Variant report

Variant	nsv902042
Chromosome Location	chr14:67213769-67351019
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	chr14:67224984-67225061	HepG2	liver:	n/a	n/a
2	ATF2	chr14:67218758-67219207	GM12878	blood:	n/a	n/a
3	ATF2	chr14:67218740-67219290	GM12878	blood:	n/a	n/a
4	BACH1	chr14:67305949-67305970	K562	blood:	n/a	n/a
5	BATF	chr14:67218719-67219305	GM12878	blood:	n/a	n/a
6	BATF	chr14:67218778-67219263	GM12878	blood:	n/a	n/a
7	BCL11A	chr14:67218813-67219271	GM12878	blood:	n/a	n/a
8	BCL11A	chr14:67219021-67219287	GM12878	blood:	n/a	n/a
9	BHLHE40	chr14:67218905-67219220	GM12878	blood:	n/a	n/a
10	BRCA1	chr14:67288110-67288222	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr14:67326090-67326343	HepG2	liver:	n/a	n/a
12	CEBPB	chr14:67280261-67280604	HepG2	liver:	n/a	chr14:67280486-67280497
13	CEBPB	chr14:67280298-67280687	IMR90	lung:	n/a	chr14:67280486-67280497
14	CEBPB	chr14:67258805-67259057	HepG2	liver:	n/a	n/a
15	CEBPB	chr14:67250550-67250614	K562	blood:	n/a	n/a
16	CEBPB	chr14:67280318-67280671	ECC-1	luminal epithelium:	n/a	chr14:67280486-67280497
17	CEBPB	chr14:67237108-67237444	HepG2	liver:	n/a	chr14:67237274-67237283 chr14:67237273-67237284 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237272-67237285 chr14:67237272-67237285
18	CEBPB	chr14:67280301-67280681	K562	blood:	n/a	chr14:67280486-67280497
19	CEBPB	chr14:67326052-67326430	HepG2	liver:	n/a	n/a
20	CEBPB	chr14:67237118-67237434	Hela-S3	cervix:	n/a	chr14:67237274-67237283 chr14:67237273-67237284 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237272-67237285 chr14:67237272-67237285
21	CEBPB	chr14:67310889-67310923	A549	lung:	n/a	n/a
22	CEBPB	chr14:67280274-67280662	A549	lung:	n/a	chr14:67280486-67280497
23	CEBPB	chr14:67237138-67237439	A549	lung:	n/a	chr14:67237274-67237283 chr14:67237273-67237284 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237272-67237285 chr14:67237272-67237285
24	CEBPB	chr14:67280306-67280665	H1-hESC	embryonic stem cell:	n/a	chr14:67280486-67280497
25	CEBPB	chr14:67280297-67280677	A549	lung:	n/a	chr14:67280486-67280497
26	CEBPB	chr14:67237101-67237436	K562	blood:	n/a	chr14:67237274-67237283 chr14:67237273-67237284 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237272-67237285 chr14:67237272-67237285
27	CEBPB	chr14:67326212-67326326	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr14:67280291-67280680	ECC-1	luminal epithelium:	n/a	chr14:67280486-67280497
29	CEBPB	chr14:67326120-67326325	HepG2	liver:	n/a	n/a
30	CEBPB	chr14:67250490-67250759	HepG2	liver:	n/a	n/a
31	CEBPB	chr14:67290366-67290605	A549	lung:	n/a	n/a
32	CEBPB	chr14:67280307-67280679	Hela-S3	cervix:	n/a	chr14:67280486-67280497
33	CEBPB	chr14:67325909-67326408	HepG2	liver:	n/a	n/a
34	CEBPB	chr14:67280182-67280792	A549	lung:	n/a	chr14:67280486-67280497
35	CEBPB	chr14:67280360-67280549	HepG2	liver:	n/a	chr14:67280486-67280497
36	CEBPB	chr14:67280308-67280682	HepG2	liver:	n/a	chr14:67280486-67280497
37	CEBPB	chr14:67280194-67280806	MCF-7	breast:	n/a	chr14:67280486-67280497
38	CEBPB	chr14:67237135-67237372	H1-hESC	embryonic stem cell:	n/a	chr14:67237274-67237283 chr14:67237273-67237284 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237272-67237285 chr14:67237272-67237285
39	CEBPB	chr14:67290364-67290658	IMR90	lung:	n/a	n/a
40	CEBPB	chr14:67250483-67250759	A549	lung:	n/a	n/a
41	CEBPB	chr14:67237139-67237466	IMR90	lung:	n/a	chr14:67237274-67237283 chr14:67237273-67237284 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237272-67237285 chr14:67237272-67237285
42	CEBPB	chr14:67326093-67326355	A549	lung:	n/a	n/a
43	CEBPB	chr14:67280214-67280811	MCF-7	breast:	n/a	chr14:67280486-67280497
44	CEBPB	chr14:67280292-67280682	HepG2	liver:	n/a	chr14:67280486-67280497
45	CTCF	chr14:67249573-67250232	MCF-7	breast:	n/a	n/a
46	CTCF	chr14:67225084-67225134	Medullo	brain:	n/a	n/a
47	CTCF	chr14:67280631-67280687	MCF-7	breast:	n/a	n/a
48	CTCF	chr14:67249700-67249850	BE2_C	brain:	n/a	n/a
