Variant report

Variant	nsv1054960
Chromosome Location	chr14:104789101-104915527
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1082)
CpG islands
(count:4035)
Chromatin interactive
region (count:83)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1082 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr14:104853315-104853690	GM12878	blood:	n/a	n/a
2	BACH1	chr14:104910308-104910836	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr14:104882766-104882975	GM12878	blood:	n/a	chr14:104882870-104882881
4	BATF	chr14:104873533-104873737	GM12878	blood:	n/a	chr14:104873580-104873591 chr14:104873618-104873629
5	BATF	chr14:104873436-104873767	GM12878	blood:	n/a	chr14:104873580-104873591 chr14:104873618-104873629
6	BATF	chr14:104853348-104853593	GM12878	blood:	n/a	n/a
7	BCL11A	chr14:104853356-104853621	GM12878	blood:	n/a	chr14:104853461-104853470
8	BCL3	chr14:104790507-104790824	GM12878	blood:	n/a	n/a
9	BCL3	chr14:104792253-104792517	GM12878	blood:	n/a	n/a
10	BCL3	chr14:104850568-104850914	GM12878	blood:	n/a	chr14:104850648-104850657
11	BCL3	chr14:104853374-104853619	GM12878	blood:	n/a	chr14:104853461-104853470
12	BCL3	chr14:104850572-104850917	GM12878	blood:	n/a	chr14:104850648-104850657
13	BCL3	chr14:104906971-104907201	GM12878	blood:	n/a	n/a
14	BCL3	chr14:104910462-104910720	GM12878	blood:	n/a	n/a
15	BCL3	chr14:104792028-104792354	GM12878	blood:	n/a	n/a
16	BCL3	chr14:104910404-104910832	GM12878	blood:	n/a	n/a
17	BCL3	chr14:104906905-104907311	GM12878	blood:	n/a	n/a
18	BCLAF1	chr14:104853385-104853683	GM12878	blood:	n/a	chr14:104853461-104853470
19	BHLHE40	chr14:104811665-104811782	GM12878	blood:	n/a	n/a
20	BHLHE40	chr14:104891140-104891268	GM12878	blood:	n/a	n/a
21	BHLHE40	chr14:104891142-104891342	K562	blood:	n/a	n/a
22	BHLHE40	chr14:104789191-104789192	K562	blood:	n/a	n/a
23	BHLHE40	chr14:104811740-104811940	HepG2	liver:	n/a	n/a
24	CBX3	chr14:104808070-104808820	HCT-116	colon:	n/a	n/a
25	CEBPB	chr14:104862743-104862899	A549	lung:	n/a	chr14:104862810-104862823
26	CEBPB	chr14:104862673-104862964	HepG2	liver:	n/a	chr14:104862810-104862823
27	CEBPB	chr14:104836980-104837263	A549	lung:	n/a	n/a
28	CEBPB	chr14:104837024-104837262	HepG2	liver:	n/a	n/a
29	CEBPB	chr14:104817900-104818104	HepG2	liver:	n/a	chr14:104818065-104818076
30	CEBPB	chr14:104862645-104863007	H1-hESC	embryonic stem cell:	n/a	chr14:104862810-104862823
31	CEBPB	chr14:104862712-104862901	Hela-S3	cervix:	n/a	chr14:104862810-104862823
32	CEBPB	chr14:104862635-104863004	MCF-7	breast:	n/a	chr14:104862810-104862823
33	CHD2	chr14:104836616-104836682	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr14:104909120-104909319	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr14:104808370-104808676	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr14:104808207-104808588	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr14:104886256-104886838	GM12878	blood:	n/a	n/a
38	CREB1	chr14:104808384-104808562	A549	lung:	n/a	n/a
39	CREB1	chr14:104886313-104886828	GM12878	blood:	n/a	n/a
40	CTCF	chr14:104808380-104808530	GM12868	blood:	n/a	chr14:104808472-104808488 chr14:104808480-104808493 chr14:104808478-104808486 chr14:104808466-104808487 chr14:104808471-104808489 chr14:104808473-104808486
41	CTCF	chr14:104808254-104808696	T-47D	breast:	n/a	chr14:104808472-104808488 chr14:104808480-104808493 chr14:104808478-104808486 chr14:104808466-104808487 chr14:104808471-104808489 chr14:104808473-104808486
42	CTCF	chr14:104811780-104811825	MCF-7	breast:	n/a	chr14:104811805-104811813
43	CTCF	chr14:104798291-104798467	GM12892	blood:	n/a	n/a
44	CTCF	chr14:104808344-104808640	MCF-7	breast:	n/a	chr14:104808472-104808488 chr14:104808480-104808493 chr14:104808478-104808486 chr14:104808466-104808487 chr14:104808471-104808489 chr14:104808473-104808486
45	CTCF	chr14:104798336-104798433	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr14:104808440-104808590	A549	lung:	n/a	chr14:104808472-104808488 chr14:104808480-104808493 chr14:104808478-104808486 chr14:104808466-104808487 chr14:104808471-104808489 chr14:104808473-104808486
