Variant report

Variant	nsv663
Chromosome Location	chr12:31941989-31986608
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:737)
CpG islands
(count:671)
Chromatin interactive
region (count:3)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:737 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:31942529-31942746	K562	blood:	n/a	n/a
2	ARID3A	chr12:31966125-31966490	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:31985993-31986444	K562	blood:	n/a	n/a
4	ATF1	chr12:31949441-31949444	K562	blood:	n/a	n/a
5	ATF1	chr12:31985887-31986386	K562	blood:	n/a	n/a
6	ATF2	chr12:31963946-31964779	GM12878	blood:	n/a	n/a
7	ATF2	chr12:31956928-31957459	GM12878	blood:	n/a	n/a
8	ATF2	chr12:31985676-31986223	GM12878	blood:	n/a	n/a
9	ATF2	chr12:31963894-31964676	GM12878	blood:	n/a	n/a
10	ATF3	chr12:31960500-31960895	GM12878	blood:	n/a	n/a
11	ATF3	chr12:31960655-31960820	GM12878	blood:	n/a	n/a
12	BATF	chr12:31957019-31957431	GM12878	blood:	n/a	n/a
13	BATF	chr12:31985768-31986139	GM12878	blood:	n/a	n/a
14	BATF	chr12:31963892-31964710	GM12878	blood:	n/a	chr12:31964200-31964209
15	BATF	chr12:31957043-31957422	GM12878	blood:	n/a	n/a
16	BATF	chr12:31963959-31964683	GM12878	blood:	n/a	chr12:31964200-31964209
17	BCL11A	chr12:31957139-31957320	GM12878	blood:	n/a	n/a
18	BCL11A	chr12:31963903-31964601	GM12878	blood:	n/a	n/a
19	BCL11A	chr12:31957022-31957369	GM12878	blood:	n/a	n/a
20	BCL11A	chr12:31985779-31986107	GM12878	blood:	n/a	n/a
21	BCL11A	chr12:31985800-31986149	GM12878	blood:	n/a	n/a
22	BCL11A	chr12:31961977-31962264	GM12878	blood:	n/a	n/a
23	BCL3	chr12:31963898-31964480	GM12878	blood:	n/a	n/a
24	BCLAF1	chr12:31985645-31986285	GM12878	blood:	n/a	n/a
25	BCLAF1	chr12:31985714-31986171	GM12878	blood:	n/a	n/a
26	BCLAF1	chr12:31963859-31964680	GM12878	blood:	n/a	n/a
27	BCLAF1	chr12:31963934-31964773	GM12878	blood:	n/a	n/a
28	BHLHE40	chr12:31961881-31962273	GM12878	blood:	n/a	n/a
29	BHLHE40	chr12:31959897-31960934	GM12878	blood:	n/a	n/a
30	BHLHE40	chr12:31957050-31957414	GM12878	blood:	n/a	n/a
31	BHLHE40	chr12:31963887-31964519	GM12878	blood:	n/a	n/a
32	BRCA1	chr12:31960519-31960597	GM12878	blood:	n/a	n/a
33	CBX3	chr12:31979017-31979313	K562	blood:	n/a	n/a
34	CBX3	chr12:31985206-31986445	K562	blood:	n/a	n/a
35	CBX3	chr12:31966202-31966664	HCT-116	colon:	n/a	n/a
36	CEBPB	chr12:31964015-31964249	HepG2	liver:	n/a	chr12:31964139-31964150
37	CEBPB	chr12:31963882-31964739	GM12878	blood:	n/a	chr12:31964139-31964150
38	CEBPB	chr12:31964020-31964328	K562	blood:	n/a	chr12:31964139-31964150
39	CEBPB	chr12:31963972-31964438	GM12878	blood:	n/a	chr12:31964139-31964150
40	CEBPB	chr12:31983292-31983336	HepG2	liver:	n/a	n/a
41	CEBPB	chr12:31964000-31964262	Hela-S3	cervix:	n/a	chr12:31964139-31964150
42	CEBPB	chr12:31973762-31974122	MCF-7	breast:	n/a	n/a
43	CEBPB	chr12:31964638-31964939	HepG2	liver:	n/a	n/a
44	CEBPB	chr12:31948842-31949042	HepG2	liver:	n/a	chr12:31948963-31948974
45	CEBPB	chr12:31948845-31949051	A549	lung:	n/a	chr12:31948963-31948974
46	CEBPB	chr12:31959392-31959420	IMR90	lung:	n/a	chr12:31959398-31959409
47	CEBPB	chr12:31964726-31964920	A549	lung:	n/a	n/a
48	CEBPB	chr12:31983258-31983329	A549	lung:	n/a	chr12:31983285-31983296
49	CEBPB	chr12:31964036-31964284	A549	lung:	n/a	chr12:31964139-31964150
50	CEBPB	chr12:31973865-31974031	HepG2	liver:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31945075-31945125	LNCaP	prostate:	n/a
2	chr12:31944836-31944886	T-47D	breast:	n/a
3	chr12:31946408-31946458	PrEC	prostate:	n/a
4	chr12:31946434-31946484	Hepatocyte	liver:	n/a
5	chr12:31944807-31944857	SK-N-SH_RA	brain:	n/a
6	chr12:31946262-31946312	NT2-D1	testis:	n/a
7	chr12:31946434-31946484	PANC-1	pancreas:	n/a
8	chr12:31946434-31946484	AG09319	gingival:	n/a
9	chr12:31945286-31945336	HL-60	blood:	n/a
10	chr12:31946262-31946312	GM19239	blood:	n/a
11	chr12:31946408-31946458	MCF10A-Er-Src	breast:	n/a
12	chr12:31945075-31945125	ovcar-3	ovarian:	n/a
13	chr12:31942768-31942818	HIPEpiC	eye:	n/a
14	chr12:31945075-31945125	AG10803	skin:	n/a
15	chr12:31944807-31944857	MCF-7	breast:	n/a
16	chr12:31946434-31946484	RPTEC	kidney:	n/a
17	chr12:31945075-31945125	HUVEC	blood vessel:	n/a
18	chr12:31944836-31944886	NHDF-neo	bronchial:	n/a
19	chr12:31945286-31945336	MCF-7	breast:	n/a
20	chr12:31942768-31942818	HL-60	blood:	n/a
21	chr12:31958950-31959000	LNCaP	prostate:	n/a
22	chr12:31944836-31944886	HepG2	liver:	n/a
23	chr12:31942768-31942818	NH-A	brain:	n/a
24	chr12:31945118-31945168	GM12892	blood:	n/a
25	chr12:31945118-31945168	GM12891	blood:	n/a
26	chr12:31945118-31945168	SAEC	small airway:	n/a
27	chr12:31944836-31944886	AG04450	lung:	fetal
28	chr12:31945286-31945336	HRE	kidney:	n/a
29	chr12:31944556-31944606	HRE	kidney:	n/a
30	chr12:31945075-31945125	HPAEpiC	pulmonary alveolar:	n/a
31	chr12:31958950-31959000	BJ	skin:	n/a
32	chr12:31946434-31946484	HEK293	kidney:	embryo
33	chr12:31958950-31959000	CMK	blood:	n/a
34	chr12:31946262-31946312	GM06990	blood:	n/a
35	chr12:31942768-31942818	HEEpiC	esophagus:	n/a
