Variant report

Variant	nsv976845
Chromosome Location	chr14:77621865-77649191
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:307)
CpG islands
(count:854)
Chromatin interactive
region (count:31)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr14:77647709-77648274	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr14:77624605-77624993	H1-hESC	embryonic stem cell:	n/a	chr14:77624707-77624721
3	BACH1	chr14:77647926-77648568	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr14:77622103-77622443	GM12878	blood:	n/a	n/a
5	BCL3	chr14:77624624-77625044	GM12878	blood:	n/a	n/a
6	BCL3	chr14:77624563-77625093	GM12878	blood:	n/a	n/a
7	BHLHE40	chr14:77624625-77624700	K562	blood:	n/a	n/a
8	CBX3	chr14:77636309-77636879	HCT-116	colon:	n/a	n/a
9	CBX3	chr14:77636389-77636702	K562	blood:	n/a	n/a
10	CBX3	chr14:77636348-77636770	K562	blood:	n/a	n/a
11	CBX3	chr14:77636277-77636735	HCT-116	colon:	n/a	n/a
12	CEBPB	chr14:77622961-77623347	HepG2	liver:	n/a	chr14:77623106-77623117
13	CEBPB	chr14:77631284-77631561	Hela-S3	cervix:	n/a	chr14:77631413-77631424
14	CEBPB	chr14:77623364-77623387	K562	blood:	n/a	chr14:77623373-77623384
15	CEBPB	chr14:77631294-77631495	IMR90	lung:	n/a	chr14:77631413-77631424
16	CEBPB	chr14:77631284-77631577	A549	lung:	n/a	chr14:77631413-77631424
17	CEBPB	chr14:77623107-77623127	A549	lung:	n/a	n/a
18	CEBPB	chr14:77622947-77623396	HepG2	liver:	n/a	chr14:77623373-77623384 chr14:77623106-77623117
19	CEBPB	chr14:77631311-77631573	HepG2	liver:	n/a	chr14:77631413-77631424
20	CEBPB	chr14:77631392-77631489	K562	blood:	n/a	chr14:77631413-77631424
21	CEBPB	chr14:77622997-77623198	HepG2	liver:	n/a	chr14:77623106-77623117
22	CEBPB	chr14:77622998-77623221	HepG2	liver:	n/a	chr14:77623106-77623117
23	CHD2	chr14:77647712-77648186	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr14:77647846-77648263	A549	lung:	n/a	n/a
25	CREB1	chr14:77647622-77648449	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr14:77647522-77648391	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTBP2	chr14:77647662-77648717	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr14:77648609-77648704	GM12891	blood:	n/a	n/a
29	CTCF	chr14:77648560-77648710	HEEpiC	esophagus:	n/a	n/a
30	CTCF	chr14:77624556-77624623	Gliobla	brain:	n/a	chr14:77624572-77624581 chr14:77624569-77624582
31	CTCF	chr14:77624756-77624951	GM19239	blood:	n/a	n/a
32	CTCF	chr14:77648540-77648690	SAEC	small airway:	n/a	n/a
33	CTCF	chr14:77648540-77648690	Caco-2	colon:	n/a	n/a
34	CTCF	chr14:77624520-77624670	AG04449	skin:	n/a	chr14:77624572-77624581 chr14:77624569-77624582
35	CTCF	chr14:77624440-77624590	SK-N-SH_RA	brain:	n/a	chr14:77624572-77624581 chr14:77624569-77624582
36	CTCF	chr14:77648500-77648650	HRE	kidney:	n/a	n/a
37	CTCF	chr14:77648560-77648710	Caco-2	colon:	n/a	n/a
38	CTCF	chr14:77630527-77630617	HepG2	liver:	n/a	n/a
39	CTCF	chr14:77648617-77648693	GM12878	blood:	n/a	n/a
40	CTCF	chr14:77648623-77648694	GM19240	blood:	n/a	n/a
41	CTCF	chr14:77630548-77630619	GM10266	blood:	n/a	n/a
42	CTCF	chr14:77624440-77624590	HepG2	liver:	n/a	chr14:77624572-77624581 chr14:77624569-77624582
43	CTCF	chr14:77630460-77630610	MCF-7	breast:	n/a	n/a
44	CTCF	chr14:77630569-77630582	MCF-7	breast:	n/a	n/a
45	CTCF	chr14:77648580-77648730	GM12868	blood:	n/a	n/a
46	CTCF	chr14:77648380-77648530	GM06990	blood:	n/a	n/a
47	CTCF	chr14:77624528-77624822	H1-hESC	embryonic stem cell:	n/a	chr14:77624572-77624581 chr14:77624569-77624582
48	CTCF	chr14:77630280-77630430	A549	lung:	n/a	n/a
49	CTCF	chr14:77630547-77630657	K562	blood:	n/a	n/a
50	CTCF	chr14:77648660-77648810	BE2_C	brain:	n/a	chr14:77648732-77648741

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:77647704-77647754	AG04450	lung:	fetal
2	chr14:77647063-77647113	ProgFib	skin:	n/a
3	chr14:77647704-77647754	HEK293	kidney:	embryo
4	chr14:77648283-77648333	HCT-116	colon:	n/a
5	chr14:77648007-77648057	HRCEpiC	kidney:	n/a
6	chr14:77648491-77648541	HMEC	breast:	n/a
7	chr14:77647482-77647532	NB4	blood:	n/a
8	chr14:77647983-77648033	HCM	heart:	n/a
9	chr14:77648199-77648249	SK-N-MC	brain:	n/a
10	chr14:77647704-77647754	HRE	kidney:	n/a
11	chr14:77645945-77645995	A549	lung:	n/a
12	chr14:77647063-77647113	AG09319	gingival:	n/a
13	chr14:77648283-77648333	A549	lung:	n/a
14	chr14:77648283-77648333	GM12891	blood:	n/a
15	chr14:77647482-77647532	ECC-1	luminal epithelium:	n/a
