 chr12:41793842-41793853
3	CEBPB	chr12:41793794-41793971	K562	blood:	n/a	chr12:41793843-41793852 chr12:41793842-41793853
4	CEBPB	chr12:41793798-41793998	H1-hESC	embryonic stem cell:	n/a	chr12:41793843-41793852 chr12:41793842-41793853
5	CEBPB	chr12:41788187-41788427	HepG2	liver:	n/a	chr12:41788258-41788269
6	CEBPB	chr12:41793692-41794032	HepG2	liver:	n/a	chr12:41793843-41793852 chr12:41793842-41793853
7	CEBPB	chr12:41793682-41794026	IMR90	lung:	n/a	chr12:41793843-41793852 chr12:41793842-41793853
8	CEBPB	chr12:41793716-41794026	Hela-S3	cervix:	n/a	chr12:41793843-41793852 chr12:41793842-41793853
9	CREB1	chr12:41799994-41800397	GM12878	blood:	n/a	n/a
10	CTCF	chr12:41804540-41804690	HRE	kidney:	n/a	n/a
11	CTCF	chr12:41803460-41803610	HL-60	blood:	n/a	n/a
12	CTCF	chr12:41803500-41803650	HepG2	liver:	n/a	n/a
13	CTCF	chr12:41803560-41803710	GM12873	blood:	n/a	n/a
14	CTCF	chr12:41793426-41793498	Fibrobl	skin:	n/a	n/a
15	CTCF	chr12:41803500-41803650	HCT-116	colon:	n/a	n/a
16	CTCF	chr12:41803520-41803670	GM12874	blood:	n/a	n/a
17	CTCF	chr12:41803520-41803670	GM12871	blood:	n/a	n/a
18	CTCF	chr12:41803520-41803670	RPTEC	kidney:	n/a	n/a
19	CTCF	chr12:41803460-41803610	RPTEC	kidney:	n/a	n/a
20	CTCF	chr12:41803560-41803710	HEK293	kidney:	n/a	n/a
21	E2F4	chr12:41807109-41807353	MCF10A-Er-Src	breast:	n/a	n/a
22	ELK1	chr12:41795423-41795483	Hela-S3	cervix:	n/a	n/a
23	FOS	chr12:41796626-41796908	MCF10A-Er-Src	breast:	n/a	chr12:41796783-41796795 chr12:41796783-41796794 chr12:41796785-41796794 chr12:41796784-41796794 chr12:41796784-41796793
24	FOS	chr12:41796620-41796960	MCF10A-Er-Src	breast:	n/a	chr12:41796783-41796795 chr12:41796783-41796794 chr12:41796785-41796794 chr12:41796784-41796794 chr12:41796784-41796793
25	FOS	chr12:41796631-41796894	MCF10A-Er-Src	breast:	n/a	chr12:41796783-41796795 chr12:41796783-41796794 chr12:41796785-41796794 chr12:41796784-41796794 chr12:41796784-41796793
26	FOS	chr12:41796596-41796986	HUVEC	blood vessel:	n/a	chr12:41796783-41796795 chr12:41796783-41796794 chr12:41796785-41796794 chr12:41796784-41796794 chr12:41796784-41796793
27	FOS	chr12:41796681-41796931	MCF10A-Er-Src	breast:	n/a	chr12:41796783-41796795 chr12:41796783-41796794 chr12:41796785-41796794 chr12:41796784-41796794 chr12:41796784-41796793
28	GATA3	chr12:41786387-41786508	SH-SY5Y	brain:	n/a	n/a
29	JUN	chr12:41796615-41796937	HepG2	liver:	n/a	chr12:41796783-41796795 chr12:41796785-41796794 chr12:41796784-41796794 chr12:41796784-41796793
30	JUND	chr12:41796587-41797116	SK-N-SH	brain:	n/a	chr12:41796783-41796794 chr12:41796783-41796795 chr12:41796785-41796794 chr12:41796784-41796794 chr12:41796784-41796793
31	JUND	chr12:41796617-41796960	HepG2	liver:	n/a	chr12:41796783-41796794 chr12:41796783-41796795 chr12:41796785-41796794 chr12:41796784-41796794 chr12:41796784-41796793
32	MAFK	chr12:41809691-41809703	HepG2	liver:	n/a	n/a
33	MAFK	chr12:41784986-41785223	HepG2	liver:	n/a	n/a
34	MAFK	chr12:41789234-41789347	HepG2	liver:	n/a	n/a
35	MAFK	chr12:41785071-41785206	HepG2	liver:	n/a	n/a
36	MAFK	chr12:41794680-41794681	IMR90	lung:	n/a	n/a
37	MAFK	chr12:41796670-41796700	HepG2	liver:	n/a	n/a
38	MAX	chr12:41808556-41808884	H1-hESC	embryonic stem cell:	n/a	n/a
39	MAX	chr12:41801080-41801327	H1-hESC	embryonic stem cell:	n/a	chr12:41801206-41801215 chr12:41801202-41801211
40	MAX	chr12:41808661-41808897	H1-hESC	embryonic stem cell:	n/a	n/a
41	MAZ	chr12:41803542-41803544	HepG2	liver:	n/a	n/a
42	MYC	chr12:41794748-41794844	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr12:41799052-41799444	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr12:41787040-41787100	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr12:41807448-41807612	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr12:41809230-41809366	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr12:41800922-41801530	H1-neurons	neurons:	n/a	n/a
48	POLR2A	chr12:41800388-41800610	ProgFib	skin:	n/a	n/a
49	POLR2A	chr12:41790489-41790746	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr12:41794992-41795082	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:41797234-41797284	BE2_C	brain:	n/a
2	chr12:41797234-41797284	CMK	blood:	n/a
3	chr12:41797234-41797284	RPTEC	kidney:	n/a
4	chr12:41797234-41797284	A549	lung:	n/a
5	chr12:41797234-41797284	GM12891	blood:	n/a
6	chr12:41797234-41797284	SKMC	muscle:	n/a
7	chr12:41797234-41797284	HCF	heart:	n/a
8	chr12:41797234-41797284	LNCaP	prostate:	n/a
9	chr12:41797234-41797284	NT2-D1	testis:	n/a
10	chr12:41797234-41797284	NHBE	bronchial:	n/a
11	chr12:41797234-41797284	GM12878	blood:	n/a
12	chr12:41797234-41797284	NH-A	brain:	n/a
13	chr12:41797234-41797284	AG09309	skin:	n/a
14	chr12:41797234-41797284	GM06990	blood:	n/a
15	chr12:41797234-41797284	HMEC	breast:	n/a
16	chr12:41797234-41797284	ECC-1	luminal epithelium:	n/a
17	chr12:41797234-41797284	U87	brain:	n/a
18	chr12:41797234-41797284	PrEC	prostate:	n/a
19	chr12:41797234-41797284	HRE	kidney:	n/a
20	chr12:41797234-41797284	HCPEpiC	choroid plexus:	n/a
21	chr12:41797234-41797284	HNPCEpiC	eye:	n/a
22	chr12:41797234-41797284	AG10803	skin:	n/a
23	chr12:41797234-41797284	HUVEC	blood vessel:	n/a
