Variant report

Variant	nsv1023502
Chromosome Location	chr5:179086091-179105316
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:765)
CpG islands
(count:305)
Chromatin interactive
region (count:60)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:765 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:179095553-179095777	K562	blood:	n/a	n/a
2	ARID3A	chr5:179095445-179095794	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:179105219-179105743	HepG2	liver:	n/a	n/a
4	ATF1	chr5:179094425-179094603	K562	blood:	n/a	n/a
5	ATF2	chr5:179105206-179105959	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr5:179105197-179106298	GM12878	blood:	n/a	n/a
7	ATF2	chr5:179105100-179105843	GM12878	blood:	n/a	n/a
8	ATF2	chr5:179104979-179106509	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr5:179095433-179095694	K562	blood:	n/a	n/a
10	ATF3	chr5:179105154-179105824	A549	lung:	n/a	n/a
11	ATF3	chr5:179095468-179095775	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr5:179105263-179105777	HepG2	liver:	n/a	n/a
13	ATF3	chr5:179105309-179105835	A549	lung:	n/a	n/a
14	BACH1	chr5:179105168-179105658	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL3	chr5:179104929-179105840	A549	lung:	n/a	chr5:179105186-179105195
16	BCL3	chr5:179104994-179105597	A549	lung:	n/a	chr5:179105186-179105195
17	BCLAF1	chr5:179105260-179106595	GM12878	blood:	n/a	n/a
18	BCLAF1	chr5:179104797-179106301	GM12878	blood:	n/a	chr5:179105186-179105195
19	BHLHE40	chr5:179105159-179105877	K562	blood:	n/a	n/a
20	BHLHE40	chr5:179095414-179095737	K562	blood:	n/a	n/a
21	BHLHE40	chr5:179105243-179106458	GM12878	blood:	n/a	n/a
22	BRCA1	chr5:179095579-179095636	HepG2	liver:	n/a	n/a
23	BRCA1	chr5:179105297-179105711	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr5:179105232-179106295	K562	blood:	n/a	n/a
25	CBX3	chr5:179095362-179095789	K562	blood:	n/a	n/a
26	CCNT2	chr5:179105071-179106185	K562	blood:	n/a	chr5:179105167-179105176
27	CEBPB	chr5:179105248-179105805	IMR90	lung:	n/a	chr5:179105576-179105587
28	CEBPB	chr5:179105052-179105860	K562	blood:	n/a	chr5:179105576-179105587
29	CEBPB	chr5:179104989-179106198	GM12878	blood:	n/a	chr5:179105576-179105587
30	CEBPB	chr5:179095478-179095643	K562	blood:	n/a	n/a
31	CEBPB	chr5:179105235-179105847	HepG2	liver:	n/a	chr5:179105576-179105587
32	CEBPB	chr5:179105270-179105828	Hela-S3	cervix:	n/a	chr5:179105576-179105587
33	CEBPB	chr5:179097467-179097624	K562	blood:	n/a	n/a
34	CEBPB	chr5:179105282-179105787	A549	lung:	n/a	chr5:179105576-179105587
35	CEBPB	chr5:179105214-179105938	A549	lung:	n/a	chr5:179105576-179105587
36	CEBPB	chr5:179099688-179099703	K562	blood:	n/a	n/a
37	CEBPB	chr5:179099517-179099718	HepG2	liver:	n/a	chr5:179099685-179099696
38	CEBPB	chr5:179105254-179105809	HepG2	liver:	n/a	chr5:179105576-179105587
39	CEBPB	chr5:179105269-179105900	ECC-1	luminal epithelium:	n/a	chr5:179105576-179105587
40	CEBPB	chr5:179105180-179106019	MCF-7	breast:	n/a	chr5:179105576-179105587
41	CEBPB	chr5:179105266-179105897	MCF-7	breast:	n/a	chr5:179105576-179105587
42	CEBPD	chr5:179105268-179105704	HepG2	liver:	n/a	n/a
43	CEBPD	chr5:179105225-179105778	HepG2	liver:	n/a	n/a
44	CEBPD	chr5:179105226-179105874	K562	blood:	n/a	n/a
45	CHD1	chr5:179104935-179105901	GM12878	blood:	n/a	n/a
46	CHD1	chr5:179105002-179105411	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr5:179105218-179105841	HepG2	liver:	n/a	n/a
48	CHD2	chr5:179105150-179106540	GM12878	blood:	n/a	n/a
49	CHD2	chr5:179105082-179105511	K562	blood:	n/a	n/a
50	CHD2	chr5:179105181-179105784	Hela-S3	cervix:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179105010-179105060	PFSK-1	brain:	n/a
2	chr5:179104144-179104194	HL-60	blood:	n/a
3	chr5:179089038-179089088	SAEC	small airway:	n/a
4	chr5:179104144-179104194	AG10803	skin:	n/a
5	chr5:179089038-179089088	CMK	blood:	n/a
6	chr5:179105290-179105340	SK-N-SH	brain:	n/a
