Variant report

Variant	nsv518936
Chromosome Location	chr1:179847402-179858333
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1047)
CpG islands
(count:1039)
Chromatin interactive
region (count:43)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1047 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:179851266-179852143	K562	blood:	n/a	n/a
2	ARID3A	chr1:179850320-179852316	HepG2	liver:	n/a	chr1:179850758-179850774
3	ARID3A	chr1:179846614-179847471	K562	blood:	n/a	n/a
4	ARID3A	chr1:179849058-179849997	K562	blood:	n/a	chr1:179849295-179849311
5	ATF1	chr1:179852882-179853255	K562	blood:	n/a	n/a
6	ATF1	chr1:179851118-179852130	K562	blood:	n/a	n/a
7	ATF2	chr1:179852432-179853269	GM12878	blood:	n/a	n/a
8	ATF2	chr1:179851073-179852302	H1-hESC	embryonic stem cell:	n/a	chr1:179851622-179851633
9	ATF2	chr1:179851160-179852280	GM12878	blood:	n/a	chr1:179851622-179851633
10	ATF2	chr1:179851247-179852208	GM12878	blood:	n/a	chr1:179851622-179851633
11	ATF2	chr1:179851000-179852273	H1-hESC	embryonic stem cell:	n/a	chr1:179851622-179851633
12	ATF2	chr1:179852414-179853231	GM12878	blood:	n/a	n/a
13	ATF3	chr1:179852936-179853175	K562	blood:	n/a	n/a
14	ATF3	chr1:179851254-179852058	K562	blood:	n/a	n/a
15	ATF3	chr1:179851272-179852130	K562	blood:	n/a	n/a
16	ATF3	chr1:179851435-179852205	A549	lung:	n/a	n/a
17	ATF3	chr1:179850884-179852151	A549	lung:	n/a	n/a
18	BACH1	chr1:179851347-179852374	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr1:179851735-179852063	K562	blood:	n/a	n/a
20	BATF	chr1:179851664-179852200	GM12878	blood:	n/a	n/a
21	BATF	chr1:179852838-179853186	GM12878	blood:	n/a	chr1:179853000-179853008
22	BCL11A	chr1:179851660-179852147	GM12878	blood:	n/a	n/a
23	BCL11A	chr1:179851712-179852058	GM12878	blood:	n/a	n/a
24	BCL3	chr1:179850964-179852214	A549	lung:	n/a	chr1:179851493-179851506
25	BCL3	chr1:179850608-179852213	A549	lung:	n/a	chr1:179851493-179851506
26	BCLAF1	chr1:179850999-179852705	GM12878	blood:	n/a	chr1:179851493-179851506 chr1:179852343-179852356
27	BCLAF1	chr1:179851101-179852175	K562	blood:	n/a	chr1:179851493-179851506
28	BCLAF1	chr1:179851125-179852269	GM12878	blood:	n/a	chr1:179851493-179851506
29	BCLAF1	chr1:179848803-179849319	GM12878	blood:	n/a	chr1:179849154-179849163
30	BCLAF1	chr1:179851195-179852110	K562	blood:	n/a	chr1:179851493-179851506
31	BHLHE40	chr1:179846836-179847488	K562	blood:	n/a	n/a
32	BHLHE40	chr1:179850807-179852395	K562	blood:	n/a	n/a
33	BHLHE40	chr1:179850831-179852211	GM12878	blood:	n/a	n/a
34	BRCA1	chr1:179851706-179852062	HepG2	liver:	n/a	n/a
35	BRCA1	chr1:179850535-179852341	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr1:179851420-179852227	GM12878	blood:	n/a	n/a
37	BRCA1	chr1:179851676-179852234	H1-hESC	embryonic stem cell:	n/a	n/a
38	CBX3	chr1:179850746-179852315	K562	blood:	n/a	n/a
39	CBX3	chr1:179846232-179847480	K562	blood:	n/a	n/a
40	CBX3	chr1:179851209-179852256	K562	blood:	n/a	n/a
41	CCNT2	chr1:179852773-179853105	K562	blood:	n/a	n/a
42	CCNT2	chr1:179851118-179852422	K562	blood:	n/a	chr1:179851302-179851311 chr1:179852345-179852354
43	CEBPB	chr1:179850711-179852126	K562	blood:	n/a	n/a
44	CEBPB	chr1:179849069-179849093	A549	lung:	n/a	n/a
45	CEBPB	chr1:179851018-179851221	HepG2	liver:	n/a	n/a
46	CEBPB	chr1:179851708-179852059	GM12878	blood:	n/a	n/a
47	CEBPB	chr1:179846766-179847472	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr1:179846606-179847465	GM12878	blood:	n/a	n/a
49	CEBPB	chr1:179846887-179847492	K562	blood:	n/a	n/a
50	CEBPB	chr1:179847117-179847458	HepG2	liver:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:179851219-179851269	SK-N-SH_RA	brain:	n/a
2	chr1:179851994-179852044	MCF10A-Er-Src	breast:	n/a
3	chr1:179851219-179851269	SK-N-SH_RA	brain:	n/a
4	chr1:179851994-179852044	MCF10A-Er-Src	breast:	n/a
5	chr1:179851094-179851144	T-47D	breast:	n/a
