Variant report

Variant	nsv1045451
Chromosome Location	chr14:21340639-21402584
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	ATF1	chr14:21349520-21349644	K562	blood:	n/a	n/a
2	BCLAF1	chr14:21341818-21342245	GM12878	blood:	n/a	chr14:21341956-21341969
3	BCLAF1	chr14:21341829-21342279	GM12878	blood:	n/a	chr14:21341956-21341969
4	BHLHE40	chr14:21341894-21342031	K562	blood:	n/a	chr14:21341954-21341970
5	CBX3	chr14:21341821-21342185	K562	blood:	n/a	n/a
6	CEBPB	chr14:21390712-21390883	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr14:21387328-21387608	MCF-7	breast:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
8	CEBPB	chr14:21390806-21390847	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr14:21387199-21387544	A549	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
10	CEBPB	chr14:21390675-21390974	A549	lung:	n/a	n/a
11	CEBPB	chr14:21362130-21362293	A549	lung:	n/a	chr14:21362250-21362261
12	CEBPB	chr14:21390780-21390974	K562	blood:	n/a	n/a
13	CEBPB	chr14:21390663-21390987	HepG2	liver:	n/a	n/a
14	CEBPB	chr14:21362247-21362271	H1-hESC	embryonic stem cell:	n/a	chr14:21362250-21362261
15	CEBPB	chr14:21359339-21359538	K562	blood:	n/a	chr14:21359447-21359460
16	CEBPB	chr14:21341852-21342195	K562	blood:	n/a	n/a
17	CEBPB	chr14:21362091-21362409	HepG2	liver:	n/a	chr14:21362250-21362261
18	CEBPB	chr14:21372661-21372946	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr14:21387197-21387553	H1-hESC	embryonic stem cell:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
20	CEBPB	chr14:21341896-21342213	MCF-7	breast:	n/a	n/a
21	CEBPB	chr14:21341881-21342104	HepG2	liver:	n/a	n/a
22	CEBPB	chr14:21341854-21342226	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr14:21341851-21342133	K562	blood:	n/a	n/a
24	CEBPB	chr14:21387196-21387557	Hela-S3	cervix:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
25	CEBPB	chr14:21341785-21342305	A549	lung:	n/a	n/a
26	CEBPB	chr14:21387140-21387598	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
27	CEBPB	chr14:21362168-21362307	Hela-S3	cervix:	n/a	chr14:21362250-21362261
28	CEBPB	chr14:21387189-21387569	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
29	CEBPB	chr14:21362153-21362361	IMR90	lung:	n/a	chr14:21362250-21362261
30	CEBPB	chr14:21387233-21387541	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
31	CEBPB	chr14:21387183-21387567	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
32	CEBPB	chr14:21387301-21387487	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
33	CEBPB	chr14:21341879-21342172	HepG2	liver:	n/a	n/a
34	CEBPB	chr14:21373948-21374221	HepG2	liver:	n/a	chr14:21374057-21374070
35	CEBPB	chr14:21390705-21391054	MCF-7	breast:	n/a	n/a
36	CEBPB	chr14:21387278-21387542	IMR90	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
37	CEBPB	chr14:21362201-21362274	K562	blood:	n/a	chr14:21362250-21362261
38	CEBPB	chr14:21344519-21344558	HepG2	liver:	n/a	chr14:21344532-21344543
39	CEBPB	chr14:21387296-21387479	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
40	CEBPB	chr14:21387184-21387565	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
41	CEBPD	chr14:21387228-21387447	HepG2	liver:	n/a	chr14:21387366-21387377 chr14:21387368-21387377
42	CREB1	chr14:21341735-21342321	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr14:21341864-21342173	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr14:21402266-21402821	HCT-116	colon:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
45	CTCF	chr14:21372720-21372870	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr14:21372601-21372892	K562	blood:	n/a	n/a
47	CTCF	chr14:21402480-21402630	AG04450	lung:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
48	CTCF	chr14:21341860-21342010	GM12864	blood:	n/a	chr14:21341957-21341973 chr14:21341958-21341971 chr14:21341956-21341974
49	CTCF	chr14:21402392-21402645	GM12892	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
50	CTCF	chr14:21402420-21402570	HEEpiC	esophagus:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21358233-21358283	T-47D	breast:	n/a
2	chr14:21359737-21359787	HMEC	breast:	n/a
3	chr14:21359737-21359787	GM19239	blood:	n/a
4	chr14:21341871-21341921	HepG2	liver:	n/a
5	chr14:21386453-21386503	Jurkat	blood:	n/a
6	chr14:21359295-21359345	HL-60	blood:	n/a
7	chr14:21358099-21358149	HUVEC	blood vessel:	n/a
8	chr14:21359295-21359345	U87	brain:	n/a
9	chr14:21358099-21358149	PANC-1	pancreas:	n/a
10	chr14:21342066-21342116	HCF	heart:	n/a
11	chr14:21386453-21386503	HRPEpiC	eye:	n/a
12	chr14:21386453-21386503	SK-N-MC	brain:	n/a
13	chr14:21359737-21359787	HEK293	kidney:	embryo
14	chr14:21358099-21358149	HAEpiC	amniotic membrane:	n/a
15	chr14:21342066-21342116	SK-N-MC	brain:	n/a
16	chr14:21341871-21341921	HEEpiC	esophagus:	n/a
17	chr14:21359737-21359787	NHDF-neo	bronchial:	n/a
18	chr14:21358099-21358149	NB4	blood:	n/a
19	chr14:21386453-21386503	NHDF-neo	bronchial:	n/a
20	chr14:21358233-21358283	HRCEpiC	kidney:	n/a
21	chr14:21386453-21386503	AG09319	gingival:	n/a
22	chr14:21342066-21342116	HRPEpiC	eye:	n/a
23	chr14:21358233-21358283	HPAEpiC	pulmonary alveolar:	n/a
24	chr14:21359943-21359993	AG04450	lung:	fetal
25	chr14:21359737-21359787	BJ	skin:	n/a
26	chr14:21341871-21341921	AG10803	skin:	n/a
27	chr14:21358233-21358283	SK-N-MC	brain:	n/a
28	chr14:21359943-21359993	LNCaP	prostate:	n/a
29	chr14:21342066-21342116	AG04449	skin:	fetal
30	chr14:21341871-21341921	Jurkat	blood:	n/a
