Variant report

Variant	esv2755601
Chromosome Location	chr1:191091343-191282343
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:645)
CpG islands
(count:122)
Chromatin interactive
region (count:32)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:645 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:191159156-191159163	K562	blood:	n/a	n/a
2	ATF1	chr1:191122236-191122374	K562	blood:	n/a	n/a
3	ATF2	chr1:191143328-191144013	GM12878	blood:	n/a	n/a
4	BACH1	chr1:191274761-191274805	K562	blood:	n/a	n/a
5	BACH1	chr1:191253401-191253595	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr1:191143439-191143828	GM12878	blood:	n/a	n/a
7	BATF	chr1:191143451-191143751	GM12878	blood:	n/a	n/a
8	BCL11A	chr1:191143469-191143830	GM12878	blood:	n/a	n/a
9	BCLAF1	chr1:191143259-191143906	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:191143231-191143785	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:191259569-191259784	K562	blood:	n/a	n/a
12	CBX3	chr1:191253357-191253679	K562	blood:	n/a	n/a
13	CBX3	chr1:191275577-191275852	K562	blood:	n/a	n/a
14	CBX3	chr1:191120966-191121245	K562	blood:	n/a	n/a
15	CBX3	chr1:191253318-191253712	K562	blood:	n/a	n/a
16	CBX3	chr1:191126404-191126763	K562	blood:	n/a	n/a
17	CBX3	chr1:191186779-191187146	K562	blood:	n/a	n/a
18	CEBPB	chr1:191226088-191226421	K562	blood:	n/a	chr1:191226236-191226247
19	CEBPB	chr1:191248512-191248886	HepG2	liver:	n/a	chr1:191248692-191248703
20	CEBPB	chr1:191274516-191274867	IMR90	lung:	n/a	chr1:191274702-191274713
21	CEBPB	chr1:191248541-191248874	Hela-S3	cervix:	n/a	chr1:191248692-191248703
22	CEBPB	chr1:191274526-191274855	HepG2	liver:	n/a	chr1:191274702-191274713
23	CEBPB	chr1:191248450-191248950	A549	lung:	n/a	chr1:191248692-191248703
24	CEBPB	chr1:191226072-191226414	IMR90	lung:	n/a	chr1:191226236-191226247
25	CEBPB	chr1:191248490-191248817	K562	blood:	n/a	chr1:191248692-191248703
26	CEBPB	chr1:191248505-191248880	A549	lung:	n/a	chr1:191248692-191248703
27	CEBPB	chr1:191109185-191109537	K562	blood:	n/a	chr1:191109350-191109361
28	CEBPB	chr1:191269951-191270221	HepG2	liver:	n/a	chr1:191270075-191270086
29	CEBPB	chr1:191248382-191248980	MCF-7	breast:	n/a	chr1:191248692-191248703
30	CEBPB	chr1:191204015-191204017	K562	blood:	n/a	n/a
31	CEBPB	chr1:191134018-191134308	K562	blood:	n/a	n/a
32	CEBPB	chr1:191248480-191248906	ECC-1	luminal epithelium:	n/a	chr1:191248692-191248703
33	CEBPB	chr1:191226146-191226379	H1-hESC	embryonic stem cell:	n/a	chr1:191226236-191226247
34	CEBPB	chr1:191248507-191248874	K562	blood:	n/a	chr1:191248692-191248703
35	CEBPB	chr1:191248505-191248873	H1-hESC	embryonic stem cell:	n/a	chr1:191248692-191248703
36	CEBPB	chr1:191109191-191109512	IMR90	lung:	n/a	chr1:191109350-191109361
37	CEBPB	chr1:191128063-191128248	HepG2	liver:	n/a	chr1:191128163-191128174
38	CEBPB	chr1:191274527-191274827	A549	lung:	n/a	chr1:191274702-191274713
39	CEBPB	chr1:191226100-191226380	A549	lung:	n/a	chr1:191226236-191226247
40	CEBPB	chr1:191274454-191274930	ECC-1	luminal epithelium:	n/a	chr1:191274702-191274713
41	CEBPB	chr1:191128034-191128422	IMR90	lung:	n/a	chr1:191128163-191128174
42	CEBPB	chr1:191109240-191109499	HepG2	liver:	n/a	chr1:191109350-191109361
43	CEBPB	chr1:191226089-191226409	HepG2	liver:	n/a	chr1:191226236-191226247
44	CEBPB	chr1:191248508-191248878	A549	lung:	n/a	chr1:191248692-191248703
45	CEBPB	chr1:191211379-191211586	K562	blood:	n/a	n/a
46	CEBPB	chr1:191109247-191109477	A549	lung:	n/a	chr1:191109350-191109361
47	CEBPB	chr1:191128031-191128288	K562	blood:	n/a	chr1:191128163-191128174
48	CEBPB	chr1:191096019-191096306	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr1:191274508-191274875	ECC-1	luminal epithelium:	n/a	chr1:191274702-191274713
50	CEBPB	chr1:191248509-191248885	IMR90	lung:	n/a	chr1:191248692-191248703

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:191120792-191120842	Hepatocyte	liver:	n/a
2	chr1:191120792-191120842	HMEC	breast:	n/a
3	chr1:191120792-191120842	PrEC	prostate:	n/a
4	chr1:191120830-191120880	ovcar-3	ovarian:	n/a
5	chr1:191120830-191120880	BJ	skin:	n/a
6	chr1:191120830-191120880	T-47D	breast:	n/a
7	chr1:191120830-191120880	NT2-D1	testis:	n/a
8	chr1:191120830-191120880	AG04450	lung:	fetal
9	chr1:191120792-191120842	HEEpiC	esophagus:	n/a
10	chr1:191120830-191120880	HCF	heart:	n/a
11	chr1:191120830-191120880	PANC-1	pancreas:	n/a
12	chr1:191120792-191120842	GM12878	blood:	n/a
13	chr1:191120830-191120880	NHDF-neo	bronchial:	n/a
14	chr1:191120792-191120842	MCF-7	breast:	n/a
