Variant report

Variant	nsv530660
Chromosome Location	chr14:44259180-44862269
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1834)
CpG islands
(count:305)
Chromatin interactive
region (count:74)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1834 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:44369215-44370041	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:44786027-44786367	K562	blood:	n/a	n/a
3	ARID3A	chr14:44479441-44480344	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:44264895-44265217	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:44370996-44371623	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:44368064-44368187	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:44786011-44786505	HepG2	liver:	n/a	n/a
8	ATF1	chr14:44786110-44786462	K562	blood:	n/a	n/a
9	ATF3	chr14:44786185-44786384	HepG2	liver:	n/a	n/a
10	ATF3	chr14:44786000-44786531	HCT-116	colon:	n/a	n/a
11	ATF3	chr14:44786197-44786335	K562	blood:	n/a	n/a
12	ATF3	chr14:44786082-44786534	A549	lung:	n/a	n/a
13	ATF3	chr14:44786091-44786377	K562	blood:	n/a	n/a
14	ATF3	chr14:44786106-44786596	HCT-116	colon:	n/a	n/a
15	BACH1	chr14:44632100-44632238	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr14:44786178-44786410	GM12878	blood:	n/a	n/a
17	BATF	chr14:44786155-44786410	GM12878	blood:	n/a	n/a
18	BCL11A	chr14:44342534-44342783	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL11A	chr14:44673306-44673565	H1-hESC	embryonic stem cell:	n/a	n/a
20	BCL3	chr14:44786061-44786449	GM12878	blood:	n/a	n/a
21	BHLHE40	chr14:44786155-44786484	K562	blood:	n/a	n/a
22	BHLHE40	chr14:44435424-44435438	GM12878	blood:	n/a	n/a
23	BHLHE40	chr14:44786136-44786463	HepG2	liver:	n/a	n/a
24	BHLHE40	chr14:44361529-44361580	GM12878	blood:	n/a	n/a
25	BHLHE40	chr14:44369547-44369744	HepG2	liver:	n/a	n/a
26	BRCA1	chr14:44618833-44619126	H1-hESC	embryonic stem cell:	n/a	n/a
27	CBX3	chr14:44785944-44786626	HCT-116	colon:	n/a	n/a
28	CEBPB	chr14:44675063-44675294	HepG2	liver:	n/a	chr14:44675185-44675198 chr14:44675185-44675198 chr14:44675186-44675197 chr14:44675185-44675196
29	CEBPB	chr14:44498824-44499447	IMR90	lung:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44498983-44498994 chr14:44499340-44499351
30	CEBPB	chr14:44319227-44319428	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr14:44319705-44320031	A549	lung:	n/a	chr14:44319833-44319844
32	CEBPB	chr14:44801504-44801823	HepG2	liver:	n/a	chr14:44801651-44801662 chr14:44801651-44801664
33	CEBPB	chr14:44862132-44862411	HepG2	liver:	n/a	chr14:44862299-44862316 chr14:44862302-44862315
34	CEBPB	chr14:44822915-44823413	MCF-7	breast:	n/a	chr14:44823024-44823035
35	CEBPB	chr14:44452992-44453227	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr14:44369514-44369863	H1-hESC	embryonic stem cell:	n/a	chr14:44369691-44369702
37	CEBPB	chr14:44845840-44846035	A549	lung:	n/a	n/a
38	CEBPB	chr14:44444697-44444949	HepG2	liver:	n/a	chr14:44444844-44444855
39	CEBPB	chr14:44370974-44371424	MCF-7	breast:	n/a	chr14:44371181-44371194 chr14:44371182-44371193
40	CEBPB	chr14:44560924-44561243	H1-hESC	embryonic stem cell:	n/a	chr14:44561060-44561071
41	CEBPB	chr14:44560929-44561184	K562	blood:	n/a	chr14:44561060-44561071
42	CEBPB	chr14:44448312-44448448	HepG2	liver:	n/a	chr14:44448367-44448378
43	CEBPB	chr14:44479304-44479659	ECC-1	luminal epithelium:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
44	CEBPB	chr14:44319690-44320016	IMR90	lung:	n/a	chr14:44319833-44319844
45	CEBPB	chr14:44364978-44365636	HepG2	liver:	n/a	n/a
46	CEBPB	chr14:44804468-44804813	HepG2	liver:	n/a	chr14:44804642-44804653
47	CEBPB	chr14:44478929-44479169	A549	lung:	n/a	n/a
48	CEBPB	chr14:44478922-44479578	IMR90	lung:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
49	CEBPB	chr14:44785988-44786493	A549	lung:	n/a	n/a
50	CEBPB	chr14:44599593-44600126	A549	lung:	n/a	chr14:44599949-44599960

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:44408417-44408467	AG09319	gingival:	n/a
2	chr14:44853952-44854002	Hela-S3	cervix:	n/a
