Variant report

Variant	nsv830565
Chromosome Location	chr5:180067633-180191643
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:876)
CpG islands
(count:2630)
Chromatin interactive
region (count:45)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:876 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:180144959-180145359	GM12878	blood:	n/a	n/a
2	BATF	chr5:180097198-180097443	GM12878	blood:	n/a	n/a
3	BATF	chr5:180169789-180169977	GM12878	blood:	n/a	n/a
4	BATF	chr5:180145040-180145312	GM12878	blood:	n/a	chr5:180145207-180145218
5	BATF	chr5:180145061-180145379	GM12878	blood:	n/a	chr5:180145207-180145218
6	BCL11A	chr5:180145000-180145348	GM12878	blood:	n/a	chr5:180145235-180145244
7	BCL11A	chr5:180085399-180085773	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:180145100-180145299	GM12878	blood:	n/a	chr5:180145235-180145244
9	BCL3	chr5:180097085-180097491	GM12878	blood:	n/a	n/a
10	CBX3	chr5:180127492-180127736	K562	blood:	n/a	n/a
11	CEBPB	chr5:180131341-180131657	K562	blood:	n/a	n/a
12	CEBPD	chr5:180131384-180131803	K562	blood:	n/a	n/a
13	CREB1	chr5:180075851-180076164	A549	lung:	n/a	n/a
14	CREB1	chr5:180144917-180145413	GM12878	blood:	n/a	n/a
15	CREB1	chr5:180144836-180145451	GM12878	blood:	n/a	n/a
16	CTCF	chr5:180145712-180146044	ECC-1	luminal epithelium:	n/a	n/a
17	CTCF	chr5:180145800-180145950	GM12866	blood:	n/a	n/a
18	CTCF	chr5:180145820-180145970	GM12869	blood:	n/a	n/a
19	CTCF	chr5:180076012-180076052	GM20000	blood:	n/a	n/a
20	CTCF	chr5:180145801-180146020	GM10248	blood:	n/a	n/a
21	CTCF	chr5:180146197-180146332	ProgFib	skin:	n/a	n/a
22	CTCF	chr5:180075960-180076110	GM12875	blood:	n/a	chr5:180076001-180076019 chr5:180076003-180076016
23	CTCF	chr5:180146300-180146450	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr5:180097660-180097810	NHDF-neo	bronchial:	n/a	chr5:180097737-180097755 chr5:180097732-180097753
25	CTCF	chr5:180110429-180110440	Medullo	brain:	n/a	n/a
26	CTCF	chr5:180100406-180100496	GM19240	blood:	n/a	chr5:180100461-180100470 chr5:180100458-180100476 chr5:180100461-180100474
27	CTCF	chr5:180100380-180100530	WERI-Rb-1	eye:	n/a	chr5:180100461-180100470 chr5:180100458-180100476 chr5:180100461-180100474
28	CTCF	chr5:180075900-180076050	HepG2	liver:	n/a	chr5:180076001-180076019 chr5:180076003-180076016
29	CTCF	chr5:180100391-180100512	GM12892	blood:	n/a	chr5:180100461-180100470 chr5:180100458-180100476 chr5:180100461-180100474
30	CTCF	chr5:180100433-180100508	LNCaP	prostate:	n/a	chr5:180100461-180100470 chr5:180100458-180100476 chr5:180100461-180100474
31	CTCF	chr5:180075961-180076097	GM13977	blood:	n/a	chr5:180076001-180076019 chr5:180076003-180076016
32	CTCF	chr5:180075940-180076090	WERI-Rb-1	eye:	n/a	chr5:180076001-180076019 chr5:180076003-180076016
33	CTCF	chr5:180110360-180110510	GM06990	blood:	n/a	n/a
34	CTCF	chr5:180145800-180145950	A549	lung:	n/a	n/a
35	CTCF	chr5:180145790-180146025	LNCaP	prostate:	n/a	n/a
36	CTCF	chr5:180100360-180100510	HBMEC	blood vessel:	n/a	chr5:180100461-180100470 chr5:180100458-180100476 chr5:180100461-180100474
37	CTCF	chr5:180145820-180145970	HCT-116	colon:	n/a	n/a
38	CTCF	chr5:180110340-180110490	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr5:180075811-180076142	A549	lung:	n/a	chr5:180076001-180076019 chr5:180076003-180076016
40	CTCF	chr5:180110361-180110490	HepG2	liver:	n/a	n/a
41	CTCF	chr5:180097597-180097883	GM12878	blood:	n/a	chr5:180097737-180097755 chr5:180097732-180097753
42	CTCF	chr5:180097609-180097878	GM13977	blood:	n/a	chr5:180097737-180097755 chr5:180097732-180097753
43	CTCF	chr5:180097465-180097983	A549	lung:	n/a	chr5:180097737-180097755 chr5:180097732-180097753
44	CTCF	chr5:180145806-180146001	Lung_OC	lung:	n/a	n/a
45	CTCF	chr5:180100400-180100550	HCPEpiC	choroid plexus:	n/a	chr5:180100461-180100470 chr5:180100458-180100476 chr5:180100461-180100474
