Variant report

Variant	esv3381082
Chromosome Location	chr1:227029266-227059927
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:571)
CpG islands
(count:736)
Chromatin interactive
region (count:11)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:571 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:227057940-227058295	K562	blood:	n/a	n/a
2	ATF3	chr1:227057988-227058398	K562	blood:	n/a	chr1:227058187-227058196
3	BACH1	chr1:227057909-227058331	K562	blood:	n/a	n/a
4	BACH1	chr1:227057896-227058744	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr1:227057895-227059083	GM12878	blood:	n/a	chr1:227058884-227058897 chr1:227058689-227058705 chr1:227058385-227058401 chr1:227058559-227058575
6	BHLHE40	chr1:227057896-227059411	K562	blood:	n/a	chr1:227058884-227058897 chr1:227058689-227058705 chr1:227058385-227058401 chr1:227058559-227058575
7	BHLHE40	chr1:227058301-227059310	HepG2	liver:	n/a	chr1:227058884-227058897 chr1:227058689-227058705 chr1:227058385-227058401 chr1:227058559-227058575
8	BHLHE40	chr1:227058700-227059037	A549	lung:	n/a	chr1:227058884-227058897
9	BRCA1	chr1:227058551-227058644	GM12878	blood:	n/a	n/a
10	BRCA1	chr1:227057790-227058505	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr1:227058745-227058914	HepG2	liver:	n/a	n/a
12	CBX3	chr1:227057693-227058352	K562	blood:	n/a	n/a
13	CBX3	chr1:227057889-227058213	K562	blood:	n/a	n/a
14	CBX3	chr1:227058402-227058887	K562	blood:	n/a	n/a
15	CCNT2	chr1:227058077-227058973	K562	blood:	n/a	n/a
16	CEBPB	chr1:227039012-227039016	K562	blood:	n/a	n/a
17	CEBPB	chr1:227053349-227054015	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr1:227052080-227052366	HepG2	liver:	n/a	n/a
19	CEBPB	chr1:227057947-227058601	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr1:227058084-227058275	K562	blood:	n/a	n/a
21	CHD1	chr1:227033611-227033639	GM12878	blood:	n/a	n/a
22	CHD2	chr1:227057977-227058825	K562	blood:	n/a	chr1:227058695-227058705
23	CHD2	chr1:227057876-227058813	Hela-S3	cervix:	n/a	chr1:227058695-227058705
24	CHD2	chr1:227058322-227058624	GM12878	blood:	n/a	n/a
25	CREB1	chr1:227057896-227058709	A549	lung:	n/a	n/a
26	CREB1	chr1:227057900-227058698	HepG2	liver:	n/a	n/a
27	CREB1	chr1:227057847-227058456	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr1:227057896-227058388	GM12878	blood:	n/a	n/a
29	CREB1	chr1:227057901-227058441	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr1:227057793-227058578	K562	blood:	n/a	n/a
31	CTBP2	chr1:227058033-227059017	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr1:227058800-227058950	AG04450	lung:	n/a	n/a
33	CTCF	chr1:227058480-227058630	HepG2	liver:	n/a	chr1:227058559-227058572
34	CTCF	chr1:227058480-227058630	K562	blood:	n/a	chr1:227058559-227058572
35	CTCF	chr1:227058488-227058619	GM19239	blood:	n/a	chr1:227058559-227058572
36	CTCF	chr1:227058660-227058810	K562	blood:	n/a	n/a
37	CTCF	chr1:227058445-227058681	K562	blood:	n/a	chr1:227058559-227058572
38	CTCF	chr1:227058140-227058290	GM12867	blood:	n/a	n/a
39	CTCF	chr1:227058480-227058630	Hela-S3	cervix:	n/a	chr1:227058559-227058572
40	CTCF	chr1:227058018-227058066	K562	blood:	n/a	n/a
41	CTCF	chr1:227058440-227058590	GM12867	blood:	n/a	chr1:227058559-227058572
42	CTCF	chr1:227058100-227058155	Fibrobl	skin:	n/a	n/a
43	CTCF	chr1:227058480-227058630	AG09309	skin:	n/a	chr1:227058559-227058572
44	CTCF	chr1:227058440-227058590	Caco-2	colon:	n/a	chr1:227058559-227058572
45	CTCF	chr1:227058520-227058670	AG04450	lung:	n/a	chr1:227058559-227058572
46	CTCF	chr1:227058440-227058590	HepG2	liver:	n/a	chr1:227058559-227058572
47	CTCF	chr1:227058513-227058602	GM12892	blood:	n/a	chr1:227058559-227058572
48	CTCF	chr1:227058535-227058567	Gliobla	brain:	n/a	n/a
49	CTCF	chr1:227058500-227058650	SK-N-SH_RA	brain:	n/a	chr1:227058559-227058572
50	CTCF	chr1:227058480-227058630	GM12869	blood:	n/a	chr1:227058559-227058572

