Variant report

Variant	nsv830558
Chromosome Location	chr5:178624391-178805604
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1593)
CpG islands
(count:5931)
Chromatin interactive
region (count:60)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1593 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:178729527-178729868	K562	blood:	n/a	n/a
2	ATF1	chr5:178658394-178658571	K562	blood:	n/a	n/a
3	ATF2	chr5:178753597-178754030	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr5:178688256-178688623	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr5:178763657-178763929	K562	blood:	n/a	n/a
6	BACH1	chr5:178770779-178771405	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr5:178688361-178688719	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr5:178782018-178782023	K562	blood:	n/a	n/a
9	BACH1	chr5:178753623-178753861	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr5:178650528-178650927	GM12878	blood:	n/a	n/a
11	BCL3	chr5:178746298-178746633	GM12878	blood:	n/a	n/a
12	BCL3	chr5:178746077-178746614	GM12878	blood:	n/a	n/a
13	BCL3	chr5:178650193-178650886	GM12878	blood:	n/a	n/a
14	BHLHE40	chr5:178703014-178703214	K562	blood:	n/a	n/a
15	BHLHE40	chr5:178800328-178800428	K562	blood:	n/a	n/a
16	BHLHE40	chr5:178703446-178703646	K562	blood:	n/a	n/a
17	BHLHE40	chr5:178712032-178712059	K562	blood:	n/a	n/a
18	BHLHE40	chr5:178695327-178695745	HepG2	liver:	n/a	n/a
19	BHLHE40	chr5:178763708-178763938	K562	blood:	n/a	n/a
20	BHLHE40	chr5:178655800-178656133	K562	blood:	n/a	n/a
21	BHLHE40	chr5:178691705-178692905	HepG2	liver:	n/a	chr5:178692685-178692701 chr5:178692599-178692615
22	BHLHE40	chr5:178639943-178640216	K562	blood:	n/a	n/a
23	BHLHE40	chr5:178722893-178723057	K562	blood:	n/a	chr5:178723031-178723040 chr5:178723031-178723040
24	BRCA1	chr5:178754565-178754676	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr5:178729517-178729803	K562	blood:	n/a	n/a
26	CCNT2	chr5:178702918-178703113	K562	blood:	n/a	n/a
27	CCNT2	chr5:178771882-178771973	K562	blood:	n/a	n/a
28	CCNT2	chr5:178772466-178772783	K562	blood:	n/a	n/a
29	CEBPB	chr5:178692736-178692932	K562	blood:	n/a	chr5:178692842-178692853
30	CEBPB	chr5:178628227-178628571	IMR90	lung:	n/a	chr5:178628403-178628414
31	CEBPB	chr5:178628215-178628562	K562	blood:	n/a	chr5:178628403-178628414
32	CEBPB	chr5:178691969-178692038	HepG2	liver:	n/a	n/a
33	CEBPB	chr5:178648671-178648772	K562	blood:	n/a	chr5:178648732-178648743
34	CEBPB	chr5:178670851-178671041	HepG2	liver:	n/a	n/a
35	CEBPB	chr5:178692711-178693040	ECC-1	luminal epithelium:	n/a	chr5:178692842-178692853
36	CEBPB	chr5:178692661-178693037	HepG2	liver:	n/a	chr5:178692842-178692853
37	CEBPB	chr5:178731436-178731883	IMR90	lung:	n/a	n/a
38	CEBPB	chr5:178688334-178688561	K562	blood:	n/a	n/a
39	CEBPB	chr5:178695368-178695660	HepG2	liver:	n/a	n/a
40	CEBPB	chr5:178791997-178792197	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr5:178628243-178628559	HepG2	liver:	n/a	chr5:178628403-178628414
42	CEBPB	chr5:178786289-178786460	HepG2	liver:	n/a	chr5:178786328-178786339
43	CEBPB	chr5:178692707-178692953	Hela-S3	cervix:	n/a	chr5:178692842-178692853
44	CEBPB	chr5:178692734-178692920	HepG2	liver:	n/a	chr5:178692842-178692853
45	CEBPB	chr5:178692696-178693007	H1-hESC	embryonic stem cell:	n/a	chr5:178692842-178692853
46	CEBPB	chr5:178771987-178772057	IMR90	lung:	n/a	n/a
47	CEBPB	chr5:178628311-178628506	A549	lung:	n/a	chr5:178628403-178628414
48	CEBPB	chr5:178705701-178705882	HepG2	liver:	n/a	n/a
49	CEBPB	chr5:178786162-178786480	Hela-S3	cervix:	n/a	chr5:178786328-178786339
50	CEBPB	chr5:178688281-178688621	IMR90	lung:	n/a	n/a