31	chr14:21358233-21358283	SAEC	small airway:	n/a
32	chr14:21358233-21358283	GM12892	blood:	n/a
33	chr14:21359943-21359993	ProgFib	skin:	n/a
34	chr14:21341871-21341921	PFSK-1	brain:	n/a
35	chr14:21359943-21359993	Hela-S3	cervix:	n/a
36	chr14:21358099-21358149	HCF	heart:	n/a
37	chr14:21358233-21358283	SK-N-SH	brain:	n/a
38	chr14:21341871-21341921	ECC-1	luminal epithelium:	n/a
39	chr14:21341871-21341921	GM12878	blood:	n/a
40	chr14:21359295-21359345	HAEpiC	amniotic membrane:	n/a
41	chr14:21341871-21341921	HCF	heart:	n/a
42	chr14:21342066-21342116	ProgFib	skin:	n/a
43	chr14:21341871-21341921	SK-N-SH	brain:	n/a
44	chr14:21359295-21359345	HepG2	liver:	n/a
45	chr14:21358099-21358149	HMEC	breast:	n/a
46	chr14:21359943-21359993	HRCEpiC	kidney:	n/a
47	chr14:21358099-21358149	A549	lung:	n/a
48	chr14:21341871-21341921	HMEC	breast:	n/a
49	chr14:21359737-21359787	HepG2	liver:	n/a
50	chr14:21359295-21359345	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:21345187..21348103-chr14:21455224..21457829,2	K562	blood:
2	chr14:21325580..21326139-chr14:21341851..21342353,2	MCF-7	breast:
3	chr14:21341929..21342586-chr14:21439203..21440051,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDRG2-2	chr14:21384925-21385029	ENSG00000258772
2	lnc-RNASE1-1	chr14:21341350-21341529	ENSG00000259130
3	lnc-RNASE1-1	chr14:21343696-21343927	ENSG00000258642.1
4	lnc-RNASE3-1	chr14:21387795-21388335	ENSG00000136315
5	lnc-NDRG2-2	chr14:21396396-21396739	ENSG00000258772
6	lnc-RNASE1-1	chr14:21340531-21340720	ENSG00000259130
7	lnc-RNASE1-1	chr14:21341718-21341751	ENSG00000259130
8	lnc-NDRG2-3	chr14:21366144-21366340	ENSG00000258918
9	lnc-RNASE1-1	chr14:21343696-21343904	XLOC_010966
10	lnc-RNASE3-1	chr14:21387500-21387563	ENSG00000136315
11	lnc-RNASE1-1	chr14:21341079-21342995	XLOC_010966
12	lnc-RNASE1-1	chr14:21342464-21342995	ENSG00000258642.1

Variant related genes	Relation type
ENSG00000258772	TF binding region
ENSG00000136315	TF binding region
ENSG00000258642	TF binding region
RNASE3	TF binding region
ENSG00000259130	TF binding region
ENSG00000258772	CpG island
ENSG00000136315	CpG island
ENSG00000258642	CpG island
RNASE3	CpG island
ENSG00000259130	CpG island

Extended variants
information (count: 1875 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1875 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576293490	chr14:21340702-21340703	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs537897472	chr14:21340710-21340711	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs75322289	chr14:21340721-21340722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547846717	chr14:21340725-21340726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs58691612	chr14:21340739-21340740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148425780	chr14:21340763-21340764	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556117762	chr14:21340768-21340769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs58179497	chr14:21340819-21340820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538930497	chr14:21340942-21340943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183870783	chr14:21340955-21340956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564614293	chr14:21341050-21341051	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372212989	chr14:21341076-21341077	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533554669	chr14:21341083-21341084	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs550428272	chr14:21341125-21341126	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs6571499	chr14:21341149-21341150	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs189224917	chr14:21341153-21341154	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs369476382	chr14:21341196-21341197	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs548134004	chr14:21341197-21341198	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs533651486	chr14:21341208-21341209	Active TSS Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs540332233	chr14:21341226-21341227	Active TSS Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs561805269	chr14:21341241-21341242	Active TSS Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs567971862	chr14:21341365-21341366	Active TSS Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs573775717	chr14:21341385-21341386	Active TSS Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs533836157	chr14:21341433-21341434	Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs551490458	chr14:21341463-21341464	Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs117271587	chr14:21341538-21341539	Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs568921456	chr14:21341574-21341575	Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs191514141	chr14:21341587-21341588	Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs11622628	chr14:21341637-21341638	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs141666069	chr14:21341685-21341686	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs551355617	chr14:21341745-21341746	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs116793119	chr14:21341855-21341856	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs535404090	chr14:21341866-21341867	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs114825219	chr14:21341893-21341894	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs572354329	chr14:21341951-21341952	