47	CTCF	chr14:104808295-104808641	K562	blood:	n/a	chr14:104808472-104808488 chr14:104808480-104808493 chr14:104808478-104808486 chr14:104808466-104808487 chr14:104808471-104808489 chr14:104808473-104808486
48	CTCF	chr14:104791938-104791954	GM19239	blood:	n/a	n/a
49	CTCF	chr14:104798340-104798490	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr14:104852660-104852810	GM12873	blood:	n/a	chr14:104852711-104852720 chr14:104852742-104852751

(count:4035 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:104866284-104866334	AG04449	skin:	fetal
2	chr14:104893636-104893686	NH-A	brain:	n/a
3	chr14:104895709-104895759	HepG2	liver:	n/a
4	chr14:104808516-104808566	AG10803	skin:	n/a
5	chr14:104902678-104902728	PANC-1	pancreas:	n/a
6	chr14:104799486-104799536	AG10803	skin:	n/a
7	chr14:104889005-104889055	ECC-1	luminal epithelium:	n/a
8	chr14:104789524-104789574	HAEpiC	amniotic membrane:	n/a
9	chr14:104862559-104862609	HMEC	breast:	n/a
10	chr14:104866284-104866334	AG04449	skin:	fetal
11	chr14:104893636-104893686	NH-A	brain:	n/a
12	chr14:104895709-104895759	HepG2	liver:	n/a
13	chr14:104808516-104808566	AG10803	skin:	n/a
14	chr14:104902678-104902728	PANC-1	pancreas:	n/a
15	chr14:104799486-104799536	AG10803	skin:	n/a
16	chr14:104889005-104889055	ECC-1	luminal epithelium:	n/a
17	chr14:104789524-104789574	HAEpiC	amniotic membrane:	n/a
18	chr14:104862559-104862609	HMEC	breast:	n/a
19	chr14:104808474-104808524	SAEC	small airway:	n/a
20	chr14:104852104-104852154	ProgFib	skin:	n/a
21	chr14:104900453-104900503	HRE	kidney:	n/a
22	chr14:104824167-104824217	HUVEC	blood vessel:	n/a
23	chr14:104854790-104854840	T-47D	breast:	n/a
24	chr14:104862680-104862730	Caco-2	colon:	n/a
25	chr14:104824475-104824525	SK-N-MC	brain:	n/a
26	chr14:104837550-104837600	SK-N-SH_RA	brain:	n/a
27	chr14:104897068-104897118	HL-60	blood:	n/a
28	chr14:104789371-104789421	Jurkat	blood:	n/a
29	chr14:104789371-104789421	HRE	kidney:	n/a
30	chr14:104800950-104801000	Hepatocyte	liver:	n/a
31	chr14:104837070-104837120	GM12891	blood:	n/a
32	chr14:104896560-104896610	HIPEpiC	eye:	n/a
33	chr14:104837070-104837120	AG09309	skin:	n/a
34	chr14:104852706-104852756	HCT-116	colon:	n/a
35	chr14:104889116-104889166	CMK	blood:	n/a
36	chr14:104866284-104866334	Hela-S3	cervix:	n/a
37	chr14:104900453-104900503	AG09309	skin:	n/a
38	chr14:104800746-104800796	HCM	heart:	n/a
39	chr14:104889116-104889166	PANC-1	pancreas:	n/a
40	chr14:104800568-104800618	SAEC	small airway:	n/a
41	chr14:104862559-104862609	Jurkat	blood:	n/a
42	chr14:104864723-104864773	AG04449	skin:	fetal
43	chr14:104789524-104789574	HL-60	blood:	n/a
44	chr14:104909505-104909555	AoSMC	blood vessel:	n/a
45	chr14:104789261-104789311	HIPEpiC	eye:	n/a
46	chr14:104851903-104851953	ECC-1	luminal epithelium:	n/a
47	chr14:104865792-104865842	NHBE	bronchial:	n/a
48	chr14:104866636-104866686	Hepatocyte	liver:	n/a
49	chr14:104862680-104862730	SK-N-SH_RA	brain:	n/a
50	chr14:104852775-104852825	MCF10A-Er-Src	breast:	n/a

(count:83 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:104827640..104830097-chr14:104849702..104851434,2	MCF-7	breast:
2	chr14:104913762..104916000-chr14:104927543..104930360,2	MCF-7	breast:
3	chr14:104650176..104652362-chr14:104808842..104810389,2	MCF-7	breast:
4	chr14:104820971..104823040-chr14:104824214..104826295,2	MCF-7	breast:
5	chr14:104852349..104854257-chr14:104854522..104857044,2	MCF-7	breast:
6	chr14:104837762..104840619-chr14:104842293..104845118,2	MCF-7	breast:
7	chr14:104820971..104823040-chr14:104824214..104826295,2	MCF-7	breast:
8	chr14:104808040..104808889-chr14:104836311..104836990,2	MCF-7	breast:
9	chr14:104852349..104854257-chr14:104854522..104857044,2	MCF-7	breast:
10	chr14:104898141..104899816-chr14:104900937..104903488,2	MCF-7	breast:
11	chr14:104841247..104842926-chr14:104851671..104854407,2	MCF-7	breast:
12	chr14:104810225..104812544-chr14:104838511..104840510,3	MCF-7	breast:
13	chr14:104818033..104822202-chr14:104826990..104831579,5	MCF-7	breast:
