Variant report

Variant	nsv899389
Chromosome Location	chr12:85430187-85499132
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	BRCA1	chr12:85430006-85430438	H1-hESC	embryonic stem cell:	n/a	n/a
2	CBX3	chr12:85486417-85486899	HCT-116	colon:	n/a	n/a
3	CCNT2	chr12:85446186-85446386	K562	blood:	n/a	n/a
4	CEBPB	chr12:85451200-85451523	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr12:85451209-85451528	A549	lung:	n/a	n/a
6	CEBPB	chr12:85451182-85451527	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr12:85451199-85451430	ECC-1	luminal epithelium:	n/a	n/a
8	CEBPB	chr12:85451223-85451554	K562	blood:	n/a	n/a
9	CEBPB	chr12:85451193-85451587	MCF-7	breast:	n/a	n/a
10	CEBPB	chr12:85451207-85451539	HepG2	liver:	n/a	n/a
11	CHD2	chr12:85429936-85430402	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr12:85429910-85430498	Hela-S3	cervix:	n/a	n/a
13	CREB1	chr12:85430009-85430335	A549	lung:	n/a	n/a
14	CREB1	chr12:85430000-85430187	A549	lung:	n/a	n/a
15	CTCF	chr12:85451240-85451390	GM12871	blood:	n/a	chr12:85451321-85451342 chr12:85451333-85451340 chr12:85451327-85451343 chr12:85451326-85451344
16	CTCF	chr12:85470800-85470950	HAc	cerebellar:	n/a	n/a
17	CTCF	chr12:85451220-85451370	GM12801	blood:	n/a	chr12:85451321-85451342 chr12:85451333-85451340 chr12:85451327-85451343 chr12:85451326-85451344
18	CTCF	chr12:85451162-85451399	A549	lung:	n/a	chr12:85451321-85451342 chr12:85451333-85451340 chr12:85451327-85451343 chr12:85451326-85451344
19	CTCF	chr12:85451180-85451330	NHDF-neo	bronchial:	n/a	n/a
20	CTCF	chr12:85468529-85468599	Lung_OC	lung:	n/a	n/a
21	CTCF	chr12:85470489-85470661	Pancreas_OC	pancreas:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
22	CTCF	chr12:85451231-85451467	GM10248	blood:	n/a	chr12:85451321-85451342 chr12:85451333-85451340 chr12:85451327-85451343 chr12:85451326-85451344
23	CTCF	chr12:85470542-85470710	Gliobla	brain:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
24	CTCF	chr12:85470860-85471010	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr12:85451280-85451430	GM12864	blood:	n/a	chr12:85451321-85451342 chr12:85451333-85451340 chr12:85451327-85451343 chr12:85451326-85451344
26	CTCF	chr12:85451260-85451410	GM12878	blood:	n/a	chr12:85451321-85451342 chr12:85451333-85451340 chr12:85451327-85451343 chr12:85451326-85451344
27	CTCF	chr12:85470501-85470653	GM10248	blood:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
28	CTCF	chr12:85451260-85451410	GM12865	blood:	n/a	chr12:85451321-85451342 chr12:85451333-85451340 chr12:85451327-85451343 chr12:85451326-85451344
29	CTCF	chr12:85470560-85470710	Hela-S3	cervix:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
30	CTCF	chr12:85470600-85470750	HCT-116	colon:	n/a	n/a
31	CTCF	chr12:85470520-85470670	AG04450	lung:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
32	CTCF	chr12:85470940-85471090	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr12:85470440-85470590	HAc	cerebellar:	n/a	chr12:85470580-85470588
34	CTCF	chr12:85451180-85451330	HVMF	connective:	n/a	n/a
35	CTCF	chr12:85470200-85470350	HCM	heart:	n/a	n/a
36	CTCF	chr12:85470540-85470690	HCPEpiC	choroid plexus:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
37	CTCF	chr12:85470460-85470610	GM12870	blood:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
38	CTCF	chr12:85470440-85470590	GM12868	blood:	n/a	chr12:85470580-85470588
39	CTCF	chr12:85451260-85451410	GM12870	blood:	n/a	chr12:85451321-85451342 chr12:85451333-85451340 chr12:85451327-85451343 chr12:85451326-85451344
40	CTCF	chr12:85470520-85470670	HPF	lung:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
41	CTCF	chr12:85470540-85470690	GM12872	blood:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
42	CTCF	chr12:85451240-85451390	HCPEpiC	choroid plexus:	n/a	chr12:85451321-85451342 chr12:85451333-85451340 chr12:85451327-85451343 chr12:85451326-85451344
43	CTCF	chr12:85470620-85470770	AG04450	lung:	n/a	n/a
44	CTCF	chr12:85470520-85470670	AG10803	skin:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
45	CTCF	chr12:85451260-85451410	WERI-Rb-1	eye:	n/a	chr12:85451321-85451342 chr12:85451333-85451340 chr12:85451327-85451343 chr12:85451326-85451344
