Variant report

Variant	nsv1040560
Chromosome Location	chr12:11370919-11588024
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:629)
CpG islands
(count:1037)
Chromatin interactive
region (count:25)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:629 , 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	ATF1	chr12:11501400-11501725	K562	blood:	n/a	n/a
2	BCL3	chr12:11501361-11501642	GM12878	blood:	n/a	n/a
3	BCL3	chr12:11501365-11501771	GM12878	blood:	n/a	n/a
4	BRCA1	chr12:11388624-11388659	GM12878	blood:	n/a	n/a
5	CBX3	chr12:11569521-11569734	K562	blood:	n/a	n/a
6	CEBPB	chr12:11584855-11585296	MCF-7	breast:	n/a	chr12:11585039-11585052
7	CEBPB	chr12:11458075-11458297	HepG2	liver:	n/a	chr12:11458153-11458164
8	CEBPB	chr12:11550382-11550647	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:11584903-11585301	MCF-7	breast:	n/a	chr12:11585039-11585052
10	CEBPB	chr12:11478711-11479007	HepG2	liver:	n/a	chr12:11478828-11478841 chr12:11478830-11478839 chr12:11478828-11478839 chr12:11478829-11478840
11	CEBPB	chr12:11538442-11538474	A549	lung:	n/a	n/a
12	CEBPB	chr12:11423258-11423283	HepG2	liver:	n/a	chr12:11423268-11423279
13	CEBPB	chr12:11457994-11458258	A549	lung:	n/a	chr12:11458153-11458164
14	CEBPB	chr12:11550359-11550619	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr12:11538413-11538520	HepG2	liver:	n/a	chr12:11538466-11538477 chr12:11538464-11538475
16	CEBPB	chr12:11514261-11514433	Hela-S3	cervix:	n/a	chr12:11514316-11514325
17	CREB1	chr12:11501275-11501755	HepG2	liver:	n/a	n/a
18	CREB1	chr12:11501156-11501972	K562	blood:	n/a	n/a
19	CREB1	chr12:11501341-11501827	HepG2	liver:	n/a	n/a
20	CREB1	chr12:11501322-11501785	K562	blood:	n/a	n/a
21	CREB1	chr12:11501439-11501709	A549	lung:	n/a	n/a
22	CTCF	chr12:11381300-11381450	K562	blood:	n/a	n/a
23	CTCF	chr12:11500920-11501070	GM12872	blood:	n/a	n/a
24	CTCF	chr12:11459054-11459110	GM20000	blood:	n/a	n/a
25	CTCF	chr12:11500720-11500870	BE2_C	brain:	n/a	n/a
26	CTCF	chr12:11381280-11381430	AG09319	gingival:	n/a	n/a
27	CTCF	chr12:11381320-11381470	GM12865	blood:	n/a	n/a
28	CTCF	chr12:11500800-11500950	GM12865	blood:	n/a	n/a
29	CTCF	chr12:11381260-11381410	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr12:11381260-11381410	HVMF	connective:	n/a	n/a
31	CTCF	chr12:11381260-11381410	BJ	skin:	n/a	n/a
32	CTCF	chr12:11409039-11409105	GM10248	blood:	n/a	n/a
33	CTCF	chr12:11381280-11381430	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr12:11545778-11545816	GM12891	blood:	n/a	n/a
35	CTCF	chr12:11500840-11500990	GM12875	blood:	n/a	n/a
36	CTCF	chr12:11381260-11381410	GM12801	blood:	n/a	n/a
37	CTCF	chr12:11381200-11381350	HVMF	connective:	n/a	n/a
38	CTCF	chr12:11492997-11493057	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr12:11381204-11381530	Gliobla	brain:	n/a	n/a
40	CTCF	chr12:11569479-11569545	MCF-7	breast:	n/a	n/a
41	CTCF	chr12:11377857-11378090	K562	blood:	n/a	chr12:11377955-11377968 chr12:11377948-11377969
42	CTCF	chr12:11377890-11378028	HUVEC	blood vessel:	n/a	chr12:11377955-11377968 chr12:11377948-11377969
43	CTCF	chr12:11381340-11381490	GM12872	blood:	n/a	n/a
44	CTCF	chr12:11381300-11381450	GM12870	blood:	n/a	n/a
45	CTCF	chr12:11381300-11381450	SAEC	small airway:	n/a	n/a
46	CTCF	chr12:11381300-11381450	AG09319	gingival:	n/a	n/a
47	CTCF	chr12:11500800-11500950	GM12874	blood:	n/a	n/a
48	CTCF	chr12:11505978-11506004	Lung_OC	lung:	n/a	n/a
49	CTCF	chr12:11381280-11381430	HMF	breast:	n/a	n/a
50	CTCF	chr12:11381193-11381605	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11420895-11420945	RPTEC	kidney:	n/a
2	chr12:11548867-11548917	ProgFib	skin:	n/a
3	chr12:11422897-11422947	HRE	kidney:	n/a
4	chr12:11464607-11464657	HPAEpiC	pulmonary alveolar:	n/a
5	chr12:11422897-11422947	HNPCEpiC	eye:	n/a
6	chr12:11549192-11549242	HRCEpiC	kidney:	n/a
7	chr12:11423120-11423170	HIPEpiC	eye:	n/a
8	chr12:11509583-11509633	PrEC	prostate:	n/a
9	chr12:11463844-11463894	A549	lung:	n/a
10	chr12:11508049-11508099	NB4	blood:	n/a
11	chr12:11548019-11548069	CMK	blood:	n/a
12	chr12:11423120-11423170	A549	lung:	n/a
13	chr12:11460710-11460760	HRCEpiC	kidney:	n/a
14	chr12:11463379-11463429	PrEC	prostate:	n/a
15	chr12:11460710-11460760	MCF-7	breast:	n/a
16	chr12:11460710-11460760	HUVEC	blood vessel:	n/a
17	chr12:11463937-11463987	K562	blood:	n/a
18	chr12:11548019-11548069	Caco-2	colon:	n/a
19	chr12:11463937-11463987	AG04450	lung:	fetal
20	chr12:11423020-11423070	K562	blood:	n/a
