Variant report

Variant	nsv456345
Chromosome Location	chr14:78380390-78398891
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:210)
CpG islands
(count:183)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:210 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:78389927-78390312	K562	blood:	n/a	n/a
2	ARID3A	chr14:78388472-78388487	K562	blood:	n/a	n/a
3	ARID3A	chr14:78384908-78385258	K562	blood:	n/a	n/a
4	ATF1	chr14:78389966-78390359	K562	blood:	n/a	n/a
5	ATF1	chr14:78384742-78385161	K562	blood:	n/a	n/a
6	ATF3	chr14:78380398-78380683	K562	blood:	n/a	n/a
7	ATF3	chr14:78395759-78395981	K562	blood:	n/a	n/a
8	BACH1	chr14:78380360-78380732	K562	blood:	n/a	n/a
9	BACH1	chr14:78389655-78390258	K562	blood:	n/a	n/a
10	BHLHE40	chr14:78389440-78389462	K562	blood:	n/a	n/a
11	BHLHE40	chr14:78380444-78380917	K562	blood:	n/a	n/a
12	BHLHE40	chr14:78384611-78385134	K562	blood:	n/a	n/a
13	BHLHE40	chr14:78389737-78390326	K562	blood:	n/a	n/a
14	BHLHE40	chr14:78390684-78391026	K562	blood:	n/a	n/a
15	CBX3	chr14:78389425-78390411	K562	blood:	n/a	n/a
16	CBX3	chr14:78386661-78386986	K562	blood:	n/a	n/a
17	CBX3	chr14:78380372-78380995	K562	blood:	n/a	n/a
18	CCNT2	chr14:78389919-78390490	K562	blood:	n/a	n/a
19	CCNT2	chr14:78384890-78385149	K562	blood:	n/a	n/a
20	CEBPB	chr14:78383807-78384162	K562	blood:	n/a	chr14:78383983-78383996 chr14:78383983-78383994 chr14:78383980-78383997 chr14:78383985-78383996
21	CEBPB	chr14:78383038-78383271	K562	blood:	n/a	chr14:78383161-78383174
22	CEBPB	chr14:78383844-78384121	HepG2	liver:	n/a	chr14:78383983-78383996 chr14:78383983-78383994 chr14:78383980-78383997 chr14:78383985-78383996
23	CEBPB	chr14:78383800-78384186	K562	blood:	n/a	chr14:78383983-78383996 chr14:78383983-78383994 chr14:78383980-78383997 chr14:78383985-78383996
24	CEBPB	chr14:78389975-78390291	K562	blood:	n/a	n/a
25	CEBPB	chr14:78384762-78385175	K562	blood:	n/a	n/a
26	CHD2	chr14:78395737-78395903	K562	blood:	n/a	n/a
27	CHD2	chr14:78380339-78380906	K562	blood:	n/a	n/a
28	CTCF	chr14:78387214-78387247	GM10248	blood:	n/a	n/a
29	CUX1	chr14:78389571-78390176	K562	blood:	n/a	n/a
30	CUX1	chr14:78380335-78380962	K562	blood:	n/a	n/a
31	CUX1	chr14:78384664-78385204	K562	blood:	n/a	n/a
32	E2F6	chr14:78380627-78380976	K562	blood:	n/a	n/a
33	E2F6	chr14:78383012-78383196	K562	blood:	n/a	n/a
34	EGR1	chr14:78390400-78390630	K562	blood:	n/a	n/a
35	EGR1	chr14:78390288-78390727	K562	blood:	n/a	n/a
36	EP300	chr14:78380418-78380737	K562	blood:	n/a	n/a
37	EP300	chr14:78389934-78390262	SK-N-SH_RA	brain:	n/a	n/a
38	EP300	chr14:78389969-78390234	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr14:78389922-78390539	K562	blood:	n/a	n/a
40	EP300	chr14:78384959-78385434	MCF-7	breast:	n/a	n/a
41	EP300	chr14:78381302-78381311	K562	blood:	n/a	n/a
42	EP300	chr14:78384876-78385121	K562	blood:	n/a	n/a
43	EP300	chr14:78387618-78391805	SK-N-SH	brain:	n/a	chr14:78391351-78391367
44	EP300	chr14:78384720-78385260	K562	blood:	n/a	n/a
45	EP300	chr14:78380321-78381004	K562	blood:	n/a	chr14:78380768-78380775
46	FOSL1	chr14:78380375-78380681	K562	blood:	n/a	n/a
47	GATA1	chr14:78380349-78380806	PBDE	blood:	n/a	n/a
48	GATA1	chr14:78389753-78390290	PBDE	blood:	n/a	chr14:78390098-78390105 chr14:78390096-78390106 chr14:78390082-78390093 chr14:78390091-78390112 chr14:78390098-78390105 chr14:78390098-78390105 chr14:78390093-78390109
49	GATA1	chr14:78389406-78390471	K562	blood:	n/a	chr14:78390098-78390105 chr14:78390096-78390106 chr14:78390082-78390093 chr14:78390091-78390112 chr14:78390098-78390105 chr14:78390098-78390105 chr14:78390093-78390109
50	GATA2	chr14:78387696-78388780	SH-SY5Y	brain:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:78389529-78389579	HCM	heart:	n/a
2	chr14:78388728-78388778	LNCaP	prostate:	n/a
3	chr14:78388736-78388786	SAEC	small airway:	n/a
4	chr14:78388728-78388778	HMEC	breast:	n/a
5	chr14:78388736-78388786	AG04449	skin:	fetal
6	chr14:78388736-78388786	PANC-1	pancreas:	n/a
7	chr14:78388736-78388786	SK-N-SH_RA	brain:	n/a
8	chr14:78389529-78389579	NHBE	bronchial:	n/a
9	chr14:78388728-78388778	NH-A	brain:	n/a
