Variant report

Variant	nsv564269
Chromosome Location	chr14:35596092-35613619
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	ARID3A	chr14:35609838-35610282	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:35613218-35613555	HepG2	liver:	n/a	n/a
3	BRCA1	chr14:35613335-35613393	GM12878	blood:	n/a	n/a
4	CBX3	chr14:35602269-35602685	K562	blood:	n/a	n/a
5	CBX3	chr14:35602360-35602546	K562	blood:	n/a	n/a
6	CEBPB	chr14:35612292-35612467	HepG2	liver:	n/a	chr14:35612414-35612425
7	CEBPB	chr14:35612279-35612564	HepG2	liver:	n/a	chr14:35612414-35612425
8	CEBPB	chr14:35613295-35613593	HepG2	liver:	n/a	n/a
9	CEBPB	chr14:35601915-35601965	HepG2	liver:	n/a	chr14:35601943-35601954
10	CEBPB	chr14:35605476-35605702	HepG2	liver:	n/a	n/a
11	CHD2	chr14:35613402-35613558	GM12878	blood:	n/a	n/a
12	CTCF	chr14:35602808-35603034	HepG2	liver:	n/a	n/a
13	CTCF	chr14:35610000-35610150	GM12873	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
14	CTCF	chr14:35610040-35610190	HCFaa	heart:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
15	CTCF	chr14:35609921-35610231	H1-hESC	embryonic stem cell:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
16	CTCF	chr14:35610000-35610150	HRE	kidney:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
17	CTCF	chr14:35610060-35610210	HCM	heart:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
18	CTCF	chr14:35610040-35610190	GM06990	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
19	CTCF	chr14:35610026-35610195	K562	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
20	CTCF	chr14:35610100-35610250	HCM	heart:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
21	CTCF	chr14:35603381-35603557	MCF-7	breast:	n/a	n/a
22	CTCF	chr14:35610060-35610210	HMF	breast:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
23	CTCF	chr14:35603900-35604050	HepG2	liver:	n/a	n/a
24	CTCF	chr14:35610031-35610194	GM12878	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
25	CTCF	chr14:35603453-35603537	GM12891	blood:	n/a	n/a
26	CTCF	chr14:35610020-35610170	AG10803	skin:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
27	CTCF	chr14:35610060-35610210	GM12864	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
28	CTCF	chr14:35602960-35603110	RPTEC	kidney:	n/a	n/a
29	CTCF	chr14:35603280-35603430	HMEC	breast:	n/a	n/a
30	CTCF	chr14:35609900-35610050	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr14:35603312-35603548	HepG2	liver:	n/a	n/a
32	CTCF	chr14:35609836-35610408	HCT-116	colon:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
33	CTCF	chr14:35610040-35610190	HFF-Myc	foreskin:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
34	CTCF	chr14:35610049-35610175	GM10266	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
35	CTCF	chr14:35602860-35603010	HepG2	liver:	n/a	n/a
36	CTCF	chr14:35599453-35599504	LNCaP	prostate:	n/a	n/a
37	CTCF	chr14:35603420-35603570	MCF-7	breast:	n/a	n/a
38	CTCF	chr14:35610040-35610190	GM12874	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
39	CTCF	chr14:35610060-35610210	AG04449	skin:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
40	CTCF	chr14:35610042-35610185	SK-N-SH_RA	brain:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
41	CTCF	chr14:35610040-35610190	HPAF	blood vessel:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
42	CTCF	chr14:35610060-35610210	HMEC	breast:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
43	CTCF	chr14:35603438-35603480	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr14:35609980-35610130	HepG2	liver:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
45	CTCF	chr14:35610051-35610190	Hela-S3	cervix:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
46	CTCF	chr14:35609977-35610231	Pancreas_OC	pancreas:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
47	CTCF	chr14:35603300-35603450	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr14:35610080-35610230	HRPEpiC	eye:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
49	CTCF	chr14:35603410-35603544	MCF-7	breast:	n/a	n/a
50	CTCF	chr14:35603360-35603510	HEK293	kidney:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:35607146..35612253-chr14:35870483..35876264,6	MCF-7	breast:
2	chr14:35610009..35610550-chr14:36156270..36157192,2	K562	blood:
3	chr14:35593618..35595181-chr14:35595674..35598084,2	K562	blood:
4	chr14:35591181..35592726-chr14:35595848..35598610,3	MCF-7	breast:
5	chr14:35605217..35606991-chr14:35607370..35609971,2	MCF-7	breast:
6	chr14:35591208..35595473-chr14:35600554..35604133,4	K562	blood:
7	chr14:35509776..35510382-chr14:35602542..35603513,2	MCF-7	breast:
8	chr14:35603102..35605461-chr14:35881286..35882903,2	MCF-7	breast:
9	chr14:35593883..35596766-chr14:35627445..35630133,2	MCF-7	breast:
10	chr14:35589606..35593451-chr14:35594804..35598522,5	K562	blood:
11	chr14:35604060..35606513-chr14:35608346..35611320,2	K562	blood:
12	chr14:35593860..35596443-chr14:35605517..35607732,2	MCF-7	breast:
13	chr14:35593860..35596443-chr14:35605517..35607732,2	MCF-7	breast:
14	chr14:35609923..35610592-chr14:35882131..35883118,2	K562	blood:
15	chr14:35604060..35606513-chr14:35608346..35611320,2	K562	blood:
16	chr14:35342813..35344956-chr14:35595359..35597712,2	K562	blood:
17	chr14:35610882..35612765-chr14:35874078..35876845,2	MCF-7	breast:
18	chr14:35604150..35607008-chr14:35873146..35874686,2	MCF-7	breast:
19	chr14:35605217..35606991-chr14:35607370..35609971,2	MCF-7	breast:
20	chr14:35590804..35592605-chr14:35605460..35607939,2	K562	blood:
21	chr14:35590482..35592799-chr14:35601392..35603277,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP2R3C-1	chr14:35613227-35613686	NONHSAT036366

