Variant report

Variant	esv18643
Chromosome Location	chr12:118499231-118500113
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:118499313-118499469	HepG2	liver:	n/a	n/a
2	ATF2	chr12:118499805-118500513	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr12:118499702-118500613	A549	lung:	n/a	n/a
4	BHLHE40	chr12:118498966-118499934	K562	blood:	n/a	n/a
5	BHLHE40	chr12:118498816-118499605	GM12878	blood:	n/a	n/a
6	BRCA1	chr12:118499462-118499467	GM12878	blood:	n/a	n/a
7	CBX3	chr12:118499675-118500583	K562	blood:	n/a	n/a
8	CCNT2	chr12:118499778-118500178	K562	blood:	n/a	n/a
9	CEBPD	chr12:118498842-118499509	K562	blood:	n/a	n/a
10	CEBPD	chr12:118498939-118499437	K562	blood:	n/a	n/a
11	CHD1	chr12:118499841-118500826	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD1	chr12:118499070-118499918	GM12878	blood:	n/a	chr12:118499202-118499212
13	CHD1	chr12:118499207-118499605	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr12:118499081-118499584	GM12878	blood:	n/a	chr12:118499202-118499212
15	CHD2	chr12:118499815-118500344	K562	blood:	n/a	n/a
16	CHD2	chr12:118498584-118500446	Hela-S3	cervix:	n/a	chr12:118499202-118499212
17	CHD2	chr12:118499282-118499492	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTBP2	chr12:118499801-118500695	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr12:118499889-118499917	GM12891	blood:	n/a	n/a
20	CTCF	chr12:118499100-118499250	GM12864	blood:	n/a	n/a
21	CTCF	chr12:118499840-118500110	SK-N-SH_RA	brain:	n/a	n/a
22	CTCF	chr12:118499940-118500090	AG10803	skin:	n/a	n/a
23	CUX1	chr12:118499921-118500334	K562	blood:	n/a	n/a
24	CUX1	chr12:118499344-118499436	K562	blood:	n/a	n/a
25	E2F4	chr12:118498915-118500652	K562	blood:	n/a	chr12:118499157-118499166 chr12:118500198-118500209 chr12:118499582-118499594 chr12:118499157-118499169
26	E2F4	chr12:118499521-118499680	MCF10A-Er-Src	breast:	n/a	chr12:118499582-118499594
27	E2F4	chr12:118499891-118500285	MCF10A-Er-Src	breast:	n/a	chr12:118500198-118500209
28	E2F6	chr12:118499874-118500425	A549	lung:	n/a	n/a
29	E2F6	chr12:118499831-118500548	A549	lung:	n/a	n/a
30	E2F6	chr12:118499440-118499576	K562	blood:	n/a	n/a
31	EBF1	chr12:118499367-118499518	GM12878	blood:	n/a	chr12:118499372-118499383
32	EGR1	chr12:118498798-118499312	MCF-7	breast:	n/a	chr12:118499152-118499165 chr12:118499152-118499165 chr12:118499200-118499210 chr12:118499155-118499164 chr12:118498949-118498963
33	EGR1	chr12:118498765-118499238	ECC-1	luminal epithelium:	n/a	chr12:118499152-118499165 chr12:118499152-118499165 chr12:118499200-118499210 chr12:118499155-118499164 chr12:118498949-118498963
34	EGR1	chr12:118498496-118499307	K562	blood:	n/a	chr12:118499152-118499165 chr12:118499152-118499165 chr12:118499200-118499210 chr12:118499155-118499164 chr12:118498949-118498963
35	EGR1	chr12:118498128-118499513	HCT-116	colon:	n/a	chr12:118499152-118499165 chr12:118499152-118499165 chr12:118498367-118498381 chr12:118499200-118499210 chr12:118499155-118499164 chr12:118498949-118498963
36	EGR1	chr12:118499593-118500075	K562	blood:	n/a	chr12:118499656-118499669 chr12:118499834-118499847 chr12:118499655-118499670
37	EGR1	chr12:118498144-118499441	K562	blood:	n/a	chr12:118499152-118499165 chr12:118499152-118499165 chr12:118498367-118498381 chr12:118499200-118499210 chr12:118499155-118499164 chr12:118498949-118498963
38	EGR1	chr12:118498787-118499538	H1-hESC	embryonic stem cell:	n/a	chr12:118499152-118499165 chr12:118499152-118499165 chr12:118499200-118499210 chr12:118499155-118499164 chr12:118498949-118498963
39	ELF1	chr12:118499689-118500338	GM12878	blood:	n/a	n/a
40	ELF1	chr12:118499698-118500255	K562	blood:	n/a	n/a
