Variant report

Variant	nsv564179
Chromosome Location	chr14:31919728-31972289
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:637)
CpG islands
(count:671)
Chromatin interactive
region (count:29)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:637 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:31925760-31927934	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:31926692-31926973	K562	blood:	n/a	n/a
3	ATF1	chr14:31926120-31926865	K562	blood:	n/a	n/a
4	ATF2	chr14:31958860-31959365	GM12878	blood:	n/a	n/a
5	BACH1	chr14:31926111-31926143	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr14:31969113-31969289	GM12878	blood:	n/a	n/a
7	BCL3	chr14:31925991-31926652	A549	lung:	n/a	n/a
8	BCLAF1	chr14:31926271-31926791	GM12878	blood:	n/a	n/a
9	BHLHE40	chr14:31926046-31926988	K562	blood:	n/a	n/a
10	BHLHE40	chr14:31927411-31928024	HepG2	liver:	n/a	n/a
11	BHLHE40	chr14:31926041-31926306	GM12878	blood:	n/a	n/a
12	BHLHE40	chr14:31927568-31927695	K562	blood:	n/a	n/a
13	BHLHE40	chr14:31926519-31926988	GM12878	blood:	n/a	n/a
14	BHLHE40	chr14:31926028-31927013	HepG2	liver:	n/a	n/a
15	BRCA1	chr14:31926624-31926988	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr14:31926086-31926643	HepG2	liver:	n/a	n/a
17	CCNT2	chr14:31925188-31925343	K562	blood:	n/a	n/a
18	CCNT2	chr14:31926229-31926887	K562	blood:	n/a	n/a
19	CEBPB	chr14:31927588-31927796	H1-hESC	embryonic stem cell:	n/a	chr14:31927770-31927781
20	CEBPB	chr14:31927555-31927968	MCF-7	breast:	n/a	chr14:31927770-31927781
21	CEBPB	chr14:31927395-31928100	MCF-7	breast:	n/a	chr14:31927770-31927781
22	CEBPB	chr14:31926006-31926819	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:31927299-31927966	HepG2	liver:	n/a	chr14:31927770-31927781
24	CEBPB	chr14:31926004-31926891	HepG2	liver:	n/a	n/a
25	CEBPB	chr14:31925985-31926709	HepG2	liver:	n/a	n/a
26	CEBPB	chr14:31926492-31926814	HepG2	liver:	n/a	n/a
27	CEBPB	chr14:31927518-31927890	HepG2	liver:	n/a	chr14:31927770-31927781
28	CEBPB	chr14:31963434-31963492	HepG2	liver:	n/a	chr14:31963452-31963463
29	CEBPB	chr14:31927445-31927920	HepG2	liver:	n/a	chr14:31927770-31927781
30	CEBPB	chr14:31925935-31926927	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr14:31927333-31927968	HepG2	liver:	n/a	chr14:31927770-31927781
32	CEBPD	chr14:31926093-31926858	HepG2	liver:	n/a	n/a
33	CEBPD	chr14:31926004-31926865	HepG2	liver:	n/a	n/a
34	CHD1	chr14:31925940-31926644	GM12878	blood:	n/a	n/a
35	CHD1	chr14:31925862-31926595	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr14:31926052-31926858	GM12878	blood:	n/a	n/a
37	CHD2	chr14:31925986-31926975	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr14:31958944-31959261	GM12878	blood:	n/a	n/a
39	CHD2	chr14:31926398-31926598	K562	blood:	n/a	n/a
40	CHD2	chr14:31926126-31926820	HepG2	liver:	n/a	n/a
41	CHD2	chr14:31962333-31962472	GM12878	blood:	n/a	n/a
42	CHD2	chr14:31926114-31926772	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr14:31927110-31927919	HepG2	liver:	n/a	n/a
44	CREB1	chr14:31925928-31927039	HepG2	liver:	n/a	n/a
45	CREB1	chr14:31926352-31926870	A549	lung:	n/a	n/a
46	CREB1	chr14:31926552-31926798	A549	lung:	n/a	n/a
47	CTCF	chr14:31926080-31926230	HepG2	liver:	n/a	n/a
48	CTCF	chr14:31926718-31926898	MCF-7	breast:	n/a	n/a
49	CTCF	chr14:31926680-31926830	SAEC	small airway:	n/a	n/a
50	CTCF	chr14:31926773-31926846	ProgFib	skin:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:31926862-31926912	HUVEC	blood vessel:	n/a
2	chr14:31926792-31926842	HAEpiC	amniotic membrane:	n/a
3	chr14:31927974-31928024	GM19239	blood:	n/a
4	chr14:31926789-31926839	AG09309	skin:	n/a
5	chr14:31926483-31926533	GM12878	blood:	n/a
6	chr14:31926792-31926842	ProgFib	skin:	n/a
7	chr14:31926862-31926912	A549	lung:	n/a
8	chr14:31929696-31929746	GM12878	blood:	n/a
9	chr14:31926862-31926912	Hela-S3	cervix:	n/a
10	chr14:31927974-31928024	HMEC	breast:	n/a
11	chr14:31927974-31928024	GM12878	blood:	n/a
12	chr14:31926564-31926614	SK-N-SH	brain:	n/a
13	chr14:31926862-31926912	SKMC	muscle:	n/a
14	chr14:31926776-31926826	K562	blood:	n/a
15	chr14:31926564-31926614	HRCEpiC	kidney:	n/a
16	chr14:31929696-31929746	LNCaP	prostate:	n/a
17	chr14:31926299-31926349	HNPCEpiC	eye:	n/a
18	chr14:31926299-31926349	PrEC	prostate:	n/a
19	chr14:31927974-31928024	PFSK-1	brain:	n/a
