Variant report

Variant	esv1825092
Chromosome Location	chr14:104005264-104022171
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:947)
CpG islands
(count:366)
Chromatin interactive
region (count:36)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:947 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr14:104008631-104009577	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr14:104008628-104009560	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr14:104009192-104009278	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr14:104013141-104013279	K562	blood:	n/a	n/a
5	BCL3	chr14:104005675-104006079	A549	lung:	n/a	chr14:104005788-104005801
6	BCL3	chr14:104006448-104007282	A549	lung:	n/a	chr14:104006908-104006921
7	BCL3	chr14:104006674-104007310	A549	lung:	n/a	chr14:104006908-104006921
8	BCL3	chr14:104009007-104009557	A549	lung:	n/a	n/a
9	BCL3	chr14:104013048-104013611	A549	lung:	n/a	n/a
10	BHLHE40	chr14:104013187-104013524	GM12878	blood:	n/a	n/a
11	BHLHE40	chr14:104013135-104013517	K562	blood:	n/a	n/a
12	BHLHE40	chr14:104010014-104010420	HepG2	liver:	n/a	chr14:104010174-104010183 chr14:104010175-104010184 chr14:104010175-104010184 chr14:104010169-104010190
13	BHLHE40	chr14:104010100-104010240	K562	blood:	n/a	chr14:104010174-104010183 chr14:104010175-104010184 chr14:104010175-104010184 chr14:104010169-104010190
14	BHLHE40	chr14:104017963-104018166	K562	blood:	n/a	n/a
15	BHLHE40	chr14:104021319-104021556	K562	blood:	n/a	n/a
16	BHLHE40	chr14:104015812-104016627	HepG2	liver:	n/a	chr14:104016139-104016148
17	BHLHE40	chr14:104013183-104013504	HepG2	liver:	n/a	n/a
18	BRCA1	chr14:104005264-104005367	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr14:104013253-104013311	HepG2	liver:	n/a	n/a
20	BRCA1	chr14:104009136-104009452	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr14:104006747-104007212	Hela-S3	cervix:	n/a	n/a
22	CCNT2	chr14:104013174-104013552	K562	blood:	n/a	n/a
23	CEBPB	chr14:104009098-104009477	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr14:104013104-104013435	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr14:104006320-104007313	Hela-S3	cervix:	n/a	chr14:104006440-104006453
26	CEBPB	chr14:104009168-104009329	Hela-S3	cervix:	n/a	n/a
27	CHD1	chr14:104008957-104009037	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD1	chr14:104013004-104013497	IMR90	lung:	n/a	n/a
29	CHD2	chr14:104008764-104009587	H1-hESC	embryonic stem cell:	n/a	chr14:104009112-104009122
30	CHD2	chr14:104013101-104013383	K562	blood:	n/a	n/a
31	CHD2	chr14:104008488-104009660	Hela-S3	cervix:	n/a	chr14:104009112-104009122
32	CHD2	chr14:104010721-104010843	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr14:104006629-104007364	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr14:104013165-104013478	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr14:104005226-104005343	HepG2	liver:	n/a	n/a
36	CHD2	chr14:104013162-104013466	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr14:104005291-104005545	K562	blood:	n/a	n/a
38	CHD2	chr14:104010047-104010120	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr14:104007755-104007934	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr14:104013245-104013414	HepG2	liver:	n/a	n/a
41	CHD2	chr14:104008226-104008233	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr14:104008719-104009652	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr14:104009010-104009622	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr14:104009064-104009526	ECC-1	luminal epithelium:	n/a	n/a
45	CREB1	chr14:104013054-104013371	A549	lung:	n/a	n/a
46	CTBP2	chr14:104008571-104010001	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr14:104013860-104014010	BJ	skin:	n/a	n/a
48	CTCF	chr14:104013240-104013390	HA-sp	spinal cord:	n/a	chr14:104013283-104013299 chr14:104013277-104013298 chr14:104013282-104013300 chr14:104013284-104013297 chr14:104013285-104013295
49	CTCF	chr14:104013150-104013431	Hela-S3	cervix:	n/a	chr14:104013283-104013299 chr14:104013277-104013298 chr14:104013282-104013300 chr14:104013284-104013297 chr14:104013285-104013295
50	CTCF	chr14:104009820-104009970	Hela-S3	cervix:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:104012008-104012058	SAEC	small airway:	n/a
2	chr14:104009727-104009777	HPAEpiC	pulmonary alveolar:	n/a
3	chr14:104010865-104010915	SK-N-MC	brain:	n/a
4	chr14:104018735-104018785	HCPEpiC	choroid plexus:	n/a
5	chr14:104010839-104010889	GM12891	blood:	n/a
6	chr14:104010865-104010915	ovcar-3	ovarian:	n/a
7	chr14:104010865-104010915	AG04449	skin:	fetal
8	chr14:104009727-104009777	HCF	heart:	n/a
