Variant report

Variant	esv1828838
Chromosome Location	chr3:17646794-17757960
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1239)
CpG islands
(count:305)
Chromatin interactive
region (count:101)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1239 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:17662995-17662997	K562	blood:	n/a	n/a
2	ARID3A	chr3:17680833-17681044	K562	blood:	n/a	n/a
3	ARID3A	chr3:17661446-17661826	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:17673539-17674340	K562	blood:	n/a	n/a
5	ARID3A	chr3:17734937-17735178	K562	blood:	n/a	n/a
6	ARID3A	chr3:17680767-17681726	HepG2	liver:	n/a	n/a
7	ATF1	chr3:17673982-17674275	K562	blood:	n/a	n/a
8	ATF1	chr3:17734896-17735339	K562	blood:	n/a	n/a
9	ATF2	chr3:17719752-17720261	GM12878	blood:	n/a	n/a
10	ATF2	chr3:17719869-17720228	GM12878	blood:	n/a	n/a
11	ATF3	chr3:17673904-17674346	K562	blood:	n/a	n/a
12	ATF3	chr3:17680608-17681751	A549	lung:	n/a	n/a
13	ATF3	chr3:17677049-17677503	A549	lung:	n/a	n/a
14	ATF3	chr3:17680668-17681742	A549	lung:	n/a	n/a
15	ATF3	chr3:17681150-17681679	HCT-116	colon:	n/a	n/a
16	ATF3	chr3:17754178-17754326	GM12878	blood:	n/a	n/a
17	BACH1	chr3:17673982-17674292	K562	blood:	n/a	n/a
18	BACH1	chr3:17676636-17676646	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr3:17674103-17674135	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr3:17673986-17674216	GM12878	blood:	n/a	n/a
21	BATF	chr3:17697294-17697587	GM12878	blood:	n/a	n/a
22	BATF	chr3:17719836-17720148	GM12878	blood:	n/a	chr3:17720079-17720089
23	BATF	chr3:17719740-17720156	GM12878	blood:	n/a	chr3:17720079-17720089
24	BCL11A	chr3:17719823-17720178	GM12878	blood:	n/a	n/a
25	BCL3	chr3:17680262-17681764	A549	lung:	n/a	n/a
26	BCL3	chr3:17681131-17681708	A549	lung:	n/a	n/a
27	BHLHE40	chr3:17734856-17735321	K562	blood:	n/a	n/a
28	BHLHE40	chr3:17681315-17681561	HepG2	liver:	n/a	n/a
29	BHLHE40	chr3:17681358-17681439	K562	blood:	n/a	n/a
30	BHLHE40	chr3:17676851-17676996	K562	blood:	n/a	n/a
31	BHLHE40	chr3:17677262-17677542	K562	blood:	n/a	n/a
32	BHLHE40	chr3:17681161-17681672	HepG2	liver:	n/a	n/a
33	BHLHE40	chr3:17680864-17681154	K562	blood:	n/a	n/a
34	BRCA1	chr3:17677219-17677434	Hela-S3	cervix:	n/a	n/a
35	CBX3	chr3:17734796-17735400	K562	blood:	n/a	n/a
36	CBX3	chr3:17734345-17735445	K562	blood:	n/a	n/a
37	CBX3	chr3:17680940-17681805	HCT-116	colon:	n/a	n/a
38	CBX3	chr3:17673887-17674282	HCT-116	colon:	n/a	n/a
39	CBX3	chr3:17646425-17646996	HCT-116	colon:	n/a	n/a
40	CBX3	chr3:17676453-17676798	K562	blood:	n/a	n/a
41	CCNT2	chr3:17734888-17735176	K562	blood:	n/a	n/a
42	CCNT2	chr3:17706948-17707136	K562	blood:	n/a	n/a
43	CEBPB	chr3:17649245-17649772	A549	lung:	n/a	n/a
44	CEBPB	chr3:17686504-17686892	K562	blood:	n/a	chr3:17686694-17686705 chr3:17686693-17686704
45	CEBPB	chr3:17673932-17674300	IMR90	lung:	n/a	n/a
46	CEBPB	chr3:17673976-17674264	A549	lung:	n/a	n/a
47	CEBPB	chr3:17663508-17663763	IMR90	lung:	n/a	n/a
48	CEBPB	chr3:17686456-17686972	MCF-7	breast:	n/a	chr3:17686694-17686705 chr3:17686693-17686704
49	CEBPB	chr3:17715664-17716107	HCT-116	colon:	n/a	chr3:17715765-17715776 chr3:17715767-17715776 chr3:17715767-17715776 chr3:17715767-17715776
50	CEBPB	chr3:17649444-17649733	A549	lung:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:17686199-17686249	ECC-1	luminal epithelium:	n/a
2	chr3:17680687-17680737	HRE	kidney:	n/a
3	chr3:17742212-17742262	NB4	blood:	n/a
4	chr3:17680687-17680737	PrEC	prostate:	n/a
5	chr3:17742789-17742839	MCF-7	breast:	n/a
6	chr3:17666379-17666429	AG04450	lung:	fetal
7	chr3:17680687-17680737	U87	brain:	n/a
8	chr3:17686199-17686249	Caco-2	colon:	n/a