20	chr14:31929696-31929746	SK-N-MC	brain:	n/a
21	chr14:31926792-31926842	ECC-1	luminal epithelium:	n/a
22	chr14:31926564-31926614	Hela-S3	cervix:	n/a
23	chr14:31927974-31928024	MCF10A-Er-Src	breast:	n/a
24	chr14:31926483-31926533	HMEC	breast:	n/a
25	chr14:31926299-31926349	SK-N-SH	brain:	n/a
26	chr14:31926789-31926839	AG04450	lung:	fetal
27	chr14:31926483-31926533	HL-60	blood:	n/a
28	chr14:31927974-31928024	K562	blood:	n/a
29	chr14:31923667-31923717	HRPEpiC	eye:	n/a
30	chr14:31926483-31926533	Jurkat	blood:	n/a
31	chr14:31927974-31928024	BJ	skin:	n/a
32	chr14:31927974-31928024	AoSMC	blood vessel:	n/a
33	chr14:31926216-31926266	BJ	skin:	n/a
34	chr14:31926564-31926614	LNCaP	prostate:	n/a
35	chr14:31926216-31926266	HMEC	breast:	n/a
36	chr14:31929696-31929746	SK-N-SH	brain:	n/a
37	chr14:31926862-31926912	HMEC	breast:	n/a
38	chr14:31926299-31926349	HRCEpiC	kidney:	n/a
39	chr14:31927974-31928024	NH-A	brain:	n/a
40	chr14:31929696-31929746	IMR90	lung:	fetal
41	chr14:31926789-31926839	HepG2	liver:	n/a
42	chr14:31927974-31928024	PrEC	prostate:	n/a
43	chr14:31929696-31929746	MCF10A-Er-Src	breast:	n/a
44	chr14:31926792-31926842	Hepatocyte	liver:	n/a
45	chr14:31926792-31926842	HRPEpiC	eye:	n/a
46	chr14:31926299-31926349	GM12891	blood:	n/a
47	chr14:31929696-31929746	ovcar-3	ovarian:	n/a
48	chr14:31926789-31926839	NH-A	brain:	n/a
49	chr14:31929696-31929746	SK-N-SH_RA	brain:	n/a
50	chr14:31926299-31926349	Hepatocyte	liver:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:31676519..31677499-chr14:31926219..31927033,2	HCT-116	colon:
2	chr11:65189842..65190451-chr14:31926170..31926697,2	Hela-S3	cervix:
3	chr14:31918485..31921453-chr14:31921609..31924237,3	MCF-7	breast:
4	chr14:31950717..31953457-chr14:31954097..31956557,2	MCF-7	breast:
5	chr14:31947442..31950402-chr14:31952570..31954101,2	K562	blood:
6	chr14:31926057..31926979-chr20:2632755..2633485,2	NB4	blood:
7	chr14:31923625..31927013-chr14:32030157..32032112,3	K562	blood:
8	chr14:31915577..31920525-chr14:31924298..31927871,6	MCF-7	breast:
9	chr14:31675457..31678157-chr14:31923548..31926271,3	MCF-7	breast:
10	chr11:122932393..122933144-chr14:31926505..31927244,2	NB4	blood:
11	chr14:31924768..31927652-chr14:31950974..31952580,2	K562	blood:
12	chr14:31925687..31926473-chr17:8076447..8076967,2	Hela-S3	cervix:
13	chr14:31914833..31916596-chr14:31919367..31920967,2	MCF-7	breast:
14	chr14:31857830..31860114-chr14:31922683..31925572,2	K562	blood:
15	chr14:31926128..31926628-chr21:34851837..34852441,2	HCT-116	colon:
16	chr14:31888318..31891005-chr14:31919529..31921805,3	MCF-7	breast:
17	chr14:31926509..31929146-chr14:31940368..31943663,3	MCF-7	breast:
18	chr14:31881996..31884911-chr14:31918681..31921369,2	MCF-7	breast:
19	chr14:31887046..31892106-chr14:31923824..31928892,9	K562	blood:
20	chr14:31888413..31890616-chr14:31917360..31920011,3	MCF-7	breast:
21	chr14:31917093..31923585-chr14:31924368..31929094,11	MCF-7	breast:
22	chr14:31925036..31927590-chr14:31947189..31950405,3	MCF-7	breast:
23	chr14:31925030..31927583-chr14:31933327..31936225,2	MCF-7	breast:
24	chr14:31872181..31874850-chr14:31924970..31926788,2	K562	blood:
25	chr14:31494077..31496185-chr14:31924915..31927180,2	K562	blood:
26	chr14:31887818..31891601-chr14:31923594..31927929,15	K562	blood:
27	chr14:31918485..31921453-chr14:31921609..31924237,3	MCF-7	breast:
28	chr14:31926644..31929603-chr14:31946033..31947573,2	K562	blood:
29	chr14:31913970..31917383-chr14:31917651..31919831,3	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP4S1-2	chr14:31959233-31959309	XLOC_010789
2	lnc-NUBPL-1	chr14:31921313-31922089	ENSG00000250365
3	lnc-C14orf126-7	chr14:31932001-31932577	NONHSAT036283

No data

Variant related genes	Relation type
NUBPL	TF binding region
ENSG00000239323	TF binding region
ENSG00000203546	TF binding region
DTD2	TF binding region
GPR33	TF binding region
NUBPL	CpG island
ENSG00000239323	CpG island
ENSG00000203546	CpG island
DTD2	CpG island
GPR33	CpG island
ENSG00000129480	chromatin interactions
ENSG00000109971	chromatin interactions
ENSG00000257155	chromatin interactions
ENSG00000151413	chromatin interactions
ENSG00000250365	chromatin interactions
ENSG00000200463	chromatin interactions
ENSG00000101361	chromatin interactions
ENSG00000142188	chromatin interactions
ENSG00000092148	chromatin interactions
