Variant report

Variant	nsv975626
Chromosome Location	chr12:31937678-31972436
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:669)
CpG islands
(count:671)
Chromatin interactive
region (count:4)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:669 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:31966125-31966490	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:31942529-31942746	K562	blood:	n/a	n/a
3	ATF1	chr12:31949441-31949444	K562	blood:	n/a	n/a
4	ATF2	chr12:31956928-31957459	GM12878	blood:	n/a	n/a
5	ATF2	chr12:31963946-31964779	GM12878	blood:	n/a	n/a
6	ATF2	chr12:31963894-31964676	GM12878	blood:	n/a	n/a
7	ATF3	chr12:31960500-31960895	GM12878	blood:	n/a	n/a
8	ATF3	chr12:31960655-31960820	GM12878	blood:	n/a	n/a
9	BATF	chr12:31963959-31964683	GM12878	blood:	n/a	chr12:31964200-31964209
10	BATF	chr12:31963892-31964710	GM12878	blood:	n/a	chr12:31964200-31964209
11	BATF	chr12:31957043-31957422	GM12878	blood:	n/a	n/a
12	BATF	chr12:31957019-31957431	GM12878	blood:	n/a	n/a
13	BCL11A	chr12:31963903-31964601	GM12878	blood:	n/a	n/a
14	BCL11A	chr12:31957022-31957369	GM12878	blood:	n/a	n/a
15	BCL11A	chr12:31961977-31962264	GM12878	blood:	n/a	n/a
16	BCL11A	chr12:31957139-31957320	GM12878	blood:	n/a	n/a
17	BCL3	chr12:31963898-31964480	GM12878	blood:	n/a	n/a
18	BCLAF1	chr12:31963934-31964773	GM12878	blood:	n/a	n/a
19	BCLAF1	chr12:31963859-31964680	GM12878	blood:	n/a	n/a
20	BHLHE40	chr12:31959897-31960934	GM12878	blood:	n/a	n/a
21	BHLHE40	chr12:31957050-31957414	GM12878	blood:	n/a	n/a
22	BHLHE40	chr12:31961881-31962273	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:31963887-31964519	GM12878	blood:	n/a	n/a
24	BRCA1	chr12:31960519-31960597	GM12878	blood:	n/a	n/a
25	CBX3	chr12:31966202-31966664	HCT-116	colon:	n/a	n/a
26	CEBPB	chr12:31964015-31964249	HepG2	liver:	n/a	chr12:31964139-31964150
27	CEBPB	chr12:31948842-31949042	HepG2	liver:	n/a	chr12:31948963-31948974
28	CEBPB	chr12:31963882-31964739	GM12878	blood:	n/a	chr12:31964139-31964150
29	CEBPB	chr12:31938038-31938681	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr12:31964726-31964920	A549	lung:	n/a	n/a
31	CEBPB	chr12:31959392-31959420	IMR90	lung:	n/a	chr12:31959398-31959409
32	CEBPB	chr12:31964036-31964284	A549	lung:	n/a	chr12:31964139-31964150
33	CEBPB	chr12:31964756-31964886	IMR90	lung:	n/a	n/a
34	CEBPB	chr12:31964744-31964931	K562	blood:	n/a	n/a
35	CEBPB	chr12:31964020-31964328	K562	blood:	n/a	chr12:31964139-31964150
36	CEBPB	chr12:31963972-31964438	GM12878	blood:	n/a	chr12:31964139-31964150
37	CEBPB	chr12:31964000-31964262	Hela-S3	cervix:	n/a	chr12:31964139-31964150
38	CEBPB	chr12:31938174-31938682	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr12:31964638-31964939	HepG2	liver:	n/a	n/a
40	CEBPB	chr12:31948845-31949051	A549	lung:	n/a	chr12:31948963-31948974
41	CHD1	chr12:31959908-31960927	GM12878	blood:	n/a	n/a
42	CHD1	chr12:31957083-31957326	GM12878	blood:	n/a	n/a
43	CHD2	chr12:31957046-31957443	GM12878	blood:	n/a	n/a
44	CHD2	chr12:31959862-31960902	GM12878	blood:	n/a	n/a
45	CREB1	chr12:31963892-31964795	GM12878	blood:	n/a	n/a
46	CREB1	chr12:31963902-31964606	GM12878	blood:	n/a	n/a
47	CREB1	chr12:31938215-31938793	ECC-1	luminal epithelium:	n/a	n/a
48	CTCF	chr12:31942605-31942727	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr12:31966340-31966490	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr12:31966249-31966615	K562	blood:	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	chr12:31944807-31944857	HUVEC	blood vessel:	n/a
2	chr12:31946262-31946312	RPTEC	kidney:	n/a
3	chr12:31946434-31946484	RPTEC	kidney:	n/a
4	chr12:31946262-31946312	IMR90	lung:	fetal
5	chr12:31946434-31946484	HUVEC	blood vessel:	n/a
6	chr12:31946408-31946458	GM12878	blood:	n/a
7	chr12:31944807-31944857	GM06990	blood:	n/a
8	chr12:31946408-31946458	CMK	blood:	n/a
9	chr12:31944556-31944606	AG09309	skin:	n/a
10	chr12:31944556-31944606	HIPEpiC	eye:	n/a
11	chr12:31945286-31945336	SKMC	muscle:	n/a
12	chr12:31945075-31945125	PFSK-1	brain:	n/a
13	chr12:31946434-31946484	CMK	blood:	n/a
14	chr12:31945075-31945125	SK-N-SH	brain:	n/a
15	chr12:31944807-31944857	AG09309	skin:	n/a
16	chr12:31945286-31945336	HCM	heart:	n/a
17	chr12:31945118-31945168	HRCEpiC	kidney:	n/a
18	chr12:31958950-31959000	GM12878	blood:	n/a
19	chr12:31945118-31945168	AG04449	skin:	fetal
20	chr12:31942768-31942818	ECC-1	luminal epithelium:	n/a
21	chr12:31944556-31944606	SKMC	muscle:	n/a
22	chr12:31944807-31944857	HNPCEpiC	eye:	n/a
23	chr12:31944556-31944606	NH-A	brain:	n/a
24	chr12:31958950-31959000	HepG2	liver:	n/a
25	chr12:31942768-31942818	Caco-2	colon:	n/a
26	chr12:31942768-31942818	HCT-116	colon:	n/a
27	chr12:31946408-31946458	BE2_C	brain:	n/a
28	chr12:31946408-31946458	ovcar-3	ovarian:	n/a
29	chr12:31945075-31945125	ECC-1	luminal epithelium:	n/a
30	chr12:31942768-31942818	LNCaP	prostate:	n/a
31	chr12:31945075-31945125	MCF10A-Er-Src	breast:	n/a