9	chr14:104018735-104018785	NB4	blood:	n/a
10	chr14:104010839-104010889	HCF	heart:	n/a
11	chr14:104012008-104012058	HepG2	liver:	n/a
12	chr14:104018735-104018785	Hepatocyte	liver:	n/a
13	chr14:104009727-104009777	MCF-7	breast:	n/a
14	chr14:104010865-104010915	AoSMC	blood vessel:	n/a
15	chr14:104010865-104010915	GM12892	blood:	n/a
16	chr14:104009727-104009777	AG04450	lung:	fetal
17	chr14:104012008-104012058	HL-60	blood:	n/a
18	chr14:104012008-104012058	HCT-116	colon:	n/a
19	chr14:104010865-104010915	BJ	skin:	n/a
20	chr14:104012008-104012058	HCM	heart:	n/a
21	chr14:104007538-104007588	RPTEC	kidney:	n/a
22	chr14:104018735-104018785	HAEpiC	amniotic membrane:	n/a
23	chr14:104018735-104018785	HepG2	liver:	n/a
24	chr14:104012008-104012058	PFSK-1	brain:	n/a
25	chr14:104018735-104018785	GM12891	blood:	n/a
26	chr14:104007538-104007588	BE2_C	brain:	n/a
27	chr14:104010865-104010915	PrEC	prostate:	n/a
28	chr14:104009727-104009777	HUVEC	blood vessel:	n/a
29	chr14:104012008-104012058	HEEpiC	esophagus:	n/a
30	chr14:104012008-104012058	Hela-S3	cervix:	n/a
31	chr14:104010865-104010915	HRPEpiC	eye:	n/a
32	chr14:104012008-104012058	BE2_C	brain:	n/a
33	chr14:104010839-104010889	GM12878	blood:	n/a
34	chr14:104007538-104007588	HMEC	breast:	n/a
35	chr14:104010865-104010915	SKMC	muscle:	n/a
36	chr14:104009727-104009777	NHDF-neo	bronchial:	n/a
37	chr14:104010865-104010915	NHDF-neo	bronchial:	n/a
38	chr14:104007538-104007588	A549	lung:	n/a
39	chr14:104009727-104009777	SKMC	muscle:	n/a
40	chr14:104018735-104018785	HRCEpiC	kidney:	n/a
41	chr14:104018735-104018785	Hela-S3	cervix:	n/a
42	chr14:104010839-104010889	HRCEpiC	kidney:	n/a
43	chr14:104009727-104009777	ovcar-3	ovarian:	n/a
44	chr14:104009727-104009777	HNPCEpiC	eye:	n/a
45	chr14:104009727-104009777	A549	lung:	n/a
46	chr14:104010865-104010915	HEEpiC	esophagus:	n/a
47	chr14:104018735-104018785	AG04450	lung:	fetal
48	chr14:104010839-104010889	HUVEC	blood vessel:	n/a
49	chr14:104012008-104012058	GM19239	blood:	n/a
50	chr14:104010839-104010889	AG09309	skin:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:103967396..103969451-chr14:104009245..104011145,2	MCF-7	breast:
2	chr14:103987382..103988017-chr14:104013265..104013800,2	K562	blood:
3	chr14:103989521..103992471-chr14:104020578..104022117,2	K562	blood:
4	chr14:103801342..103804122-chr14:104010938..104012453,2	K562	blood:
5	chr14:104005293..104008024-chr14:104095001..104096983,2	K562	blood:
6	chr14:104018005..104022715-chr14:104023184..104028959,7	K562	blood:
7	chr14:103984597..103986282-chr14:104012561..104013842,22	MCF-7	breast:
8	chr14:104006138..104009668-chr14:104023103..104027300,4	K562	blood:
9	chr14:103967247..103969712-chr14:104012689..104014722,2	MCF-7	breast:
10	chr14:103991343..103994487-chr14:104021014..104023570,3	MCF-7	breast:
11	chr14:103966852..103969165-chr14:104004136..104006723,2	MCF-7	breast:
12	chr1:935421..935993-chr14:104006660..104007419,2	Hela-S3	cervix:
13	chr12:56552118..56552624-chr14:104006836..104007485,2	Hela-S3	cervix:
14	chr14:104014533..104016298-chr14:104025800..104028102,2	K562	blood:
15	chr14:104007446..104009155-chr14:104027649..104030499,2	K562	blood:
16	chr14:103966239..103967223-chr14:104012598..104013775,9	K562	blood:
17	chr14:103984635..103986409-chr14:104012608..104013744,13	MCF-7	breast:
18	chr14:104013569..104015477-chr14:104021457..104023719,2	K562	blood:
19	chr14:103964404..103966727-chr14:104006569..104008780,2	K562	blood:
20	chr14:104016689..104020988-chr14:104027518..104030448,6	MCF-7	breast:
21	chr14:104002894..104005189-chr14:104020540..104022849,2	K562	blood:
22	chr14:103966209..103967132-chr14:104012771..104013734,5	MCF-7	breast:
23	chr14:104013569..104015477-chr14:104021457..104023719,2	K562	blood:
24	chr14:103987063..103988176-chr14:104012776..104013601,3	MCF-7	breast:
25	chr14:103984576..103985603-chr14:104012806..104013775,10	K562	blood:
26	chr14:103799669..103802148-chr14:104015889..104018791,2	MCF-7	breast:
27	chr14:104005381..104007221-chr14:104349678..104351959,2	K562	blood:
28	chr14:103966734..103968731-chr14:104012541..104016540,3	MCF-7	breast:
29	chr14:103964170..103966734-chr14:104015429..104018902,3	MCF-7	breast:
30	chr14:103977025..103977552-chr14:104012965..104013507,2	MCF-7	breast:
31	chr14:104003474..104006501-chr14:104024765..104028078,3	MCF-7	breast:
32	chr14:104013318..104015138-chr14:104023392..104025223,2	MCF-7	breast:
33	chr14:104022023..104026446-chr14:104027134..104030443,10	MCF-7	breast:
34	chr14:104021728..104024444-chr14:104089391..104091550,2	K562	blood:
35	chr14:104013579..104015507-chr14:104018184..104020087,2	K562	blood:
36	chr14:104009722..104012574-chr14:104026131..104028003,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLC1-1	chr14:104019758-104020199	ENSG00000258851.1

No data

Variant related genes	Relation type
RNU7-160P	TF binding region
ENSG00000258851	TF binding region
RNU7-160P	CpG island
ENSG00000258851	CpG island
ENSG00000126214	chromatin interactions
ENSG00000166165	chromatin interactions
ENSG00000188290	chromatin interactions
ENSG00000092841	chromatin interactions
ENSG00000258851	chromatin interactions
ENSG00000075413	chromatin interactions
ENSG00000256053	chromatin interactions
ENSG00000166170	chromatin interactions
ENSG00000100664	chromatin interactions

Extended variants
information (count: 775 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:775 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568504118	chr14:104005316-104005317	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs552989177	chr14:104005320-104005321	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs537797942	chr14:104005368-104005369	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs548443165	chr14:104005436-104005437	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs568197793	chr14:104005504-104005505	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs533954770	chr14:104005536-104005537	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs553528283	chr14:104005545-104005546	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs566926074	chr14:104005547-104005548	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs539047548	chr14:104005574-104005575	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs559036502	chr14:104005581-104005582	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs377313067	chr14:104005622-104005623	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs575570725	chr14:104005706-104005707	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs369131516	chr14:104005722-104005723	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs117082826	chr14:104005730-104005731	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs555207757	chr14:104005735-104005736	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs574953842	chr14:104005755-104005756	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs540773805	chr14:104005787-104005788	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs559824829	chr14:104005794-104005795	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs532115586	chr14:104005818-104005819	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs545490574	chr14:104005841-104005842	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs562172740	chr14:104005871-104005872	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs73359286	chr14:104005903-104005904	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs548205622	chr14:104005904-104005905	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs142381336	chr14:104005905-104005906	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs151275149	chr14:104005943-104005944	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs547577145	chr14:104005959-104005960	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs570654118	chr14:104005960-104005961	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs539160330	chr14:104006031-104006032	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs189389159	chr14:104006093-104006094	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs569171309	chr14:104006095-104006096	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs538208785	chr14:104006107-104006108	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs554965913	chr14:104006110-104006111	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs553764457	chr14:104006130-104006131	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs11621037	chr14:104006160-104006161	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs540515661	chr14:104006161-104006162	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs377508503	chr14:104006168-104006169	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs553991765	chr14:104006180-104006181	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs577002537	chr14:104006212-104006213	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs545968792	chr14:104006217-104006218	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs545529165	chr14:104006230-104006231	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs60076449	chr14:104006235-104006236	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs397942478	