Variant report

Variant	nsv526200
Chromosome Location	chr14:32308511-32454372
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1963)
CpG islands
(count:610)
Chromatin interactive
region (count:38)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1963 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:32336820-32337151	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:32435269-32435821	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:32363573-32363850	K562	blood:	n/a	n/a
4	ARID3A	chr14:32435419-32435511	K562	blood:	n/a	n/a
5	ARID3A	chr14:32324410-32324953	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:32405430-32405611	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:32410542-32410944	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:32406936-32407273	K562	blood:	n/a	n/a
9	ARID3A	chr14:32436746-32437119	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:32395314-32395700	HepG2	liver:	n/a	n/a
11	ARID3A	chr14:32413392-32414034	HepG2	liver:	n/a	n/a
12	ARID3A	chr14:32406856-32407357	HepG2	liver:	n/a	n/a
13	ARID3A	chr14:32328061-32328458	HepG2	liver:	n/a	n/a
14	ARID3A	chr14:32371343-32371443	HepG2	liver:	n/a	n/a
15	ARID3A	chr14:32399791-32399991	HepG2	liver:	n/a	n/a
16	ARID3A	chr14:32364687-32364887	HepG2	liver:	n/a	n/a
17	ARID3A	chr14:32371298-32371463	K562	blood:	n/a	n/a
18	ARID3A	chr14:32420002-32420133	K562	blood:	n/a	n/a
19	ATF1	chr14:32406911-32407288	K562	blood:	n/a	n/a
20	ATF1	chr14:32396643-32396811	K562	blood:	n/a	n/a
21	ATF1	chr14:32363503-32363948	K562	blood:	n/a	n/a
22	ATF1	chr14:32370963-32371540	K562	blood:	n/a	n/a
23	ATF1	chr14:32346315-32346347	K562	blood:	n/a	n/a
24	ATF1	chr14:32372421-32372751	K562	blood:	n/a	n/a
25	ATF2	chr14:32406895-32407392	GM12878	blood:	n/a	n/a
26	ATF3	chr14:32406991-32407216	K562	blood:	n/a	n/a
27	ATF3	chr14:32324566-32324812	HepG2	liver:	n/a	n/a
28	ATF3	chr14:32399677-32400179	A549	lung:	n/a	n/a
29	ATF3	chr14:32371180-32371540	K562	blood:	n/a	n/a
30	ATF3	chr14:32406922-32407305	K562	blood:	n/a	n/a
31	ATF3	chr14:32371304-32371469	K562	blood:	n/a	n/a
32	BACH1	chr14:32406875-32407361	K562	blood:	n/a	chr14:32407162-32407176
33	BACH1	chr14:32401901-32402010	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr14:32407027-32407290	H1-hESC	embryonic stem cell:	n/a	chr14:32407162-32407176
35	BATF	chr14:32406904-32407398	GM12878	blood:	n/a	chr14:32407137-32407147 chr14:32407140-32407151
36	BATF	chr14:32406928-32407345	GM12878	blood:	n/a	chr14:32407137-32407147 chr14:32407140-32407151
37	BATF	chr14:32312682-32312995	GM12878	blood:	n/a	chr14:32312694-32312704
38	BCL11A	chr14:32406965-32407373	GM12878	blood:	n/a	chr14:32407102-32407111
39	BCL11A	chr14:32406983-32407282	GM12878	blood:	n/a	chr14:32407102-32407111
40	BCLAF1	chr14:32406918-32407313	GM12878	blood:	n/a	chr14:32407102-32407111
41	BCLAF1	chr14:32395264-32395602	GM12878	blood:	n/a	n/a
42	BHLHE40	chr14:32385414-32385519	HepG2	liver:	n/a	n/a
43	BHLHE40	chr14:32406967-32407309	GM12878	blood:	n/a	n/a
44	BHLHE40	chr14:32403994-32404312	HepG2	liver:	n/a	n/a
45	BHLHE40	chr14:32385333-32385552	K562	blood:	n/a	n/a
46	BHLHE40	chr14:32404049-32404249	A549	lung:	n/a	n/a
47	BHLHE40	chr14:32437752-32437933	GM12878	blood:	n/a	n/a
48	BHLHE40	chr14:32346581-32346736	HepG2	liver:	n/a	n/a
49	BHLHE40	chr14:32435380-32435580	K562	blood:	n/a	n/a
50	BHLHE40	chr14:32406943-32407315	HepG2	liver:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:32413698-32413748	ProgFib	skin:	n/a
2	chr14:32328771-32328821	SAEC	small airway:	n/a
3	chr14:32350324-32350374	H1-hESC	embryonic stem cell:	embryo
4	chr14:32435490-32435540	Jurkat	blood:	n/a
5	chr14:32363503-32363553	NH-A	brain:	n/a
6	chr14:32350324-32350374	HCM	heart:	n/a
7	chr14:32396820-32396870	BJ	skin:	n/a
8	chr14:32364560-32364610	ECC-1	luminal epithelium:	n/a
9	chr14:32350324-32350374	SK-N-SH	brain:	n/a
10	chr14:32435490-32435540	ECC-1	luminal epithelium:	n/a
11	chr14:32404458-32404508	SK-N-MC	brain:	n/a
12	chr14:32413698-32413748	NHDF-neo	bronchial:	n/a
13	chr14:32350428-32350478	RPTEC	kidney:	n/a
14	chr14:32435490-32435540	LNCaP	prostate:	n/a
15	chr14:32350324-32350374	NH-A	brain:	n/a
16	chr14:32413698-32413748	HCF	heart:	n/a
17	chr14:32413698-32413748	AG10803	skin:	n/a
18	chr14:32420205-32420255	RPTEC	kidney:	n/a
