Variant report

Variant	nsv1039046
Chromosome Location	chr12:117170989-117225635
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1126)
CpG islands
(count:1957)
Chromatin interactive
region (count:42)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1126 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:117175750-117176341	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:117172197-117172531	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:117173962-117174516	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:117175930-117176220	K562	blood:	n/a	n/a
5	ATF1	chr12:117175804-117176263	K562	blood:	n/a	n/a
6	ATF1	chr12:117197531-117197877	K562	blood:	n/a	n/a
7	ATF2	chr12:117175763-117176311	GM12878	blood:	n/a	n/a
8	ATF3	chr12:117175646-117176242	K562	blood:	n/a	chr12:117175986-117176006
9	ATF3	chr12:117175670-117176187	K562	blood:	n/a	chr12:117175986-117176006
10	ATF3	chr12:117175774-117176251	A549	lung:	n/a	chr12:117175986-117176006
11	ATF3	chr12:117175974-117176161	GM12878	blood:	n/a	chr12:117175986-117176006
12	ATF3	chr12:117222139-117222376	K562	blood:	n/a	n/a
13	ATF3	chr12:117175659-117176327	GM12878	blood:	n/a	chr12:117175986-117176006
14	ATF3	chr12:117175692-117176197	HepG2	liver:	n/a	chr12:117175986-117176006
15	ATF3	chr12:117175779-117175931	GM12878	blood:	n/a	n/a
16	ATF3	chr12:117175687-117176254	H1-hESC	embryonic stem cell:	n/a	chr12:117175986-117176006
17	ATF3	chr12:117175744-117176333	H1-hESC	embryonic stem cell:	n/a	chr12:117175986-117176006
18	BACH1	chr12:117174351-117174490	K562	blood:	n/a	n/a
19	BACH1	chr12:117209577-117209696	K562	blood:	n/a	n/a
20	BACH1	chr12:117197545-117198049	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr12:117197646-117198094	K562	blood:	n/a	n/a
22	BCL3	chr12:117175779-117176346	A549	lung:	n/a	chr12:117175891-117175900
23	BCL3	chr12:117175816-117176507	A549	lung:	n/a	chr12:117175891-117175900
24	BCLAF1	chr12:117175687-117176590	GM12878	blood:	n/a	chr12:117175891-117175900
25	BHLHE40	chr12:117175589-117176433	GM12878	blood:	n/a	n/a
26	BHLHE40	chr12:117197551-117197921	K562	blood:	n/a	n/a
27	BHLHE40	chr12:117175648-117176366	HepG2	liver:	n/a	n/a
28	BHLHE40	chr12:117175493-117176406	K562	blood:	n/a	n/a
29	BHLHE40	chr12:117174926-117175126	K562	blood:	n/a	chr12:117175069-117175085
30	BHLHE40	chr12:117221957-117222209	K562	blood:	n/a	n/a
31	BHLHE40	chr12:117173947-117174427	GM12878	blood:	n/a	n/a
32	BHLHE40	chr12:117174018-117174413	HepG2	liver:	n/a	n/a
33	BHLHE40	chr12:117175838-117176188	A549	lung:	n/a	n/a
34	BHLHE40	chr12:117174046-117174273	K562	blood:	n/a	n/a
35	BRCA1	chr12:117175897-117176064	HepG2	liver:	n/a	n/a
36	BRCA1	chr12:117175433-117176578	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr12:117175902-117176487	GM12878	blood:	n/a	n/a
38	BRCA1	chr12:117175841-117176266	H1-hESC	embryonic stem cell:	n/a	n/a
39	CBX3	chr12:117175775-117176288	K562	blood:	n/a	n/a
40	CBX3	chr12:117197494-117197850	K562	blood:	n/a	n/a
41	CBX3	chr12:117221897-117222455	K562	blood:	n/a	n/a
42	CBX3	chr12:117222132-117222436	K562	blood:	n/a	n/a
43	CBX3	chr12:117197454-117197882	K562	blood:	n/a	n/a
44	CCNT2	chr12:117175605-117176191	K562	blood:	n/a	n/a
45	CEBPB	chr12:117173956-117174505	MCF-7	breast:	n/a	n/a
46	CEBPB	chr12:117175956-117176192	GM12878	blood:	n/a	chr12:117176119-117176127
47	CEBPB	chr12:117175763-117176406	IMR90	lung:	n/a	chr12:117176119-117176127
48	CEBPB	chr12:117211904-117212147	A549	lung:	n/a	chr12:117212032-117212043
49	CEBPB	chr12:117175845-117176225	HepG2	liver:	n/a	chr12:117176119-117176127
50	CEBPB	chr12:117211466-117211649	A549	lung:	n/a	chr12:117211544-117211555

(count:1957 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:117173003-117173053	SK-N-MC	brain:	n/a
2	chr12:117175884-117175934	HCPEpiC	choroid plexus:	n/a
3	chr12:117175957-117176007	K562	blood:	n/a
4	chr12:117176435-117176485	SKMC	muscle:	n/a
5	chr12:117187890-117187940	PrEC	prostate:	n/a
6	chr12:117173003-117173053	SK-N-MC	brain:	n/a
7	chr12:117175884-117175934	HCPEpiC	choroid plexus:	n/a
8	chr12:117175957-117176007	K562	blood:	n/a
9	chr12:117176435-117176485	SKMC	muscle:	n/a
10	chr12:117187890-117187940	PrEC	prostate:	n/a
11	chr12:117176563-117176613	PANC-1	pancreas:	n/a
12	chr12:117176038-117176088	HEEpiC	esophagus:	n/a
13	chr12:117187868-117187918	Hepatocyte	liver:	n/a
14	chr12:117204781-117204831	SKMC	muscle:	n/a
15	chr12:117180235-117180285	PFSK-1	brain:	n/a
16	chr12:117175042-117175092	HCF	heart:	n/a
17	chr12:117188015-117188065	GM12892	blood:	n/a
18	chr12:117175042-117175092	PFSK-1	brain:	n/a
19	chr12:117187838-117187888	AG04449	skin:	fetal
20	chr12:117190080-117190130	H1-hESC	embryonic stem cell:	embryo
