Variant report

Variant	esv3391296
Chromosome Location	chr14:78017218-78017807
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	CTCF	chr14:78017800-78017950	HFF	foreskin:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
2	CTCF	chr14:78017780-78017930	Hela-S3	cervix:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
3	CTCF	chr14:78017656-78018088	GM12878	blood:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
4	CTCF	chr14:78017800-78017950	GM12872	blood:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
5	CTCF	chr14:78017800-78017950	SAEC	small airway:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
6	CTCF	chr14:78017800-78017950	A549	lung:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
7	CTCF	chr14:78017770-78017980	GM13977	blood:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
8	CTCF	chr14:78017741-78018010	Medullo	brain:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
9	CTCF	chr14:78017740-78017890	HCM	heart:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
10	CTCF	chr14:78017760-78017910	GM12870	blood:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
11	CTCF	chr14:78017780-78017930	AG04449	skin:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
12	CTCF	chr14:78017674-78018078	IMR90	lung:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
13	CTCF	chr14:78017800-78017950	HMF	breast:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
14	CTCF	chr14:78017670-78018180	SK-N-SH	brain:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
15	CTCF	chr14:78017756-78017998	LNCaP	prostate:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
16	CTCF	chr14:78017697-78017948	A549	lung:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
17	CTCF	chr14:78017780-78017930	Caco-2	colon:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
18	CTCF	chr14:78017800-78017950	GM12873	blood:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
19	CTCF	chr14:78017752-78018010	GM12878	blood:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
20	CTCF	chr14:78017800-78017950	NHLF	lung:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
21	CTCF	chr14:78017780-78017930	GM06990	blood:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
22	CTCF	chr14:78017780-78017930	HCFaa	heart:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
23	CTCF	chr14:78017760-78017910	GM12869	blood:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
24	CTCF	chr14:78017769-78017990	GM10266	blood:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
25	CTCF	chr14:78017780-78017930	HAc	cerebellar:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
26	CTCF	chr14:78017800-78017950	HEK293	kidney:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
27	CTCF	chr14:78017760-78017910	HVMF	connective:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
28	CTCF	chr14:78017800-78017950	HMEC	breast:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
29	CTCF	chr14:78017686-78018174	MCF-7	breast:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
30	CTCF	chr14:78017800-78017950	WERI-Rb-1	eye:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
31	CTCF	chr14:78017780-78017930	AG04450	lung:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
32	CTCF	chr14:78017717-78018023	A549	lung:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
33	CTCF	chr14:78017780-78017930	HEK293	kidney:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
34	CTCF	chr14:78017780-78017930	AG10803	skin:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
35	CTCF	chr14:78017756-78017998	Pancreas_OC	pancreas:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
36	CTCF	chr14:78017780-78017930	BJ	skin:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
37	CTCF	chr14:78017735-78018025	HUVEC	blood vessel:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
38	CTCF	chr14:78017772-78017980	Gliobla	brain:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
39	CTCF	chr14:78017800-78017950	MCF-7	breast:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
40	CTCF	chr14:78017754-78017968	T-47D	breast:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
41	CTCF	chr14:78017780-78017930	HMF	breast:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
42	CTCF	chr14:78017720-78017967	ECC-1	luminal epithelium:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
43	CTCF	chr14:78017735-78018013	A549	lung:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
44	CTCF	chr14:78017780-78017930	HCPEpiC	choroid plexus:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
45	CTCF	chr14:78017760-78017910	HFF-Myc	foreskin:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
46	CTCF	chr14:78017759-78017976	GM10248	blood:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
47	CTCF	chr14:78017800-78017950	HUVEC	blood vessel:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
48	CTCF	chr14:78017760-78017910	HEEpiC	esophagus:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
49	CTCF	chr14:78017770-78017979	MCF-7	breast:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877
50	CTCF	chr14:78017780-78017930	SK-N-SH_RA	brain:	n/a	chr14:78017860-78017878 chr14:78017855-78017876 chr14:78017862-78017875 chr14:78017863-78017873 chr14:78017861-78017877

No.	Distal block	Cell Line	Cell type
1	chr14:78013266..78015094-chr14:78015615..78018423,2	MCF-7	breast:
2	chr14:77864538..77867025-chr14:78015900..78017650,2	MCF-7	breast:
3	chr14:77841219..77843906-chr14:78015874..78017760,2	MCF-7	breast:
4	chr14:77922995..77924910-chr14:78015324..78017998,2	MCF-7	breast:

Variant related genes	Relation type
RN7SL587P	TF binding region
ENSG00000100583	chromatin interactions
ENSG00000100580	chromatin interactions
ENSG00000100591	chromatin interactions
ENSG00000151445	chromatin interactions
ENSG00000240233	chromatin interactions

