Variant report

Variant	esv1810757
Chromosome Location	chr1:242965934-243167667
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	chr1:242996994-242996997	K562	blood:	n/a	n/a
5	BACH1	chr1:243122482-243122506	K562	blood:	n/a	n/a
6	BCL11A	chr1:242976721-242977165	GM12878	blood:	n/a	chr1:242976959-242976968
7	BCL11A	chr1:243153505-243153675	GM12878	blood:	n/a	n/a
8	BCL11A	chr1:242976760-242977140	GM12878	blood:	n/a	chr1:242976959-242976968
9	BHLHE40	chr1:242976782-242977230	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:243031757-243031938	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:243087986-243088483	K562	blood:	n/a	n/a
12	BRCA1	chr1:242997383-242997489	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr1:243053418-243053739	K562	blood:	n/a	n/a
14	CBX3	chr1:243100093-243100300	K562	blood:	n/a	n/a
15	CBX3	chr1:243130209-243130606	K562	blood:	n/a	n/a
16	CBX3	chr1:243087941-243088379	K562	blood:	n/a	n/a
17	CCNT2	chr1:243129321-243129526	K562	blood:	n/a	n/a
18	CCNT2	chr1:243087975-243088306	K562	blood:	n/a	n/a
19	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
20	CEBPB	chr1:243072449-243072662	HepG2	liver:	n/a	chr1:243072592-243072603
21	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
22	CEBPB	chr1:242998320-242998357	HepG2	liver:	n/a	chr1:242998327-242998338
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	chr1:242998985-242999533	A549	lung:	n/a	n/a
25	CEBPB	chr1:243072507-243072681	IMR90	lung:	n/a	chr1:243072592-243072603
26	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
27	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
28	CEBPB	chr1:243105260-243105310	HepG2	liver:	n/a	chr1:243105272-243105283
29	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
30	CEBPB	chr1:243072543-243072743	K562	blood:	n/a	chr1:243072592-243072603
31	CEBPB	chr1:243105243-243105313	A549	lung:	n/a	chr1:243105272-243105283
32	CEBPB	chr1:243088005-243088218	K562	blood:	n/a	n/a
33	CEBPB	chr1:243148513-243148717	K562	blood:	n/a	n/a
34	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
35	CHD1	chr1:242976654-242977278	GM12878	blood:	n/a	n/a
36	CHD2	chr1:243087993-243088116	K562	blood:	n/a	n/a
37	CHD2	chr1:242976690-242977268	GM12878	blood:	n/a	n/a
38	CHD2	chr1:243005456-243005619	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr1:243080927-243080928	K562	blood:	n/a	n/a
40	CHD2	chr1:242991732-242991777	HepG2	liver:	n/a	n/a
41	CTCF	chr1:243100162-243100338	GM13977	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
42	CTCF	chr1:243043213-243043217	K562	blood:	n/a	n/a
43	CTCF	chr1:243100220-243100370	GM06990	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
44	CTCF	chr1:243166373-243166711	K562	blood:	n/a	chr1:243166447-243166465 chr1:243166448-243166464
45	CTCF	chr1:243063909-243063983	ProgFib	skin:	n/a	n/a
46	CTCF	chr1:243100124-243100378	MCF-7	breast:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
47	CTCF	chr1:243099979-243100540	MCF-7	breast:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
48	CTCF	chr1:243100160-243100310	MCF-7	breast:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
49	CTCF	chr1:243100180-243100330	GM12868	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
50	CTCF	chr1:243100200-243100350	GM12865	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:243053934-243053984	HNPCEpiC	eye:	n/a
2	chr1:243053934-243053984	HNPCEpiC	eye:	n/a
3	chr1:243138527-243138577	LNCaP	prostate:	n/a
4	chr1:243057080-243057130	ovcar-3	ovarian:	n/a
5	chr1:243050875-243050925	NHBE	bronchial:	n/a
6	chr1:243053934-243053984	SKMC	muscle:	n/a
7	chr1:243054071-243054121	HMEC	breast:	n/a
8	chr1:243138527-243138577	HCF	heart:	n/a
9	chr1:243050875-243050925	Caco-2	colon:	n/a
10	chr1:243053934-243053984	HPAEpiC	pulmonary alveolar:	n/a
11	chr1:243053673-243053723	AG09309	skin:	n/a