9	chr3:17686199-17686249	HMEC	breast:	n/a
10	chr3:17666379-17666429	HPAEpiC	pulmonary alveolar:	n/a
11	chr3:17680687-17680737	HIPEpiC	eye:	n/a
12	chr3:17686199-17686249	ProgFib	skin:	n/a
13	chr3:17742789-17742839	HEEpiC	esophagus:	n/a
14	chr3:17742212-17742262	BJ	skin:	n/a
15	chr3:17742212-17742262	GM12892	blood:	n/a
16	chr3:17680687-17680737	Caco-2	colon:	n/a
17	chr3:17742212-17742262	BE2_C	brain:	n/a
18	chr3:17742789-17742839	LNCaP	prostate:	n/a
19	chr3:17686199-17686249	HNPCEpiC	eye:	n/a
20	chr3:17666379-17666429	HCT-116	colon:	n/a
21	chr3:17742789-17742839	GM12892	blood:	n/a
22	chr3:17742789-17742839	Hela-S3	cervix:	n/a
23	chr3:17742212-17742262	AG09319	gingival:	n/a
24	chr3:17742789-17742839	AG04449	skin:	fetal
25	chr3:17686199-17686249	SAEC	small airway:	n/a
26	chr3:17742789-17742839	HEK293	kidney:	embryo
27	chr3:17686199-17686249	Hepatocyte	liver:	n/a
28	chr3:17666379-17666429	CMK	blood:	n/a
29	chr3:17742212-17742262	Hela-S3	cervix:	n/a
30	chr3:17686199-17686249	ovcar-3	ovarian:	n/a
31	chr3:17686199-17686249	NH-A	brain:	n/a
32	chr3:17686199-17686249	HL-60	blood:	n/a
33	chr3:17666379-17666429	NHBE	bronchial:	n/a
34	chr3:17742212-17742262	PANC-1	pancreas:	n/a
35	chr3:17686199-17686249	BJ	skin:	n/a
36	chr3:17680687-17680737	GM19239	blood:	n/a
37	chr3:17742212-17742262	RPTEC	kidney:	n/a
38	chr3:17742212-17742262	HIPEpiC	eye:	n/a
39	chr3:17680687-17680737	PFSK-1	brain:	n/a
40	chr3:17742212-17742262	HCT-116	colon:	n/a
41	chr3:17742212-17742262	U87	brain:	n/a
42	chr3:17686199-17686249	A549	lung:	n/a
43	chr3:17686199-17686249	SKMC	muscle:	n/a
44	chr3:17686199-17686249	Jurkat	blood:	n/a
45	chr3:17742212-17742262	SKMC	muscle:	n/a
46	chr3:17742789-17742839	HL-60	blood:	n/a
47	chr3:17742212-17742262	Jurkat	blood:	n/a
48	chr3:17742212-17742262	Hepatocyte	liver:	n/a
49	chr3:17686199-17686249	HCF	heart:	n/a
50	chr3:17666379-17666429	HAEpiC	amniotic membrane:	n/a

(count:101 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:17743159..17745302-chr3:17783350..17785711,2	K562	blood:
2	chr3:17668314..17670997-chr3:17674062..17676778,5	K562	blood:
3	chr3:17644530..17646231-chr3:17650472..17652535,2	K562	blood:
4	chr3:17675340..17678330-chr3:17685687..17687246,2	K562	blood:
5	chr3:17731991..17733864-chr3:17783866..17786187,2	K562	blood:
6	chr3:17651090..17652832-chr3:17671455..17674137,2	K562	blood:
7	chr3:17648313..17650341-chr3:17782722..17784711,2	MCF-7	breast:
8	chr3:17728906..17731016-chr3:17783302..17786090,2	K562	blood:
9	chr3:17677327..17679225-chr3:17680575..17682681,2	K562	blood:
10	chr3:17729939..17731943-chr3:17732995..17734878,2	MCF-7	breast:
11	chr3:17697081..17699650-chr3:17703020..17705438,2	K562	blood:
12	chr3:17667671..17669916-chr3:17678475..17680012,2	MCF-7	breast:
13	chr3:17685895..17687359-chr3:17882432..17883403,5	MCF-7	breast:
14	chr3:17686538..17687204-chr7:20296816..20297526,2	MCF-7	breast:
15	chr3:17729939..17731943-chr3:17732995..17734878,2	MCF-7	breast:
16	chr3:17749020..17751309-chr3:17782613..17784937,2	MCF-7	breast:
17	chr3:17705149..17707396-chr3:17708581..17710185,2	K562	blood:
18	chr3:17681620..17683339-chr3:17686946..17688450,2	K562	blood:
19	chr3:17686325..17687848-chr3:17882370..17883316,8	K562	blood:
20	chr3:17753992..17758136-chr3:17779432..17782585,3	K562	blood:
21	chr3:17726443..17728457-chr3:17731343..17734227,2	K562	blood:
22	chr3:17697081..17699650-chr3:17703020..17705438,2	K562	blood:
23	chr3:17668314..17670732-chr3:17674253..17676778,2	K562	blood:
24	chr3:17726443..17728457-chr3:17731343..17734227,2	K562	blood:
25	chr3:17675340..17678330-chr3:17685687..17687246,2	K562	blood:
26	chr3:17662482..17664001-chr3:17666148..17668577,2	K562	blood:
27	chr3:17646023..17648164-chr3:17782827..17784866,2	MCF-7	breast:
28	chr3:17472331..17474427-chr3:17733760..17736029,2	MCF-7	breast:
29	chr3:17671191..17673216-chr3:17880235..17883064,2	K562	blood:
30	chr3:17659334..17661547-chr3:17665428..17668300,2	MCF-7	breast:
31	chr3:17701833..17704472-chr3:17708885..17710880,2	MCF-7	breast:
32	chr3:17686300..17687006-chr3:17728236..17728848,2	MCF-7	breast:
33	chr3:17672884..17675384-chr3:17683158..17685612,2	K562	blood:
34	chr3:17748021..17751254-chr3:17782290..17784175,4	MCF-7	breast:
35	chr3:17700032..17702372-chr3:17706466..17709394,2	MCF-7	breast:
36	chr3:17681918..17684024-chr3:17685231..17687253,2	MCF-7	breast:
37	chr3:17703859..17706608-chr3:17724124..17726176,2	K562	blood:
38	chr3:17472375..17473059-chr3:17727721..17728808,3	MCF-7	breast:
39	chr3:17751258..17753632-chr3:17763558..17765356,2	K562	blood:
40	chr3:17752527..17754058-chr3:17756146..17757899,2	K562	blood:
41	chr3:17682592..17685089-chr3:17685251..17686866,2	K562	blood:
42	chr3:17734868..17735782-chr3:17882598..17883359,3	MCF-7	breast:
43	chr3:17710199..17712453-chr3:17724629..17727105,2	MCF-7	breast:
44	chr3:17734657..17735373-chr3:17852073..17852702,2	MCF-7	breast:
45	chr3:17661913..17664495-chr3:17666006..17668523,2	MCF-7	breast:
46	chr3:17668314..17670997-chr3:17674062..17676778,5	K562	blood:
47	chr3:17751695..17753389-chr3:17765736..17768612,2	K562	blood:
48	chr3:17661913..17664495-chr3:17666006..17668523,2	MCF-7	breast:
49	chr3:17752527..17754058-chr3:17756146..17757899,2	K562	blood:
50	chr3:17648652..17650282-chr3:17668047..17670129,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SATB1-8	chr3:17665341-17665405	NONHSAT088551
2	lnc-SATB1-8	chr3:17665341-17665405	NONHSAT088552
3	lnc-SATB1-8	chr3:17688453-17688548	NONHSAT088552
4	lnc-SATB1-8	chr3:17741470-17741506	NONHSAT088552
5	lnc-SATB1-8	chr3:17664140-17664257	NONHSAT088551
6	lnc-SATB1-8	chr3:17664140-17664257	NONHSAT088554
7	lnc-SATB1-8	chr3:17664140-17664257	NONHSAT088553
8	lnc-SATB1-8	chr3:17665341-17665405	NONHSAT088553
9	lnc-SATB1-8	chr3:17714037-17714167	NONHSAT088555
10	lnc-SATB1-8	chr3:17685533-17685612	NONHSAT088556
11	lnc-SATB1-8	chr3:17688453-17688548	NONHSAT088556
12	lnc-SATB1-8	chr3:17664140-17664257	NONHSAT088552
13	lnc-SATB1-8	chr3:17665341-17665405	NONHSAT088554
14	lnc-SATB1-8	chr3:17665207-17665405	NONHSAT088555

No data

Variant related genes	Relation type
TBC1D5	TF binding region
ENSG00000271841	TF binding region
ENSG00000233133	TF binding region
TBC1D5	CpG island
ENSG00000271841	CpG island
ENSG00000233133	CpG island
ENSG00000233133	chromatin interactions
ENSG00000238923	chromatin interactions
ENSG00000271841	chromatin interactions
ENSG00000131374	chromatin interactions
ENSG00000111678	chromatin interactions
CMTM3	miRNA target sites
MED22	miRNA target sites

Extended variants
information (count: 4236 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:4236 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139622309	chr3:17646807-17646808	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs374764994	chr3:17646822-17646823	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs145250606	chr3:17646830-17646831	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs147580934	chr3:17646833-17646834	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs571709621	chr3:17646995-17646996	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs537186657	chr3:17647019-17647020	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs578180481	chr3:17647039-17647040	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs142094176	