6	chr1:179852195-179852245	HEEpiC	esophagus:	n/a
7	chr1:179847685-179847735	HEEpiC	esophagus:	n/a
8	chr1:179852419-179852469	SK-N-MC	brain:	n/a
9	chr1:179851019-179851069	HIPEpiC	eye:	n/a
10	chr1:179847685-179847735	AoSMC	blood vessel:	n/a
11	chr1:179851103-179851153	HRPEpiC	eye:	n/a
12	chr1:179851575-179851625	SAEC	small airway:	n/a
13	chr1:179851391-179851441	H1-hESC	embryonic stem cell:	embryo
14	chr1:179851575-179851625	RPTEC	kidney:	n/a
15	chr1:179851103-179851153	CMK	blood:	n/a
16	chr1:179851019-179851069	U87	brain:	n/a
17	chr1:179852419-179852469	Caco-2	colon:	n/a
18	chr1:179851019-179851069	HEK293	kidney:	embryo
19	chr1:179851385-179851435	BJ	skin:	n/a
20	chr1:179851385-179851435	AG09309	skin:	n/a
21	chr1:179851994-179852044	MCF-7	breast:	n/a
22	chr1:179851825-179851875	HRPEpiC	eye:	n/a
23	chr1:179851019-179851069	GM19239	blood:	n/a
24	chr1:179851219-179851269	HEK293	kidney:	embryo
25	chr1:179847685-179847735	Jurkat	blood:	n/a
26	chr1:179851103-179851153	PFSK-1	brain:	n/a
27	chr1:179851019-179851069	PANC-1	pancreas:	n/a
28	chr1:179851103-179851153	HL-60	blood:	n/a
29	chr1:179851825-179851875	A549	lung:	n/a
30	chr1:179856239-179856289	HNPCEpiC	eye:	n/a
31	chr1:179847685-179847735	NH-A	brain:	n/a
32	chr1:179851094-179851144	Hela-S3	cervix:	n/a
33	chr1:179851234-179851284	HRCEpiC	kidney:	n/a
34	chr1:179851234-179851284	LNCaP	prostate:	n/a
35	chr1:179851535-179851585	HCPEpiC	choroid plexus:	n/a
36	chr1:179851103-179851153	AG09319	gingival:	n/a
37	chr1:179851234-179851284	HCF	heart:	n/a
38	chr1:179851535-179851585	HCT-116	colon:	n/a
39	chr1:179851825-179851875	HL-60	blood:	n/a
40	chr1:179851391-179851441	GM06990	blood:	n/a
41	chr1:179851575-179851625	IMR90	lung:	fetal
42	chr1:179851103-179851153	U87	brain:	n/a
43	chr1:179851385-179851435	AG09319	gingival:	n/a
44	chr1:179851575-179851625	AG09319	gingival:	n/a
45	chr1:179851825-179851875	HUVEC	blood vessel:	n/a
46	chr1:179851234-179851284	Hepatocyte	liver:	n/a
47	chr1:179851234-179851284	NHDF-neo	bronchial:	n/a
48	chr1:179852195-179852245	NT2-D1	testis:	n/a
49	chr1:179852195-179852245	AG10803	skin:	n/a
50	chr1:179856239-179856289	HCPEpiC	choroid plexus:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:179849806..179852481-chr17:56735365..56738310,2	MCF-7	breast:
2	chr1:179851198..179852026-chr3:49203059..49203856,2	HCT-116	colon:
3	chr1:179851121..179851836-chr16:67223607..67224107,2	Hela-S3	cervix:
4	chr1:179855626..179859704-chr1:179868315..179870321,3	K562	blood:
5	chr1:179856867..179859704-chr1:179868315..179870029,2	K562	blood:
6	chr1:179851199..179852167-chr15:73925572..73926175,2	Hela-S3	cervix:
7	chr1:179848142..179854405-chr1:179919774..179927189,17	MCF-7	breast:
8	chr1:179845348..179847730-chr1:179923811..179926342,3	MCF-7	breast:
9	chr1:179844894..179847778-chr1:180122782..180124340,2	K562	blood:
10	chr1:179851204..179851993-chr18:2655318..2656099,2	Hela-S3	cervix:
11	chr1:179843719..179847778-chr1:180121939..180127812,8	K562	blood:
12	chr1:179832603..179840385-chr1:179843229..179848672,10	MCF-7	breast:
13	chr1:179850599..179851124-chr17:27052630..27053629,2	Hela-S3	cervix:
14	chr1:179856725..179858627-chr1:179861974..179863939,2	K562	blood:
15	chr1:179857047..179859272-chr1:179914724..179916523,2	K562	blood:
16	chr1:179849600..179851970-chr1:180040830..180043217,3	K562	blood:
17	chr1:179847679..179853408-chr1:179922379..179926886,15	MCF-7	breast:
18	chr1:179849016..179853452-chr1:179922333..179928502,16	K562	blood:
19	chr1:179845449..179848601-chr1:179867688..179872232,4	K562	blood:
20	chr1:179851119..179851848-chr3:150479575..150480206,2	Hela-S3	cervix:
21	chr1:179849896..179853295-chr1:179868800..179873439,8	K562	blood:
22	chr1:179851188..179852119-chr7:45025474..45026402,2	Hela-S3	cervix:
23	chr1:179850318..179852494-chr17:27276905..27279440,2	MCF-7	breast:
24	chr1:179853596..179856683-chr1:179859981..179861933,3	MCF-7	breast:
25	chr1:179851750..179853316-chr1:179871986..179873575,2	MCF-7	breast:
26	chr1:179851260..179852079-chr8:98787810..98788460,2	Hela-S3	cervix:
27	chr1:179833317..179835863-chr1:179849395..179853272,4	MCF-7	breast:
28	chr1:179851639..179853343-chr1:181059453..181061374,2	K562	blood:
29	chr1:179850172..179852530-chr1:180041069..180043217,2	K562	blood:
30	chr1:179850917..179851836-chr5:176874454..176875296,2	Hela-S3	cervix:
31	chr1:179854286..179855981-chr1:179868215..179870330,2	MCF-7	breast:
32	chr1:179848758..179850478-chr1:179862468..179865015,2	MCF-7	breast:
33	chr1:179851412..179851962-chr6:27113794..27114759,2	Hela-S3	cervix:
34	chr1:179850426..179852030-chr1:179871802..179874421,2	MCF-7	breast:
35	chr1:179850478..179853234-chr1:179853885..179855815,2	MCF-7	breast:
36	chr1:179857167..179860041-chr1:179939702..179942440,2	K562	blood:
37	chr1:179850058..179853356-chr1:179869131..179876291,8	K562	blood:
38	chr1:179851119..179851675-chrX:133506676..133507425,2	Hela-S3	cervix:
39	chr1:179849895..179854138-chr1:179857075..179860267,5	MCF-7	breast:
40	chr1:179844528..179853403-chr1:179920065..179927793,25	K562	blood:
41	chr1:179851935..179852739-chr6:30584601..30585176,2	Hela-S3	cervix:
42	chr1:179850793..179851495-chr16:89574636..89575309,2	Hela-S3	cervix:
43	chr1:179849468..179853023-chr1:180122560..180126275,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEP350-3	chr1:179853827-179853904	NONHSAT008228
2	lnc-CEP350-3	chr1:179853103-179853163	NONHSAT008227
3	lnc-CEP350-3	chr1:179853827-179853904	NONHSAT008227
4	lnc-CEP350-3	chr1:179853072-179853163	NONHSAT008226
5	lnc-TOR1AIP2-5	chr1:179850742-179851730	ENSG00000272906.1
6	lnc-CEP350-3	chr1:179856964-179857094	NONHSAT008226
7	lnc-CEP350-3	chr1:179853827-179853904	NONHSAT008226
8	lnc-CEP350-3	chr1:179853120-179853163	NONHSAT008228

No data

Variant related genes	Relation type
TOR1AIP2	TF binding region
TOR1AIP1	TF binding region
ENSG00000272906	TF binding region
TOR1AIP2	CpG island
TOR1AIP1	CpG island
ENSG00000272906	CpG island
ENSG00000160606	chromatin interactions
ENSG00000177352	chromatin interactions
ENSG00000232956	chromatin interactions
ENSG00000272906	chromatin interactions
ENSG00000135837	chromatin interactions
ENSG00000109118	chromatin interactions
ENSG00000197903	chromatin interactions
ENSG00000156642	chromatin interactions
ENSG00000179761	chromatin interactions
ENSG00000258664	chromatin interactions
ENSG00000156531	chromatin interactions
ENSG00000244265	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000101596	chromatin interactions
ENSG00000104341	chromatin interactions
ENSG00000204569	chromatin interactions
ENSG00000179044	chromatin interactions
ENSG00000116260	chromatin interactions
ENSG00000266405	chromatin interactions
ENSG00000246334	chromatin interactions
ENSG00000264916	chromatin interactions
ENSG00000260360	chromatin interactions
ENSG00000272198	chromatin interactions
ENSG00000143337	chromatin interactions
ENSG00000197912	chromatin interactions
ENSG00000160602	chromatin interactions

Extended variants
information (count: 439 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1144575	chr1:179847402-179847403	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574696363	chr1:179847459-179847460	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs576425122	chr1:179847479-179847480	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs373046078	chr1:179847505-179847506	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs76807187	chr1:179847590-179847591	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs2249346	chr1:179847635-179847636	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs553331183	chr1:179847688-179847689	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs559034004	