Variant report

Variant	nsv973021
Chromosome Location	chr12:9389409-9393436
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:80)
CpG islands
(count:306)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:80 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr12:9389926-9390245	Hela-S3	cervix:	n/a	chr12:9390075-9390086
2	CTCF	chr12:9392766-9392829	Lung_OC	lung:	n/a	n/a
3	CTCF	chr12:9390880-9391030	GM12872	blood:	n/a	n/a
4	CTCF	chr12:9392708-9392771	Fibrobl	skin:	n/a	n/a
5	CTCF	chr12:9392680-9392830	GM12871	blood:	n/a	n/a
6	EBF1	chr12:9392318-9392638	GM12878	blood:	n/a	n/a
7	EBF1	chr12:9392346-9392678	GM12878	blood:	n/a	n/a
8	FOS	chr12:9389873-9390328	MCF10A-Er-Src	breast:	n/a	chr12:9390209-9390218
9	FOS	chr12:9389873-9390313	MCF10A-Er-Src	breast:	n/a	chr12:9390209-9390218
10	FOS	chr12:9389875-9390358	MCF10A-Er-Src	breast:	n/a	chr12:9390209-9390218
11	FOS	chr12:9389891-9390311	MCF10A-Er-Src	breast:	n/a	chr12:9390209-9390218
12	GTF3C2	chr12:9389804-9390163	Hela-S3	cervix:	n/a	n/a
13	HEY1	chr12:9392740-9393099	HepG2	liver:	n/a	n/a
14	HEY1	chr12:9392818-9393079	K562	blood:	n/a	n/a
15	HEY1	chr12:9392817-9393063	HepG2	liver:	n/a	n/a
16	HEY1	chr12:9392805-9393070	K562	blood:	n/a	n/a
17	HEY1	chr12:9391846-9392081	K562	blood:	n/a	n/a
18	HEY1	chr12:9392345-9392663	K562	blood:	n/a	n/a
19	JUND	chr12:9389999-9390151	HepG2	liver:	n/a	chr12:9390048-9390059
20	JUND	chr12:9389889-9390261	Hela-S3	cervix:	n/a	chr12:9390048-9390059 chr12:9390209-9390218
21	PAX5	chr12:9392343-9392615	GM12878	blood:	n/a	n/a
22	POLR2A	chr12:9392239-9393195	GM12892	blood:	n/a	n/a
23	POLR2A	chr12:9391779-9392735	GM12878	blood:	n/a	n/a
24	POLR2A	chr12:9392808-9393096	GM12878	blood:	n/a	n/a
25	POLR2A	chr12:9392773-9393141	GM12891	blood:	n/a	n/a
26	POLR2A	chr12:9392854-9393111	U87	brain:	n/a	n/a
27	POLR2A	chr12:9392324-9392712	GM12891	blood:	n/a	n/a
28	POLR2A	chr12:9392760-9393164	GM12891	blood:	n/a	n/a
29	POLR2A	chr12:9392807-9392837	A549	lung:	n/a	n/a
30	POLR2A	chr12:9392739-9393109	SK-N-MC	brain:	n/a	n/a
31	POLR2A	chr12:9392612-9393072	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr12:9392262-9393245	GM12892	blood:	n/a	n/a
33	POLR2A	chr12:9391852-9392168	GM12891	blood:	n/a	n/a
34	POLR2A	chr12:9392688-9393105	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr12:9392661-9393190	GM12892	blood:	n/a	n/a
36	POLR2A	chr12:9392745-9393086	GM12891	blood:	n/a	n/a
37	POLR2A	chr12:9391850-9392298	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr12:9392740-9393114	GM12878	blood:	n/a	n/a
39	POLR2A	chr12:9392360-9392580	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr12:9392395-9392554	GM12878	blood:	n/a	n/a
41	POLR2A	chr12:9392810-9393108	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr12:9392176-9392328	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr12:9392855-9392937	A549	lung:	n/a	n/a