7	chr5:179089038-179089088	HRPEpiC	eye:	n/a
8	chr5:179105290-179105340	Hela-S3	cervix:	n/a
9	chr5:179104144-179104194	MCF-7	breast:	n/a
10	chr5:179105290-179105340	T-47D	breast:	n/a
11	chr5:179104144-179104194	HCPEpiC	choroid plexus:	n/a
12	chr5:179105170-179105220	SK-N-MC	brain:	n/a
13	chr5:179104144-179104194	GM19239	blood:	n/a
14	chr5:179089038-179089088	SK-N-MC	brain:	n/a
15	chr5:179105010-179105060	Hepatocyte	liver:	n/a
16	chr5:179105170-179105220	ovcar-3	ovarian:	n/a
17	chr5:179104144-179104194	GM12878	blood:	n/a
18	chr5:179105010-179105060	PANC-1	pancreas:	n/a
19	chr5:179105290-179105340	NHDF-neo	bronchial:	n/a
20	chr5:179104144-179104194	HCF	heart:	n/a
21	chr5:179105010-179105060	GM12891	blood:	n/a
22	chr5:179105290-179105340	GM12878	blood:	n/a
23	chr5:179105170-179105220	HMEC	breast:	n/a
24	chr5:179105290-179105340	HRE	kidney:	n/a
25	chr5:179089038-179089088	Jurkat	blood:	n/a
26	chr5:179089038-179089088	PANC-1	pancreas:	n/a
27	chr5:179105290-179105340	PANC-1	pancreas:	n/a
28	chr5:179089038-179089088	HepG2	liver:	n/a
29	chr5:179105170-179105220	GM12878	blood:	n/a
30	chr5:179105170-179105220	SK-N-SH	brain:	n/a
31	chr5:179105170-179105220	ECC-1	luminal epithelium:	n/a
32	chr5:179105170-179105220	HCF	heart:	n/a
33	chr5:179105010-179105060	SK-N-MC	brain:	n/a
34	chr5:179104144-179104194	HCT-116	colon:	n/a
35	chr5:179089038-179089088	U87	brain:	n/a
36	chr5:179089038-179089088	SK-N-SH	brain:	n/a
37	chr5:179105170-179105220	HEEpiC	esophagus:	n/a
38	chr5:179105170-179105220	PrEC	prostate:	n/a
39	chr5:179089038-179089088	GM12892	blood:	n/a
40	chr5:179089038-179089088	HCF	heart:	n/a
41	chr5:179104144-179104194	Jurkat	blood:	n/a
42	chr5:179104144-179104194	HRE	kidney:	n/a
43	chr5:179105290-179105340	MCF-7	breast:	n/a
44	chr5:179089038-179089088	PFSK-1	brain:	n/a
45	chr5:179105010-179105060	GM12892	blood:	n/a
46	chr5:179105290-179105340	NHBE	bronchial:	n/a
47	chr5:179105290-179105340	SK-N-MC	brain:	n/a
48	chr5:179089038-179089088	SK-N-SH_RA	brain:	n/a
49	chr5:179105290-179105340	AG09319	gingival:	n/a
50	chr5:179089038-179089088	ECC-1	luminal epithelium:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:179038960..179041938-chr5:179093606..179095921,3	K562	blood:
2	chr17:62502005..62502822-chr5:179104873..179105477,2	HCT-116	colon:
3	chr5:179100989..179111182-chr5:179122076..179128627,19	K562	blood:
4	chr5:179101603..179111989-chr5:179122927..179129527,32	MCF-7	breast:
5	chr5:179049811..179051331-chr5:179093984..179095608,2	K562	blood:
6	chr5:179104067..179106595-chr5:179220718..179223236,3	MCF-7	breast:
7	chr5:179049220..179051845-chr5:179089709..179092137,2	K562	blood:
8	chr5:179096128..179097947-chr5:179132698..179134223,2	K562	blood:
9	chr5:179064378..179067657-chr5:179095247..179097749,4	K562	blood:
10	chr5:179104047..179107935-chr5:179157751..179161258,3	K562	blood:
11	chr5:179047959..179050192-chr5:179084037..179087067,3	K562	blood:
12	chr5:179032379..179035248-chr5:179088409..179090962,2	MCF-7	breast:
13	chr5:179084083..179087060-chr5:179094227..179096251,2	K562	blood:
14	chr5:178980836..178983768-chr5:179095589..179098241,2	MCF-7	breast:
15	chr5:179094562..179097080-chr5:179122833..179124461,2	MCF-7	breast:
16	chr5:179048487..179050192-chr5:179084037..179087067,3	K562	blood:
17	chr5:179038046..179040249-chr5:179091057..179092681,2	K562	blood:
18	chr5:179049036..179051561-chr5:179096691..179099581,2	K562	blood:
19	chr5:179038238..179040444-chr5:179101128..179103965,2	K562	blood:
20	chr5:179085578..179087269-chr5:179124562..179126084,2	MCF-7	breast:
21	chr1:32671254..32672166-chr5:179105011..179105570,2	Hela-S3	cervix:
22	chr5:179102777..179105502-chr5:179129566..179131277,2	MCF-7	breast:
23	chr5:179048811..179053260-chr5:179101652..179108160,8	MCF-7	breast:
24	chr5:179049332..179050368-chr5:179095139..179096218,4	MCF-7	breast:
25	chr5:179047581..179051358-chr5:179102429..179108878,16	K562	blood:
26	chr5:179047219..179049310-chr5:179100956..179102522,2	K562	blood:
27	chr5:179104105..179106791-chr5:179194829..179197317,2	K562	blood:
28	chr5:179048902..179051476-chr5:179093984..179097643,6	K562	blood:
29	chr5:179032616..179037685-chr5:179101606..179106447,5	K562	blood:
30	chr5:179042046..179045911-chr5:179093714..179097156,4	K562	blood:
31	chr5:179091330..179094019-chr5:179094233..179096513,3	K562	blood:
32	chr5:179091330..179094019-chr5:179094233..179096513,3	K562	blood:
33	chr5:179085577..179087271-chr5:179159837..179161552,2	K562	blood:
34	chr5:179104081..179106481-chr5:179247871..179249548,2	K562	blood:
35	chr5:179049533..179052334-chr5:179104256..179107492,4	MCF-7	breast:
36	chr5:179048865..179051290-chr5:179093625..179096792,3	MCF-7	breast:
37	chr5:179085589..179087601-chr5:179105143..179107865,2	MCF-7	breast:
38	chr5:179048484..179051740-chr5:179086105..179090360,4	MCF-7	breast:
39	chr5:179095526..179096093-chr5:179105184..179105999,2	K562	blood:
40	chr5:179102368..179107935-chr5:179157286..179161555,5	K562	blood:
41	chr5:179104088..179107429-chr5:179222108..179224529,3	MCF-7	breast:
42	chr5:179037627..179040262-chr5:179091207..179093202,2	K562	blood:
43	chr5:179050030..179052067-chr5:179087390..179090621,3	MCF-7	breast:
44	chr5:179097480..179099129-chr5:179124027..179126055,2	K562	blood:
45	chr5:179101962..179108661-chr5:179122383..179128408,19	MCF-7	breast:
46	chr5:179098847..179102050-chr5:179104228..179106166,3	K562	blood:
47	chr5:179048142..179050752-chr5:179095144..179097340,5	MCF-7	breast:
48	chr5:179048156..179052144-chr5:179103013..179109071,12	K562	blood:
49	chr5:179103716..179105834-chr5:179232132..179234075,2	MCF-7	breast:
50	chr5:178986726..178988892-chr5:179104044..179106638,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC136604.1-1	chr5:179091324-179091433	XLOC_004677
2	lnc-AC136604.1-1	chr5:179091386-179091418	XLOC_004677
3	lnc-AC136604.1-1	chr5:179101947-179102346	NONHSAT105614
4	lnc-AC136604.1-1	chr5:179095218-179095672	XLOC_004677
5	lnc-CBY3-1	chr5:179089955-179090287	ncRnaDb_ncrna_FR353964_1
6	lnc-AC136604.1-1	chr5:179091324-179091431	XLOC_004677
7	lnc-AC136604.1-1	chr5:179089976-179090159	XLOC_004677
8	lnc-AC136604.1-1	chr5:179094877-179096772	NONHSAT105614
9	lnc-AC136604.1-1	chr5:179089976-179090104	XLOC_004677

No data

Variant related genes	Relation type
CANX	TF binding region
HMGB3P22	TF binding region
CANX	CpG island
HMGB3P22	CpG island
ENSG00000139370	chromatin interactions
ENSG00000176783	chromatin interactions
ENSG00000127022	chromatin interactions
ENSG00000213316	chromatin interactions
ENSG00000160051	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000161013	chromatin interactions
ENSG00000258890	chromatin interactions
ENSG00000250999	chromatin interactions
ENSG00000224066	chromatin interactions
ENSG00000161021	chromatin interactions
ENSG00000225051	chromatin interactions
ENSG00000173113	chromatin interactions
ENSG00000108654	chromatin interactions
ENSG00000161011	chromatin interactions
KREMEN1	miRNA target sites

Extended variants
information (count: 738 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:738 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542281590	chr5:179086097-179086098	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs530183726	chr5:179086130-179086131	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs541975232	chr5:179086131-179086132	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs560480146	chr5:179086148-179086149	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs111423228	chr5:179086152-179086153	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs182854118	chr5:179086156-179086157	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs552496366	chr5:179086161-179086162	