Variant report

Variant	nsv902074
Chromosome Location	chr14:69339691-69360631
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:392)
CpG islands
(count:551)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:392 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr14:69340227-69340392	A549	lung:	n/a	n/a
2	CEBPB	chr14:69341102-69341418	HepG2	liver:	n/a	n/a
3	CEBPB	chr14:69341145-69341345	K562	blood:	n/a	n/a
4	CEBPB	chr14:69340146-69340426	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr14:69341093-69341425	IMR90	lung:	n/a	n/a
6	CEBPB	chr14:69357231-69357540	HepG2	liver:	n/a	n/a
7	CEBPB	chr14:69341121-69341424	A549	lung:	n/a	n/a
8	CREB1	chr14:69350931-69351624	A549	lung:	n/a	n/a
9	CTCF	chr14:69359887-69359976	GM12892	blood:	n/a	chr14:69359926-69359944
10	CTCF	chr14:69352760-69352910	A549	lung:	n/a	n/a
11	CTCF	chr14:69341635-69341736	Kidney_OC	kidney:	n/a	n/a
12	CTCF	chr14:69355180-69355330	Caco-2	colon:	n/a	n/a
13	CTCF	chr14:69352660-69352810	AG04450	lung:	n/a	chr14:69352702-69352715
14	CTCF	chr14:69359540-69359690	HCPEpiC	choroid plexus:	n/a	chr14:69359589-69359597
15	CTCF	chr14:69355260-69355410	HPAF	blood vessel:	n/a	n/a
16	CTCF	chr14:69354880-69355030	MCF-7	breast:	n/a	n/a
17	CTCF	chr14:69359860-69360010	BJ	skin:	n/a	chr14:69359926-69359944
18	CTCF	chr14:69355013-69355036	Lung_OC	lung:	n/a	n/a
19	CTCF	chr14:69352760-69352910	AG04450	lung:	n/a	n/a
20	CTCF	chr14:69358561-69358636	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr14:69354940-69355090	A549	lung:	n/a	chr14:69355033-69355042 chr14:69355032-69355045 chr14:69355035-69355048
22	CTCF	chr14:69355180-69355330	HRE	kidney:	n/a	n/a
23	CTCF	chr14:69341601-69341759	GM12892	blood:	n/a	n/a
24	CTCF	chr14:69352772-69352814	MCF-7	breast:	n/a	n/a
25	CTCF	chr14:69341511-69341554	GM12892	blood:	n/a	n/a
26	CTCF	chr14:69355040-69355058	ProgFib	skin:	n/a	n/a
27	CTCF	chr14:69352780-69352930	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr14:69355180-69355330	AG04449	skin:	n/a	n/a
29	CTCF	chr14:69341540-69341690	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr14:69355049-69355116	NHEK	skin:	n/a	n/a
31	CTCF	chr14:69341600-69341750	SAEC	small airway:	n/a	n/a
32	CTCF	chr14:69354920-69355070	HMEC	breast:	n/a	chr14:69355033-69355042 chr14:69355032-69355045 chr14:69355035-69355048
33	CTCF	chr14:69352620-69352770	HPAF	blood vessel:	n/a	chr14:69352702-69352715
34	CTCF	chr14:69340340-69340490	BE2_C	brain:	n/a	n/a
35	CTCF	chr14:69354940-69355090	HRPEpiC	eye:	n/a	chr14:69355033-69355042 chr14:69355032-69355045 chr14:69355035-69355048
36	CTCF	chr14:69352760-69352910	BJ	skin:	n/a	n/a
37	CTCF	chr14:69355020-69355170	RPTEC	kidney:	n/a	chr14:69355033-69355042 chr14:69355032-69355045 chr14:69355035-69355048
38	CTCF	chr14:69352780-69352930	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr14:69352760-69352910	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr14:69352771-69352807	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr14:69355006-69355058	H1-hESC	embryonic stem cell:	n/a	chr14:69355033-69355042 chr14:69355032-69355045 chr14:69355035-69355048
42	CTCF	chr14:69354960-69355110	RPTEC	kidney:	n/a	chr14:69355033-69355042 chr14:69355032-69355045 chr14:69355035-69355048
43	CTCF	chr14:69355011-69355044	Kidney_OC	kidney:	n/a	chr14:69355033-69355042
44	CTCF	chr14:69359880-69360030	HMF	breast:	n/a	chr14:69359926-69359944
45	CTCF	chr14:69355080-69355230	BJ	skin:	n/a	n/a
46	CTCF	chr14:69359780-69359930	HepG2	liver:	n/a	n/a
47	CTCF	chr14:69352680-69352830	HepG2	liver:	n/a	chr14:69352702-69352715
48	CTCF	chr14:69341640-69341790	HCT-116	colon:	n/a	n/a
49	CTCF	chr14:69355160-69355310	HAc	cerebellar:	n/a	n/a
50	CTCF	chr14:69359460-69359610	NHEK	skin:	n/a	chr14:69359589-69359597

