Variant report

Variant	esv21432
Chromosome Location	chr10:96856006-96996043
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2217)
CpG islands
(count:1041)
Chromatin interactive
region (count:30)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2217 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:96868876-96868910	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:96995827-96996075	K562	blood:	n/a	n/a
3	ARID3A	chr10:96937886-96938999	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:96943386-96943426	K562	blood:	n/a	n/a
5	ARID3A	chr10:96941575-96941858	HepG2	liver:	n/a	n/a
6	ARID3A	chr10:96968456-96968849	HepG2	liver:	n/a	n/a
7	ARID3A	chr10:96968566-96968766	K562	blood:	n/a	n/a
8	ATF2	chr10:96989260-96990956	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr10:96943280-96943679	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr10:96943372-96943658	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr10:96995637-96996580	GM12878	blood:	n/a	n/a
12	ATF2	chr10:96943278-96943673	GM12878	blood:	n/a	n/a
13	ATF2	chr10:96989170-96991319	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr10:96955730-96956135	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr10:96995746-96996625	GM12878	blood:	n/a	n/a
16	ATF3	chr10:96995671-96995931	K562	blood:	n/a	n/a
17	ATF3	chr10:96989222-96989972	A549	lung:	n/a	n/a
18	ATF3	chr10:96943347-96943798	A549	lung:	n/a	n/a
19	ATF3	chr10:96990627-96990956	GM12878	blood:	n/a	n/a
20	BACH1	chr10:96943380-96943878	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr10:96894893-96894920	K562	blood:	n/a	n/a
22	BACH1	chr10:96991400-96991618	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr10:96989434-96990974	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr10:96995707-96996669	GM12878	blood:	n/a	chr10:96995925-96995935 chr10:96995979-96995989
25	BATF	chr10:96974644-96974850	GM12878	blood:	n/a	n/a
26	BATF	chr10:96995787-96996547	GM12878	blood:	n/a	chr10:96995925-96995935 chr10:96995979-96995989
27	BCL11A	chr10:96995730-96996479	GM12878	blood:	n/a	chr10:96996172-96996181 chr10:96995923-96995932 chr10:96995981-96995990 chr10:96995924-96995933
28	BCL3	chr10:96989110-96989992	A549	lung:	n/a	n/a
29	BCL3	chr10:96995658-96996450	GM12878	blood:	n/a	chr10:96996172-96996181 chr10:96995923-96995932 chr10:96995981-96995990 chr10:96995924-96995933
30	BCL3	chr10:96943282-96944065	A549	lung:	n/a	chr10:96943335-96943344 chr10:96943340-96943353 chr10:96943317-96943330 chr10:96943334-96943347 chr10:96943337-96943350
31	BCL3	chr10:96943398-96943752	GM12878	blood:	n/a	n/a
32	BCL3	chr10:96989196-96989903	A549	lung:	n/a	n/a
33	BCL3	chr10:96990626-96991073	GM12878	blood:	n/a	n/a
34	BCLAF1	chr10:96942994-96943820	GM12878	blood:	n/a	chr10:96943335-96943344 chr10:96943340-96943353 chr10:96943317-96943330 chr10:96943334-96943347 chr10:96943337-96943350
35	BCLAF1	chr10:96990333-96991038	GM12878	blood:	n/a	n/a
36	BCLAF1	chr10:96995638-96996727	GM12878	blood:	n/a	chr10:96996172-96996181 chr10:96995923-96995932 chr10:96995981-96995990 chr10:96995924-96995933
37	BCLAF1	chr10:96995898-96996581	GM12878	blood:	n/a	chr10:96996172-96996181 chr10:96995923-96995932 chr10:96995981-96995990 chr10:96995924-96995933
38	BCLAF1	chr10:96943300-96943894	GM12878	blood:	n/a	chr10:96943335-96943344 chr10:96943340-96943353 chr10:96943317-96943330 chr10:96943334-96943347 chr10:96943337-96943350
39	BHLHE40	chr10:96892675-96893155	K562	blood:	n/a	n/a
40	BHLHE40	chr10:96892767-96893282	HepG2	liver:	n/a	n/a
41	BHLHE40	chr10:96995795-96996691	GM12878	blood:	n/a	chr10:96996198-96996219
42	BHLHE40	chr10:96943199-96943888	K562	blood:	n/a	chr10:96943258-96943274 chr10:96943337-96943353 chr10:96943336-96943352 chr10:96943328-96943344
