Variant report

Variant	esv3357072
Chromosome Location	chr12:118540094-118543142
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:391)
CpG islands
(count:550)
Chromatin interactive
region (count:12)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr12:118541814-118542344	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr12:118541182-118541904	A549	lung:	n/a	chr12:118541198-118541211 chr12:118541680-118541693
3	BHLHE40	chr12:118540927-118541296	GM12878	blood:	n/a	chr12:118541198-118541214
4	BRCA1	chr12:118541655-118541768	Hela-S3	cervix:	n/a	n/a
5	CCNT2	chr12:118541453-118542116	K562	blood:	n/a	chr12:118541719-118541728
6	CEBPB	chr12:118539737-118540443	MCF-7	breast:	n/a	chr12:118539865-118539876
7	CEBPB	chr12:118540763-118542351	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr12:118539743-118540392	Hela-S3	cervix:	n/a	chr12:118539865-118539876
9	CEBPD	chr12:118541548-118541978	HepG2	liver:	n/a	n/a
10	CHD1	chr12:118540672-118541676	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr12:118541601-118541627	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr12:118541902-118542029	HepG2	liver:	n/a	n/a
13	CHD2	chr12:118542242-118542442	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr12:118539906-118540329	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr12:118540915-118542346	Hela-S3	cervix:	n/a	chr12:118541717-118541727
16	CREB1	chr12:118541029-118542250	A549	lung:	n/a	n/a
17	CTBP2	chr12:118541112-118542192	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr12:118541080-118541230	BJ	skin:	n/a	n/a
19	CTCF	chr12:118541720-118541870	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr12:118541320-118541470	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr12:118541400-118541550	GM12865	blood:	n/a	n/a
22	CTCF	chr12:118541340-118541490	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr12:118541680-118541830	HCM	heart:	n/a	n/a
24	CTCF	chr12:118541340-118541490	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr12:118541960-118542110	AG04449	skin:	n/a	n/a
26	CTCF	chr12:118541160-118541310	A549	lung:	n/a	n/a
27	CTCF	chr12:118541380-118541530	AG04449	skin:	n/a	n/a
28	CTCF	chr12:118540060-118540210	HMEC	breast:	n/a	n/a
29	CTCF	chr12:118541640-118541790	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr12:118541340-118541490	HepG2	liver:	n/a	n/a
31	CTCF	chr12:118541680-118541830	AG10803	skin:	n/a	n/a
32	CTCF	chr12:118541360-118541510	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr12:118541660-118541810	SAEC	small airway:	n/a	n/a
34	CTCF	chr12:118541460-118541610	AG09319	gingival:	n/a	n/a
35	CTCF	chr12:118541640-118541790	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr12:118541340-118541490	BJ	skin:	n/a	n/a
37	CTCF	chr12:118541320-118541470	GM12865	blood:	n/a	n/a
38	CTCF	chr12:118541460-118541610	AG04450	lung:	n/a	n/a
39	CTCF	chr12:118541680-118541830	HMEC	breast:	n/a	n/a
40	CTCF	chr12:118541660-118541810	Caco-2	colon:	n/a	n/a
41	CTCF	chr12:118541600-118541750	Caco-2	colon:	n/a	n/a
42	CTCF	chr12:118541360-118541510	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr12:118540120-118540270	HMEC	breast:	n/a	n/a
44	CTCF	chr12:118541400-118541550	GM12878	blood:	n/a	n/a
45	CTCF	chr12:118541423-118541495	MCF-7	breast:	n/a	n/a
46	CTCF	chr12:118541660-118541810	AG04449	skin:	n/a	n/a
47	CTCF	chr12:118541480-118541630	K562	blood:	n/a	n/a
48	CTCF	chr12:118541740-118541890	GM12865	blood:	n/a	n/a
49	CTCF	chr12:118541620-118541770	HEK293	kidney:	n/a	n/a
50	CTCF	chr12:118541400-118541550	AG04449	skin:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:118541298-118541348	HPAEpiC	pulmonary alveolar:	n/a
