Variant report

Variant	nsv482170
Chromosome Location	chr14:24505710-24520580
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	chr14:24505981-24506248	HepG2	liver:	n/a	n/a
2	ATF2	chr14:24505949-24506263	GM12878	blood:	n/a	n/a
3	BATF	chr14:24506427-24506735	GM12878	blood:	n/a	n/a
4	BATF	chr14:24506432-24506750	GM12878	blood:	n/a	n/a
5	BCL3	chr14:24505902-24506304	A549	lung:	n/a	n/a
6	BHLHE40	chr14:24505965-24506313	GM12878	blood:	n/a	n/a
7	BRCA1	chr14:24505981-24506214	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr14:24505919-24506258	H1-hESC	embryonic stem cell:	n/a	chr14:24506174-24506185
9	CEBPB	chr14:24505953-24506379	MCF-7	breast:	n/a	chr14:24506174-24506185
10	CEBPB	chr14:24505928-24506341	A549	lung:	n/a	chr14:24506174-24506185
11	CEBPB	chr14:24506005-24506241	ECC-1	luminal epithelium:	n/a	chr14:24506174-24506185
12	CEBPB	chr14:24505923-24506358	A549	lung:	n/a	chr14:24506174-24506185
13	CEBPB	chr14:24506005-24506217	HepG2	liver:	n/a	chr14:24506174-24506185
14	CEBPB	chr14:24505955-24506340	MCF-7	breast:	n/a	chr14:24506174-24506185
15	CEBPB	chr14:24505959-24506192	HepG2	liver:	n/a	chr14:24506174-24506185
16	CEBPB	chr14:24505949-24506410	HepG2	liver:	n/a	chr14:24506174-24506185
17	CEBPB	chr14:24505832-24506370	GM12878	blood:	n/a	chr14:24506174-24506185
18	CEBPB	chr14:24505883-24506354	Hela-S3	cervix:	n/a	chr14:24506174-24506185
19	CEBPD	chr14:24505867-24506262	HepG2	liver:	n/a	n/a
20	CEBPD	chr14:24505874-24506366	HepG2	liver:	n/a	n/a
21	CEBPD	chr14:24505308-24505800	HepG2	liver:	n/a	n/a
22	CHD1	chr14:24505868-24506176	GM12878	blood:	n/a	n/a
23	CHD2	chr14:24505969-24506247	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr14:24505991-24506252	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr14:24506007-24506172	HepG2	liver:	n/a	n/a
26	CTCF	chr14:24505845-24505851	GM12878	blood:	n/a	n/a
27	CTCF	chr14:24505962-24506266	GM12892	blood:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
28	CTCF	chr14:24506020-24506170	GM12865	blood:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
29	CTCF	chr14:24506040-24506190	HEEpiC	esophagus:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
30	CTCF	chr14:24505980-24506130	HVMF	connective:	n/a	n/a
31	CTCF	chr14:24505924-24506279	ECC-1	luminal epithelium:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
32	CTCF	chr14:24506040-24506190	Caco-2	colon:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
33	CTCF	chr14:24506100-24506250	GM12801	blood:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
34	CTCF	chr14:24510561-24510585	GM13976	blood:	n/a	n/a
35	CTCF	chr14:24506040-24506190	MCF-7	breast:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
36	CTCF	chr14:24506080-24506230	HRPEpiC	eye:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
37	CTCF	chr14:24506008-24506215	H1-hESC	embryonic stem cell:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
38	CTCF	chr14:24506017-24506263	LNCaP	prostate:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
39	CTCF	chr14:24506040-24506190	GM12874	blood:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
40	CTCF	chr14:24506040-24506190	HMF	breast:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
41	CTCF	chr14:24506688-24506699	GM10266	blood:	n/a	n/a
42	CTCF	chr14:24506060-24506210	GM12871	blood:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
43	CTCF	chr14:24506020-24506170	GM12870	blood:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
44	CTCF	chr14:24506040-24506190	GM12864	blood:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
45	CTCF	chr14:24506080-24506230	HAc	cerebellar:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
46	CTCF	chr14:24506020-24506170	GM12866	blood:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
47	CTCF	chr14:24506000-24506150	GM12878	blood:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
48	CTCF	chr14:24506040-24506190	AoAF	blood vessel:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
49	CTCF	chr14:24506010-24506268	GM13977	blood:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
50	CTCF	chr14:24506040-24506190	HCFaa	heart:	n/a	chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24509703-24509753	PANC-1	pancreas:	n/a