21	chr12:117188015-117188065	HCPEpiC	choroid plexus:	n/a
22	chr12:117187838-117187888	AG09309	skin:	n/a
23	chr12:117188015-117188065	ovcar-3	ovarian:	n/a
24	chr12:117187868-117187918	HRE	kidney:	n/a
25	chr12:117186815-117186865	BJ	skin:	n/a
26	chr12:117176047-117176097	AG04450	lung:	fetal
27	chr12:117176367-117176417	GM06990	blood:	n/a
28	chr12:117176113-117176163	SKMC	muscle:	n/a
29	chr12:117175859-117175909	PrEC	prostate:	n/a
30	chr12:117174758-117174808	MCF10A-Er-Src	breast:	n/a
31	chr12:117175884-117175934	K562	blood:	n/a
32	chr12:117176563-117176613	A549	lung:	n/a
33	chr12:117175954-117176004	IMR90	lung:	fetal
34	chr12:117188277-117188327	ProgFib	skin:	n/a
35	chr12:117176047-117176097	ovcar-3	ovarian:	n/a
36	chr12:117176294-117176344	GM12878	blood:	n/a
37	chr12:117190080-117190130	HCF	heart:	n/a
38	chr12:117175828-117175878	GM19239	blood:	n/a
39	chr12:117187838-117187888	SAEC	small airway:	n/a
40	chr12:117188015-117188065	HL-60	blood:	n/a
41	chr12:117174758-117174808	BJ	skin:	n/a
42	chr12:117175957-117176007	SK-N-SH_RA	brain:	n/a
43	chr12:117175954-117176004	GM06990	blood:	n/a
44	chr12:117175636-117175686	NHDF-neo	bronchial:	n/a
45	chr12:117188015-117188065	H1-hESC	embryonic stem cell:	embryo
46	chr12:117176294-117176344	HMEC	breast:	n/a
47	chr12:117175828-117175878	AoSMC	blood vessel:	n/a
48	chr12:117188015-117188065	Jurkat	blood:	n/a
49	chr12:117175954-117176004	SAEC	small airway:	n/a
50	chr12:117176113-117176163	HIPEpiC	eye:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:117172847..117175842-chr12:117176495..117179141,3	MCF-7	breast:
2	chr12:117172640..117175052-chr12:117251934..117254803,2	MCF-7	breast:
3	chr12:117174361..117176592-chr12:117201588..117204152,2	K562	blood:
4	chr12:117189265..117191529-chr12:117194956..117197970,3	K562	blood:
5	chr12:117189265..117191529-chr12:117194956..117197970,3	K562	blood:
6	chr12:117201753..117204739-chr12:117206043..117208953,2	MCF-7	breast:
7	chr12:117175239..117175990-chr9:34329401..34330121,2	NB4	blood:
8	chr12:117171214..117173165-chr12:117362456..117365349,2	MCF-7	breast:
9	chr12:117207905..117210327-chr12:117210901..117212728,2	K562	blood:
10	chr12:31478801..31479401-chr12:117175467..117175974,2	NB4	blood:
11	chr12:117168142..117171595-chr12:117173878..117178564,5	K562	blood:
12	chr12:117207922..117210742-chr12:117210782..117213183,2	MCF-7	breast:
13	chr12:117150536..117152971-chr12:117172971..117174579,2	MCF-7	breast:
14	chr12:117169181..117172410-chr12:117172557..117176005,5	MCF-7	breast:
15	chr12:117211246..117213116-chr12:117248453..117251134,2	MCF-7	breast:
16	chr12:117214324..117217304-chr12:117220516..117222283,2	K562	blood:
17	chr12:117211223..117211938-chr12:117300747..117301762,3	MCF-7	breast:
18	chr12:117172693..117174490-chr12:117177320..117180266,3	MCF-7	breast:
19	chr12:117217330..117219094-chr12:117250590..117252479,2	K562	blood:
20	chr12:117174551..117177201-chr12:117210571..117213552,2	MCF-7	breast:
21	chr12:117172693..117174490-chr12:117177320..117180266,3	MCF-7	breast:
22	chr12:117211331..117213827-chr12:117255904..117257677,2	MCF-7	breast:
23	chr12:117206430..117208950-chr12:117256822..117258508,2	MCF-7	breast:
24	chr12:117211010..117211823-chr12:117393204..117393940,3	MCF-7	breast:
25	chr12:117208783..117211588-chr12:117216119..117217810,2	MCF-7	breast:
26	chr12:117174783..117176988-chr12:117316113..117318785,2	MCF-7	breast:
27	chr12:117174912..117176575-chr12:117346883..117348986,2	MCF-7	breast:
28	chr12:117208783..117211588-chr12:117216119..117217810,2	MCF-7	breast:
29	chr12:117207905..117210327-chr12:117210901..117212728,2	K562	blood:
30	chr12:117155609..117158442-chr12:117174031..117175991,2	MCF-7	breast:
31	chr12:117155749..117159803-chr12:117174359..117177084,5	MCF-7	breast:
32	chr12:117217400..117220428-chr12:117221372..117224735,3	K562	blood:
33	chr12:117174714..117176386-chr12:117186480..117189521,3	MCF-7	breast:
34	chr12:117175863..117177827-chr12:117180239..117183137,3	MCF-7	breast:
35	chr12:117201753..117204739-chr12:117206043..117208953,2	MCF-7	breast:
36	chr12:117214324..117217304-chr12:117220516..117222283,2	K562	blood:
37	chr12:117187713..117190765-chr12:117193491..117197822,3	K562	blood:
38	chr12:117217400..117220350-chr12:117221372..117223420,2	K562	blood:
39	chr12:117169208..117171523-chr12:117172734..117175670,2	MCF-7	breast:
40	chr12:117207922..117210742-chr12:117210782..117213183,2	MCF-7	breast:
41	chr12:117172045..117174104-chr12:117174584..117176997,3	K562	blood:
42	chr12:117165095..117168822-chr12:117170823..117173766,4	MCF-7	breast:

No data

Variant related genes	Relation type
RNU6-558P	TF binding region