14	chr14:104903421..104906757-chr14:104907729..104911933,3	MCF-7	breast:
15	chr14:104818033..104822202-chr14:104826990..104831579,5	MCF-7	breast:
16	chr14:104803247..104805895-chr14:104810944..104812693,2	MCF-7	breast:
17	chr14:104903421..104906757-chr14:104907729..104911933,3	MCF-7	breast:
18	chr14:104828202..104830108-chr14:104833873..104835498,2	K562	blood:
19	chr14:104890913..104893677-chr14:104894092..104896751,2	MCF-7	breast:
20	chr14:104816456..104819206-chr14:104822482..104825637,3	MCF-7	breast:
21	chr14:104604366..104607521-chr14:104837580..104840047,4	MCF-7	breast:
22	chr14:104824690..104827500-chr14:105019187..105021176,2	MCF-7	breast:
23	chr14:104808137..104810517-chr14:104838226..104840189,2	MCF-7	breast:
24	chr14:104898141..104899816-chr14:104900937..104903488,2	MCF-7	breast:
25	chr14:104797978..104799771-chr14:104802827..104805475,2	MCF-7	breast:
26	chr14:104803247..104805895-chr14:104810944..104812693,2	MCF-7	breast:
27	chr14:104894876..104896838-chr14:104897650..104900830,3	MCF-7	breast:
28	chr14:104809922..104812049-chr14:104902257..104904031,2	MCF-7	breast:
29	chr14:104827640..104830097-chr14:104849702..104851434,2	MCF-7	breast:
30	chr14:104812965..104815337-chr14:104815556..104818475,2	MCF-7	breast:
31	chr14:104893761..104895389-chr14:104914243..104917076,2	MCF-7	breast:
32	chr14:104808612..104811334-chr14:105028919..105032790,3	MCF-7	breast:
33	chr14:104808040..104808889-chr14:104836311..104836990,2	MCF-7	breast:
34	chr14:104604293..104606398-chr14:104806693..104809135,2	MCF-7	breast:
35	chr14:104810513..104812777-chr14:104821342..104823710,2	MCF-7	breast:
36	chr14:104809922..104812049-chr14:104902257..104904031,2	MCF-7	breast:
37	chr14:104634157..104636948-chr14:104811497..104813606,2	MCF-7	breast:
38	chr14:104893761..104895389-chr14:104914243..104917076,2	MCF-7	breast:
39	chr14:104890951..104893457-chr14:104909378..104911636,2	MCF-7	breast:
40	chr14:104575835..104578265-chr14:104818122..104819690,2	MCF-7	breast:
41	chr14:104890951..104893457-chr14:104909378..104911636,2	MCF-7	breast:
42	chr14:104894876..104896838-chr14:104897650..104900830,3	MCF-7	breast:
43	chr14:104654764..104655392-chr14:104812527..104813058,2	MCF-7	breast:
44	chr14:104792609..104796456-chr14:104799877..104802767,4	MCF-7	breast:
45	chr14:104890275..104892805-chr14:104894264..104895980,2	MCF-7	breast:
46	chr14:104862114..104865269-chr14:104866594..104868712,3	MCF-7	breast:
47	chr14:104820148..104824002-chr14:104833372..104835893,3	MCF-7	breast:
48	chr14:104797978..104799771-chr14:104802827..104805475,2	MCF-7	breast:
49	chr14:104596286..104598130-chr14:104827828..104829835,2	MCF-7	breast:
50	chr14:104694371..104697146-chr14:104809063..104811864,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-614O9.3.1-1	chr14:104843878-104844157	ENSG00000258598
2	lnc-RP11-614O9.3.1-2	chr14:104824919-104825367	NONHSAT040256
3	lnc-RP11-614O9.3.1-1	chr14:104845218-104845288	ENSG00000258598
4	lnc-RP11-614O9.3.1-1	chr14:104842867-104843033	ENSG00000258598
5	lnc-RP11-614O9.3.1-2	chr14:104828079-104828393	NONHSAT040256

No data

Variant related genes	Relation type
RNU6-684P	TF binding region
ENSG00000258598	TF binding region
CEND1P1	TF binding region
RNU6-684P	CpG island
ENSG00000258598	CpG island
CEND1P1	CpG island
ENSG00000258986	chromatin interactions
ENSG00000166183	chromatin interactions
ENSG00000066735	chromatin interactions
ENSG00000184640	chromatin interactions
ENSG00000222761	chromatin interactions
ENSG00000258748	chromatin interactions
ENSG00000258598	chromatin interactions

Extended variants
