Variant report

Variant	nsv901510
Chromosome Location	chr14:25476170-25526309
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:811)
CpG islands
(count:612)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:811 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:25519099-25519144	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:25501686-25502161	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:25476440-25476640	K562	blood:	n/a	n/a
4	ARID3A	chr14:25476282-25476539	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:25504361-25504969	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:25517182-25517745	K562	blood:	n/a	n/a
7	ARID3A	chr14:25507001-25507029	HepG2	liver:	n/a	n/a
8	ATF1	chr14:25517415-25517757	K562	blood:	n/a	n/a
9	ATF1	chr14:25476380-25476674	K562	blood:	n/a	n/a
10	ATF3	chr14:25517401-25517686	K562	blood:	n/a	n/a
11	BACH1	chr14:25517483-25517764	K562	blood:	n/a	n/a
12	BACH1	chr14:25512084-25512541	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr14:25519180-25519718	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr14:25476396-25476625	GM12878	blood:	n/a	chr14:25476510-25476521
15	BATF	chr14:25476363-25476710	GM12878	blood:	n/a	chr14:25476510-25476521 chr14:25476620-25476629
16	BATF	chr14:25502275-25502551	GM12878	blood:	n/a	n/a
17	BATF	chr14:25525970-25526204	GM12878	blood:	n/a	n/a
18	BCLAF1	chr14:25501621-25501962	GM12878	blood:	n/a	n/a
19	BHLHE40	chr14:25518960-25519311	GM12878	blood:	n/a	chr14:25519094-25519110 chr14:25519236-25519252
20	BHLHE40	chr14:25510800-25511004	K562	blood:	n/a	n/a
21	BHLHE40	chr14:25518980-25519578	HepG2	liver:	n/a	chr14:25519094-25519110 chr14:25519236-25519252
22	BHLHE40	chr14:25504434-25504751	HepG2	liver:	n/a	n/a
23	BHLHE40	chr14:25501704-25502009	GM12878	blood:	n/a	n/a
24	BHLHE40	chr14:25476675-25476700	K562	blood:	n/a	n/a
25	BRCA1	chr14:25476137-25476719	Hela-S3	cervix:	n/a	n/a
26	CCNT2	chr14:25516822-25517806	K562	blood:	n/a	n/a
27	CCNT2	chr14:25519078-25519498	K562	blood:	n/a	chr14:25519458-25519467 chr14:25519465-25519474 chr14:25519270-25519279
28	CEBPB	chr14:25498082-25498357	IMR90	lung:	n/a	chr14:25498176-25498187
29	CEBPB	chr14:25511761-25511940	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr14:25498071-25498266	K562	blood:	n/a	chr14:25498176-25498187
31	CEBPB	chr14:25511617-25511909	IMR90	lung:	n/a	chr14:25511633-25511645
32	CEBPB	chr14:25476002-25476746	IMR90	lung:	n/a	n/a
33	CEBPB	chr14:25524312-25524649	HepG2	liver:	n/a	chr14:25524492-25524505
34	CEBPB	chr14:25518635-25518960	IMR90	lung:	n/a	chr14:25518797-25518814
35	CEBPB	chr14:25494180-25494338	A549	lung:	n/a	n/a
36	CEBPB	chr14:25500245-25500262	A549	lung:	n/a	n/a
37	CEBPB	chr14:25498066-25498339	HepG2	liver:	n/a	chr14:25498176-25498187
38	CEBPB	chr14:25525397-25526089	IMR90	lung:	n/a	n/a
39	CEBPB	chr14:25517347-25517638	K562	blood:	n/a	n/a
40	CEBPB	chr14:25501745-25502287	HepG2	liver:	n/a	n/a
41	CEBPB	chr14:25500214-25500414	HepG2	liver:	n/a	chr14:25500295-25500306 chr14:25500289-25500300 chr14:25500287-25500300 chr14:25500287-25500298 chr14:25500289-25500300
42	CEBPB	chr14:25511626-25511923	HepG2	liver:	n/a	chr14:25511633-25511645
43	CEBPB	chr14:25511683-25511903	K562	blood:	n/a	n/a
44	CEBPB	chr14:25518649-25518910	H1-hESC	embryonic stem cell:	n/a	chr14:25518797-25518814
45	CEBPB	chr14:25501987-25502166	A549	lung:	n/a	n/a
46	CEBPB	chr14:25518728-25518987	HepG2	liver:	n/a	chr14:25518797-25518814
47	CEBPD	chr14:25517310-25517711	K562	blood:	n/a	n/a
48	CEBPD	chr14:25519167-25519522	HepG2	liver:	n/a	n/a
49	CEBPD	chr14:25518938-25519662	HepG2	liver:	n/a	n/a
50	CHD1	chr14:25500204-25500363	GM12878	blood:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:25518624-25518674	HL-60	blood:	n/a
2	chr14:25516343-25516393	HEK293	kidney:	embryo
3	chr14:25518624-25518674	HL-60	blood:	n/a
4	chr14:25516343-25516393	HEK293	kidney:	embryo
5	chr14:25519484-25519534	ECC-1	luminal epithelium:	n/a
6	chr14:25522307-25522357	NHDF-neo	bronchial:	n/a
