Variant report

Variant	esv1836556
Chromosome Location	chr12:9555805-9714330
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1468)
CpG islands
(count:1652)
Chromatin interactive
region (count:8)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:9621679-9621874	HepG2	liver:	n/a	n/a
2	ATF3	chr12:9608285-9608446	K562	blood:	n/a	n/a
3	BACH1	chr12:9600846-9601058	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr12:9601742-9601759	K562	blood:	n/a	n/a
5	BACH1	chr12:9600477-9600495	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr12:9599040-9599656	GM12878	blood:	n/a	chr12:9599254-9599262
7	BATF	chr12:9599060-9599517	GM12878	blood:	n/a	chr12:9599254-9599262
8	BATF	chr12:9593967-9594189	GM12878	blood:	n/a	n/a
9	BATF	chr12:9560636-9560925	GM12878	blood:	n/a	n/a
10	BATF	chr12:9600026-9601051	GM12878	blood:	n/a	n/a
11	BATF	chr12:9627069-9627370	GM12878	blood:	n/a	chr12:9627229-9627240
12	BATF	chr12:9574493-9574708	GM12878	blood:	n/a	n/a
13	BATF	chr12:9623145-9623344	GM12878	blood:	n/a	n/a
14	BATF	chr12:9594018-9594252	GM12878	blood:	n/a	n/a
15	BATF	chr12:9627071-9627414	GM12878	blood:	n/a	chr12:9627229-9627240
16	BCL11A	chr12:9599859-9600445	GM12878	blood:	n/a	chr12:9600117-9600126
17	BCL11A	chr12:9599928-9600111	GM12878	blood:	n/a	n/a
18	BCL11A	chr12:9600168-9600488	GM12878	blood:	n/a	n/a
19	BCL11A	chr12:9598941-9599450	GM12878	blood:	n/a	chr12:9599009-9599018
20	BCL11A	chr12:9600454-9600822	GM12878	blood:	n/a	chr12:9600809-9600818
21	BCL11A	chr12:9600546-9600932	GM12878	blood:	n/a	chr12:9600809-9600818 chr12:9600810-9600823
22	BCL11A	chr12:9599028-9599550	GM12878	blood:	n/a	n/a
23	BCL11A	chr12:9564505-9564797	GM12878	blood:	n/a	n/a
24	BHLHE40	chr12:9621680-9621866	K562	blood:	n/a	n/a
25	BHLHE40	chr12:9608196-9608405	K562	blood:	n/a	n/a
26	BHLHE40	chr12:9600844-9601336	K562	blood:	n/a	chr12:9600944-9600960
27	BHLHE40	chr12:9564391-9564639	GM12878	blood:	n/a	n/a
28	BRCA1	chr12:9621725-9621746	GM12878	blood:	n/a	n/a
29	BRCA1	chr12:9600585-9600802	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr12:9602352-9602776	K562	blood:	n/a	n/a
31	CBX3	chr12:9599960-9601079	K562	blood:	n/a	n/a
32	CBX3	chr12:9602101-9602849	K562	blood:	n/a	n/a
33	CEBPB	chr12:9699995-9700109	A549	lung:	n/a	n/a
34	CEBPB	chr12:9626823-9627139	HepG2	liver:	n/a	chr12:9626967-9626978
35	CEBPB	chr12:9626847-9627088	A549	lung:	n/a	chr12:9626967-9626978
36	CEBPB	chr12:9626864-9627128	K562	blood:	n/a	chr12:9626967-9626978
37	CEBPB	chr12:9646117-9646284	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr12:9621705-9621858	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr12:9626831-9627127	Hela-S3	cervix:	n/a	chr12:9626967-9626978
40	CEBPB	chr12:9699973-9700136	IMR90	lung:	n/a	n/a
41	CEBPB	chr12:9621719-9621810	K562	blood:	n/a	n/a
42	CEBPB	chr12:9621651-9621793	HepG2	liver:	n/a	n/a
43	CEBPB	chr12:9561882-9562084	HepG2	liver:	n/a	n/a
44	CEBPB	chr12:9600111-9600908	GM12878	blood:	n/a	chr12:9600576-9600588
45	CEBPB	chr12:9626941-9627031	K562	blood:	n/a	chr12:9626967-9626978
46	CEBPB	chr12:9621557-9621862	HepG2	liver:	n/a	n/a
47	CEBPB	chr12:9635038-9635326	IMR90	lung:	n/a	chr12:9635144-9635153 chr12:9635144-9635153 chr12:9635144-9635153
48	CEBPB	chr12:9600431-9601043	Hela-S3	cervix:	n/a	chr12:9600576-9600588
49	CEBPD	chr12:9600207-9600646	K562	blood:	n/a	n/a
50	CEBPD	chr12:9600756-9601125	K562	blood:	n/a	n/a

(count:1652 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9601149-9601199	SK-N-MC	brain:	n/a
2	chr12:9601031-9601081	Caco-2	colon:	n/a
3	chr12:9557205-9557255	HPAEpiC	pulmonary alveolar:	n/a
4	chr12:9559402-9559452	K562	blood:	n/a
5	chr12:9601066-9601116	AG09319	gingival:	n/a
6	chr12:9601149-9601199	SK-N-MC	brain:	n/a
7	chr12:9601031-9601081	Caco-2	colon:	n/a
8	chr12:9557205-9557255	HPAEpiC	pulmonary alveolar:	n/a
9	chr12:9559402-9559452	K562	blood:	n/a
10	chr12:9601066-9601116	AG09319	gingival:	n/a
11	chr12:9559402-9559452	Hela-S3	cervix:	n/a
12	chr12:9568315-9568365	AoSMC	blood vessel:	n/a
13	chr12:9568315-9568365	SKMC	muscle:	n/a
14	chr12:9600941-9600991	HMEC	breast:	n/a