chr3:17647044-17647045	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs115583892	chr3:17647100-17647101	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs542867819	chr3:17647112-17647113	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs553271418	chr3:17647155-17647156	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs369466753	chr3:17647179-17647180	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs370776607	chr3:17647207-17647208	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs373841056	chr3:17647222-17647223	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs573212117	chr3:17647237-17647238	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs188253128	chr3:17647244-17647245	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs564774773	chr3:17647250-17647251	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs551891625	chr3:17647289-17647290	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs117572665	chr3:17647316-17647317	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs552656856	chr3:17647416-17647417	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs149664414	chr3:17647454-17647455	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs547344525	chr3:17647463-17647464	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs550192116	chr3:17647469-17647470	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs560654621	chr3:17647474-17647475	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs371901844	chr3:17647559-17647560	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs180918478	chr3:17647564-17647565	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs557839822	chr3:17647579-17647580	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs529411016	chr3:17647580-17647581	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs374610345	chr3:17647596-17647597	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs115239841	chr3:17647609-17647610	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs116653565	chr3:17647633-17647634	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs74630636	chr3:17647634-17647635	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs145485069	chr3:17647655-17647656	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs117893100	chr3:17647656-17647657	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs114819240	chr3:17647660-17647661	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs184954483	chr3:17647662-17647663	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs190436268	chr3:17647670-17647671	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs368989705	chr3:17647671-17647672	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs567778271	chr3:17647701-17647702	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs536437579	chr3:17647712-17647713	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs553234633	chr3:17647751-17647752	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs373700997	chr3:17647760-17647761	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs573173084	chr3:17647780-17647781	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs538596994	chr3:17647865-17647866	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs573426574	chr3:17647875-17647876	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs573148047	chr3:17647893-17647894	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs541058010	chr3:17647902-17647903	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs554244611	chr3:17647935-17647936	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs558824156	chr3:17647938-17647939	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs148824748	chr3:17647974-17647975	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	21364760	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1361 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:17616000-17663600	Weak transcription	Left Ventricle	heart