43	BHLHE40	chr10:96892748-96893037	GM12878	blood:	n/a	n/a
44	BHLHE40	chr10:96943258-96943763	GM12878	blood:	n/a	chr10:96943258-96943274 chr10:96943337-96943353 chr10:96943336-96943352 chr10:96943328-96943344
45	BRCA1	chr10:96943494-96943557	H1-hESC	embryonic stem cell:	n/a	n/a
46	BRCA1	chr10:96939156-96939188	H1-hESC	embryonic stem cell:	n/a	n/a
47	BRCA1	chr10:96989389-96989480	H1-hESC	embryonic stem cell:	n/a	n/a
48	CBX3	chr10:96995675-96996459	HCT-116	colon:	n/a	n/a
49	CBX3	chr10:96943302-96943679	K562	blood:	n/a	n/a
50	CBX3	chr10:96989210-96990027	HCT-116	colon:	n/a	n/a

(count:1041 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:96943563-96943613	PFSK-1	brain:	n/a
2	chr10:96943842-96943892	NT2-D1	testis:	n/a
3	chr10:96943196-96943246	MCF-7	breast:	n/a
4	chr10:96953447-96953497	Jurkat	blood:	n/a
5	chr10:96943563-96943613	PFSK-1	brain:	n/a
6	chr10:96943842-96943892	NT2-D1	testis:	n/a
7	chr10:96943196-96943246	MCF-7	breast:	n/a
8	chr10:96953447-96953497	Jurkat	blood:	n/a
9	chr10:96954252-96954302	NHDF-neo	bronchial:	n/a
10	chr10:96953953-96954003	PFSK-1	brain:	n/a
11	chr10:96980135-96980185	HAEpiC	amniotic membrane:	n/a
12	chr10:96989650-96989700	HMEC	breast:	n/a
13	chr10:96990543-96990593	HNPCEpiC	eye:	n/a
14	chr10:96953447-96953497	U87	brain:	n/a
15	chr10:96991431-96991481	AG09309	skin:	n/a
16	chr10:96954252-96954302	HRPEpiC	eye:	n/a
17	chr10:96943842-96943892	AG09319	gingival:	n/a
18	chr10:96991505-96991555	RPTEC	kidney:	n/a
19	chr10:96943563-96943613	MCF-7	breast:	n/a
20	chr10:96946522-96946572	PrEC	prostate:	n/a
21	chr10:96943130-96943180	CMK	blood:	n/a
22	chr10:96943563-96943613	GM12891	blood:	n/a
23	chr10:96946522-96946572	U87	brain:	n/a
24	chr10:96991461-96991511	HAEpiC	amniotic membrane:	n/a
25	chr10:96953447-96953497	SK-N-SH	brain:	n/a
26	chr10:96946522-96946572	HEEpiC	esophagus:	n/a
27	chr10:96953953-96954003	HNPCEpiC	eye:	n/a
28	chr10:96953953-96954003	GM12892	blood:	n/a
29	chr10:96946522-96946572	NT2-D1	testis:	n/a
30	chr10:96953447-96953497	HEK293	kidney:	embryo
31	chr10:96990858-96990908	PANC-1	pancreas:	n/a
32	chr10:96943196-96943246	NHDF-neo	bronchial:	n/a
33	chr10:96954252-96954302	AG09309	skin:	n/a
34	chr10:96988478-96988528	HepG2	liver:	n/a
35	chr10:96990700-96990750	HPAEpiC	pulmonary alveolar:	n/a
36	chr10:96980135-96980185	Hepatocyte	liver:	n/a
37	chr10:96943842-96943892	T-47D	breast:	n/a
38	chr10:96990543-96990593	T-47D	breast:	n/a
39	chr10:96990700-96990750	HCT-116	colon:	n/a
40	chr10:96988478-96988528	AG10803	skin:	n/a
41	chr10:96990543-96990593	GM06990	blood:	n/a
42	chr10:96991505-96991555	HUVEC	blood vessel:	n/a
43	chr10:96943196-96943246	SK-N-MC	brain:	n/a
44	chr10:96991505-96991555	HRE	kidney:	n/a
45	chr10:96988478-96988528	HMEC	breast:	n/a
46	chr10:96991505-96991555	PFSK-1	brain:	n/a
47	chr10:96946522-96946572	Caco-2	colon:	n/a
48	chr10:96991505-96991555	BJ	skin:	n/a
49	chr10:96980135-96980185	A549	lung:	n/a
50	chr10:96943130-96943180	GM12878	blood:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:96944739..96947695-chr10:96950554..96953637,4	MCF-7	breast:
2	chr10:96930488..96932812-chr10:96939629..96941375,2	K562	blood:
3	chr10:96944739..96947695-chr10:96950554..96953637,4	MCF-7	breast:
4	chr10:96977704..96978224-chr3:16493125..16493645,2	MCF-7	breast:
5	chr10:96983667..96985290-chr10:96987249..96989514,2	MCF-7	breast:
6	chr10:96941976..96944883-chr10:96989765..96992078,3	MCF-7	breast:
7	chr10:96975681..96977490-chr10:97052151..97054934,2	K562	blood:
8	chr10:96389495..96390471-chr10:96935594..96936525,3	MCF-7	breast:
9	chr10:96950676..96951601-chr12:66448498..66449065,2	MCF-7	breast:
10	chr10:96983644..96985637-chr10:96989361..96991556,3	K562	blood:
11	chr10:96943335..96943883-chr10:96990715..96991433,2	MCF-7	breast:
