Variant report

Variant	nsv819606
Chromosome Location	chr14:24573080-24579171
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:24578996-24579645	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:24577980-24578387	HepG2	liver:	n/a	n/a
3	ATF1	chr14:24578053-24578348	K562	blood:	n/a	n/a
4	ATF2	chr14:24578012-24578494	GM12878	blood:	n/a	n/a
5	BCLAF1	chr14:24577916-24578431	GM12878	blood:	n/a	n/a
6	BCLAF1	chr14:24577922-24578426	GM12878	blood:	n/a	n/a
7	BHLHE40	chr14:24578016-24578378	GM12878	blood:	n/a	n/a
8	BHLHE40	chr14:24578078-24578338	K562	blood:	n/a	n/a
9	BHLHE40	chr14:24578035-24578376	HepG2	liver:	n/a	n/a
10	CBX3	chr14:24574190-24574504	K562	blood:	n/a	n/a
11	CBX3	chr14:24578024-24578468	K562	blood:	n/a	n/a
12	CEBPB	chr14:24576896-24577075	HepG2	liver:	n/a	chr14:24576960-24576971
13	CEBPB	chr14:24575233-24575366	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr14:24579121-24579681	HepG2	liver:	n/a	chr14:24579385-24579396
15	CTCF	chr14:24578120-24578270	HL-60	blood:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
16	CTCF	chr14:24578120-24578270	HEK293	kidney:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
17	CTCF	chr14:24578120-24578270	SAEC	small airway:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
18	CTCF	chr14:24578002-24578416	H1-hESC	embryonic stem cell:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
19	CTCF	chr14:24578024-24578329	T-47D	breast:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
20	CTCF	chr14:24578140-24578290	GM12866	blood:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
21	CTCF	chr14:24578077-24578378	A549	lung:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
22	CTCF	chr14:24578160-24578310	GM12801	blood:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
23	CTCF	chr14:24578140-24578290	AG09319	gingival:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
24	CTCF	chr14:24578160-24578310	HUVEC	blood vessel:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
25	CTCF	chr14:24578140-24578290	HBMEC	blood vessel:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
26	CTCF	chr14:24578053-24578362	MCF-7	breast:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
27	CTCF	chr14:24578100-24578250	GM12870	blood:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
28	CTCF	chr14:24578085-24578331	HepG2	liver:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
29	CTCF	chr14:24578160-24578310	WI-38	lung:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
30	CTCF	chr14:24578093-24578339	GM13976	blood:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
31	CTCF	chr14:24578140-24578290	BJ	skin:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
32	CTCF	chr14:24578065-24578334	GM19239	blood:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
33	CTCF	chr14:24578160-24578310	AG09309	skin:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
34	CTCF	chr14:24577851-24578550	MCF-7	breast:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
35	CTCF	chr14:24578120-24578308	H1-hESC	embryonic stem cell:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
36	CTCF	chr14:24578076-24578362	GM10266	blood:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
37	CTCF	chr14:24578120-24578270	Hela-S3	cervix:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
38	CTCF	chr14:24578058-24578344	A549	lung:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
39	CTCF	chr14:24577940-24578090	HAc	cerebellar:	n/a	n/a
40	CTCF	chr14:24578140-24578290	GM12869	blood:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
41	CTCF	chr14:24578100-24578250	HRPEpiC	eye:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
42	CTCF	chr14:24578140-24578290	Caco-2	colon:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
43	CTCF	chr14:24578140-24578290	HCT-116	colon:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
44	CTCF	chr14:24578086-24578347	GM10248	blood:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
45	CTCF	chr14:24578039-24578358	GM12878	blood:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
46	CTCF	chr14:24578098-24578327	GM20000	blood:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
47	CTCF	chr14:24578070-24578325	MCF-7	breast:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
48	CTCF	chr14:24578180-24578330	GM12867	blood:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
49	CTCF	chr14:24578140-24578290	HepG2	liver:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213
50	CTCF	chr14:24578065-24578354	Lung_OC	lung:	n/a	chr14:24578190-24578211 chr14:24578196-24578212 chr14:24578197-24578210 chr14:24578200-24578208 chr14:24578195-24578213