chr14:104006258-104006259	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs372975281	chr14:104006259-104006260	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs4906334	chr14:104006260-104006261	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs139479901	chr14:104006261-104006262	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs562570113	chr14:104006336-104006337	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs12880077	chr14:104006342-104006343	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs113244487	chr14:104006353-104006354	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs142330073	chr14:104006374-104006375	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs181076127	chr14:104006375-104006376	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21364760	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:939 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:103996800-104023400	Weak transcription	Primary B cells from cord blood	blood
2	chr14:103997200-104005400	Weak transcription	Fetal Lung	lung
3	chr14:103997600-104006800	Weak transcription	Small Intestine	intestine
4	chr14:103997600-104013000	Weak transcription	K562	blood
5	chr14:103999400-104006800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr14:104000600-104008000	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr14:104001200-104006600	Weak transcription	Primary T cells from cord blood	blood
8	chr14:104001400-104007600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr14:104002000-104006200	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr14:104002000-104006400	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr14:104002000-104006800	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr14:104002000-104008200	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr14:104002000-104012800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr14:104002200-104006800	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr14:104002200-104008200	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr14:104002200-104022600	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr14:104002400-104006600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr14:104002400-104009800	Weak transcription	Liver	Liver
19	chr14:104002400-104013000	Weak transcription	Dnd41	blood
20	chr14:104002600-104005400	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr14:104002600-104005400	Weak transcription	Ovary	ovary
22	chr14:104002800-104005600	Weak transcription	Thymus	Thymus
23	chr14:104002800-104006600	Enhancers	HSMMtube	muscle
24	chr14:104002800-104023400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr14:104003000-104006000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr14:104003000-104008000	Weak transcription	Fetal Brain Female	brain
27	chr14:104003000-104008800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr14:104003000-104018400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr14:104003200-104005800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr14:104003200-104006400	Enhancers	HSMM	muscle
31	chr14:104003200-104006600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr14:104003200-104010600	Enhancers	NHDF-Ad	bronchial
33	chr14:104003400-104005600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr14:104003400-104005800	Weak transcription	NHEK	skin
35	chr14:104003400-104010000	Weak transcription	Spleen	Spleen
36	chr14:104003600-104006800	Enhancers	NH-A	brain
37	chr14:104003800-104005600	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr14:104003800-104009000	Enhancers	Fetal Muscle Leg	muscle
39	chr14:104004000-104006000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr14:104004000-104006400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr14:104004000-104006800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr14:104004000-104008200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr14:104004000-104008800	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr14:104004200-104006000	Enhancers	Gastric	stomach
45	chr14:104004200-104006800	Weak transcription	Fetal Intestine Large	intestine
46	chr14:104004200-104008200	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr14:104004200-104011400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr14:104004400-104005400	Strong transcription	Fetal Intestine Small	intestine
49	chr14:104004400-104006600	Enhancers	A549	lung
50	chr14:104004400-104006800	Enhancers	Brain Hippocampus Middle	brain

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