36	chr12:31945075-31945125	H1-hESC	embryonic stem cell:	embryo
37	chr12:31942768-31942818	RPTEC	kidney:	n/a
38	chr12:31944836-31944886	CMK	blood:	n/a
39	chr12:31946408-31946458	SK-N-MC	brain:	n/a
40	chr12:31945118-31945168	HCF	heart:	n/a
41	chr12:31945286-31945336	HRPEpiC	eye:	n/a
42	chr12:31944556-31944606	HUVEC	blood vessel:	n/a
43	chr12:31946434-31946484	GM12892	blood:	n/a
44	chr12:31944836-31944886	A549	lung:	n/a
45	chr12:31958950-31959000	Hela-S3	cervix:	n/a
46	chr12:31946408-31946458	HAEpiC	amniotic membrane:	n/a
47	chr12:31945118-31945168	NB4	blood:	n/a
48	chr12:31945286-31945336	HNPCEpiC	eye:	n/a
49	chr12:31946408-31946458	GM12891	blood:	n/a
50	chr12:31946434-31946484	HCM	heart:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:31935950..31938716-chr12:31941172..31943567,2	MCF-7	breast:
2	chr12:31834834..31835708-chr12:31965985..31966914,2	MCF-7	breast:
3	chr12:31744029..31745765-chr12:31984895..31986736,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C12orf35-12	chr12:31967425-31967510	NONHSAT027579
2	lnc-C12orf35-12	chr12:31970854-31970979	NONHSAT027579

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	H3F3C	hsa-miR-1	chr12:31944121-31944142

Variant related genes	Relation type
ENSG00000252204	TF binding region
H3F3C	TF binding region
RNU6-1069P	TF binding region
ENSG00000252204	CpG island
H3F3C	CpG island
RNU6-1069P	CpG island
ENSG00000255867	chromatin interactions
ENSG00000170456	chromatin interactions

Extended variants
information (count: 1984 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1984 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144551404	chr12:31942020-31942021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs79124760	chr12:31942023-31942024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs575120419	chr12:31942033-31942034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs146547186	chr12:31942056-31942057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12311180	chr12:31942072-31942073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10506079	chr12:31942106-31942107	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs573113193	chr12:31942114-31942115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141249559	chr12:31942130-31942131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575922588	chr12:31942179-31942180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs10506078	chr12:31942194-31942195	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs531089956	chr12:31942199-31942200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191415858	chr12:31942287-31942288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs73074013	chr12:31942289-31942290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566391696	chr12:31942324-31942325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532116473	chr12:31942343-31942344	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552303114	chr12:31942474-31942475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565739770	chr12:31942500-31942501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564993696	chr12:31942502-31942503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs141879399	chr12:31942503-31942504	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528328857	chr12:31942551-31942552	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142330690	chr12:31942605-31942606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs116253521	chr12:31942616-31942617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532008072	chr12:31942617-31942618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536929144	chr12:31942620-31942621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11051593	chr12:31942624-31942625	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs570516799	chr12:31942658-31942659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183540691	chr12:31942677-31942678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572162707	chr12:31942741-31942742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553094559	chr12:31942747-31942748	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12426434	chr12:31942787-31942788	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs542437412	chr12:31942852-31942853	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555666413	chr12:31942883-31942884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575761067	chr12:31942911-31942912	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187838122	chr12:31942940-31942941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192275992	chr12:31942987-31942988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576916336	chr12:31943023-31943024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564035937	chr12:31943027-31943028	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558346026	chr12:31943039-31943040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs199501099	chr12:31943040-31943041	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548101626	chr12:31943070-31943071	