Variant report

Variant	esv3376106
Chromosome Location	chr12:67461510-67464058
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:311)
CpG islands
(count:428)
Chromatin interactive
region (count:12)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:311 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr12:67463489-67463633	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD1	chr12:67462775-67462869	H1-hESC	embryonic stem cell:	n/a	n/a
3	CHD1	chr12:67463318-67463403	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD2	chr12:67463690-67463734	HepG2	liver:	n/a	n/a
5	CHD2	chr12:67463554-67463960	H1-hESC	embryonic stem cell:	n/a	n/a
6	CREB1	chr12:67462779-67463089	A549	lung:	n/a	n/a
7	CREB1	chr12:67463186-67463537	A549	lung:	n/a	n/a
8	CTBP2	chr12:67463348-67464145	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr12:67462880-67463030	AG04450	lung:	n/a	n/a
10	CTCF	chr12:67462840-67462990	HPF	lung:	n/a	n/a
11	CTCF	chr12:67463287-67463369	Kidney_OC	kidney:	n/a	n/a
12	CTCF	chr12:67462220-67462370	NHEK	skin:	n/a	n/a
13	CTCF	chr12:67462220-67462370	HAc	cerebellar:	n/a	n/a
14	CTCF	chr12:67462320-67462470	HAc	cerebellar:	n/a	n/a
15	CTCF	chr12:67463280-67463430	HPAF	blood vessel:	n/a	n/a
16	CTCF	chr12:67462267-67462308	GM10266	blood:	n/a	n/a
17	CTCF	chr12:67463240-67463390	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr12:67461420-67461570	NHEK	skin:	n/a	chr12:67461457-67461475 chr12:67461458-67461474
19	CTCF	chr12:67462200-67462350	HRE	kidney:	n/a	n/a
20	CTCF	chr12:67462140-67462290	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr12:67462100-67462250	BE2_C	brain:	n/a	n/a
22	CTCF	chr12:67462140-67462290	HMEC	breast:	n/a	n/a
23	CTCF	chr12:67462160-67462400	A549	lung:	n/a	n/a
24	CTCF	chr12:67462140-67462290	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr12:67463320-67463470	HCM	heart:	n/a	n/a
26	CTCF	chr12:67463359-67463367	GM12892	blood:	n/a	n/a
27	CTCF	chr12:67463280-67463430	GM12868	blood:	n/a	n/a
28	CTCF	chr12:67463276-67463509	MCF-7	breast:	n/a	n/a
29	CTCF	chr12:67462820-67462970	HCFaa	heart:	n/a	n/a
30	CTCF	chr12:67463240-67463390	AG04449	skin:	n/a	n/a
31	CTCF	chr12:67462263-67462337	GM12891	blood:	n/a	n/a
32	CTCF	chr12:67463540-67463690	NHEK	skin:	n/a	chr12:67463678-67463686
33	CTCF	chr12:67462220-67462370	HRE	kidney:	n/a	n/a
34	CTCF	chr12:67462940-67463090	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr12:67463331-67463415	GM19240	blood:	n/a	n/a
36	CTCF	chr12:67462880-67463030	HMEC	breast:	n/a	n/a
37	CTCF	chr12:67463180-67463330	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr12:67463260-67463410	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr12:67462188-67462389	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr12:67462920-67463070	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr12:67463260-67463410	Caco-2	colon:	n/a	n/a
42	CTCF	chr12:67462100-67462250	HCM	heart:	n/a	n/a
43	CTCF	chr12:67462240-67462390	AG09319	gingival:	n/a	n/a
44	CTCF	chr12:67463240-67463390	HepG2	liver:	n/a	n/a
45	CTCF	chr12:67462219-67462360	MCF-7	breast:	n/a	n/a
46	CTCF	chr12:67461360-67461510	WERI-Rb-1	eye:	n/a	chr12:67461457-67461475 chr12:67461458-67461474
47	CTCF	chr12:67462900-67463050	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr12:67462920-67463070	GM12865	blood:	n/a	n/a
49	CTCF	chr12:67463300-67463450	GM12865	blood:	n/a	n/a