15	chr1:191120830-191120880	ECC-1	luminal epithelium:	n/a
16	chr1:191120830-191120880	GM06990	blood:	n/a
17	chr1:191120792-191120842	AG09309	skin:	n/a
18	chr1:191120792-191120842	SKMC	muscle:	n/a
19	chr1:191120830-191120880	HCT-116	colon:	n/a
20	chr1:191120792-191120842	HRE	kidney:	n/a
21	chr1:191120830-191120880	RPTEC	kidney:	n/a
22	chr1:191120792-191120842	HCPEpiC	choroid plexus:	n/a
23	chr1:191120792-191120842	HL-60	blood:	n/a
24	chr1:191120792-191120842	PANC-1	pancreas:	n/a
25	chr1:191120830-191120880	A549	lung:	n/a
26	chr1:191120830-191120880	GM19239	blood:	n/a
27	chr1:191120830-191120880	PrEC	prostate:	n/a
28	chr1:191120830-191120880	HepG2	liver:	n/a
29	chr1:191120830-191120880	Caco-2	colon:	n/a
30	chr1:191120830-191120880	NHBE	bronchial:	n/a
31	chr1:191120792-191120842	HepG2	liver:	n/a
32	chr1:191120792-191120842	NHBE	bronchial:	n/a
33	chr1:191120830-191120880	AoSMC	blood vessel:	n/a
34	chr1:191120830-191120880	AG04449	skin:	fetal
35	chr1:191120792-191120842	Hela-S3	cervix:	n/a
36	chr1:191120792-191120842	SK-N-SH_RA	brain:	n/a
37	chr1:191120830-191120880	SAEC	small airway:	n/a
38	chr1:191120792-191120842	K562	blood:	n/a
39	chr1:191120830-191120880	BE2_C	brain:	n/a
40	chr1:191120830-191120880	Hepatocyte	liver:	n/a
41	chr1:191120830-191120880	PFSK-1	brain:	n/a
42	chr1:191120830-191120880	SK-N-SH	brain:	n/a
43	chr1:191120792-191120842	PFSK-1	brain:	n/a
44	chr1:191120792-191120842	LNCaP	prostate:	n/a
45	chr1:191120792-191120842	SAEC	small airway:	n/a
46	chr1:191120792-191120842	U87	brain:	n/a
47	chr1:191120792-191120842	Jurkat	blood:	n/a
48	chr1:191120792-191120842	AG04449	skin:	fetal
49	chr1:191120830-191120880	GM12892	blood:	n/a
50	chr1:191120830-191120880	HMEC	breast:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:191262328..191265076-chr1:191299134..191300928,2	K562	blood:
2	chr1:191212442..191214167-chr1:191217333..191219833,2	MCF-7	breast:
3	chr1:191117376..191119882-chr1:191120970..191122736,2	MCF-7	breast:
4	chr1:191250975..191253394-chr1:191254576..191256855,3	K562	blood:
5	chr1:191191547..191193153-chr1:191196709..191199112,2	K562	blood:
6	chr1:191154442..191156572-chr1:191159468..191162029,2	K562	blood:
7	chr1:191121690..191123350-chr1:191124411..191127560,3	K562	blood:
8	chr1:191235053..191236832-chr1:191299467..191301857,2	MCF-7	breast:
9	chr1:191088572..191091264-chr1:191094632..191096483,2	MCF-7	breast:
10	chr1:191139593..191142388-chr1:191149120..191151841,2	MCF-7	breast:
11	chr1:191251451..191253394-chr1:191255335..191256855,2	K562	blood:
12	chr1:191245868..191248178-chr1:191250282..191252170,2	K562	blood:
13	chr1:191160823..191162731-chr1:191477898..191480311,2	K562	blood:
14	chr1:191121690..191123350-chr1:191124411..191127560,3	K562	blood:
15	chr1:191157793..191160088-chr1:191162179..191165102,2	K562	blood:
16	chr1:191154442..191156572-chr1:191159468..191162029,2	K562	blood:
17	chr1:191277227..191279088-chr1:191280511..191283131,2	K562	blood:
18	chr1:191117376..191119882-chr1:191120970..191122736,2	MCF-7	breast:
19	chr1:191078284..191080144-chr1:191088639..191091448,2	K562	blood:
20	chr1:191250975..191253394-chr1:191254576..191256855,3	K562	blood:
21	chr1:191150998..191152501-chr1:191156325..191158082,2	K562	blood:
22	chr1:191102072..191104300-chr1:191107376..191108877,2	K562	blood:
23	chr1:191123228..191125504-chr1:191129557..191132140,2	K562	blood:
24	chr1:191245868..191248178-chr1:191250282..191252170,2	K562	blood:
25	chr1:191123228..191125504-chr1:191129557..191132140,2	K562	blood:
26	chr1:191212442..191214167-chr1:191217333..191219833,2	MCF-7	breast:
27	chr1:191102072..191104300-chr1:191107376..191108877,2	K562	blood:
28	chr1:191139593..191142388-chr1:191149120..191151841,2	MCF-7	breast:
29	chr1:191150998..191152501-chr1:191156325..191158082,2	K562	blood:
30	chr1:191157793..191160088-chr1:191162179..191165102,2	K562	blood:
31	chr1:191277227..191279088-chr1:191280511..191283131,2	K562	blood:
32	chr1:191251451..191253394-chr1:191255335..191256855,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM5C-10	chr1:191148651-191148869	NONHSAT008516
2	lnc-FAM5C-9	chr1:191115155-191116091	NONHSAT008514
3	lnc-FAM5C-12	chr1:191190289-191190442	ENSG00000233882.2
4	lnc-FAM5C-11	chr1:191173053-191173173	NONHSAT008517
5	lnc-RGS18-2	chr1:191190289-191190442	XLOC_000506
6	lnc-RGS18-2	chr1:191197453-191197597	XLOC_000506
7	lnc-FAM5C-12	chr1:191197453-191197597	ENSG00000233882.2
8	lnc-FAM5C-11	chr1:191183856-191184010	NONHSAT008517