7	chr14:25517974-25518024	K562	blood:	n/a
8	chr14:25522307-25522357	SK-N-SH_RA	brain:	n/a
9	chr14:25517974-25518024	SK-N-SH_RA	brain:	n/a
10	chr14:25518624-25518674	LNCaP	prostate:	n/a
11	chr14:25519778-25519828	HEEpiC	esophagus:	n/a
12	chr14:25520721-25520771	HRCEpiC	kidney:	n/a
13	chr14:25519611-25519661	LNCaP	prostate:	n/a
14	chr14:25522307-25522357	NB4	blood:	n/a
15	chr14:25511763-25511813	AG04450	lung:	fetal
16	chr14:25519484-25519534	NT2-D1	testis:	n/a
17	chr14:25512111-25512161	T-47D	breast:	n/a
18	chr14:25519611-25519661	HPAEpiC	pulmonary alveolar:	n/a
19	chr14:25519611-25519661	AoSMC	blood vessel:	n/a
20	chr14:25520721-25520771	GM12878	blood:	n/a
21	chr14:25511763-25511813	HPAEpiC	pulmonary alveolar:	n/a
22	chr14:25518624-25518674	HIPEpiC	eye:	n/a
23	chr14:25516343-25516393	AG09309	skin:	n/a
24	chr14:25520721-25520771	PFSK-1	brain:	n/a
25	chr14:25522307-25522357	HEK293	kidney:	embryo
26	chr14:25517974-25518024	HCM	heart:	n/a
27	chr14:25516343-25516393	SK-N-SH_RA	brain:	n/a
28	chr14:25511763-25511813	GM06990	blood:	n/a
29	chr14:25519484-25519534	HEEpiC	esophagus:	n/a
30	chr14:25512111-25512161	H1-hESC	embryonic stem cell:	embryo
31	chr14:25520721-25520771	MCF-7	breast:	n/a
32	chr14:25512111-25512161	GM12878	blood:	n/a
33	chr14:25522307-25522357	AG04450	lung:	fetal
34	chr14:25511763-25511813	RPTEC	kidney:	n/a
35	chr14:25511763-25511813	AG04449	skin:	fetal
36	chr14:25518624-25518674	AoSMC	blood vessel:	n/a
37	chr14:25520721-25520771	NHDF-neo	bronchial:	n/a
38	chr14:25517974-25518024	PFSK-1	brain:	n/a
39	chr14:25517974-25518024	HepG2	liver:	n/a
40	chr14:25519611-25519661	MCF-7	breast:	n/a
41	chr14:25519484-25519534	HRPEpiC	eye:	n/a
42	chr14:25518624-25518674	HRCEpiC	kidney:	n/a
43	chr14:25522307-25522357	HL-60	blood:	n/a
44	chr14:25516343-25516393	CMK	blood:	n/a
45	chr14:25512111-25512161	GM19239	blood:	n/a
46	chr14:25518624-25518674	GM19239	blood:	n/a
47	chr14:25522307-25522357	HNPCEpiC	eye:	n/a
48	chr14:25518624-25518674	HCT-116	colon:	n/a
49	chr14:25520721-25520771	HEK293	kidney:	embryo
50	chr14:25519611-25519661	HRE	kidney:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:25474104..25476985-chr14:25480254..25482757,2	MCF-7	breast:
2	chr14:25511682..25512314-chr14:25602148..25602701,2	MCF-7	breast:
3	chr14:25475307..25477626-chr14:25483489..25485932,2	MCF-7	breast:
4	chr14:25286732..25287686-chr14:25511790..25512486,5	MCF-7	breast:
5	chr14:25422370..25423189-chr14:25504381..25505293,2	MCF-7	breast:
6	chr14:25474104..25476985-chr14:25480254..25482757,2	MCF-7	breast:
7	chr14:25475307..25477626-chr14:25483489..25485932,2	MCF-7	breast:
8	chr14:25274769..25276064-chr14:25511769..25512775,13	MCF-7	breast:
9	chr14:24834687..24835397-chr14:25511870..25512753,2	MCF-7	breast:
10	chr14:25462000..25464102-chr14:25486404..25488622,2	K562	blood:
11	chr14:25203732..25204545-chr14:25511727..25512593,3	MCF-7	breast:
12	chr14:25179326..25179885-chr14:25512037..25512719,2	MCF-7	breast:
13	chr14:25516181..25518992-chr14:25521102..25522786,2	K562	blood:
14	chr14:25434060..25436749-chr14:25474798..25476702,2	K562	blood:
15	chr14:25517771..25520520-chr14:25522589..25526544,3	MCF-7	breast:
16	chr14:25501777..25502348-chr14:25601749..25602573,2	MCF-7	breast:
17	chr14:25275348..25276037-chr14:25510991..25511724,2	MCF-7	breast:
18	chr14:25286735..25287246-chr14:25511793..25512726,2	MCF-7	breast:

No data

Variant related genes	Relation type
STXBP6	TF binding region
STXBP6	CpG island
ENSG00000100968	chromatin interactions
ENSG00000168952	chromatin interactions

Extended variants