2	chr14:24509703-24509753	PANC-1	pancreas:	n/a
3	chr14:24505898-24505948	CMK	blood:	n/a
4	chr14:24509703-24509753	CMK	blood:	n/a
5	chr14:24505743-24505793	AoSMC	blood vessel:	n/a
6	chr14:24505898-24505948	SKMC	muscle:	n/a
7	chr14:24517260-24517310	HCPEpiC	choroid plexus:	n/a
8	chr14:24517260-24517310	GM12891	blood:	n/a
9	chr14:24509703-24509753	RPTEC	kidney:	n/a
10	chr14:24505743-24505793	CMK	blood:	n/a
11	chr14:24505743-24505793	GM12892	blood:	n/a
12	chr14:24505743-24505793	HIPEpiC	eye:	n/a
13	chr14:24505743-24505793	HCT-116	colon:	n/a
14	chr14:24506241-24506291	NHBE	bronchial:	n/a
15	chr14:24505671-24505721	HCM	heart:	n/a
16	chr14:24506241-24506291	NT2-D1	testis:	n/a
17	chr14:24517260-24517310	GM12878	blood:	n/a
18	chr14:24506241-24506291	AG04449	skin:	fetal
19	chr14:24506241-24506291	BJ	skin:	n/a
20	chr14:24505898-24505948	HRE	kidney:	n/a
21	chr14:24505898-24505948	A549	lung:	n/a
22	chr14:24505743-24505793	T-47D	breast:	n/a
23	chr14:24505898-24505948	GM12891	blood:	n/a
24	chr14:24517260-24517310	HNPCEpiC	eye:	n/a
25	chr14:24506241-24506291	HEEpiC	esophagus:	n/a
26	chr14:24506241-24506291	HCPEpiC	choroid plexus:	n/a
27	chr14:24517260-24517310	HMEC	breast:	n/a
28	chr14:24505898-24505948	AG04449	skin:	fetal
29	chr14:24505671-24505721	CMK	blood:	n/a
30	chr14:24505898-24505948	HRCEpiC	kidney:	n/a
31	chr14:24505671-24505721	GM12891	blood:	n/a
32	chr14:24505671-24505721	HRCEpiC	kidney:	n/a
33	chr14:24509703-24509753	HIPEpiC	eye:	n/a
34	chr14:24517260-24517310	NB4	blood:	n/a
35	chr14:24505743-24505793	AG04450	lung:	fetal
36	chr14:24506241-24506291	GM19239	blood:	n/a
37	chr14:24505671-24505721	HRPEpiC	eye:	n/a
38	chr14:24506241-24506291	LNCaP	prostate:	n/a
39	chr14:24517260-24517310	MCF10A-Er-Src	breast:	n/a
40	chr14:24505743-24505793	HEEpiC	esophagus:	n/a
41	chr14:24509703-24509753	H1-hESC	embryonic stem cell:	embryo
42	chr14:24505671-24505721	K562	blood:	n/a
43	chr14:24517260-24517310	Caco-2	colon:	n/a
44	chr14:24505898-24505948	HCT-116	colon:	n/a
45	chr14:24506241-24506291	Jurkat	blood:	n/a
46	chr14:24517260-24517310	NT2-D1	testis:	n/a
47	chr14:24517260-24517310	RPTEC	kidney:	n/a
48	chr14:24506241-24506291	ovcar-3	ovarian:	n/a
49	chr14:24505743-24505793	HEK293	kidney:	embryo
50	chr14:24505671-24505721	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:24503791..24508058-chr14:24562194..24566408,5	MCF-7	breast:
2	chr14:24519308..24521603-chr14:24550146..24552325,2	K562	blood:
3	chr14:24504490..24506127-chr14:24583788..24585514,2	MCF-7	breast:
4	chr14:24504090..24505966-chr14:24768791..24770568,2	MCF-7	breast:
5	chr14:24422701..24424551-chr14:24504249..24506129,2	MCF-7	breast:
6	chr14:24505359..24507247-chr14:24702110..24704400,2	MCF-7	breast:
7	chr14:24519379..24521106-chr14:24565277..24567591,2	MCF-7	breast:
8	chr14:24520169..24522570-chr14:24571507..24573400,2	MCF-7	breast:
9	chr14:24519146..24523502-chr14:24549476..24554002,6	MCF-7	breast:
10	chr14:24509752..24511803-chr14:24562900..24565443,2	MCF-7	breast:
11	chr14:24505124..24506975-chr14:24520204..24522367,2	MCF-7	breast:
12	chr14:24511940..24516638-chr14:24519281..24522769,4	MCF-7	breast:
13	chr14:24505124..24506975-chr14:24520204..24522367,2	MCF-7	breast:
14	chr14:24519207..24521902-chr14:24608488..24612189,3	MCF-7	breast:
15	chr14:24509893..24511543-chr14:24520701..24522909,2	MCF-7	breast:
16	chr14:24519507..24523114-chr14:24581353..24584961,4	MCF-7	breast:
17	chr14:24519595..24523490-chr14:24615649..24620329,4	MCF-7	breast:
18	chr14:24519494..24523801-chr14:24562244..24565641,8	MCF-7	breast:

Variant related genes	Relation type
ENSG00000225766	TF binding region
LRRC16B	TF binding region
ENSG00000225766	CpG island
LRRC16B	CpG island
ENSG00000259321	chromatin interactions
ENSG00000100889	chromatin interactions
ENSG00000196943	chromatin interactions
ENSG00000100911	chromatin interactions
ENSG00000100897	chromatin interactions
ENSG00000129535	chromatin interactions
ENSG00000092098	chromatin interactions
ENSG00000100938	chromatin interactions
ENSG00000186648	chromatin interactions
ENSG00000225766	chromatin interactions
ENSG00000157379	chromatin interactions
ENSG00000100908	chromatin interactions
ENSG00000157326	chromatin interactions
