Variant report

Variant	nsv832330
Chromosome Location	chr12:11077678-11206957
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:634)
CpG islands
(count:1710)
Chromatin interactive
region (count:13)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:634 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:11168444-11168649	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:11176072-11176303	HepG2	liver:	n/a	n/a
3	ATF1	chr12:11101214-11101301	K562	blood:	n/a	n/a
4	BACH1	chr12:11094869-11095246	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr12:11078726-11078738	K562	blood:	n/a	n/a
6	BACH1	chr12:11078901-11079081	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr12:11186566-11186883	GM12878	blood:	n/a	n/a
8	BATF	chr12:11134866-11135249	GM12878	blood:	n/a	n/a
9	BATF	chr12:11134883-11135228	GM12878	blood:	n/a	n/a
10	BATF	chr12:11186631-11186911	GM12878	blood:	n/a	n/a
11	BCL11A	chr12:11186584-11186913	GM12878	blood:	n/a	n/a
12	BHLHE40	chr12:11134926-11135203	GM12878	blood:	n/a	n/a
13	BHLHE40	chr12:11168360-11168714	HepG2	liver:	n/a	n/a
14	BRCA1	chr12:11168480-11168660	HepG2	liver:	n/a	n/a
15	CEBPB	chr12:11092983-11093349	A549	lung:	n/a	chr12:11093153-11093164
16	CEBPB	chr12:11121449-11121832	IMR90	lung:	n/a	chr12:11121638-11121649
17	CEBPB	chr12:11122383-11122390	HepG2	liver:	n/a	n/a
18	CEBPB	chr12:11170024-11170162	HepG2	liver:	n/a	chr12:11170139-11170150
19	CEBPB	chr12:11121485-11121799	Hela-S3	cervix:	n/a	chr12:11121638-11121649
20	CEBPB	chr12:11167458-11167736	HepG2	liver:	n/a	chr12:11167582-11167593
21	CEBPB	chr12:11148042-11148079	K562	blood:	n/a	n/a
22	CEBPB	chr12:11092903-11093336	ECC-1	luminal epithelium:	n/a	chr12:11093153-11093164
23	CEBPB	chr12:11121480-11121817	ECC-1	luminal epithelium:	n/a	chr12:11121638-11121649
24	CEBPB	chr12:11093033-11093259	H1-hESC	embryonic stem cell:	n/a	chr12:11093153-11093164
25	CEBPB	chr12:11092932-11093388	A549	lung:	n/a	chr12:11093153-11093164
26	CEBPB	chr12:11107460-11107606	HepG2	liver:	n/a	n/a
27	CEBPB	chr12:11092966-11093356	Hela-S3	cervix:	n/a	chr12:11093153-11093164
28	CEBPB	chr12:11121545-11121715	A549	lung:	n/a	chr12:11121638-11121649
29	CEBPB	chr12:11121480-11121758	HepG2	liver:	n/a	chr12:11121638-11121649
30	CEBPB	chr12:11092983-11093376	ECC-1	luminal epithelium:	n/a	chr12:11093153-11093164
31	CEBPB	chr12:11092983-11093299	HepG2	liver:	n/a	chr12:11093153-11093164
32	CEBPB	chr12:11135657-11135714	HepG2	liver:	n/a	n/a
33	CEBPB	chr12:11092967-11093366	IMR90	lung:	n/a	chr12:11093153-11093164
34	CHD2	chr12:11094919-11095112	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr12:11101840-11101990	NHLF	lung:	n/a	n/a
36	CTCF	chr12:11178800-11178950	GM12864	blood:	n/a	n/a
37	CTCF	chr12:11178820-11178970	AG09309	skin:	n/a	n/a
38	CTCF	chr12:11147020-11147170	GM12869	blood:	n/a	n/a
39	CTCF	chr12:11112564-11112604	K562	blood:	n/a	n/a
40	CTCF	chr12:11086780-11086930	HCM	heart:	n/a	n/a
41	CTCF	chr12:11086660-11086810	HFF	foreskin:	n/a	n/a
42	CTCF	chr12:11094980-11095130	HMEC	breast:	n/a	n/a
43	CTCF	chr12:11178840-11178990	AG04449	skin:	n/a	n/a
44	CTCF	chr12:11112461-11112655	A549	lung:	n/a	n/a
45	CTCF	chr12:11178820-11178970	HCFaa	heart:	n/a	n/a
46	CTCF	chr12:11178800-11178950	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr12:11086800-11086878	K562	blood:	n/a	n/a
48	CTCF	chr12:11112440-11112590	AG09319	gingival:	n/a	n/a
49	CTCF	chr12:11083470-11083512	MCF-7	breast:	n/a	n/a
50	CTCF	chr12:11086738-11086891	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1710 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11176574-11176624	Hela-S3	cervix:	n/a
2	chr12:11184347-11184397	AoSMC	blood vessel:	n/a
3	chr12:11176574-11176624	Hela-S3	cervix:	n/a
4	chr12:11184347-11184397	AoSMC	blood vessel:	n/a
5	chr12:11151224-11151274	PFSK-1	brain:	n/a
6	chr12:11184415-11184465	PrEC	prostate:	n/a
7	chr12:11081604-11081654	HNPCEpiC	eye:	n/a
8	chr12:11139710-11139760	NHBE	bronchial:	n/a
9	chr12:11176574-11176624	GM12891	blood:	n/a
10	chr12:11091149-11091199	NHBE	bronchial:	n/a
11	chr12:11151224-11151274	Caco-2	colon:	n/a
12	chr12:11184149-11184199	HAEpiC	amniotic membrane:	n/a
13	chr12:11081943-11081993	ProgFib	skin:	n/a
