Variant report

Variant	esv1353226
Chromosome Location	chr1:144533511-144533514
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:381)
CpG islands
(count:0)
Chromatin interactive
region (count:54)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:381 , 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	ARID3A	chr1:144532762-144534541	K562	blood:	n/a	n/a
2	ARID3A	chr1:144533334-144534462	HepG2	liver:	n/a	n/a
3	ATF1	chr1:144533100-144534496	K562	blood:	n/a	n/a
4	ATF2	chr1:144533212-144534565	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr1:144533459-144534584	GM12878	blood:	n/a	n/a
6	ATF2	chr1:144533382-144534573	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr1:144533458-144534609	GM12878	blood:	n/a	n/a
8	ATF3	chr1:144533095-144534612	K562	blood:	n/a	chr1:144533784-144533797 chr1:144533946-144533955 chr1:144533783-144533798
9	ATF3	chr1:144533135-144534621	A549	lung:	n/a	chr1:144533784-144533797 chr1:144533946-144533955 chr1:144533783-144533798
10	ATF3	chr1:144533311-144534469	A549	lung:	n/a	chr1:144533784-144533797 chr1:144533946-144533955 chr1:144533783-144533798
11	BACH1	chr1:144532785-144534560	K562	blood:	n/a	n/a
12	BACH1	chr1:144532809-144534499	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL3	chr1:144533245-144534596	A549	lung:	n/a	chr1:144533775-144533783
14	BCL3	chr1:144533414-144534775	K562	blood:	n/a	chr1:144533775-144533783
15	BCL3	chr1:144533167-144534598	A549	lung:	n/a	chr1:144533775-144533783
16	BCLAF1	chr1:144533324-144534619	GM12878	blood:	n/a	chr1:144533775-144533783
17	BCLAF1	chr1:144533122-144534615	K562	blood:	n/a	chr1:144533775-144533783
18	BCLAF1	chr1:144532781-144534769	K562	blood:	n/a	chr1:144533775-144533783
19	BHLHE40	chr1:144533305-144534550	GM12878	blood:	n/a	n/a
20	BHLHE40	chr1:144533242-144534538	K562	blood:	n/a	n/a
21	BHLHE40	chr1:144533255-144534490	HepG2	liver:	n/a	n/a
22	BRCA1	chr1:144533161-144534406	HepG2	liver:	n/a	n/a
23	BRCA1	chr1:144533309-144534465	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr1:144532555-144534695	K562	blood:	n/a	n/a
25	CBX3	chr1:144532664-144534621	K562	blood:	n/a	n/a
26	CBX3	chr1:144533427-144534452	HCT-116	colon:	n/a	n/a
27	CEBPB	chr1:144533447-144534520	HCT-116	colon:	n/a	n/a
28	CEBPB	chr1:144533478-144534551	K562	blood:	n/a	n/a
29	CEBPB	chr1:144533495-144534512	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr1:144532777-144534619	K562	blood:	n/a	chr1:144533148-144533159
31	CEBPB	chr1:144533417-144534515	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr1:144533329-144534661	GM12878	blood:	n/a	n/a
33	CEBPB	chr1:144533319-144534472	A549	lung:	n/a	n/a
34	CEBPD	chr1:144533386-144534576	K562	blood:	n/a	n/a
35	CEBPD	chr1:144533429-144534825	K562	blood:	n/a	n/a
36	CEBPD	chr1:144533474-144534437	HepG2	liver:	n/a	n/a
37	CHD2	chr1:144533467-144534489	Hela-S3	cervix:	n/a	chr1:144533773-144533780 chr1:144533947-144533957
38	CHD2	chr1:144533247-144534482	H1-hESC	embryonic stem cell:	n/a	chr1:144533773-144533780 chr1:144533947-144533957
39	CHD2	chr1:144533290-144534431	HepG2	liver:	n/a	chr1:144533773-144533780 chr1:144533947-144533957
40	CHD2	chr1:144533501-144534636	K562	blood:	n/a	chr1:144533773-144533780 chr1:144533947-144533957
41	CREB1	chr1:144533448-144534457	HepG2	liver:	n/a	chr1:144533784-144533797
42	CREB1	chr1:144533440-144534457	K562	blood:	n/a	chr1:144533784-144533797
43	CREB1	chr1:144533442-144534411	ECC-1	luminal epithelium:	n/a	chr1:144533784-144533797
44	CREB1	chr1:144533472-144534467	H1-hESC	embryonic stem cell:	n/a	chr1:144533784-144533797
45	CREB1	chr1:144533381-144534537	HepG2	liver:	n/a	chr1:144533784-144533797
46	CREB1	chr1:144533341-144534464	ECC-1	luminal epithelium:	n/a	chr1:144533784-144533797
47	CREB1	chr1:144533461-144534351	A549	lung:	n/a	chr1:144533784-144533797
48	CREB1	chr1:144533506-144534473	GM12878	blood:	n/a	chr1:144533784-144533797
49	CREB1	chr1:144533471-144534461	GM12878	blood:	n/a	chr1:144533784-144533797
50	CREB1	chr1:144533381-144534491	H1-hESC	embryonic stem cell:	n/a	chr1:144533784-144533797