46	CTCF	chr5:180145776-180146045	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr5:180145840-180145990	AG04449	skin:	n/a	n/a
48	CTCF	chr5:180100394-180100510	GM19239	blood:	n/a	chr5:180100461-180100470 chr5:180100458-180100476 chr5:180100461-180100474
49	CTCF	chr5:180145788-180146006	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr5:180097680-180097830	MCF-7	breast:	n/a	chr5:180097737-180097755 chr5:180097732-180097753

(count:2630 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:180101440-180101490	Hela-S3	cervix:	n/a
2	chr5:180071816-180071866	SK-N-SH	brain:	n/a
3	chr5:180111966-180112016	Caco-2	colon:	n/a
4	chr5:180071930-180071980	GM06990	blood:	n/a
5	chr5:180071816-180071866	PrEC	prostate:	n/a
6	chr5:180076982-180077032	HMEC	breast:	n/a
7	chr5:180097910-180097960	SK-N-MC	brain:	n/a
8	chr5:180101440-180101490	Hela-S3	cervix:	n/a
9	chr5:180071816-180071866	SK-N-SH	brain:	n/a
10	chr5:180111966-180112016	Caco-2	colon:	n/a
11	chr5:180071930-180071980	GM06990	blood:	n/a
12	chr5:180071816-180071866	PrEC	prostate:	n/a
13	chr5:180076982-180077032	HMEC	breast:	n/a
14	chr5:180097910-180097960	SK-N-MC	brain:	n/a
15	chr5:180074582-180074632	ProgFib	skin:	n/a
16	chr5:180071916-180071966	SK-N-SH_RA	brain:	n/a
17	chr5:180167566-180167616	Jurkat	blood:	n/a
18	chr5:180113357-180113407	ECC-1	luminal epithelium:	n/a
19	chr5:180076168-180076218	HL-60	blood:	n/a
20	chr5:180073780-180073830	RPTEC	kidney:	n/a
21	chr5:180101281-180101331	K562	blood:	n/a
22	chr5:180167566-180167616	HAEpiC	amniotic membrane:	n/a
23	chr5:180079228-180079278	BE2_C	brain:	n/a
24	chr5:180166492-180166542	HRCEpiC	kidney:	n/a
25	chr5:180076982-180077032	AG10803	skin:	n/a
26	chr5:180076982-180077032	GM12878	blood:	n/a
27	chr5:180073137-180073187	AG04450	lung:	fetal
28	chr5:180166694-180166744	RPTEC	kidney:	n/a
29	chr5:180071756-180071806	HNPCEpiC	eye:	n/a
30	chr5:180074582-180074632	HL-60	blood:	n/a
31	chr5:180073780-180073830	HMEC	breast:	n/a
32	chr5:180111966-180112016	NHDF-neo	bronchial:	n/a
33	chr5:180111800-180111850	HCM	heart:	n/a
34	chr5:180077359-180077409	HNPCEpiC	eye:	n/a
35	chr5:180113357-180113407	ovcar-3	ovarian:	n/a
36	chr5:180167965-180168015	HPAEpiC	pulmonary alveolar:	n/a
37	chr5:180077359-180077409	LNCaP	prostate:	n/a
38	chr5:180071756-180071806	BE2_C	brain:	n/a
39	chr5:180085446-180085496	NT2-D1	testis:	n/a
40	chr5:180073780-180073830	HEK293	kidney:	embryo
41	chr5:180167132-180167182	RPTEC	kidney:	n/a
42	chr5:180073137-180073187	HRCEpiC	kidney:	n/a
43	chr5:180076168-180076218	NHBE	bronchial:	n/a
44	chr5:180166492-180166542	NHDF-neo	bronchial:	n/a
45	chr5:180071756-180071806	HepG2	liver:	n/a
46	chr5:180072420-180072470	Jurkat	blood:	n/a
47	chr5:180112929-180112979	HAEpiC	amniotic membrane:	n/a
48	chr5:180101143-180101193	HEK293	kidney:	embryo
49	chr5:180076905-180076955	HCPEpiC	choroid plexus:	n/a
50	chr5:180167132-180167182	LNCaP	prostate:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:180092442..180094516-chr5:180097000..180098654,2	K562	blood:
2	chr5:180168086..180169925-chr5:180190599..180192805,2	K562	blood:
3	chr5:180038293..180038846-chr5:180097248..180097778,2	K562	blood:
4	chr3:18286488..18287319-chr5:180097543..180098157,2	MCF-7	breast:
5	chr5:179553744..179554692-chr5:180097393..180098230,2	MCF-7	breast:
6	chr5:180092442..180094516-chr5:180097000..180098654,2	K562	blood:
7	chr5:180171538..180174150-chr5:180179388..180180987,2	K562	blood:
8	chr5:180091768..180093922-chr5:180095583..180097208,2	K562	blood:
9	chr5:180168390..180170515-chr5:180204872..180207367,2	K562	blood:
10	chr5:180136617..180138276-chr5:180153652..180155749,2	K562	blood:
11	chr5:180154735..180156600-chr5:180159240..180161653,2	MCF-7	breast:
12	chr5:180153993..180156519-chr5:180159947..180161759,2	K562	blood:
13	chr5:180067823..180069604-chr5:180072708..180075164,2	K562	blood:
14	chr5:180171538..180174150-chr5:180179388..180180987,2	K562	blood:
15	chr5:180136617..180138276-chr5:180153652..180155749,2	K562	blood:
16	chr5:180170663..180173512-chr5:180175093..180176860,2	K562	blood:
17	chr5:180147687..180149481-chr5:180151717..180153867,2	K562	blood:
18	chr5:180168086..180169925-chr5:180190599..180192805,2	K562	blood:
19	chr5:180076787..180079357-chr5:180092252..180095157,2	K562	blood:
20	chr5:180170663..180173512-chr5:180175093..180176860,2	K562	blood:
21	chr5:179720167..179721132-chr5:180096980..180097838,2	K562	blood:
22	chr5:180158275..180159905-chr5:180163258..180165205,2	K562	blood:
23	chr5:180143140..180144948-chr5:180229622..180231793,2	K562	blood:
24	chr5:180094037..180096535-chr5:180099976..180102790,2	K562	blood:
25	chr5:180113673..180116367-chr5:180119581..180121156,3	K562	blood:
26	chr5:180048663..180050730-chr5:180113911..180116171,2	K562	blood:
27	chr5:180091768..180093922-chr5:180095583..180097208,2	K562	blood:
28	chr5:180067823..180069604-chr5:180072708..180075164,2	K562	blood:
29	chr5:180094037..180096535-chr5:180099976..180102790,2	K562	blood:
30	chr5:180076787..180079357-chr5:180092252..180095157,2	K562	blood:
31	chr5:180146148..180147851-chr5:180235768..180238086,2	K562	blood:
32	chr5:180158275..180159905-chr5:180163258..180165205,2	K562	blood:
33	chr5:180130605..180132994-chr5:180134010..180136773,2	MCF-7	breast:
34	chr5:180172009..180174376-chr5:180240608..180243076,2	MCF-7	breast:
35	chr5:180083705..180084315-chr6:10033064..10033612,2	MCF-7	breast:
36	chr5:180097643..180098351-chr5:180145367..180146387,3	MCF-7	breast:
37	chr5:180147687..180149481-chr5:180151717..180153867,2	K562	blood:
38	chr5:180097643..180098351-chr5:180145367..180146387,3	MCF-7	breast:
39	chr5:180065065..180066811-chr5:180072819..180075038,2	K562	blood:
40	chr5:180114639..180117305-chr5:180118582..180121501,2	MCF-7	breast:
41	chr5:180022631..180025317-chr5:180096101..180098291,2	MCF-7	breast:
42	chr5:180153993..180156519-chr5:180159947..180161759,2	K562	blood:
43	chr5:180130605..180132994-chr5:180134010..180136773,2	MCF-7	breast:
44	chr5:180032730..180033573-chr5:180097208..180098138,2	MCF-7	breast:
45	chr5:180037911..180038640-chr5:180145288..180145999,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FLT4-1	chr5:180098892-180099598	NONHSAT105695
2	lnc-CNOT6-3	chr5:180111765-180111906	NONHSAT105706
3	lnc-OR2Y1-2	chr5:180189565-180191201	ucscGeneNc_uc003mmj_1
4	lnc-CNOT6-3	chr5:180112649-180113546	XLOC_004682
5	lnc-BTNL8-8	chr5:180190563-180190835	ucscGeneNc_uc003mmk_2
6	lnc-CNOT6-3	chr5:180111766-180111906	XLOC_004682
7	lnc-OR2Y1-1	chr5:180155280-180155484	expReg_chr5_11028_-
8	lnc-CNOT6-3	chr5:180112648-180113546	NONHSAT105706

No data

Variant related genes	Relation type
FLT4	TF binding region
OR2AI1P	TF binding region
RNU1-17P	TF binding region
ENSG00000248717	TF binding region
OR2Y1	TF binding region
ENSG00000251352	TF binding region
FLT4	CpG island
OR2AI1P	CpG island
RNU1-17P	CpG island
ENSG00000248717	CpG island
OR2Y1	CpG island
ENSG00000251352	CpG island
ENSG00000131446	chromatin interactions
ENSG00000037280	chromatin interactions
ENSG00000236791	chromatin interactions
ENSG00000248367	chromatin interactions
ENSG00000199892	chromatin interactions

Extended variants
information (count: 3503 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:3503 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs307806	chr5:180067675-180067676	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs149503590	chr5:180067679-180067680	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs144288153	chr5:180067689-180067690	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs565442472	chr5:180067713-180067714	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535967482	chr5:180067726-180067727	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs72818990	