ENSG00000100478	chromatin interactions
ENSG00000214943	chromatin interactions
ENSG00000196792	chromatin interactions
ENSG00000203546	chromatin interactions
ENSG00000245532	chromatin interactions
ENSG00000221062	chromatin interactions
ENSG00000129493	chromatin interactions

Extended variants
information (count: 1721 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1721 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7157390	chr14:31919728-31919729	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184222021	chr14:31919785-31919786	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs532729867	chr14:31919842-31919843	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs147773546	chr14:31919852-31919853	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs560093192	chr14:31919879-31919880	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs530378494	chr14:31920035-31920036	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs187419446	chr14:31920087-31920088	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs570494039	chr14:31920103-31920104	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs534595049	chr14:31920134-31920135	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs55748651	chr14:31920151-31920152	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs116681717	chr14:31920159-31920160	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs78701558	chr14:31920168-31920169	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs79235129	chr14:31920170-31920171	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs75326097	chr14:31920171-31920172	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs191498050	chr14:31920181-31920182	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs184765944	chr14:31920191-31920192	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs570592332	chr14:31920300-31920301	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs534811883	chr14:31920310-31920311	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs190016338	chr14:31920327-31920328	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs568023218	chr14:31920380-31920381	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs535330552	chr14:31920384-31920385	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs574645035	chr14:31920412-31920413	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs141072133	chr14:31920415-31920416	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs541736541	chr14:31920422-31920423	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs180797493	chr14:31920441-31920442	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs184580402	chr14:31920526-31920527	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs559007280	chr14:31920537-31920538	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs577222406	chr14:31920558-31920559	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs565765079	chr14:31920586-31920587	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs190267324	chr14:31920589-31920590	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs181962635	chr14:31920595-31920596	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs530441356	chr14:31920620-31920621	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs111959891	chr14:31920627-31920628	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs542521971	chr14:31920640-31920641	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs563309206	chr14:31920643-31920644	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs142508129	chr14:31920644-31920645	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs71430960	chr14:31920652-31920653	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs371878049	chr14:31920653-31920654	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs552030262	chr14:31920654-31920655	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs570527500	chr14:31920655-31920656	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs71971493	chr14:31920658-31920659	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs34116335	chr14:31920667-31920668	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs71115010	chr14:31920668-31920669	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs76309235	chr14:31920669-31920670	