3	chr14:44853952-44854002	AG04450	lung:	fetal
4	chr14:44408473-44408523	H1-hESC	embryonic stem cell:	embryo
5	chr14:44408339-44408389	MCF-7	breast:	n/a
6	chr14:44418808-44418858	AoSMC	blood vessel:	n/a
7	chr14:44418808-44418858	HEK293	kidney:	embryo
8	chr14:44853952-44854002	HEEpiC	esophagus:	n/a
9	chr14:44408339-44408389	SK-N-SH_RA	brain:	n/a
10	chr14:44408473-44408523	AG09309	skin:	n/a
11	chr14:44408473-44408523	HRPEpiC	eye:	n/a
12	chr14:44408417-44408467	GM19239	blood:	n/a
13	chr14:44408473-44408523	NB4	blood:	n/a
14	chr14:44408473-44408523	HRCEpiC	kidney:	n/a
15	chr14:44418808-44418858	HCT-116	colon:	n/a
16	chr14:44418808-44418858	PrEC	prostate:	n/a
17	chr14:44408339-44408389	HIPEpiC	eye:	n/a
18	chr14:44418808-44418858	GM19239	blood:	n/a
19	chr14:44418808-44418858	HEEpiC	esophagus:	n/a
20	chr14:44418808-44418858	HUVEC	blood vessel:	n/a
21	chr14:44408339-44408389	NT2-D1	testis:	n/a
22	chr14:44408473-44408523	NH-A	brain:	n/a
23	chr14:44853952-44854002	LNCaP	prostate:	n/a
24	chr14:44418808-44418858	CMK	blood:	n/a
25	chr14:44853952-44854002	PFSK-1	brain:	n/a
26	chr14:44408473-44408523	NHDF-neo	bronchial:	n/a
27	chr14:44853952-44854002	SAEC	small airway:	n/a
28	chr14:44408339-44408389	HEEpiC	esophagus:	n/a
29	chr14:44408417-44408467	HRCEpiC	kidney:	n/a
30	chr14:44408473-44408523	HCT-116	colon:	n/a
31	chr14:44408339-44408389	T-47D	breast:	n/a
32	chr14:44408339-44408389	GM19239	blood:	n/a
33	chr14:44853952-44854002	ECC-1	luminal epithelium:	n/a
34	chr14:44418808-44418858	SK-N-SH_RA	brain:	n/a
35	chr14:44418808-44418858	K562	blood:	n/a
36	chr14:44408417-44408467	LNCaP	prostate:	n/a
37	chr14:44408417-44408467	NHDF-neo	bronchial:	n/a
38	chr14:44853952-44854002	GM12878	blood:	n/a
39	chr14:44408417-44408467	AG10803	skin:	n/a
40	chr14:44853952-44854002	HUVEC	blood vessel:	n/a
41	chr14:44408473-44408523	GM12892	blood:	n/a
42	chr14:44418808-44418858	HNPCEpiC	eye:	n/a
43	chr14:44408417-44408467	MCF-7	breast:	n/a
44	chr14:44853952-44854002	HAEpiC	amniotic membrane:	n/a
45	chr14:44408417-44408467	AoSMC	blood vessel:	n/a
46	chr14:44408417-44408467	Hela-S3	cervix:	n/a
47	chr14:44408417-44408467	MCF10A-Er-Src	breast:	n/a
48	chr14:44408339-44408389	HCPEpiC	choroid plexus:	n/a
49	chr14:44408339-44408389	AG04449	skin:	fetal
50	chr14:44408473-44408523	HCF	heart:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:44364217..44368954-chr14:44370108..44373061,4	MCF-7	breast:
2	chr14:44606810..44610792-chr14:44612494..44615788,3	K562	blood:
3	chr14:44302474..44305350-chr6:53571306..53573841,2	MCF-7	breast:
4	chr14:44368312..44369942-chr14:44371630..44373482,2	MCF-7	breast:
5	chr14:44248792..44250657-chr14:44368815..44370864,2	MCF-7	breast:
6	chr14:44857399..44860693-chr14:44862169..44864634,3	K562	blood:
7	chr14:44803036..44805789-chr14:44807681..44809917,2	MCF-7	breast:
8	chr14:44785511..44787603-chr14:44801475..44804165,2	MCF-7	breast:
9	chr14:44838166..44839882-chr14:44873785..44875324,2	MCF-7	breast:
10	chr14:44372607..44374197-chr14:44383168..44385135,2	MCF-7	breast:
11	chr14:44370633..44373508-chr14:44616084..44618482,2	MCF-7	breast:
12	chr14:44600217..44602036-chr14:44604194..44606588,2	K562	blood:
13	chr14:44659162..44661192-chr14:44662497..44664945,3	MCF-7	breast:
14	chr14:44262315..44264828-chr17:56707799..56709684,2	MCF-7	breast:
15	chr14:44250330..44252060-chr14:44369516..44373246,3	MCF-7	breast:
16	chr14:44659162..44661192-chr14:44662497..44664945,3	MCF-7	breast:
17	chr14:44562970..44563903-chr14:44618440..44619350,3	MCF-7	breast:
18	chr14:44834762..44837688-chr14:44839758..44841386,2	MCF-7	breast:
19	chr14:43972518..43973359-chr14:44264541..44265550,6	MCF-7	breast:
20	chr14:44799704..44802515-chr14:44803665..44805548,2	K562	blood:
21	chr14:44600217..44602036-chr14:44604194..44606588,2	K562	blood:
22	chr14:44836359..44838272-chr14:44839234..44841841,2	K562	blood:
23	chr14:43972805..43973364-chr14:44367745..44368249,2	MCF-7	breast:
24	chr14:44803036..44805789-chr14:44807681..44809917,2	MCF-7	breast:
25	chr14:44364217..44368954-chr14:44370108..44373061,4	MCF-7	breast:
26	chr14:44370894..44373377-chr14:44375088..44376684,2	MCF-7	breast:
27	chr14:44430928..44433388-chr14:44437033..44439809,2	MCF-7	breast:
28	chr14:44785511..44787603-chr14:44801475..44804165,2	MCF-7	breast:
29	chr14:44836359..44838272-chr14:44839234..44841841,3	K562	blood:
30	chr14:44856514..44860245-chr14:44862169..44864602,3	K562	blood:
31	chr14:44430928..44433388-chr14:44437033..44439809,2	MCF-7	breast:
32	chr14:44799704..44802515-chr14:44803665..44805548,2	K562	blood:
33	chr14:44429802..44430574-chr20:39327036..39327797,2	MCF-7	breast:
34	chr14:44369406..44371311-chr14:44371355..44373381,2	MCF-7	breast:
35	chr14:44836359..44838272-chr14:44839234..44841841,3	K562	blood:
36	chr14:44118768..44119290-chr14:44370795..44371415,2	MCF-7	breast:
37	chr11:64084683..64085194-chr14:44328405..44329034,2	MCF-7	breast:
38	chr14:43380269..43381028-chr14:44264574..44265376,2	MCF-7	breast:
39	chr14:44755644..44758887-chr14:44761125..44763162,3	K562	blood:
40	chr14:44370894..44373377-chr14:44375088..44376684,2	MCF-7	breast:
41	chr14:44364361..44366552-chr14:44370416..44373233,2	MCF-7	breast:
42	chr14:44370246..44372256-chr14:44617257..44619025,2	MCF-7	breast:
43	chr14:44569949..44570449-chr8:101630587..101631141,2	MCF-7	breast:
44	chr14:44249152..44254471-chr14:44260369..44263257,5	MCF-7	breast:
45	chr14:44480170..44481920-chr14:44484152..44486382,2	MCF-7	breast:
46	chr14:44754776..44756782-chr14:44760420..44763272,3	MCF-7	breast:
47	chr14:44118185..44120883-chr14:44261367..44263957,2	MCF-7	breast:
48	chr14:44370633..44373508-chr14:44616084..44618482,2	MCF-7	breast:
49	chr14:44369406..44371311-chr14:44371355..44373381,2	MCF-7	breast:
50	chr14:44838612..44839205-chr14:44974588..44975472,2	MCF-7	breast:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSCB-6	chr14:44622425-44622966	l_977_chr14:44621312-44622966_testes
2	lnc-FSCB-6	chr14:44621821-44621918	l_977_chr14:44621312-44622966_testes
3	lnc-C14orf28-3	chr14:44270413-44270454	NONHSAT036601
4	lnc-FSCB-5	chr14:44760200-44760921	NONHSAT036604
5	lnc-FSCB-2	chr14:44518586-44518710	ENSG00000258969
6	lnc-FSCB-6	chr14:44621313-44621629	l_977_chr14:44621312-44622966_testes
7	lnc-FSCB-7	chr14:44546737-44547087	NONHSAT036603
8	lnc-FSCB-2	chr14:44853680-44853748	ENSG00000258969
9	lnc-FSCB-9	chr14:44304444-44304588	l_976_chr14:44304204-44307081_thyroid
10	lnc-FSCB-9	chr14:44326723-44326896	l_976_chr14:44304204-44307081_thyroid
11	lnc-FSCB-9	chr14:44304205-44304400	l_976_chr14:44304204-44307081_thyroid
12	lnc-FSCB-9	chr14:44336883-44336965	l_976_chr14:44304204-44307081_thyroid
13	lnc-FSCB-1	chr14:44862209-44862941	XLOC_011006
14	lnc-FSCB-1	chr14:44861702-44861893	XLOC_011006
15	lnc-FSCB-8	chr14:44477505-44479523	ucscGeneNc_uc001wvs_1
16	lnc-FSCB-1	chr14:44861745-44861893	ENSG00000259126
17	lnc-C14orf28-3	chr14:44266689-44266858	NONHSAT036601
18	lnc-FSCB-6	chr14:44622029-44622354	l_977_chr14:44621312-44622966_testes
19	lnc-FSCB-2	chr14:44464984-44465046	ENSG00000258969
20	lnc-FSCB-9	chr14:44305172-44305287	l_976_chr14:44304204-44307081_thyroid
21	lnc-FSCB-9	chr14:44337342-44337506	l_976_chr14:44304204-44307081_thyroid
22	lnc-FSCB-9	chr14:44306948-44307084	l_976_chr14:44304204-44307081_thyroid
23	lnc-FSCB-1	chr14:44861734-44861893	ENSG00000259126

No data

Variant related genes	Relation type
ENSG00000259137	TF binding region
ENSG00000259019	TF binding region
ENSG00000259148	TF binding region
ENSG00000258969	TF binding region
ENSG00000259137	CpG island
ENSG00000259019	CpG island
ENSG00000259148	CpG island
ENSG00000258969	CpG island
ENSG00000259148	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000259126	chromatin interactions
ENSG00000178096	chromatin interactions
ENSG00000173113	chromatin interactions
ENSG00000187790	chromatin interactions
ENSG00000184270	chromatin interactions
ENSG00000229771	chromatin interactions
ENSG00000174226	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000253740	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000100442	chromatin interactions
FAM134B	miRNA target sites