2	chr3:17632400-17668200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr3:17633000-17667600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr3:17633600-17659600	Weak transcription	Primary B cells from peripheral blood	blood
5	chr3:17633800-17676600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr3:17634200-17647600	Weak transcription	Right Ventricle	heart
7	chr3:17634200-17659800	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr3:17639200-17676800	Weak transcription	Ovary	ovary
9	chr3:17639400-17651600	Weak transcription	Gastric	stomach
10	chr3:17641000-17659800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr3:17641400-17647600	Weak transcription	Pancreas	Pancrea
12	chr3:17641400-17659800	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr3:17641400-17660200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr3:17641400-17663000	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr3:17643800-17659800	Weak transcription	Primary B cells from cord blood	blood
16	chr3:17644000-17646800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr3:17646000-17647200	Enhancers	NHEK	skin
18	chr3:17646000-17647400	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr3:17646200-17647000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr3:17646200-17647000	Enhancers	HUVEC	blood vessel
21	chr3:17646200-17647200	Enhancers	Muscle Satellite Cultured Cells	--
22	chr3:17646200-17647200	Enhancers	HMEC	breast
23	chr3:17646200-17647200	Enhancers	NH-A	brain
24	chr3:17646200-17647400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr3:17646200-17647600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr3:17646200-17647800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr3:17646400-17647000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr3:17646400-17647000	Enhancers	HSMM	muscle
29	chr3:17646400-17647000	Enhancers	NHLF	lung
30	chr3:17646400-17647200	Enhancers	Hela-S3	cervix
31	chr3:17646400-17647400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr3:17646400-17647400	Enhancers	Osteobl	bone
33	chr3:17646400-17647800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr3:17646400-17651800	Weak transcription	Fetal Intestine Small	intestine
35	chr3:17646600-17647000	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr3:17646600-17647000	Flanking Active TSS	A549	lung
37	chr3:17646600-17647200	Enhancers	NHDF-Ad	bronchial
38	chr3:17646600-17659800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr3:17646800-17647000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr3:17646800-17647200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:17646800-17647200	Enhancers	Stomach Mucosa	stomach
42	chr3:17647000-17647800	Enhancers	A549	lung
43	chr3:17647000-17648600	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr3:17647000-17659200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr3:17647000-17670800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr3:17647400-17673800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr3:17647600-17647800	Enhancers	Psoas Muscle	Psoas
48	chr3:17647600-17648000	Enhancers	Pancreas	Pancrea
49	chr3:17647600-17648000	Enhancers	Right Ventricle	heart
50	chr3:17647600-17649000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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