Variant report

Variant	nsv978332
Chromosome Location	chr16:70398058-70410365
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:664)
CpG islands
(count:0)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:664 , 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	ATF1	chr16:70409189-70409240	K562	blood:	n/a	n/a
2	BATF	chr16:70398264-70398549	GM12878	blood:	n/a	chr16:70398416-70398424
3	BCL3	chr16:70408707-70410630	K562	blood:	n/a	chr16:70410467-70410475
4	BCL3	chr16:70408691-70409235	K562	blood:	n/a	n/a
5	BCL3	chr16:70408074-70408646	K562	blood:	n/a	n/a
6	BCL3	chr16:70409729-70410588	A549	lung:	n/a	chr16:70410467-70410475
7	BCL3	chr16:70408760-70410124	GM12878	blood:	n/a	n/a
8	BCL3	chr16:70410143-70410848	GM12878	blood:	n/a	chr16:70410467-70410475
9	BCL3	chr16:70406477-70406704	K562	blood:	n/a	n/a
10	BCL3	chr16:70406974-70407711	K562	blood:	n/a	n/a
11	BCL3	chr16:70407263-70407712	A549	lung:	n/a	n/a
12	BCL3	chr16:70406079-70406956	K562	blood:	n/a	n/a
13	BCL3	chr16:70408898-70409662	A549	lung:	n/a	n/a
14	BCL3	chr16:70409815-70410615	K562	blood:	n/a	chr16:70410467-70410475
15	BCLAF1	chr16:70409338-70409615	GM12878	blood:	n/a	n/a
16	CCNT2	chr16:70406163-70406370	K562	blood:	n/a	n/a
17	CEBPB	chr16:70400961-70401119	K562	blood:	n/a	chr16:70400988-70401001 chr16:70400990-70400999 chr16:70400988-70400999
18	CEBPB	chr16:70400946-70401035	A549	lung:	n/a	chr16:70400988-70401001 chr16:70400990-70400999 chr16:70400988-70400999
19	CEBPB	chr16:70400834-70401059	HepG2	liver:	n/a	chr16:70400988-70401001 chr16:70400990-70400999 chr16:70400988-70400999
20	CEBPB	chr16:70400873-70401059	IMR90	lung:	n/a	chr16:70400988-70401001 chr16:70400990-70400999 chr16:70400988-70400999
21	CHD2	chr16:70407472-70407638	K562	blood:	n/a	n/a
22	CHD2	chr16:70409976-70410451	K562	blood:	n/a	n/a
23	CHD2	chr16:70409152-70409486	K562	blood:	n/a	n/a
24	CTCF	chr16:70404080-70404230	RPTEC	kidney:	n/a	n/a
25	CTCF	chr16:70404074-70404279	GM13976	blood:	n/a	n/a
26	CTCF	chr16:70403955-70404269	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr16:70403836-70404367	HCT-116	colon:	n/a	n/a
28	CTCF	chr16:70404061-70404341	GM12892	blood:	n/a	n/a
29	CTCF	chr16:70403660-70403810	HMF	breast:	n/a	n/a
30	CTCF	chr16:70404080-70404230	BJ	skin:	n/a	n/a
31	CTCF	chr16:70403980-70404130	RPTEC	kidney:	n/a	n/a
32	CTCF	chr16:70403980-70404130	WI-38	lung:	n/a	n/a
33	CTCF	chr16:70403980-70404130	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr16:70404080-70404230	AG09319	gingival:	n/a	n/a
35	CTCF	chr16:70404080-70404230	NHEK	skin:	n/a	n/a
36	CTCF	chr16:70404200-70404350	HCT-116	colon:	n/a	n/a
37	CTCF	chr16:70404080-70404230	AG04450	lung:	n/a	n/a
38	CTCF	chr16:70403980-70404130	A549	lung:	n/a	n/a
39	CTCF	chr16:70403960-70404110	GM12873	blood:	n/a	n/a
40	CTCF	chr16:70404079-70404311	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr16:70404500-70404650	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr16:70403839-70404470	SK-N-SH	brain:	n/a	n/a
43	CTCF	chr16:70404080-70404230	Caco-2	colon:	n/a	n/a
44	CTCF	chr16:70403959-70404300	A549	lung:	n/a	n/a
45	CTCF	chr16:70404100-70404250	GM12870	blood:	n/a	n/a
46	CTCF	chr16:70404100-70404250	GM12866	blood:	n/a	n/a
47	CTCF	chr16:70403980-70404130	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr16:70404313-70404315	GM20000	blood:	n/a	n/a
49	CTCF	chr16:70403897-70404323	HepG2	liver:	n/a	n/a
50	CTCF	chr16:70403980-70404130	GM12873	blood:	n/a	n/a