21	chr12:11509583-11509633	AG10803	skin:	n/a
22	chr12:11509583-11509633	AG04449	skin:	fetal
23	chr12:11463937-11463987	BJ	skin:	n/a
24	chr12:11548867-11548917	NHDF-neo	bronchial:	n/a
25	chr12:11548019-11548069	NB4	blood:	n/a
26	chr12:11509583-11509633	HRE	kidney:	n/a
27	chr12:11461798-11461848	NH-A	brain:	n/a
28	chr12:11463937-11463987	IMR90	lung:	fetal
29	chr12:11423020-11423070	HRE	kidney:	n/a
30	chr12:11548867-11548917	AG09309	skin:	n/a
31	chr12:11461798-11461848	AG10803	skin:	n/a
32	chr12:11423020-11423070	H1-hESC	embryonic stem cell:	embryo
33	chr12:11463937-11463987	PrEC	prostate:	n/a
34	chr12:11463844-11463894	HRE	kidney:	n/a
35	chr12:11548867-11548917	HMEC	breast:	n/a
36	chr12:11463937-11463987	HEK293	kidney:	embryo
37	chr12:11460710-11460760	AG09319	gingival:	n/a
38	chr12:11423020-11423070	HIPEpiC	eye:	n/a
39	chr12:11549555-11549605	HMEC	breast:	n/a
40	chr12:11549555-11549605	Hepatocyte	liver:	n/a
41	chr12:11464607-11464657	SAEC	small airway:	n/a
42	chr12:11423120-11423170	NB4	blood:	n/a
43	chr12:11464607-11464657	H1-hESC	embryonic stem cell:	embryo
44	chr12:11509583-11509633	ovcar-3	ovarian:	n/a
45	chr12:11463844-11463894	BE2_C	brain:	n/a
46	chr12:11460710-11460760	HEEpiC	esophagus:	n/a
47	chr12:11463379-11463429	HL-60	blood:	n/a
48	chr12:11549192-11549242	HCPEpiC	choroid plexus:	n/a
49	chr12:11464607-11464657	HEK293	kidney:	embryo
50	chr12:11463937-11463987	MCF-7	breast:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:11386551..11388621-chr12:11390275..11392718,2	MCF-7	breast:
2	chr12:11380961..11381600-chr12:11584509..11585267,2	MCF-7	breast:
3	chr12:11380256..11382594-chr12:11395942..11397666,2	K562	blood:
4	chr12:11393394..11396191-chr12:11397306..11399582,2	K562	blood:
5	chr12:11393394..11396191-chr12:11397306..11399582,2	K562	blood:
6	chr12:11019756..11020639-chr12:11381127..11381814,2	MCF-7	breast:
7	chr12:11379156..11381655-chr12:11386557..11389546,2	MCF-7	breast:
8	chr12:11386551..11388621-chr12:11390275..11392718,2	MCF-7	breast:
9	chr12:11380800..11382351-chr12:11639202..11640262,7	K562	blood:
10	chr12:11380285..11382894-chr12:11638783..11640720,37	MCF-7	breast:
11	chr12:10902631..10903193-chr12:11380478..11381401,2	MCF-7	breast:
12	chr12:11380256..11382594-chr12:11395942..11397666,2	K562	blood:
13	chr12:11393260..11395260-chr12:11405152..11406755,2	MCF-7	breast:
14	chr12:11380955..11381831-chr12:11636473..11637250,2	MCF-7	breast:
15	chr12:11494392..11497234-chr12:11500928..11503308,2	K562	blood:
16	chr12:11393260..11395260-chr12:11405152..11406755,2	MCF-7	breast:
17	chr12:11378692..11379976-chr12:11639209..11640084,4	MCF-7	breast:
18	chr12:11382288..11384076-chr12:11390295..11392363,2	K562	blood:
19	chr12:11381972..11382582-chr12:11639477..11639992,2	MCF-7	breast:
20	chr12:11379156..11381655-chr12:11386557..11389546,2	MCF-7	breast:
21	chr12:11382288..11384076-chr12:11390295..11392363,2	K562	blood:
22	chr12:11384411..11385288-chr12:11639202..11639975,2	K562	blood:
23	chr12:11494392..11497234-chr12:11500928..11503308,2	K562	blood:
24	chr12:11380961..11381600-chr12:11584509..11585267,2	MCF-7	breast:
25	chr12:11380630..11381925-chr12:11638833..11640222,16	MCF-7	breast:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRB1-1	chr12:11583296-11583398	ENSG00000255790.1
2	lnc-PRB4-1	chr12:11462305-11462339	NONHSAT026935
3	lnc-PRB4-1	chr12:11461584-11461816	NONHSAT026935
4	lnc-PRB1-1	chr12:11552315-11552411	ENSG00000255790.1
5	lnc-PRB1-1	chr12:11584416-11584496	ENSG00000255790.1
6	lnc-PRB1-1	chr12:11559632-11559826	ENSG00000255790.1
7	lnc-PRB1-1	chr12:11584416-11584496	ENSG00000255790.1
8	lnc-PRB1-1	chr12:11584416-11584496	XLOC_010018
9	lnc-PRB4-1	chr12:11463270-11463369	NONHSAT026935
10	lnc-PRB4-2	chr12:11420927-11421082	NONHSAT026934
11	lnc-PRB1-1	chr12:11584416-11584496	ENSG00000255790.1
12	lnc-PRB4-2	chr12:11418890-11418962	NONHSAT026934
13	lnc-PRB4-2	chr12:11420109-11420359	NONHSAT026934
14	lnc-PRB1-1	chr12:11584416-11584496	XLOC_010018
15	lnc-PRB1-1	chr12:11583172-11583398	XLOC_010018
16	lnc-PRB4-2	chr12:11421567-11421602	NONHSAT026934
17	lnc-PRB4-1	chr12:11461162-11461375	NONHSAT026935
18	lnc-PRB4-2	chr12:11422540-11422641	NONHSAT026934
19	lnc-PRB1-1	chr12:11587926-11588092	ENSG00000255790.1
20	lnc-PRB1-1	chr12:11584416-11584496	ENSG00000255790.1
21	lnc-PRH2-2	chr12:11404233-11404303	ENSG00000256373
22	lnc-PRB1-1	chr12:11583186-11583398	XLOC_010018
23	lnc-PRB1-1	chr12:11552784-11552937	ENSG00000255790.1