15	chr12:9602245-9602295	BJ	skin:	n/a
16	chr12:9601031-9601081	Hela-S3	cervix:	n/a
17	chr12:9600875-9600925	GM12878	blood:	n/a
18	chr12:9602245-9602295	SK-N-MC	brain:	n/a
19	chr12:9601161-9601211	HMEC	breast:	n/a
20	chr12:9556998-9557048	AG10803	skin:	n/a
21	chr12:9618783-9618833	HCM	heart:	n/a
22	chr12:9600801-9600851	SK-N-MC	brain:	n/a
23	chr12:9597637-9597687	PFSK-1	brain:	n/a
24	chr12:9601066-9601116	NH-A	brain:	n/a
25	chr12:9600950-9601000	Hepatocyte	liver:	n/a
26	chr12:9600888-9600938	NB4	blood:	n/a
27	chr12:9601066-9601116	AG04449	skin:	fetal
28	chr12:9556998-9557048	AG04450	lung:	fetal
29	chr12:9556998-9557048	HCM	heart:	n/a
30	chr12:9600888-9600938	HRPEpiC	eye:	n/a
31	chr12:9557316-9557366	AG04449	skin:	fetal
32	chr12:9601149-9601199	NB4	blood:	n/a
33	chr12:9600801-9600851	AG09319	gingival:	n/a
34	chr12:9600453-9600503	HL-60	blood:	n/a
35	chr12:9605181-9605231	AG09309	skin:	n/a
36	chr12:9600875-9600925	AoSMC	blood vessel:	n/a
37	chr12:9602245-9602295	SK-N-SH	brain:	n/a
38	chr12:9605181-9605231	Hela-S3	cervix:	n/a
39	chr12:9600950-9601000	HEEpiC	esophagus:	n/a
40	chr12:9571130-9571180	HL-60	blood:	n/a
41	chr12:9559693-9559743	H1-hESC	embryonic stem cell:	embryo
42	chr12:9573914-9573964	GM12878	blood:	n/a
43	chr12:9568315-9568365	CMK	blood:	n/a
44	chr12:9557205-9557255	AoSMC	blood vessel:	n/a
45	chr12:9559402-9559452	Hepatocyte	liver:	n/a
46	chr12:9568315-9568365	HCF	heart:	n/a
47	chr12:9605181-9605231	AG04449	skin:	fetal
48	chr12:9602245-9602295	ECC-1	luminal epithelium:	n/a
49	chr12:9600060-9600110	NH-A	brain:	n/a
50	chr12:9573914-9573964	HNPCEpiC	eye:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:9436150..9437103-chr12:9600374..9601086,2	Hela-S3	cervix:
2	chr12:9620489..9621323-chr12:31206721..31207493,2	MCF-7	breast:
3	chr12:9471764..9473665-chr12:9564371..9566160,2	MCF-7	breast:
4	chr12:9620209..9621328-chr12:31206996..31207808,4	MCF-7	breast:
5	chr12:9530894..9532008-chr12:9621312..9622244,4	MCF-7	breast:
6	chr12:9436185..9436710-chr12:9599925..9600582,2	MCF-7	breast:
7	chr12:9471846..9472542-chr12:9564639..9565202,2	MCF-7	breast:
8	chr12:9436030..9436711-chr12:9600583..9601103,2	HCT-116	colon:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLRB1-3	chr12:9596229-9596278	NONHSAT026827
2	lnc-CLEC2D-2	chr12:9600969-9601474	XLOC_009653
3	lnc-KLRB1-3	chr12:9596155-9596205	NONHSAT026827
4	lnc-PZP-12	chr12:9565722-9566137	NONHSAT026823
5	lnc-PZP-12	chr12:9558904-9559128	NONHSAT026823
6	lnc-KLRB1-2	chr12:9690763-9691239	l_603_chr12:9690762-9691933_testes
7	lnc-KLRB1-2	chr12:9691704-9691933	l_603_chr12:9690762-9691933_testes
8	lnc-CLEC2D-2	chr12:9613920-9614245	XLOC_009653
9	lnc-CLEC2D-2	chr12:9600944-9601474	FPKM1_group_5754_transcript_1
10	lnc-PZP-12	chr12:9561452-9561545	NONHSAT026823
11	lnc-PZP-12	chr12:9561452-9561545	NONHSAT026825
12	lnc-KLRB1-3	chr12:9596676-9596721	NONHSAT026827
13	lnc-PZP-12	chr12:9559865-9560050	NONHSAT026823
14	lnc-PZP-12	chr12:9564668-9564845	NONHSAT026825
15	lnc-CLEC2D-2	chr12:9613919-9614245	FPKM1_group_5754_transcript_1
16	lnc-PZP-12	chr12:9565722-9566143	NONHSAT026825
17	lnc-PZP-12	chr12:9567399-9567447	NONHSAT026817
18	lnc-KLRB1-3	chr12:9600578-9600808	NONHSAT026827
19	lnc-PZP-12	chr12:9566315-9566384	NONHSAT026823

No data

Variant related genes	Relation type
ENSG00000212432	TF binding region
DDX12P	TF binding region
ENSG00000266633	TF binding region
ENSG00000256673	TF binding region
ENSG00000256975	TF binding region
ENSG00000214776	TF binding region
ENSG00000212432	CpG island
DDX12P	CpG island
ENSG00000266633	CpG island
ENSG00000256673	CpG island
ENSG00000256975	CpG island
ENSG00000214776	CpG island
ENSG00000111788	chromatin interactions
CALU	miRNA target sites
CASP7	miRNA target sites

Extended variants
information (count: 3653 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3653 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199765431	chr12:9555812-9555813	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
2	rs181513985	chr12:9555816-9555817	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs187098742	chr12:9555827-9555828	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