32	chr12:31944556-31944606	HEK293	kidney:	embryo
33	chr12:31946262-31946312	SK-N-SH_RA	brain:	n/a
34	chr12:31942768-31942818	H1-hESC	embryonic stem cell:	embryo
35	chr12:31944836-31944886	H1-hESC	embryonic stem cell:	embryo
36	chr12:31958950-31959000	ECC-1	luminal epithelium:	n/a
37	chr12:31944807-31944857	PANC-1	pancreas:	n/a
38	chr12:31944836-31944886	Hela-S3	cervix:	n/a
39	chr12:31945118-31945168	AG09319	gingival:	n/a
40	chr12:31944556-31944606	HUVEC	blood vessel:	n/a
41	chr12:31946434-31946484	AG09309	skin:	n/a
42	chr12:31942768-31942818	PrEC	prostate:	n/a
43	chr12:31946408-31946458	PrEC	prostate:	n/a
44	chr12:31946408-31946458	HMEC	breast:	n/a
45	chr12:31945118-31945168	NB4	blood:	n/a
46	chr12:31946262-31946312	HRPEpiC	eye:	n/a
47	chr12:31944836-31944886	NHBE	bronchial:	n/a
48	chr12:31944807-31944857	HCPEpiC	choroid plexus:	n/a
49	chr12:31946434-31946484	T-47D	breast:	n/a
50	chr12:31946262-31946312	AG04450	lung:	fetal

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:31834834..31835708-chr12:31965985..31966914,2	MCF-7	breast:
2	chr12:31935950..31938716-chr12:31941172..31943567,2	MCF-7	breast:
3	chr12:31935950..31938716-chr12:31941172..31943567,2	MCF-7	breast:
4	chr12:31936081..31938454-chr12:31945043..31947470,2	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
ENSG00000188375	chromatin interactions

Extended variants
information (count: 1584 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1584 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12227719	chr12:31937743-31937744	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574386003	chr12:31937793-31937794	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs541876862	chr12:31937935-31937936	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs184752902	chr12:31937964-31937965	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs189260099	chr12:31937984-31937985	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs79449542	chr12:31937988-31937989	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs34658509	chr12:31938061-31938062	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs543996930	chr12:31938092-31938093	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs114060677	chr12:31938107-31938108	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs77528307	chr12:31938112-31938113	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs184919678	chr12:31938123-31938124	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs1259761	chr12:31938129-31938130	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs529130158	chr12:31938251-31938252	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs549390986	chr12:31938253-31938254	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs569173144	chr12:31938267-31938268	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs559662215	chr12:31938294-31938295	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs538208658	chr12:31938321-31938322	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs16918937	chr12:31938381-31938382	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs571726586	chr12:31938423-31938424	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs556454645	chr12:31938435-31938436	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs189763236	chr12:31938493-31938494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142856368	chr12:31938524-31938525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536562016	chr12:31938535-31938536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556790927	chr12:31938567-31938568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs114363024	chr12:31938588-31938589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544154901	chr12:31938611-31938612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs16918939	chr12:31938614-31938615	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs181186164	chr12:31938655-31938656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540065726	chr12:31938685-31938686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562113448	chr12:31938699-31938700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559898624	chr12:31938759-31938760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529019017	chr12:31938783-31938784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371793589	chr12:31938784-31938785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186155718	chr12:31938810-31938811	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144734719	chr12:31938817-31938818	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374656352	chr12:31938846-31938847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535662722	chr12:31938860-31938861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531614939	chr12:31938870-31938871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188002948	chr12:31938886-31938887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571800212	