12	chr10:96892392..96893419-chr10:97122731..97123707,5	MCF-7	breast:
13	chr10:96985157..96986698-chr10:96990407..96993016,2	MCF-7	breast:
14	chr10:96892834..96893336-chr10:97122788..97123738,2	K562	blood:
15	chr10:96930488..96932812-chr10:96939629..96941375,2	K562	blood:
16	chr10:96389607..96390553-chr10:96935620..96936165,2	MCF-7	breast:
17	chr10:96980306..96982138-chr10:96989812..96992321,2	MCF-7	breast:
18	chr10:96983483..96986000-chr10:96988928..96992913,3	MCF-7	breast:
19	chr10:96989917..96992480-chr10:96995874..96997561,2	MCF-7	breast:
20	chr10:96989099..96991002-chr10:97047738..97051859,4	MCF-7	breast:
21	chr10:96988601..96990244-chr10:96996425..96998002,2	K562	blood:
22	chr10:96941976..96944883-chr10:96989765..96992078,3	MCF-7	breast:
23	chr10:96961108..96962057-chr10:97002638..97003736,3	MCF-7	breast:
24	chr10:96942861..96945609-chr10:96947623..96949502,2	K562	blood:
25	chr10:96723396..96724119-chr10:96892337..96892982,2	MCF-7	breast:
26	chr10:96983667..96985290-chr10:96987249..96989514,2	MCF-7	breast:
27	chr10:96943335..96943883-chr10:96990715..96991433,2	MCF-7	breast:
28	chr10:96943146..96943822-chr10:96960689..96961635,2	MCF-7	breast:
29	chr10:96968177..96969122-chr10:97002506..97003338,4	MCF-7	breast:
30	chr10:96951132..96952713-chr10:96952994..96955144,2	K562	blood:

(count:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDLIM1-1	chr10:96990423-96990825	NONHSAT015754
2	lnc-PDLIM1-1	chr10:96990423-96990825	NONHSAT015752
3	lnc-PDLIM1-3	chr10:96980413-96980891	ucscGeneNc_uc001kkg_1
4	lnc-PDLIM1-1	chr10:96988595-96988626	NONHSAT015754
5	lnc-PDLIM1-3	chr10:96976459-96978173	ucscGeneNc_uc001kkg_1
6	lnc-CYP2C8-2	chr10:96892983-96893041	NONHSAT015747
7	lnc-CYP2C8-2	chr10:96892355-96892444	NONHSAT015747
8	lnc-PDLIM1-1	chr10:96988000-96988183	ENSG00000234026
9	lnc-CYP2C8-2	chr10:96894018-96894165	NONHSAT015747
10	lnc-PDLIM1-2	chr10:96904028-96904175	ENSG00000231829.2
11	lnc-PDLIM1-2	chr10:96928138-96928182	ENSG00000231829.2
12	lnc-PDLIM1-1	chr10:96990423-96990901	ENSG00000234026
13	lnc-PDLIM1-2	chr10:96928138-96928182	XLOC_008910
14	lnc-CYP2C8-2	chr10:96891672-96891750	NONHSAT015747
15	lnc-PDLIM1-1	chr10:96985248-96985468	NONHSAT015752
16	lnc-PDLIM1-2	chr10:96902431-96903051	XLOC_008910
17	lnc-PDLIM1-2	chr10:96902993-96903051	ENSG00000231829.2
18	lnc-PDLIM1-2	chr10:96904028-96904175	XLOC_008910
19	lnc-PDLIM1-1	chr10:96988095-96988183	NONHSAT015752
20	lnc-PDLIM1-2	chr10:96902365-96902454	XLOC_008910
21	lnc-CYP2C8-2	chr10:96918128-96918172	NONHSAT015747
22	lnc-PDLIM1-1	chr10:96990423-96990901	NONHSAT015753
23	lnc-PDLIM1-2	chr10:96902367-96902454	ENSG00000231829.2
24	lnc-PDLIM1-2	chr10:96904028-96904243	XLOC_008910
25	lnc-PDLIM1-2	chr10:96901682-96901761	ENSG00000231829.2
26	lnc-PDLIM1-2	chr10:96902993-96903051	XLOC_008910
27	lnc-PDLIM1-2	chr10:96901682-96901760	XLOC_008910
28	lnc-PDLIM1-1	chr10:96986469-96988183	NONHSAT015753

No data

Variant related genes	Relation type
ENSG00000234026	TF binding region
PAWRP1	TF binding region
C10orf129	TF binding region
ENSG00000231829	TF binding region
ENSG00000234026	CpG island
PAWRP1	CpG island
C10orf129	CpG island
ENSG00000231829	CpG island
ENSG00000234026	chromatin interactions
ENSG00000225533	chromatin interactions
ENSG00000107438	chromatin interactions
ENSG00000173124	chromatin interactions

Extended variants
