Variant report

Variant	esv3435334
Chromosome Location	chr1:228401150-228401577
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:399)
CpG islands
(count:183)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:399 , 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	ATF3	chr1:228401191-228401451	K562	blood:	n/a	n/a
2	BACH1	chr1:228401243-228401328	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr1:228401080-228401459	A549	lung:	n/a	n/a
4	BCLAF1	chr1:228401157-228401400	GM12878	blood:	n/a	n/a
5	BHLHE40	chr1:228401158-228401469	K562	blood:	n/a	n/a
6	BHLHE40	chr1:228401203-228401535	GM12878	blood:	n/a	n/a
7	BRCA1	chr1:228401265-228401396	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr1:228401247-228401364	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr1:228401269-228401307	GM12878	blood:	n/a	n/a
10	CBX3	chr1:228401095-228401450	K562	blood:	n/a	n/a
11	CBX3	chr1:228401045-228401572	K562	blood:	n/a	n/a
12	CCNT2	chr1:228401152-228401498	K562	blood:	n/a	n/a
13	CEBPB	chr1:228401196-228401409	A549	lung:	n/a	n/a
14	CEBPB	chr1:228401243-228401395	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr1:228401206-228401485	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr1:228401189-228401413	IMR90	lung:	n/a	n/a
17	CEBPB	chr1:228401282-228401391	K562	blood:	n/a	n/a
18	CHD1	chr1:228400776-228401951	IMR90	lung:	n/a	n/a
19	CHD2	chr1:228401212-228401551	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr1:228401228-228401428	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr1:228401212-228401376	K562	blood:	n/a	n/a
22	CREB1	chr1:228401077-228401473	A549	lung:	n/a	n/a
23	CREB1	chr1:228400704-228401652	K562	blood:	n/a	n/a
24	CREB1	chr1:228400960-228401650	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr1:228401066-228401635	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr1:228401188-228401429	A549	lung:	n/a	n/a
27	CREB1	chr1:228401171-228401649	GM12878	blood:	n/a	n/a
28	CTCF	chr1:228401240-228401390	K562	blood:	n/a	n/a
29	CTCF	chr1:228400942-228401707	A549	lung:	n/a	n/a
30	CTCF	chr1:228400930-228401753	SK-N-SH	brain:	n/a	n/a
31	CTCF	chr1:228401203-228401483	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr1:228401260-228401410	GM12866	blood:	n/a	n/a
33	CTCF	chr1:228401280-228401430	GM12870	blood:	n/a	n/a
34	CTCF	chr1:228401225-228401480	Lung_OC	lung:	n/a	n/a
35	CTCF	chr1:228401280-228401430	HMEC	breast:	n/a	n/a
36	CTCF	chr1:228401280-228401430	HRE	kidney:	n/a	n/a
37	CTCF	chr1:228401300-228401450	GM12872	blood:	n/a	n/a
38	CTCF	chr1:228401300-228401450	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr1:228401082-228401619	MCF-7	breast:	n/a	n/a
40	CTCF	chr1:228401263-228401477	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr1:228401280-228401430	GM12867	blood:	n/a	n/a
42	CTCF	chr1:228401300-228401450	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr1:228401280-228401430	BE2_C	brain:	n/a	n/a
44	CTCF	chr1:228401222-228401516	LNCaP	prostate:	n/a	n/a
45	CTCF	chr1:228401300-228401450	HFF	foreskin:	n/a	n/a
46	CTCF	chr1:228401189-228401516	GM19238	blood:	n/a	n/a
47	CTCF	chr1:228401211-228401500	GM19240	blood:	n/a	n/a
48	CTCF	chr1:228401300-228401450	K562	blood:	n/a	n/a
49	CTCF	chr1:228401000-228401150	HEK293	kidney:	n/a	n/a