41	ELF1	chr12:118499674-118500039	A549	lung:	n/a	n/a
42	ELF1	chr12:118498748-118499632	GM12878	blood:	n/a	n/a
43	ELK1	chr12:118499969-118500169	K562	blood:	n/a	n/a
44	ELK1	chr12:118499206-118499361	K562	blood:	n/a	n/a
45	ELK1	chr12:118499294-118499406	GM12878	blood:	n/a	n/a
46	EP300	chr12:118499453-118500114	GM12878	blood:	n/a	n/a
47	EP300	chr12:118499744-118500136	K562	blood:	n/a	n/a
48	EP300	chr12:118499045-118499433	K562	blood:	n/a	n/a
49	ETS1	chr12:118499891-118500454	A549	lung:	n/a	n/a
50	GABPA	chr12:118498796-118499411	SK-N-SH	brain:	n/a	chr12:118499157-118499166

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:118499294-118499344	PANC-1	pancreas:	n/a
2	chr12:118499723-118499773	ProgFib	skin:	n/a
3	chr12:118499294-118499344	HepG2	liver:	n/a
4	chr12:118499723-118499773	AoSMC	blood vessel:	n/a
5	chr12:118499294-118499344	GM12878	blood:	n/a
6	chr12:118499294-118499344	NHBE	bronchial:	n/a
7	chr12:118499294-118499344	HRE	kidney:	n/a
8	chr12:118499294-118499344	BJ	skin:	n/a
9	chr12:118499723-118499773	BJ	skin:	n/a
10	chr12:118499723-118499773	U87	brain:	n/a
11	chr12:118499723-118499773	PrEC	prostate:	n/a
12	chr12:118499723-118499773	HAEpiC	amniotic membrane:	n/a
13	chr12:118499294-118499344	HRCEpiC	kidney:	n/a
14	chr12:118499723-118499773	BE2_C	brain:	n/a
15	chr12:118499723-118499773	MCF10A-Er-Src	breast:	n/a
16	chr12:118499723-118499773	SK-N-SH_RA	brain:	n/a
17	chr12:118499294-118499344	AoSMC	blood vessel:	n/a
18	chr12:118499723-118499773	NT2-D1	testis:	n/a
19	chr12:118499723-118499773	PFSK-1	brain:	n/a
20	chr12:118499723-118499773	IMR90	lung:	fetal
21	chr12:118499723-118499773	SKMC	muscle:	n/a
22	chr12:118499723-118499773	AG09319	gingival:	n/a
23	chr12:118499294-118499344	HPAEpiC	pulmonary alveolar:	n/a
24	chr12:118499723-118499773	SK-N-SH	brain:	n/a
25	chr12:118499294-118499344	GM06990	blood:	n/a
26	chr12:118499723-118499773	ECC-1	luminal epithelium:	n/a
27	chr12:118499294-118499344	NH-A	brain:	n/a
28	chr12:118499723-118499773	HCF	heart:	n/a
29	chr12:118499723-118499773	HPAEpiC	pulmonary alveolar:	n/a
30	chr12:118499723-118499773	RPTEC	kidney:	n/a
31	chr12:118499294-118499344	HIPEpiC	eye:	n/a
32	chr12:118499723-118499773	GM12892	blood:	n/a
33	chr12:118499723-118499773	NHDF-neo	bronchial:	n/a
34	chr12:118499294-118499344	SK-N-SH_RA	brain:	n/a
35	chr12:118499723-118499773	HEK293	kidney:	embryo
36	chr12:118499294-118499344	NHDF-neo	bronchial:	n/a
37	chr12:118499294-118499344	HMEC	breast:	n/a
38	chr12:118499723-118499773	GM12878	blood:	n/a
39	chr12:118499294-118499344	SKMC	muscle:	n/a
40	chr12:118499294-118499344	GM12892	blood:	n/a
41	chr12:118499294-118499344	T-47D	breast:	n/a
42	chr12:118499294-118499344	ovcar-3	ovarian:	n/a
43	chr12:118499294-118499344	SAEC	small airway:	n/a
44	chr12:118499294-118499344	HEK293	kidney:	embryo
45	chr12:118499294-118499344	HEEpiC	esophagus:	n/a
46	chr12:118499294-118499344	NB4	blood:	n/a
47	chr12:118499294-118499344	Caco-2	colon:	n/a
48	chr12:118499723-118499773	Hela-S3	cervix:	n/a
49	chr12:118499723-118499773	HNPCEpiC	eye:	n/a
50	chr12:118499294-118499344	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chr11:65193091..65193924-chr12:118499181..118499883,2	Hela-S3	cervix:
2	chr12:118499104..118499911-chr2:28614266..28615159,2	Hela-S3	cervix:
3	chr12:118498692..118501195-chr12:118558625..118560440,2	MCF-7	breast:
4	chr10:33623927..33624428-chr12:118499255..118500110,2	Hela-S3	cervix:
5	chr12:118498235..118500819-chr9:19378763..19380360,2	MCF-7	breast:
6	chr1:109642248..109642947-chr12:118498776..118499544,2	Hela-S3	cervix:
7	chr12:118450883..118457954-chr12:118495063..118502199,13	K562	blood:
8	chr12:118453031..118454691-chr12:118496978..118499714,2	K562	blood:
9	chr12:118499217..118500774-chr12:118572851..118574591,2	MCF-7	breast:
10	chr12:118499092..118500000-chr6:30524301..30524884,2	Hela-S3	cervix:
11	chr12:118497389..118502867-chr12:118535601..118543920,23	MCF-7	breast:
12	chr12:118498119..118500024-chr12:118572981..118575568,2	K562	blood:
13	chr12:118498416..118504096-chr12:118537510..118543393,12	MCF-7	breast:
14	chr12:118496436..118502396-chr12:118572063..118576805,10	MCF-7	breast:
15	chr12:118499112..118499998-chr19:39902716..39903531,2	Hela-S3	cervix:

Variant related genes	Relation type
WSB2	TF binding region
WSB2	CpG island
ENSG00000176834	chromatin interactions
ENSG00000270066	chromatin interactions
ENSG00000137154	chromatin interactions
ENSG00000090924	chromatin interactions
ENSG00000111445	chromatin interactions
ENSG00000099250	chromatin interactions
ENSG00000204576	chromatin interactions
ENSG00000089220	chromatin interactions

Extended variants
information (count: 30 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7484410	chr12:118499251-118499252	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs540621991	chr12:118499254-118499255	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs112890460	chr12:118499255-118499256	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs79950936	chr12:118499274-118499275	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs145096561	chr12:118499320-118499321	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs138986796	chr12:118499340-118499341	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs552923602	chr12:118499362-118499363	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs60432513	chr12:118499386-118499387	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs374294553	chr12:118499436-118499437	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs552118289	chr12:118499488-118499489	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs60550237	chr12:118499494-118499495	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	mRNA abundance
12	rs118101112	chr12:118499497-118499498	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs111860506	chr12:118499499-118499500	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs550724850	chr12:118499598-118499599	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs148182603	chr12:118499630-118499631	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs567622902	chr12:118499682-118499683	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs142029014	chr12:118499710-118499711	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs556592808	chr12:118499784-118499785	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs576488518	chr12:118499802-118499803	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs539214663	chr12:118499808-118499809	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs71452629	chr12:118499834-118499835	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs558772930	chr12:118499876-118499877	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs572310544	chr12:118499901-118499902	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs541287831	chr12:118499940-118499941	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs77531942	chr12:118499956-118499957	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs190284903	chr12:118500035-118500036	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs543082034	chr12:118500053-118500054	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs74803373	chr12:118500057-118500058	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs146334925	chr12:118500058-118500059	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs139226769	