Variant report

Variant	esv1804459
Chromosome Location	chr1:242955371-243170610
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:243088083-243088303	K562	blood:	n/a	n/a
2	ATF1	chr1:243148543-243148578	K562	blood:	n/a	n/a
3	ATF2	chr1:242976778-242977056	GM12878	blood:	n/a	n/a
4	BACH1	chr1:243122482-243122506	K562	blood:	n/a	n/a
5	BACH1	chr1:242996994-242996997	K562	blood:	n/a	n/a
6	BCL11A	chr1:242976721-242977165	GM12878	blood:	n/a	chr1:242976959-242976968
7	BCL11A	chr1:242976760-242977140	GM12878	blood:	n/a	chr1:242976959-242976968
8	BCL11A	chr1:243153505-243153675	GM12878	blood:	n/a	n/a
9	BCL11A	chr1:243169760-243169972	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:243087986-243088483	K562	blood:	n/a	n/a
11	BHLHE40	chr1:243031757-243031938	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:242976782-242977230	GM12878	blood:	n/a	n/a
13	BRCA1	chr1:242997383-242997489	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr1:243053418-243053739	K562	blood:	n/a	n/a
15	CBX3	chr1:243087941-243088379	K562	blood:	n/a	n/a
16	CBX3	chr1:243100093-243100300	K562	blood:	n/a	n/a
17	CBX3	chr1:243130209-243130606	K562	blood:	n/a	n/a
18	CCNT2	chr1:243087975-243088306	K562	blood:	n/a	n/a
19	CCNT2	chr1:243129321-243129526	K562	blood:	n/a	n/a
20	CEBPB	chr1:243118268-243118571	HepG2	liver:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
21	CEBPB	chr1:243118303-243118616	K562	blood:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
22	CEBPB	chr1:243072507-243072681	IMR90	lung:	n/a	chr1:243072592-243072603
23	CEBPB	chr1:243118300-243118585	A549	lung:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
24	CEBPB	chr1:243072449-243072662	HepG2	liver:	n/a	chr1:243072592-243072603
25	CEBPB	chr1:242998320-242998357	HepG2	liver:	n/a	chr1:242998327-242998338
26	CEBPB	chr1:243118255-243118634	K562	blood:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
27	CEBPB	chr1:243148513-243148717	K562	blood:	n/a	n/a
28	CEBPB	chr1:243088005-243088218	K562	blood:	n/a	n/a
29	CEBPB	chr1:243105260-243105310	HepG2	liver:	n/a	chr1:243105272-243105283
30	CEBPB	chr1:242955789-242955931	A549	lung:	n/a	n/a
31	CEBPB	chr1:243105243-243105313	A549	lung:	n/a	chr1:243105272-243105283
32	CEBPB	chr1:243118344-243118540	K562	blood:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
33	CEBPB	chr1:243072543-243072743	K562	blood:	n/a	chr1:243072592-243072603
34	CEBPB	chr1:243118280-243118602	IMR90	lung:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
35	CEBPB	chr1:243118288-243118578	Hela-S3	cervix:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
36	CEBPB	chr1:242998985-242999533	A549	lung:	n/a	n/a
37	CHD1	chr1:242976654-242977278	GM12878	blood:	n/a	n/a
38	CHD2	chr1:243080927-243080928	K562	blood:	n/a	n/a
39	CHD2	chr1:243087993-243088116	K562	blood:	n/a	n/a
40	CHD2	chr1:243005456-243005619	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr1:242991732-242991777	HepG2	liver:	n/a	n/a
42	CHD2	chr1:242976690-242977268	GM12878	blood:	n/a	n/a
43	CTCF	chr1:242991680-242991830	HepG2	liver:	n/a	chr1:242991719-242991740
44	CTCF	chr1:243166431-243166522	MCF-7	breast:	n/a	chr1:243166447-243166465 chr1:243166448-243166464
45	CTCF	chr1:243133190-243133243	GM10248	blood:	n/a	n/a
46	CTCF	chr1:243100160-243100310	HMEC	breast:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
47	CTCF	chr1:243100140-243100290	GM12865	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
48	CTCF	chr1:243100117-243100462	T-47D	breast:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
49	CTCF	chr1:243148098-243148195	MCF-7	breast:	n/a	n/a
50	CTCF	chr1:243005469-243005679	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:243053934-243053984	BE2_C	brain:	n/a
2	chr1:243053865-243053915	SK-N-SH_RA	brain:	n/a
3	chr1:243053934-243053984	BE2_C	brain:	n/a
4	chr1:243053865-243053915	SK-N-SH_RA	brain:	n/a
5	chr1:243138527-243138577	HMEC	breast:	n/a
6	chr1:243053425-243053475	MCF10A-Er-Src	breast:	n/a
7	chr1:243050875-243050925	PFSK-1	brain:	n/a
8	chr1:243057080-243057130	K562	blood:	n/a
9	chr1:243053673-243053723	AoSMC	blood vessel:	n/a
10	chr1:243054071-243054121	HCF	heart:	n/a
11	chr1:243053934-243053984	HEEpiC	esophagus:	n/a
12	chr1:243138527-243138577	ovcar-3	ovarian:	n/a
13	chr1:243050875-243050925	HAEpiC	amniotic membrane:	n/a
14	chr1:243054071-243054121	NB4	blood:	n/a
15	chr1:243138527-243138577	HCT-116	colon:	n/a
16	chr1:243053673-243053723	PFSK-1	brain:	n/a
17	chr1:243053934-243053984	K562	blood:	n/a
18	chr1:243053865-243053915	A549	lung:	n/a
19	chr1:243053425-243053475	HIPEpiC	eye:	n/a
20	chr1:243139525-243139575	U87	brain:	n/a
21	chr1:243139525-243139575	PFSK-1	brain:	n/a
22	chr1:243139525-243139575	HRE	kidney:	n/a
23	chr1:243053425-243053475	HCT-116	colon:	n/a
24	chr1:243053425-243053475	MCF-7	breast:	n/a
25	chr1:243053934-243053984	AG10803	skin:	n/a
26	chr1:243139525-243139575	GM12891	blood:	n/a
27	chr1:243053425-243053475	A549	lung:	n/a
28	chr1:243057080-243057130	GM19239	blood:	n/a
29	chr1:243057080-243057130	AG04449	skin:	fetal
30	chr1:243057080-243057130	NT2-D1	testis:	n/a
31	chr1:243053865-243053915	MCF10A-Er-Src	breast:	n/a
32	chr1:243053865-243053915	HCPEpiC	choroid plexus:	n/a
33	chr1:243054071-243054121	HMEC	breast:	n/a
34	chr1:243053934-243053984	GM12892	blood:	n/a
35	chr1:243139525-243139575	ovcar-3	ovarian:	n/a
36	chr1:243057080-243057130	HEK293	kidney:	embryo
37	chr1:243057080-243057130	HCF	heart:	n/a
38	chr1:243050875-243050925	AoSMC	blood vessel:	n/a