16	chr14:77648283-77648333	Hela-S3	cervix:	n/a
17	chr14:77647955-77648005	PFSK-1	brain:	n/a
18	chr14:77648007-77648057	CMK	blood:	n/a
19	chr14:77647983-77648033	HRCEpiC	kidney:	n/a
20	chr14:77647482-77647532	H1-hESC	embryonic stem cell:	embryo
21	chr14:77645945-77645995	AoSMC	blood vessel:	n/a
22	chr14:77648007-77648057	GM12891	blood:	n/a
23	chr14:77648199-77648249	MCF-7	breast:	n/a
24	chr14:77648491-77648541	NT2-D1	testis:	n/a
25	chr14:77648199-77648249	NT2-D1	testis:	n/a
26	chr14:77647482-77647532	MCF10A-Er-Src	breast:	n/a
27	chr14:77648007-77648057	HPAEpiC	pulmonary alveolar:	n/a
28	chr14:77647063-77647113	GM12892	blood:	n/a
29	chr14:77648199-77648249	ovcar-3	ovarian:	n/a
30	chr14:77648491-77648541	T-47D	breast:	n/a
31	chr14:77648248-77648298	HNPCEpiC	eye:	n/a
32	chr14:77648040-77648090	MCF10A-Er-Src	breast:	n/a
33	chr14:77648007-77648057	ECC-1	luminal epithelium:	n/a
34	chr14:77647063-77647113	AG09309	skin:	n/a
35	chr14:77647983-77648033	AG04449	skin:	fetal
36	chr14:77648007-77648057	Hepatocyte	liver:	n/a
37	chr14:77648248-77648298	HPAEpiC	pulmonary alveolar:	n/a
38	chr14:77647957-77648007	SKMC	muscle:	n/a
39	chr14:77647955-77648005	NB4	blood:	n/a
40	chr14:77647955-77648005	GM06990	blood:	n/a
41	chr14:77645945-77645995	AG04450	lung:	fetal
42	chr14:77624538-77624588	T-47D	breast:	n/a
43	chr14:77647983-77648033	U87	brain:	n/a
44	chr14:77647957-77648007	NHDF-neo	bronchial:	n/a
45	chr14:77645945-77645995	HPAEpiC	pulmonary alveolar:	n/a
46	chr14:77647063-77647113	HIPEpiC	eye:	n/a
47	chr14:77648040-77648090	HepG2	liver:	n/a
48	chr14:77648248-77648298	HUVEC	blood vessel:	n/a
49	chr14:77647957-77648007	HCM	heart:	n/a
50	chr14:77648040-77648090	SK-N-SH_RA	brain:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:77642180..77644687-chr14:77647056..77649855,2	MCF-7	breast:
2	chr14:77640676..77643134-chr14:77646615..77650592,3	MCF-7	breast:
3	chr14:77647339..77650955-chr14:77785389..77788358,5	MCF-7	breast:
4	chr14:77617758..77621204-chr14:77622193..77625212,3	MCF-7	breast:
5	chr14:77606589..77609950-chr14:77648751..77652223,3	MCF-7	breast:
6	chr14:77626668..77630109-chr14:77635691..77637532,3	MCF-7	breast:
7	chr14:77646079..77647711-chr14:77656807..77658749,2	MCF-7	breast:
8	chr14:77646577..77649681-chr14:77786771..77790034,4	MCF-7	breast:
9	chr14:77639432..77641882-chr14:77645275..77647716,2	MCF-7	breast:
10	chr14:77626056..77627919-chr14:77723714..77725727,2	MCF-7	breast:
11	chr14:77621398..77624327-chr14:77786933..77789294,4	MCF-7	breast:
12	chr14:77624226..77624977-chr14:77679451..77680184,2	MCF-7	breast:
13	chr14:77648815..77651444-chr14:77730169..77732622,2	MCF-7	breast:
14	chr14:77635396..77638005-chr14:77648912..77652690,3	MCF-7	breast:
15	chr14:77623679..77628078-chr14:77791213..77793958,3	MCF-7	breast:
16	chr14:77640676..77643134-chr14:77646615..77650592,3	MCF-7	breast:
17	chr14:77648085..77652144-chr14:77770230..77773335,4	MCF-7	breast:
18	chr14:77639702..77642054-chr14:77787547..77789346,2	MCF-7	breast:
19	chr14:77618647..77620331-chr14:77622173..77624872,2	K562	blood:
20	chr14:77624750..77626748-chr14:77767374..77769849,2	MCF-7	breast:
21	chr14:77635698..77637965-chr14:77784334..77787090,2	MCF-7	breast:
22	chr14:77561433..77566071-chr14:77618865..77621924,5	MCF-7	breast:
23	chr14:77644659..77647131-chr14:77754541..77756569,2	MCF-7	breast:
24	chr14:77562647..77564401-chr14:77648231..77649984,2	MCF-7	breast:
25	chr14:77615331..77626101-chr14:77782557..77793016,18	MCF-7	breast:
26	chr14:77618067..77622242-chr14:77780236..77782516,4	MCF-7	breast:
27	chr14:77626668..77630109-chr14:77635691..77637532,3	MCF-7	breast:
28	chr14:77646733..77650700-chr14:77767687..77771144,4	MCF-7	breast:
29	chr14:77646354..77648830-chr14:77666464..77668226,2	MCF-7	breast:
30	chr14:77635396..77638005-chr14:77648912..77652690,3	MCF-7	breast:
31	chr14:77642180..77644687-chr14:77647056..77649855,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZDHHC22-1	chr14:77639418-77639995	NONHSAT037963
2	lnc-KIAA1737-5	chr14:77642199-77642317	NONHSAT037964

No data

Variant related genes	Relation type
ENSG00000258552	TF binding region
TMEM63C	TF binding region
ENSG00000258552	CpG island
TMEM63C	CpG island
ENSG00000269883	chromatin interactions
ENSG00000259164	chromatin interactions
ENSG00000177108	chromatin interactions
