Variant report

Variant	nsv899037
Chromosome Location	chr12:41777144-41819215
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	chr12:41811200-41811531	HepG2	liver:	n/a	chr12:41811371-41811382
2	CEBPB	chr12:41793716-41794026	Hela-S3	cervix:	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	chr12:41793692-41794032	HepG2	liver:	n/a	chr12:41793843-41793852 chr12:41793842-41793853
5	CEBPB	chr12:41793677-41794018	A549	lung:	n/a	chr12:41793843-41793852 chr12:41793842-41793853
6	CEBPB	chr12:41804428-41804688	A549	lung:	n/a	n/a
7	CEBPB	chr12:41811221-41811487	IMR90	lung:	n/a	chr12:41811371-41811382
8	CEBPB	chr12:41778988-41779077	A549	lung:	n/a	n/a
9	CEBPB	chr12:41793798-41793998	H1-hESC	embryonic stem cell:	n/a	chr12:41793843-41793852 chr12:41793842-41793853
10	CEBPB	chr12:41811273-41811516	A549	lung:	n/a	chr12:41811371-41811382
11	CEBPB	chr12:41793682-41794026	IMR90	lung:	n/a	chr12:41793843-41793852 chr12:41793842-41793853
12	CEBPB	chr12:41788187-41788427	HepG2	liver:	n/a	chr12:41788258-41788269
13	CREB1	chr12:41799994-41800397	GM12878	blood:	n/a	n/a
14	CTCF	chr12:41803500-41803650	HepG2	liver:	n/a	n/a
15	CTCF	chr12:41803500-41803650	HCT-116	colon:	n/a	n/a
16	CTCF	chr12:41803460-41803610	RPTEC	kidney:	n/a	n/a
17	CTCF	chr12:41803520-41803670	GM12874	blood:	n/a	n/a
18	CTCF	chr12:41803460-41803610	HL-60	blood:	n/a	n/a
19	CTCF	chr12:41803560-41803710	GM12873	blood:	n/a	n/a
20	CTCF	chr12:41793426-41793498	Fibrobl	skin:	n/a	n/a
21	CTCF	chr12:41803520-41803670	RPTEC	kidney:	n/a	n/a
22	CTCF	chr12:41803560-41803710	HEK293	kidney:	n/a	n/a
23	CTCF	chr12:41804540-41804690	HRE	kidney:	n/a	n/a
24	CTCF	chr12:41803520-41803670	GM12871	blood:	n/a	n/a
25	E2F4	chr12:41807109-41807353	MCF10A-Er-Src	breast:	n/a	n/a
26	EBF1	chr12:41783444-41783535	GM12878	blood:	n/a	n/a
27	ELK1	chr12:41795423-41795483	Hela-S3	cervix:	n/a	n/a
28	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
29	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
30	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
31	FOS	chr12:41796596-41796986	HUVEC	blood vessel:	n/a	chr12:41796783-41796795 chr12:41796783-41796794 chr12:41796785-41796794 chr12:41796784-41796794 chr12:41796784-41796793
32	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
33	GATA3	chr12:41786387-41786508	SH-SY5Y	brain:	n/a	n/a
34	GATA3	chr12:41778321-41778444	SH-SY5Y	brain:	n/a	n/a
35	JUN	chr12:41796615-41796937	HepG2	liver:	n/a	chr12:41796783-41796795 chr12:41796785-41796794 chr12:41796784-41796794 chr12:41796784-41796793
36	JUN	chr12:41783121-41783225	H1-hESC	embryonic stem cell:	n/a	n/a
37	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
38	JUND	chr12:41796617-41796960	HepG2	liver:	n/a	chr12:41796783-41796794 chr12:41796783-41796795 chr12:41796785-41796794 chr12:41796784-41796794 chr12:41796784-41796793
39	KAP1	chr12:41817838-41818374	K562	blood:	n/a	n/a
40	MAFF	chr12:41813337-41813666	K562	blood:	n/a	chr12:41813480-41813498
41	MAFF	chr12:41813309-41813680	HepG2	liver:	n/a	chr12:41813480-41813498
42	MAFK	chr12:41784986-41785223	HepG2	liver:	n/a	n/a
