Variant report

Variant	nsv518956
Chromosome Location	chr14:31958761-31983371
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	chr14:31979345-31979767	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:31979285-31979597	K562	blood:	n/a	n/a
3	ATF2	chr14:31958860-31959365	GM12878	blood:	n/a	n/a
4	BCL11A	chr14:31969113-31969289	GM12878	blood:	n/a	n/a
5	CEBPB	chr14:31974300-31974414	HepG2	liver:	n/a	chr14:31974329-31974340
6	CEBPB	chr14:31973580-31973763	HepG2	liver:	n/a	chr14:31973660-31973671
7	CEBPB	chr14:31974196-31974374	K562	blood:	n/a	chr14:31974329-31974340
8	CEBPB	chr14:31973571-31973809	IMR90	lung:	n/a	chr14:31973660-31973671
9	CEBPB	chr14:31963434-31963492	HepG2	liver:	n/a	chr14:31963452-31963463
10	CEBPB	chr14:31979609-31979839	HepG2	liver:	n/a	n/a
11	CHD2	chr14:31958944-31959261	GM12878	blood:	n/a	n/a
12	CHD2	chr14:31962333-31962472	GM12878	blood:	n/a	n/a
13	CTCF	chr14:31979460-31979610	AG10803	skin:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
14	CTCF	chr14:31979688-31979696	Spleen_OC	spleen:	n/a	n/a
15	CTCF	chr14:31979520-31979670	Caco-2	colon:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
16	CTCF	chr14:31979480-31979630	SK-N-SH_RA	brain:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
17	CTCF	chr14:31979500-31979650	GM12865	blood:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
18	CTCF	chr14:31979460-31979610	SAEC	small airway:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
19	CTCF	chr14:31979540-31979690	HVMF	connective:	n/a	n/a
20	CTCF	chr14:31979440-31979590	AG09309	skin:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
21	CTCF	chr14:31981517-31981561	Pancreas_OC	pancreas:	n/a	n/a
22	CTCF	chr14:31979560-31979710	RPTEC	kidney:	n/a	n/a
23	CTCF	chr14:31979480-31979630	GM12867	blood:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
24	CTCF	chr14:31979347-31979771	GM12878	blood:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
25	CTCF	chr14:31979480-31979630	BJ	skin:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
26	CTCF	chr14:31979460-31979610	GM12872	blood:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
27	CTCF	chr14:31978760-31978910	WI-38	lung:	n/a	n/a
28	CTCF	chr14:31979460-31979610	HCPEpiC	choroid plexus:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
29	CTCF	chr14:31979660-31979810	HEK293	kidney:	n/a	n/a
30	CTCF	chr14:31979500-31979650	HPF	lung:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
31	CTCF	chr14:31979480-31979630	GM12869	blood:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
32	CTCF	chr14:31979397-31979731	MCF-7	breast:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
33	CTCF	chr14:31963460-31963610	HepG2	liver:	n/a	n/a
34	CTCF	chr14:31979440-31979590	AG04449	skin:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
35	CTCF	chr14:31978890-31978908	GM13977	blood:	n/a	n/a
36	CTCF	chr14:31979480-31979630	HRE	kidney:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
37	CTCF	chr14:31979313-31979830	HepG2	liver:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
38	CTCF	chr14:31979480-31979630	AG04450	lung:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
39	CTCF	chr14:31979400-31979550	GM12865	blood:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
40	CTCF	chr14:31979103-31980200	A549	lung:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
41	CTCF	chr14:31979480-31979630	HCFaa	heart:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
42	CTCF	chr14:31979540-31979690	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr14:31979480-31979630	GM12873	blood:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
44	CTCF	chr14:31979460-31979610	GM12871	blood:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
45	CTCF	chr14:31979480-31979630	AG09319	gingival:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
46	CTCF	chr14:31977580-31977730	HepG2	liver:	n/a	n/a
47	CTCF	chr14:31979433-31979634	K562	blood:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
48	CTCF	chr14:31979420-31979570	GM12865	blood:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
49	CTCF	chr14:31979460-31979610	GM12868	blood:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544
50	CTCF	chr14:31979480-31979630	MCF-7	breast:	n/a	chr14:31979527-31979543 chr14:31979528-31979549 chr14:31979529-31979538 chr14:31979526-31979544