No data

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:144519367..144521165-chr1:144533246..144535069,2	K562	blood:
2	chr1:144532823..144535244-chr1:149858258..149860447,2	K562	blood:
3	chr1:144532778..144535743-chr1:145042899..145044977,2	K562	blood:
4	chr1:144532824..144535385-chr1:148554860..148558437,3	K562	blood:
5	chr1:144532854..144535765-chr1:148603401..148605214,4	K562	blood:
6	chr1:17229738..17235929-chr1:144531729..144537089,21	K562	blood:
7	chr1:144530771..144535863-chr1:144988447..145007040,21	K562	blood:
8	chr1:144533449..144534234-chr6:16128957..16129770,2	NB4	blood:
9	chr1:144532662..144534458-chr1:147992705..147994526,2	K562	blood:
10	chr1:144532638..144534225-chr1:148240014..148241848,2	K562	blood:
11	chr1:21113288..21114044-chr1:144533309..144534299,4	Hela-S3	cervix:
12	chr1:144532970..144534328-chr1:149194157..149195181,24	Hela-S3	cervix:
13	chr1:17221575..17223414-chr1:144532305..144534142,2	K562	blood:
14	chr1:144530771..144535713-chr1:149191808..149196822,37	K562	blood:
15	chr1:144533498..144535527-chr14:56140284..56141806,2	K562	blood:
16	chr1:144533511..144534156-chr5:175815538..175816077,2	Hela-S3	cervix:
17	chr1:144532605..144534445-chr1:149782477..149783992,2	K562	blood:
18	chr1:144532709..144537146-chr1:146553385..146558827,17	K562	blood:
19	chr1:144532638..144535862-chr1:149213391..149217052,12	K562	blood:
20	chr1:144531583..144535759-chr1:149193159..149196806,32	K562	blood:
21	chr1:144532552..144536277-chr1:145382371..145384278,4	K562	blood:
22	chr1:144526974..144536279-chr1:149221211..149226185,98	K562	blood:
23	chr1:144531660..144535087-chr14:56140285..56143287,3	K562	blood:
24	chr1:144532574..144534383-chr1:150253333..150256090,2	K562	blood:
25	chr1:144532469..144535862-chr1:149213317..149216794,14	K562	blood:
26	chr1:144532552..144536277-chr1:145382371..145384454,4	K562	blood:
27	chr1:17221440..17223414-chr1:144532305..144534146,3	K562	blood:
28	chr1:144533458..144534448-chr1:149194159..149194696,17	HCT-116	colon:
29	chr1:144532556..144534353-chr1:147805518..147808374,3	K562	blood:
30	chr1:144531838..144533805-chr1:150206614..150208710,2	K562	blood:
31	chr1:17229738..17236634-chr1:144531729..144537089,21	K562	blood:
32	chr1:144532467..144535281-chr5:137799571..137801976,2	K562	blood:
33	chr1:144529973..144534952-chr1:149221200..149225268,6	MCF-7	breast:
34	chr1:144526732..144539178-chr1:149221186..149225476,28	MCF-7	breast:
35	chr1:120428374..120430929-chr1:144532739..144535945,3	K562	blood:
36	chr1:144532746..144535679-chr1:148240132..148243070,2	K562	blood:
37	chr1:144530904..144535858-chr1:144986921..144991934,7	K562	blood:
38	chr1:144532760..144535263-chr22:43009936..43012552,2	K562	blood:
39	chr1:144532329..144535680-chr1:145012343..145016063,5	K562	blood:
40	chr1:144533506..144534133-chr11:72524969..72526154,3	Hela-S3	cervix:
41	chr1:144533169..144534313-chr11:65266374..65267027,4	Hela-S3	cervix:
42	chr1:45187271..45188987-chr1:144532926..144535604,2	K562	blood:
43	chr1:144532828..144535619-chr1:148602130..148606442,4	K562	blood:
44	chr1:144531278..144537146-chr1:146553717..146557612,11	K562	blood:
45	chr1:144533474..144535721-chr1:145039954..145042434,2	K562	blood:
46	chr1:144532329..144536270-chr1:145012343..145016063,6	K562	blood:
47	chr1:144532285..144535839-chr1:144994993..144998864,6	K562	blood:
48	chr1:144527325..144537192-chr1:149221188..149227183,106	K562	blood:
49	chr1:144532673..144535225-chr1:149604575..149607265,3	K562	blood:
50	chr1:144531697..144534436-chr1:149784086..149786783,2	K562	blood:

No data

Variant related genes	Relation type
RNU1-59P	TF binding region
ENSG00000207501	chromatin interactions
ENSG00000242663	chromatin interactions
ENSG00000007944	chromatin interactions
ENSG00000143401	chromatin interactions
ENSG00000146066	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000212456	chromatin interactions
ENSG00000272426	chromatin interactions
ENSG00000127483	chromatin interactions
ENSG00000268172	chromatin interactions
ENSG00000199377	chromatin interactions
ENSG00000236943	chromatin interactions
ENSG00000207005	chromatin interactions
ENSG00000048162	chromatin interactions
ENSG00000159208	chromatin interactions
ENSG00000251562	chromatin interactions
ENSG00000207349	chromatin interactions
ENSG00000232956	chromatin interactions
ENSG00000184270	chromatin interactions
ENSG00000202408	chromatin interactions
ENSG00000223380	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000230832	chromatin interactions
ENSG00000269501	chromatin interactions
ENSG00000178104	chromatin interactions
ENSG00000126777	chromatin interactions
ENSG00000252656	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000203814	chromatin interactions
ENSG00000178096	chromatin interactions
ENSG00000120738	chromatin interactions
ENSG00000168010	chromatin interactions
ENSG00000252826	chromatin interactions
ENSG00000232151	chromatin interactions
ENSG00000100227	chromatin interactions
ENSG00000196544	chromatin interactions
ENSG00000183598	chromatin interactions
ENSG00000243452	chromatin interactions
ENSG00000226446	chromatin interactions
ENSG00000202496	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000207205	chromatin interactions
ENSG00000270022	chromatin interactions

Extended variants
information (count: 2 )
Associated
traits (count: 165 )

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs66523280	chr1:144533512-144533513	Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	43 gene(s)	Overlapped CNVs	n/a
2	rs10596116	chr1:144533514-144533515	Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	44 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:165)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Williams Syndrome	20824207	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	18522746	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Cancer	17440070	CNVD

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144528800-144533800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:144529400-144533800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:144530800-144533600	Strong transcription	HSMM	muscle
4	chr1:144532800-144533800	Flanking Active TSS	K562	blood
5	chr1:144532800-144534400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr1:144532800-144534600	ZNF genes & repeats	Spleen	Spleen
7	chr1:144532800-144534800	ZNF genes & repeats	Right Atrium	heart
8	chr1:144533000-144533600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr1:144533000-144533600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr1:144533000-144533600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
11	chr1:144533000-144533600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
12	chr1:144533000-144533600	Flanking Active TSS	Brain Anterior Caudate	brain
13	chr1:144533000-144534200	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
14	chr1:144533000-144534400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr1:144533200-144533600	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:144533200-144533600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
17	chr1:144533200-144533600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
18	chr1:144533200-144533600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
19	chr1:144533200-144533600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
20	chr1:144533200-144533600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
21	chr1:144533200-144533600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr1:144533200-144533600	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr1:144533200-144533600	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
24	chr1:144533200-144533600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr1:144533200-144533600	Flanking Bivalent TSS/Enh	Liver	Liver
26	chr1:144533200-144533600	Flanking Active TSS	Brain Angular Gyrus	brain
27	chr1:144533200-144533600	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain
28	chr1:144533200-144533600	Flanking Active TSS	Brain Substantia Nigra	brain
29	chr1:144533200-144533600	Flanking Bivalent TSS/Enh	Colon Smooth Muscle	Colon
30	chr1:144533200-144533600	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
31	chr1:144533200-144533600	Flanking Bivalent TSS/Enh	Fetal Heart	heart
32	chr1:144533200-144533600	Flanking Active TSS	A549	lung
33	chr1:144533200-144533600	Flanking Active TSS	Hela-S3	cervix
34	chr1:144533200-144533800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
35	chr1:144533200-144533800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr1:144533200-144533800	Flanking Active TSS	Fetal Brain Female	brain
37	chr1:144533200-144533800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
38	chr1:144533200-144534000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr1:144533200-144534000	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr1:144533200-144534000	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr1:144533200-144534000	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
42	chr1:144533200-144534200	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
43	chr1:144533200-144534200	Flanking Active TSS	HMEC	breast
44	chr1:144533200-144534200	Bivalent/Poised TSS	Osteobl	bone
45	chr1:144533200-144534400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
46	chr1:144533200-144534400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
47	chr1:144533200-144534400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
48	chr1:144533200-144534400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
49	chr1:144533200-144534400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr1:144533200-144534400	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain

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