24	chr12:41797234-41797284	HEEpiC	esophagus:	n/a
25	chr12:41797234-41797284	HRPEpiC	eye:	n/a
26	chr12:41797234-41797284	PANC-1	pancreas:	n/a
27	chr12:41797234-41797284	PFSK-1	brain:	n/a
28	chr12:41797234-41797284	HIPEpiC	eye:	n/a
29	chr12:41797234-41797284	H1-hESC	embryonic stem cell:	embryo
30	chr12:41797234-41797284	ProgFib	skin:	n/a
31	chr12:41797234-41797284	Jurkat	blood:	n/a
32	chr12:41797234-41797284	HEK293	kidney:	embryo
33	chr12:41797234-41797284	SAEC	small airway:	n/a
34	chr12:41797234-41797284	Hepatocyte	liver:	n/a
35	chr12:41797234-41797284	ovcar-3	ovarian:	n/a
36	chr12:41797234-41797284	NHDF-neo	bronchial:	n/a
37	chr12:41797234-41797284	AoSMC	blood vessel:	n/a
38	chr12:41797234-41797284	GM12892	blood:	n/a
39	chr12:41797234-41797284	HCT-116	colon:	n/a
40	chr12:41797234-41797284	BJ	skin:	n/a
41	chr12:41797234-41797284	MCF10A-Er-Src	breast:	n/a
42	chr12:41797234-41797284	HRCEpiC	kidney:	n/a
43	chr12:41797234-41797284	AG04450	lung:	fetal
44	chr12:41797234-41797284	SK-N-SH_RA	brain:	n/a
45	chr12:41797234-41797284	HCM	heart:	n/a
46	chr12:41797234-41797284	HPAEpiC	pulmonary alveolar:	n/a
47	chr12:41797234-41797284	IMR90	lung:	fetal
48	chr12:41797234-41797284	GM19239	blood:	n/a
49	chr12:41797234-41797284	Hela-S3	cervix:	n/a
50	chr12:41797234-41797284	HAEpiC	amniotic membrane:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GXYLT1-2	chr12:41805327-41805677	ENSG00000257228.1
2	lnc-GXYLT1-2	chr12:41806203-41806279	ENSG00000257228.1
3	lnc-GXYLT1-2	chr12:41806016-41806086	ENSG00000257228.1
4	lnc-GXYLT1-2	chr12:41806815-41806888	ENSG00000257228.1
5	lnc-GXYLT1-2	chr12:41806016-41806086	ENSG00000257228.1
6	lnc-GXYLT1-2	chr12:41806203-41806338	ENSG00000257228.1
7	lnc-GXYLT1-2	chr12:41803269-41803764	ENSG00000257228.1

Variant related genes	Relation type
ENSG00000257228	TF binding region
ENSG00000257228	CpG island

Extended variants
information (count: 958 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:958 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11180882	chr12:41784997-41784998	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181280421	chr12:41785009-41785010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373278006	chr12:41785014-41785015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141488713	chr12:41785020-41785021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545103956	chr12:41785080-41785081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548610986	chr12:41785097-41785098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs557622137	chr12:41785122-41785123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575876363	chr12:41785161-41785162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543367195	chr12:41785230-41785231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561583831	chr12:41785235-41785236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146196415	chr12:41785244-41785245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73274455	chr12:41785277-41785278	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs370574791	chr12:41785307-41785308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532501736	chr12:41785379-41785380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184331565	chr12:41785431-41785432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35907625	chr12:41785440-41785441	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374598595	chr12:41785462-41785463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs139189084	chr12:41785511-41785512	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12228172	chr12:41785576-41785577	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs116459922	chr12:41785583-41785584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572244344	chr12:41785615-41785616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149492578	chr12:41785627-41785628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73126890	chr12:41785683-41785684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552756277	chr12:41785688-41785689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189608278	chr12:41785689-41785690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182016464	chr12:41785695-41785696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538755181	chr12:41785778-41785779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7957823	chr12:41785792-41785793	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs7960955	chr12:41785843-41785844	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs536803065	chr12:41785853-41785854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187266764	chr12:41785867-41785868	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551105226	chr12:41785878-41785879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35506579	chr12:41785923-41785924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190964921	chr12:41785938-41785939	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181404042	chr12:41785942-41785943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369662941	chr12:41785982-41785983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535103560	