24	lnc-PRB1-1	chr12:11583144-11583398	ENSG00000255790.1
25	lnc-PRB1-1	chr12:11554419-11554457	ENSG00000255790.1
26	lnc-PRB1-1	chr12:11587926-11588092	XLOC_010018

No data

Variant related genes	Relation type
PRB4	TF binding region
PRB2	TF binding region
PRB1	TF binding region
PRB3	TF binding region
PRB4	CpG island
PRB2	CpG island
PRB1	CpG island
PRB3	CpG island
ENSG00000255790	chromatin interactions
ENSG00000256888	chromatin interactions
ARID5B	miRNA target sites

Extended variants
information (count: 7056 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:7056 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556933700	chr12:11370938-11370939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs573652951	chr12:11370948-11370949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138912285	chr12:11371026-11371027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149419369	chr12:11371090-11371091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553827702	chr12:11371123-11371124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187713757	chr12:11371148-11371149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536166346	chr12:11371163-11371164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556049316	chr12:11371164-11371165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116149329	chr12:11371171-11371172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs143818716	chr12:11371208-11371209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558257894	chr12:11371222-11371223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2008542	chr12:11371234-11371235	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs540293913	chr12:11371256-11371257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201100043	chr12:11371274-11371275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528435958	chr12:11371321-11371322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs148078643	chr12:11371374-11371375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540851988	chr12:11371379-11371380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75085797	chr12:11371442-11371443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562633926	chr12:11371461-11371462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535572842	chr12:11371496-11371497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531572193	chr12:11371504-11371505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551267640	chr12:11371598-11371599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141847830	chr12:11371601-11371602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192369076	chr12:11371624-11371625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547475823	chr12:11371632-11371633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs115117048	chr12:11371715-11371716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536251843	chr12:11371749-11371750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs556058974	chr12:11371755-11371756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558524	chr12:11371756-11371757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569427691	chr12:11371786-11371787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184418191	chr12:11371789-11371790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548188710	chr12:11371835-11371836	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs188481151	chr12:11371873-11371874	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs147254354	chr12:11371878-11371879	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs192727214	chr12:11371914-11371915	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs117084008	chr12:11371924-11371925	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs550051048	chr12:11371978-11371979	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs562832299	chr12:11371981-11371982	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs531532278	chr12:11372061-11372062	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs371957105	chr12:11372089-11372090	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs563587363	chr12:11372099-11372100	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs531082633	chr12:11372170-11372171	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs528863372	chr12:11372176-11372177	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs545256336	chr12:11372187-11372188	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs139117690	chr12:11372224-11372225	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs527438097	chr12:11372266-11372267	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs547561689	chr12:11372270-11372271	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs567361081	chr12:11372315-11372316	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs550494097	chr12:11372334-11372335	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs549532973	chr12:11372358-11372359	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Acute myeloid leukemia	17237825	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	22522925	CNVD