chr1:179847690-179847691	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs4651052	chr1:179847719-179847720	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs548190096	chr1:179847734-179847735	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs567828955	chr1:179847765-179847766	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs2318388	chr1:179847877-179847878	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs144342737	chr1:179848056-179848057	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs552749511	chr1:179848092-179848093	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs55851972	chr1:179848097-179848098	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs574497957	chr1:179848116-179848117	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs541628150	chr1:179848138-179848139	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs148761052	chr1:179848145-179848146	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs80215449	chr1:179848154-179848155	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs141586138	chr1:179848155-179848156	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs76179816	chr1:179848211-179848212	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs534678600	chr1:179848276-179848277	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs546109385	chr1:179848335-179848336	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs554962292	chr1:179848343-179848344	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs574773193	chr1:179848349-179848350	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs543699464	chr1:179848364-179848365	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs372899810	chr1:179848401-179848402	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs576590906	chr1:179848469-179848470	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs564381931	chr1:179848478-179848479	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs545598964	chr1:179848489-179848490	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs138965376	chr1:179848502-179848503	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs35343684	chr1:179848547-179848548	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs558996181	chr1:179848551-179848552	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs369228848	chr1:179848552-179848553	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs150898098	chr1:179848559-179848560	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs140330459	chr1:179848575-179848576	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs367697449	chr1:179848586-179848587	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs530469062	chr1:179848700-179848701	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs112986640	chr1:179848720-179848721	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs189302359	chr1:179848758-179848759	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs570372510	chr1:179848777-179848778	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs532706474	chr1:179848783-179848784	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs552823581	chr1:179848784-179848785	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs566003453	chr1:179848823-179848824	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs537571420	chr1:179848889-179848890	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs535100313	chr1:179848901-179848902	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs530587017	chr1:179848973-179848974	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs545825113	chr1:179848979-179848980	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs144190417	chr1:179848991-179848992	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs12239940	chr1:179849002-179849003	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Breast cancer	16397240	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	23248035	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:992 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179845200-179847600	Active TSS	HUES6 Cell Line	embryonic stem cell