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs528131446	chr14:31920745-31920746	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs546404368	chr14:31920755-31920756	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs117579788	chr14:31920756-31920757	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs372518015	chr14:31920780-31920781	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs535387547	chr14:31920795-31920796	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs185930465	chr14:31920803-31920804	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	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:877 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31890400-31921200	Weak transcription	Psoas Muscle	Psoas
2	chr14:31890400-31925800	Weak transcription	Right Ventricle	heart
3	chr14:31890600-31920600	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr14:31890600-31922400	Weak transcription	Brain Angular Gyrus	brain
5	chr14:31890800-31920800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr14:31890800-31925200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr14:31900400-31920200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr14:31901200-31921200	Weak transcription	Brain Substantia Nigra	brain
9	chr14:31901200-31922400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr14:31901800-31920400	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr14:31904600-31920600	Weak transcription	Left Ventricle	heart
12	chr14:31904600-31925200	Weak transcription	Fetal Brain Male	brain
13	chr14:31905000-31920600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr14:31905200-31925800	Weak transcription	NHDF-Ad	bronchial
15	chr14:31907000-31925200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr14:31908000-31920000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr14:31909800-31920800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr14:31910600-31924400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr14:31911000-31919800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr14:31911000-31920800	Weak transcription	Ovary	ovary
21	chr14:31911000-31925200	Weak transcription	Rectal Smooth Muscle	rectum
22	chr14:31911000-31925200	Weak transcription	K562	blood
23	chr14:31911200-31920800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr14:31911200-31925800	Weak transcription	Fetal Intestine Small	intestine
25	chr14:31911400-31921000	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr14:31911400-31921000	Weak transcription	HMEC	breast
27	chr14:31911600-31921200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr14:31911600-31925200	Weak transcription	Placenta	Placenta
29	chr14:31911600-31926000	Weak transcription	Lung	lung
30	chr14:31911800-31921000	Weak transcription	Fetal Kidney	kidney
31	chr14:31912000-31920600	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr14:31912000-31925800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr14:31912200-31920600	Weak transcription	NH-A	brain
34	chr14:31912200-31921000	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr14:31912200-31925200	Weak transcription	HSMMtube	muscle
36	chr14:31912200-31925200	Weak transcription	NHLF	lung
37	chr14:31913000-31921200	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr14:31913200-31920800	Weak transcription	Brain Germinal Matrix	brain
39	chr14:31913600-31925200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr14:31913800-31923600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr14:31914000-31926000	Weak transcription	Small Intestine	intestine
42	chr14:31914400-31920600	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr14:31914800-31922600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr14:31914800-31922600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr14:31914800-31925200	Weak transcription	Fetal Stomach	stomach
46	chr14:31915200-31921200	Weak transcription	Fetal Intestine Large	intestine
47	chr14:31915200-31921200	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr14:31915200-31925200	Weak transcription	Primary T cells from cord blood	blood
49	chr14:31915400-31920000	Weak transcription	Duodenum Mucosa	Duodenum
50	chr14:31915400-31922600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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