50	CTCF	chr12:67463420-67463570	GM12869	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:67462881-67462931	HEK293	kidney:	embryo
2	chr12:67462881-67462931	HEK293	kidney:	embryo
3	chr12:67461690-67461740	HL-60	blood:	n/a
4	chr12:67462522-67462572	NH-A	brain:	n/a
5	chr12:67462881-67462931	HEEpiC	esophagus:	n/a
6	chr12:67461558-67461608	SK-N-SH	brain:	n/a
7	chr12:67462881-67462931	HPAEpiC	pulmonary alveolar:	n/a
8	chr12:67463828-67463878	NHDF-neo	bronchial:	n/a
9	chr12:67461690-67461740	PFSK-1	brain:	n/a
10	chr12:67463828-67463878	ECC-1	luminal epithelium:	n/a
11	chr12:67462881-67462931	U87	brain:	n/a
12	chr12:67463258-67463308	Caco-2	colon:	n/a
13	chr12:67463281-67463331	Caco-2	colon:	n/a
14	chr12:67461690-67461740	GM12878	blood:	n/a
15	chr12:67462881-67462931	BJ	skin:	n/a
16	chr12:67462522-67462572	GM19239	blood:	n/a
17	chr12:67461558-67461608	HEEpiC	esophagus:	n/a
18	chr12:67462522-67462572	LNCaP	prostate:	n/a
19	chr12:67463828-67463878	T-47D	breast:	n/a
20	chr12:67463281-67463331	SK-N-SH_RA	brain:	n/a
21	chr12:67462881-67462931	BE2_C	brain:	n/a
22	chr12:67462881-67462931	HNPCEpiC	eye:	n/a
23	chr12:67463828-67463878	SK-N-MC	brain:	n/a
24	chr12:67463828-67463878	Caco-2	colon:	n/a
25	chr12:67463258-67463308	HepG2	liver:	n/a
26	chr12:67463828-67463878	HRE	kidney:	n/a
27	chr12:67463828-67463878	GM12892	blood:	n/a
28	chr12:67463258-67463308	GM12892	blood:	n/a
29	chr12:67462522-67462572	MCF10A-Er-Src	breast:	n/a
30	chr12:67461690-67461740	ovcar-3	ovarian:	n/a
31	chr12:67463258-67463308	GM12878	blood:	n/a
32	chr12:67463281-67463331	RPTEC	kidney:	n/a
33	chr12:67463281-67463331	HIPEpiC	eye:	n/a
34	chr12:67463281-67463331	Jurkat	blood:	n/a
35	chr12:67463281-67463331	NT2-D1	testis:	n/a
36	chr12:67462881-67462931	GM12891	blood:	n/a
37	chr12:67463828-67463878	AG10803	skin:	n/a
38	chr12:67462881-67462931	AG04450	lung:	fetal
39	chr12:67462881-67462931	HUVEC	blood vessel:	n/a
40	chr12:67462881-67462931	Jurkat	blood:	n/a
41	chr12:67463281-67463331	SAEC	small airway:	n/a
42	chr12:67462522-67462572	GM12878	blood:	n/a
43	chr12:67461558-67461608	ECC-1	luminal epithelium:	n/a
44	chr12:67463258-67463308	AG04449	skin:	fetal
45	chr12:67461690-67461740	GM06990	blood:	n/a
46	chr12:67463258-67463308	H1-hESC	embryonic stem cell:	embryo
47	chr12:67463258-67463308	ProgFib	skin:	n/a
48	chr12:67462522-67462572	SK-N-SH_RA	brain:	n/a
49	chr12:67463258-67463308	PANC-1	pancreas:	n/a
50	chr12:67463828-67463878	ProgFib	skin:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:67297865..67298411-chr12:67461007..67461777,2	MCF-7	breast:
2	chr12:67459525..67462456-chr12:67462804..67465110,3	MCF-7	breast:
3	chr12:67460777..67464522-chr12:67661841..67665703,9	MCF-7	breast:
4	chr12:67461965..67464455-chr12:67489883..67491932,2	MCF-7	breast:
5	chr12:67463389..67464966-chr12:67474386..67476237,2	MCF-7	breast:
6	chr12:67461284..67462231-chr12:67613205..67614026,3	MCF-7	breast:
7	chr12:67427801..67429631-chr12:67463165..67465076,2	MCF-7	breast:
8	chr12:67461087..67461964-chr12:67614042..67614668,2	MCF-7	breast:
9	chr12:67462768..67464522-chr12:67660868..67664362,4	MCF-7	breast:
10	chr12:67448355..67449925-chr12:67462962..67464949,2	MCF-7	breast:
11	chr12:67441847..67445341-chr12:67460170..67462670,3	MCF-7	breast:
12	chr12:67310671..67312914-chr12:67463080..67465006,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CAND1-3	chr12:67463830-67463879	l_674_chr12:67463829-67473923_lymphNode
2	lnc-GRIP1-1	chr12:67462830-67462942	ENSG00000256248