43	MAFK	chr12:41813326-41813666	K562	blood:	n/a	chr12:41813482-41813493 chr12:41813481-41813495 chr12:41813482-41813498 chr12:41813482-41813493 chr12:41813483-41813494 chr12:41813482-41813497
44	MAFK	chr12:41785071-41785206	HepG2	liver:	n/a	n/a
45	MAFK	chr12:41809691-41809703	HepG2	liver:	n/a	n/a
46	MAFK	chr12:41813398-41813641	Hela-S3	cervix:	n/a	chr12:41813482-41813493 chr12:41813481-41813495 chr12:41813482-41813498 chr12:41813482-41813493 chr12:41813483-41813494 chr12:41813482-41813497
47	MAFK	chr12:41789234-41789347	HepG2	liver:	n/a	n/a
48	MAFK	chr12:41796670-41796700	HepG2	liver:	n/a	n/a
49	MAFK	chr12:41813321-41813663	H1-hESC	embryonic stem cell:	n/a	chr12:41813482-41813493 chr12:41813481-41813495 chr12:41813482-41813498 chr12:41813482-41813493 chr12:41813483-41813494 chr12:41813482-41813497
50	MAFK	chr12:41794680-41794681	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:41797234-41797284	AG09309	skin:	n/a
2	chr12:41797234-41797284	AG09309	skin:	n/a
3	chr12:41797234-41797284	HPAEpiC	pulmonary alveolar:	n/a
4	chr12:41797234-41797284	A549	lung:	n/a
5	chr12:41797234-41797284	AG04450	lung:	fetal
6	chr12:41797234-41797284	NHBE	bronchial:	n/a
7	chr12:41797234-41797284	GM12892	blood:	n/a
8	chr12:41797234-41797284	HNPCEpiC	eye:	n/a
9	chr12:41797234-41797284	GM06990	blood:	n/a
10	chr12:41797234-41797284	HRE	kidney:	n/a
11	chr12:41797234-41797284	SAEC	small airway:	n/a
12	chr12:41797234-41797284	HL-60	blood:	n/a
13	chr12:41797234-41797284	Hela-S3	cervix:	n/a
14	chr12:41797234-41797284	BE2_C	brain:	n/a
15	chr12:41797234-41797284	NB4	blood:	n/a
16	chr12:41797234-41797284	HUVEC	blood vessel:	n/a
17	chr12:41797234-41797284	AoSMC	blood vessel:	n/a
18	chr12:41797234-41797284	HCT-116	colon:	n/a
19	chr12:41797234-41797284	NT2-D1	testis:	n/a
20	chr12:41797234-41797284	HCPEpiC	choroid plexus:	n/a
21	chr12:41797234-41797284	HRCEpiC	kidney:	n/a
22	chr12:41797234-41797284	U87	brain:	n/a
23	chr12:41797234-41797284	HCM	heart:	n/a
24	chr12:41797234-41797284	HepG2	liver:	n/a
25	chr12:41797234-41797284	SK-N-SH_RA	brain:	n/a
26	chr12:41797234-41797284	BJ	skin:	n/a
27	chr12:41797234-41797284	AG09319	gingival:	n/a
28	chr12:41797234-41797284	HIPEpiC	eye:	n/a
29	chr12:41797234-41797284	Caco-2	colon:	n/a
30	chr12:41797234-41797284	Jurkat	blood:	n/a
31	chr12:41797234-41797284	GM19239	blood:	n/a
32	chr12:41797234-41797284	ovcar-3	ovarian:	n/a
33	chr12:41797234-41797284	CMK	blood:	n/a
34	chr12:41797234-41797284	H1-hESC	embryonic stem cell:	embryo
35	chr12:41797234-41797284	PrEC	prostate:	n/a
36	chr12:41797234-41797284	HEEpiC	esophagus:	n/a
37	chr12:41797234-41797284	LNCaP	prostate:	n/a
38	chr12:41797234-41797284	K562	blood:	n/a
39	chr12:41797234-41797284	SK-N-MC	brain:	n/a
40	chr12:41797234-41797284	ECC-1	luminal epithelium:	n/a
41	chr12:41797234-41797284	SK-N-SH	brain:	n/a
42	chr12:41797234-41797284	SKMC	muscle:	n/a
43	chr12:41797234-41797284	T-47D	breast:	n/a
44	chr12:41797234-41797284	GM12891	blood:	n/a
45	chr12:41797234-41797284	PFSK-1	brain:	n/a
46	chr12:41797234-41797284	NH-A	brain:	n/a
47	chr12:41797234-41797284	AG04449	skin:	fetal
48	chr12:41797234-41797284	MCF-7	breast:	n/a
49	chr12:41797234-41797284	HEK293	kidney:	embryo
50	chr12:41797234-41797284	PANC-1	pancreas:	n/a