14	chr12:11139710-11139760	HMEC	breast:	n/a
15	chr12:11140560-11140610	SK-N-SH_RA	brain:	n/a
16	chr12:11184005-11184055	BE2_C	brain:	n/a
17	chr12:11184037-11184087	Hela-S3	cervix:	n/a
18	chr12:11151224-11151274	HRCEpiC	kidney:	n/a
19	chr12:11151430-11151480	GM12891	blood:	n/a
20	chr12:11092816-11092866	HCT-116	colon:	n/a
21	chr12:11184347-11184397	HMEC	breast:	n/a
22	chr12:11184149-11184199	AoSMC	blood vessel:	n/a
23	chr12:11091149-11091199	ProgFib	skin:	n/a
24	chr12:11081943-11081993	Hepatocyte	liver:	n/a
25	chr12:11151622-11151672	GM12892	blood:	n/a
26	chr12:11093283-11093333	AG09309	skin:	n/a
27	chr12:11127185-11127235	HepG2	liver:	n/a
28	chr12:11184037-11184087	HAEpiC	amniotic membrane:	n/a
29	chr12:11080457-11080507	NT2-D1	testis:	n/a
30	chr12:11184415-11184465	HMEC	breast:	n/a
31	chr12:11081604-11081654	HIPEpiC	eye:	n/a
32	chr12:11080457-11080507	T-47D	breast:	n/a
33	chr12:11184347-11184397	HRPEpiC	eye:	n/a
34	chr12:11174898-11174948	NHBE	bronchial:	n/a
35	chr12:11184005-11184055	HEEpiC	esophagus:	n/a
36	chr12:11184149-11184199	SAEC	small airway:	n/a
37	chr12:11140560-11140610	PFSK-1	brain:	n/a
38	chr12:11093283-11093333	HAEpiC	amniotic membrane:	n/a
39	chr12:11176386-11176436	GM12878	blood:	n/a
40	chr12:11184037-11184087	HCM	heart:	n/a
41	chr12:11149362-11149412	T-47D	breast:	n/a
42	chr12:11080457-11080507	SAEC	small airway:	n/a
43	chr12:11174898-11174948	ECC-1	luminal epithelium:	n/a
44	chr12:11081943-11081993	NHBE	bronchial:	n/a
45	chr12:11139710-11139760	LNCaP	prostate:	n/a
46	chr12:11151522-11151572	HNPCEpiC	eye:	n/a
47	chr12:11139962-11140012	HL-60	blood:	n/a
48	chr12:11176574-11176624	PrEC	prostate:	n/a
49	chr12:11139304-11139354	CMK	blood:	n/a
50	chr12:11184415-11184465	HepG2	liver:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:11058073..11060923-chr12:11099457..11101619,2	K562	blood:
2	chr12:11158423..11160257-chr12:11164352..11165951,2	MCF-7	breast:
3	chr12:11157746..11159406-chr12:11165545..11167423,2	K562	blood:
4	chr12:11158423..11160257-chr12:11164352..11165951,2	MCF-7	breast:
5	chr12:11169301..11171201-chr12:11322573..11325255,2	MCF-7	breast:
6	chr12:11091072..11093170-chr12:11322389..11325259,3	MCF-7	breast:
7	chr12:11111049..11113421-chr12:11322867..11324787,2	MCF-7	breast:
8	chr12:11154648..11156385-chr12:11157901..11159498,2	K562	blood:
9	chr12:11157746..11159406-chr12:11165545..11167423,2	K562	blood:
10	chr12:11009323..11011109-chr12:11168207..11170860,2	K562	blood:
11	chr12:11153714..11156559-chr12:11162296..11164278,2	MCF-7	breast:
12	chr12:11154648..11156385-chr12:11157901..11159498,2	K562	blood:
13	chr12:11153714..11156559-chr12:11162296..11164278,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRH1-1	chr12:11187381-11187484	NONHSAT026912
2	lnc-PRH1-1	chr12:11126254-11126320	NONHSAT026912
3	lnc-PRH1-1	chr12:11199619-11199787	NONHSAT026907
4	lnc-PRH1-1	chr12:11126254-11126320	NONHSAT026907
5	lnc-PRH1-1	chr12:11199619-11199713	NONHSAT026914
6	lnc-PRH1-1	chr12:11199619-11199640	NONHSAT026908
7	lnc-PRH1-1	chr12:11090007-11091176	NONHSAT026912
8	lnc-PRH1-1	chr12:11126254-11126320	NONHSAT026908
9	lnc-PRH1-1	chr12:11187381-11187484	NR_037918
10	lnc-PRH1-1	chr12:11199619-11199736	NONHSAT026915
11	lnc-TAS2R50-1	chr12:11117024-11117951	NONHSAT026913
12	lnc-PRH1-1	chr12:11125883-11126320	NONHSAT026914
13	lnc-PRH1-1	chr12:11126254-11126305	NONHSAT026910
14	lnc-PRH1-1	chr12:11158533-11158868	NONHSAT026915
15	lnc-PRH1-1	chr12:11199619-11199787	NR_037918
16	lnc-PRH1-1	chr12:11126254-11126320	NR_037918
17	lnc-PRH1-1	chr12:11199612-11199787	NONHSAT026916
18	lnc-PRH1-1	chr12:11199619-11199787	NONHSAT026912
19	lnc-TAS2R46-1	chr12:11200931-11201855	NONHSAT026917

No data

Variant related genes	Relation type
TAS2R14	TF binding region
TAS2R19	TF binding region
TAS2R31	TF binding region
ENSG00000268301	TF binding region
TAS2R15	TF binding region
TAS2R20	TF binding region
TAS2R50	TF binding region
PRR4	TF binding region
TAS2R63P	TF binding region
PRH2	TF binding region
TAS2R14	CpG island
TAS2R19	CpG island
TAS2R31	CpG island
ENSG00000268301	CpG island
TAS2R15	CpG island
TAS2R20	CpG island
TAS2R50	CpG island
PRR4	CpG island
TAS2R63P	CpG island
PRH2	CpG island