(count:736 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:227051345-227051395	HNPCEpiC	eye:	n/a
2	chr1:227056896-227056946	GM12891	blood:	n/a
3	chr1:227058070-227058120	IMR90	lung:	fetal
4	chr1:227058595-227058645	GM12892	blood:	n/a
5	chr1:227051345-227051395	HNPCEpiC	eye:	n/a
6	chr1:227056896-227056946	GM12891	blood:	n/a
7	chr1:227058070-227058120	IMR90	lung:	fetal
8	chr1:227058595-227058645	GM12892	blood:	n/a
9	chr1:227058426-227058476	MCF-7	breast:	n/a
10	chr1:227058905-227058955	SK-N-SH_RA	brain:	n/a
11	chr1:227056896-227056946	HCF	heart:	n/a
12	chr1:227058941-227058991	ovcar-3	ovarian:	n/a
13	chr1:227059463-227059513	U87	brain:	n/a
14	chr1:227058595-227058645	PrEC	prostate:	n/a
15	chr1:227056896-227056946	SK-N-SH	brain:	n/a
16	chr1:227058046-227058096	HUVEC	blood vessel:	n/a
17	chr1:227058905-227058955	SK-N-MC	brain:	n/a
18	chr1:227056896-227056946	AG10803	skin:	n/a
19	chr1:227058070-227058120	HAEpiC	amniotic membrane:	n/a
20	chr1:227051345-227051395	HCF	heart:	n/a
21	chr1:227058905-227058955	HRPEpiC	eye:	n/a
22	chr1:227054129-227054179	HUVEC	blood vessel:	n/a
23	chr1:227054129-227054179	H1-hESC	embryonic stem cell:	embryo
24	chr1:227059463-227059513	H1-hESC	embryonic stem cell:	embryo
25	chr1:227058905-227058955	HepG2	liver:	n/a
26	chr1:227056896-227056946	HRE	kidney:	n/a
27	chr1:227051345-227051395	HepG2	liver:	n/a
28	chr1:227059109-227059159	SAEC	small airway:	n/a
29	chr1:227058941-227058991	PrEC	prostate:	n/a
30	chr1:227058754-227058804	Jurkat	blood:	n/a
31	chr1:227059109-227059159	NHBE	bronchial:	n/a
32	chr1:227059109-227059159	NB4	blood:	n/a
33	chr1:227058046-227058096	ECC-1	luminal epithelium:	n/a
34	chr1:227058046-227058096	Hela-S3	cervix:	n/a
35	chr1:227059463-227059513	HCF	heart:	n/a
36	chr1:227058595-227058645	CMK	blood:	n/a
37	chr1:227058905-227058955	HEK293	kidney:	embryo
38	chr1:227058941-227058991	Jurkat	blood:	n/a
39	chr1:227058595-227058645	GM06990	blood:	n/a
40	chr1:227058426-227058476	AG10803	skin:	n/a
41	chr1:227058046-227058096	SK-N-SH_RA	brain:	n/a
42	chr1:227058905-227058955	Hela-S3	cervix:	n/a
43	chr1:227058905-227058955	HPAEpiC	pulmonary alveolar:	n/a
44	chr1:227058941-227058991	SK-N-SH	brain:	n/a
45	chr1:227051345-227051395	GM12891	blood:	n/a
46	chr1:227059109-227059159	H1-hESC	embryonic stem cell:	embryo
47	chr1:227051345-227051395	SK-N-SH	brain:	n/a
48	chr1:227051345-227051395	SKMC	muscle:	n/a
49	chr1:227059463-227059513	SKMC	muscle:	n/a
50	chr1:227058595-227058645	Jurkat	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:227044512..227048863-chr1:227049496..227051817,3	K562	blood:
2	chr1:227022576..227024779-chr1:227029976..227031514,2	K562	blood:
3	chr1:227058393..227060106-chr1:227070481..227073137,2	MCF-7	breast:
4	chr1:227051915..227054203-chr1:227056473..227058361,2	K562	blood:
5	chr1:227031005..227032884-chr1:227503623..227506611,2	MCF-7	breast:
6	chr1:227058010..227060717-chr1:227127922..227130467,2	K562	blood:
7	chr1:227044512..227048863-chr1:227049496..227051817,3	K562	blood:
8	chr1:227044580..227047261-chr1:227056474..227058125,2	MCF-7	breast:
9	chr1:227045661..227050211-chr1:227053920..227059739,5	K562	blood:
10	chr1:227045661..227048469-chr1:227054532..227056179,2	K562	blood:
11	chr1:227045661..227048469-chr1:227054532..227056179,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADCK3-4	chr1:227058564-227059105	NONHSAT009905
2	lnc-CDC42BPA-3	chr1:227049124-227049418	NONHSAT009904
3	lnc-CDC42BPA-3	chr1:227058063-227058176	NONHSAT009904