50	CTCF	chr1:228401260-228401410	HMF	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:228401278-228401328	SK-N-MC	brain:	n/a
2	chr1:228401186-228401236	NHDF-neo	bronchial:	n/a
3	chr1:228401278-228401328	ovcar-3	ovarian:	n/a
4	chr1:228401572-228401622	HL-60	blood:	n/a
5	chr1:228401186-228401236	Hepatocyte	liver:	n/a
6	chr1:228401278-228401328	LNCaP	prostate:	n/a
7	chr1:228401278-228401328	MCF-7	breast:	n/a
8	chr1:228401278-228401328	ProgFib	skin:	n/a
9	chr1:228401572-228401622	T-47D	breast:	n/a
10	chr1:228401186-228401236	RPTEC	kidney:	n/a
11	chr1:228401572-228401622	GM12891	blood:	n/a
12	chr1:228401278-228401328	HMEC	breast:	n/a
13	chr1:228401572-228401622	HEK293	kidney:	embryo
14	chr1:228401572-228401622	SAEC	small airway:	n/a
15	chr1:228401278-228401328	IMR90	lung:	fetal
16	chr1:228401278-228401328	MCF10A-Er-Src	breast:	n/a
17	chr1:228401278-228401328	BJ	skin:	n/a
18	chr1:228401278-228401328	GM19239	blood:	n/a
19	chr1:228401572-228401622	AG04450	lung:	fetal
20	chr1:228401186-228401236	ECC-1	luminal epithelium:	n/a
21	chr1:228401572-228401622	HEEpiC	esophagus:	n/a
22	chr1:228401186-228401236	PANC-1	pancreas:	n/a
23	chr1:228401186-228401236	HEK293	kidney:	embryo
24	chr1:228401572-228401622	HCF	heart:	n/a
25	chr1:228401186-228401236	HRPEpiC	eye:	n/a
26	chr1:228401572-228401622	PFSK-1	brain:	n/a
27	chr1:228401186-228401236	T-47D	breast:	n/a
28	chr1:228401186-228401236	AG09309	skin:	n/a
29	chr1:228401278-228401328	K562	blood:	n/a
30	chr1:228401278-228401328	SAEC	small airway:	n/a
31	chr1:228401278-228401328	NHDF-neo	bronchial:	n/a
32	chr1:228401572-228401622	NT2-D1	testis:	n/a
33	chr1:228401186-228401236	Jurkat	blood:	n/a
34	chr1:228401278-228401328	BE2_C	brain:	n/a
35	chr1:228401572-228401622	HNPCEpiC	eye:	n/a
36	chr1:228401186-228401236	SKMC	muscle:	n/a
37	chr1:228401278-228401328	AG04449	skin:	fetal
38	chr1:228401278-228401328	HepG2	liver:	n/a
39	chr1:228401278-228401328	Hepatocyte	liver:	n/a
40	chr1:228401186-228401236	HPAEpiC	pulmonary alveolar:	n/a
41	chr1:228401572-228401622	HRPEpiC	eye:	n/a
42	chr1:228401186-228401236	GM12892	blood:	n/a
43	chr1:228401572-228401622	LNCaP	prostate:	n/a
44	chr1:228401186-228401236	HRCEpiC	kidney:	n/a
45	chr1:228401572-228401622	SK-N-SH	brain:	n/a
46	chr1:228401572-228401622	RPTEC	kidney:	n/a
47	chr1:228401278-228401328	AoSMC	blood vessel:	n/a
48	chr1:228401186-228401236	GM19239	blood:	n/a
49	chr1:228401278-228401328	AG10803	skin:	n/a
50	chr1:228401278-228401328	HRPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:228399724..228401498-chr1:228644939..228647172,2	MCF-7	breast:
2	chr1:228400118..228403034-chr1:228591844..228593875,2	MCF-7	breast:
3	chr1:228400987..228403639-chr1:228644070..228647036,3	K562	blood:
4	chr1:228400809..228401396-chr19:36631414..36632120,2	Hela-S3	cervix:
5	chr1:228270338..228271968-chr1:228400103..228402238,2	MCF-7	breast:
6	chr1:228352180..228354320-chr1:228400730..228402843,3	MCF-7	breast:
7	chr1:228360767..228363057-chr1:228399837..228402220,2	MCF-7	breast:
8	chr1:228401076..228403639-chr1:228645192..228647036,2	K562	blood:
9	chr1:228400032..228401961-chr1:228675104..228677391,2	MCF-7	breast:
10	chr1:228399534..228402324-chr1:228461653..228463776,2	MCF-7	breast:
11	chr1:228352301..228356055-chr1:228400478..228402839,5	K562	blood:
12	chr1:228399573..228401373-chr1:228480199..228482605,2	K562	blood:

No data

Variant related genes	Relation type
C1orf145	TF binding region
OBSCN	TF binding region
C1orf145	CpG island
OBSCN	CpG island
ENSG00000269890	chromatin interactions
ENSG00000154358	chromatin interactions
ENSG00000143761	chromatin interactions
ENSG00000196890	chromatin interactions
ENSG00000269934	chromatin interactions
ENSG00000154370	chromatin interactions
ENSG00000181873	chromatin interactions
ENSG00000203684	chromatin interactions
ENSG00000168159	chromatin interactions
ENSG00000126247	chromatin interactions
ENSG00000181218	chromatin interactions

Extended variants
information (count: 20 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569727649	chr1:228401183-228401184	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
2	rs373759154	chr1:228401205-228401206	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
3	rs368823490	chr1:228401221-228401222	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
4	rs372423540	chr1:228401224-228401225	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
5	rs375552745	chr1:228401244-228401245	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
6	rs368219464	chr1:228401262-228401263	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
7	rs552489989	chr1:228401265-228401266	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
8	rs565988095	chr1:228401287-228401288	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
9	rs534969020	chr1:228401292-228401293	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
10	rs372465829	chr1:228401313-228401314	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
11	rs377725925	chr1:228401328-228401329	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
12	rs185717159	chr1:228401329-228401330	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
13	rs369341013	chr1:228401350-228401351	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
14	rs201231167	chr1:228401352-228401353	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
15	rs369113665	chr1:228401417-228401418	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
16	rs577357081	chr1:228401443-228401444	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
17	rs539656738	chr1:228401450-228401451	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
18	rs553206774	chr1:228401470-228401471	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
19	rs573225139	chr1:228401534-228401535	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
20	rs3121190	chr1:228401556-228401557	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:93)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	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
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Melanoma	17363583	CNVD

Chromatin state (count:181 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228395800-228405200	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
2	chr1:228398800-228402000	Active TSS	Psoas Muscle	Psoas
3	chr1:228400000-228401800	Active TSS	Thymus	Thymus
4	chr1:228400000-228402400	Active TSS	H9 Cell Line	embryonic stem cell
5	chr1:228400000-228402600	Active TSS	HUES64 Cell Line	embryonic stem cell
6	chr1:228400200-228401200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
7	chr1:228400200-228401200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:228400200-228401400	Flanking Active TSS	Primary B cells from cord blood	blood
9	chr1:228400200-228401400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr1:228400200-228401800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr1:228400200-228401800	Active TSS	Brain Angular Gyrus	brain
12	chr1:228400200-228402200	Active TSS	iPS-18 Cell Line	embryonic stem cell
13	chr1:228400200-228402600	Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr1:228400400-228401200	Enhancers	Liver	Liver
15	chr1:228400400-228401400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
16	chr1:228400400-228401400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
17	chr1:228400400-228401400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr1:228400400-228401400	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
19	chr1:228400400-228401400	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
20	chr1:228400400-228401600	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
21	chr1:228400400-228401800	Active TSS	Primary T helper naive cells from peripheral blood	blood
22	chr1:228400400-228401800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
23	chr1:228400400-228402000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
24	chr1:228400400-228402000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr1:228400400-228402000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr1:228400400-228402000	Active TSS	Fetal Kidney	kidney
27	chr1:228400400-228402000	Active TSS	NHEK	skin
28	chr1:228400400-228402200	Active TSS	iPS-15b Cell Line	embryonic stem cell
29	chr1:228400400-228402400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr1:228400400-228403200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr1:228400600-228401400	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr1:228400600-228401400	Active TSS	Primary T cells from cord blood	blood
33	chr1:228400600-228401600	Active TSS	Breast Myoepithelial Primary Cells	Breast
34	chr1:228400600-228401600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr1:228400600-228401600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr1:228400600-228401600	Active TSS	Right Atrium	heart
37	chr1:228400600-228401600	Active TSS	Dnd41	blood
38	chr1:228400600-228401800	Active TSS	ES-I3 Cell Line	embryonic stem cell
39	chr1:228400600-228401800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr1:228400600-228401800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr1:228400600-228401800	Active TSS	Fetal Intestine Small	intestine
42	chr1:228400600-228401800	Active TSS	Fetal Thymus	thymus
43	chr1:228400600-228401800	Active TSS	Gastric	stomach
44	chr1:228400600-228402000	Active TSS	H1 Cell Line	embryonic stem cell
45	chr1:228400600-228402000	Active TSS	HUES48 Cell Line	embryonic stem cell
46	chr1:228400600-228402000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr1:228400600-228402000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
48	chr1:228400600-228402000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr1:228400600-228402000	Active TSS	Brain Substantia Nigra	brain
50	chr1:228400600-228402000	Active TSS	Duodenum Mucosa	Duodenum

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