information (count: 4152 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:4152 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10786187	chr10:96856010-96856011	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs74715140	chr10:96856015-96856016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs10786188	chr10:96856022-96856023	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs546267198	chr10:96856039-96856040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559329823	chr10:96856071-96856072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548996839	chr10:96856078-96856079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs192527244	chr10:96856079-96856080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs145719773	chr10:96856088-96856089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148948933	chr10:96856142-96856143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs185571329	chr10:96856145-96856146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs11188179	chr10:96856172-96856173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs59277980	chr10:96856221-96856222	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs189230195	chr10:96856250-96856251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539205745	chr10:96856286-96856287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553012302	chr10:96856311-96856312	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs367576569	chr10:96856335-96856336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181026318	chr10:96856439-96856440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs185860116	chr10:96856453-96856454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs555322699	chr10:96856463-96856464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528100316	chr10:96856483-96856484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs575139514	chr10:96856499-96856500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs551341313	chr10:96856500-96856501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571541734	chr10:96856519-96856520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536817884	chr10:96856551-96856552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs543845713	chr10:96856552-96856553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs78967886	chr10:96856569-96856570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs2094294	chr10:96856611-96856612	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs752415	chr10:96856628-96856629	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs188722433	chr10:96856639-96856640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs555720708	chr10:96856650-96856651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs377024819	chr10:96856681-96856682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs752416	chr10:96856685-96856686	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs752417	chr10:96856695-96856696	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs561660051	chr10:96856698-96856699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181153573	chr10:96856726-96856727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs550460816	chr10:96856752-96856753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs570382702	chr10:96856810-96856811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2094293	chr10:96856853-96856854	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs943315	chr10:96856976-96856977	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs143726627	chr10:96856977-96856978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2860951	chr10:96856996-96856997	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs555159022	chr10:96856997-96856998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544014877	chr10:96857017-96857018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs200111680	chr10:96857021-96857022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs138012100	chr10:96857025-96857026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549682671	chr10:96857029-96857030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs372609023	