ENSG00000165548	chromatin interactions
ENSG00000201384	chromatin interactions
ENSG00000221754	chromatin interactions
ENSG00000198894	chromatin interactions
ENSG00000258552	chromatin interactions
ENSG00000009830	chromatin interactions
ENSG00000100577	chromatin interactions

Extended variants
information (count: 1079 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1079 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555205153	chr14:77621890-77621891	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs189936796	chr14:77621917-77621918	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs528040311	chr14:77621919-77621920	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs567564400	chr14:77621929-77621930	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs559530826	chr14:77621934-77621935	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs112224801	chr14:77621942-77621943	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs386779017	chr14:77621964-77621965	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs2023502	chr14:77621966-77621967	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs374368806	chr14:77621969-77621970	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs376146240	chr14:77621976-77621977	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs532370864	chr14:77622041-77622042	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs564327214	chr14:77622139-77622140	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs578007290	chr14:77622151-77622152	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs188306183	chr14:77622174-77622175	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs551129501	chr14:77622176-77622177	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs562924426	chr14:77622197-77622198	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs531638304	chr14:77622234-77622235	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs17105411	chr14:77622256-77622257	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs561889550	chr14:77622257-77622258	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs572353731	chr14:77622308-77622309	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs527832054	chr14:77622411-77622412	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs139746732	chr14:77622422-77622423	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs202081484	chr14:77622462-77622463	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs200368147	chr14:77622463-77622464	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs373859759	chr14:77622464-77622465	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs201507940	chr14:77622468-77622469	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs158109	chr14:77622470-77622471	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs569616743	chr14:77622489-77622490	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs12883659	chr14:77622509-77622510	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs548618153	chr14:77622534-77622535	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs180698265	chr14:77622537-77622538	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs552196227	chr14:77622540-77622541	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs377207146	chr14:77622569-77622570	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs12885136	chr14:77622585-77622586	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs372826665	chr14:77622603-77622604	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs61990326	chr14:77622604-77622605	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs186265070	chr14:77622612-77622613	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs553406520	chr14:77622620-77622621	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs557010757	chr14:77622622-77622623	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs368830132	chr14:77622626-77622627	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs376935885	chr14:77622638-77622639	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs11434884	chr14:77622639-77622640	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs67335288	chr14:77622640-77622641	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs141021919	chr14:77622706-77622707	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs166967	