ENSG00000215256	chromatin interactions

Extended variants
information (count: 729 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:729 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371416349	chr14:24505717-24505718	Active TSS Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs577988643	chr14:24505719-24505720	Active TSS Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs8005834	chr14:24505722-24505723	Active TSS Flanking Active TSS	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs557180142	chr14:24505727-24505728	Active TSS Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs574260536	chr14:24505729-24505730	Active TSS Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs200625178	chr14:24505735-24505736	Active TSS Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs556461153	chr14:24505740-24505741	Active TSS Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs543261626	chr14:24505748-24505749	Active TSS Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs374626236	chr14:24505751-24505752	Active TSS Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs145675272	chr14:24505764-24505765	Active TSS Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs573556548	chr14:24505784-24505785	Active TSS Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs372557477	chr14:24505789-24505790	Active TSS Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs371755645	chr14:24505802-24505803	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs374800603	chr14:24505807-24505808	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs368624982	chr14:24505822-24505823	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs112435648	chr14:24505836-24505837	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs375426884	chr14:24505842-24505843	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs369681534	chr14:24505867-24505868	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs369829744	chr14:24505878-24505879	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs113048202	chr14:24505885-24505886	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs566915788	chr14:24505889-24505890	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs550621363	chr14:24505934-24505935	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs144856253	chr14:24505951-24505952	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs8009086	chr14:24505963-24505964	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs8010483	chr14:24505984-24505985	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs566373975	chr14:24505993-24505994	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs538912044	chr14:24505994-24505995	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs184301184	chr14:24506011-24506012	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs571571932	chr14:24506037-24506038	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs567942514	chr14:24506044-24506045	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs2277477	chr14:24506073-24506074	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs2277478	chr14:24506076-24506077	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs574168905	chr14:24506080-24506081	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs536771448	chr14:24506082-24506083	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs553602105	chr14:24506096-24506097	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs573519768	chr14:24506106-24506107	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs578057827	chr14:24506126-24506127	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs62000815	chr14:24506140-24506141	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs575142601	chr14:24506173-24506174	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs188132712	chr14:24506231-24506232	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs560575141	chr14:24506241-24506242	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs533051938	chr14:24506264-24506265	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs8009760	chr14:24506296-24506297	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs539978027	chr14:24506297-24506298	