No data

Variant related genes	Relation type
ENSG00000261642	TF binding region
HNRNPA1P46	TF binding region
ENSG00000233882	TF binding region
ENSG00000271187	TF binding region
ENSG00000261642	CpG island
HNRNPA1P46	CpG island
ENSG00000233882	CpG island
ENSG00000271187	CpG island
ENSG00000233882	chromatin interactions
GSK3B	miRNA target sites
BCOR	miRNA target sites

Extended variants
information (count: 1481 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1481 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147995989	chr1:191095207-191095208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs544631736	chr1:191095208-191095209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78252696	chr1:191095210-191095211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs79751997	chr1:191095245-191095246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs186637020	chr1:191095270-191095271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150124976	chr1:191095309-191095310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532692249	chr1:191095317-191095318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553443652	chr1:191095369-191095370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569498866	chr1:191095370-191095371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531895317	chr1:191095390-191095391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs374557748	chr1:191095406-191095407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs191846752	chr1:191095456-191095457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs34466908	chr1:191095487-191095488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574795679	chr1:191095492-191095493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533913672	chr1:191095537-191095538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs553860475	chr1:191095581-191095582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs10920893	chr1:191095628-191095629	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs528966951	chr1:191095669-191095670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550607397	chr1:191095687-191095688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138373830	chr1:191095709-191095710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556072182	chr1:191095717-191095718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576316479	chr1:191095721-191095722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2168081	chr1:191095755-191095756	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs375191664	chr1:191095808-191095809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2123962	chr1:191095842-191095843	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs371753449	chr1:191095878-191095879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201251750	chr1:191095879-191095880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376481851	chr1:191095889-191095890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7551940	chr1:191095891-191095892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs7549554	chr1:191095898-191095899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7551941	chr1:191095899-191095900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2123963	chr1:191095931-191095932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188389883	chr1:191095951-191095952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2123964	chr1:191095953-191095954	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs536070830	chr1:191095978-191095979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549607030	chr1:191095998-191095999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527252389	chr1:191096216-191096217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs193054244	chr1:191096224-191096225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs1902036	chr1:191096227-191096228	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs570564220	chr1:191096250-191096251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs113962687	chr1:191096255-191096256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs185624586	chr1:191096280-191096281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs190783986	chr1:191096328-191096329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs151017659	chr1:191103429-191103430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569912441	chr1:191103471-191103472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs561056691	chr1:191103502-191103503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs533849767	chr1:191103609-191103610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs564344078	chr1:191103639-191103640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs35674355	chr1:191103656-191103657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs77348174	chr1:191103684-191103685	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