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:31974893-31974943	ECC-1	luminal epithelium:	n/a
2	chr14:31974893-31974943	HNPCEpiC	eye:	n/a
3	chr14:31974893-31974943	PrEC	prostate:	n/a
4	chr14:31974893-31974943	AG09309	skin:	n/a
5	chr14:31974893-31974943	ovcar-3	ovarian:	n/a
6	chr14:31974893-31974943	SK-N-SH	brain:	n/a
7	chr14:31974893-31974943	HMEC	breast:	n/a
8	chr14:31974893-31974943	NHDF-neo	bronchial:	n/a
9	chr14:31974893-31974943	AoSMC	blood vessel:	n/a
10	chr14:31974893-31974943	AG09319	gingival:	n/a
11	chr14:31974893-31974943	Hela-S3	cervix:	n/a
12	chr14:31974893-31974943	MCF-7	breast:	n/a
13	chr14:31974893-31974943	Hepatocyte	liver:	n/a
14	chr14:31974893-31974943	NHBE	bronchial:	n/a
15	chr14:31974893-31974943	GM06990	blood:	n/a
16	chr14:31974893-31974943	IMR90	lung:	fetal
17	chr14:31974893-31974943	BJ	skin:	n/a
18	chr14:31974893-31974943	GM12878	blood:	n/a
19	chr14:31974893-31974943	HepG2	liver:	n/a
20	chr14:31974893-31974943	PFSK-1	brain:	n/a
21	chr14:31974893-31974943	GM12892	blood:	n/a
22	chr14:31974893-31974943	AG04450	lung:	fetal
23	chr14:31974893-31974943	HAEpiC	amniotic membrane:	n/a
24	chr14:31974893-31974943	H1-hESC	embryonic stem cell:	embryo
25	chr14:31974893-31974943	CMK	blood:	n/a
26	chr14:31974893-31974943	HCPEpiC	choroid plexus:	n/a
27	chr14:31974893-31974943	A549	lung:	n/a
28	chr14:31974893-31974943	K562	blood:	n/a
29	chr14:31974893-31974943	NH-A	brain:	n/a
30	chr14:31974893-31974943	HIPEpiC	eye:	n/a
31	chr14:31974893-31974943	HRE	kidney:	n/a
32	chr14:31974893-31974943	U87	brain:	n/a
33	chr14:31974893-31974943	MCF10A-Er-Src	breast:	n/a
34	chr14:31974893-31974943	NT2-D1	testis:	n/a
35	chr14:31974893-31974943	AG04449	skin:	fetal
36	chr14:31974893-31974943	HPAEpiC	pulmonary alveolar:	n/a
37	chr14:31974893-31974943	BE2_C	brain:	n/a
38	chr14:31974893-31974943	T-47D	breast:	n/a
39	chr14:31974893-31974943	HCF	heart:	n/a
40	chr14:31974893-31974943	SK-N-MC	brain:	n/a
41	chr14:31974893-31974943	Caco-2	colon:	n/a
42	chr14:31974893-31974943	SAEC	small airway:	n/a
43	chr14:31974893-31974943	GM12891	blood:	n/a
44	chr14:31974893-31974943	RPTEC	kidney:	n/a
45	chr14:31974893-31974943	GM19239	blood:	n/a
46	chr14:31974893-31974943	HEK293	kidney:	embryo
47	chr14:31974893-31974943	Jurkat	blood:	n/a
48	chr14:31974893-31974943	AG10803	skin:	n/a
49	chr14:31974893-31974943	PANC-1	pancreas:	n/a
50	chr14:31974893-31974943	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:31979147..31979905-chr14:32256388..32256891,2	MCF-7	breast:
2	chr14:31979520..31980020-chr14:32542725..32543442,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP4S1-2	chr14:31959233-31959309	XLOC_010789

Variant related genes	Relation type
NUBPL	TF binding region
NUBPL	CpG island

Extended variants
information (count: 735 )
Associated
traits (count: 69 )