Variant related genes	Relation type
PPP2R3C	TF binding region
ENSG00000100906	chromatin interactions
ENSG00000258790	chromatin interactions
ENSG00000259090	chromatin interactions
ENSG00000092020	chromatin interactions
ENSG00000100890	chromatin interactions
ENSG00000198604	chromatin interactions
ENSG00000258738	chromatin interactions

Extended variants
information (count: 657 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:657 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10147080	chr14:35596092-35596093	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537982091	chr14:35596113-35596114	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs557785381	chr14:35596132-35596133	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs185739521	chr14:35596149-35596150	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs533782232	chr14:35596184-35596185	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs191298837	chr14:35596188-35596189	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs573903710	chr14:35596204-35596205	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs566823827	chr14:35596258-35596259	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs145712594	chr14:35596271-35596272	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs56027918	chr14:35596284-35596285	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs72664840	chr14:35596323-35596324	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs545051090	chr14:35596324-35596325	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs565046827	chr14:35596325-35596326	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs544911175	chr14:35596326-35596327	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs527644637	chr14:35596353-35596354	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs541048691	chr14:35596395-35596396	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs561400342	chr14:35596409-35596410	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs182666759	chr14:35596433-35596434	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs78537249	chr14:35596441-35596442	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs570278828	chr14:35596467-35596468	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs532758630	chr14:35596478-35596479	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs561615928	chr14:35596506-35596507	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs551457295	chr14:35596544-35596545	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs140431277	chr14:35596558-35596559	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs57818081	chr14:35596605-35596606	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs370473221	chr14:35596607-35596608	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs373695121	chr14:35596622-35596623	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs571383144	chr14:35596688-35596689	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs200601862	chr14:35596696-35596697	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs376175469	chr14:35596714-35596715	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs149121781	chr14:35596805-35596806	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs567435926	chr14:35596859-35596860	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs536592569	chr14:35596881-35596882	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs148995973	chr14:35596917-35596918	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs187988315	chr14:35596923-35596924	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs577878030	chr14:35596951-35596952	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs558598060	chr14:35597003-35597004	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs190727192	chr14:35597024-35597025	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs530095294	chr14:35597043-35597044	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs386776402	chr14:35597067-35597068	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs115225522	chr14:35597068-35597069	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs561375334	chr14:35597078-35597079	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs116106616	chr14:35597100-35597101	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs7158416	chr14:35597149-35597150	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs560464876	chr14:35597197-35597198	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs183438665	chr14:35597242-35597243	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs527627721	chr14:35597314-35597315	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs532720964	chr14:35597320-35597321	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs552829687	chr14:35597322-35597323	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs562154645	chr14:35597331-35597332	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Glioma	24330732	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21858162	CNVD
Lung cancer	21569311	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Lung adenocarcinoma	17982442	CNVD