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
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
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	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
Hepatocellular carcinoma	18803288	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
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	17086460	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	17086460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:191095200-191095600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:191095200-191096000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:191096200-191096400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr1:191103400-191104000	Enhancers	HUVEC	blood vessel
5	chr1:191103800-191104000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr1:191103800-191104400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr1:191103800-191104400	Active TSS	Stomach Smooth Muscle	stomach
8	chr1:191104000-191104400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr1:191104000-191104400	Flanking Active TSS	HUVEC	blood vessel
10	chr1:191104200-191104600	Enhancers	Colon Smooth Muscle	Colon
11	chr1:191104400-191105000	Enhancers	HUVEC	blood vessel
12	chr1:191120400-191120800	Enhancers	Placenta	Placenta
13	chr1:191121800-191122400	Enhancers	GM12878-XiMat	blood
14	chr1:191123600-191124600	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr1:191123800-191124800	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr1:191124000-191124600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr1:191124000-191124600	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr1:191124200-191124600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr1:191124200-191124600	Active TSS	K562	blood
20	chr1:191128400-191130200	Weak transcription	Fetal Kidney	kidney
21	chr1:191129200-191129600	Enhancers	Placenta	Placenta
22	chr1:191129600-191129800	Active TSS	HSMM	muscle
23	chr1:191129800-191130000	Flanking Active TSS	HSMM	muscle
24	chr1:191130200-191130600	ZNF genes & repeats	Fetal Kidney	kidney
25	chr1:191140800-191141000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr1:191141600-191141800	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr1:191141800-191142800	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr1:191142600-191143000	Enhancers	Dnd41	blood
29	chr1:191142600-191144000	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr1:191142800-191143800	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr1:191142800-191144000	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr1:191142800-191144400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr1:191143000-191143400	Enhancers	GM12878-XiMat	blood
34	chr1:191143000-191143600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr1:191143000-191143800	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr1:191143000-191144000	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr1:191143000-191144000	Flanking Active TSS	Dnd41	blood
38	chr1:191143200-191143400	Active TSS	Colon Smooth Muscle	Colon
39	chr1:191143200-191143600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr1:191143200-191143600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr1:191143200-191144000	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr1:191143200-191144200	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr1:191143400-191143600	Flanking Active TSS	Colon Smooth Muscle	Colon
44	chr1:191143400-191143600	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr1:191143400-191143800	Enhancers	H9 Cell Line	embryonic stem cell
46	chr1:191143400-191144000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr1:191143400-191144200	Flanking Active TSS	GM12878-XiMat	blood
48	chr1:191143400-191144400	Enhancers	Primary B cells from peripheral blood	blood
49	chr1:191143400-191145400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:191143600-191144000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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