No.	Distal block	Cell Line	Cell type
1	chr14:24577316..24580506-chr14:24613504..24618387,7	MCF-7	breast:
2	chr14:24570842..24573550-chr14:24657440..24659369,2	MCF-7	breast:
3	chr14:24563398..24564210-chr14:24577622..24578539,2	NB4	blood:
4	chr14:24532041..24534501-chr14:24576665..24578239,2	MCF-7	breast:
5	chr14:24576432..24578231-chr14:24737364..24740268,2	K562	blood:
6	chr14:24578447..24580118-chr14:24606078..24608916,2	MCF-7	breast:
7	chr14:24527348..24529329-chr14:24572772..24574744,2	K562	blood:
8	chr14:23937083..23939130-chr14:24576354..24578004,2	MCF-7	breast:
9	chr14:24576568..24579822-chr14:24581236..24586094,9	MCF-7	breast:
10	chr14:24576561..24578362-chr14:24614861..24616418,2	K562	blood:
11	chr14:24520169..24522570-chr14:24571507..24573400,2	MCF-7	breast:
12	chr14:24527119..24528160-chr14:24577459..24578694,4	K562	blood:
13	chr14:24527104..24528114-chr14:24577764..24578949,8	MCF-7	breast:
14	chr14:24575156..24579604-chr14:24581629..24585415,10	K562	blood:
15	chr14:24521386..24523883-chr14:24578349..24580057,2	MCF-7	breast:
16	chr14:24527305..24528103-chr14:24577802..24578457,2	MCF-7	breast:
17	chr14:24572871..24573418-chr5:179321477..179322120,2	NB4	blood:
18	chr14:24572111..24574244-chr14:24608030..24610822,2	MCF-7	breast:
19	chr14:24519001..24521647-chr14:24574102..24575661,2	MCF-7	breast:
20	chr14:24538248..24540912-chr14:24574170..24576704,2	K562	blood:
21	chr14:24575682..24577445-chr14:24635634..24638482,2	K562	blood:
22	chr14:24526373..24527932-chr14:24577955..24579478,2	MCF-7	breast:
23	chr14:24572731..24575018-chr14:24581882..24584441,3	K562	blood:

Variant related genes	Relation type
DCAF11	TF binding region
ENSG00000100949	chromatin interactions
ENSG00000100897	chromatin interactions
ENSG00000092010	chromatin interactions
ENSG00000196497	chromatin interactions
ENSG00000100908	chromatin interactions
ENSG00000100911	chromatin interactions
ENSG00000129535	chromatin interactions
ENSG00000092098	chromatin interactions
ENSG00000186648	chromatin interactions
ENSG00000100889	chromatin interactions
ENSG00000259321	chromatin interactions
ENSG00000129460	chromatin interactions
ENSG00000100884	chromatin interactions

Extended variants
information (count: 220 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:220 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186959087	chr14:24573086-24573087	ZNF genes & repeats Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs200658873	chr14:24573092-24573093	ZNF genes & repeats Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs549471476	chr14:24573094-24573095	ZNF genes & repeats Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs529585074	chr14:24573103-24573104	ZNF genes & repeats Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs113945997	chr14:24573107-24573108	ZNF genes & repeats Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs11538428	chr14:24573120-24573121	ZNF genes & repeats Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs144940239	chr14:24573135-24573136	ZNF genes & repeats Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs142085278	chr14:24573151-24573152	ZNF genes & repeats Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs201279659	chr14:24573156-24573157	ZNF genes & repeats Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs145739132	chr14:24573157-24573158	ZNF genes & repeats Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs372280326	chr14:24573214-24573215	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs376387392	chr14:24573226-24573227	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs371133998	chr14:24573283-24573284	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs552917819	chr14:24573290-24573291	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs569631551	chr14:24573292-24573293	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs150461115	chr14:24573377-24573378	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs568099632	chr14:24573391-24573392	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs533719341	chr14:24573512-24573513	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs547163386	chr14:24573513-24573514	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs138196716	chr14:24573609-24573610	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs190405902	chr14:24573610-24573611	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs556188574	chr14:24573620-24573621	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs373832858	chr14:24573683-24573684	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs59451696	chr14:24573698-24573699	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs569231576	chr14:24573707-24573708	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs537893646	chr14:24573711-24573712	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs149166240	chr14:24573717-24573718	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs146297963	chr14:24573721-24573722	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs79750495	chr14:24573802-24573803	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs56146037	chr14:24573803-24573804	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs55785827	chr14:24573836-24573837	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs375795839	chr14:24573849-24573850	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs7160211	chr14:24573857-24573858	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs181304998	chr14:24573861-24573862	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs200193501	chr14:24573862-24573863	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs531323574	chr14:24573915-24573916	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs541491445	chr14:24573998-24573999	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs561748676	chr14:24574006-24574007	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs527353426	chr14:24574008-24574009	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs148069394	chr14:24574009-24574010	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs570265912	chr14:24574045-24574046	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs533007017	chr14:24574051-24574052	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs550039980	chr14:24574060-24574061	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs574701666	chr14:24574089-24574090	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs185329747	chr14:24574107-24574108	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs538216710	chr14:24574146-24574147	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs554636862	chr14:24574166-24574167	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs369505752	chr14:24574174-24574175	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs534242710	chr14:24574182-24574183	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs571863318	chr14:24574187-24574188	ZNF genes & repeats Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21390271	CNVD