39	chr1:243053934-243053984	HUVEC	blood vessel:	n/a
40	chr1:243054071-243054121	HRE	kidney:	n/a
41	chr1:243053425-243053475	HCM	heart:	n/a
42	chr1:243053934-243053984	HCM	heart:	n/a
43	chr1:243057080-243057130	Jurkat	blood:	n/a
44	chr1:243054071-243054121	Caco-2	colon:	n/a
45	chr1:243139525-243139575	T-47D	breast:	n/a
46	chr1:243057080-243057130	ovcar-3	ovarian:	n/a
47	chr1:243050875-243050925	HCF	heart:	n/a
48	chr1:243053934-243053984	HCT-116	colon:	n/a
49	chr1:243050875-243050925	HNPCEpiC	eye:	n/a
50	chr1:243057080-243057130	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:243019974..243021671-chr1:243028235..243030687,2	K562	blood:
2	chr1:243003845..243005366-chr1:243007691..243009298,2	K562	blood:
3	chr1:243028922..243031643-chr1:243036505..243039074,2	K562	blood:
4	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:
5	chr1:243028922..243031643-chr1:243036505..243039074,2	K562	blood:
6	chr1:243003845..243005366-chr1:243007691..243009298,2	K562	blood:
7	chr1:242989477..242991101-chr1:242991941..242994002,2	K562	blood:
8	chr1:242617838..242618342-chr1:242955947..242956813,2	MCF-7	breast:
9	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:
10	chr1:243019974..243021671-chr1:243028235..243030687,2	K562	blood:
11	chr1:242989477..242991101-chr1:242991941..242994002,2	K562	blood:
12	chr1:242998388..243001295-chr1:243002456..243004745,2	K562	blood:
13	chr1:242998388..243001295-chr1:243002456..243004745,2	K562	blood:
14	chr1:242991254..242992220-chr1:243099841..243100636,3	MCF-7	breast:
15	chr1:243028092..243030417-chr1:243031884..243034309,2	K562	blood:
16	chr1:242991254..242992220-chr1:243099841..243100636,3	MCF-7	breast:
17	chr1:243028092..243030417-chr1:243031884..243034309,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEP170-9	chr1:243076807-243077141	expReg_chr1_22678_-
2	lnc-CEP170-3	chr1:243169714-243169980	XLOC_001282
3	lnc-CEP170-9	chr1:243070564-243075269	refGeneNc_994_NR_026778
4	lnc-CEP170-8	chr1:243077153-243077520	expReg_chr1_22679_-
5	lnc-CEP170-9	chr1:243076529-243076866	refGeneNc_994_NR_026778
6	lnc-CEP170-3	chr1:243169147-243169576	XLOC_001282
7	lnc-CEP170-7	chr1:243078426-243078834	expReg_chr1_22680_-

Variant related genes	Relation type
ENSG00000230199	TF binding region
ENSG00000270818	TF binding region
ENSG00000264972	TF binding region
ENSG00000230199	CpG island
ENSG00000270818	CpG island
ENSG00000264972	CpG island
LEFTY2	miRNA target sites

Extended variants
information (count: 2832 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2832 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78424850	chr1:242955390-242955391	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs570873158	chr1:242955394-242955395	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs192560856	chr1:242955395-242955396	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs371024487	chr1:242955429-242955430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12752277	chr1:242955437-242955438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs12751141	chr1:242955471-242955472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs12751150	chr1:242955487-242955488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12733675	chr1:242955508-242955509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12751297	chr1:242955563-242955564	Weak transcription	n/a	n/a	Overlapped CNVs	disease
10	rs556722012	chr1:242955623-242955624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184541804	chr1:242955654-242955655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs188154184	chr1:242955655-242955656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370645680	chr1:242955668-242955669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2809866	chr1:242955841-242955842	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs574598540	chr1:242955876-242955877	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs192503928	chr1:242955920-242955921	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs553319235	chr1:242955930-242955931	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs12092159	chr1:242955934-242955935	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs184426665	chr1:242955943-242955944	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs562291743	chr1:242955973-242955974	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs142797973	chr1:242955978-242955979	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs562285991	chr1:242963608-242963609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572750361	chr1:242963609-242963610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184615688	chr1:242963613-242963614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141172497	chr1:242963630-242963631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376765055	chr1:242963665-242963666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs71652434	chr1:242963666-242963667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1034212	chr1:242963677-242963678	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs543549631	chr1:242963680-242963681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs190101436	chr1:242963689-242963690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs150292103	chr1:242963743-242963744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs2151550	chr1:242963753-242963754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs78881088	