information (count: 1784 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1784 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs912304	chr14:25476170-25476171	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs541736774	chr14:25476183-25476184	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs563455868	chr14:25476225-25476226	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs570505079	chr14:25476233-25476234	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs185805375	chr14:25476236-25476237	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs550431111	chr14:25476270-25476271	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs79118848	chr14:25476289-25476290	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs76383489	chr14:25476347-25476348	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs190210621	chr14:25476367-25476368	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs144957809	chr14:25476368-25476369	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs149023652	chr14:25476421-25476422	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs1957762	chr14:25476431-25476432	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs183351735	chr14:25476472-25476473	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs151103266	chr14:25476490-25476491	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs114467024	chr14:25476544-25476545	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs141471715	chr14:25476569-25476570	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs559520939	chr14:25476617-25476618	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs145101899	chr14:25476640-25476641	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs116398504	chr14:25476670-25476671	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs564284918	chr14:25476675-25476676	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs562571753	chr14:25476748-25476749	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs577767203	chr14:25476755-25476756	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs370514736	chr14:25476856-25476857	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs528672045	chr14:25476890-25476891	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs186206731	chr14:25476907-25476908	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs115574698	chr14:25476908-25476909	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs529527907	chr14:25476922-25476923	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs549733324	chr14:25476981-25476982	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs566256404	chr14:25477016-25477017	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs551493354	chr14:25477024-25477025	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs564011657	chr14:25477095-25477096	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs191059287	chr14:25477128-25477129	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs140676650	chr14:25477143-25477144	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs182345679	chr14:25477156-25477157	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs189235521	chr14:25477205-25477206	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs556655068	chr14:25477271-25477272	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs192498723	chr14:25477285-25477286	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs183165660	chr14:25477392-25477393	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs571239089	chr14:25477396-25477397	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs572695150	chr14:25477427-25477428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs7141216	chr14:25477438-25477439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs138225141	chr14:25477540-25477541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11848412	chr14:25477632-25477633	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs187451743	chr14:25477634-25477635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192053636	chr14:25477704-25477705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184950768	chr14:25477723-25477724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs546591323	chr14:25477735-25477736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529316452	chr14:25477784-25477785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs549696784	chr14:25477785-25477786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs111543946	chr14:25478038-25478039	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Cancer	20164920	CNVD
