Variant report

Variant	esv3341718
Chromosome Location	chr12:117318119-117320417
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:235)
CpG islands
(count:1102)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:235 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCLAF1	chr12:117318774-117319117	GM12878	blood:	n/a	n/a
2	CCNT2	chr12:117318736-117319509	K562	blood:	n/a	chr12:117319333-117319342 chr12:117319297-117319306
3	CEBPB	chr12:117318771-117319456	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr12:117319134-117319481	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD1	chr12:117318512-117318933	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr12:117318777-117319006	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr12:117318747-117319521	Hela-S3	cervix:	n/a	chr12:117319435-117319445 chr12:117319298-117319308
8	CREB1	chr12:117318718-117319134	A549	lung:	n/a	n/a
9	CTBP2	chr12:117317825-117318426	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTBP2	chr12:117319876-117320529	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTBP2	chr12:117318637-117319669	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr12:117318880-117319030	GM12873	blood:	n/a	n/a
13	CTCF	chr12:117318834-117319061	GM19240	blood:	n/a	n/a
14	CTCF	chr12:117320240-117320390	A549	lung:	n/a	n/a
15	CTCF	chr12:117318900-117319050	GM12870	blood:	n/a	n/a
16	CTCF	chr12:117318874-117319053	ProgFib	skin:	n/a	n/a
17	CTCF	chr12:117318793-117319151	MCF-7	breast:	n/a	n/a
18	CTCF	chr12:117318812-117319058	A549	lung:	n/a	n/a
19	CTCF	chr12:117318840-117318990	AG09319	gingival:	n/a	n/a
20	CTCF	chr12:117318829-117318963	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr12:117318795-117319107	MCF-7	breast:	n/a	n/a
22	CTCF	chr12:117318834-117319045	Spleen_OC	spleen:	n/a	n/a
23	CTCF	chr12:117318800-117319074	LNCaP	prostate:	n/a	n/a
24	CTCF	chr12:117318740-117318890	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr12:117318880-117319030	HCT-116	colon:	n/a	n/a
26	CTCF	chr12:117318742-117319092	T-47D	breast:	n/a	n/a
27	CTCF	chr12:117318726-117319041	GM12878	blood:	n/a	n/a
28	CTCF	chr12:117318878-117319022	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr12:117318742-117319077	HepG2	liver:	n/a	n/a
30	CTCF	chr12:117318781-117319081	MCF-7	breast:	n/a	n/a
31	CTCF	chr12:117318718-117319072	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr12:117318860-117319010	GM12865	blood:	n/a	n/a
33	CTCF	chr12:117318740-117318890	Caco-2	colon:	n/a	n/a
34	CTCF	chr12:117318793-117319081	GM12892	blood:	n/a	n/a
35	CTCF	chr12:117318840-117319069	Gliobla	brain:	n/a	n/a
36	CTCF	chr12:117318920-117319070	GM12869	blood:	n/a	n/a
37	CTCF	chr12:117318840-117319038	GM12878	blood:	n/a	n/a
38	CTCF	chr12:117318860-117319010	GM12864	blood:	n/a	n/a
39	CTCF	chr12:117318828-117319034	MCF-7	breast:	n/a	n/a
40	CTCF	chr12:117318810-117319076	NHEK	skin:	n/a	n/a
41	CTCF	chr12:117318820-117319038	GM19239	blood:	n/a	n/a
42	CTCF	chr12:117318757-117319099	K562	blood:	n/a	n/a
43	CTCF	chr12:117318823-117319044	GM13977	blood:	n/a	n/a
44	CTCF	chr12:117318511-117319350	A549	lung:	n/a	chr12:117319323-117319336
45	CTCF	chr12:117318620-117318770	GM12874	blood:	n/a	n/a
46	CTCF	chr12:117318826-117319010	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr12:117318760-117318910	GM06990	blood:	n/a	n/a
48	CTCF	chr12:117318900-117319050	GM12868	blood:	n/a	n/a
49	CTCF	chr12:117320270-117321093	HCT-116	colon:	n/a	n/a
50	CTCF	chr12:117318820-117318970	GM12865	blood:	n/a	n/a

