Variant report

Variant	esv3345810
Chromosome Location	chr14:31599017-31622767
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:129)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:129 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr14:31607526-31607846	MCF-7	breast:	n/a	chr14:31607662-31607673 chr14:31607660-31607671 chr14:31607660-31607673 chr14:31607660-31607673
2	CEBPB	chr14:31607491-31607810	Hela-S3	cervix:	n/a	chr14:31607662-31607673 chr14:31607660-31607671 chr14:31607660-31607673 chr14:31607660-31607673
3	CEBPB	chr14:31606554-31607023	HCT-116	colon:	n/a	n/a
4	CEBPB	chr14:31606528-31606850	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr14:31607499-31607843	IMR90	lung:	n/a	chr14:31607662-31607673 chr14:31607660-31607671 chr14:31607660-31607673 chr14:31607660-31607673
6	CEBPB	chr14:31607490-31607827	HepG2	liver:	n/a	chr14:31607662-31607673 chr14:31607660-31607671 chr14:31607660-31607673 chr14:31607660-31607673
7	CEBPB	chr14:31611571-31612110	ECC-1	luminal epithelium:	n/a	n/a
8	CEBPB	chr14:31607643-31607735	H1-hESC	embryonic stem cell:	n/a	chr14:31607662-31607673 chr14:31607660-31607671 chr14:31607660-31607673 chr14:31607660-31607673
9	CEBPB	chr14:31607533-31607760	A549	lung:	n/a	chr14:31607662-31607673 chr14:31607660-31607671 chr14:31607660-31607673 chr14:31607660-31607673
10	CEBPD	chr14:31620077-31620399	K562	blood:	n/a	n/a
11	CTCF	chr14:31604100-31604250	NB4	blood:	n/a	n/a
12	CTCF	chr14:31615891-31615960	Kidney_OC	kidney:	n/a	n/a
13	E2F4	chr14:31604266-31604337	MCF10A-Er-Src	breast:	n/a	n/a
14	EP300	chr14:31611605-31612241	ECC-1	luminal epithelium:	n/a	n/a
15	FOS	chr14:31606674-31606736	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr14:31606514-31606816	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr14:31606536-31606772	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr14:31606608-31606715	MCF10A-Er-Src	breast:	n/a	n/a
19	GATA3	chr14:31609031-31609155	SH-SY5Y	brain:	n/a	n/a
20	GATA3	chr14:31599122-31599286	SH-SY5Y	brain:	n/a	n/a
21	GTF3C2	chr14:31606557-31606890	Hela-S3	cervix:	n/a	n/a
22	IRF1	chr14:31620820-31621401	K562	blood:	n/a	n/a
23	IRF1	chr14:31620977-31621295	K562	blood:	n/a	n/a
24	JUN	chr14:31613420-31613580	K562	blood:	n/a	n/a
25	JUN	chr14:31613880-31614041	H1-hESC	embryonic stem cell:	n/a	n/a
26	JUN	chr14:31610741-31610790	HepG2	liver:	n/a	chr14:31610748-31610761
27	JUND	chr14:31606510-31606983	HCT-116	colon:	n/a	n/a
28	MAFF	chr14:31620712-31621074	K562	blood:	n/a	chr14:31620888-31620906
29	MAFF	chr14:31620780-31621047	HepG2	liver:	n/a	chr14:31620888-31620906
30	MAFF	chr14:31599198-31599332	HepG2	liver:	n/a	n/a
31	MAFK	chr14:31620718-31621103	K562	blood:	n/a	chr14:31620889-31620904
32	MAFK	chr14:31600264-31600459	HepG2	liver:	n/a	n/a
33	MAFK	chr14:31620734-31621026	IMR90	lung:	n/a	chr14:31620889-31620904
34	MAFK	chr14:31620753-31621013	HepG2	liver:	n/a	chr14:31620889-31620904
35	MAFK	chr14:31620730-31621076	HepG2	liver:	n/a	chr14:31620889-31620904
36	MAFK	chr14:31599141-31599407	HepG2	liver:	n/a	n/a
37	MAFK	chr14:31599143-31599343	HepG2	liver:	n/a	n/a
38	MAFK	chr14:31607307-31607506	HepG2	liver:	n/a	n/a
39	MAX	chr14:31611584-31612224	ECC-1	luminal epithelium:	n/a	n/a
40	MYC	chr14:31606850-31606932	MCF-7	breast:	n/a	n/a
41	MYC	chr14:31620843-31620849	K562	blood:	n/a	n/a
42	NFIC	chr14:31611474-31612199	ECC-1	luminal epithelium:	n/a	n/a
43	NFIC	chr14:31611499-31612183	ECC-1	luminal epithelium:	n/a	n/a
44	POLR2A	chr14:31620790-31620823	HepG2	liver:	n/a	n/a
45	POLR2A	chr14:31621517-31621871	HepG2	liver:	n/a	n/a
46	POLR2A	chr14:31615913-31615947	MCF-7	breast:	n/a	n/a
47	POLR2A	chr14:31618536-31618606	A549	lung:	n/a	n/a
48	POLR2A	chr14:31618592-31618604	MCF-7	breast:	n/a	n/a
49	POLR2A	chr14:31615430-31615578	HepG2	liver:	n/a	n/a
50	POLR2A	chr14:31610702-31610760	ProgFib	skin:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:31607371-31607421	H1-hESC	embryonic stem cell:	embryo
2	chr14:31607371-31607421	BE2_C	brain:	n/a