Chromatin state (count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24564200-24575200	Weak transcription	Aorta	Aorta
2	chr14:24564800-24582600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr14:24565000-24575200	Weak transcription	HUVEC	blood vessel
4	chr14:24565000-24578000	Weak transcription	Brain Anterior Caudate	brain
5	chr14:24565000-24582600	Weak transcription	HSMM	muscle
6	chr14:24565200-24574000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
7	chr14:24565200-24575000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr14:24565200-24576000	Weak transcription	Fetal Kidney	kidney
9	chr14:24565200-24576800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr14:24565200-24577800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr14:24565200-24578000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr14:24565200-24578000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr14:24565200-24578000	Weak transcription	Brain Angular Gyrus	brain
14	chr14:24565200-24578000	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr14:24565200-24578000	Weak transcription	Hela-S3	cervix
16	chr14:24565200-24578000	Weak transcription	NHDF-Ad	bronchial
17	chr14:24565200-24582600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr14:24565200-24582600	Weak transcription	Left Ventricle	heart
19	chr14:24565800-24574200	Strong transcription	H1 Cell Line	embryonic stem cell
20	chr14:24565800-24574200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
21	chr14:24565800-24574400	Strong transcription	HUES48 Cell Line	embryonic stem cell
22	chr14:24566000-24573200	Strong transcription	Sigmoid Colon	Sigmoid Colon
23	chr14:24566000-24573600	Genic enhancers	Liver	Liver
24	chr14:24566000-24574200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr14:24566200-24573200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr14:24566200-24573400	Strong transcription	Rectal Mucosa Donor 31	rectum
27	chr14:24566200-24573800	Strong transcription	Dnd41	blood
28	chr14:24566200-24574000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr14:24566200-24574400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr14:24566400-24574000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr14:24566400-24575000	Strong transcription	Primary B cells from peripheral blood	blood
32	chr14:24566800-24573200	Strong transcription	Spleen	Spleen
33	chr14:24567000-24573600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
34	chr14:24567000-24574000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr14:24567200-24573400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr14:24567200-24573400	Strong transcription	Primary T cells from cord blood	blood
37	chr14:24567200-24573600	Strong transcription	Colonic Mucosa	Colon
38	chr14:24567200-24573600	Strong transcription	Rectal Mucosa Donor 29	rectum
39	chr14:24567200-24573600	Strong transcription	GM12878-XiMat	blood
40	chr14:24567200-24574200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr14:24567200-24574400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr14:24567200-24574400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr14:24567200-24574600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr14:24567200-24574800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr14:24567400-24573600	Strong transcription	Duodenum Smooth Muscle	Duodenum
46	chr14:24568200-24582600	Weak transcription	Right Ventricle	heart
47	chr14:24568200-24582600	Weak transcription	Stomach Mucosa	stomach
48	chr14:24568400-24577600	Weak transcription	Fetal Thymus	thymus
49	chr14:24568600-24573200	Strong transcription	Lung	lung
50	chr14:24568600-24577800	Weak transcription	Brain Substantia Nigra	brain

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