chr12:118500063-118500064	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 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:178 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118496800-118501600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr12:118497000-118499800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr12:118497000-118500400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr12:118497000-118501000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr12:118497000-118501000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr12:118497200-118500400	Active TSS	HSMMtube	muscle
7	chr12:118497200-118500800	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr12:118497200-118501200	Active TSS	H1 Cell Line	embryonic stem cell
9	chr12:118497400-118500000	Active TSS	NHLF	lung
10	chr12:118497400-118500600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr12:118497400-118500600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr12:118497400-118500600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr12:118497400-118500600	Active TSS	Fetal Intestine Large	intestine
14	chr12:118497400-118501000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
15	chr12:118497400-118501000	Active TSS	H9 Cell Line	embryonic stem cell
16	chr12:118497400-118501000	Active TSS	Aorta	Aorta
17	chr12:118497400-118501000	Active TSS	Brain Inferior Temporal Lobe	brain
18	chr12:118497400-118501200	Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr12:118497400-118501400	Active TSS	iPS-15b Cell Line	embryonic stem cell
20	chr12:118497600-118500000	Active TSS	Fetal Muscle Trunk	muscle
21	chr12:118497600-118500600	Active TSS	Psoas Muscle	Psoas
22	chr12:118497600-118500800	Active TSS	Esophagus	oesophagus
23	chr12:118497600-118500800	Active TSS	Left Ventricle	heart
24	chr12:118497600-118501400	Active TSS	HUES64 Cell Line	embryonic stem cell
25	chr12:118497800-118500000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr12:118497800-118500400	Active TSS	Fetal Stomach	stomach
27	chr12:118497800-118500400	Active TSS	Lung	lung
28	chr12:118497800-118500600	Active TSS	Fetal Intestine Small	intestine
29	chr12:118497800-118500800	Active TSS	Brain Hippocampus Middle	brain
30	chr12:118497800-118500800	Active TSS	Fetal Kidney	kidney
31	chr12:118497800-118500800	Active TSS	Ovary	ovary
32	chr12:118497800-118501000	Active TSS	Duodenum Smooth Muscle	Duodenum
33	chr12:118497800-118501200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr12:118498000-118500000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr12:118498000-118500000	Active TSS	HSMM	muscle
36	chr12:118498000-118500400	Active TSS	Muscle Satellite Cultured Cells	--
37	chr12:118498000-118500400	Active TSS	Gastric	stomach
38	chr12:118498000-118500600	Active TSS	Brain Cingulate Gyrus	brain
39	chr12:118498000-118500600	Active TSS	Thymus	Thymus
40	chr12:118498000-118500600	Active TSS	NHDF-Ad	bronchial
41	chr12:118498000-118500800	Active TSS	Pancreas	Pancrea
42	chr12:118498000-118500800	Active TSS	HepG2	liver
43	chr12:118498000-118501000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr12:118498000-118501000	Active TSS	Brain Angular Gyrus	brain
45	chr12:118498000-118501000	Active TSS	Small Intestine	intestine
46	chr12:118498000-118501000	Active TSS	Stomach Smooth Muscle	stomach
47	chr12:118498000-118501200	Active TSS	iPS-18 Cell Line	embryonic stem cell
48	chr12:118498200-118499800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr12:118498200-118499800	Active TSS	Skeletal Muscle Male	skeletal muscle
50	chr12:118498200-118499800	Active TSS	HMEC	breast

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