ENSG00000111215	chromatin interactions
ENSG00000256537	chromatin interactions
ENSG00000256712	chromatin interactions
ENSG00000212127	chromatin interactions

Extended variants
information (count: 5679 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:5679 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572903420	chr12:11077738-11077739	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs535331624	chr12:11077749-11077750	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs555342829	chr12:11077753-11077754	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs575219427	chr12:11077774-11077775	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs186154994	chr12:11077799-11077800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563928893	chr12:11077809-11077810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577233792	chr12:11077811-11077812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139332228	chr12:11077820-11077821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200114278	chr12:11077843-11077844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190549140	chr12:11077854-11077855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570955647	chr12:11077861-11077862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368646058	chr12:11077912-11077913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541578634	chr12:11077937-11077938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530853620	chr12:11077959-11077960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536725878	chr12:11078047-11078048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570657384	chr12:11078080-11078081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532864625	chr12:11078104-11078105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs546762474	chr12:11078119-11078120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113817605	chr12:11078214-11078215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182732212	chr12:11078231-11078232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536561065	chr12:11078276-11078277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373995855	chr12:11078335-11078336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555406238	chr12:11078366-11078367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568631687	chr12:11078369-11078370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537766072	chr12:11078388-11078389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553284874	chr12:11078408-11078409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188268452	chr12:11078501-11078502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545980365	chr12:11078510-11078511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553094607	chr12:11078592-11078593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371257198	chr12:11078609-11078610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541791588	chr12:11078738-11078739	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs192691442	chr12:11078761-11078762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78598784	chr12:11078776-11078777	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs149713796	chr12:11078798-11078799	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs183007828	chr12:11078824-11078825	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs145583490	chr12:11078842-11078843	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs546825824	chr12:11078844-11078845	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs566526174	chr12:11078893-11078894	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs141403403	chr12:11078929-11078930	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs577894135	chr12:11078934-11078935	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs548966018	chr12:11078972-11078973	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs74062405	chr12:11079049-11079050	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs116234620	chr12:11079050-11079051	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs557684959	chr12:11079068-11079069	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs7297167	