chr12:41786037-41786038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs56290808	chr12:41786038-41786039	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs576267996	chr12:41786045-41786046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs368811420	chr12:41786078-41786079	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs57395098	chr12:41786089-41786090	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs12300045	chr12:41786096-41786097	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs146887438	chr12:41786111-41786112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10785262	chr12:41786194-41786195	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs528421410	chr12:41786206-41786207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532189863	chr12:41786251-41786252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs59508383	chr12:41786267-41786268	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs571288538	chr12:41786307-41786308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538595749	chr12:41786323-41786324	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190093756	chr12:41786327-41786328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
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
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
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	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
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:41776200-41787400	Weak transcription	Aorta	Aorta
2	chr12:41784400-41785000	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr12:41785400-41787000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr12:41787400-41787800	ZNF genes & repeats	Aorta	Aorta
5	chr12:41790400-41790600	Enhancers	Brain Germinal Matrix	brain
6	chr12:41790600-41791200	Weak transcription	Brain Germinal Matrix	brain
7	chr12:41791200-41792200	Enhancers	Brain Germinal Matrix	brain
8	chr12:41792200-41792400	Weak transcription	Brain Germinal Matrix	brain
9	chr12:41792400-41792800	Enhancers	Brain Germinal Matrix	brain
10	chr12:41792800-41793600	Weak transcription	Brain Germinal Matrix	brain
11	chr12:41793600-41794200	Enhancers	Brain Substantia Nigra	brain
12	chr12:41793600-41794400	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr12:41793600-41794400	Enhancers	Brain Germinal Matrix	brain
14	chr12:41793800-41794200	Enhancers	Brain Hippocampus Middle	brain
15	chr12:41793800-41794400	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr12:41794200-41794400	Enhancers	Colon Smooth Muscle	Colon
17	chr12:41795400-41795600	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr12:41795600-41796600	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr12:41796600-41797000	Active TSS	Brain Anterior Caudate	brain
20	chr12:41796600-41797200	Enhancers	HUVEC	blood vessel
21	chr12:41796600-41797800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr12:41796800-41797800	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr12:41797000-41797600	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr12:41797000-41797800	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr12:41797000-41798000	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr12:41797000-41798400	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr12:41797000-41800600	Weak transcription	Brain Anterior Caudate	brain
28	chr12:41797200-41797800	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr12:41797600-41798200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr12:41797800-41798400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr12:41798200-41798400	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr12:41798400-41798600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr12:41798600-41799200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr12:41799200-41799600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
35	chr12:41799800-41800400	Weak transcription	Brain Hippocampus Middle	brain
36	chr12:41800000-41800800	Enhancers	Fetal Brain Male	brain
37	chr12:41800600-41800800	Enhancers	Brain Angular Gyrus	brain
38	chr12:41800600-41800800	Enhancers	Brain Anterior Caudate	brain
39	chr12:41800600-41801200	Enhancers	Brain Substantia Nigra	brain
40	chr12:41800600-41801600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr12:41800600-41801800	Enhancers	Fetal Brain Female	brain
42	chr12:41800600-41802200	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr12:41800800-41801000	Enhancers	Brain Cingulate Gyrus	brain
44	chr12:41800800-41801000	Enhancers	Brain Hippocampus Middle	brain
45	chr12:41800800-41801000	Active TSS	Brain Inferior Temporal Lobe	brain
46	chr12:41800800-41801000	Flanking Active TSS	Fetal Brain Male	brain
47	chr12:41800800-41801200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr12:41800800-41801200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr12:41800800-41801200	Flanking Active TSS	Brain Anterior Caudate	brain
50	chr12:41800800-41801200	Enhancers	Brain Germinal Matrix	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links