Variant report

Variant	nsv1052996
Chromosome Location	chr12:74710909-74891621
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1366)
CpG islands
(count:122)
Chromatin interactive
region (count:75)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1366 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:74826796-74826833	K562	blood:	n/a	n/a
2	ARID3A	chr12:74809466-74809749	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:74759175-74759298	HepG2	liver:	n/a	n/a
4	ATF1	chr12:74793868-74794034	K562	blood:	n/a	n/a
5	ATF1	chr12:74802714-74802755	K562	blood:	n/a	n/a
6	ATF1	chr12:74818651-74818803	K562	blood:	n/a	n/a
7	ATF1	chr12:74825653-74825916	K562	blood:	n/a	n/a
8	ATF3	chr12:74764528-74765038	A549	lung:	n/a	n/a
9	ATF3	chr12:74794732-74795182	HCT-116	colon:	n/a	n/a
10	BACH1	chr12:74859437-74859442	K562	blood:	n/a	n/a
11	BCL3	chr12:74795748-74796682	A549	lung:	n/a	n/a
12	BCL3	chr12:74867773-74868041	GM12878	blood:	n/a	n/a
13	BCLAF1	chr12:74759438-74759660	GM12878	blood:	n/a	n/a
14	BHLHE40	chr12:74881949-74882475	GM12878	blood:	n/a	n/a
15	BRCA1	chr12:74732633-74732644	HepG2	liver:	n/a	n/a
16	CBX3	chr12:74786973-74787524	HCT-116	colon:	n/a	n/a
17	CBX3	chr12:74795707-74796687	HCT-116	colon:	n/a	n/a
18	CBX3	chr12:74786964-74787539	HCT-116	colon:	n/a	n/a
19	CBX3	chr12:74731744-74732185	HCT-116	colon:	n/a	n/a
20	CBX3	chr12:74731580-74732163	HCT-116	colon:	n/a	n/a
21	CCNT2	chr12:74813681-74813941	K562	blood:	n/a	n/a
22	CEBPB	chr12:74728409-74729025	HCT-116	colon:	n/a	n/a
23	CEBPB	chr12:74795874-74796525	A549	lung:	n/a	n/a
24	CEBPB	chr12:74775754-74776054	A549	lung:	n/a	chr12:74775919-74775930
25	CEBPB	chr12:74796081-74796596	A549	lung:	n/a	n/a
26	CEBPB	chr12:74794812-74795217	A549	lung:	n/a	chr12:74795016-74795027
27	CEBPB	chr12:74717021-74717301	K562	blood:	n/a	chr12:74717187-74717200 chr12:74717187-74717200 chr12:74717189-74717200 chr12:74717243-74717256
28	CEBPB	chr12:74795959-74796632	HCT-116	colon:	n/a	n/a
29	CEBPB	chr12:74718452-74718672	K562	blood:	n/a	chr12:74718562-74718573
30	CEBPB	chr12:74794779-74795280	A549	lung:	n/a	chr12:74795016-74795027
31	CEBPB	chr12:74753040-74753109	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr12:74794851-74795187	H1-hESC	embryonic stem cell:	n/a	chr12:74795016-74795027
33	CEBPB	chr12:74816311-74816671	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr12:74794688-74795314	HCT-116	colon:	n/a	chr12:74795016-74795027
35	CEBPB	chr12:74795808-74796796	HCT-116	colon:	n/a	n/a
36	CEBPB	chr12:74862173-74862510	IMR90	lung:	n/a	chr12:74862345-74862356
37	CEBPB	chr12:74764643-74764946	HepG2	liver:	n/a	chr12:74764787-74764798 chr12:74764786-74764799
38	CEBPB	chr12:74718420-74718696	HepG2	liver:	n/a	chr12:74718562-74718573
39	CEBPB	chr12:74725757-74726048	HepG2	liver:	n/a	n/a
40	CEBPB	chr12:74725734-74726056	IMR90	lung:	n/a	n/a
41	CEBPB	chr12:74846869-74847181	HepG2	liver:	n/a	chr12:74847028-74847039
42	CEBPB	chr12:74816368-74816662	IMR90	lung:	n/a	n/a
43	CEBPB	chr12:74739933-74740109	K562	blood:	n/a	chr12:74740041-74740052 chr12:74740043-74740052
44	CEBPB	chr12:74794840-74795215	A549	lung:	n/a	chr12:74795016-74795027
45	CEBPB	chr12:74764596-74765004	A549	lung:	n/a	chr12:74764787-74764798 chr12:74764786-74764799
46	CEBPB	chr12:74775762-74776092	IMR90	lung:	n/a	chr12:74775919-74775930
47	CEBPB	chr12:74865017-74865309	A549	lung:	n/a	n/a
48	CEBPB	chr12:74764664-74764940	K562	blood:	n/a	chr12:74764787-74764798 chr12:74764786-74764799
49	CEBPB	chr12:74764688-74765029	A549	lung:	n/a	chr12:74764787-74764798 chr12:74764786-74764799
50	CEBPB	chr12:74862249-74862420	HepG2	liver:	n/a	chr12:74862345-74862356