No data

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:70400513..70403701-chr16:70406827..70410088,3	MCF-7	breast:
2	chr16:70403834..70405811-chr16:70505768..70508585,2	MCF-7	breast:
3	chr16:70409390..70411008-chr16:70493324..70495460,2	MCF-7	breast:
4	chr16:70397691..70399397-chr16:70409002..70410941,2	K562	blood:
5	chr16:70406454..70409078-chr16:70491898..70493398,2	MCF-7	breast:
6	chr16:70399401..70401287-chr16:70555885..70558751,2	MCF-7	breast:
7	chr16:70402213..70405460-chr16:70405653..70409896,4	K562	blood:
8	chr16:70398049..70400170-chr16:70401389..70403852,4	MCF-7	breast:
9	chr16:70409036..70411924-chr16:70413991..70417469,3	K562	blood:
10	chr16:70405289..70407200-chr16:70415529..70417121,2	K562	blood:
11	chr16:70403865..70404598-chr16:70414555..70415060,2	MCF-7	breast:
12	chr16:70402621..70404136-chr16:70529533..70532181,2	K562	blood:
13	chr16:70405164..70407624-chr16:70497254..70499481,2	MCF-7	breast:
14	chr16:70400513..70403701-chr16:70406827..70410088,3	MCF-7	breast:
15	chr16:70379903..70382135-chr16:70398083..70399782,2	MCF-7	breast:
16	chr16:70386987..70389423-chr16:70409457..70411415,2	MCF-7	breast:
17	chr16:70403504..70406044-chr16:70486900..70491075,3	MCF-7	breast:
18	chr16:70408470..70409240-chr9:7799247..7799915,2	NB4	blood:
19	chr16:70405086..70408024-chr17:60101921..60103638,2	MCF-7	breast:
20	chr16:70397078..70399883-chr16:70405233..70409142,3	MCF-7	breast:
21	chr16:70407385..70408894-chr16:70556676..70558799,2	MCF-7	breast:
22	chr16:70403494..70406143-chr16:70569820..70571486,2	K562	blood:
23	chr16:70408425..70412469-chr16:70501223..70503201,4	MCF-7	breast:
24	chr16:70402213..70407234-chr16:70407266..70410953,6	K562	blood:
25	chr16:70373940..70375897-chr16:70406795..70408435,2	MCF-7	breast:
26	chr16:70402213..70405460-chr16:70405653..70409896,4	K562	blood:
27	chr16:70382796..70385300-chr16:70408811..70411389,2	K562	blood:
28	chr16:70404267..70407170-chr16:70413763..70415301,2	K562	blood:
29	chr16:70408756..70411643-chr16:70690769..70692311,2	MCF-7	breast:
30	chr16:70401435..70404109-chr16:70556506..70558662,2	K562	blood:
31	chr16:70409061..70411371-chr16:70561272..70563423,2	MCF-7	breast:
32	chr16:70380932..70385143-chr16:70404657..70409914,6	MCF-7	breast:
33	chr16:70403683..70405364-chr16:70556846..70558413,2	MCF-7	breast:
34	chr16:70402213..70407234-chr16:70407266..70410953,6	K562	blood:
35	chr16:70406308..70408837-chr16:70511303..70514267,2	MCF-7	breast:
36	chr16:70407277..70408933-chr16:70493231..70495760,2	MCF-7	breast:

No data

Variant related genes	Relation type
DDX19A	TF binding region
ENSG00000260111	TF binding region
ENSG00000189091	chromatin interactions
ENSG00000157353	chromatin interactions
ENSG00000103051	chromatin interactions
ENSG00000168872	chromatin interactions
ENSG00000221514	chromatin interactions
ENSG00000261777	chromatin interactions