chr12:31938894-31938895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148258164	chr12:31938947-31938948	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547878983	chr12:31939039-31939040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567883712	chr12:31939096-31939097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10844012	chr12:31939113-31939114	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs141348649	chr12:31939125-31939126	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs370735493	chr12:31939141-31939142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545853793	chr12:31939160-31939161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181896028	chr12:31939191-31939192	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560324629	chr12:31939214-31939215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs186232528	chr12:31939267-31939268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	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:343 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31937000-31938800	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr12:31937400-31942000	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr12:31938400-31939400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
4	chr12:31938800-31939200	Enhancers	Primary T cells from cord blood	blood
5	chr12:31938800-31939200	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr12:31938800-31939200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr12:31938800-31939200	Enhancers	Fetal Kidney	kidney
8	chr12:31938800-31939400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
9	chr12:31939200-31941800	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr12:31939200-31942600	Weak transcription	Primary T cells from cord blood	blood
11	chr12:31939200-31947600	Weak transcription	Fetal Kidney	kidney
12	chr12:31939400-31939800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr12:31939400-31942200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr12:31939800-31940000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr12:31940000-31942200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr12:31940400-31941000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr12:31941800-31944600	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr12:31942000-31942800	Enhancers	Primary B cells from peripheral blood	blood
19	chr12:31942000-31944600	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr12:31942200-31943200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr12:31942200-31943800	Enhancers	Primary T cells fromperipheralblood	blood
22	chr12:31942200-31944400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr12:31942200-31944800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr12:31942400-31942800	Enhancers	Placenta	Placenta
25	chr12:31942600-31943000	Enhancers	Placenta Amnion	Placenta Amnion
26	chr12:31942600-31943800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr12:31942600-31944600	Enhancers	Primary T cells from cord blood	blood
28	chr12:31942600-31944600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr12:31942600-31944600	Enhancers	Primary T helper naive cells from peripheral blood	blood
30	chr12:31942600-31944600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
31	chr12:31942800-31944200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr12:31942800-31944400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
33	chr12:31942800-31944400	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr12:31942800-31956600	Weak transcription	Primary B cells from peripheral blood	blood
35	chr12:31943000-31943400	Enhancers	Fetal Thymus	thymus
36	chr12:31943800-31944600	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr12:31943800-31944600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr12:31944200-31945000	Active TSS	HUVEC	blood vessel
39	chr12:31944200-31949600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr12:31944400-31949200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr12:31944400-31949400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr12:31944400-31949400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr12:31944600-31945200	Enhancers	Primary T cells fromperipheralblood	blood
44	chr12:31944600-31945200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr12:31944600-31949200	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr12:31944600-31949200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr12:31944600-31949400	Weak transcription	Primary T cells from cord blood	blood
48	chr12:31944600-31949400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr12:31944600-31949400	Weak transcription	Primary T helper cells fromperipheralblood	blood
50	chr12:31944600-31949600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

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