44	POLR2A	chr12:9392359-9392659	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr12:9391816-9393165	GM12878	blood:	n/a	n/a
46	POLR2A	chr12:9392836-9393081	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr12:9392307-9392664	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr12:9392770-9393104	GM12878	blood:	n/a	n/a
49	POLR2A	chr12:9392720-9392896	GM12878	blood:	n/a	n/a
50	POLR2A	chr12:9392849-9393057	A549	lung:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9389499-9389549	Hela-S3	cervix:	n/a
2	chr12:9389499-9389549	Hela-S3	cervix:	n/a
3	chr12:9392651-9392701	NT2-D1	testis:	n/a
4	chr12:9391348-9391398	IMR90	lung:	fetal
5	chr12:9389499-9389549	T-47D	breast:	n/a
6	chr12:9392948-9392998	LNCaP	prostate:	n/a
7	chr12:9392651-9392701	NHBE	bronchial:	n/a
8	chr12:9392948-9392998	AG09309	skin:	n/a
9	chr12:9392847-9392897	HEEpiC	esophagus:	n/a
10	chr12:9391348-9391398	ovcar-3	ovarian:	n/a
11	chr12:9392847-9392897	GM06990	blood:	n/a
12	chr12:9389499-9389549	AoSMC	blood vessel:	n/a
13	chr12:9392948-9392998	AG04449	skin:	fetal
14	chr12:9389499-9389549	Jurkat	blood:	n/a
15	chr12:9391348-9391398	PANC-1	pancreas:	n/a
16	chr12:9392948-9392998	MCF10A-Er-Src	breast:	n/a
17	chr12:9391348-9391398	GM12878	blood:	n/a
18	chr12:9392948-9392998	HRCEpiC	kidney:	n/a
19	chr12:9392948-9392998	GM06990	blood:	n/a
20	chr12:9392651-9392701	Hepatocyte	liver:	n/a
21	chr12:9392847-9392897	HMEC	breast:	n/a
22	chr12:9391348-9391398	AG10803	skin:	n/a
23	chr12:9392651-9392701	BJ	skin:	n/a
24	chr12:9391348-9391398	AG09309	skin:	n/a
25	chr12:9392651-9392701	AoSMC	blood vessel:	n/a
26	chr12:9392651-9392701	SK-N-MC	brain:	n/a
27	chr12:9392948-9392998	HCF	heart:	n/a
28	chr12:9392651-9392701	H1-hESC	embryonic stem cell:	embryo
29	chr12:9389499-9389549	HMEC	breast:	n/a
30	chr12:9392948-9392998	GM19239	blood:	n/a
31	chr12:9392651-9392701	HRE	kidney:	n/a
32	chr12:9392847-9392897	SK-N-SH_RA	brain:	n/a
33	chr12:9392948-9392998	ovcar-3	ovarian:	n/a
34	chr12:9392948-9392998	IMR90	lung:	fetal
35	chr12:9389499-9389549	HRCEpiC	kidney:	n/a
36	chr12:9392651-9392701	NH-A	brain:	n/a
37	chr12:9392651-9392701	HCT-116	colon:	n/a
38	chr12:9392948-9392998	SK-N-SH	brain:	n/a
39	chr12:9391348-9391398	SKMC	muscle:	n/a
40	chr12:9392651-9392701	GM12891	blood:	n/a
41	chr12:9392651-9392701	ProgFib	skin:	n/a
42	chr12:9391348-9391398	AG04450	lung:	fetal
43	chr12:9392847-9392897	HCPEpiC	choroid plexus:	n/a
44	chr12:9391348-9391398	HCPEpiC	choroid plexus:	n/a
45	chr12:9389499-9389549	HCM	heart:	n/a
46	chr12:9392948-9392998	HIPEpiC	eye:	n/a
47	chr12:9389499-9389549	H1-hESC	embryonic stem cell:	embryo
48	chr12:9392948-9392998	AoSMC	blood vessel:	n/a
49	chr12:9392847-9392897	NHDF-neo	bronchial:	n/a
50	chr12:9392847-9392897	HIPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:9389499..9391072-chr12:9394393..9395954,2	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1244	chr12:9392068-9392093	MIMAT0005896