3	chr14:31607371-31607421	HUVEC	blood vessel:	n/a
4	chr14:31607371-31607421	HAEpiC	amniotic membrane:	n/a
5	chr14:31607371-31607421	AG09309	skin:	n/a
6	chr14:31607371-31607421	ECC-1	luminal epithelium:	n/a
7	chr14:31607371-31607421	RPTEC	kidney:	n/a
8	chr14:31607371-31607421	Hela-S3	cervix:	n/a
9	chr14:31607371-31607421	NB4	blood:	n/a
10	chr14:31607371-31607421	SK-N-SH	brain:	n/a
11	chr14:31607371-31607421	A549	lung:	n/a
12	chr14:31607371-31607421	SAEC	small airway:	n/a
13	chr14:31607371-31607421	HEEpiC	esophagus:	n/a
14	chr14:31607371-31607421	AG10803	skin:	n/a
15	chr14:31607371-31607421	PANC-1	pancreas:	n/a
16	chr14:31607371-31607421	GM06990	blood:	n/a
17	chr14:31607371-31607421	Jurkat	blood:	n/a
18	chr14:31607371-31607421	Caco-2	colon:	n/a
19	chr14:31607371-31607421	SKMC	muscle:	n/a
20	chr14:31607371-31607421	AG04450	lung:	fetal
21	chr14:31607371-31607421	AG09319	gingival:	n/a
22	chr14:31607371-31607421	HCM	heart:	n/a
23	chr14:31607371-31607421	GM12878	blood:	n/a
24	chr14:31607371-31607421	HNPCEpiC	eye:	n/a
25	chr14:31607371-31607421	HIPEpiC	eye:	n/a
26	chr14:31607371-31607421	HL-60	blood:	n/a
27	chr14:31607371-31607421	NHBE	bronchial:	n/a
28	chr14:31607371-31607421	MCF-7	breast:	n/a
29	chr14:31607371-31607421	AG04449	skin:	fetal
30	chr14:31607371-31607421	HRPEpiC	eye:	n/a
31	chr14:31607371-31607421	K562	blood:	n/a
32	chr14:31607371-31607421	PFSK-1	brain:	n/a
33	chr14:31607371-31607421	U87	brain:	n/a
34	chr14:31607371-31607421	SK-N-MC	brain:	n/a
35	chr14:31607371-31607421	HPAEpiC	pulmonary alveolar:	n/a
36	chr14:31607371-31607421	BJ	skin:	n/a
37	chr14:31607371-31607421	ProgFib	skin:	n/a
38	chr14:31607371-31607421	ovcar-3	ovarian:	n/a
39	chr14:31607371-31607421	HRE	kidney:	n/a
40	chr14:31607371-31607421	GM12891	blood:	n/a
41	chr14:31607371-31607421	SK-N-SH_RA	brain:	n/a
42	chr14:31607371-31607421	IMR90	lung:	fetal
43	chr14:31607371-31607421	Hepatocyte	liver:	n/a
44	chr14:31607371-31607421	PrEC	prostate:	n/a
45	chr14:31607371-31607421	NHDF-neo	bronchial:	n/a
46	chr14:31607371-31607421	GM12892	blood:	n/a
47	chr14:31607371-31607421	HMEC	breast:	n/a
48	chr14:31607371-31607421	AoSMC	blood vessel:	n/a
49	chr14:31607371-31607421	HCF	heart:	n/a
50	chr14:31607371-31607421	MCF10A-Er-Src	breast:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:31601205..31602720-chr14:31611086..31613417,2	MCF-7	breast:
2	chr14:31612683..31614896-chr14:31619951..31622680,2	MCF-7	breast:
3	chr14:31605351..31607300-chr14:31607732..31611422,3	MCF-7	breast:
4	chr14:31590905..31593026-chr14:31610871..31613579,2	MCF-7	breast:
5	chr14:31344003..31345728-chr14:31604211..31605992,2	K562	blood:
6	chr14:31600570..31602295-chr14:31607545..31609357,2	K562	blood:
7	chr14:31601478..31601997-chr3:62322077..62322936,2	MCF-7	breast:
8	chr14:31592178..31594075-chr14:31598650..31601042,2	K562	blood:
9	chr14:31621746..31624641-chr14:31675931..31678702,3	MCF-7	breast:
10	chr14:31612683..31614896-chr14:31619951..31622680,2	MCF-7	breast:
11	chr14:31592934..31595654-chr14:31599577..31602427,2	MCF-7	breast:
12	chr14:31600570..31602295-chr14:31607545..31609357,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STRN3-11	chr14:31614377-31615656	l_960_NR_027263

No data

Variant related genes	Relation type
RNU6-541P	TF binding region
HECTD1	TF binding region
RNU6-541P	CpG island
HECTD1	CpG island
ENSG00000207440	chromatin interactions
ENSG00000092148	chromatin interactions

Extended variants