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs111489530	chr5:179086185-179086186	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs531387359	chr5:179086198-179086199	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs549973617	chr5:179086216-179086217	Weak transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs555592903	chr5:179086222-179086223	Weak transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs367636986	chr5:179086234-179086235	Weak transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs55765420	chr5:179086236-179086237	Weak transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs67516170	chr5:179086237-179086238	Weak transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs545118009	chr5:179086250-179086251	Weak transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs191571079	chr5:179086321-179086322	Weak transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs182905731	chr5:179086347-179086348	Weak transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs565335826	chr5:179086378-179086379	Weak transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs539088771	chr5:179086416-179086417	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs73336088	chr5:179086476-179086477	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs73336089	chr5:179086498-179086499	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs538179166	chr5:179086499-179086500	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs111599056	chr5:179086519-179086520	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs111838052	chr5:179086527-179086528	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs200712542	chr5:179086536-179086537	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs61608275	chr5:179086548-179086549	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs386695659	chr5:179086561-179086562	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs28796419	chr5:179086564-179086565	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs560615045	chr5:179086587-179086588	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs143547402	chr5:179086593-179086594	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs546251701	chr5:179086613-179086614	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs72824570	chr5:179086624-179086625	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs188061752	chr5:179086666-179086667	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs549821398	chr5:179086711-179086712	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs76597794	chr5:179086715-179086716	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs28797599	chr5:179086735-179086736	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs28819678	chr5:179086753-179086754	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs73336090	chr5:179086787-179086788	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs531224091	chr5:179086788-179086789	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs539025602	chr5:179086827-179086828	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs115444800	chr5:179086832-179086833	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs28833246	chr5:179086833-179086834	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs143889765	chr5:179086842-179086843	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs556580315	chr5:179086854-179086855	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs10079107	chr5:179086861-179086862	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs10479548	chr5:179086931-179086932	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs190749728	chr5:179086959-179086960	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs147251680	chr5:179086965-179086966	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs372570402	chr5:179086970-179086971	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs112067572	chr5:179086987-179086988	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