information (count: 5421 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:5421 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191854772	chr14:104789160-104789161	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs375237728	chr14:104789174-104789175	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs138481318	chr14:104789215-104789216	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs369576991	chr14:104789217-104789218	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs558152825	chr14:104789233-104789234	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs527852846	chr14:104789261-104789262	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs578101869	chr14:104789278-104789279	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs543837559	chr14:104789299-104789300	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs548131224	chr14:104789305-104789306	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs4906449	chr14:104789323-104789324	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs529368704	chr14:104789331-104789332	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs148841644	chr14:104789338-104789339	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs374970291	chr14:104789356-104789357	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs143490434	chr14:104789366-104789367	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs137937133	chr14:104789373-104789374	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs571198318	chr14:104789374-104789375	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs530469446	chr14:104789400-104789401	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs550112960	chr14:104789401-104789402	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs567038740	chr14:104789428-104789429	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs184699191	chr14:104789444-104789445	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs552771998	chr14:104789472-104789473	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs34199752	chr14:104789532-104789533	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs542014503	chr14:104789534-104789535	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs116859311	chr14:104789538-104789539	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs368971529	chr14:104789547-104789548	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs373216437	chr14:104789569-104789570	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs143417699	chr14:104789632-104789633	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs147547367	chr14:104789633-104789634	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs557355429	chr14:104789637-104789638	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs190030558	chr14:104789648-104789649	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs138516637	chr14:104789650-104789651	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs559575409	chr14:104789675-104789676	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs549742473	chr14:104789681-104789682	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs181789437	chr14:104789689-104789690	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs143998540	chr14:104789764-104789765	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs71419835	chr14:104789785-104789786	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs61997111	chr14:104789797-104789798	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs530676292	chr14:104789831-104789832	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs60725466	chr14:104789838-104789839	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs11454455	chr14:104789881-104789882	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs397725772	chr14:104789884-104789885	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs6576030	chr14:104789894-104789895	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs560578864	chr14:104789917-104789918	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs535589582	chr14:104789936-104789937	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs8008637	chr14:104789976-104789977	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs546716748	chr14:104789988-104789989	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs566444059	chr14:104789990-104789991	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs535227014	chr14:104790005-104790006	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs150657500	chr14:104790016-104790017	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571987858	chr14:104790042-104790043	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	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