chr5:180067727-180067728	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs572563514	chr5:180067731-180067732	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs112160445	chr5:180067751-180067752	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540947168	chr5:180067760-180067761	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188762305	chr5:180067768-180067769	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567976800	chr5:180067782-180067783	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543721434	chr5:180067785-180067786	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562523176	chr5:180067851-180067852	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs575899335	chr5:180067856-180067857	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs541915050	chr5:180067868-180067869	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs74445224	chr5:180067870-180067871	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs527384961	chr5:180067871-180067872	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs547220428	chr5:180067885-180067886	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs192212536	chr5:180067888-180067889	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs182831146	chr5:180067890-180067891	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs533273669	chr5:180067901-180067902	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs549780686	chr5:180067927-180067928	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs376414216	chr5:180067962-180067963	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs11249740	chr5:180067968-180067969	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs549395755	chr5:180067979-180067980	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs143633662	chr5:180067997-180067998	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs535105724	chr5:180067998-180067999	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs11750142	chr5:180068009-180068010	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs578088331	chr5:180068013-180068014	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs139777069	chr5:180068026-180068027	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs557327806	chr5:180068034-180068035	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs574263628	chr5:180068125-180068126	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs541473999	chr5:180068127-180068128	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs79778505	chr5:180068154-180068155	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs370400747	chr5:180068155-180068156	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs187252973	chr5:180068168-180068169	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs184269	chr5:180068239-180068240	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs532938587	chr5:180068250-180068251	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs550058455	chr5:180068252-180068253	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs563480896	chr5:180068261-180068262	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs74575417	chr5:180068279-180068280	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs560772826	chr5:180068325-180068326	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs549433091	chr5:180068364-180068365	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs566044202	chr5:180068371-180068372	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs535143947	chr5:180068419-180068420	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs551851103	chr5:180068480-180068481	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs571817805	chr5:180068561-180068562	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs13354902	chr5:180068571-180068572	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs375743409	chr5:180068583-180068584	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs550731202	chr5:180068597-180068598	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	17440070	CNVD