Chromatin state (count:557 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35592200-35600000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:35592400-35603000	Weak transcription	Ovary	ovary
3	chr14:35592600-35599800	Weak transcription	Fetal Muscle Trunk	muscle
4	chr14:35592600-35602800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr14:35592600-35602800	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr14:35592600-35602800	Weak transcription	Spleen	Spleen
7	chr14:35592600-35603000	Weak transcription	Esophagus	oesophagus
8	chr14:35592600-35603000	Weak transcription	Gastric	stomach
9	chr14:35592600-35603200	Weak transcription	Left Ventricle	heart
10	chr14:35592600-35603200	Weak transcription	Pancreas	Pancrea
11	chr14:35592600-35603400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr14:35592600-35625200	Weak transcription	Small Intestine	intestine
13	chr14:35592800-35603200	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr14:35592800-35611000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr14:35593000-35596200	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr14:35593000-35596800	Weak transcription	HSMM	muscle
17	chr14:35593000-35598000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr14:35593000-35601000	Weak transcription	Psoas Muscle	Psoas
19	chr14:35593000-35601400	Weak transcription	Brain Germinal Matrix	brain
20	chr14:35593000-35601400	Weak transcription	Fetal Muscle Leg	muscle
21	chr14:35593000-35602800	Weak transcription	Adipose Nuclei	Adipose
22	chr14:35593000-35602800	Weak transcription	Placenta	Placenta
23	chr14:35593000-35602800	Weak transcription	Lung	lung
24	chr14:35593000-35602800	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr14:35593000-35603400	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr14:35593000-35603400	Weak transcription	Right Atrium	heart
27	chr14:35593000-35603800	Weak transcription	Brain Anterior Caudate	brain
28	chr14:35593000-35603800	Weak transcription	Right Ventricle	heart
29	chr14:35593000-35605200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr14:35593000-35610200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr14:35593000-35613400	Weak transcription	Stomach Mucosa	stomach
32	chr14:35593000-35638200	Weak transcription	Fetal Brain Male	brain
33	chr14:35593000-35660400	Weak transcription	Stomach Smooth Muscle	stomach
34	chr14:35593200-35596200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr14:35593200-35596600	Weak transcription	NHDF-Ad	bronchial
36	chr14:35593200-35596800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr14:35593200-35596800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr14:35593200-35596800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr14:35593200-35596800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr14:35593200-35597000	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr14:35593200-35599200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr14:35593200-35599200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr14:35593200-35599600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr14:35593200-35600200	Weak transcription	Primary B cells from peripheral blood	blood
45	chr14:35593200-35601600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr14:35593200-35601600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr14:35593200-35602400	Weak transcription	Fetal Brain Female	brain
48	chr14:35593200-35602600	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr14:35593200-35602800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr14:35593200-35602800	Weak transcription	Aorta	Aorta

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