4	rs189518826	chr12:9555843-9555844	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs148228982	chr12:9555864-9555865	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs71441752	chr12:9555877-9555878	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs71441751	chr12:9555879-9555880	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs549208888	chr12:9555888-9555889	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs71441750	chr12:9555896-9555897	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs71441749	chr12:9555901-9555902	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs61914450	chr12:9555934-9555935	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs61914451	chr12:9555937-9555938	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs115248798	chr12:9555944-9555945	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs537048655	chr12:9555974-9555975	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
15	rs113910830	chr12:9555980-9555981	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
16	rs114481207	chr12:9555987-9555988	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs185949636	chr12:9556008-9556009	Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs141198189	chr12:9556011-9556012	Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs113512093	chr12:9556017-9556018	Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
20	rs573494541	chr12:9556030-9556031	Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
21	rs189550872	chr12:9556031-9556032	Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
22	rs545590906	chr12:9556041-9556042	Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs182245475	chr12:9556047-9556048	Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs186134372	chr12:9556056-9556057	Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
25	rs564174910	chr12:9556086-9556087	Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs190997775	chr12:9556098-9556099	Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs183362060	chr12:9556117-9556118	Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
28	rs111839455	chr12:9556120-9556121	Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs549791575	chr12:9556145-9556146	Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs202167025	chr12:9556147-9556148	Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs111620642	chr12:9556158-9556159	Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs73242964	chr12:9556174-9556175	Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs370979386	chr12:9556201-9556202	Weak transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
34	rs146196539	chr12:9556203-9556204	Weak transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
35	rs376729055	chr12:9556221-9556222	Weak transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
36	rs371648213	chr12:9556478-9556479	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs112576881	chr12:9556525-9556526	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs111622031	chr12:9556526-9556527	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
39	rs192693178	chr12:9556528-9556529	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs374525767	chr12:9556567-9556568	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs548988392	chr12:9556582-9556583	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs112568424	chr12:9556633-9556634	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs113978975	chr12:9556675-9556676	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs79093479	chr12:9556700-9556701	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs183080591	chr12:9556735-9556736	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs115631690	chr12:9556745-9556746	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs150520636	chr12:9556761-9556762	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs113710776	chr12:9556766-9556767	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs74062835	chr12:9556783-9556784	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs139581533	chr12:9556786-9556787	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21611746	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Obesity	21131291	CNVD