10	chr14:78388736-78388786	RPTEC	kidney:	n/a
11	chr14:78388728-78388778	A549	lung:	n/a
12	chr14:78388736-78388786	HepG2	liver:	n/a
13	chr14:78388736-78388786	GM06990	blood:	n/a
14	chr14:78389529-78389579	HNPCEpiC	eye:	n/a
15	chr14:78388736-78388786	NT2-D1	testis:	n/a
16	chr14:78388736-78388786	GM12892	blood:	n/a
17	chr14:78389529-78389579	H1-hESC	embryonic stem cell:	embryo
18	chr14:78388736-78388786	ProgFib	skin:	n/a
19	chr14:78388736-78388786	H1-hESC	embryonic stem cell:	embryo
20	chr14:78388728-78388778	HPAEpiC	pulmonary alveolar:	n/a
21	chr14:78389529-78389579	PANC-1	pancreas:	n/a
22	chr14:78388728-78388778	HCM	heart:	n/a
23	chr14:78388728-78388778	ECC-1	luminal epithelium:	n/a
24	chr14:78388736-78388786	HCPEpiC	choroid plexus:	n/a
25	chr14:78389529-78389579	AG04450	lung:	fetal
26	chr14:78389529-78389579	MCF10A-Er-Src	breast:	n/a
27	chr14:78388728-78388778	CMK	blood:	n/a
28	chr14:78388736-78388786	Hepatocyte	liver:	n/a
29	chr14:78388736-78388786	HEK293	kidney:	embryo
30	chr14:78388728-78388778	ovcar-3	ovarian:	n/a
31	chr14:78389529-78389579	GM06990	blood:	n/a
32	chr14:78389529-78389579	GM12891	blood:	n/a
33	chr14:78389529-78389579	LNCaP	prostate:	n/a
34	chr14:78389529-78389579	AG04449	skin:	fetal
35	chr14:78388728-78388778	RPTEC	kidney:	n/a
36	chr14:78388728-78388778	T-47D	breast:	n/a
37	chr14:78388736-78388786	NB4	blood:	n/a
38	chr14:78388728-78388778	H1-hESC	embryonic stem cell:	embryo
39	chr14:78389529-78389579	U87	brain:	n/a
40	chr14:78388736-78388786	HIPEpiC	eye:	n/a
41	chr14:78388728-78388778	BE2_C	brain:	n/a
42	chr14:78388736-78388786	SK-N-MC	brain:	n/a
43	chr14:78388728-78388778	HEK293	kidney:	embryo
44	chr14:78388728-78388778	NT2-D1	testis:	n/a
45	chr14:78388728-78388778	GM12891	blood:	n/a
46	chr14:78388728-78388778	AG04450	lung:	fetal
47	chr14:78388736-78388786	HCM	heart:	n/a
48	chr14:78388728-78388778	HEEpiC	esophagus:	n/a
49	chr14:78388728-78388778	HRE	kidney:	n/a
50	chr14:78388728-78388778	GM12878	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:78382649..78385767-chr14:78387779..78390139,4	K562	blood:
2	chr14:78391749..78395575-chr14:78398550..78402914,3	K562	blood:
3	chr14:78394289..78396703-chr14:78398863..78401449,2	K562	blood:
4	chr14:78380542..78382156-chr14:78382539..78385215,4	K562	blood:
5	chr14:78391749..78395575-chr14:78398550..78402914,3	K562	blood:
6	chr14:78394289..78396703-chr14:78398863..78401449,2	K562	blood:
7	chr14:78379164..78381775-chr14:78388793..78390991,2	K562	blood:
8	chr14:78380586..78382152-chr14:78382643..78384269,2	K562	blood:
9	chr14:78388179..78390818-chr14:78392390..78394664,2	MCF-7	breast:
10	chr14:78374932..78377581-chr14:78382548..78385109,2	K562	blood:
11	chr14:78383178..78385641-chr14:78388639..78391453,2	K562	blood:
12	chr14:78380586..78382152-chr14:78382643..78384269,2	K562	blood:
13	chr14:78395022..78397820-chr14:78443504..78445248,2	MCF-7	breast:
14	chr14:78375925..78378556-chr14:78379735..78381780,2	MCF-7	breast:
15	chr14:78344966..78346676-chr14:78382145..78384614,2	K562	blood:
16	chr14:78380542..78382156-chr14:78382539..78385215,4	K562	blood:
17	chr14:78392307..78394224-chr14:78398932..78400488,2	K562	blood:
18	chr14:78396385..78399196-chr14:78423059..78425223,2	K562	blood:

No data

Variant related genes	Relation type
ADCK1	TF binding region
ADCK1	CpG island
ENSG00000063761	chromatin interactions

Extended variants
information (count: 735 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:735 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8015618	chr14:78380390-78380391	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs78521521	chr14:78380414-78380415	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