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
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:579 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179084600-179086200	Active TSS	Fetal Brain Female	brain
2	chr5:179084800-179086200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr5:179084800-179086200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr5:179084800-179086400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr5:179085400-179086200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr5:179085400-179086200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr5:179085400-179086200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr5:179085400-179086200	Active TSS	Brain Angular Gyrus	brain
9	chr5:179085400-179086200	Flanking Active TSS	Dnd41	blood
10	chr5:179085800-179086200	Enhancers	Primary B cells from peripheral blood	blood
11	chr5:179085800-179086200	Enhancers	Liver	Liver
12	chr5:179085800-179086800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr5:179085800-179087000	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr5:179085800-179087000	Enhancers	Primary T cells fromperipheralblood	blood
15	chr5:179085800-179087000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr5:179085800-179090000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr5:179085800-179090000	Weak transcription	Lung	lung
18	chr5:179085800-179090200	Weak transcription	Adipose Nuclei	Adipose
19	chr5:179085800-179090400	Weak transcription	Colon Smooth Muscle	Colon
20	chr5:179085800-179090600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr5:179085800-179090800	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr5:179085800-179090800	Weak transcription	Fetal Lung	lung
23	chr5:179085800-179090800	Weak transcription	Gastric	stomach
24	chr5:179085800-179090800	Weak transcription	Ovary	ovary
25	chr5:179085800-179091200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr5:179085800-179091200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr5:179085800-179091200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr5:179085800-179091200	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr5:179085800-179091400	Weak transcription	Spleen	Spleen
30	chr5:179085800-179092000	Weak transcription	Colonic Mucosa	Colon
31	chr5:179085800-179092200	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr5:179085800-179092200	Weak transcription	Thymus	Thymus
33	chr5:179085800-179099200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr5:179085800-179099400	Weak transcription	Aorta	Aorta
35	chr5:179085800-179103800	Weak transcription	GM12878-XiMat	blood
36	chr5:179085800-179104000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr5:179085800-179104200	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr5:179085800-179104200	Weak transcription	A549	lung
39	chr5:179085800-179104600	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr5:179085800-179104600	Weak transcription	Brain Hippocampus Middle	brain
41	chr5:179085800-179104600	Weak transcription	Esophagus	oesophagus
42	chr5:179085800-179104600	Weak transcription	Fetal Kidney	kidney
43	chr5:179085800-179104800	Weak transcription	Right Ventricle	heart
44	chr5:179085800-179105000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr5:179086000-179086200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr5:179086000-179086200	Enhancers	Fetal Intestine Small	intestine
47	chr5:179086000-179086200	Enhancers	Fetal Muscle Trunk	muscle
48	chr5:179086000-179086200	Enhancers	Fetal Stomach	stomach
49	chr5:179086000-179086200	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr5:179086000-179086200	Enhancers	HUVEC	blood vessel

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