19	chr14:32363503-32363553	HL-60	blood:	n/a
20	chr14:32396820-32396870	NT2-D1	testis:	n/a
21	chr14:32328771-32328821	NHBE	bronchial:	n/a
22	chr14:32350428-32350478	BJ	skin:	n/a
23	chr14:32350428-32350478	IMR90	lung:	fetal
24	chr14:32350324-32350374	ECC-1	luminal epithelium:	n/a
25	chr14:32328771-32328821	NT2-D1	testis:	n/a
26	chr14:32404458-32404508	LNCaP	prostate:	n/a
27	chr14:32404458-32404508	SKMC	muscle:	n/a
28	chr14:32350324-32350374	IMR90	lung:	fetal
29	chr14:32420205-32420255	ECC-1	luminal epithelium:	n/a
30	chr14:32413698-32413748	AG04449	skin:	fetal
31	chr14:32420205-32420255	Hepatocyte	liver:	n/a
32	chr14:32350428-32350478	HEEpiC	esophagus:	n/a
33	chr14:32404458-32404508	HCF	heart:	n/a
34	chr14:32404458-32404508	HepG2	liver:	n/a
35	chr14:32364560-32364610	HEEpiC	esophagus:	n/a
36	chr14:32420205-32420255	HAEpiC	amniotic membrane:	n/a
37	chr14:32350324-32350374	Hela-S3	cervix:	n/a
38	chr14:32364560-32364610	CMK	blood:	n/a
39	chr14:32435490-32435540	HUVEC	blood vessel:	n/a
40	chr14:32363503-32363553	HCPEpiC	choroid plexus:	n/a
41	chr14:32363503-32363553	SAEC	small airway:	n/a
42	chr14:32328771-32328821	HEEpiC	esophagus:	n/a
43	chr14:32404458-32404508	HCT-116	colon:	n/a
44	chr14:32413698-32413748	NB4	blood:	n/a
45	chr14:32396820-32396870	AG10803	skin:	n/a
46	chr14:32328771-32328821	HNPCEpiC	eye:	n/a
47	chr14:32328771-32328821	HCPEpiC	choroid plexus:	n/a
48	chr14:32350324-32350374	HIPEpiC	eye:	n/a
49	chr14:32328771-32328821	HL-60	blood:	n/a
50	chr14:32350324-32350374	NT2-D1	testis:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:32369516..32371564-chr14:32376698..32378777,2	MCF-7	breast:
2	chr14:32404299..32405896-chr14:32722271..32724714,2	MCF-7	breast:
3	chr14:32394986..32395973-chr14:32938340..32938867,2	K562	blood:
4	chr14:32340007..32341798-chr14:32343859..32345846,2	K562	blood:
5	chr14:32452982..32453943-chr14:32542808..32543419,2	MCF-7	breast:
6	chr14:32369516..32371564-chr14:32376698..32378777,2	MCF-7	breast:
7	chr14:32303855..32305860-chr14:32313557..32315760,2	MCF-7	breast:
8	chr14:32394037..32396201-chr16:75304956..75307730,2	MCF-7	breast:
9	chr14:32405775..32408648-chr14:32433205..32435677,2	K562	blood:
10	chr14:32395062..32396238-chr14:32721028..32721952,3	MCF-7	breast:
11	chr14:32341518..32343411-chr14:32344329..32346208,2	MCF-7	breast:
12	chr14:32404853..32406467-chr14:32545391..32547317,2	MCF-7	breast:
13	chr14:32341518..32343411-chr14:32344329..32346208,2	MCF-7	breast:
14	chr14:32394989..32395944-chr14:32721409..32721963,3	K562	blood:
15	chr14:32407172..32410124-chr14:32413888..32415450,2	MCF-7	breast:
16	chr14:32405775..32408648-chr14:32433205..32435677,2	K562	blood:
17	chr14:32394915..32396057-chr14:32721234..32722134,5	MCF-7	breast:
18	chr14:32412347..32415225-chr14:32417011..32419996,3	MCF-7	breast:
19	chr14:32418462..32421329-chr14:32545887..32548430,2	MCF-7	breast:
20	chr14:32407297..32408889-chr14:32413240..32415265,2	K562	blood:
21	chr14:32388285..32389795-chr14:32392007..32393966,2	K562	blood:
22	chr14:32360805..32362723-chr14:32544749..32546621,2	K562	blood:
23	chr14:32404484..32405348-chr14:32542806..32543426,2	MCF-7	breast:
24	chr14:32316314..32318915-chr14:32319714..32322323,3	K562	blood:
25	chr14:32428349..32431269-chr14:32434384..32437911,3	K562	blood:
26	chr14:32414286..32416412-chr14:32544564..32547544,2	MCF-7	breast:
27	chr14:32409592..32411316-chr14:32413977..32416384,2	K562	blood:
28	chr14:32385965..32386716-chr8:88512662..88513393,2	MCF-7	breast:
29	chr14:32316314..32318915-chr14:32319714..32322323,3	K562	blood:
30	chr14:32415369..32417109-chr14:32417144..32419896,2	MCF-7	breast:
31	chr14:32403221..32404535-chr14:32721037..32721949,6	MCF-7	breast:
32	chr14:32340007..32341798-chr14:32343859..32345846,2	K562	blood:
33	chr14:32394502..32396600-chr14:32540991..32542877,2	K562	blood:
34	chr14:32415369..32417109-chr14:32417144..32419896,2	MCF-7	breast:
35	chr14:32404021..32404551-chr14:32713638..32714218,2	MCF-7	breast:
36	chr14:32403773..32404594-chr14:32713792..32714300,2	MCF-7	breast:
37	chr14:32388285..32389795-chr14:32392007..32393966,2	K562	blood:
38	chr14:32428349..32431269-chr14:32434384..32437911,3	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C14orf126-3	chr14:32398586-32399352	ENSG00000257472