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559534307	chr12:31943079-31943080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528149878	chr12:31943174-31943175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529356539	chr12:31943218-31943219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563109530	chr12:31943222-31943223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs1797739	chr12:31943223-31943224	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs552343051	chr12:31943252-31943253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs151265790	chr12:31943301-31943302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs373583716	chr12:31943303-31943304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs530686662	chr12:31943327-31943328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs11051594	chr12:31943340-31943341	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	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
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
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
microdeletion syndrome	16199537	CNVD
Chordoma	18071362	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:465 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31937400-31942000	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr12:31939200-31942600	Weak transcription	Primary T cells from cord blood	blood
3	chr12:31939200-31947600	Weak transcription	Fetal Kidney	kidney
4	chr12:31939400-31942200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr12:31940000-31942200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr12:31941800-31944600	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr12:31942000-31942800	Enhancers	Primary B cells from peripheral blood	blood
8	chr12:31942000-31944600	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr12:31942200-31943200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr12:31942200-31943800	Enhancers	Primary T cells fromperipheralblood	blood
11	chr12:31942200-31944400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr12:31942200-31944800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr12:31942400-31942800	Enhancers	Placenta	Placenta
14	chr12:31942600-31943000	Enhancers	Placenta Amnion	Placenta Amnion
15	chr12:31942600-31943800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr12:31942600-31944600	Enhancers	Primary T cells from cord blood	blood
17	chr12:31942600-31944600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr12:31942600-31944600	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr12:31942600-31944600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr12:31942800-31944200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
21	chr12:31942800-31944400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr12:31942800-31944400	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr12:31942800-31956600	Weak transcription	Primary B cells from peripheral blood	blood
24	chr12:31943000-31943400	Enhancers	Fetal Thymus	thymus
25	chr12:31943800-31944600	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr12:31943800-31944600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr12:31944200-31945000	Active TSS	HUVEC	blood vessel
28	chr12:31944200-31949600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr12:31944400-31949200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr12:31944400-31949400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr12:31944400-31949400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr12:31944600-31945200	Enhancers	Primary T cells fromperipheralblood	blood
33	chr12:31944600-31945200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr12:31944600-31949200	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr12:31944600-31949200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr12:31944600-31949400	Weak transcription	Primary T cells from cord blood	blood
37	chr12:31944600-31949400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr12:31944600-31949400	Weak transcription	Primary T helper cells fromperipheralblood	blood
39	chr12:31944600-31949600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr12:31944800-31949200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr12:31945200-31949400	Weak transcription	Primary T cells fromperipheralblood	blood
42	chr12:31947600-31947800	Flanking Active TSS	Fetal Kidney	kidney
43	chr12:31947600-31947800	Enhancers	Fetal Thymus	thymus
44	chr12:31947800-31948000	Enhancers	Fetal Kidney	kidney
45	chr12:31948000-31948200	Flanking Active TSS	Fetal Kidney	kidney
46	chr12:31949200-31949600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr12:31949200-31949800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr12:31949200-31950600	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr12:31949200-31950800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
50	chr12:31949200-31951000	Enhancers	Primary T killer naive cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links