2	chr12:118541298-118541348	HPAEpiC	pulmonary alveolar:	n/a
3	chr12:118542069-118542119	GM12878	blood:	n/a
4	chr12:118542069-118542119	GM19239	blood:	n/a
5	chr12:118541298-118541348	AG10803	skin:	n/a
6	chr12:118541731-118541781	AG09309	skin:	n/a
7	chr12:118541585-118541635	GM12878	blood:	n/a
8	chr12:118542069-118542119	NHBE	bronchial:	n/a
9	chr12:118541247-118541297	ECC-1	luminal epithelium:	n/a
10	chr12:118541247-118541297	NHDF-neo	bronchial:	n/a
11	chr12:118542027-118542077	HPAEpiC	pulmonary alveolar:	n/a
12	chr12:118541247-118541297	AG10803	skin:	n/a
13	chr12:118541585-118541635	ECC-1	luminal epithelium:	n/a
14	chr12:118541298-118541348	AG04449	skin:	fetal
15	chr12:118541731-118541781	ProgFib	skin:	n/a
16	chr12:118541247-118541297	K562	blood:	n/a
17	chr12:118541585-118541635	Jurkat	blood:	n/a
18	chr12:118542027-118542077	NHDF-neo	bronchial:	n/a
19	chr12:118541298-118541348	NHBE	bronchial:	n/a
20	chr12:118541298-118541348	HNPCEpiC	eye:	n/a
21	chr12:118541247-118541297	Hela-S3	cervix:	n/a
22	chr12:118541851-118541901	AG04450	lung:	fetal
23	chr12:118541851-118541901	PFSK-1	brain:	n/a
24	chr12:118541585-118541635	HEK293	kidney:	embryo
25	chr12:118541731-118541781	NHBE	bronchial:	n/a
26	chr12:118541298-118541348	T-47D	breast:	n/a
27	chr12:118540222-118540272	HEEpiC	esophagus:	n/a
28	chr12:118541247-118541297	U87	brain:	n/a
29	chr12:118542069-118542119	LNCaP	prostate:	n/a
30	chr12:118541722-118541772	U87	brain:	n/a
31	chr12:118541247-118541297	GM12878	blood:	n/a
32	chr12:118541722-118541772	AoSMC	blood vessel:	n/a
33	chr12:118542027-118542077	HIPEpiC	eye:	n/a
34	chr12:118542069-118542119	HUVEC	blood vessel:	n/a
35	chr12:118540222-118540272	SAEC	small airway:	n/a
36	chr12:118541851-118541901	CMK	blood:	n/a
37	chr12:118541722-118541772	AG10803	skin:	n/a
38	chr12:118541247-118541297	NH-A	brain:	n/a
39	chr12:118542027-118542077	GM19239	blood:	n/a
40	chr12:118541247-118541297	AoSMC	blood vessel:	n/a
41	chr12:118542069-118542119	GM06990	blood:	n/a
42	chr12:118542027-118542077	PFSK-1	brain:	n/a
43	chr12:118541298-118541348	HCPEpiC	choroid plexus:	n/a
44	chr12:118541731-118541781	HRE	kidney:	n/a
45	chr12:118541585-118541635	AG10803	skin:	n/a
46	chr12:118542069-118542119	AG10803	skin:	n/a
47	chr12:118541247-118541297	AG09319	gingival:	n/a
48	chr12:118541298-118541348	SK-N-MC	brain:	n/a
49	chr12:118541247-118541297	SK-N-MC	brain:	n/a
50	chr12:118541585-118541635	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:118500316..118502003-chr12:118542187..118545128,2	K562	blood:
2	chr12:118536275..118537815-chr12:118538077..118540227,2	MCF-7	breast:
3	chr12:118538419..118540104-chr12:118573597..118576258,3	MCF-7	breast:
4	chr1:202857759..202858556-chr12:118541187..118542115,2	HCT-116	colon:
5	chr12:51157194..51157900-chr12:118541616..118542435,2	Hela-S3	cervix:
6	chr12:118540025..118541851-chr12:118573172..118576109,2	MCF-7	breast:
7	chr12:118498416..118504096-chr12:118537510..118543393,12	MCF-7	breast:
8	chr12:118490377..118492216-chr12:118538475..118541095,2	MCF-7	breast:
9	chr12:117627165..117629540-chr12:118540302..118543294,2	MCF-7	breast:
10	chr12:118540506..118543698-chr12:118572832..118575450,7	MCF-7	breast:
11	chr12:118497389..118502867-chr12:118535601..118543920,23	MCF-7	breast:
12	chr12:118539824..118542719-chr12:118557194..118560231,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAOK3-1	chr12:118539412-118540975	NONHSAT031022
2	lnc-TAOK3-1	chr12:118540794-118540861	NONHSAT031023
3	lnc-TAOK3-1	chr12:118541398-118541810	NONHSAT031022