2	lnc-C14orf126-3	chr14:32395007-32395475	ENSG00000257472

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	NUBPL	hsa-miR-24-3p	chr14:32329735-32329757

Variant related genes	Relation type
NUBPL	TF binding region
ENSG00000257472	TF binding region
ENSG00000258474	TF binding region
NUBPL	CpG island
ENSG00000257472	CpG island
ENSG00000258474	CpG island
ENSG00000100852	chromatin interactions
ENSG00000258474	chromatin interactions
ENSG00000258655	chromatin interactions

Extended variants
information (count: 5265 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:5265 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1959071	chr14:32308511-32308512	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs146613265	chr14:32308513-32308514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116335828	chr14:32308569-32308570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186066550	chr14:32308650-32308651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113065280	chr14:32308654-32308655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111950818	chr14:32308695-32308696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554828090	chr14:32308712-32308713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192220145	chr14:32308722-32308723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs117265861	chr14:32308731-32308732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562530323	chr14:32308738-32308739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543603879	chr14:32308741-32308742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558675941	chr14:32308742-32308743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181961291	chr14:32308745-32308746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142462688	chr14:32308760-32308761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559420215	chr14:32308763-32308764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371020964	chr14:32308765-32308766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs118139856	chr14:32308773-32308774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563564954	chr14:32308777-32308778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs114143598	chr14:32308799-32308800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533183004	chr14:32308850-32308851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs151336758	chr14:32308920-32308921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140602751	chr14:32308996-32308997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185972048	chr14:32309015-32309016	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559585081	chr14:32309098-32309099	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528312434	chr14:32309125-32309126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535271001	chr14:32309169-32309170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375460751	chr14:32309192-32309193	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs8023131	chr14:32309226-32309227	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs566201180	chr14:32309247-32309248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs118017685	chr14:32309302-32309303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs190642152	chr14:32309326-32309327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569715752	chr14:32309330-32309331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558943767	chr14:32309340-32309341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs79563705	chr14:32309341-32309342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs117693770	chr14:32309357-32309358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577337233	chr14:32309373-32309374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs34384458	chr14:32309386-32309387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541637950	chr14:32309410-32309411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552776212	chr14:32309414-32309415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113443745	chr14:32309434-32309435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs367709874	chr14:32309437-32309438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115090817	