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
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	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
Breast cancer	21364760	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:1234 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:25463200-25476600	Weak transcription	Placenta	Placenta
2	chr14:25471200-25476200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr14:25472200-25476200	Enhancers	HSMM	muscle
4	chr14:25473000-25476400	Weak transcription	Brain Anterior Caudate	brain
5	chr14:25473000-25477800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr14:25473200-25476200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr14:25473400-25476600	Weak transcription	Adipose Nuclei	Adipose
8	chr14:25473400-25476600	Weak transcription	Fetal Muscle Leg	muscle
9	chr14:25473400-25477200	Enhancers	Fetal Intestine Small	intestine
10	chr14:25473400-25477800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr14:25473400-25478600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr14:25473400-25478800	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr14:25473400-25479200	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr14:25473600-25476200	Weak transcription	Brain Angular Gyrus	brain
15	chr14:25473600-25476200	Weak transcription	Brain Cingulate Gyrus	brain
16	chr14:25473600-25476200	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr14:25473600-25476400	Weak transcription	Brain Hippocampus Middle	brain
18	chr14:25473600-25478600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr14:25473800-25478000	Weak transcription	Fetal Brain Male	brain
20	chr14:25473800-25478200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr14:25474200-25476200	Weak transcription	Duodenum Mucosa	Duodenum
22	chr14:25474200-25476600	Weak transcription	Pancreas	Pancrea
23	chr14:25474200-25476600	Weak transcription	Right Atrium	heart
24	chr14:25474200-25476600	Weak transcription	Right Ventricle	heart
25	chr14:25474200-25476800	Weak transcription	Brain Substantia Nigra	brain
26	chr14:25474200-25477800	Enhancers	HepG2	liver
27	chr14:25474800-25476200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr14:25474800-25477400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr14:25475200-25476200	Enhancers	HSMMtube	muscle
30	chr14:25475200-25477200	Enhancers	Fetal Intestine Large	intestine
31	chr14:25475200-25478000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr14:25475200-25480800	Enhancers	Placenta Amnion	Placenta Amnion
33	chr14:25475400-25477400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr14:25475400-25478800	Enhancers	Fetal Heart	heart
35	chr14:25475600-25476200	Enhancers	NH-A	brain
36	chr14:25475600-25476600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr14:25475600-25476600	Weak transcription	Left Ventricle	heart
38	chr14:25475600-25477400	Enhancers	Stomach Mucosa	stomach
39	chr14:25475600-25478800	Weak transcription	Lung	lung
40	chr14:25475600-25479400	Enhancers	Fetal Lung	lung
41	chr14:25475800-25476400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
42	chr14:25475800-25476400	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr14:25475800-25477000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr14:25475800-25477000	Enhancers	NHLF	lung
45	chr14:25475800-25477200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr14:25475800-25477200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr14:25475800-25477200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
48	chr14:25475800-25477200	Enhancers	NHDF-Ad	bronchial
49	chr14:25475800-25477200	Enhancers	Osteobl	bone
50	chr14:25475800-25477400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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