Schizophrenia	21346763	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:868 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:180046200-180071800	Weak transcription	Liver	Liver
2	chr5:180046400-180072200	Weak transcription	Right Atrium	heart
3	chr5:180056800-180068400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr5:180065400-180069600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr5:180066400-180075600	Enhancers	Spleen	Spleen
6	chr5:180066600-180068600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr5:180066600-180068600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
8	chr5:180066600-180068800	Enhancers	Lung	lung
9	chr5:180066800-180068000	Enhancers	Fetal Muscle Leg	muscle
10	chr5:180066800-180068000	Enhancers	Placenta	Placenta
11	chr5:180067200-180069400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr5:180067400-180067800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr5:180067400-180068200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
14	chr5:180067600-180068200	Weak transcription	Right Ventricle	heart
15	chr5:180067600-180068600	Bivalent Enhancer	Adipose Nuclei	Adipose
16	chr5:180067600-180072200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
17	chr5:180067800-180068800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr5:180068200-180068600	Bivalent Enhancer	Right Ventricle	heart
19	chr5:180068800-180069400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr5:180068800-180071800	Weak transcription	Lung	lung
21	chr5:180069400-180069600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr5:180069400-180069800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr5:180069600-180069800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr5:180069600-180070600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr5:180069800-180070000	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr5:180069800-180070400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr5:180070200-180072600	Bivalent Enhancer	Placenta	Placenta
28	chr5:180070400-180070600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr5:180070600-180071600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr5:180070600-180073400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr5:180071200-180071600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
32	chr5:180071200-180073600	Bivalent Enhancer	Adipose Nuclei	Adipose
33	chr5:180071200-180074600	Bivalent Enhancer	Fetal Muscle Leg	muscle
34	chr5:180071400-180071600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr5:180071400-180074200	Enhancers	HUVEC	blood vessel
36	chr5:180071600-180072000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr5:180071600-180073200	Bivalent Enhancer	K562	blood
38	chr5:180071800-180072000	Enhancers	Liver	Liver
39	chr5:180071800-180072000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
40	chr5:180071800-180072000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
41	chr5:180071800-180072800	Bivalent Enhancer	Right Ventricle	heart
42	chr5:180071800-180073000	Enhancers	Lung	lung
43	chr5:180071800-180075200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
44	chr5:180072000-180072600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr5:180072000-180072800	Enhancers	Primary hematopoietic stem cells	blood
46	chr5:180072000-180074400	Enhancers	Left Ventricle	heart
47	chr5:180072200-180072400	Enhancers	Right Atrium	heart
48	chr5:180072200-180072600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr5:180072200-180072600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr5:180072400-180072600	Weak transcription	Right Atrium	heart

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