chr14:32309438-32309439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535757892	chr14:32309494-32309495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112393078	chr14:32309505-32309506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557662637	chr14:32309507-32309508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546092971	chr14:32309513-32309514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35411605	chr14:32309537-32309538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564434256	chr14:32309595-32309596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs150095668	chr14:32309596-32309597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138644921	chr14:32309618-32309619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1779 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32250600-32322400	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr14:32281800-32330200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr14:32291000-32310400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr14:32294200-32328800	Weak transcription	Ovary	ovary
5	chr14:32294800-32328000	Weak transcription	Left Ventricle	heart
6	chr14:32295000-32332800	Weak transcription	Primary hematopoietic stem cells	blood
7	chr14:32297400-32325800	Weak transcription	Primary B cells from cord blood	blood
8	chr14:32298200-32322000	Weak transcription	Primary T cells from cord blood	blood
9	chr14:32299000-32325800	Weak transcription	Fetal Stomach	stomach
10	chr14:32304200-32319600	Weak transcription	HepG2	liver
11	chr14:32304400-32312200	Weak transcription	Esophagus	oesophagus
12	chr14:32304600-32312200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr14:32304600-32312400	Weak transcription	HUVEC	blood vessel
14	chr14:32305600-32309000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr14:32309000-32309200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr14:32309200-32330000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr14:32311600-32313000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr14:32311600-32328000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr14:32311800-32313200	Enhancers	GM12878-XiMat	blood
20	chr14:32312200-32312400	Enhancers	Esophagus	oesophagus
21	chr14:32312200-32312400	Enhancers	Rectal Mucosa Donor 29	rectum
22	chr14:32312200-32312600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr14:32312200-32312600	Enhancers	Colonic Mucosa	Colon
24	chr14:32312200-32312600	Enhancers	Fetal Brain Female	brain
25	chr14:32312200-32312600	Enhancers	Sigmoid Colon	Sigmoid Colon
26	chr14:32312200-32312800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr14:32312200-32313000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr14:32312200-32313000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr14:32312200-32313000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr14:32312200-32313000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr14:32312200-32313000	Enhancers	HSMM	muscle
32	chr14:32312200-32313200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr14:32312200-32313200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr14:32312200-32313200	Enhancers	Stomach Mucosa	stomach
35	chr14:32312200-32313200	Enhancers	HMEC	breast
36	chr14:32312200-32313200	Enhancers	HSMMtube	muscle
37	chr14:32312200-32313200	Enhancers	NHEK	skin
38	chr14:32312200-32313800	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr14:32312400-32312600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
40	chr14:32312400-32312800	Enhancers	Psoas Muscle	Psoas
41	chr14:32312400-32313000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr14:32312400-32313000	Enhancers	Fetal Intestine Large	intestine
43	chr14:32312400-32313000	Enhancers	Hela-S3	cervix
44	chr14:32312400-32313000	Enhancers	HUVEC	blood vessel
45	chr14:32312400-32313200	Enhancers	Muscle Satellite Cultured Cells	--
46	chr14:32312600-32313200	Enhancers	A549	lung
47	chr14:32312600-32313400	Active TSS	Rectal Mucosa Donor 29	rectum
48	chr14:32312600-32318000	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr14:32313000-32323800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr14:32313000-32327200	Weak transcription	Fetal Intestine Large	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links