Extended variants
information (count: 8023 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:8023 , 50 per page) page: 1 2 3 4 5 6 7 ... 161

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560554889	chr14:44259183-44259184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs144822497	chr14:44259196-44259197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552472713	chr14:44259210-44259211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138590389	chr14:44259223-44259224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531209692	chr14:44259272-44259273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541739073	chr14:44259276-44259277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548854607	chr14:44259283-44259284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184428226	chr14:44259286-44259287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs4584742	chr14:44259289-44259290	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs568138980	chr14:44259333-44259334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs189204118	chr14:44259400-44259401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181184313	chr14:44259439-44259440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565761183	chr14:44259446-44259447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12590334	chr14:44259489-44259490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs7155339	chr14:44259505-44259506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10484242	chr14:44259509-44259510	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs17114395	chr14:44259549-44259550	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs189130847	chr14:44259573-44259574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12588034	chr14:44259626-44259627	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs147986050	chr14:44259675-44259676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs141990594	chr14:44259677-44259678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567876349	chr14:44259678-44259679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536854470	chr14:44259715-44259716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572321574	chr14:44259794-44259795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs147326213	chr14:44259796-44259797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376288759	chr14:44259807-44259808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139200070	chr14:44259811-44259812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143198108	chr14:44259812-44259813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147522362	chr14:44259813-44259814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs546013233	chr14:44259939-44259940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561555966	chr14:44259943-44259944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs180704098	chr14:44259944-44259945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185956307	chr14:44259952-44259953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573202773	chr14:44259967-44259968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531498653	chr14:44259997-44259998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192164101	chr14:44259999-44260000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536284927	chr14:44260026-44260027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150517435	chr14:44260038-44260039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139294813	chr14:44260039-44260040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75099276	chr14:44260044-44260045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537379419	chr14:44260063-44260064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs61998442	chr14:44260098-44260099	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs150018306	chr14:44260162-44260163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs58590384	chr14:44260173-44260174	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs144212999	