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	17426248	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1045 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104783800-104789400	Enhancers	Fetal Lung	lung
2	chr14:104786800-104793200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:104787600-104789200	Weak transcription	Fetal Brain Male	brain
4	chr14:104788000-104789200	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr14:104788400-104792000	Weak transcription	Spleen	Spleen
6	chr14:104788600-104790000	Enhancers	Brain Germinal Matrix	brain
7	chr14:104788800-104789600	Bivalent Enhancer	Fetal Stomach	stomach
8	chr14:104788800-104789600	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
9	chr14:104789000-104789200	Bivalent Enhancer	Brain Anterior Caudate	brain
10	chr14:104789000-104789200	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
11	chr14:104789200-104789400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr14:104789200-104789400	Enhancers	Brain Anterior Caudate	brain
13	chr14:104789200-104789400	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr14:104789200-104790200	Enhancers	Fetal Brain Male	brain
15	chr14:104789200-104790800	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr14:104789400-104789600	Bivalent Enhancer	Colonic Mucosa	Colon
17	chr14:104789400-104789600	Enhancers	Fetal Intestine Small	intestine
18	chr14:104789400-104789800	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr14:104789400-104790200	Enhancers	Duodenum Mucosa	Duodenum
20	chr14:104789400-104790600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr14:104789600-104790000	Enhancers	Colonic Mucosa	Colon
22	chr14:104789600-104790000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
23	chr14:104789800-104790200	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr14:104790000-104790200	Flanking Active TSS	Colonic Mucosa	Colon
25	chr14:104790000-104790400	Enhancers	Rectal Mucosa Donor 29	rectum
26	chr14:104790200-104790400	Enhancers	Colonic Mucosa	Colon
27	chr14:104790200-104790600	Weak transcription	Fetal Brain Male	brain
28	chr14:104790600-104791000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr14:104790600-104791000	Bivalent/Poised TSS	Fetal Lung	lung
30	chr14:104790600-104791000	Enhancers	Pancreas	Pancrea
31	chr14:104790600-104791200	ZNF genes & repeats	Fetal Brain Male	brain
32	chr14:104791000-104792000	Weak transcription	Pancreas	Pancrea
33	chr14:104792000-104792200	Bivalent Enhancer	Fetal Kidney	kidney
34	chr14:104792000-104792200	Enhancers	Pancreas	Pancrea
35	chr14:104792000-104792400	Bivalent/Poised TSS	Fetal Lung	lung
36	chr14:104792000-104792400	ZNF genes & repeats	Spleen	Spleen
37	chr14:104792200-104792400	ZNF genes & repeats	Esophagus	oesophagus
38	chr14:104792400-104794800	Weak transcription	Spleen	Spleen
39	chr14:104793200-104794200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr14:104793400-104794000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr14:104793600-104793800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
42	chr14:104793600-104794000	Enhancers	Adipose Nuclei	Adipose
43	chr14:104794200-104794600	Enhancers	Adipose Nuclei	Adipose
44	chr14:104794200-104798000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr14:104794800-104795000	ZNF genes & repeats	Spleen	Spleen
46	chr14:104794800-104795200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr14:104794800-104795400	Enhancers	Ovary	ovary
48	chr14:104798000-104798400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr14:104798000-104799600	Enhancers	Spleen	Spleen
50	chr14:104798200-104798400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin

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