information (count: 893 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:893 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373929092	chr14:31599070-31599071	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs367786150	chr14:31599106-31599107	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs539768702	chr14:31599157-31599158	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs565443200	chr14:31599239-31599240	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs58204331	chr14:31599278-31599279	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs548060712	chr14:31599322-31599323	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs75858941	chr14:31599356-31599357	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs544442982	chr14:31599357-31599358	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs529738198	chr14:31599368-31599369	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs547875651	chr14:31599388-31599389	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs569761631	chr14:31599397-31599398	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs374625344	chr14:31599401-31599402	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs185942440	chr14:31599413-31599414	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs551969752	chr14:31599464-31599465	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs189667026	chr14:31599488-31599489	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs181216262	chr14:31599490-31599491	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs564364695	chr14:31599553-31599554	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs376703131	chr14:31599555-31599556	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs10133173	chr14:31599561-31599562	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs59860266	chr14:31599567-31599568	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs143821977	chr14:31599589-31599590	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs186941700	chr14:31599600-31599601	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs572781863	chr14:31599667-31599668	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs554649023	chr14:31599672-31599673	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs540212494	chr14:31599684-31599685	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs553945728	chr14:31599685-31599686	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs77896262	chr14:31599835-31599836	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs74042164	chr14:31599869-31599870	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs147256969	chr14:31599880-31599881	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs532889461	chr14:31599915-31599916	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs74042165	chr14:31599923-31599924	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs35920813	chr14:31600011-31600012	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs368513885	chr14:31600022-31600023	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs541258500	chr14:31600054-31600055	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs560043599	chr14:31600056-31600057	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs530308721	chr14:31600074-31600075	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs371938128	chr14:31600077-31600078	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs573781988	chr14:31600092-31600093	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs538151665	chr14:31600234-31600235	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs71430920	chr14:31600235-31600236	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs76187544	chr14:31600248-31600249	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs397852443	chr14:31600249-31600250	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs199760699	chr14:31600250-31600251	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs541845386	chr14:31600321-31600322	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs563104674	chr14:31600330-31600331	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs149785279	chr14:31600364-31600365	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs551808966	chr14:31600371-31600372	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs570202421	chr14:31600385-31600386	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs528316343	chr14:31600387-31600388	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs544282466	chr14:31600399-31600400	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	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