ENSG00000239374	TF binding region
RNFT2	TF binding region
C12orf49	TF binding region
RNU6-558P	CpG island
ENSG00000239374	CpG island
RNFT2	CpG island
C12orf49	CpG island
ENSG00000174989	chromatin interactions
ENSG00000135119	chromatin interactions
ENSG00000139146	chromatin interactions
ENSG00000111412	chromatin interactions
ENSG00000239374	chromatin interactions
ENSG00000201382	chromatin interactions
ENSG00000164978	chromatin interactions
ENSG00000135116	chromatin interactions

Extended variants
information (count: 2185 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2185 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs429963	chr12:117170989-117170990	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181670389	chr12:117171017-117171018	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs532364575	chr12:117171040-117171041	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs2117962	chr12:117171051-117171052	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs535399633	chr12:117171088-117171089	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs555057287	chr12:117171090-117171091	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs574952476	chr12:117171091-117171092	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs544407059	chr12:117171099-117171100	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs564339976	chr12:117171112-117171113	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs578227019	chr12:117171113-117171114	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs371467210	chr12:117171135-117171136	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs375753339	chr12:117171136-117171137	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs367670533	chr12:117171142-117171143	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs372880373	chr12:117171144-117171145	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs375849235	chr12:117171148-117171149	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs369658042	chr12:117171151-117171152	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs373018507	chr12:117171161-117171162	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs374961675	chr12:117171163-117171164	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs369149578	chr12:117171168-117171169	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs372660239	chr12:117171178-117171179	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs7315716	chr12:117171179-117171180	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs185960875	chr12:117171234-117171235	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs189913797	chr12:117171239-117171240	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs527438383	chr12:117171241-117171242	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs71442996	chr12:117171250-117171251	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs374615029	chr12:117171258-117171259	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs138833022	chr12:117171259-117171260	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs182548032	chr12:117171268-117171269	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs367734391	chr12:117171269-117171270	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs112710772	chr12:117171278-117171279	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs546597657	chr12:117171292-117171293	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs566723333	chr12:117171354-117171355	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs535113281	chr12:117171357-117171358	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs185625444	chr12:117171392-117171393	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs537386118	chr12:117171408-117171409	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs191008435	chr12:117171450-117171451	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs537540499	chr12:117171498-117171499	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs182678383	chr12:117171515-117171516	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs578094424	chr12:117171558-117171559	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs113392414	chr12:117171587-117171588	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs567303149	chr12:117171588-117171589	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs540796196	chr12:117171653-117171654	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs188990061	chr12:117171654-117171655	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs2101869	chr12:117171669-117171670	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs543088854	chr12:117171674-117171675	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs562859610	chr12:117171725-117171726	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs531874246	chr12:117171770-117171771	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs545493163	chr12:117171785-117171786	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs565352325	chr12:117171795-117171796	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs552966669	chr12:117171827-117171828	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	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