chr14:77622721-77622722	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs561802704	chr14:77622832-77622833	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs190779206	chr14:77622833-77622834	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs373085267	chr14:77622841-77622842	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs371638438	chr14:77622843-77622844	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs541197418	chr14:77622844-77622845	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Biliary cancer	19435499	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Intracranial aneurysm	16715129	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:77613800-77624800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr14:77615400-77624200	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr14:77618200-77624200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr14:77620200-77624000	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr14:77620400-77622400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr14:77620600-77622000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr14:77620600-77622000	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr14:77620600-77622000	Enhancers	Brain Hippocampus Middle	brain
9	chr14:77620800-77622000	Enhancers	Fetal Brain Male	brain
10	chr14:77620800-77622000	Bivalent Enhancer	Fetal Muscle Leg	muscle
11	chr14:77621200-77622600	Enhancers	Brain Germinal Matrix	brain
12	chr14:77621200-77624200	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr14:77621200-77624200	Weak transcription	Fetal Brain Female	brain
14	chr14:77621400-77622000	Enhancers	Fetal Heart	heart
15	chr14:77621400-77622200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr14:77621400-77622200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr14:77621400-77624200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr14:77621400-77624200	Weak transcription	Brain Substantia Nigra	brain
19	chr14:77621400-77624600	Weak transcription	Esophagus	oesophagus
20	chr14:77621600-77622000	Enhancers	Left Ventricle	heart
21	chr14:77621600-77622000	Enhancers	Right Atrium	heart
22	chr14:77621600-77623400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr14:77621600-77624200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr14:77621600-77624200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr14:77621600-77624200	Weak transcription	Brain Anterior Caudate	brain
26	chr14:77621600-77624200	Weak transcription	Brain Cingulate Gyrus	brain
27	chr14:77621800-77622000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
28	chr14:77621800-77622200	Weak transcription	Brain Angular Gyrus	brain
29	chr14:77621800-77624000	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr14:77622000-77624000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr14:77622000-77624200	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr14:77622000-77624200	Weak transcription	Brain Hippocampus Middle	brain
33	chr14:77622000-77624200	Weak transcription	Fetal Brain Male	brain
34	chr14:77622000-77624800	Weak transcription	Left Ventricle	heart
35	chr14:77622000-77624800	Weak transcription	Right Atrium	heart
36	chr14:77622200-77622400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr14:77622200-77622400	Enhancers	Brain Angular Gyrus	brain
38	chr14:77622200-77622400	Bivalent Enhancer	Fetal Intestine Large	intestine
39	chr14:77622200-77624000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr14:77622200-77624200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
41	chr14:77622400-77624200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr14:77622400-77624200	Weak transcription	Brain Angular Gyrus	brain
43	chr14:77622600-77623000	Weak transcription	Brain Germinal Matrix	brain
44	chr14:77623000-77623200	Enhancers	Brain Germinal Matrix	brain
45	chr14:77623200-77624200	Weak transcription	Brain Germinal Matrix	brain
46	chr14:77623400-77624200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr14:77624000-77624200	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr14:77624000-77624400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr14:77624000-77624600	Enhancers	H9 Cell Line	embryonic stem cell
50	chr14:77624000-77624600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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