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:74796989-74797039	A549	lung:	n/a
2	chr12:74796989-74797039	NH-A	brain:	n/a
3	chr12:74796989-74797039	Hepatocyte	liver:	n/a
4	chr12:74796989-74797039	AG04450	lung:	fetal
5	chr12:74796989-74797039	HMEC	breast:	n/a
6	chr12:74796989-74797039	PrEC	prostate:	n/a
7	chr12:74796989-74797039	MCF-7	breast:	n/a
8	chr12:74796989-74797039	HAEpiC	amniotic membrane:	n/a
9	chr12:74796919-74796969	H1-hESC	embryonic stem cell:	embryo
10	chr12:74796919-74796969	AG04450	lung:	fetal
11	chr12:74796989-74797039	HRE	kidney:	n/a
12	chr12:74796919-74796969	LNCaP	prostate:	n/a
13	chr12:74796919-74796969	AG10803	skin:	n/a
14	chr12:74796989-74797039	U87	brain:	n/a
15	chr12:74796989-74797039	PFSK-1	brain:	n/a
16	chr12:74796919-74796969	SKMC	muscle:	n/a
17	chr12:74796989-74797039	HRPEpiC	eye:	n/a
18	chr12:74796919-74796969	HMEC	breast:	n/a
19	chr12:74796919-74796969	K562	blood:	n/a
20	chr12:74796919-74796969	PrEC	prostate:	n/a
21	chr12:74796989-74797039	AG10803	skin:	n/a
22	chr12:74796989-74797039	MCF10A-Er-Src	breast:	n/a
23	chr12:74796989-74797039	IMR90	lung:	fetal
24	chr12:74796989-74797039	HL-60	blood:	n/a
25	chr12:74796919-74796969	BJ	skin:	n/a
26	chr12:74796989-74797039	NHBE	bronchial:	n/a
27	chr12:74796919-74796969	ProgFib	skin:	n/a
28	chr12:74796989-74797039	GM06990	blood:	n/a
29	chr12:74796989-74797039	GM12892	blood:	n/a
30	chr12:74796919-74796969	NHBE	bronchial:	n/a
31	chr12:74796989-74797039	PANC-1	pancreas:	n/a
32	chr12:74796989-74797039	RPTEC	kidney:	n/a
33	chr12:74796989-74797039	BE2_C	brain:	n/a
34	chr12:74796919-74796969	U87	brain:	n/a
35	chr12:74796919-74796969	MCF10A-Er-Src	breast:	n/a
36	chr12:74796919-74796969	HIPEpiC	eye:	n/a
37	chr12:74796919-74796969	NH-A	brain:	n/a
38	chr12:74796989-74797039	HNPCEpiC	eye:	n/a
39	chr12:74796919-74796969	NHDF-neo	bronchial:	n/a
40	chr12:74796919-74796969	HCF	heart:	n/a
41	chr12:74796919-74796969	AG09309	skin:	n/a
42	chr12:74796919-74796969	T-47D	breast:	n/a
43	chr12:74796919-74796969	HPAEpiC	pulmonary alveolar:	n/a
44	chr12:74796919-74796969	Jurkat	blood:	n/a
45	chr12:74796919-74796969	SK-N-SH_RA	brain:	n/a
46	chr12:74796989-74797039	NB4	blood:	n/a
47	chr12:74796989-74797039	AG09309	skin:	n/a
48	chr12:74796919-74796969	GM12891	blood:	n/a
49	chr12:74796919-74796969	IMR90	lung:	fetal
50	chr12:74796989-74797039	BJ	skin:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:74806359..74807259-chr12:75040526..75041195,3	MCF-7	breast:
2	chr12:74717186..74718789-chr12:74720353..74721970,2	K562	blood:
3	chr12:74841181..74842984-chr12:74844069..74845768,2	MCF-7	breast:
4	chr12:74728722..74730831-chr12:74734863..74737720,2	K562	blood:
5	chr12:74790241..74792314-chr12:74792608..74794740,2	K562	blood:
6	chr12:74886784..74889473-chr12:74901933..74904935,3	MCF-7	breast:
7	chr12:74784205..74786048-chr12:74789309..74790953,2	MCF-7	breast:
8	chr12:74855468..74859118-chr12:74859957..74863080,3	MCF-7	breast:
9	chr12:74790902..74793392-chr12:74837126..74839228,2	K562	blood:
10	chr12:74722908..74725146-chr12:74726519..74728134,2	K562	blood:
11	chr12:74809074..74809733-chr12:74930798..74931679,2	MCF-7	breast:
12	chr12:74505546..74506081-chr12:74710850..74711455,2	MCF-7	breast:
13	chr12:74767533..74770103-chr12:74773203..74774977,2	K562	blood:
14	chr12:74735826..74737720-chr12:74741864..74744419,2	K562	blood:
15	chr12:74773013..74775445-chr12:74931117..74932872,2	MCF-7	breast:
16	chr12:74886086..74889072-chr12:74890768..74893334,2	K562	blood:
17	chr12:74735518..74737270-chr12:74738700..74740204,2	K562	blood:
18	chr12:74415343..74416036-chr12:74759116..74760027,3	MCF-7	breast:
19	chr12:74806364..74807139-chr12:74930822..74931570,3	MCF-7	breast:
20	chr12:74733054..74735137-chr12:74736132..74739051,2	MCF-7	breast:
21	chr12:74735518..74737270-chr12:74738700..74740204,2	K562	blood:
22	chr12:74790827..74794195-chr12:74799790..74803789,4	K562	blood:
23	chr12:74808967..74810071-chr12:74930722..74931602,5	MCF-7	breast:
24	chr12:74799398..74801033-chr12:74804670..74806463,2	K562	blood:
25	chr12:74809152..74809679-chr12:75040399..75041156,3	MCF-7	breast:
26	chr12:74784205..74786048-chr12:74789309..74790953,2	MCF-7	breast:
27	chr12:74790827..74794195-chr12:74799790..74803789,4	K562	blood:
28	chr12:74805449..74807207-chr12:74930003..74932862,2	K562	blood:
29	chr12:74505239..74506034-chr12:74759124..74759988,3	MCF-7	breast:
30	chr12:74795006..74795737-chr7:112051152..112051706,2	MCF-7	breast:
31	chr12:74854045..74856877-chr12:74857073..74859373,2	MCF-7	breast:
32	chr12:74764014..74766511-chr12:74767490..74770061,2	K562	blood:
33	chr12:74505191..74505755-chr12:74710574..74711440,3	MCF-7	breast:
34	chr12:74415389..74416204-chr12:74806037..74807059,3	MCF-7	breast:
35	chr12:74767533..74770103-chr12:74773203..74774977,2	K562	blood:
36	chr12:74683740..74685933-chr12:74788608..74790315,2	K562	blood:
37	chr12:74735511..74737326-chr12:74742061..74744419,2	K562	blood:
38	chr12:74744747..74747636-chr12:74751430..74753414,2	MCF-7	breast:
39	chr12:74790902..74793392-chr12:74837126..74839228,2	K562	blood:
40	chr12:74710734..74711407-chr12:74759142..74759810,2	MCF-7	breast:
41	chr12:74869489..74872190-chr12:74878705..74880923,2	MCF-7	breast:
42	chr12:74808031..74810219-chr12:74931221..74933935,2	MCF-7	breast:
43	chr12:74728722..74730831-chr12:74734863..74737720,2	K562	blood:
44	chr12:74780034..74781968-chr12:74784353..74786746,2	K562	blood:
45	chr12:74877290..74879814-chr12:74930783..74933713,2	MCF-7	breast:
46	chr12:74766974..74769221-chr12:74772181..74774631,2	MCF-7	breast:
47	chr12:74723847..74726680-chr12:74730834..74733309,2	MCF-7	breast:
48	chr12:74855922..74856922-chrX:16789379..16790137,2	HCT-116	colon:
49	chr12:74505591..74506172-chr12:74759484..74759999,2	MCF-7	breast:
50	chr12:74722908..74725146-chr12:74726519..74728134,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNC2-2	chr12:74771343-74771412	ENSG00000251138
2	lnc-KCNC2-2	chr12:74767700-74767836	NONHSAT029508
3	lnc-KCNC2-2	chr12:74715315-74715474	ENSG00000251138
4	lnc-KCNC2-2	chr12:74796249-74796315	ENSG00000251138
5	lnc-KCNC2-2	chr12:74771343-74771407	NONHSAT029508
6	lnc-KCNC2-8	chr12:74747664-74747926	expReg_chr12_6787_-

No data

Variant related genes	Relation type
ENSG00000251138	TF binding region
ENSG00000251138	CpG island
ENSG00000257386	chromatin interactions
ENSG00000253719	chromatin interactions
SNAPIN	miRNA target sites
SLC2A3	miRNA target sites
MTMR9	miRNA target sites

Extended variants
information (count: 3554 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:3554 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190370346	chr12:74710960-74710961	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs565794072	chr12:74710961-74710962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201640153	chr12:74711022-74711023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138867387	chr12:74711030-74711031	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551448395	chr12:74711073-74711074	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542235162	chr12:74711086-74711087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181175871	chr12:74711089-74711090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185586636	chr12:74711106-74711107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375254782	