3	rs148500047	chr14:78380436-78380437	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs61990752	chr14:78380437-78380438	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs56374507	chr14:78380533-78380534	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs10147707	chr14:78380555-78380556	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs549806519	chr14:78380645-78380646	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs565938975	chr14:78380682-78380683	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs182784298	chr14:78380692-78380693	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs529186338	chr14:78380698-78380699	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs533685513	chr14:78380715-78380716	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs565879063	chr14:78380727-78380728	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs142809423	chr14:78380737-78380738	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs112811997	chr14:78380740-78380741	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs558869782	chr14:78380787-78380788	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs570926101	chr14:78380788-78380789	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs539421276	chr14:78380798-78380799	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs373336190	chr14:78380810-78380811	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs576063158	chr14:78380825-78380826	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs151052294	chr14:78380826-78380827	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs555686936	chr14:78380882-78380883	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs558559824	chr14:78380884-78380885	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs10150472	chr14:78380965-78380966	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs541625553	chr14:78380966-78380967	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs563980947	chr14:78380995-78380996	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs577682245	chr14:78381008-78381009	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs543574763	chr14:78381111-78381112	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs116217569	chr14:78381138-78381139	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs528941052	chr14:78381254-78381255	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs188353274	chr14:78381274-78381275	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs71131604	chr14:78381275-78381276	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs398025840	chr14:78381280-78381281	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs199854147	chr14:78381283-78381284	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs79322622	chr14:78381284-78381285	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs112366336	chr14:78381405-78381406	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs113379082	chr14:78381440-78381441	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs551574230	chr14:78381474-78381475	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs570823484	chr14:78381508-78381509	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs34034949	chr14:78381526-78381527	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs36000775	chr14:78381527-78381528	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs35146672	chr14:78381528-78381529	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs75178616	chr14:78381540-78381541	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs192554524	chr14:78381562-78381563	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs549890844	chr14:78381563-78381564	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs569711896	chr14:78381594-78381595	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs542407449	chr14:78381599-78381600	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs372984859	chr14:78381617-78381618	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs555602644	chr14:78381635-78381636	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs558075619	chr14:78381671-78381672	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs577762445	chr14:78381678-78381679	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
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