No data

Variant related genes	Relation type
ENSG00000256248	TF binding region
ENSG00000256248	CpG island
ENSG00000256248	chromatin interactions
ENSG00000111530	chromatin interactions
ENSG00000257083	chromatin interactions

Extended variants
information (count: 92 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:92 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139449110	chr12:67461511-67461512	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs547847993	chr12:67461533-67461534	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs116684223	chr12:67461635-67461636	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs372207238	chr12:67461645-67461646	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs142540043	chr12:67461668-67461669	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs144011624	chr12:67461682-67461683	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs535520062	chr12:67461690-67461691	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs201268293	chr12:67461696-67461697	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs553712056	chr12:67461714-67461715	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs565890193	chr12:67461773-67461774	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs78566517	chr12:67461787-67461788	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs567643868	chr12:67461795-67461796	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs1526835	chr12:67461802-67461803	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs527574844	chr12:67461850-67461851	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs543460911	chr12:67461885-67461886	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs148666393	chr12:67461953-67461954	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs58119930	chr12:67461974-67461975	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs541490800	chr12:67462050-67462051	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs188892508	chr12:67462057-67462058	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs533586701	chr12:67462059-67462060	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs545576743	chr12:67462062-67462063	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs563974148	chr12:67462069-67462070	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs73318965	chr12:67462090-67462091	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs549842961	chr12:67462091-67462092	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs568040665	chr12:67462107-67462108	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs528855768	chr12:67462160-67462161	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs116048787	chr12:67462187-67462188	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs565599259	chr12:67462268-67462269	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs539625154	chr12:67462283-67462284	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs116371300	chr12:67462308-67462309	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs372085567	chr12:67462313-67462314	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs193251189	chr12:67462315-67462316	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs142844462	chr12:67462361-67462362	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs7298268	chr12:67462393-67462394	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs534673244	chr12:67462446-67462447	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs553439751	chr12:67462523-67462524	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs577999143	chr12:67462524-67462525	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs545664418	chr12:67462527-67462528	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs563863705	chr12:67462528-67462529	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs185338187	chr12:67462546-67462547	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs543365191	chr12:67462594-67462595	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs117125692	chr12:67462617-67462618	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs561390472	chr12:67462643-67462644	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs529172455	chr12:67462647-67462648	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs57351839	chr12:67462648-67462649	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs7301580	chr12:67462695-67462696	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs375939812	chr12:67462732-67462733	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs140701340	chr12:67462900-67462901	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
49	rs559448710	chr12:67462946-67462947	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs532879928	chr12:67462991-67462992	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	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
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21364760	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	22048815	CNVD
Congenital anomalies of the kidney and urinary tract	21113617	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Myxofibrosarcoma	16751306	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Lung cancer	17925434	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Disease	21505450	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma multiforme	19115005	CNVD
Cancer	20164920	CNVD

Chromatin state (count:479 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:67460800-67461600	Active TSS	Placenta	Placenta
2	chr12:67461000-67461800	Bivalent/Poised TSS	Brain Angular Gyrus	brain
3	chr12:67461000-67462000	Flanking Active TSS	HMEC	breast
4	chr12:67461000-67462200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr12:67461000-67462400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr12:67461200-67461600	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr12:67461200-67461600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
8	chr12:67461200-67461600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
9	chr12:67461200-67461600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
10	chr12:67461200-67461600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr12:67461200-67461600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
12	chr12:67461200-67461800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr12:67461200-67461800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
14	chr12:67461200-67461800	Bivalent Enhancer	NH-A	brain
15	chr12:67461200-67462000	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr12:67461200-67462000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr12:67461200-67462400	Flanking Active TSS	Brain Germinal Matrix	brain
18	chr12:67461200-67462400	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
19	chr12:67461200-67462400	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
20	chr12:67461200-67462400	Flanking Active TSS	Fetal Brain Female	brain
21	chr12:67461200-67463800	Active TSS	Fetal Kidney	kidney
22	chr12:67461400-67461600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr12:67461400-67461600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr12:67461400-67461600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
25	chr12:67461400-67461600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr12:67461400-67461600	Active TSS	Rectal Smooth Muscle	rectum
27	chr12:67461400-67461600	Enhancers	Stomach Smooth Muscle	stomach
28	chr12:67461400-67461800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
29	chr12:67461400-67461800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr12:67461400-67461800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
31	chr12:67461400-67461800	Bivalent/Poised TSS	Primary T cells from cord blood	blood
32	chr12:67461400-67461800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr12:67461400-67461800	Bivalent Enhancer	Fetal Intestine Small	intestine
34	chr12:67461400-67461800	Enhancers	A549	lung
35	chr12:67461400-67462000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
36	chr12:67461400-67462000	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
37	chr12:67461400-67462000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
38	chr12:67461400-67462200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
39	chr12:67461400-67462200	Bivalent/Poised TSS	Brain Anterior Caudate	brain
40	chr12:67461400-67462200	Enhancers	Placenta Amnion	Placenta Amnion
41	chr12:67461400-67462400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
42	chr12:67461400-67462400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr12:67461400-67462400	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
44	chr12:67461400-67462400	Flanking Active TSS	Fetal Brain Male	brain
45	chr12:67461400-67462400	Flanking Active TSS	NHEK	skin
46	chr12:67461400-67462600	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
47	chr12:67461400-67463600	Active TSS	Colon Smooth Muscle	Colon
48	chr12:67461400-67464000	Active TSS	H9 Cell Line	embryonic stem cell
49	chr12:67461600-67461800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr12:67461600-67461800	Flanking Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell

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