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs559873811	chr14:24506298-24506299	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs192324350	chr14:24506355-24506356	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs557956573	chr14:24506366-24506367	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs148959991	chr14:24506394-24506395	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs74036736	chr14:24506408-24506409	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs550972418	chr14:24506411-24506412	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 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:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24505000-24506200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:24505000-24506200	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr14:24505000-24506200	Active TSS	iPS-18 Cell Line	embryonic stem cell
4	chr14:24505000-24506200	Active TSS	Brain Anterior Caudate	brain
5	chr14:24505000-24506200	Active TSS	Stomach Smooth Muscle	stomach
6	chr14:24505000-24506200	Active TSS	A549	lung
7	chr14:24505000-24506400	Active TSS	HUES64 Cell Line	embryonic stem cell
8	chr14:24505000-24506600	Flanking Active TSS	Dnd41	blood
9	chr14:24505200-24505800	Active TSS	Primary T helper cells fromperipheralblood	blood
10	chr14:24505200-24505800	Active TSS	Fetal Lung	lung
11	chr14:24505200-24505800	Active TSS	Fetal Stomach	stomach
12	chr14:24505200-24505800	Flanking Active TSS	Fetal Thymus	thymus
13	chr14:24505200-24506000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr14:24505200-24506000	Active TSS	Fetal Brain Female	brain
15	chr14:24505200-24506000	Active TSS	GM12878-XiMat	blood
16	chr14:24505200-24506200	Active TSS	H1 Cell Line	embryonic stem cell
17	chr14:24505200-24506200	Active TSS	H9 Cell Line	embryonic stem cell
18	chr14:24505200-24506200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr14:24505200-24506200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr14:24505200-24506200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr14:24505200-24506200	Active TSS	iPS-15b Cell Line	embryonic stem cell
22	chr14:24505200-24506200	Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr14:24505200-24506200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr14:24505200-24506200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
25	chr14:24505200-24506200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr14:24505200-24506200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr14:24505200-24506200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
28	chr14:24505200-24506200	Active TSS	Primary T helper cells PMA-I stimulated	--
29	chr14:24505200-24506200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr14:24505200-24506200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr14:24505200-24506200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr14:24505200-24506200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr14:24505200-24506200	Active TSS	Brain Cingulate Gyrus	brain
34	chr14:24505200-24506200	Active TSS	Brain Hippocampus Middle	brain
35	chr14:24505200-24506200	Active TSS	Brain Inferior Temporal Lobe	brain
36	chr14:24505200-24506200	Active TSS	Colon Smooth Muscle	Colon
37	chr14:24505200-24506200	Active TSS	Duodenum Mucosa	Duodenum
38	chr14:24505200-24506200	Active TSS	Fetal Heart	heart
39	chr14:24505200-24506200	Active TSS	Fetal Intestine Large	intestine
40	chr14:24505200-24506200	Active TSS	Left Ventricle	heart
41	chr14:24505200-24506200	Active TSS	Psoas Muscle	Psoas
42	chr14:24505200-24506200	Active TSS	Rectal Mucosa Donor 29	rectum
43	chr14:24505200-24506200	Active TSS	Rectal Mucosa Donor 31	rectum
44	chr14:24505200-24506200	Active TSS	Rectal Smooth Muscle	rectum
45	chr14:24505200-24506200	Active TSS	Right Ventricle	heart
46	chr14:24505200-24506200	Active TSS	Small Intestine	intestine
47	chr14:24505200-24506200	Active TSS	Hela-S3	cervix
48	chr14:24505200-24506200	Active TSS	Osteobl	bone
49	chr14:24505200-24506400	Active TSS	ES-I3 Cell Line	embryonic stem cell
50	chr14:24505200-24506400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived

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