(count:1102 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:117319785-117319835	AG04450	lung:	fetal
2	chr12:117319188-117319238	HNPCEpiC	eye:	n/a
3	chr12:117318251-117318301	NH-A	brain:	n/a
4	chr12:117319264-117319314	SKMC	muscle:	n/a
5	chr12:117319785-117319835	AG04450	lung:	fetal
6	chr12:117319188-117319238	HNPCEpiC	eye:	n/a
7	chr12:117318251-117318301	NH-A	brain:	n/a
8	chr12:117319264-117319314	SKMC	muscle:	n/a
9	chr12:117319785-117319835	MCF-7	breast:	n/a
10	chr12:117318659-117318709	BE2_C	brain:	n/a
11	chr12:117318832-117318882	Caco-2	colon:	n/a
12	chr12:117319577-117319627	H1-hESC	embryonic stem cell:	embryo
13	chr12:117318251-117318301	HPAEpiC	pulmonary alveolar:	n/a
14	chr12:117319264-117319314	MCF-7	breast:	n/a
15	chr12:117319395-117319445	AG04449	skin:	fetal
16	chr12:117318251-117318301	SK-N-SH_RA	brain:	n/a
17	chr12:117318832-117318882	PFSK-1	brain:	n/a
18	chr12:117319193-117319243	SK-N-SH_RA	brain:	n/a
19	chr12:117319856-117319906	AoSMC	blood vessel:	n/a
20	chr12:117319193-117319243	T-47D	breast:	n/a
21	chr12:117319246-117319296	RPTEC	kidney:	n/a
22	chr12:117320134-117320184	HEEpiC	esophagus:	n/a
23	chr12:117320299-117320349	HL-60	blood:	n/a
24	chr12:117319395-117319445	RPTEC	kidney:	n/a
25	chr12:117320134-117320184	ProgFib	skin:	n/a
26	chr12:117319264-117319314	HCF	heart:	n/a
27	chr12:117318832-117318882	HNPCEpiC	eye:	n/a
28	chr12:117320316-117320366	ovcar-3	ovarian:	n/a
29	chr12:117318251-117318301	GM06990	blood:	n/a
30	chr12:117319785-117319835	NB4	blood:	n/a
31	chr12:117320299-117320349	U87	brain:	n/a
32	chr12:117320299-117320349	Jurkat	blood:	n/a
33	chr12:117319914-117319964	H1-hESC	embryonic stem cell:	embryo
34	chr12:117319577-117319627	AG09309	skin:	n/a
35	chr12:117320316-117320366	GM12891	blood:	n/a
36	chr12:117318251-117318301	AG04449	skin:	fetal
37	chr12:117319785-117319835	H1-hESC	embryonic stem cell:	embryo
38	chr12:117319246-117319296	NB4	blood:	n/a
39	chr12:117319246-117319296	HMEC	breast:	n/a
40	chr12:117319246-117319296	A549	lung:	n/a
41	chr12:117318548-117318598	NT2-D1	testis:	n/a
42	chr12:117319246-117319296	K562	blood:	n/a
43	chr12:117320316-117320366	SKMC	muscle:	n/a
44	chr12:117319264-117319314	HEEpiC	esophagus:	n/a
45	chr12:117320003-117320053	RPTEC	kidney:	n/a
46	chr12:117320134-117320184	BE2_C	brain:	n/a
47	chr12:117318251-117318301	HEK293	kidney:	embryo
48	chr12:117318416-117318466	MCF-7	breast:	n/a
49	chr12:117319577-117319627	HIPEpiC	eye:	n/a
50	chr12:117319188-117319238	AoSMC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:117317029..117319301-chr12:117346996..117349580,2	MCF-7	breast:
2	chr12:117174783..117176988-chr12:117316113..117318785,2	MCF-7	breast:

No data

Variant related genes	Relation type
HRK	TF binding region
HRK	CpG island
ENSG00000111412	chromatin interactions
ENSG00000174989	chromatin interactions
ENSG00000135119	chromatin interactions