No data

Variant related genes	Relation type
PSEN2	TF binding region
PSEN2	CpG island
ENSG00000143776	chromatin interactions
ENSG00000163050	chromatin interactions
ENSG00000143801	chromatin interactions

Extended variants
information (count: 1095 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1095 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572286615	chr1:227029313-227029314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs560072280	chr1:227029356-227029357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542806502	chr1:227029384-227029385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561172932	chr1:227029407-227029408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531686233	chr1:227029431-227029432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543693914	chr1:227029457-227029458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573606982	chr1:227029471-227029472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564760246	chr1:227029516-227029517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532109411	chr1:227029520-227029521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547194483	chr1:227029563-227029564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs77387618	chr1:227029583-227029584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575862333	chr1:227029584-227029585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs74139840	chr1:227029587-227029588	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs182394644	chr1:227029617-227029618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187393584	chr1:227029641-227029642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201700620	chr1:227029694-227029695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538187523	chr1:227029708-227029709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375950892	chr1:227029709-227029710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs1539045	chr1:227029710-227029711	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
20	rs376807840	chr1:227029711-227029712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201756542	chr1:227029712-227029713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556795302	chr1:227029722-227029723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs3927712	chr1:227029726-227029727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs3927711	chr1:227029728-227029729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs3927710	chr1:227029730-227029731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs3927709	chr1:227029734-227029735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538989482	chr1:227029735-227029736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs59174106	chr1:227029740-227029741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561775544	chr1:227029743-227029744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs60602411	chr1:227029750-227029751	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs572528781	chr1:227029752-227029753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543143158	chr1:227029758-227029759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559640515	chr1:227029767-227029768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551054612	chr1:227029770-227029771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576286352	chr1:227029782-227029783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543378442	chr1:227029785-227029786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565156170	chr1:227029786-227029787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs61585264	chr1:227029791-227029792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs199881491	chr1:227029792-227029793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532024094	chr1:227029795-227029796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs72262357	chr1:227029809-227029810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552909903	chr1:227029815-227029816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs34791705	chr1:227029816-227029817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200270915	chr1:227029817-227029818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551590954	chr1:227029829-227029830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533143583	chr1:227029858-227029859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190661052	chr1:227029870-227029871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372138064	chr1:227029871-227029872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201489873	chr1:227029896-227029897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577708009	chr1:227029897-227029898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Acute lymphoblastic leukemia	21098271	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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:741 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:227026800-227034200	Weak transcription	HMEC	breast
2	chr1:227026800-227043800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:227027000-227034400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:227028000-227034200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr1:227033000-227034800	Enhancers	GM12878-XiMat	blood
6	chr1:227034200-227034800	Enhancers	Thymus	Thymus
7	chr1:227034200-227035000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr1:227034200-227035000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr1:227034200-227035000	Enhancers	HMEC	breast
10	chr1:227034200-227035200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr1:227034200-227035400	Enhancers	NHEK	skin
12	chr1:227034400-227034800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr1:227034400-227035200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr1:227034600-227035000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr1:227034800-227035000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr1:227034800-227035200	Enhancers	NHDF-Ad	bronchial
17	chr1:227035000-227036600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr1:227035000-227039800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr1:227035800-227036000	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr1:227035800-227036200	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr1:227035800-227036600	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr1:227035800-227037600	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr1:227035800-227037600	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr1:227036000-227037000	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr1:227036000-227037200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr1:227036200-227037200	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr1:227036400-227037200	Enhancers	H1 Cell Line	embryonic stem cell
28	chr1:227036600-227036800	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr1:227036600-227037000	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr1:227036800-227037000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr1:227037000-227037200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr1:227037000-227037400	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr1:227037000-227037600	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr1:227037200-227037800	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr1:227037200-227038600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr1:227037200-227043600	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr1:227037400-227038600	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr1:227037600-227039000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr1:227037600-227039200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr1:227037600-227043800	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr1:227037800-227038600	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr1:227038600-227039200	Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr1:227038600-227039400	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr1:227038600-227039600	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr1:227039000-227039600	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr1:227039200-227039600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr1:227039200-227039600	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr1:227039400-227044000	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr1:227039600-227043800	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr1:227043600-227044200	Enhancers	H1 Cell Line	embryonic stem cell

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