Variant report

Variant	nsv528041
Chromosome Location	chr1:180154776-180163390
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr1:180157245-180157730	HepG2	liver:	n/a	n/a
2	BHLHE40	chr1:180157355-180158219	K562	blood:	n/a	n/a
3	BRCA1	chr1:180157382-180157663	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr1:180157372-180157602	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr1:180162028-180162181	K562	blood:	n/a	n/a
6	CHD2	chr1:180157402-180157711	Hela-S3	cervix:	n/a	n/a
7	CHD2	chr1:180157347-180157621	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr1:180157370-180157582	A549	lung:	n/a	chr1:180157389-180157397 chr1:180157495-180157511
9	CTCF	chr1:180157420-180157570	Hela-S3	cervix:	n/a	chr1:180157495-180157511
10	CTCF	chr1:180157440-180157590	GM12871	blood:	n/a	chr1:180157495-180157511
11	CTCF	chr1:180157400-180157550	GM12875	blood:	n/a	chr1:180157495-180157511
12	CTCF	chr1:180157440-180157590	RPTEC	kidney:	n/a	chr1:180157495-180157511
13	CTCF	chr1:180157400-180157550	HUVEC	blood vessel:	n/a	chr1:180157495-180157511
14	CTCF	chr1:180157440-180157590	HRPEpiC	eye:	n/a	chr1:180157495-180157511
15	CTCF	chr1:180157316-180157632	MCF-7	breast:	n/a	chr1:180157389-180157397 chr1:180157495-180157511
16	CTCF	chr1:180157339-180157635	A549	lung:	n/a	chr1:180157389-180157397 chr1:180157495-180157511
17	CTCF	chr1:180157420-180157570	AG09309	skin:	n/a	chr1:180157495-180157511
18	CTCF	chr1:180157317-180157639	MCF-7	breast:	n/a	chr1:180157389-180157397 chr1:180157495-180157511
19	CTCF	chr1:180157440-180157590	BJ	skin:	n/a	chr1:180157495-180157511
20	CTCF	chr1:180157380-180157530	WI-38	lung:	n/a	chr1:180157389-180157397 chr1:180157495-180157511
21	CTCF	chr1:180157420-180157570	HBMEC	blood vessel:	n/a	chr1:180157495-180157511
22	CTCF	chr1:180157350-180157646	Hela-S3	cervix:	n/a	chr1:180157389-180157397 chr1:180157495-180157511
23	CTCF	chr1:180157359-180157608	GM13977	blood:	n/a	chr1:180157389-180157397 chr1:180157495-180157511
24	CTCF	chr1:180157370-180157642	HUVEC	blood vessel:	n/a	chr1:180157389-180157397 chr1:180157495-180157511
25	CTCF	chr1:180157150-180158081	A549	lung:	n/a	chr1:180157389-180157397 chr1:180157495-180157511
26	CTCF	chr1:180157440-180157590	AG04449	skin:	n/a	chr1:180157495-180157511
27	CTCF	chr1:180157286-180157713	A549	lung:	n/a	chr1:180157389-180157397 chr1:180157495-180157511
28	CTCF	chr1:180157460-180157610	GM12869	blood:	n/a	chr1:180157495-180157511
29	CTCF	chr1:180157440-180157590	GM12865	blood:	n/a	chr1:180157495-180157511
30	CTCF	chr1:180157306-180157702	K562	blood:	n/a	chr1:180157389-180157397 chr1:180157495-180157511
31	CTCF	chr1:180157420-180157570	AG09319	gingival:	n/a	chr1:180157495-180157511
32	CTCF	chr1:180157440-180157590	A549	lung:	n/a	chr1:180157495-180157511
33	CTCF	chr1:180157400-180157550	HCM	heart:	n/a	chr1:180157495-180157511
34	CTCF	chr1:180157440-180157590	SAEC	small airway:	n/a	chr1:180157495-180157511
35	CTCF	chr1:180158260-180158410	AG04449	skin:	n/a	n/a
36	CTCF	chr1:180157400-180157550	GM12870	blood:	n/a	chr1:180157495-180157511
37	CTCF	chr1:180157460-180157610	BE2_C	brain:	n/a	chr1:180157495-180157511
38	CTCF	chr1:180157440-180157590	HMF	breast:	n/a	chr1:180157495-180157511
39	CTCF	chr1:180157309-180157706	HepG2	liver:	n/a	chr1:180157389-180157397 chr1:180157495-180157511
40	CTCF	chr1:180157420-180157570	K562	blood:	n/a	chr1:180157495-180157511
41	CTCF	chr1:180157420-180157570	HA-sp	spinal cord:	n/a	chr1:180157495-180157511
42	CTCF	chr1:180157281-180157721	H1-hESC	embryonic stem cell:	n/a	chr1:180157389-180157397 chr1:180157495-180157511
43	CTCF	chr1:180157321-180157721	MCF-7	breast:	n/a	chr1:180157389-180157397 chr1:180157495-180157511
44	CTCF	chr1:180157440-180157590	HCT-116	colon:	n/a	chr1:180157495-180157511
45	CTCF	chr1:180157299-180157624	T-47D	breast:	n/a	chr1:180157389-180157397 chr1:180157495-180157511
46	CTCF	chr1:180157400-180157550	GM12864	blood:	n/a	chr1:180157495-180157511
47	CTCF	chr1:180157383-180157633	Kidney_OC	kidney:	n/a	chr1:180157389-180157397 chr1:180157495-180157511
48	CTCF	chr1:180157162-180157764	MCF-7	breast:	n/a	chr1:180157389-180157397 chr1:180157495-180157511
49	CTCF	chr1:180157307-180157729	K562	blood:	n/a	chr1:180157389-180157397 chr1:180157495-180157511
50	CTCF	chr1:180157440-180157590	GM12874	blood:	n/a	chr1:180157495-180157511

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:180161452-180161502	HEK293	kidney:	embryo
2	chr1:180161452-180161502	BE2_C	brain:	n/a
3	chr1:180157401-180157451	GM12878	blood:	n/a
4	chr1:180157401-180157451	SAEC	small airway:	n/a
5	chr1:180157401-180157451	HPAEpiC	pulmonary alveolar:	n/a
6	chr1:180157401-180157451	Caco-2	colon:	n/a