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs541475644	chr14:21341976-21341977	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs371335910	chr14:21341979-21341980	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs537452658	chr14:21341997-21341998	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs372150312	chr14:21342010-21342011	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs183125295	chr14:21342030-21342031	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs578162222	chr14:21342047-21342048	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs544001091	chr14:21342051-21342052	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs187063049	chr14:21342074-21342075	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs529549258	chr14:21342090-21342091	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs549414676	chr14:21342092-21342093	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs560308201	chr14:21342107-21342108	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs560041840	chr14:21342108-21342109	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs527282534	chr14:21342135-21342136	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs191834234	chr14:21342152-21342153	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs72488260	chr14:21342236-21342237	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	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
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	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
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
Mortal	21835882	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:266 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21337200-21341600	Weak transcription	Brain Substantia Nigra	brain
2	chr14:21337600-21341600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr14:21338800-21341600	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr14:21340200-21341200	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr14:21341200-21341400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr14:21341200-21341400	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr14:21341200-21341600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
8	chr14:21341200-21342200	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr14:21341200-21342200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr14:21341200-21342200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr14:21341200-21342600	Active TSS	ES-I3 Cell Line	embryonic stem cell
12	chr14:21341200-21342600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr14:21341200-21343200	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr14:21341400-21341600	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr14:21341400-21341600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
16	chr14:21341400-21341600	Enhancers	Brain Cingulate Gyrus	brain
17	chr14:21341400-21341600	Enhancers	Dnd41	blood
18	chr14:21341400-21341800	Enhancers	Primary T cells from cord blood	blood
19	chr14:21341400-21342200	Active TSS	H1 Cell Line	embryonic stem cell
20	chr14:21341400-21342200	Enhancers	Primary B cells from peripheral blood	blood
21	chr14:21341400-21342200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr14:21341400-21342200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
23	chr14:21341400-21342200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr14:21341400-21342400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
25	chr14:21341400-21342400	Enhancers	Primary hematopoietic stem cells	blood
26	chr14:21341400-21342400	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr14:21341400-21342400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr14:21341400-21342400	Enhancers	Brain Anterior Caudate	brain
29	chr14:21341400-21342600	Enhancers	Primary B cells from cord blood	blood
30	chr14:21341400-21342600	Enhancers	Spleen	Spleen
31	chr14:21341400-21342600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
32	chr14:21341600-21341800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
33	chr14:21341600-21341800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr14:21341600-21341800	Flanking Active TSS	Brain Cingulate Gyrus	brain
35	chr14:21341600-21342000	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr14:21341600-21342000	Flanking Active TSS	Brain Substantia Nigra	brain
37	chr14:21341600-21342000	Enhancers	Colon Smooth Muscle	Colon
38	chr14:21341600-21342000	Active TSS	GM12878-XiMat	blood
39	chr14:21341600-21342000	Enhancers	HUVEC	blood vessel
40	chr14:21341600-21342200	Active TSS	HUES6 Cell Line	embryonic stem cell
41	chr14:21341600-21342200	Active TSS	HUES64 Cell Line	embryonic stem cell
42	chr14:21341600-21342200	Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr14:21341600-21342200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr14:21341600-21342200	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr14:21341600-21342200	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr14:21341600-21342200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr14:21341600-21342200	Enhancers	Duodenum Mucosa	Duodenum
48	chr14:21341600-21342200	Active TSS	Duodenum Smooth Muscle	Duodenum
49	chr14:21341600-21342200	Active TSS	Fetal Kidney	kidney
50	chr14:21341600-21342200	Active TSS	Rectal Mucosa Donor 29	rectum

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