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

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

Extended variants
information (count: 1484 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1484 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1458176	chr12:41777144-41777145	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538514130	chr12:41777214-41777215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73126876	chr12:41777246-41777247	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs541536728	chr12:41777328-41777329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs145358854	chr12:41777362-41777363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554040459	chr12:41777370-41777371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73274436	chr12:41777409-41777410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572256208	chr12:41777415-41777416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370845577	chr12:41777440-41777441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201887030	chr12:41777528-41777529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs189980039	chr12:41777572-41777573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs146815179	chr12:41777613-41777614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142487208	chr12:41777624-41777625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150522594	chr12:41777630-41777631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139310192	chr12:41777653-41777654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531341029	chr12:41777658-41777659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183300384	chr12:41777693-41777694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372405211	chr12:41777717-41777718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187070484	chr12:41777734-41777735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs77378759	chr12:41777771-41777772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs199820633	chr12:41777828-41777829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192349158	chr12:41777844-41777845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377076533	chr12:41777865-41777866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547073742	chr12:41777867-41777868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183248882	chr12:41777868-41777869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533334508	chr12:41777915-41777916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140555427	chr12:41777942-41777943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375660539	chr12:41777957-41777958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552051216	chr12:41777961-41777962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570211931	chr12:41777980-41777981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537737669	chr12:41777991-41777992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572495507	chr12:41778047-41778048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139511871	chr12:41778054-41778055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528768948	chr12:41778133-41778134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535160939	chr12:41778187-41778188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs77549587	chr12:41778222-41778223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572227557	chr12:41778243-41778244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188664649	chr12:41778356-41778357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs542706013	chr12:41778360-41778361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558043096	chr12:41778370-41778371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576303927	chr12:41778371-41778372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543289221	chr12:41778372-41778373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191658854	chr12:41778385-41778386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182660116	chr12:41778391-41778392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540746324	chr12:41778411-41778412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558973313	chr12:41778424-41778425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533580473	chr12:41778435-41778436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551726140	chr12:41778439-41778440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143307375	chr12:41778453-41778454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs75092832	chr12:41778481-41778482	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:136 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:41776200-41787400	Weak transcription	Aorta	Aorta
2	chr12:41779000-41779200	Enhancers	Gastric	stomach
3	chr12:41784400-41785000	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr12:41785400-41787000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr12:41787400-41787800	ZNF genes & repeats	Aorta	Aorta
6	chr12:41790400-41790600	Enhancers	Brain Germinal Matrix	brain
7	chr12:41790600-41791200	Weak transcription	Brain Germinal Matrix	brain
8	chr12:41791200-41792200	Enhancers	Brain Germinal Matrix	brain
9	chr12:41792200-41792400	Weak transcription	Brain Germinal Matrix	brain
10	chr12:41792400-41792800	Enhancers	Brain Germinal Matrix	brain
11	chr12:41792800-41793600	Weak transcription	Brain Germinal Matrix	brain
12	chr12:41793600-41794200	Enhancers	Brain Substantia Nigra	brain
13	chr12:41793600-41794400	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr12:41793600-41794400	Enhancers	Brain Germinal Matrix	brain
15	chr12:41793800-41794200	Enhancers	Brain Hippocampus Middle	brain
16	chr12:41793800-41794400	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr12:41794200-41794400	Enhancers	Colon Smooth Muscle	Colon
18	chr12:41795400-41795600	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr12:41795600-41796600	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr12:41796600-41797000	Active TSS	Brain Anterior Caudate	brain
21	chr12:41796600-41797200	Enhancers	HUVEC	blood vessel
22	chr12:41796600-41797800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr12:41796800-41797800	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr12:41797000-41797600	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr12:41797000-41797800	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr12:41797000-41798000	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr12:41797000-41798400	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr12:41797000-41800600	Weak transcription	Brain Anterior Caudate	brain
29	chr12:41797200-41797800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr12:41797600-41798200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr12:41797800-41798400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr12:41798200-41798400	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr12:41798400-41798600	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr12:41798600-41799200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr12:41799200-41799600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
36	chr12:41799800-41800400	Weak transcription	Brain Hippocampus Middle	brain
37	chr12:41800000-41800800	Enhancers	Fetal Brain Male	brain
38	chr12:41800600-41800800	Enhancers	Brain Angular Gyrus	brain
39	chr12:41800600-41800800	Enhancers	Brain Anterior Caudate	brain
40	chr12:41800600-41801200	Enhancers	Brain Substantia Nigra	brain
41	chr12:41800600-41801600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr12:41800600-41801800	Enhancers	Fetal Brain Female	brain
43	chr12:41800600-41802200	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr12:41800800-41801000	Enhancers	Brain Cingulate Gyrus	brain
45	chr12:41800800-41801000	Enhancers	Brain Hippocampus Middle	brain
46	chr12:41800800-41801000	Active TSS	Brain Inferior Temporal Lobe	brain
47	chr12:41800800-41801000	Flanking Active TSS	Fetal Brain Male	brain
48	chr12:41800800-41801200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr12:41800800-41801200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr12:41800800-41801200	Flanking Active TSS	Brain Anterior Caudate	brain

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