Variant report

Variant	nsv564266
Chromosome Location	chr14:35594442-35611552
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	CBX3	chr14:35602269-35602685	K562	blood:	n/a	n/a
3	CBX3	chr14:35602360-35602546	K562	blood:	n/a	n/a
4	CEBPB	chr14:35601915-35601965	HepG2	liver:	n/a	chr14:35601943-35601954
5	CEBPB	chr14:35605476-35605702	HepG2	liver:	n/a	n/a
6	CTCF	chr14:35610040-35610190	GM12801	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
7	CTCF	chr14:35609980-35610130	HepG2	liver:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
8	CTCF	chr14:35610082-35610179	LNCaP	prostate:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
9	CTCF	chr14:35609900-35610050	AG09309	skin:	n/a	n/a
10	CTCF	chr14:35609940-35610090	GM12873	blood:	n/a	n/a
11	CTCF	chr14:35610042-35610185	SK-N-SH_RA	brain:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
12	CTCF	chr14:35602860-35603010	HepG2	liver:	n/a	n/a
13	CTCF	chr14:35610031-35610194	GM12878	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
14	CTCF	chr14:35609963-35610210	HepG2	liver:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
15	CTCF	chr14:35610049-35610175	GM10266	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
16	CTCF	chr14:35599453-35599504	LNCaP	prostate:	n/a	n/a
17	CTCF	chr14:35609900-35610373	GM12878	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
18	CTCF	chr14:35610020-35610170	AG10803	skin:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
19	CTCF	chr14:35603438-35603480	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr14:35610020-35610170	HVMF	connective:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
21	CTCF	chr14:35603300-35603450	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr14:35603387-35603552	MCF-7	breast:	n/a	n/a
23	CTCF	chr14:35609980-35610130	GM12864	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
24	CTCF	chr14:35602900-35603050	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr14:35603900-35604050	HepG2	liver:	n/a	n/a
26	CTCF	chr14:35609960-35610110	HMEC	breast:	n/a	n/a
27	CTCF	chr14:35610060-35610210	BE2_C	brain:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
28	CTCF	chr14:35609980-35610130	GM06990	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
29	CTCF	chr14:35610065-35610168	GM13976	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
30	CTCF	chr14:35610060-35610210	HMF	breast:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
31	CTCF	chr14:35610029-35610233	Lung_OC	lung:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
32	CTCF	chr14:35609960-35610110	GM12865	blood:	n/a	n/a
33	CTCF	chr14:35603453-35603537	GM12891	blood:	n/a	n/a
34	CTCF	chr14:35610040-35610190	RPTEC	kidney:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
35	CTCF	chr14:35610060-35610210	GM12864	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
36	CTCF	chr14:35603400-35603550	HepG2	liver:	n/a	n/a
37	CTCF	chr14:35603400-35603550	HVMF	connective:	n/a	n/a
38	CTCF	chr14:35610000-35610150	HPF	lung:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
39	CTCF	chr14:35609759-35610458	HepG2	liver:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
40	CTCF	chr14:35603320-35603470	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr14:35609953-35610237	HUVEC	blood vessel:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
42	CTCF	chr14:35610040-35610176	LNCaP	prostate:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
43	CTCF	chr14:35610060-35610210	AG04449	skin:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
44	CTCF	chr14:35610018-35610210	Kidney_OC	kidney:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
45	CTCF	chr14:35610100-35610250	HVMF	connective:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
46	CTCF	chr14:35609980-35610130	HCPEpiC	choroid plexus:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
47	CTCF	chr14:35610004-35610180	A549	lung:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
48	CTCF	chr14:35610040-35610190	HCFaa	heart:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
49	CTCF	chr14:35603240-35603565	MCF-7	breast:	n/a	n/a
50	CTCF	chr14:35610040-35610190	WI-38	lung:	n/a	chr14:35610106-35610124 chr14:35610108-35610129

No.	Distal block	Cell Line	Cell type
1	chr14:35609923..35610592-chr14:35882131..35883118,2	K562	blood:
2	chr14:35593883..35596766-chr14:35627445..35630133,2	MCF-7	breast:
3	chr14:35603102..35605461-chr14:35881286..35882903,2	MCF-7	breast:
4	chr14:35604060..35606513-chr14:35608346..35611320,2	K562	blood:
5	chr14:35591658..35595888-chr14:35872338..35875561,5	K562	blood:
6	chr14:35509776..35510382-chr14:35602542..35603513,2	MCF-7	breast:
7	chr14:35591181..35592726-chr14:35595848..35598610,3	MCF-7	breast:
8	chr14:35605217..35606991-chr14:35607370..35609971,2	MCF-7	breast:
9	chr14:35593618..35595181-chr14:35595674..35598084,2	K562	blood:
10	chr14:35589606..35593451-chr14:35594804..35598522,5	K562	blood:
11	chr14:35590804..35592605-chr14:35605460..35607939,2	K562	blood:
12	chr14:35605217..35606991-chr14:35607370..35609971,2	MCF-7	breast:
13	chr14:35593618..35595181-chr14:35595674..35598084,2	K562	blood:
14	chr14:35590482..35592799-chr14:35601392..35603277,2	MCF-7	breast:
15	chr14:35604060..35606513-chr14:35608346..35611320,2	K562	blood:
16	chr14:35593860..35596443-chr14:35605517..35607732,2	MCF-7	breast:
17	chr14:35592944..35595456-chr14:35809160..35811582,2	K562	blood:
18	chr14:35589827..35591407-chr14:35592886..35594751,2	K562	blood:
19	chr14:35342813..35344956-chr14:35595359..35597712,2	K562	blood:
20	chr14:35607146..35612253-chr14:35870483..35876264,6	MCF-7	breast:
21	chr14:35610882..35612765-chr14:35874078..35876845,2	MCF-7	breast:
22	chr14:35610009..35610550-chr14:36156270..36157192,2	K562	blood:
23	chr14:35604150..35607008-chr14:35873146..35874686,2	MCF-7	breast:
24	chr14:35450019..35452754-chr14:35591061..35594828,4	K562	blood:
25	chr14:35593860..35596443-chr14:35605517..35607732,2	MCF-7	breast:
26	chr14:35591208..35595473-chr14:35600554..35604133,4	K562	blood:

Variant related genes	Relation type
PPP2R3C	TF binding region
ENSG00000258790	chromatin interactions
ENSG00000258704	chromatin interactions
ENSG00000100906	chromatin interactions
ENSG00000258738	chromatin interactions
ENSG00000198604	chromatin interactions
ENSG00000092020	chromatin interactions
ENSG00000259090	chromatin interactions
ENSG00000100890	chromatin interactions
ENSG00000100883	chromatin interactions

Extended variants
information (count: 643 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:643 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10141085	chr14:35594442-35594443	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs192078391	chr14:35594453-35594454	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs139712827	chr14:35594495-35594496	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs560547016	chr14:35594539-35594540	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs183994244	chr14:35594563-35594564	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs113168692	chr14:35594594-35594595	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs373421514	chr14:35594664-35594665	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs112805449	chr14:35594693-35594694	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs549350120	chr14:35594718-35594719	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs569204235	chr14:35594755-35594756	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs375792500	chr14:35594794-35594795	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs11156874	chr14:35594803-35594804	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs551750451	chr14:35594806-35594807	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs189687579	chr14:35594881-35594882	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs534103130	chr14:35594912-35594913	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs145426857	chr14:35594929-35594930	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs549010167	chr14:35594956-35594957	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs372913414	chr14:35594959-35594960	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs147702691	chr14:35594970-35594971	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs117765529	chr14:35594985-35594986	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs35804187	chr14:35594987-35594988	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs555442547	chr14:35595015-35595016	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs180904699	chr14:35595021-35595022	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs544209969	chr14:35595093-35595094	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs564345742	chr14:35595100-35595101	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs578019886	chr14:35595144-35595145	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs540414624	chr14:35595151-35595152	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs560429683	chr14:35595159-35595160	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs142452296	chr14:35595168-35595169	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs377124247	chr14:35595195-35595196	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs549163511	chr14:35595206-35595207	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs563011669	chr14:35595284-35595285	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs559233793	chr14:35595316-35595317	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs35300567	chr14:35595321-35595322	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs531575344	chr14:35595324-35595325	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs551331435	chr14:35595327-35595328	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs566362270	chr14:35595328-35595329	