Extended variants
information (count: 40 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:40 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs60221235	chr14:78017222-78017223	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs187917653	chr14:78017223-78017224	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs555414773	chr14:78017238-78017239	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs201659405	chr14:78017261-78017262	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs397702108	chr14:78017274-78017275	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs535200018	chr14:78017314-78017315	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs72683265	chr14:78017318-78017319	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs36063635	chr14:78017321-78017322	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs534814038	chr14:78017322-78017323	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs557768528	chr14:78017328-78017329	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs58990038	chr14:78017332-78017333	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs530486990	chr14:78017348-78017349	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs539854796	chr14:78017357-78017358	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs191181826	chr14:78017378-78017379	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs17824700	chr14:78017397-78017398	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs549430989	chr14:78017427-78017428	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs58905756	chr14:78017457-78017458	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs138965882	chr14:78017489-78017490	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs377193750	chr14:78017501-78017502	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs541566157	chr14:78017511-78017512	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs564635352	chr14:78017518-78017519	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs533413024	chr14:78017552-78017553	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs549389194	chr14:78017585-78017586	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs562976562	chr14:78017594-78017595	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs528848197	chr14:78017602-78017603	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs561600794	chr14:78017610-78017611	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs368803572	chr14:78017630-78017631	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs534525122	chr14:78017658-78017659	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs551517533	chr14:78017659-78017660	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs149751853	chr14:78017685-78017686	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs11282740	chr14:78017686-78017687	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs398070549	chr14:78017694-78017695	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs141542999	chr14:78017695-78017696	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs140683103	chr14:78017697-78017698	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs78765593	chr14:78017733-78017734	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs11347331	chr14:78017734-78017735	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs77509896	chr14:78017738-78017739	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs571470769	chr14:78017783-78017784	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs8003639	chr14:78017788-78017789	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs557279632	chr14:78017804-78017805	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	22209245	CNVD
Prostate cancer	22553170	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:77970200-78047200	Weak transcription	Fetal Heart	heart
2	chr14:77972000-78018000	Weak transcription	Hela-S3	cervix
3	chr14:77978800-78042200	Weak transcription	Fetal Brain Male	brain
4	chr14:77987400-78021000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr14:77987800-78060000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr14:77988400-78029400	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr14:77997800-78018800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr14:78002200-78020800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr14:78006800-78019000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr14:78008200-78019000	Strong transcription	Primary T helper cells fromperipheralblood	blood
11	chr14:78009600-78019400	Strong transcription	Primary T cells fromperipheralblood	blood
12	chr14:78009600-78021200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr14:78009600-78030000	Strong transcription	Primary neutrophils fromperipheralblood	blood
14	chr14:78009800-78050800	Weak transcription	Psoas Muscle	Psoas
15	chr14:78010000-78018800	Strong transcription	NH-A	brain
16	chr14:78010000-78019800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr14:78010000-78029800	Strong transcription	Primary T cells from cord blood	blood
18	chr14:78010200-78019000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr14:78010200-78020400	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr14:78010200-78026800	Weak transcription	Stomach Mucosa	stomach
21	chr14:78010400-78018600	Strong transcription	Muscle Satellite Cultured Cells	--
22	chr14:78010400-78030000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr14:78010600-78019200	Strong transcription	Rectal Mucosa Donor 29	rectum
24	chr14:78010600-78025000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr14:78010800-78018600	Strong transcription	Primary T helper cells PMA-I stimulated	--
26	chr14:78010800-78019000	Strong transcription	Primary monocytes fromperipheralblood	blood
27	chr14:78011000-78020000	Strong transcription	Primary B cells from peripheral blood	blood
28	chr14:78011000-78031800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
29	chr14:78011200-78019000	Strong transcription	Osteobl	bone
30	chr14:78011200-78045800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr14:78011400-78019000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr14:78011400-78037400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr14:78012800-78019000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr14:78013000-78017400	Strong transcription	Small Intestine	intestine
35	chr14:78013000-78018800	Strong transcription	Duodenum Mucosa	Duodenum
36	chr14:78013200-78030600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr14:78013200-78066200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr14:78013400-78017800	Weak transcription	Fetal Brain Female	brain
39	chr14:78013400-78025800	Strong transcription	HSMM	muscle
40	chr14:78013600-78018400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr14:78013600-78018800	Strong transcription	Rectal Mucosa Donor 31	rectum
42	chr14:78013600-78026200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr14:78013800-78019200	Strong transcription	Fetal Stomach	stomach
44	chr14:78014000-78018800	Strong transcription	HUES6 Cell Line	embryonic stem cell
45	chr14:78014400-78018800	Strong transcription	Fetal Intestine Large	intestine
46	chr14:78014600-78018800	Strong transcription	H1 Cell Line	embryonic stem cell
47	chr14:78014600-78018800	Strong transcription	GM12878-XiMat	blood
48	chr14:78014600-78019400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
49	chr14:78015000-78017400	Strong transcription	Lung	lung
50	chr14:78015000-78018800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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