(count:5931 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178692691-178692741	Jurkat	blood:	n/a
2	chr5:178651200-178651250	MCF-7	breast:	n/a
3	chr5:178759017-178759067	HEEpiC	esophagus:	n/a
4	chr5:178771329-178771379	SKMC	muscle:	n/a
5	chr5:178656491-178656541	A549	lung:	n/a
6	chr5:178803207-178803257	GM06990	blood:	n/a
7	chr5:178667709-178667759	AG04450	lung:	fetal
8	chr5:178680976-178681026	SK-N-MC	brain:	n/a
9	chr5:178767472-178767522	HL-60	blood:	n/a
10	chr5:178685787-178685837	GM19239	blood:	n/a
11	chr5:178656269-178656319	AG09319	gingival:	n/a
12	chr5:178753803-178753853	NH-A	brain:	n/a
13	chr5:178704915-178704965	GM19239	blood:	n/a
14	chr5:178752999-178753049	HIPEpiC	eye:	n/a
15	chr5:178692691-178692741	Jurkat	blood:	n/a
16	chr5:178651200-178651250	MCF-7	breast:	n/a
17	chr5:178759017-178759067	HEEpiC	esophagus:	n/a
18	chr5:178771329-178771379	SKMC	muscle:	n/a
19	chr5:178656491-178656541	A549	lung:	n/a
20	chr5:178803207-178803257	GM06990	blood:	n/a
21	chr5:178667709-178667759	AG04450	lung:	fetal
22	chr5:178680976-178681026	SK-N-MC	brain:	n/a
23	chr5:178767472-178767522	HL-60	blood:	n/a
24	chr5:178685787-178685837	GM19239	blood:	n/a
25	chr5:178656269-178656319	AG09319	gingival:	n/a
26	chr5:178753803-178753853	NH-A	brain:	n/a
27	chr5:178704915-178704965	GM19239	blood:	n/a
28	chr5:178752999-178753049	HIPEpiC	eye:	n/a
29	chr5:178631497-178631547	ovcar-3	ovarian:	n/a
30	chr5:178759017-178759067	GM12892	blood:	n/a
31	chr5:178631741-178631791	ECC-1	luminal epithelium:	n/a
32	chr5:178667879-178667929	PrEC	prostate:	n/a
33	chr5:178770629-178770679	AG04450	lung:	fetal
34	chr5:178801647-178801697	HL-60	blood:	n/a
35	chr5:178632502-178632552	HRE	kidney:	n/a
36	chr5:178736443-178736493	SK-N-SH	brain:	n/a
37	chr5:178771776-178771826	SK-N-SH	brain:	n/a
38	chr5:178658477-178658527	ProgFib	skin:	n/a
39	chr5:178631845-178631895	HEEpiC	esophagus:	n/a
40	chr5:178680976-178681026	K562	blood:	n/a
41	chr5:178651519-178651569	Hela-S3	cervix:	n/a
42	chr5:178702842-178702892	AG04450	lung:	fetal
43	chr5:178801647-178801697	T-47D	breast:	n/a
44	chr5:178687780-178687830	HCPEpiC	choroid plexus:	n/a
45	chr5:178767472-178767522	PrEC	prostate:	n/a
46	chr5:178772203-178772253	SK-N-SH	brain:	n/a
47	chr5:178784097-178784147	HNPCEpiC	eye:	n/a
48	chr5:178799709-178799759	LNCaP	prostate:	n/a
49	chr5:178658501-178658551	GM06990	blood:	n/a
50	chr5:178656491-178656541	HRE	kidney:	n/a