No data

Variant related genes	Relation type
VSIG10	TF binding region
VSIG10	CpG island
ENSG00000089220	chromatin interactions
ENSG00000176834	chromatin interactions
ENSG00000176871	chromatin interactions
ENSG00000123268	chromatin interactions
ENSG00000135108	chromatin interactions
ENSG00000183155	chromatin interactions

Extended variants
information (count: 113 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:113 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188331682	chr12:118540099-118540100	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
2	rs559614089	chr12:118540112-118540113	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs528450546	chr12:118540127-118540128	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs550438105	chr12:118540156-118540157	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs142474359	chr12:118540189-118540190	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs77101661	chr12:118540193-118540194	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs568614108	chr12:118540206-118540207	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs139087449	chr12:118540223-118540224	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs551227133	chr12:118540234-118540235	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
10	rs538833639	chr12:118540235-118540236	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
11	rs192066332	chr12:118540264-118540265	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
12	rs557472513	chr12:118540273-118540274	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
13	rs35935640	chr12:118540397-118540398	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
14	rs11068826	chr12:118540402-118540403	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs182448430	chr12:118540408-118540409	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
16	rs76338032	chr12:118540410-118540411	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
17	rs187144569	chr12:118540422-118540423	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
18	rs567586536	chr12:118540470-118540471	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
19	rs74759940	chr12:118540528-118540529	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs536585005	chr12:118540548-118540549	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
21	rs61943495	chr12:118540552-118540553	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
22	rs553131417	chr12:118540553-118540554	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
23	rs191744607	chr12:118540565-118540566	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
24	rs537525308	chr12:118540600-118540601	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
25	rs77378935	chr12:118540627-118540628	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
26	rs142883878	chr12:118540651-118540652	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
27	rs112616262	chr12:118540683-118540684	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
28	rs144621266	chr12:118540692-118540693	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
29	rs367781366	chr12:118540703-118540704	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
30	rs148026322	chr12:118540705-118540706	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
31	rs573973290	chr12:118540773-118540774	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
32	rs539228662	chr12:118540777-118540778	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
33	rs182110760	chr12:118540789-118540790	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
34	rs562043656	chr12:118540868-118540869	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
35	rs557679354	chr12:118540922-118540923	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
36	rs531050677	chr12:118540950-118540951	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
37	rs550764953	chr12:118540956-118540957	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
38	rs558733290	chr12:118541030-118541031	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs564710631	chr12:118541039-118541040	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs533316178	chr12:118541071-118541072	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs547166386	chr12:118541097-118541098	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs566862233	chr12:118541103-118541104	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs575713335	chr12:118541107-118541108	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs187903949	chr12:118541109-118541110	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs568484372	chr12:118541124-118541125	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs71450259	chr12:118541131-118541132	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs137991960	chr12:118541132-118541133	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs537960267	chr12:118541137-118541138	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs12372214	chr12:118541166-118541167	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs557523250	chr12:118541181-118541182	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
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
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
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	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
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Neuroblastoma	20406844	CNVD
Medulloblastoma	16783165	CNVD
mental retardation	16760730	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21045234	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD

Chromatin state (count:465 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118500800-118540800	Weak transcription	Brain Cingulate Gyrus	brain
2	chr12:118501000-118540200	Weak transcription	HUVEC	blood vessel
3	chr12:118501000-118540800	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr12:118501000-118540800	Weak transcription	NH-A	brain
5	chr12:118501200-118540400	Weak transcription	Brain Germinal Matrix	brain
6	chr12:118501200-118540800	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr12:118501200-118541000	Weak transcription	Aorta	Aorta
8	chr12:118501600-118540400	Weak transcription	NHLF	lung
9	chr12:118502200-118540800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr12:118502200-118540800	Weak transcription	Brain Anterior Caudate	brain
11	chr12:118514600-118540400	Weak transcription	Fetal Heart	heart
12	chr12:118515800-118540800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr12:118515800-118540800	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr12:118517600-118540800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr12:118517600-118540800	Weak transcription	Stomach Smooth Muscle	stomach
16	chr12:118518600-118540800	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr12:118519000-118540400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr12:118519000-118540800	Weak transcription	Colon Smooth Muscle	Colon
19	chr12:118519400-118540600	Weak transcription	Rectal Smooth Muscle	rectum
20	chr12:118519600-118540200	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr12:118520200-118540600	Weak transcription	Liver	Liver
22	chr12:118528000-118540400	Weak transcription	Dnd41	blood
23	chr12:118528800-118540400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr12:118528800-118540800	Weak transcription	Lung	lung
25	chr12:118529000-118540600	Weak transcription	Spleen	Spleen
26	chr12:118529600-118540800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr12:118530400-118540400	Weak transcription	Fetal Lung	lung
28	chr12:118532000-118540400	Weak transcription	Ovary	ovary
29	chr12:118532600-118540800	Weak transcription	Brain Hippocampus Middle	brain
30	chr12:118533600-118540200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr12:118533600-118540400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr12:118533600-118540400	Weak transcription	Fetal Stomach	stomach
33	chr12:118536400-118540200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr12:118536400-118540600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr12:118536600-118540800	Weak transcription	Right Atrium	heart
36	chr12:118537000-118541000	Weak transcription	Gastric	stomach
37	chr12:118537000-118541000	Weak transcription	Small Intestine	intestine
38	chr12:118537400-118540800	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr12:118537600-118540400	Weak transcription	Fetal Intestine Small	intestine
40	chr12:118539600-118540200	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr12:118539600-118540200	Enhancers	Psoas Muscle	Psoas
42	chr12:118539600-118540400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr12:118539600-118540400	Enhancers	Colonic Mucosa	Colon
44	chr12:118539600-118540400	Enhancers	Pancreas	Pancrea
45	chr12:118539600-118540400	Enhancers	HMEC	breast
46	chr12:118539600-118540400	Enhancers	NHEK	skin
47	chr12:118539600-118540800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr12:118539600-118540800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr12:118539600-118540800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr12:118539600-118540800	Enhancers	Placenta	Placenta

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