Extended variants
information (count: 81 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:81 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76841485	chr12:117318245-117318246	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs78254244	chr12:117318246-117318247	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs12311024	chr12:117318273-117318274	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs534326446	chr12:117318274-117318275	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs568739393	chr12:117318276-117318277	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs12311027	chr12:117318286-117318287	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs574469645	chr12:117318324-117318325	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs181457135	chr12:117318327-117318328	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs200442588	chr12:117318348-117318349	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs1495931	chr12:117318368-117318369	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs577011161	chr12:117318374-117318375	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs149873150	chr12:117318426-117318427	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs144974154	chr12:117318453-117318454	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs528740186	chr12:117318495-117318496	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs548311074	chr12:117318525-117318526	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs562088633	chr12:117318529-117318530	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs530939067	chr12:117318618-117318619	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs551080792	chr12:117318634-117318635	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs569907628	chr12:117318638-117318639	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs374436556	chr12:117318660-117318661	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs139859241	chr12:117318683-117318684	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs552354302	chr12:117318697-117318698	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs565850899	chr12:117318720-117318721	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs534889360	chr12:117318746-117318747	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs28489658	chr12:117318755-117318756	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs574356922	chr12:117318759-117318760	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs536788729	chr12:117318760-117318761	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs542812903	chr12:117318827-117318828	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs556633190	chr12:117318870-117318871	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs576481353	chr12:117318882-117318883	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs79110608	chr12:117318883-117318884	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs545994190	chr12:117318891-117318892	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs12311393	chr12:117318899-117318900	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs573483316	chr12:117318929-117318930	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs542490181	chr12:117318937-117318938	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs561976658	chr12:117318968-117318969	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs530919893	chr12:117318969-117318970	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs12228937	chr12:117318971-117318972	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs146607495	chr12:117319202-117319203	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs564574409	chr12:117319218-117319219	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs533425450	chr12:117319243-117319244	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs576685133	chr12:117319339-117319340	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs112676943	chr12:117319340-117319341	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs565845522	chr12:117319341-117319342	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs528408712	chr12:117319342-117319343	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs533781669	chr12:117319457-117319458	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs548453443	chr12:117319494-117319495	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs545468480	chr12:117319502-117319503	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs557860526	chr12:117319506-117319507	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs371814986	chr12:117319520-117319521	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:443 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117316000-117320200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
2	chr12:117316200-117318400	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr12:117316200-117318600	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
4	chr12:117316200-117318800	Flanking Active TSS	Primary B cells from cord blood	blood
5	chr12:117316200-117320000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
6	chr12:117316200-117320200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
7	chr12:117316200-117320400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
8	chr12:117316200-117320400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
9	chr12:117316400-117318400	Enhancers	Pancreas	Pancrea
10	chr12:117316400-117318600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr12:117316400-117318600	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
12	chr12:117316400-117318600	Bivalent Enhancer	Fetal Brain Male	brain
13	chr12:117316400-117318800	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr12:117316400-117318800	Enhancers	Gastric	stomach
15	chr12:117316400-117319000	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr12:117316400-117319400	Bivalent Enhancer	Lung	lung
17	chr12:117316400-117320200	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr12:117316600-117318600	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr12:117316600-117318600	Bivalent/Poised TSS	HSMMtube	muscle
20	chr12:117316600-117318800	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
21	chr12:117316600-117320000	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr12:117316800-117318800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr12:117316800-117318800	Bivalent/Poised TSS	NHDF-Ad	bronchial
24	chr12:117316800-117319600	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
25	chr12:117316800-117320200	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr12:117317000-117318200	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
27	chr12:117317000-117318600	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
28	chr12:117317000-117318600	Bivalent Enhancer	Stomach Mucosa	stomach
29	chr12:117317000-117318600	Flanking Active TSS	Hela-S3	cervix
30	chr12:117317000-117318800	Bivalent/Poised TSS	Primary mononuclear cells fromperipheralblood	Blood
31	chr12:117317000-117319000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
32	chr12:117317000-117320000	Bivalent Enhancer	Placenta	Placenta
33	chr12:117317200-117318200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr12:117317200-117318200	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
35	chr12:117317200-117318600	Bivalent Enhancer	Duodenum Mucosa	Duodenum
36	chr12:117317200-117318600	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
37	chr12:117317200-117318800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
38	chr12:117317400-117318400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
39	chr12:117317400-117318400	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
40	chr12:117317400-117318400	Bivalent/Poised TSS	Brain Anterior Caudate	brain
41	chr12:117317400-117318400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
42	chr12:117317400-117318400	Bivalent Enhancer	Fetal Muscle Leg	muscle
43	chr12:117317400-117319600	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr12:117317600-117318200	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
45	chr12:117317600-117318200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr12:117317600-117318400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
47	chr12:117317600-117318400	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
48	chr12:117317600-117318600	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr12:117317600-117318600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
50	chr12:117317600-117318600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood

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