chr12:74711117-74711118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556695954	chr12:74711266-74711267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs76662843	chr12:74711325-74711326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188727128	chr12:74711331-74711332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs369288270	chr12:74711364-74711365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573064019	chr12:74711370-74711371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs537115795	chr12:74711374-74711375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs17831577	chr12:74711457-74711458	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs570839141	chr12:74711459-74711460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75310599	chr12:74711461-74711462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554767046	chr12:74711541-74711542	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139124962	chr12:74711571-74711572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11614020	chr12:74711592-74711593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs145658219	chr12:74711593-74711594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377463820	chr12:74711596-74711597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373350452	chr12:74711600-74711601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111966769	chr12:74711604-74711605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs386376988	chr12:74711608-74711609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs59915726	chr12:74711611-74711612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142299226	chr12:74711640-74711641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542173670	chr12:74711752-74711753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs180694286	chr12:74711911-74711912	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185505536	chr12:74711912-74711913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530067361	chr12:74711952-74711953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs150354032	chr12:74711964-74711965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560455570	chr12:74711981-74711982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs75650494	chr12:74711982-74711983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191940988	chr12:74712000-74712001	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571285207	chr12:74712064-74712065	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530539118	chr12:74712066-74712067	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550676628	chr12:74712107-74712108	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567255344	chr12:74712114-74712115	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113863992	chr12:74712125-74712126	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138051346	chr12:74712186-74712187	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7953924	chr12:74712274-74712275	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs117155985	chr12:74712285-74712286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538787482	chr12:74712310-74712311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs11180015	chr12:74712319-74712320	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs575666756	chr12:74712360-74712361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149503774	chr12:74712410-74712411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs370063669	chr12:74712437-74712438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs11180016	chr12:74712451-74712452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