7	chr1:180157401-180157451	ProgFib	skin:	n/a
8	chr1:180161452-180161502	GM19239	blood:	n/a
9	chr1:180161452-180161502	MCF10A-Er-Src	breast:	n/a
10	chr1:180157401-180157451	LNCaP	prostate:	n/a
11	chr1:180157401-180157451	HMEC	breast:	n/a
12	chr1:180157401-180157451	GM12892	blood:	n/a
13	chr1:180157401-180157451	SK-N-MC	brain:	n/a
14	chr1:180157401-180157451	HL-60	blood:	n/a
15	chr1:180157401-180157451	HRPEpiC	eye:	n/a
16	chr1:180161452-180161502	T-47D	breast:	n/a
17	chr1:180157401-180157451	PrEC	prostate:	n/a
18	chr1:180161452-180161502	HRPEpiC	eye:	n/a
19	chr1:180157401-180157451	HEEpiC	esophagus:	n/a
20	chr1:180161452-180161502	SKMC	muscle:	n/a
21	chr1:180157401-180157451	HEK293	kidney:	embryo
22	chr1:180161452-180161502	HRE	kidney:	n/a
23	chr1:180161452-180161502	HCT-116	colon:	n/a
24	chr1:180157401-180157451	RPTEC	kidney:	n/a
25	chr1:180161452-180161502	NB4	blood:	n/a
26	chr1:180161452-180161502	HUVEC	blood vessel:	n/a
27	chr1:180161452-180161502	AG10803	skin:	n/a
28	chr1:180157401-180157451	AG09319	gingival:	n/a
29	chr1:180157401-180157451	T-47D	breast:	n/a
30	chr1:180161452-180161502	Hepatocyte	liver:	n/a
31	chr1:180161452-180161502	MCF-7	breast:	n/a
32	chr1:180161452-180161502	RPTEC	kidney:	n/a
33	chr1:180161452-180161502	PFSK-1	brain:	n/a
34	chr1:180161452-180161502	NT2-D1	testis:	n/a
35	chr1:180157401-180157451	Hela-S3	cervix:	n/a
36	chr1:180161452-180161502	A549	lung:	n/a
37	chr1:180161452-180161502	AG09309	skin:	n/a
38	chr1:180161452-180161502	HepG2	liver:	n/a
39	chr1:180161452-180161502	AG04449	skin:	fetal
40	chr1:180157401-180157451	NH-A	brain:	n/a
41	chr1:180161452-180161502	SK-N-MC	brain:	n/a
42	chr1:180161452-180161502	GM12878	blood:	n/a
43	chr1:180157401-180157451	HCM	heart:	n/a
44	chr1:180157401-180157451	NT2-D1	testis:	n/a
45	chr1:180157401-180157451	IMR90	lung:	fetal
46	chr1:180161452-180161502	HMEC	breast:	n/a
47	chr1:180161452-180161502	HCPEpiC	choroid plexus:	n/a
48	chr1:180161452-180161502	AG04450	lung:	fetal
49	chr1:180161452-180161502	HCF	heart:	n/a
50	chr1:180157401-180157451	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:180163252..180165050-chr1:180165265..180167767,3	K562	blood:
2	chr1:180161313..180163848-chr1:180192967..180194620,2	MCF-7	breast:
3	chr1:180151242..180153585-chr1:180154166..180155979,2	MCF-7	breast:
4	chr1:180151479..180154072-chr1:180156282..180158155,2	MCF-7	breast:
5	chr1:180160033..180161907-chr1:180449286..180451690,2	MCF-7	breast:
6	chr1:180155609..180157306-chr1:180443324..180446117,2	MCF-7	breast:
7	chr1:180160617..180162181-chr1:180163324..180165275,2	K562	blood:
8	chr1:180157727..180159234-chr1:180178003..180180666,2	K562	blood:
9	chr1:180157909..180159726-chr1:180159740..180161747,2	K562	blood:
10	chr1:180123298..180125650-chr1:180161810..180164469,2	MCF-7	breast:
11	chr1:180155367..180159115-chr1:180198321..180200996,3	MCF-7	breast:
12	chr1:180143979..180145920-chr1:180152234..180155000,2	MCF-7	breast:
13	chr1:180157064..180157810-chr1:180212292..180213377,3	MCF-7	breast:
14	chr1:179785444..179788071-chr1:180162529..180164673,3	K562	blood:
15	chr1:180148498..180150410-chr1:180153485..180156039,2	MCF-7	breast:
16	chr1:180153240..180155932-chr1:180156941..180159298,3	K562	blood:
17	chr1:180157851..180159409-chr1:180159735..180161240,2	K562	blood:
18	chr1:180157564..180158553-chr1:180385566..180386276,2	MCF-7	breast:
19	chr1:180157851..180159409-chr1:180159735..180161240,2	K562	blood:
20	chr1:180152753..180155932-chr1:180156941..180161376,5	K562	blood:
21	chr1:180162538..180164961-chr1:180165083..180167591,3	K562	blood:
22	chr1:180157396..180157988-chr1:180200314..180201082,2	MCF-7	breast:
23	chr1:180153240..180155932-chr1:180156941..180159298,3	K562	blood:
24	chr1:180155464..180157247-chr1:180221856..180223365,2	K562	blood:
25	chr1:180157990..180162959-chr1:180199986..180202950,5	MCF-7	breast:
26	chr1:180152760..180154935-chr1:180161699..180163252,2	K562	blood:
27	chr1:180157909..180159726-chr1:180159740..180161747,2	K562	blood:
28	chr1:180152760..180154935-chr1:180161699..180163252,2	K562	blood:
29	chr1:180157472..180157976-chr1:180220457..180221410,2	K562	blood:
30	chr1:180155978..180158084-chr1:180185932..180188850,2	K562	blood:
31	chr1:180160617..180162181-chr1:180163324..180165275,2	K562	blood:
32	chr1:180161207..180162897-chr1:180165029..180166628,2	K562	blood:
33	chr1:180157764..180160729-chr1:180196773..180199044,2	MCF-7	breast:
34	chr1:180152753..180155932-chr1:180156941..180161376,5	K562	blood:
35	chr1:180156740..180157798-chr1:180384923..180385820,3	MCF-7	breast:
36	chr1:180158876..180161561-chr1:180163823..180167690,5	MCF-7	breast:
37	chr1:180156865..180157706-chr1:180384959..180385623,2	K562	blood:
38	chr1:180155164..180157473-chr1:180197827..180200176,2	MCF-7	breast:
39	chr1:180157048..180157967-chr1:180446543..180447542,2	K562	blood:
40	chr1:180147709..180148394-chr1:180157374..180157997,3	K562	blood:
41	chr1:180157807..180161991-chr1:180470088..180472888,3	MCF-7	breast:
42	chr1:180159949..180162056-chr1:180168756..180171575,2	K562	blood:
43	chr1:180157104..180157974-chr1:180212363..180213260,6	MCF-7	breast:
44	chr1:180150202..180151825-chr1:180157652..180159202,2	MCF-7	breast:
45	chr1:180157037..180158401-chr1:180451224..180451939,3	K562	blood:

Variant related genes	Relation type
QSOX1	TF binding region
QSOX1	CpG island
ENSG00000121454	chromatin interactions
ENSG00000135847	chromatin interactions
ENSG00000116260	chromatin interactions
ENSG00000229407	chromatin interactions

Extended variants
information (count: 402 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:402 , 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	rs3842890	chr1:180154776-180154777	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs74393558	chr1:180154806-180154807	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536153165	chr1:180154821-180154822	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs139478846	chr1:180154822-180154823	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs569859935	chr1:180154847-180154848	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs28637163	chr1:180154850-180154851	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs149985978	chr1:180154854-180154855	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558810119	chr1:180154874-180154875	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs3835559	chr1:180154880-180154881	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs529759190	chr1:180154959-180154960	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535918970	chr1:180154989-180154990	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572151179	chr1:180155012-180155013	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557501825	chr1:180155067-180155068	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs534744404	chr1:180155075-180155076	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370961992	chr1:180155137-180155138	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs186142995	chr1:180155148-180155149	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs375873436	chr1:180155168-180155169	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs370405608	chr1:180155169-180155170	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs201329109	chr1:180155172-180155173	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs367672526	chr1:180155173-180155174	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs145881420	chr1:180155223-180155224	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs543057324	chr1:180155254-180155255	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs200808149	chr1:180155259-180155260	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs371348842	chr1:180155260-180155261	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs189319097	chr1:180155276-180155277	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs201013348	chr1:180155287-180155288	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs565169426	chr1:180155289-180155290	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs527768719	chr1:180155298-180155299	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs547917068	chr1:180155308-180155309	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs144365485	chr1:180155323-180155324	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs200032419	chr1:180155327-180155328	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs201981215	chr1:180155351-180155352	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs375497597	chr1:180155354-180155355	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs181979697	chr1:180155358-180155359	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs369665220	chr1:180155365-180155366	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs532478331	chr1:180155373-180155374	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs552385046	chr1:180155374-180155375	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs2298207	chr1:180155376-180155377	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs3216058	chr1:180155383-180155384	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs397840181	chr1:180155384-180155385	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs534706929	chr1:180155407-180155408	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs535239190	