small cell lung cancer	20016488	CNVD
Incontinentia Pigmenti	22033527	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Cancer	21272361	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:963 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9541400-9557200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr12:9541800-9557400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr12:9544800-9593200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr12:9545400-9573800	Weak transcription	Fetal Intestine Small	intestine
5	chr12:9545400-9575600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr12:9546200-9559400	Weak transcription	A549	lung
7	chr12:9547000-9558600	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr12:9547200-9556800	Weak transcription	Fetal Stomach	stomach
9	chr12:9547400-9556600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr12:9547400-9557400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr12:9549400-9558800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr12:9549400-9559200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr12:9549400-9564000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr12:9551400-9557000	Weak transcription	Dnd41	blood
15	chr12:9555200-9556200	Active TSS	Right Ventricle	heart
16	chr12:9555200-9557600	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr12:9555400-9556000	Enhancers	Primary B cells from peripheral blood	blood
18	chr12:9555400-9556000	Enhancers	Primary T cells fromperipheralblood	blood
19	chr12:9555600-9556000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
20	chr12:9555600-9556000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr12:9555600-9556000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr12:9555600-9556200	Active TSS	Thymus	Thymus
23	chr12:9555600-9559400	Weak transcription	Colonic Mucosa	Colon
24	chr12:9555800-9556000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
25	chr12:9555800-9556200	Active TSS	Breast Myoepithelial Primary Cells	Breast
26	chr12:9555800-9557400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr12:9555800-9557400	Weak transcription	Fetal Muscle Trunk	muscle
28	chr12:9555800-9557800	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr12:9555800-9558400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr12:9556000-9556400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr12:9556000-9556600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr12:9556200-9558400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr12:9556400-9557400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr12:9556600-9557200	ZNF genes & repeats	Fetal Thymus	thymus
35	chr12:9556600-9557800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr12:9556800-9557400	ZNF genes & repeats	Fetal Stomach	stomach
37	chr12:9557000-9557600	ZNF genes & repeats	Dnd41	blood
38	chr12:9557200-9557600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr12:9557200-9557800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr12:9557200-9557800	Bivalent/Poised TSS	Right Ventricle	heart
41	chr12:9557400-9557600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr12:9557400-9557600	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
43	chr12:9557400-9557800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
44	chr12:9557400-9557800	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr12:9557400-9557800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr12:9557400-9557800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr12:9557400-9558400	Weak transcription	Fetal Stomach	stomach
48	chr12:9557400-9558600	Strong transcription	Fetal Muscle Trunk	muscle
49	chr12:9557400-9559200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr12:9557400-9559400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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