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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Hepatocellular carcinoma	16750200	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Biliary cancer	19435499	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Intracranial aneurysm	16715129	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	22209245	CNVD
Prostate cancer	22553170	CNVD
Cancer	20164919	CNVD
Breast cancer	21509527	CNVD
Autism	22543975	CNVD

Chromatin state (count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78327800-78400600	Weak transcription	Colonic Mucosa	Colon
2	chr14:78349200-78397200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr14:78349200-78407200	Weak transcription	Colon Smooth Muscle	Colon
4	chr14:78352600-78398800	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr14:78354800-78391600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr14:78355000-78390800	Weak transcription	Spleen	Spleen
7	chr14:78355000-78391600	Weak transcription	Esophagus	oesophagus
8	chr14:78355600-78398000	Weak transcription	Rectal Smooth Muscle	rectum
9	chr14:78356000-78393600	Weak transcription	Duodenum Mucosa	Duodenum
10	chr14:78356000-78398600	Weak transcription	Fetal Intestine Large	intestine
11	chr14:78356200-78390800	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr14:78356800-78399600	Weak transcription	Thymus	Thymus
13	chr14:78357000-78398600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr14:78359200-78399600	Weak transcription	HSMMtube	muscle
15	chr14:78359200-78399800	Weak transcription	Primary B cells from cord blood	blood
16	chr14:78359400-78384200	Weak transcription	Right Ventricle	heart
17	chr14:78359800-78390800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr14:78364000-78398800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr14:78366000-78393000	Weak transcription	Aorta	Aorta
20	chr14:78367400-78399200	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr14:78369200-78392000	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr14:78369400-78397400	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr14:78369600-78394000	Weak transcription	Liver	Liver
24	chr14:78369800-78384200	Weak transcription	Left Ventricle	heart
25	chr14:78370000-78380400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr14:78370000-78397600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr14:78372800-78399200	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr14:78373000-78383800	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr14:78373000-78395200	Weak transcription	Primary B cells from peripheral blood	blood
30	chr14:78374200-78390200	Weak transcription	Lung	lung
31	chr14:78374800-78391000	Weak transcription	Ovary	ovary
32	chr14:78375200-78391000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr14:78375200-78391600	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr14:78375400-78400800	Weak transcription	NHEK	skin
35	chr14:78375600-78397800	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr14:78376000-78384400	Weak transcription	Right Atrium	heart
37	chr14:78376000-78392200	Weak transcription	Fetal Intestine Small	intestine
38	chr14:78376600-78386600	Weak transcription	Adipose Nuclei	Adipose
39	chr14:78376800-78384400	Weak transcription	Gastric	stomach
40	chr14:78377000-78384600	Weak transcription	Brain Hippocampus Middle	brain
41	chr14:78377000-78392000	Weak transcription	Fetal Muscle Leg	muscle
42	chr14:78377000-78393200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr14:78377200-78398600	Weak transcription	Brain Substantia Nigra	brain
44	chr14:78377200-78399600	Weak transcription	Fetal Muscle Trunk	muscle
45	chr14:78377800-78390200	Weak transcription	Stomach Smooth Muscle	stomach
46	chr14:78378000-78380800	Weak transcription	Primary T cells from cord blood	blood
47	chr14:78378800-78380400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr14:78378800-78381000	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr14:78379000-78380600	Enhancers	H1 Cell Line	embryonic stem cell
50	chr14:78379000-78380600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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