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	rs2183631	chr14:31958761-31958762	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs575257832	chr14:31958781-31958782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546055566	chr14:31958866-31958867	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs139303031	chr14:31958907-31958908	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs150045440	chr14:31958913-31958914	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs540465821	chr14:31958935-31958936	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs10139022	chr14:31958956-31958957	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs528964979	chr14:31959017-31959018	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs181533486	chr14:31959030-31959031	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs144326643	chr14:31959038-31959039	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs532970637	chr14:31959043-31959044	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs1013394	chr14:31959086-31959087	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs75305514	chr14:31959117-31959118	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs202160146	chr14:31959203-31959204	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs144893980	chr14:31959224-31959225	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs548892237	chr14:31959266-31959267	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
17	rs567484648	chr14:31959298-31959299	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
18	rs544306672	chr14:31959437-31959438	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs535550504	chr14:31959473-31959474	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs77971576	chr14:31959479-31959480	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs113550740	chr14:31959498-31959499	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs557444175	chr14:31959543-31959544	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs568872792	chr14:31959568-31959569	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs116622913	chr14:31959607-31959608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557775956	chr14:31959621-31959622	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573190107	chr14:31959639-31959640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79194714	chr14:31959641-31959642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114806415	chr14:31959663-31959664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372569341	chr14:31959673-31959674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs115662893	chr14:31959681-31959682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574196252	chr14:31959793-31959794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs57110356	chr14:31959827-31959828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565065253	chr14:31959833-31959834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200454329	chr14:31959844-31959845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186145219	chr14:31959848-31959849	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535987624	chr14:31959856-31959857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373418668	chr14:31959909-31959910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142007408	chr14:31959961-31959962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs72672700	chr14:31960000-31960001	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs77522360	chr14:31960008-31960009	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369206811	chr14:31960022-31960023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373514443	chr14:31960101-31960102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549282349	chr14:31960109-31960110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560459865	chr14:31960276-31960277	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533256019	chr14:31960289-31960290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560884982	chr14:31960331-31960332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs72672702	chr14:31960359-31960360	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs117662819	chr14:31960434-31960435	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569006495	chr14:31960489-31960490	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs151178374	chr14:31960499-31960500	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
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
Esophageal cancer	20955586	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
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21990379	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31953400-31960400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr14:31955800-31961200	Enhancers	Primary B cells from cord blood	blood
3	chr14:31956400-31963800	Enhancers	Primary B cells from peripheral blood	blood
4	chr14:31957600-31959400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr14:31957800-31960000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr14:31957800-31960200	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr14:31958600-31959000	Enhancers	GM12878-XiMat	blood
8	chr14:31959000-31959600	Flanking Active TSS	GM12878-XiMat	blood
9	chr14:31959200-31959600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr14:31959400-31959600	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr14:31959400-31959600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr14:31959400-31960200	Enhancers	Fetal Brain Male	brain
13	chr14:31959600-31959800	Enhancers	GM12878-XiMat	blood
14	chr14:31959600-31961800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr14:31959800-31961800	Weak transcription	GM12878-XiMat	blood
16	chr14:31960000-31960200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr14:31960400-31960600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
18	chr14:31960400-31961600	Enhancers	HepG2	liver
19	chr14:31961200-31961600	Weak transcription	Primary B cells from cord blood	blood
20	chr14:31961600-31962200	Bivalent Enhancer	HepG2	liver
21	chr14:31961600-31962600	Enhancers	HMEC	breast
22	chr14:31961600-31962800	Enhancers	Primary B cells from cord blood	blood
23	chr14:31961800-31962200	Enhancers	Hela-S3	cervix
24	chr14:31961800-31962400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr14:31961800-31962600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr14:31961800-31962800	Enhancers	GM12878-XiMat	blood
27	chr14:31962000-31962200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr14:31962000-31962400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr14:31962000-31962600	Enhancers	Esophagus	oesophagus
30	chr14:31962000-31962600	Enhancers	NHEK	skin
31	chr14:31962000-31968000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr14:31962200-31963400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr14:31962400-31962600	Enhancers	A549	lung
34	chr14:31963400-31963600	Enhancers	GM12878-XiMat	blood
35	chr14:31963400-31964400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr14:31972000-31974200	Enhancers	Fetal Heart	heart
37	chr14:31972400-31972600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr14:31972400-31972600	Enhancers	Aorta	Aorta
39	chr14:31972400-31974200	Weak transcription	Right Atrium	heart
40	chr14:31972600-31973400	Weak transcription	Aorta	Aorta
41	chr14:31972800-31974000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr14:31973000-31974400	Enhancers	Fetal Brain Male	brain
43	chr14:31973400-31973800	Enhancers	Aorta	Aorta
44	chr14:31973400-31976200	Enhancers	Ovary	ovary
45	chr14:31973600-31974400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr14:31973600-31974800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr14:31973800-31974000	Weak transcription	Aorta	Aorta
48	chr14:31973800-31974400	Enhancers	Left Ventricle	heart
49	chr14:31973800-31974400	Enhancers	Lung	lung
50	chr14:31974000-31974200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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