49	CTCF	chr14:67334874-67334990	LNCaP	prostate:	n/a	chr14:67334895-67334913 chr14:67334897-67334918 chr14:67334896-67334912
50	CTCF	chr14:67225040-67225190	HCPEpiC	choroid plexus:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:67292488-67292538	HPAEpiC	pulmonary alveolar:	n/a
2	chr14:67292488-67292538	GM12878	blood:	n/a
3	chr14:67292488-67292538	GM19239	blood:	n/a
4	chr14:67292488-67292538	PrEC	prostate:	n/a
5	chr14:67292488-67292538	NH-A	brain:	n/a
6	chr14:67292488-67292538	HCT-116	colon:	n/a
7	chr14:67292488-67292538	Hela-S3	cervix:	n/a
8	chr14:67292488-67292538	HCM	heart:	n/a
9	chr14:67292488-67292538	NHBE	bronchial:	n/a
10	chr14:67292488-67292538	HL-60	blood:	n/a
11	chr14:67292488-67292538	HCPEpiC	choroid plexus:	n/a
12	chr14:67292488-67292538	RPTEC	kidney:	n/a
13	chr14:67292488-67292538	ECC-1	luminal epithelium:	n/a
14	chr14:67292488-67292538	SAEC	small airway:	n/a
15	chr14:67292488-67292538	NHDF-neo	bronchial:	n/a
16	chr14:67292488-67292538	LNCaP	prostate:	n/a
17	chr14:67292488-67292538	H1-hESC	embryonic stem cell:	embryo
18	chr14:67292488-67292538	HUVEC	blood vessel:	n/a
19	chr14:67292488-67292538	AG04449	skin:	fetal
20	chr14:67292488-67292538	HCF	heart:	n/a
21	chr14:67292488-67292538	MCF10A-Er-Src	breast:	n/a
22	chr14:67292488-67292538	SKMC	muscle:	n/a
23	chr14:67292488-67292538	GM06990	blood:	n/a
24	chr14:67292488-67292538	NT2-D1	testis:	n/a
25	chr14:67292488-67292538	SK-N-SH	brain:	n/a
26	chr14:67292488-67292538	A549	lung:	n/a
27	chr14:67292488-67292538	HAEpiC	amniotic membrane:	n/a
28	chr14:67292488-67292538	HRCEpiC	kidney:	n/a
29	chr14:67292488-67292538	HepG2	liver:	n/a
30	chr14:67292488-67292538	NB4	blood:	n/a
31	chr14:67292488-67292538	PANC-1	pancreas:	n/a
32	chr14:67292488-67292538	IMR90	lung:	fetal
33	chr14:67292488-67292538	AG09319	gingival:	n/a
34	chr14:67292488-67292538	Hepatocyte	liver:	n/a
35	chr14:67292488-67292538	AG10803	skin:	n/a
36	chr14:67292488-67292538	AoSMC	blood vessel:	n/a
37	chr14:67292488-67292538	BE2_C	brain:	n/a
38	chr14:67292488-67292538	BJ	skin:	n/a
39	chr14:67292488-67292538	MCF-7	breast:	n/a
40	chr14:67292488-67292538	SK-N-SH_RA	brain:	n/a
41	chr14:67292488-67292538	K562	blood:	n/a
42	chr14:67292488-67292538	HEK293	kidney:	embryo
43	chr14:67292488-67292538	AG09309	skin:	n/a
44	chr14:67292488-67292538	HRE	kidney:	n/a
45	chr14:67292488-67292538	SK-N-MC	brain:	n/a
46	chr14:67292488-67292538	ProgFib	skin:	n/a
47	chr14:67292488-67292538	CMK	blood:	n/a
48	chr14:67292488-67292538	AG04450	lung:	fetal
49	chr14:67292488-67292538	HMEC	breast:	n/a
50	chr14:67292488-67292538	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:67290864..67292814-chr14:67296432..67298009,2	MCF-7	breast:
2	chr14:67273370..67275073-chr14:67291638..67294473,2	K562	blood:
3	chr14:67221145..67223857-chr14:67240535..67242119,2	K562	blood:
4	chr14:67091099..67091710-chr14:67212729..67213799,3	MCF-7	breast:
5	chr14:67347067..67349521-chr14:67447070..67449089,2	MCF-7	breast:
6	chr14:67249480..67250181-chr17:59494053..59494794,2	MCF-7	breast:
7	chr14:67292902..67294544-chr14:67295956..67298374,2	MCF-7	breast:
8	chr14:67292902..67294544-chr14:67295956..67298374,2	MCF-7	breast:
9	chr14:67221145..67223857-chr14:67240535..67242119,2	K562	blood:
10	chr14:67310130..67311981-chr14:67312589..67315388,2	MCF-7	breast:
11	chr14:67247462..67249948-chr14:67251250..67254048,2	MCF-7	breast:
12	chr14:67273370..67275073-chr14:67291638..67294473,2	K562	blood:
13	chr14:67310130..67311981-chr14:67312589..67315388,2	MCF-7	breast:
14	chr14:67297492..67297992-chr6:10786994..10787529,2	MCF-7	breast:
15	chr14:67247462..67249948-chr14:67251250..67254048,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM71D-3	chr14:67227250-67227736	NONHSAT037427

Variant related genes	Relation type
GPHN	TF binding region
ENSG00000258796	TF binding region
GPHN	CpG island
ENSG00000258796	CpG island
ENSG00000171723	chromatin interactions

Extended variants
