Variant report

Variant	nsv902368
Chromosome Location	chr14:104839816-104947517
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:493)
CpG islands
(count:3665)
Chromatin interactive
region (count:49)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:493 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	BACH1	chr14:104927523-104927809	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr14:104928581-104928716	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr14:104873533-104873737	GM12878	blood:	n/a	chr14:104873580-104873591 chr14:104873618-104873629
6	BATF	chr14:104882766-104882975	GM12878	blood:	n/a	chr14:104882870-104882881
7	BATF	chr14:104853348-104853593	GM12878	blood:	n/a	n/a
8	BATF	chr14:104873436-104873767	GM12878	blood:	n/a	chr14:104873580-104873591 chr14:104873618-104873629
9	BCL11A	chr14:104853356-104853621	GM12878	blood:	n/a	chr14:104853461-104853470
10	BCL3	chr14:104937880-104938837	GM12878	blood:	n/a	n/a
11	BCL3	chr14:104850568-104850914	GM12878	blood:	n/a	chr14:104850648-104850657
12	BCL3	chr14:104853374-104853619	GM12878	blood:	n/a	chr14:104853461-104853470
13	BCL3	chr14:104906905-104907311	GM12878	blood:	n/a	n/a
14	BCL3	chr14:104906971-104907201	GM12878	blood:	n/a	n/a
15	BCL3	chr14:104937869-104938923	GM12878	blood:	n/a	n/a
16	BCL3	chr14:104910404-104910832	GM12878	blood:	n/a	n/a
17	BCL3	chr14:104910462-104910720	GM12878	blood:	n/a	n/a
18	BCL3	chr14:104850572-104850917	GM12878	blood:	n/a	chr14:104850648-104850657
19	BCLAF1	chr14:104853385-104853683	GM12878	blood:	n/a	chr14:104853461-104853470
20	BHLHE40	chr14:104891142-104891342	K562	blood:	n/a	n/a
21	BHLHE40	chr14:104891140-104891268	GM12878	blood:	n/a	n/a
22	CEBPB	chr14:104927611-104927725	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr14:104862743-104862899	A549	lung:	n/a	chr14:104862810-104862823
24	CEBPB	chr14:104929360-104929668	A549	lung:	n/a	n/a
25	CEBPB	chr14:104862635-104863004	MCF-7	breast:	n/a	chr14:104862810-104862823
26	CEBPB	chr14:104929383-104929624	IMR90	lung:	n/a	n/a
27	CEBPB	chr14:104862712-104862901	Hela-S3	cervix:	n/a	chr14:104862810-104862823
28	CEBPB	chr14:104929365-104929595	HepG2	liver:	n/a	n/a
29	CEBPB	chr14:104862673-104862964	HepG2	liver:	n/a	chr14:104862810-104862823
30	CEBPB	chr14:104862645-104863007	H1-hESC	embryonic stem cell:	n/a	chr14:104862810-104862823
31	CHD2	chr14:104909120-104909319	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr14:104886256-104886838	GM12878	blood:	n/a	n/a
33	CREB1	chr14:104943728-104944011	A549	lung:	n/a	n/a
34	CREB1	chr14:104886313-104886828	GM12878	blood:	n/a	n/a
35	CTCF	chr14:104852540-104852690	GM06990	blood:	n/a	chr14:104852630-104852643
36	CTCF	chr14:104938416-104938544	GM19239	blood:	n/a	n/a
37	CTCF	chr14:104852640-104852790	GM12866	blood:	n/a	chr14:104852711-104852720 chr14:104852742-104852751
38	CTCF	chr14:104902220-104902370	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr14:104920787-104920790	MCF-7	breast:	n/a	n/a
40	CTCF	chr14:104852660-104852810	GM12872	blood:	n/a	chr14:104852711-104852720 chr14:104852742-104852751
41	CTCF	chr14:104852580-104852730	GM12864	blood:	n/a	chr14:104852711-104852720 chr14:104852630-104852643
42	CTCF	chr14:104939640-104939790	BE2_C	brain:	n/a	chr14:104939691-104939709 chr14:104939686-104939707 chr14:104939693-104939706
43	CTCF	chr14:104902369-104902416	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr14:104852600-104852750	GM12873	blood:	n/a	chr14:104852711-104852720 chr14:104852630-104852643
45	CTCF	chr14:104900449-104900452	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr14:104858364-104858407	GM12891	blood:	n/a	n/a
47	CTCF	chr14:104900320-104900470	GM12865	blood:	n/a	chr14:104900373-104900391
48	CTCF	chr14:104909856-104910040	HepG2	liver:	n/a	n/a
49	CTCF	chr14:104920654-104920810	MCF-7	breast:	n/a	n/a
50	CTCF	chr14:104858340-104858490	Hela-S3	cervix:	n/a	n/a