46	CTCF	chr12:85470520-85470670	GM12871	blood:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
47	CTCF	chr12:85450940-85451718	A549	lung:	n/a	chr12:85451321-85451342 chr12:85451333-85451340 chr12:85451327-85451343 chr12:85451326-85451344
48	CTCF	chr12:85451420-85451570	GM12867	blood:	n/a	n/a
49	CTCF	chr12:85470520-85470670	HRE	kidney:	n/a	chr12:85470575-85470593 chr12:85470576-85470592 chr12:85470580-85470588 chr12:85470578-85470591 chr12:85470577-85470598
50	CTCF	chr12:85451259-85451453	ProgFib	skin:	n/a	chr12:85451321-85451342 chr12:85451333-85451340 chr12:85451327-85451343 chr12:85451326-85451344

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:85430174-85430224	HEK293	kidney:	embryo
2	chr12:85430174-85430224	HEK293	kidney:	embryo
3	chr12:85430250-85430300	A549	lung:	n/a
4	chr12:85430250-85430300	Jurkat	blood:	n/a
5	chr12:85430192-85430242	AG09319	gingival:	n/a
6	chr12:85430215-85430265	HUVEC	blood vessel:	n/a
7	chr12:85430174-85430224	SK-N-SH_RA	brain:	n/a
8	chr12:85430336-85430386	AG09319	gingival:	n/a
9	chr12:85473162-85473212	AG09319	gingival:	n/a
10	chr12:85430215-85430265	ECC-1	luminal epithelium:	n/a
11	chr12:85430250-85430300	H1-hESC	embryonic stem cell:	embryo
12	chr12:85430174-85430224	AG09319	gingival:	n/a
13	chr12:85430336-85430386	SK-N-SH_RA	brain:	n/a
14	chr12:85430215-85430265	HNPCEpiC	eye:	n/a
15	chr12:85473162-85473212	NB4	blood:	n/a
16	chr12:85430174-85430224	AG04449	skin:	fetal
17	chr12:85473162-85473212	HNPCEpiC	eye:	n/a
18	chr12:85430215-85430265	HEEpiC	esophagus:	n/a
19	chr12:85430336-85430386	SAEC	small airway:	n/a
20	chr12:85473162-85473212	GM12892	blood:	n/a
21	chr12:85473162-85473212	AG10803	skin:	n/a
22	chr12:85473162-85473212	NT2-D1	testis:	n/a
23	chr12:85430215-85430265	SK-N-SH_RA	brain:	n/a
24	chr12:85430145-85430195	HEK293	kidney:	embryo
25	chr12:85430145-85430195	HCM	heart:	n/a
26	chr12:85430215-85430265	HIPEpiC	eye:	n/a
27	chr12:85430145-85430195	HUVEC	blood vessel:	n/a
28	chr12:85430215-85430265	GM12878	blood:	n/a
29	chr12:85473162-85473212	SKMC	muscle:	n/a
30	chr12:85430336-85430386	PFSK-1	brain:	n/a
31	chr12:85430145-85430195	HCT-116	colon:	n/a
32	chr12:85430145-85430195	CMK	blood:	n/a
33	chr12:85430250-85430300	AG04449	skin:	fetal
34	chr12:85430192-85430242	RPTEC	kidney:	n/a
35	chr12:85430215-85430265	HRCEpiC	kidney:	n/a
36	chr12:85430336-85430386	AoSMC	blood vessel:	n/a
37	chr12:85430192-85430242	HRE	kidney:	n/a
38	chr12:85430250-85430300	PANC-1	pancreas:	n/a
39	chr12:85430336-85430386	HCT-116	colon:	n/a
40	chr12:85430192-85430242	NT2-D1	testis:	n/a
41	chr12:85430145-85430195	NHBE	bronchial:	n/a
42	chr12:85430192-85430242	Jurkat	blood:	n/a
43	chr12:85430336-85430386	SK-N-MC	brain:	n/a
44	chr12:85430250-85430300	HepG2	liver:	n/a
45	chr12:85430250-85430300	CMK	blood:	n/a
46	chr12:85430174-85430224	GM12878	blood:	n/a
47	chr12:85430174-85430224	RPTEC	kidney:	n/a
48	chr12:85430336-85430386	GM12891	blood:	n/a
49	chr12:85430145-85430195	HCPEpiC	choroid plexus:	n/a
50	chr12:85430145-85430195	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:85268014..85268964-chr12:85450937..85451485,2	MCF-7	breast:
2	chr12:85454595..85457151-chr12:85457581..85459222,2	MCF-7	breast:
3	chr12:85268266..85268773-chr12:85451270..85451782,2	MCF-7	breast:
4	chr12:85496315..85499030-chr12:85506456..85509353,2	K562	blood:
5	chr12:85469399..85472134-chr9:139733502..139735289,2	MCF-7	breast:
6	chr12:85269198..85269791-chr12:85451134..85451813,2	MCF-7	breast:
7	chr12:85470175..85471007-chr12:86313905..86314467,2	MCF-7	breast:
8	chr12:85454595..85457151-chr12:85457581..85459222,2	MCF-7	breast:
9	chr12:85470092..85470900-chr12:85818409..85819385,3	MCF-7	breast:
10	chr12:85470147..85471061-chr12:85788737..85789303,2	MCF-7	breast:
11	chr12:85470481..85471011-chr12:86260831..86261575,2	MCF-7	breast:

Variant related genes	Relation type
LRRIQ1	TF binding region
TSPAN19	TF binding region
LRRIQ1	CpG island
TSPAN19	CpG island
ENSG00000072041	chromatin interactions

Extended variants