(count:60 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:178619900..178622290-chr5:178622494..178625423,2	MCF-7	breast:
2	chr5:178698907..178700648-chr5:178703533..178706246,2	MCF-7	breast:
3	chr5:178793109..178796105-chr5:179125384..179128079,2	K562	blood:
4	chr5:178650614..178652876-chr5:178653305..178655920,2	K562	blood:
5	chr5:178669101..178670915-chr5:178673147..178675746,2	MCF-7	breast:
6	chr5:178652878..178655223-chr5:178665952..178668603,2	K562	blood:
7	chr5:178637418..178640045-chr5:178643551..178645345,3	MCF-7	breast:
8	chr5:178694614..178696474-chr5:178699270..178701166,2	K562	blood:
9	chr5:178748584..178750238-chr5:178758412..178760319,2	MCF-7	breast:
10	chr5:178698907..178700648-chr5:178703533..178706246,2	MCF-7	breast:
11	chr5:178694647..178697268-chr5:179049140..179050881,2	MCF-7	breast:
12	chr5:178626882..178628440-chr5:178635586..178638472,2	MCF-7	breast:
13	chr5:178631257..178632902-chr5:178635722..178638591,2	K562	blood:
14	chr5:178774195..178776525-chr5:178779659..178783563,3	K562	blood:
15	chr5:178219952..178220766-chr5:178688074..178688887,3	MCF-7	breast:
16	chr5:178786828..178788661-chr5:178798258..178800552,2	K562	blood:
17	chr5:178639660..178640480-chr5:178701010..178701947,3	MCF-7	breast:
18	chr5:178669101..178670915-chr5:178673147..178675746,2	MCF-7	breast:
19	chr5:178763364..178765890-chr5:178804717..178806886,2	K562	blood:
20	chr5:178673165..178675582-chr5:178682729..178684288,2	MCF-7	breast:
21	chr5:178650614..178652876-chr5:178653305..178655920,2	K562	blood:
22	chr5:178795348..178797290-chr5:178808669..178810729,2	K562	blood:
23	chr5:178694614..178696834-chr5:178698467..178700770,2	K562	blood:
24	chr5:178780858..178782954-chr5:178784606..178786505,2	MCF-7	breast:
25	chr5:178802308..178804471-chr5:178807615..178809965,2	K562	blood:
26	chr5:178662646..178664463-chr5:178900746..178903231,2	K562	blood:
27	chr5:178719721..178723694-chr5:178743933..178746463,3	K562	blood:
28	chr5:178719721..178723694-chr5:178743933..178746463,3	K562	blood:
29	chr5:178786828..178788661-chr5:178798258..178800552,2	K562	blood:
30	chr5:178570556..178571105-chr5:178687987..178688905,2	MCF-7	breast:
31	chr5:178770291..178772174-chr5:178775649..178777213,2	MCF-7	breast:
32	chr5:178669552..178671241-chr5:178672789..178674406,2	K562	blood:
33	chr5:178545417..178547035-chr5:178698975..178701216,2	K562	blood:
34	chr5:178639660..178640480-chr5:178701010..178701947,3	MCF-7	breast:
35	chr5:178751231..178753197-chr5:178755873..178757949,2	MCF-7	breast:
36	chr5:178639654..178640533-chr5:178687929..178688900,5	MCF-7	breast:
37	chr5:178780858..178782954-chr5:178784606..178786505,2	MCF-7	breast:
38	chr5:178748584..178750238-chr5:178758412..178760319,2	MCF-7	breast:
39	chr5:178626882..178628440-chr5:178635586..178638472,2	MCF-7	breast:
40	chr5:178649094..178651976-chr5:178660819..178662665,2	MCF-7	breast:
41	chr5:178694614..178696474-chr5:178699270..178701166,2	K562	blood:
42	chr5:178652878..178655223-chr5:178665952..178668603,2	K562	blood:
43	chr5:178650071..178651966-chr5:178658345..178660809,2	MCF-7	breast:
44	chr5:178774195..178776525-chr5:178779659..178783563,3	K562	blood:
45	chr5:178687965..178688655-chr5:178920708..178921301,2	K562	blood:
46	chr5:178751231..178753197-chr5:178755873..178757949,2	MCF-7	breast:
47	chr5:178673165..178675582-chr5:178682729..178684288,2	MCF-7	breast:
48	chr5:178650071..178651966-chr5:178658345..178660809,2	MCF-7	breast:
49	chr5:178762053..178764261-chr5:178817559..178819340,2	K562	blood:
50	chr5:178799420..178802506-chr5:178805933..178808859,3	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAMTS2-1	chr5:178804601-178804929	XLOC_005105
2	lnc-RUFY1-2	chr5:178804506-178804705	ENSG00000253979
3	lnc-ADAMTS2-1	chr5:178805537-178805760	XLOC_005105

No data

Variant related genes	Relation type
ADAMTS2	TF binding region
ENSG00000253979	TF binding region
ADAMTS2	CpG island
ENSG00000253979	CpG island
ENSG00000127022	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000253163	chromatin interactions

Extended variants
information (count: 9005 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:9005 , 50 per page) page: 1 2 3 4 5 6 7 ... 181