(count:3665 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:104928472-104928522	PrEC	prostate:	n/a
2	chr14:104862559-104862609	HAEpiC	amniotic membrane:	n/a
3	chr14:104889005-104889055	K562	blood:	n/a
4	chr14:104898358-104898408	HIPEpiC	eye:	n/a
5	chr14:104927127-104927177	Hela-S3	cervix:	n/a
6	chr14:104928472-104928522	PrEC	prostate:	n/a
7	chr14:104862559-104862609	HAEpiC	amniotic membrane:	n/a
8	chr14:104889005-104889055	K562	blood:	n/a
9	chr14:104898358-104898408	HIPEpiC	eye:	n/a
10	chr14:104927127-104927177	Hela-S3	cervix:	n/a
11	chr14:104928652-104928702	PrEC	prostate:	n/a
12	chr14:104851903-104851953	AG04450	lung:	fetal
13	chr14:104852641-104852691	GM12891	blood:	n/a
14	chr14:104938987-104939037	HUVEC	blood vessel:	n/a
15	chr14:104864723-104864773	HL-60	blood:	n/a
16	chr14:104917314-104917364	HRCEpiC	kidney:	n/a
17	chr14:104900453-104900503	Hela-S3	cervix:	n/a
18	chr14:104928289-104928339	Hela-S3	cervix:	n/a
19	chr14:104928289-104928339	HepG2	liver:	n/a
20	chr14:104928289-104928339	AG09309	skin:	n/a
21	chr14:104917395-104917445	SK-N-SH_RA	brain:	n/a
22	chr14:104854940-104854990	ECC-1	luminal epithelium:	n/a
23	chr14:104856872-104856922	NH-A	brain:	n/a
24	chr14:104896090-104896140	K562	blood:	n/a
25	chr14:104928289-104928339	Jurkat	blood:	n/a
26	chr14:104852641-104852691	NB4	blood:	n/a
27	chr14:104854711-104854761	HMEC	breast:	n/a
28	chr14:104928289-104928339	HIPEpiC	eye:	n/a
29	chr14:104889005-104889055	AG09309	skin:	n/a
30	chr14:104928055-104928105	MCF10A-Er-Src	breast:	n/a
31	chr14:104928055-104928105	HRE	kidney:	n/a
32	chr14:104852706-104852756	SK-N-SH_RA	brain:	n/a
33	chr14:104854940-104854990	HCPEpiC	choroid plexus:	n/a
34	chr14:104866284-104866334	BJ	skin:	n/a
35	chr14:104896090-104896140	LNCaP	prostate:	n/a
36	chr14:104865792-104865842	Hepatocyte	liver:	n/a
37	chr14:104897068-104897118	LNCaP	prostate:	n/a
38	chr14:104917314-104917364	U87	brain:	n/a
39	chr14:104854790-104854840	BJ	skin:	n/a
40	chr14:104941923-104941973	MCF-7	breast:	n/a
41	chr14:104889116-104889166	AG09319	gingival:	n/a
42	chr14:104909505-104909555	HMEC	breast:	n/a
43	chr14:104850405-104850455	CMK	blood:	n/a
44	chr14:104852104-104852154	BE2_C	brain:	n/a
45	chr14:104854790-104854840	LNCaP	prostate:	n/a
46	chr14:104938987-104939037	K562	blood:	n/a
47	chr14:104928472-104928522	H1-hESC	embryonic stem cell:	embryo
48	chr14:104937088-104937138	IMR90	lung:	fetal
49	chr14:104928652-104928702	HRE	kidney:	n/a
50	chr14:104896001-104896051	SK-N-MC	brain:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:104894876..104896838-chr14:104897650..104900830,3	MCF-7	breast:
2	chr14:104902006..104903971-chr14:104906199..104909973,3	MCF-7	breast:
3	chr14:104890913..104893677-chr14:104894092..104896751,2	MCF-7	breast:
4	chr14:104841247..104842926-chr14:104851671..104854407,2	MCF-7	breast:
5	chr14:104917302..104919822-chr14:104924215..104925879,2	K562	blood:
6	chr14:104808137..104810517-chr14:104838226..104840189,2	MCF-7	breast:
7	chr14:104809922..104812049-chr14:104902257..104904031,2	MCF-7	breast:
8	chr14:104893761..104895389-chr14:104914243..104917076,2	MCF-7	breast:
9	chr14:104915992..104918653-chr14:104925232..104927798,2	MCF-7	breast:
10	chr14:104604366..104607521-chr14:104837580..104840047,4	MCF-7	breast:
11	chr14:104852349..104854257-chr14:104854522..104857044,2	MCF-7	breast:
12	chr14:104862114..104865269-chr14:104866594..104868712,3	MCF-7	breast:
13	chr14:104846626..104850072-chr14:104851431..104854716,4	MCF-7	breast:
14	chr14:104827640..104830097-chr14:104849702..104851434,2	MCF-7	breast:
15	chr14:104837762..104840619-chr14:104842293..104845118,2	MCF-7	breast:
16	chr14:104926023..104927806-chr14:104944745..104946610,2	MCF-7	breast:
17	chr14:104903421..104906757-chr14:104907729..104911933,3	MCF-7	breast:
18	chr14:104860512..104862041-chr14:104863587..104866008,2	K562	blood:
19	chr14:104841247..104842926-chr14:104851671..104854407,2	MCF-7	breast:
20	chr14:104935381..104936897-chr14:104942473..104945422,2	MCF-7	breast:
21	chr14:104936926..104938597-chr14:104940514..104942466,3	MCF-7	breast:
22	chr14:104898141..104899816-chr14:104900937..104903488,2	MCF-7	breast:
23	chr14:104890951..104893457-chr14:104909378..104911636,2	MCF-7	breast:
24	chr14:104890951..104893457-chr14:104909378..104911636,2	MCF-7	breast:
25	chr14:104893761..104895389-chr14:104914243..104917076,2	MCF-7	breast:
26	chr14:104842421..104844937-chr14:104846124..104848778,2	K562	blood:
27	chr14:104890913..104893677-chr14:104894092..104896751,2	MCF-7	breast:
28	chr14:104913762..104916000-chr14:104927543..104930360,2	MCF-7	breast:
29	chr14:104926023..104927806-chr14:104944745..104946610,2	MCF-7	breast:
30	chr14:104935381..104936897-chr14:104942473..104945422,2	MCF-7	breast:
31	chr14:104940339..104943047-chr14:104952341..104955339,2	MCF-7	breast:
32	chr14:104810225..104812544-chr14:104838511..104840510,3	MCF-7	breast:
33	chr14:104865956..104868004-chr14:104868266..104870745,2	K562	blood:
34	chr14:104913762..104916000-chr14:104927543..104930360,2	MCF-7	breast:
35	chr14:104903421..104906757-chr14:104907729..104911933,3	MCF-7	breast:
36	chr14:104842421..104844937-chr14:104846124..104848778,2	K562	blood:
37	chr14:104890275..104892805-chr14:104894264..104895980,2	MCF-7	breast:
38	chr14:104907597..104909438-chr14:105077013..105079589,2	K562	blood:
39	chr14:104890275..104892805-chr14:104894264..104895980,2	MCF-7	breast:
40	chr14:104902006..104903971-chr14:104906199..104909973,3	MCF-7	breast:
41	chr14:104839152..104841523-chr14:104843087..104845999,3	MCF-7	breast:
42	chr14:104846626..104850072-chr14:104851431..104854716,4	MCF-7	breast:
43	chr14:104936926..104938597-chr14:104940514..104942466,3	MCF-7	breast:
44	chr14:104907745..104909314-chr14:105070369..105072440,2	MCF-7	breast:
45	chr14:104860512..104862041-chr14:104863587..104866008,2	K562	blood:
46	chr14:104852349..104854257-chr14:104854522..104857044,2	MCF-7	breast:
47	chr14:104898141..104899816-chr14:104900937..104903488,2	MCF-7	breast:
48	chr14:104837762..104840619-chr14:104842293..104845118,2	MCF-7	breast:
49	chr14:104894876..104896838-chr14:104897650..104900830,3	MCF-7	breast:

(count:3 , 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-RP11-614O9.3.1-1	chr14:104842867-104843033	ENSG00000258598
3	lnc-RP11-614O9.3.1-1	chr14:104845218-104845288	ENSG00000258598

No data

Variant related genes	Relation type
CEND1P1	TF binding region
RNU6-684P	TF binding region
ENSG00000258598	TF binding region
CEND1P1	CpG island
RNU6-684P	CpG island
ENSG00000258598	CpG island
ENSG00000258598	chromatin interactions
ENSG00000258986	chromatin interactions
ENSG00000066735	chromatin interactions
ENSG00000213159	chromatin interactions
ENSG00000222761	chromatin interactions

Extended variants
information (count: 4500 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:4500 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4074324	chr14:104839816-104839817	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538364715	chr14:104839825-104839826	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs553466511	chr14:104839906-104839907	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs182829942	chr14:104839927-104839928	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs4074325	chr14:104839937-104839938	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs36049224	chr14:104839939-104839940	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs575194695	chr14:104839941-104839942	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs4074326	chr14:104839958-104839959	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs146864532	chr14:104839970-104839971	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs561291631	chr14:104839971-104839972	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs575009386	chr14:104840013-104840014	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs530141225	chr14:104840019-104840020	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs540600574	chr14:104840099-104840100	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs79598270	chr14:104840135-104840136	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs140669381	chr14:104840141-104840142	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs552136286	chr14:104840168-104840169	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs76197762	chr14:104840178-104840179	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs560810716	chr14:104840225-104840226	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs200432659	chr14:104840235-104840236	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs531542259	chr14:104840287-104840288	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs548058391	chr14:104840305-104840306	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs567980323	chr14:104840306-104840307	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs532845615	chr14:104840310-104840311	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs533551977	chr14:104840316-104840317	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs553303344	chr14:104840323-104840324	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs370542210	chr14:104840341-104840342	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs145760536	chr14:104840393-104840394	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs80354736	chr14:104840395-104840396	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs141005543	chr14:104840447-104840448	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs565638300	chr14:104840452-104840453	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs116317378	chr14:104840457-104840458	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs544447706	chr14:104840469-104840470	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs74088592	chr14:104840476-104840477	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs74331960	chr14:104840493-104840494	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs540637289	chr14:104840505-104840506	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs560490054	chr14:104840534-104840535	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs577308888	chr14:104840537-104840538	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs546264869	chr14:104840547-104840548	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs562571418	chr14:104840554-104840555	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs10140394	chr14:104840569-104840570	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs547940792	chr14:104840571-104840572	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs561650479	chr14:104840595-104840596	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs527576432	chr14:104840634-104840635	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs150214851	chr14:104840650-104840651	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs59696956	chr14:104840654-104840655	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs539184946	chr14:104840665-104840666	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs187251189	chr14:104840716-104840717	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs57788677	chr14:104840729-104840730	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs569619620	chr14:104840740-104840741	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs538453092	chr14:104840767-104840768	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	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
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:975 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104831000-104842000	Weak transcription	Gastric	stomach
2	chr14:104835400-104842000	Weak transcription	Fetal Brain Male	brain
3	chr14:104837600-104840200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr14:104838800-104840000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
5	chr14:104838800-104840000	Enhancers	Fetal Intestine Small	intestine
6	chr14:104839200-104840000	Enhancers	Brain Germinal Matrix	brain
7	chr14:104840200-104842000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr14:104840800-104841000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
9	chr14:104842000-104842200	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr14:104842000-104842600	Enhancers	Gastric	stomach
11	chr14:104842000-104843000	Enhancers	Brain Germinal Matrix	brain
12	chr14:104842000-104847400	Enhancers	Fetal Brain Male	brain
13	chr14:104842200-104842800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr14:104842400-104843400	Enhancers	Adipose Nuclei	Adipose
15	chr14:104842600-104850400	Weak transcription	Gastric	stomach
16	chr14:104842800-104843000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
17	chr14:104842800-104843000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
18	chr14:104842800-104846800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr14:104843000-104843400	Weak transcription	Brain Germinal Matrix	brain
20	chr14:104843400-104845000	Enhancers	Brain Germinal Matrix	brain
21	chr14:104843800-104845800	Enhancers	Fetal Brain Female	brain
22	chr14:104845000-104845200	Flanking Active TSS	Brain Germinal Matrix	brain
23	chr14:104845200-104845400	Enhancers	Brain Germinal Matrix	brain
24	chr14:104845400-104845600	Flanking Active TSS	Brain Germinal Matrix	brain
25	chr14:104845400-104845800	Enhancers	Fetal Stomach	stomach
26	chr14:104845600-104846200	Enhancers	Brain Germinal Matrix	brain
27	chr14:104845800-104846000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
28	chr14:104845800-104849200	Weak transcription	Fetal Brain Female	brain
29	chr14:104846800-104847400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr14:104847400-104849000	Weak transcription	Fetal Brain Male	brain
31	chr14:104847400-104849800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr14:104848400-104849800	Enhancers	Brain Germinal Matrix	brain
33	chr14:104849000-104849800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr14:104849000-104850000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
35	chr14:104849000-104850600	Enhancers	Fetal Brain Male	brain
36	chr14:104849200-104849400	Bivalent Enhancer	Fetal Kidney	kidney
37	chr14:104849200-104850200	Enhancers	Fetal Brain Female	brain
38	chr14:104849200-104850600	Enhancers	Fetal Lung	lung
39	chr14:104849200-104852000	Bivalent Enhancer	Fetal Stomach	stomach
40	chr14:104849200-104853800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr14:104849400-104850200	Bivalent Enhancer	Fetal Muscle Leg	muscle
42	chr14:104849400-104850800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr14:104849400-104851200	Enhancers	Spleen	Spleen
44	chr14:104849400-104852000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr14:104849400-104852200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr14:104849600-104851000	Enhancers	Ovary	ovary
47	chr14:104849600-104851000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
48	chr14:104849600-104851400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr14:104849800-104850200	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
50	chr14:104849800-104850400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain

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