information (count: 923 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:923 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35453500	chr12:85430187-85430188	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
2	rs558510967	chr12:85430191-85430192	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
3	rs151078141	chr12:85430203-85430204	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs541325395	chr12:85430213-85430214	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs558146259	chr12:85430224-85430225	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs557911832	chr12:85430300-85430301	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs575169961	chr12:85430302-85430303	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs574703469	chr12:85430307-85430308	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs74873900	chr12:85430344-85430345	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs111331871	chr12:85430365-85430366	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs563262107	chr12:85430382-85430383	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs530606617	chr12:85430417-85430418	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs141124483	chr12:85430444-85430445	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs370602703	chr12:85430445-85430446	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs112776838	chr12:85430458-85430459	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs5799718	chr12:85430526-85430527	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs543889514	chr12:85430531-85430532	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs398044606	chr12:85430536-85430537	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs150268836	chr12:85430684-85430685	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs75142967	chr12:85430711-85430712	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs528044888	chr12:85430812-85430813	Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs144911106	chr12:85430820-85430821	Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs73379726	chr12:85430864-85430865	Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs190736478	chr12:85430951-85430952	Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs148274577	chr12:85430952-85430953	Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs56897633	chr12:85430953-85430954	Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs550727306	chr12:85430958-85430959	Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs374823668	chr12:85431023-85431024	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs181669101	chr12:85431027-85431028	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs537545506	chr12:85431028-85431029	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs184400648	chr12:85431045-85431046	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs570516699	chr12:85431058-85431059	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs534660892	chr12:85431065-85431066	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs189158447	chr12:85431068-85431069	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs369099965	chr12:85431071-85431072	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs575049911	chr12:85431091-85431092	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs373063056	chr12:85431157-85431158	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs181084038	chr12:85431158-85431159	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs560055021	chr12:85431170-85431171	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs185735419	chr12:85431182-85431183	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs575291959	chr12:85431194-85431195	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs545917573	chr12:85431201-85431202	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs564127833	chr12:85431217-85431218	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs548599366	chr12:85431270-85431271	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs528107816	chr12:85431271-85431272	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs544105827	chr12:85431290-85431291	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs140779921	chr12:85431351-85431352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs554304647	chr12:85431424-85431425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs115869572	chr12:85431534-85431535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs144584863	chr12:85431555-85431556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