2	chr1:179845400-179847600	Active TSS	HUES64 Cell Line	embryonic stem cell
3	chr1:179845400-179847600	Active TSS	iPS-20b Cell Line	embryonic stem cell
4	chr1:179845400-179847600	Active TSS	K562	blood
5	chr1:179845600-179847600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:179845600-179847600	Active TSS	Pancreatic Islets	Pancreatic Islet
7	chr1:179846000-179847600	Active TSS	iPS-15b Cell Line	embryonic stem cell
8	chr1:179846000-179847800	Active TSS	GM12878-XiMat	blood
9	chr1:179846200-179847600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:179846200-179847600	Active TSS	Brain Anterior Caudate	brain
11	chr1:179846200-179847600	Active TSS	Brain Inferior Temporal Lobe	brain
12	chr1:179846600-179847600	Active TSS	Brain Substantia Nigra	brain
13	chr1:179847000-179847600	Flanking Active TSS	Dnd41	blood
14	chr1:179847000-179850800	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr1:179847200-179847600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr1:179847200-179847600	Flanking Active TSS	Brain Cingulate Gyrus	brain
17	chr1:179847200-179847600	Flanking Active TSS	A549	lung
18	chr1:179847200-179847600	Flanking Active TSS	HepG2	liver
19	chr1:179847200-179849800	Weak transcription	HSMMtube	muscle
20	chr1:179847200-179850400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr1:179847200-179850600	Weak transcription	Fetal Thymus	thymus
22	chr1:179847200-179850800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr1:179847200-179851000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr1:179847200-179851000	Weak transcription	Gastric	stomach
25	chr1:179847200-179851000	Weak transcription	Lung	lung
26	chr1:179847400-179847600	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr1:179847400-179847600	Enhancers	Primary B cells from cord blood	blood
28	chr1:179847400-179847600	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr1:179847400-179847600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr1:179847400-179847600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr1:179847400-179847600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr1:179847400-179847600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr1:179847400-179847600	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr1:179847400-179847600	Enhancers	Brain Hippocampus Middle	brain
35	chr1:179847400-179847600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr1:179847400-179847600	Enhancers	Colon Smooth Muscle	Colon
37	chr1:179847400-179847600	Enhancers	Fetal Heart	heart
38	chr1:179847400-179847600	Active TSS	Skeletal Muscle Male	skeletal muscle
39	chr1:179847400-179847600	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr1:179847400-179847600	Enhancers	Hela-S3	cervix
41	chr1:179847400-179847800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
42	chr1:179847400-179847800	Enhancers	Primary T helper cells PMA-I stimulated	--
43	chr1:179847400-179847800	Enhancers	Primary T killer memory cells from peripheral blood	blood
44	chr1:179847400-179848000	Enhancers	Stomach Mucosa	stomach
45	chr1:179847400-179849000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr1:179847400-179849000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr1:179847400-179849000	Weak transcription	Fetal Muscle Trunk	muscle
48	chr1:179847400-179849600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr1:179847400-179849800	Weak transcription	Primary T cells from cord blood	blood
50	chr1:179847400-179849800	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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