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Neuroblastoma	20406844	CNVD
Medulloblastoma	16783165	CNVD
mental retardation	16760730	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21045234	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21806811	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1349 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117147200-117174000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr12:117147400-117173600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr12:117149400-117174000	Weak transcription	K562	blood
4	chr12:117150800-117172600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr12:117157800-117174000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr12:117158200-117172000	Weak transcription	Stomach Smooth Muscle	stomach
7	chr12:117158200-117172000	Weak transcription	NH-A	brain
8	chr12:117158400-117172200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr12:117158400-117174000	Weak transcription	Psoas Muscle	Psoas
10	chr12:117158400-117174600	Weak transcription	Colon Smooth Muscle	Colon
11	chr12:117158600-117172000	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr12:117158600-117172600	Weak transcription	Rectal Smooth Muscle	rectum
13	chr12:117158600-117174200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr12:117158600-117174400	Weak transcription	Esophagus	oesophagus
15	chr12:117159000-117172000	Weak transcription	HMEC	breast
16	chr12:117159000-117174000	Weak transcription	Fetal Brain Male	brain
17	chr12:117159200-117174000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr12:117159800-117172000	Weak transcription	HSMMtube	muscle
19	chr12:117159800-117172200	Weak transcription	NHLF	lung
20	chr12:117160000-117174000	Weak transcription	Colonic Mucosa	Colon
21	chr12:117160200-117172200	Weak transcription	Primary hematopoietic stem cells	blood
22	chr12:117161000-117171400	Weak transcription	Liver	Liver
23	chr12:117161000-117171600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr12:117161000-117172000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr12:117161000-117172000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr12:117161000-117172000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr12:117161000-117172000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr12:117161000-117174000	Weak transcription	A549	lung
29	chr12:117161200-117172200	Weak transcription	HSMM	muscle
30	chr12:117161400-117172000	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr12:117164800-117174600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr12:117165000-117172000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr12:117165000-117174000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr12:117165200-117171400	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr12:117165200-117173000	Strong transcription	Primary T helper cells fromperipheralblood	blood
36	chr12:117165200-117174200	Weak transcription	Fetal Kidney	kidney
37	chr12:117165200-117174400	Weak transcription	Aorta	Aorta
38	chr12:117165400-117171600	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr12:117165400-117172000	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr12:117165400-117172000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr12:117165400-117172200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr12:117165400-117174600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
43	chr12:117165600-117171400	Weak transcription	Fetal Brain Female	brain
44	chr12:117165600-117171600	Weak transcription	Brain Hippocampus Middle	brain
45	chr12:117165600-117172000	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr12:117165600-117174000	Weak transcription	Brain Germinal Matrix	brain
47	chr12:117165800-117173200	Strong transcription	Fetal Thymus	thymus
48	chr12:117165800-117174000	Weak transcription	Fetal Heart	heart
49	chr12:117165800-117174000	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr12:117166000-117173000	Strong transcription	Rectal Mucosa Donor 29	rectum

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