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs59456453	chr5:178624457-178624458	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs562199504	chr5:178624458-178624459	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552070466	chr5:178624468-178624469	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532493670	chr5:178624486-178624487	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs550616176	chr5:178624536-178624537	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562549198	chr5:178624571-178624572	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529938538	chr5:178624586-178624587	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148122564	chr5:178624614-178624615	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs28553364	chr5:178624672-178624673	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527568886	chr5:178624673-178624674	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369594088	chr5:178624750-178624751	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73329725	chr5:178624751-178624752	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs145009996	chr5:178624830-178624831	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs28409173	chr5:178624844-178624845	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs556265898	chr5:178624882-178624883	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs112091297	chr5:178624905-178624906	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs386695587	chr5:178624907-178624908	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs114660039	chr5:178624908-178624909	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs34008687	chr5:178624912-178624913	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs536878657	chr5:178624958-178624959	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs17079197	chr5:178624961-178624962	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs142255982	chr5:178624971-178624972	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs540499495	chr5:178624989-178624990	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs558534128	chr5:178625006-178625007	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs150470542	chr5:178625007-178625008	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs564326713	chr5:178625013-178625014	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs138326577	chr5:178625037-178625038	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs563043716	chr5:178625064-178625065	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs530113247	chr5:178625140-178625141	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs542041701	chr5:178625153-178625154	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs560055377	chr5:178625154-178625155	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs527605673	chr5:178625187-178625188	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs112623884	chr5:178625212-178625213	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs375307933	chr5:178625239-178625240	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs570751263	chr5:178625249-178625250	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs368951890	chr5:178625306-178625307	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs543718932	chr5:178625313-178625314	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs531382258	chr5:178625355-178625356	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs187619504	chr5:178625377-178625378	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs377367520	chr5:178625414-178625415	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs564733855	chr5:178625415-178625416	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs115256538	chr5:178625423-178625424	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs530658605	chr5:178625452-178625453	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs192138727	chr5:178625469-178625470	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs563607649	chr5:178625477-178625478	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs555168859	chr5:178625495-178625496	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs7705793	chr5:178625525-178625526	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs534232972	chr5:178625529-178625530	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs549148499	chr5:178625531-178625532	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs558862072	chr5:178625560-178625561	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	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
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
small cell lung cancer	20016488	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3560 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178594800-178627600	Weak transcription	Right Atrium	heart
2	chr5:178607400-178636200	Weak transcription	HSMM	muscle
3	chr5:178607600-178626000	Weak transcription	HSMMtube	muscle
4	chr5:178607800-178629000	Weak transcription	NHLF	lung
5	chr5:178619000-178625000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr5:178619000-178635000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr5:178619600-178627200	Weak transcription	Fetal Intestine Small	intestine
8	chr5:178619800-178650200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr5:178620200-178650200	Weak transcription	Fetal Lung	lung
10	chr5:178620400-178636400	Weak transcription	Ovary	ovary
11	chr5:178621000-178630200	Weak transcription	Osteobl	bone
12	chr5:178622200-178631600	Weak transcription	Spleen	Spleen
13	chr5:178622600-178624600	Enhancers	Fetal Brain Male	brain
14	chr5:178622600-178629200	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr5:178622600-178630000	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr5:178622800-178625200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr5:178623000-178625000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr5:178623200-178624400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr5:178623200-178624400	Enhancers	Fetal Brain Female	brain
20	chr5:178623200-178629600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr5:178623400-178625200	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr5:178623800-178628000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr5:178623800-178633200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr5:178623800-178636000	Weak transcription	Adipose Nuclei	Adipose
25	chr5:178623800-178636000	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr5:178623800-178640600	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr5:178624000-178624400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr5:178624200-178624400	Weak transcription	Fetal Stomach	stomach
29	chr5:178624200-178625200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr5:178624200-178626000	Weak transcription	Fetal Muscle Leg	muscle
31	chr5:178624200-178627200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr5:178624400-178625800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr5:178624400-178626600	Strong transcription	Fetal Stomach	stomach
34	chr5:178624400-178627200	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr5:178624600-178624800	Enhancers	Fetal Muscle Trunk	muscle
36	chr5:178624800-178625400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr5:178625000-178626000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr5:178625000-178626800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr5:178625200-178626000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr5:178625200-178626200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr5:178625200-178626800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr5:178625800-178626600	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr5:178626000-178626200	Enhancers	Fetal Muscle Leg	muscle
44	chr5:178626000-178626400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr5:178626000-178626600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr5:178626000-178626800	Strong transcription	HSMMtube	muscle
47	chr5:178626200-178626600	Enhancers	Esophagus	oesophagus
48	chr5:178626200-178626800	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr5:178626400-178626600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
50	chr5:178626400-178628000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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