Mental retardation	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	20531469	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:136 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11362200-11371800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:11371800-11372600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:11379800-11381400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr12:11380400-11380800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr12:11381400-11381600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr12:11386400-11386800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr12:11386600-11386800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr12:11391200-11391600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr12:11391200-11391600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr12:11391200-11391600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr12:11391400-11392200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr12:11391600-11392600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr12:11392400-11392600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr12:11392600-11394000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr12:11392600-11397400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr12:11394000-11394600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr12:11394200-11394600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr12:11394200-11395200	Enhancers	HMEC	breast
19	chr12:11394600-11396200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr12:11395400-11395800	Enhancers	HepG2	liver
21	chr12:11396200-11396600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr12:11397400-11399800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr12:11398400-11405200	Weak transcription	Primary T cells from cord blood	blood
24	chr12:11398600-11399000	Active TSS	Hela-S3	cervix
25	chr12:11399800-11400400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr12:11400400-11401200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr12:11401200-11401400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr12:11402400-11410800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr12:11403600-11403800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr12:11403800-11404400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr12:11405200-11407400	Strong transcription	Primary T cells from cord blood	blood
32	chr12:11407400-11440200	Weak transcription	Primary T cells from cord blood	blood
33	chr12:11418400-11418600	Bivalent Enhancer	HUVEC	blood vessel
34	chr12:11418600-11419200	Enhancers	HUVEC	blood vessel
35	chr12:11420200-11420400	ZNF genes & repeats	Pancreas	Pancrea
36	chr12:11420400-11423000	Weak transcription	Pancreas	Pancrea
37	chr12:11422400-11422600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr12:11423000-11423200	ZNF genes & repeats	Pancreas	Pancrea
39	chr12:11424400-11425000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr12:11425000-11432400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr12:11426200-11427000	Enhancers	HMEC	breast
42	chr12:11429800-11433800	Weak transcription	Liver	Liver
43	chr12:11430600-11433200	Weak transcription	Left Ventricle	heart
44	chr12:11431000-11431200	Active TSS	Adipose Nuclei	Adipose
45	chr12:11431000-11433200	Weak transcription	Primary T cells fromperipheralblood	blood
46	chr12:11431200-11433400	Weak transcription	Adipose Nuclei	Adipose
47	chr12:11432400-11433000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr12:11433400-11434000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr12:11433400-11434200	Strong transcription	Adipose Nuclei	Adipose
50	chr12:11433800-11434000	ZNF genes & repeats	Liver	Liver

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