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:69341603-69341653	T-47D	breast:	n/a
2	chr14:69341603-69341653	HAEpiC	amniotic membrane:	n/a
3	chr14:69341603-69341653	T-47D	breast:	n/a
4	chr14:69341603-69341653	HAEpiC	amniotic membrane:	n/a
5	chr14:69341139-69341189	NHBE	bronchial:	n/a
6	chr14:69341905-69341955	HRCEpiC	kidney:	n/a
7	chr14:69354734-69354784	Jurkat	blood:	n/a
8	chr14:69341430-69341480	H1-hESC	embryonic stem cell:	embryo
9	chr14:69341738-69341788	BJ	skin:	n/a
10	chr14:69341738-69341788	AG04450	lung:	fetal
11	chr14:69341603-69341653	GM06990	blood:	n/a
12	chr14:69344852-69344902	Hela-S3	cervix:	n/a
13	chr14:69344852-69344902	CMK	blood:	n/a
14	chr14:69341738-69341788	MCF-7	breast:	n/a
15	chr14:69354819-69354869	SK-N-MC	brain:	n/a
16	chr14:69354819-69354869	GM12892	blood:	n/a
17	chr14:69344852-69344902	AG04450	lung:	fetal
18	chr14:69341905-69341955	PANC-1	pancreas:	n/a
19	chr14:69341738-69341788	RPTEC	kidney:	n/a
20	chr14:69341603-69341653	NT2-D1	testis:	n/a
21	chr14:69341738-69341788	HRE	kidney:	n/a
22	chr14:69341905-69341955	HCPEpiC	choroid plexus:	n/a
23	chr14:69351311-69351361	RPTEC	kidney:	n/a
24	chr14:69354819-69354869	NH-A	brain:	n/a
25	chr14:69344852-69344902	BJ	skin:	n/a
26	chr14:69341738-69341788	BE2_C	brain:	n/a
27	chr14:69341905-69341955	AG09309	skin:	n/a
28	chr14:69341905-69341955	GM12892	blood:	n/a
29	chr14:69341139-69341189	AG10803	skin:	n/a
30	chr14:69341905-69341955	H1-hESC	embryonic stem cell:	embryo
31	chr14:69341430-69341480	Jurkat	blood:	n/a
32	chr14:69344852-69344902	ECC-1	luminal epithelium:	n/a
33	chr14:69341430-69341480	CMK	blood:	n/a
34	chr14:69344852-69344902	PANC-1	pancreas:	n/a
35	chr14:69341139-69341189	SK-N-MC	brain:	n/a
36	chr14:69354734-69354784	U87	brain:	n/a
37	chr14:69341430-69341480	NB4	blood:	n/a
38	chr14:69354819-69354869	NHBE	bronchial:	n/a
39	chr14:69341430-69341480	SK-N-MC	brain:	n/a
40	chr14:69351311-69351361	NH-A	brain:	n/a
41	chr14:69354734-69354784	HUVEC	blood vessel:	n/a
42	chr14:69341738-69341788	Hela-S3	cervix:	n/a
43	chr14:69341905-69341955	SK-N-MC	brain:	n/a
44	chr14:69354819-69354869	HCT-116	colon:	n/a
45	chr14:69341430-69341480	PFSK-1	brain:	n/a
46	chr14:69341905-69341955	HRE	kidney:	n/a
47	chr14:69341603-69341653	HepG2	liver:	n/a
48	chr14:69354819-69354869	HIPEpiC	eye:	n/a
49	chr14:69354819-69354869	SK-N-SH	brain:	n/a
50	chr14:69354819-69354869	RPTEC	kidney:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:69258431..69260776-chr14:69342311..69344169,2	MCF-7	breast:
2	chr14:69339299..69342243-chr14:69346709..69349197,2	K562	blood:
3	chr14:69360053..69363258-chr14:69363316..69367429,3	K562	blood:
4	chr14:69335131..69337608-chr14:69359625..69361996,2	MCF-7	breast:
5	chr14:69351207..69353545-chr14:69360069..69361747,2	MCF-7	breast:
6	chr14:69343145..69344900-chr14:69346743..69349990,3	K562	blood:
7	chr14:69341893..69344810-chr14:69345203..69347658,2	MCF-7	breast:
8	chr14:69351207..69353545-chr14:69360069..69361747,2	MCF-7	breast:
9	chr14:69358005..69360954-chr14:69365847..69368420,3	MCF-7	breast:
10	chr14:69339299..69343925-chr14:69346207..69350701,5	K562	blood:
11	chr14:69342043..69343868-chr14:69343974..69346142,2	MCF-7	breast:
12	chr14:69340121..69342574-chr14:69346978..69348522,2	MCF-7	breast:
13	chr14:69334968..69337458-chr14:69339261..69341131,2	MCF-7	breast:
14	chr14:69347920..69352793-chr14:69354599..69357859,5	MCF-7	breast:
15	chr14:69344263..69347194-chr14:69349604..69352915,4	MCF-7	breast:
16	chr14:69344263..69347194-chr14:69349604..69352915,4	MCF-7	breast:
17	chr14:69347920..69352793-chr14:69354599..69357859,5	MCF-7	breast:

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ACTN1	hsa-miR-16-5p	chr14:69341084-69341106
2	ACTN1	hsa-miR-218-5p	chr14:69341238-69341257
3	ACTN1	hsa-miR-218-5p	chr14:69341244-69341237

Variant related genes	Relation type
HMGN1P3	TF binding region
BLZF2P	TF binding region
ACTN1	TF binding region
HMGN1P3	CpG island
BLZF2P	CpG island
ACTN1	CpG island
ENSG00000258967	chromatin interactions
ENSG00000258565	chromatin interactions
ENSG00000185650	chromatin interactions
ENSG00000072110	chromatin interactions

Extended variants
information (count: 937 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:937 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17106449	chr14:69339691-69339692	Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566148655	chr14:69339695-69339696	Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs539941001	chr14:69339701-69339702	Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs17835718	chr14:69339746-69339747	Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs4902664	chr14:69339768-69339769	Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs10129289	chr14:69339834-69339835	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs556215419	chr14:69339844-69339845	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs376726806	chr14:69339863-69339864	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs72171612	chr14:69339875-69339876	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs376967590	chr14:69339877-69339878	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs79886526	chr14:69339984-69339985	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs535074164	chr14:69339994-69339995	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs369767345	chr14:69340018-69340019	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs571762177	chr14:69340040-69340041	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs545502874	chr14:69340092-69340093	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs564331830	chr14:69340102-69340103	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs138054979	chr14:69340108-69340109	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs544078513	chr14:69340172-69340173	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs562208452	chr14:69340178-69340179	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs371058476	chr14:69340184-69340185	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs541387818	chr14:69340192-69340193	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs559790374	chr14:69340198-69340199	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs533145624	chr14:69340227-69340228	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs77357695	chr14:69340271-69340272	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs373103177	chr14:69340272-69340273	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs181498318	chr14:69340276-69340277	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs113130257	chr14:69340295-69340296	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs192033914	chr14:69340305-69340306	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs142167821	chr14:69340338-69340339	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs568236766	chr14:69340351-69340352	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs535366429	chr14:69340411-69340412	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs80095531	chr14:69340426-69340427	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs555892638	chr14:69340442-69340443	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs117690792	chr14:69340456-69340457	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs150141280	chr14:69340463-69340464	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs576102688	chr14:69340486-69340487	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs540587415	chr14:69340498-69340499	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs181454	chr14:69340542-69340543	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs553581911	chr14:69340555-69340556	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs11381691	chr14:69340556-69340557	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs183093818	chr14:69340561-69340562	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs368255139	chr14:69340569-69340570	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs181456	chr14:69340599-69340600	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs559777174	chr14:69340600-69340601	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs138623176	chr14:69340618-69340619	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs79940552	chr14:69340633-69340634	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs563598837	chr14:69340689-69340690	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs576373327	chr14:69340734-69340735	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs1475034	chr14:69340760-69340761	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs186265501	chr14:69340803-69340804	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD

Chromatin state (count:556 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69310800-69339800	Weak transcription	Right Ventricle	heart
2	chr14:69330000-69351000	Weak transcription	Fetal Heart	heart
3	chr14:69330200-69348200	Weak transcription	K562	blood
4	chr14:69331200-69350800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr14:69331400-69344600	Weak transcription	Brain Angular Gyrus	brain
6	chr14:69334000-69349600	Weak transcription	Fetal Kidney	kidney
7	chr14:69334000-69350800	Strong transcription	NH-A	brain
8	chr14:69334200-69346400	Weak transcription	Stomach Mucosa	stomach
9	chr14:69336200-69341400	Weak transcription	Brain Germinal Matrix	brain
10	chr14:69336200-69349600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr14:69336200-69350800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr14:69336200-69351200	Strong transcription	HSMM	muscle
13	chr14:69336400-69341400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr14:69336400-69341600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr14:69336400-69350800	Strong transcription	NHLF	lung
16	chr14:69336400-69350800	Strong transcription	Osteobl	bone
17	chr14:69336400-69358800	Strong transcription	HSMMtube	muscle
18	chr14:69336400-69364200	Strong transcription	Primary neutrophils fromperipheralblood	blood
19	chr14:69336400-69378200	Strong transcription	Primary T cells from cord blood	blood
20	chr14:69336600-69348000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr14:69336600-69350600	Strong transcription	Muscle Satellite Cultured Cells	--
22	chr14:69336600-69351000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr14:69336600-69351000	Strong transcription	Adipose Nuclei	Adipose
24	chr14:69336600-69358600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr14:69336800-69341200	Weak transcription	Fetal Brain Female	brain
26	chr14:69336800-69343800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr14:69336800-69360400	Weak transcription	Right Atrium	heart
28	chr14:69337000-69343200	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr14:69337200-69342400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr14:69337400-69341400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr14:69337400-69341400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr14:69337400-69341400	Strong transcription	Monocytes-CD14+_RO01746	blood
33	chr14:69337400-69348000	Weak transcription	Brain Substantia Nigra	brain
34	chr14:69337400-69350800	Weak transcription	Psoas Muscle	Psoas
35	chr14:69337400-69351400	Strong transcription	Fetal Muscle Trunk	muscle
36	chr14:69337400-69353000	Strong transcription	HUES6 Cell Line	embryonic stem cell
37	chr14:69337400-69404400	Weak transcription	Fetal Brain Male	brain
38	chr14:69337600-69340000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr14:69337600-69341400	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr14:69337600-69341400	Strong transcription	Fetal Intestine Small	intestine
41	chr14:69337600-69351200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr14:69337600-69353000	Strong transcription	Aorta	Aorta
43	chr14:69337600-69361200	Strong transcription	Rectal Mucosa Donor 31	rectum
44	chr14:69337800-69340400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr14:69337800-69344000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr14:69337800-69344600	Strong transcription	Stomach Smooth Muscle	stomach
47	chr14:69337800-69345400	Strong transcription	NHDF-Ad	bronchial
48	chr14:69337800-69346200	Strong transcription	Duodenum Smooth Muscle	Duodenum
49	chr14:69337800-69350600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr14:69337800-69350600	Strong transcription	A549	lung

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