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs184328569	chr14:35595334-35595335	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs189075352	chr14:35595350-35595351	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs534260507	chr14:35595365-35595366	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs547579882	chr14:35595395-35595396	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs567705866	chr14:35595398-35595399	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs536861685	chr14:35595408-35595409	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs182518532	chr14:35595413-35595414	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs12589278	chr14:35595418-35595419	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs150186250	chr14:35595437-35595438	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs557820585	chr14:35595441-35595442	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs555039904	chr14:35595464-35595465	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs78464258	chr14:35595497-35595498	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs540580828	chr14:35595528-35595529	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 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:540 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35589800-35595000	Active TSS	K562	blood
2	chr14:35592200-35600000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr14:35592400-35603000	Weak transcription	Ovary	ovary
4	chr14:35592600-35599800	Weak transcription	Fetal Muscle Trunk	muscle
5	chr14:35592600-35602800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:35592600-35602800	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr14:35592600-35602800	Weak transcription	Spleen	Spleen
8	chr14:35592600-35603000	Weak transcription	Esophagus	oesophagus
9	chr14:35592600-35603000	Weak transcription	Gastric	stomach
10	chr14:35592600-35603200	Weak transcription	Left Ventricle	heart
11	chr14:35592600-35603200	Weak transcription	Pancreas	Pancrea
12	chr14:35592600-35603400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr14:35592600-35625200	Weak transcription	Small Intestine	intestine
14	chr14:35592800-35603200	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr14:35592800-35611000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr14:35593000-35594800	Enhancers	Primary B cells from cord blood	blood
17	chr14:35593000-35595200	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr14:35593000-35595200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr14:35593000-35595400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr14:35593000-35595800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr14:35593000-35596200	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr14:35593000-35596800	Weak transcription	HSMM	muscle
23	chr14:35593000-35598000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr14:35593000-35601000	Weak transcription	Psoas Muscle	Psoas
25	chr14:35593000-35601400	Weak transcription	Brain Germinal Matrix	brain
26	chr14:35593000-35601400	Weak transcription	Fetal Muscle Leg	muscle
27	chr14:35593000-35602800	Weak transcription	Adipose Nuclei	Adipose
28	chr14:35593000-35602800	Weak transcription	Placenta	Placenta
29	chr14:35593000-35602800	Weak transcription	Lung	lung
30	chr14:35593000-35602800	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr14:35593000-35603400	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr14:35593000-35603400	Weak transcription	Right Atrium	heart
33	chr14:35593000-35603800	Weak transcription	Brain Anterior Caudate	brain
34	chr14:35593000-35603800	Weak transcription	Right Ventricle	heart
35	chr14:35593000-35605200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr14:35593000-35610200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr14:35593000-35613400	Weak transcription	Stomach Mucosa	stomach
38	chr14:35593000-35638200	Weak transcription	Fetal Brain Male	brain
39	chr14:35593000-35660400	Weak transcription	Stomach Smooth Muscle	stomach
40	chr14:35593200-35594600	Enhancers	Hela-S3	cervix
41	chr14:35593200-35594800	Enhancers	Primary T cells from cord blood	blood
42	chr14:35593200-35595800	Enhancers	Primary T helper naive cells from peripheral blood	blood
43	chr14:35593200-35595800	Weak transcription	Monocytes-CD14+_RO01746	blood
44	chr14:35593200-35596000	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr14:35593200-35596200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr14:35593200-35596600	Weak transcription	NHDF-Ad	bronchial
47	chr14:35593200-35596800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr14:35593200-35596800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr14:35593200-35596800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr14:35593200-35596800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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