No data

Variant related genes	Relation type
A2MP1	TF binding region
PTMAP4	TF binding region
LINC00987	TF binding region
A2MP1	CpG island
PTMAP4	CpG island
LINC00987	CpG island

Extended variants
information (count: 85 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:85 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs137946625	chr12:9389563-9389564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs561933349	chr12:9389567-9389568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192887298	chr12:9389698-9389699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184325654	chr12:9389709-9389710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188280814	chr12:9389748-9389749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs369603811	chr12:9389781-9389782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs60195182	chr12:9389836-9389837	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs142483868	chr12:9389845-9389846	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs531674839	chr12:9389871-9389872	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs532407431	chr12:9389941-9389942	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs145964181	chr12:9389976-9389977	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs148624578	chr12:9389984-9389985	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs372127765	chr12:9390016-9390017	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs374767149	chr12:9390273-9390274	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs12303039	chr12:9390298-9390299	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs568380504	chr12:9390442-9390443	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs180689803	chr12:9390522-9390523	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs571341013	chr12:9390524-9390525	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs538323339	chr12:9390534-9390535	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs554171073	chr12:9390541-9390542	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs113977753	chr12:9390704-9390705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142037664	chr12:9390716-9390717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs60979104	chr12:9390797-9390798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs34363	chr12:9390857-9390858	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs540076034	chr12:9390875-9390876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs34641190	chr12:9390960-9390961	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs150801242	chr12:9390970-9390971	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs139183277	chr12:9391000-9391001	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs145257057	chr12:9391044-9391045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556779474	chr12:9391101-9391102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs185341987	chr12:9391323-9391324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112504912	chr12:9391384-9391385	Weak transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
33	rs182198489	chr12:9391397-9391398	Weak transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
34	rs11838025	chr12:9391411-9391412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs544345619	chr12:9391426-9391427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186870809	chr12:9391443-9391444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191725116	chr12:9391479-9391480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183236234	chr12:9391482-9391483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185650252	chr12:9391487-9391488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535342635	chr12:9391730-9391731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371886212	chr12:9391897-9391898	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs374519075	chr12:9391898-9391899	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs35672108	chr12:9391919-9391920	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs55634098	chr12:9391979-9391980	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs200023669	chr12:9392055-9392056	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs367702648	chr12:9392072-9392073	Weak transcription	TF binding region miRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs372637179	chr12:9392095-9392096	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs377261732	chr12:9392128-9392129	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs34364	chr12:9392205-9392206	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs142155565	chr12:9392216-9392217	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Breast cancer	17133270	CNVD
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
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:155 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9374400-9392600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr12:9376200-9392600	Weak transcription	Primary T cells from cord blood	blood
3	chr12:9383400-9392600	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr12:9383800-9392600	Weak transcription	Left Ventricle	heart
5	chr12:9387000-9392600	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr12:9388400-9392600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr12:9390200-9390400	Enhancers	HepG2	liver
8	chr12:9390600-9393400	Weak transcription	HepG2	liver
9	chr12:9390800-9391200	Enhancers	Adipose Nuclei	Adipose
10	chr12:9391200-9392600	Weak transcription	Adipose Nuclei	Adipose
11	chr12:9392600-9393000	Active TSS	Primary monocytes fromperipheralblood	blood
12	chr12:9392600-9393000	Active TSS	Primary B cells from cord blood	blood
13	chr12:9392600-9393000	Active TSS	Primary B cells from peripheral blood	blood
14	chr12:9392600-9393000	Active TSS	Primary T cells fromperipheralblood	blood
15	chr12:9392600-9393000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
16	chr12:9392600-9393000	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
17	chr12:9392600-9393000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
18	chr12:9392600-9393000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr12:9392600-9393000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr12:9392600-9393000	Active TSS	Cortex derived primary cultured neurospheres	brain
21	chr12:9392600-9393000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr12:9392600-9393000	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
23	chr12:9392600-9393000	Active TSS	Brain Germinal Matrix	brain
24	chr12:9392600-9393000	Active TSS	Fetal Thymus	thymus
25	chr12:9392600-9393200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr12:9392600-9393200	Active TSS	Primary T helper naive cells from peripheral blood	blood
27	chr12:9392600-9393200	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
28	chr12:9392600-9393200	Active TSS	Primary T helper cells PMA-I stimulated	--
29	chr12:9392600-9393200	Active TSS	Primary T helper cells fromperipheralblood	blood
30	chr12:9392600-9393200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
31	chr12:9392600-9393200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr12:9392600-9393200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr12:9392600-9393200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr12:9392600-9393200	Active TSS	Esophagus	oesophagus
35	chr12:9392600-9393200	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
36	chr12:9392600-9393200	Active TSS	Fetal Kidney	kidney
37	chr12:9392600-9393200	Active TSS	Fetal Lung	lung
38	chr12:9392600-9393200	Active TSS	Lung	lung
39	chr12:9392600-9393200	Active TSS	Pancreas	Pancrea
40	chr12:9392600-9393200	Active TSS	Psoas Muscle	Psoas
41	chr12:9392600-9393200	Active TSS	Rectal Mucosa Donor 31	rectum
42	chr12:9392600-9393200	Active TSS	Right Ventricle	heart
43	chr12:9392600-9393200	Active TSS	Skeletal Muscle Female	skeletal muscle
44	chr12:9392600-9393400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr12:9392600-9393400	Active TSS	Primary T cells from cord blood	blood
46	chr12:9392600-9393400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
47	chr12:9392600-9393400	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr12:9392600-9393400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr12:9392600-9393400	Active TSS	Liver	Liver
50	chr12:9392600-9393400	Active TSS	Brain Substantia Nigra	brain

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