information (count: 4805 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:4805 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10148469	chr14:67213769-67213770	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs140188606	chr14:67213783-67213784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532262373	chr14:67213854-67213855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs112142421	chr14:67213907-67213908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565378327	chr14:67213958-67213959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373429009	chr14:67214046-67214047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs79618672	chr14:67214130-67214131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371482672	chr14:67214167-67214168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567960560	chr14:67214172-67214173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs143859468	chr14:67214220-67214221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115587816	chr14:67214221-67214222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576543134	chr14:67214268-67214269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539174236	chr14:67214276-67214277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577147152	chr14:67214290-67214291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs572525012	chr14:67214291-67214292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35180294	chr14:67214330-67214331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541445039	chr14:67214336-67214337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561232033	chr14:67214342-67214343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574696620	chr14:67214573-67214574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368460399	chr14:67214601-67214602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543331494	chr14:67214630-67214631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs563534622	chr14:67214637-67214638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs12897164	chr14:67214699-67214700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs532198885	chr14:67214752-67214753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551900381	chr14:67214785-67214786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs9783678	chr14:67214811-67214812	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs146848544	chr14:67214863-67214864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541057070	chr14:67214876-67214877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547800554	chr14:67214917-67214918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575000098	chr14:67214934-67214935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567940951	chr14:67214945-67214946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs536984894	chr14:67214951-67214952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148979495	chr14:67214979-67214980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs35036515	chr14:67214983-67214984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111958614	chr14:67215130-67215131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570274805	chr14:67215146-67215147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186292386	chr14:67215156-67215157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115542390	chr14:67215161-67215162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116355552	chr14:67215174-67215175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs8008369	chr14:67215196-67215197	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs545858374	chr14:67215222-67215223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554978411	chr14:67215226-67215227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541632939	chr14:67215230-67215231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574726483	chr14:67215238-67215239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189107802	chr14:67215239-67215240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574788417	chr14:67215269-67215270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556972297	