chr10:96857030-96857031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs11188180	chr10:96857031-96857032	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs528416509	chr10:96857102-96857103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs577200336	chr10:96857103-96857104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Intracranial aneurysm	16715129	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1461 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96855800-96856400	Enhancers	Fetal Intestine Large	intestine
2	chr10:96855800-96856400	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr10:96856000-96856200	Enhancers	Fetal Intestine Small	intestine
4	chr10:96856000-96856800	Enhancers	Stomach Mucosa	stomach
5	chr10:96856000-96858200	Enhancers	HepG2	liver
6	chr10:96856200-96857200	Weak transcription	Fetal Intestine Small	intestine
7	chr10:96856400-96857400	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr10:96856400-96857600	Weak transcription	Fetal Intestine Large	intestine
9	chr10:96856800-96857200	Weak transcription	Stomach Mucosa	stomach
10	chr10:96857200-96858000	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr10:96857200-96858200	Enhancers	Fetal Intestine Small	intestine
12	chr10:96857200-96858200	Enhancers	Stomach Mucosa	stomach
13	chr10:96857400-96858000	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr10:96857400-96858200	Enhancers	Liver	Liver
15	chr10:96857600-96857800	Enhancers	Gastric	stomach
16	chr10:96857600-96858200	Enhancers	Fetal Intestine Large	intestine
17	chr10:96869000-96871600	Enhancers	HepG2	liver
18	chr10:96871600-96876200	Weak transcription	HepG2	liver
19	chr10:96874800-96875200	Enhancers	Liver	Liver
20	chr10:96875200-96876200	Flanking Active TSS	Liver	Liver
21	chr10:96876200-96876600	Enhancers	Liver	Liver
22	chr10:96876200-96877400	Enhancers	HepG2	liver
23	chr10:96876600-96876800	Flanking Active TSS	Liver	Liver
24	chr10:96876800-96877000	Enhancers	Liver	Liver
25	chr10:96877000-96877400	Flanking Active TSS	Liver	Liver
26	chr10:96877400-96878000	Enhancers	Liver	Liver
27	chr10:96877400-96881000	Weak transcription	HepG2	liver
28	chr10:96878000-96880600	Weak transcription	Liver	Liver
29	chr10:96879200-96879800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr10:96879200-96879800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr10:96880600-96881400	Enhancers	Liver	Liver
32	chr10:96881000-96883400	Enhancers	HepG2	liver
33	chr10:96881200-96881600	Active TSS	Fetal Heart	heart
34	chr10:96881400-96881800	Flanking Active TSS	Liver	Liver
35	chr10:96881400-96882400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
36	chr10:96881400-96882400	Enhancers	Duodenum Mucosa	Duodenum
37	chr10:96881400-96882400	Enhancers	Gastric	stomach
38	chr10:96881400-96882400	Enhancers	Pancreas	Pancrea
39	chr10:96881600-96883400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr10:96881600-96883400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr10:96881800-96882000	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr10:96881800-96882200	Enhancers	HSMMtube	muscle
43	chr10:96881800-96882400	Enhancers	Fetal Stomach	stomach
44	chr10:96881800-96882600	Enhancers	Liver	Liver
45	chr10:96882000-96882200	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
46	chr10:96882000-96883400	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr10:96882200-96883400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr10:96882400-96882800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr10:96882400-96889400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr10:96882600-96883200	Weak transcription	Liver	Liver

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