Extended variants
information (count: 585 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:585 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377524292	chr16:70398089-70398090	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs182414755	chr16:70398120-70398121	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs369950995	chr16:70398176-70398177	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs568023515	chr16:70398228-70398229	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs144971879	chr16:70398256-70398257	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs553570636	chr16:70398292-70398293	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs548740594	chr16:70398318-70398319	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs571782579	chr16:70398320-70398321	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs149083739	chr16:70398340-70398341	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs557457822	chr16:70398350-70398351	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs187884976	chr16:70398351-70398352	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs144789747	chr16:70398359-70398360	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs562331355	chr16:70398372-70398373	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs371558009	chr16:70398406-70398407	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs1142618	chr16:70398467-70398468	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs1065159	chr16:70398479-70398480	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs200983393	chr16:70398489-70398490	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs1065160	chr16:70398500-70398501	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs1065161	chr16:70398515-70398516	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs1065162	chr16:70398520-70398521	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs1142619	chr16:70398524-70398525	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs1142620	chr16:70398527-70398528	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs61755352	chr16:70398533-70398534	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs369403131	chr16:70398538-70398539	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs372426215	chr16:70398560-70398561	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs375224641	chr16:70398597-70398598	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs200494353	chr16:70398598-70398599	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs533254404	chr16:70398623-70398624	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs184852041	chr16:70398713-70398714	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs570054526	chr16:70398723-70398724	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs530893771	chr16:70398724-70398725	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs549124499	chr16:70398726-70398727	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs567982796	chr16:70398755-70398756	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs575510689	chr16:70398762-70398763	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs146742531	chr16:70398782-70398783	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs114562321	chr16:70398798-70398799	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs565576484	chr16:70398840-70398841	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs140431947	chr16:70398859-70398860	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs373486221	chr16:70398906-70398907	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs1142621	chr16:70398925-70398926	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs537699457	chr16:70398938-70398939	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs1142622	chr16:70398940-70398941	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs1065163	chr16:70398949-70398950	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs1065164	chr16:70398955-70398956	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs199527052	chr16:70398961-70398962	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs1065165	chr16:70398976-70398977	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs1065166	chr16:70398979-70398980	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs139025377	chr16:70398987-70398988	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs1142624	chr16:70399009-70399010	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs201168154	chr16:70399019-70399020	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	21909424	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	20841430	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70381600-70413200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr16:70381600-70414000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr16:70382200-70413600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr16:70382600-70413000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr16:70382800-70403600	Strong transcription	Primary T helper cells PMA-I stimulated	--
6	chr16:70382800-70409800	Strong transcription	Fetal Muscle Leg	muscle
7	chr16:70382800-70410800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr16:70382800-70410800	Strong transcription	HUES64 Cell Line	embryonic stem cell
9	chr16:70383000-70403600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr16:70383000-70410200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
11	chr16:70383000-70410600	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr16:70383000-70410800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr16:70383000-70413000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr16:70383000-70413000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr16:70383000-70413000	Strong transcription	Fetal Thymus	thymus
16	chr16:70383200-70412200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr16:70383200-70413000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr16:70383200-70413400	Strong transcription	Fetal Stomach	stomach
19	chr16:70383400-70410600	Strong transcription	HUES48 Cell Line	embryonic stem cell
20	chr16:70383400-70411000	Strong transcription	Primary B cells from peripheral blood	blood
21	chr16:70383400-70411000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr16:70383600-70407600	Strong transcription	HepG2	liver
23	chr16:70383600-70412200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr16:70383600-70413200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr16:70383600-70413400	Strong transcription	Fetal Muscle Trunk	muscle
26	chr16:70383600-70413600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr16:70383800-70401000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr16:70383800-70410600	Strong transcription	Liver	Liver
29	chr16:70384200-70403600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr16:70384400-70411000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr16:70384400-70411400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr16:70384600-70413400	Strong transcription	Fetal Intestine Small	intestine
33	chr16:70385200-70403600	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr16:70385200-70407600	Strong transcription	Rectal Mucosa Donor 29	rectum
35	chr16:70385200-70410800	Strong transcription	Duodenum Mucosa	Duodenum
36	chr16:70385200-70410800	Strong transcription	Stomach Smooth Muscle	stomach
37	chr16:70385400-70410200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr16:70385600-70403600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr16:70385600-70407800	Strong transcription	Brain Anterior Caudate	brain
40	chr16:70385600-70410400	Strong transcription	Monocytes-CD14+_RO01746	blood
41	chr16:70385800-70401200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr16:70385800-70410200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
43	chr16:70386000-70413400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr16:70386200-70410400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr16:70387800-70401200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr16:70387800-70414000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
47	chr16:70388400-70402600	Strong transcription	Primary T cells fromperipheralblood	blood
48	chr16:70388400-70402600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr16:70388400-70402600	Strong transcription	Placenta Amnion	Placenta Amnion
50	chr16:70388400-70407000	Strong transcription	Fetal Brain Female	brain

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