chr12:11079085-11079086	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs145298779	chr12:11079118-11079119	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs553291459	chr12:11079148-11079149	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs367739908	chr12:11079175-11079176	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs558675279	chr12:11079200-11079201	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs187543453	chr12:11079203-11079204	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Acute myeloid leukemia	17237825	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Incontinentia Pigmenti	22033527	CNVD
Recurrent pregnancy loss	19789632	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1465 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11033800-11101600	Weak transcription	Ovary	ovary
2	chr12:11054400-11084800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:11058000-11081200	Weak transcription	Primary T cells from cord blood	blood
4	chr12:11058200-11081800	Weak transcription	Aorta	Aorta
5	chr12:11061600-11079800	Weak transcription	HepG2	liver
6	chr12:11065200-11093000	Weak transcription	Primary hematopoietic stem cells	blood
7	chr12:11069200-11094800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr12:11070600-11079600	Weak transcription	Gastric	stomach
9	chr12:11070800-11079200	Weak transcription	Left Ventricle	heart
10	chr12:11071400-11079200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr12:11072200-11092800	Weak transcription	A549	lung
12	chr12:11078000-11089400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr12:11078400-11095800	Weak transcription	Primary B cells from cord blood	blood
14	chr12:11079000-11079600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr12:11079200-11080000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:11079200-11080000	Enhancers	Left Ventricle	heart
17	chr12:11079600-11080400	Enhancers	Gastric	stomach
18	chr12:11079800-11080200	Enhancers	HepG2	liver
19	chr12:11080000-11095000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr12:11080000-11101600	Weak transcription	Left Ventricle	heart
21	chr12:11080200-11080400	Enhancers	Psoas Muscle	Psoas
22	chr12:11080200-11081200	Weak transcription	HepG2	liver
23	chr12:11080400-11095400	Weak transcription	Psoas Muscle	Psoas
24	chr12:11081200-11082000	Strong transcription	Primary T cells from cord blood	blood
25	chr12:11081200-11082200	Enhancers	Liver	Liver
26	chr12:11081200-11082200	Enhancers	HepG2	liver
27	chr12:11081800-11082400	Enhancers	Lung	lung
28	chr12:11082000-11101000	Weak transcription	Primary T cells from cord blood	blood
29	chr12:11082200-11094800	Weak transcription	HepG2	liver
30	chr12:11084800-11085400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr12:11087400-11090000	Weak transcription	Pancreas	Pancrea
32	chr12:11088000-11088200	Enhancers	Brain Substantia Nigra	brain
33	chr12:11088200-11093200	Weak transcription	Brain Substantia Nigra	brain
34	chr12:11088400-11089200	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr12:11089400-11089600	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr12:11089600-11090000	Enhancers	Fetal Brain Male	brain
37	chr12:11089600-11094800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr12:11091400-11095600	Enhancers	NHEK	skin
39	chr12:11091600-11095600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr12:11091600-11095800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr12:11091600-11095800	Enhancers	HMEC	breast
42	chr12:11092000-11092200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr12:11092000-11092600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr12:11092200-11093200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr12:11092600-11093000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr12:11092600-11093200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr12:11092600-11093400	Enhancers	Brain Cingulate Gyrus	brain
48	chr12:11092800-11093400	Enhancers	A549	lung
49	chr12:11092800-11095000	Weak transcription	GM12878-XiMat	blood
50	chr12:11093000-11093200	Enhancers	H9 Cell Line	embryonic stem cell

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