chr1:180155421-180155422	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs113276668	chr1:180155464-180155465	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs73040447	chr1:180155483-180155484	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs537018814	chr1:180155500-180155501	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs556708381	chr1:180155530-180155531	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs576310894	chr1:180155541-180155542	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs545331130	chr1:180155562-180155563	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs573514415	chr1:180155571-180155572	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs558719916	chr1:180155596-180155597	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	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
Autism	20841430	CNVD

Chromatin state (count:339 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:180125600-180159200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:180134000-180167600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:180134400-180168800	Strong transcription	Primary monocytes fromperipheralblood	blood
4	chr1:180135000-180169000	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr1:180136200-180167200	Weak transcription	Dnd41	blood
6	chr1:180137200-180155400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:180137400-180157800	Weak transcription	HSMMtube	muscle
8	chr1:180137800-180159200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr1:180138200-180158000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr1:180138200-180172800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr1:180138800-180157600	Weak transcription	K562	blood
12	chr1:180140200-180167200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr1:180142600-180157800	Strong transcription	Primary neutrophils fromperipheralblood	blood
14	chr1:180143400-180171600	Strong transcription	Fetal Stomach	stomach
15	chr1:180143800-180156000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr1:180143800-180169000	Weak transcription	Small Intestine	intestine
17	chr1:180143800-180170000	Strong transcription	Osteobl	bone
18	chr1:180144000-180166800	Weak transcription	Psoas Muscle	Psoas
19	chr1:180144200-180166400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr1:180144600-180168400	Strong transcription	Ovary	ovary
21	chr1:180144800-180161600	Strong transcription	Placenta	Placenta
22	chr1:180145200-180155400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr1:180145200-180159600	Weak transcription	Liver	Liver
24	chr1:180145200-180160800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr1:180145400-180157000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr1:180146400-180164000	Weak transcription	Right Atrium	heart
27	chr1:180147800-180166000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr1:180148000-180165400	Strong transcription	NHEK	skin
29	chr1:180148000-180168400	Strong transcription	Stomach Smooth Muscle	stomach
30	chr1:180148200-180159600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr1:180148200-180161400	Strong transcription	Rectal Mucosa Donor 31	rectum
32	chr1:180148200-180162800	Strong transcription	Sigmoid Colon	Sigmoid Colon
33	chr1:180148600-180156000	Strong transcription	HUVEC	blood vessel
34	chr1:180148600-180168800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr1:180149200-180156800	Weak transcription	NHDF-Ad	bronchial
36	chr1:180150200-180161200	Strong transcription	Rectal Mucosa Donor 29	rectum
37	chr1:180150200-180171200	Strong transcription	NHLF	lung
38	chr1:180150400-180155400	Strong transcription	HUES48 Cell Line	embryonic stem cell
39	chr1:180150400-180161200	Strong transcription	Left Ventricle	heart
40	chr1:180150400-180162400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
41	chr1:180150400-180168800	Strong transcription	Lung	lung
42	chr1:180150600-180161200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
43	chr1:180150600-180167400	Strong transcription	Adipose Nuclei	Adipose
44	chr1:180150800-180167800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr1:180150800-180168200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr1:180151000-180155200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr1:180151000-180155400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr1:180151000-180155400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr1:180151000-180155600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr1:180151000-180155800	Strong transcription	Rectal Smooth Muscle	rectum

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