chr1:242963763-242963764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs144967653	chr1:242963781-242963782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1034211	chr1:242963799-242963800	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs149063968	chr1:242963823-242963824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542372800	chr1:242963827-242963828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs111700576	chr1:242963837-242963838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs141808710	chr1:242963858-242963859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555898575	chr1:242963875-242963876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs569700698	chr1:242963910-242963911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs1034210	chr1:242963928-242963929	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs555975818	chr1:242963965-242963966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572713824	chr1:242963969-242963970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545686876	chr1:242974008-242974009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs572487610	chr1:242974023-242974024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541208226	chr1:242974083-242974084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs2780802	chr1:242974235-242974236	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs59578046	chr1:242974296-242974297	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs187514050	chr1:242974345-242974346	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	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
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	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
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
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	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
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:203 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:242953800-242955800	Weak transcription	Primary B cells from cord blood	blood
2	chr1:242955200-242955400	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
3	chr1:242955800-242956000	ZNF genes & repeats	Primary B cells from cord blood	blood
4	chr1:242963600-242964000	Enhancers	GM12878-XiMat	blood
5	chr1:242974000-242975000	Enhancers	HMEC	breast
6	chr1:242974600-242975200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr1:242976400-242976600	Enhancers	GM12878-XiMat	blood
8	chr1:242976400-242977000	Enhancers	Primary B cells from cord blood	blood
9	chr1:242976400-242977200	Enhancers	Primary B cells from peripheral blood	blood
10	chr1:242976600-242977200	Flanking Active TSS	GM12878-XiMat	blood
11	chr1:242977200-242977400	Enhancers	GM12878-XiMat	blood
12	chr1:242987200-242988800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr1:242987200-242991000	Enhancers	HMEC	breast
14	chr1:242987400-242988600	Enhancers	A549	lung
15	chr1:242987400-242988800	Enhancers	Muscle Satellite Cultured Cells	--
16	chr1:242987600-242987800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:242987600-242987800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr1:242987600-242988000	Enhancers	HSMMtube	muscle
19	chr1:242987600-242988200	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr1:242987600-242988600	Enhancers	Placenta Amnion	Placenta Amnion
21	chr1:242987600-242989000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr1:242987600-242991800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr1:242987600-242993200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr1:242987800-242988600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr1:242987800-242988600	Enhancers	Hela-S3	cervix
26	chr1:242988000-242990000	Weak transcription	HSMMtube	muscle
27	chr1:242988200-242992000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr1:242988600-242989600	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr1:242988600-242989600	Weak transcription	A549	lung
30	chr1:242988600-242989600	Weak transcription	Hela-S3	cervix
31	chr1:242988600-242991400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr1:242988800-242989200	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr1:242988800-242990000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr1:242989000-242989200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:242989000-242989200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr1:242989000-242989400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr1:242989200-242991800	Enhancers	Muscle Satellite Cultured Cells	--
38	chr1:242989400-242990600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:242989600-242990200	Enhancers	Placenta Amnion	Placenta Amnion
40	chr1:242989600-242990400	Enhancers	Hela-S3	cervix
41	chr1:242989600-242991600	Enhancers	A549	lung
42	chr1:242989800-242991600	Enhancers	NH-A	brain
43	chr1:242989800-242991800	Enhancers	Fetal Brain Male	brain
44	chr1:242990000-242990200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr1:242990000-242990200	Enhancers	HSMMtube	muscle
46	chr1:242990200-242991400	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr1:242990800-242993400	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr1:242991400-242991800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr1:242991400-242992000	Enhancers	Brain Anterior Caudate	brain
50	chr1:242991400-242992000	Enhancers	Placenta Amnion	Placenta Amnion

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