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
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	17133270	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21364760	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	20409316	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:74709800-74711200	Weak transcription	Ovary	ovary
2	chr12:74710200-74711400	Enhancers	Muscle Satellite Cultured Cells	--
3	chr12:74710400-74711200	Enhancers	Brain Germinal Matrix	brain
4	chr12:74710400-74711200	Enhancers	Fetal Heart	heart
5	chr12:74710400-74711400	Enhancers	A549	lung
6	chr12:74710400-74713200	Enhancers	Brain Substantia Nigra	brain
7	chr12:74710600-74711000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr12:74710600-74711000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
9	chr12:74710600-74711400	Enhancers	Brain Anterior Caudate	brain
10	chr12:74710600-74712200	Enhancers	Brain Cingulate Gyrus	brain
11	chr12:74710600-74712200	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr12:74710600-74712400	Enhancers	Brain Angular Gyrus	brain
13	chr12:74710600-74714200	Enhancers	Brain Hippocampus Middle	brain
14	chr12:74710800-74711200	Enhancers	Duodenum Smooth Muscle	Duodenum
15	chr12:74710800-74712000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr12:74710800-74712200	Enhancers	Fetal Stomach	stomach
17	chr12:74711200-74711400	Enhancers	Ovary	ovary
18	chr12:74711200-74711800	Enhancers	Fetal Brain Male	brain
19	chr12:74711400-74721600	Weak transcription	A549	lung
20	chr12:74712000-74712200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr12:74712200-74713600	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr12:74712200-74713800	Weak transcription	Brain Cingulate Gyrus	brain
23	chr12:74712400-74713600	Weak transcription	Brain Angular Gyrus	brain
24	chr12:74713200-74713600	Weak transcription	Brain Substantia Nigra	brain
25	chr12:74713600-74714200	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr12:74713600-74714200	Enhancers	Brain Substantia Nigra	brain
27	chr12:74713800-74714000	Enhancers	Brain Angular Gyrus	brain
28	chr12:74713800-74714000	Enhancers	Brain Cingulate Gyrus	brain
29	chr12:74721200-74722400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr12:74721600-74722200	Enhancers	A549	lung
31	chr12:74722200-74722600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr12:74722200-74722800	Enhancers	HSMMtube	muscle
33	chr12:74722200-74723000	Flanking Active TSS	A549	lung
34	chr12:74722400-74722600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr12:74722600-74728600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr12:74723000-74723400	Enhancers	A549	lung
37	chr12:74723400-74724400	Weak transcription	A549	lung
38	chr12:74725600-74726200	Enhancers	HMEC	breast
39	chr12:74726200-74731400	Weak transcription	HMEC	breast
40	chr12:74728200-74729000	Enhancers	Muscle Satellite Cultured Cells	--
41	chr12:74728400-74728800	Enhancers	A549	lung
42	chr12:74728400-74729000	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr12:74728400-74729000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr12:74728400-74729200	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr12:74728600-74728800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr12:74728600-74729000	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr12:74728600-74729000	Enhancers	HUVEC	blood vessel
48	chr12:74728800-74731600	Weak transcription	A549	lung
49	chr12:74729000-74731200	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr12:74729000-74731400	Weak transcription	HUVEC	blood vessel

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