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:664 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31563800-31650000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
2	chr14:31564800-31648600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr14:31565600-31648000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr14:31566000-31599200	Strong transcription	Fetal Muscle Trunk	muscle
5	chr14:31566000-31627400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr14:31566200-31599200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr14:31566200-31627000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr14:31566200-31635200	Strong transcription	Placenta	Placenta
9	chr14:31566200-31648200	Strong transcription	Primary neutrophils fromperipheralblood	blood
10	chr14:31567000-31620200	Strong transcription	Duodenum Smooth Muscle	Duodenum
11	chr14:31567000-31647600	Strong transcription	Duodenum Mucosa	Duodenum
12	chr14:31567000-31651200	Strong transcription	Dnd41	blood
13	chr14:31572800-31604600	Strong transcription	Fetal Intestine Large	intestine
14	chr14:31573000-31650200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr14:31573600-31608800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr14:31573800-31648200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr14:31576800-31623800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr14:31577200-31604000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr14:31588000-31623800	Weak transcription	Psoas Muscle	Psoas
20	chr14:31588600-31607600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr14:31591800-31656400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr14:31592400-31600000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr14:31592400-31607200	Weak transcription	Fetal Heart	heart
24	chr14:31593400-31600600	Strong transcription	Fetal Muscle Leg	muscle
25	chr14:31593600-31604600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr14:31593800-31599400	Strong transcription	Fetal Stomach	stomach
27	chr14:31593800-31648200	Strong transcription	HUES64 Cell Line	embryonic stem cell
28	chr14:31594000-31599200	Strong transcription	Fetal Intestine Small	intestine
29	chr14:31594200-31599200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr14:31594200-31599400	Strong transcription	Cortex derived primary cultured neurospheres	brain
31	chr14:31594400-31628600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr14:31594600-31599200	Strong transcription	Stomach Smooth Muscle	stomach
33	chr14:31594600-31604400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr14:31594600-31619800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
35	chr14:31595000-31649000	Strong transcription	HUES48 Cell Line	embryonic stem cell
36	chr14:31595200-31602800	Strong transcription	Fetal Kidney	kidney
37	chr14:31595200-31605800	Strong transcription	HMEC	breast
38	chr14:31595200-31630200	Strong transcription	HUES6 Cell Line	embryonic stem cell
39	chr14:31595400-31599200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr14:31595600-31599200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr14:31595600-31599400	Strong transcription	Left Ventricle	heart
42	chr14:31595800-31599200	Strong transcription	Osteobl	bone
43	chr14:31595800-31599400	Strong transcription	Brain Hippocampus Middle	brain
44	chr14:31595800-31600000	Strong transcription	NHEK	skin
45	chr14:31595800-31600800	Strong transcription	HUVEC	blood vessel
46	chr14:31595800-31610000	Strong transcription	Fetal Thymus	thymus
47	chr14:31596600-31606600	Strong transcription	Hela-S3	cervix
48	chr14:31596800-31606000	Strong transcription	HSMM	muscle
49	chr14:31597000-31599200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr14:31597000-31599200	Strong transcription	Fetal Brain Female	brain

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