chr14:44260220-44260221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572253295	chr14:44260221-44260222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185816802	chr14:44260248-44260249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547708236	chr14:44260250-44260251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs373473591	chr14:44260323-44260324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544836155	chr14:44260387-44260388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Mortal	21835882	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:44250200-44262800	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr14:44258800-44265400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr14:44259000-44261400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr14:44261400-44263000	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr14:44262200-44262800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr14:44262400-44262800	Enhancers	Fetal Heart	heart
7	chr14:44262400-44263400	Enhancers	Liver	Liver
8	chr14:44262800-44263400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr14:44262800-44263400	Enhancers	HepG2	liver
10	chr14:44262800-44265400	Weak transcription	Fetal Heart	heart
11	chr14:44263400-44265600	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr14:44265000-44266000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr14:44265400-44266400	Enhancers	Fetal Heart	heart
14	chr14:44265400-44266600	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr14:44265600-44266600	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr14:44266000-44266600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr14:44266000-44266600	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr14:44266600-44268000	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr14:44268400-44268600	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr14:44271800-44273000	Enhancers	Hela-S3	cervix
21	chr14:44272000-44272800	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
22	chr14:44272200-44272600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
23	chr14:44272200-44273000	Enhancers	HepG2	liver
24	chr14:44272400-44272600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr14:44272600-44275000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr14:44273000-44273800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr14:44275000-44275200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr14:44276800-44278000	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr14:44280800-44281400	Enhancers	Adipose Nuclei	Adipose
30	chr14:44302000-44303600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr14:44312400-44312800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr14:44321400-44321600	Enhancers	Fetal Brain Male	brain
33	chr14:44321600-44322600	Weak transcription	Fetal Brain Male	brain
34	chr14:44322600-44323000	Enhancers	Fetal Lung	lung
35	chr14:44322600-44323400	Enhancers	Fetal Brain Male	brain
36	chr14:44322800-44323000	Enhancers	Fetal Heart	heart
37	chr14:44323000-44324600	Weak transcription	Fetal Lung	lung
38	chr14:44323400-44324200	Weak transcription	Fetal Brain Male	brain
39	chr14:44324200-44326200	Enhancers	Fetal Brain Male	brain
40	chr14:44324600-44325200	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr14:44324600-44325400	Enhancers	Fetal Lung	lung
42	chr14:44324800-44325200	Enhancers	Fetal Stomach	stomach
43	chr14:44324800-44325600	Enhancers	Fetal Heart	heart
44	chr14:44326400-44338600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr14:44328400-44328800	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr14:44328400-44329000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr14:44328400-44329000	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr14:44328600-44329000	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr14:44336800-44337000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr14:44337000-44338000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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