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
Breast cancer	17899364	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD

Chromatin state (count:215 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:85429400-85430600	Active TSS	HUES48 Cell Line	embryonic stem cell
2	chr12:85429600-85430600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
3	chr12:85429600-85430600	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr12:85429600-85430600	Active TSS	iPS-20b Cell Line	embryonic stem cell
5	chr12:85429600-85430600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr12:85429600-85430600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr12:85429600-85430600	Active TSS	Brain Anterior Caudate	brain
8	chr12:85429600-85430600	Active TSS	Fetal Brain Female	brain
9	chr12:85429600-85430600	Active TSS	Fetal Kidney	kidney
10	chr12:85429600-85430600	Active TSS	Hela-S3	cervix
11	chr12:85429600-85430600	Active TSS	NH-A	brain
12	chr12:85429600-85430600	Active TSS	NHDF-Ad	bronchial
13	chr12:85429600-85430800	Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr12:85429600-85430800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr12:85429600-85430800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr12:85429600-85430800	Active TSS	iPS-18 Cell Line	embryonic stem cell
17	chr12:85429600-85430800	Active TSS	Brain Angular Gyrus	brain
18	chr12:85429600-85430800	Active TSS	Brain Cingulate Gyrus	brain
19	chr12:85429600-85430800	Active TSS	Brain Hippocampus Middle	brain
20	chr12:85429600-85430800	Active TSS	Brain Inferior Temporal Lobe	brain
21	chr12:85429600-85430800	Active TSS	Brain Substantia Nigra	brain
22	chr12:85429600-85430800	Active TSS	Duodenum Smooth Muscle	Duodenum
23	chr12:85429600-85430800	Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr12:85429600-85430800	Active TSS	Stomach Smooth Muscle	stomach
25	chr12:85429600-85430800	Active TSS	A549	lung
26	chr12:85429600-85430800	Active TSS	HMEC	breast
27	chr12:85429600-85431000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr12:85429600-85431000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr12:85429600-85431000	Active TSS	HUES64 Cell Line	embryonic stem cell
30	chr12:85429800-85430200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr12:85429800-85430200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr12:85429800-85430200	Flanking Bivalent TSS/Enh	HUVEC	blood vessel
33	chr12:85429800-85430400	Bivalent/Poised TSS	Primary B cells from cord blood	blood
34	chr12:85429800-85430400	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr12:85429800-85430600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr12:85429800-85430600	Bivalent/Poised TSS	Primary T cells from cord blood	blood
37	chr12:85429800-85430600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr12:85429800-85430600	Active TSS	Colon Smooth Muscle	Colon
39	chr12:85429800-85430600	Active TSS	Fetal Brain Male	brain
40	chr12:85429800-85430600	Bivalent/Poised TSS	Fetal Intestine Large	intestine
41	chr12:85429800-85430600	Active TSS	Fetal Muscle Leg	muscle
42	chr12:85429800-85430600	Active TSS	Rectal Mucosa Donor 29	rectum
43	chr12:85429800-85430600	Active TSS	Rectal Smooth Muscle	rectum
44	chr12:85429800-85430600	Active TSS	Skeletal Muscle Male	skeletal muscle
45	chr12:85429800-85430600	Bivalent/Poised TSS	HSMMtube	muscle
46	chr12:85429800-85430600	Active TSS	NHEK	skin
47	chr12:85429800-85430600	Active TSS	NHLF	lung
48	chr12:85429800-85430800	Active TSS	H1 Cell Line	embryonic stem cell
49	chr12:85429800-85430800	Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr12:85429800-85430800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell

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