chr14:67215270-67215271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs151058419	chr14:67215305-67215306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs111264784	chr14:67215313-67215314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552801249	chr14:67215342-67215343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Acute myeloid leukemia	21251322	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Autism	22495309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21611746	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67208200-67219400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr14:67212000-67213800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr14:67212200-67218600	Weak transcription	GM12878-XiMat	blood
4	chr14:67212600-67214000	Enhancers	Liver	Liver
5	chr14:67213400-67213800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr14:67213400-67213800	Enhancers	Brain Cingulate Gyrus	brain
7	chr14:67213800-67215400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr14:67214000-67224600	Weak transcription	Liver	Liver
9	chr14:67214600-67214800	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr14:67214800-67216200	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr14:67215400-67217200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr14:67216200-67216400	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr14:67216400-67223200	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr14:67217000-67217600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr14:67217200-67218800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr14:67217800-67224600	Weak transcription	Pancreas	Pancrea
17	chr14:67218600-67218800	Flanking Active TSS	GM12878-XiMat	blood
18	chr14:67218800-67219000	Enhancers	GM12878-XiMat	blood
19	chr14:67218800-67219400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr14:67219000-67219200	Flanking Active TSS	GM12878-XiMat	blood
21	chr14:67219200-67219600	Enhancers	GM12878-XiMat	blood
22	chr14:67223200-67223400	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr14:67224400-67225600	Enhancers	HepG2	liver
24	chr14:67224600-67225400	Enhancers	Liver	Liver
25	chr14:67224600-67225400	Enhancers	Duodenum Mucosa	Duodenum
26	chr14:67224600-67225400	Enhancers	Pancreas	Pancrea
27	chr14:67225200-67226400	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr14:67225200-67226600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr14:67225400-67256400	Weak transcription	Pancreas	Pancrea
30	chr14:67232200-67232400	Enhancers	Psoas Muscle	Psoas
31	chr14:67232400-67244400	Weak transcription	Psoas Muscle	Psoas
32	chr14:67237600-67238400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr14:67237600-67258800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr14:67238000-67238200	Enhancers	Liver	Liver
35	chr14:67238200-67256400	Weak transcription	Liver	Liver
36	chr14:67239600-67240000	Enhancers	HUVEC	blood vessel
37	chr14:67239800-67240000	ZNF genes & repeats	Fetal Intestine Small	intestine
38	chr14:67240000-67254800	Weak transcription	Fetal Intestine Small	intestine
39	chr14:67242600-67256200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr14:67242800-67245600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr14:67244200-67249600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr14:67247400-67249800	Weak transcription	Left Ventricle	heart
43	chr14:67248400-67259000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr14:67248800-67251400	Weak transcription	Fetal Lung	lung
45	chr14:67248800-67251800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr14:67249000-67250200	Weak transcription	Duodenum Mucosa	Duodenum
47	chr14:67249600-67250200	Enhancers	HepG2	liver
48	chr14:67249600-67250600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr14:67249800-67250400	Strong transcription	Left Ventricle	heart
50	chr14:67250200-67250400	ZNF genes & repeats	Duodenum Mucosa	Duodenum

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