12	chr1:243057080-243057130	SK-N-MC	brain:	n/a
13	chr1:243053425-243053475	K562	blood:	n/a
14	chr1:243054071-243054121	CMK	blood:	n/a
15	chr1:243053425-243053475	SAEC	small airway:	n/a
16	chr1:243053673-243053723	HUVEC	blood vessel:	n/a
17	chr1:243053934-243053984	HRE	kidney:	n/a
18	chr1:243138527-243138577	BJ	skin:	n/a
19	chr1:243138527-243138577	GM12891	blood:	n/a
20	chr1:243053865-243053915	U87	brain:	n/a
21	chr1:243053425-243053475	A549	lung:	n/a
22	chr1:243057080-243057130	BE2_C	brain:	n/a
23	chr1:243053673-243053723	SK-N-MC	brain:	n/a
24	chr1:243053934-243053984	BJ	skin:	n/a
25	chr1:243139525-243139575	Hela-S3	cervix:	n/a
26	chr1:243054071-243054121	HAEpiC	amniotic membrane:	n/a
27	chr1:243053865-243053915	ECC-1	luminal epithelium:	n/a
28	chr1:243053425-243053475	MCF-7	breast:	n/a
29	chr1:243054071-243054121	GM12891	blood:	n/a
30	chr1:243054071-243054121	GM12892	blood:	n/a
31	chr1:243139525-243139575	HCM	heart:	n/a
32	chr1:243138527-243138577	PANC-1	pancreas:	n/a
33	chr1:243054071-243054121	HRE	kidney:	n/a
34	chr1:243138527-243138577	CMK	blood:	n/a
35	chr1:243050875-243050925	HL-60	blood:	n/a
36	chr1:243139525-243139575	GM19239	blood:	n/a
37	chr1:243050875-243050925	HCPEpiC	choroid plexus:	n/a
38	chr1:243053425-243053475	ECC-1	luminal epithelium:	n/a
39	chr1:243057080-243057130	AG09309	skin:	n/a
40	chr1:243138527-243138577	HPAEpiC	pulmonary alveolar:	n/a
41	chr1:243139525-243139575	HNPCEpiC	eye:	n/a
42	chr1:243053934-243053984	NHBE	bronchial:	n/a
43	chr1:243053673-243053723	HCF	heart:	n/a
44	chr1:243050875-243050925	ovcar-3	ovarian:	n/a
45	chr1:243053425-243053475	ProgFib	skin:	n/a
46	chr1:243139525-243139575	A549	lung:	n/a
47	chr1:243139525-243139575	MCF-7	breast:	n/a
48	chr1:243053934-243053984	NT2-D1	testis:	n/a
49	chr1:243054071-243054121	LNCaP	prostate:	n/a
50	chr1:243139525-243139575	NB4	blood:	n/a

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

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

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

Extended variants
information (count: 2654 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2654 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545686876	chr1:242974008-242974009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs572487610	chr1:242974023-242974024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541208226	chr1:242974083-242974084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs2780802	chr1:242974235-242974236	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs59578046	chr1:242974296-242974297	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs187514050	chr1:242974345-242974346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2780801	chr1:242974392-242974393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2780800	chr1:242974401-242974402	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs548144290	chr1:242974461-242974462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs192929139	chr1:242974498-242974499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs183981123	chr1:242974499-242974500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188661446	chr1:242974502-242974503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs570565034	chr1:242974510-242974511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs12131075	chr1:242974542-242974543	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs147032426	chr1:242974544-242974545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs12123385	chr1:242974623-242974624	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs184461207	chr1:242974626-242974627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs548829614	chr1:242974630-242974631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535807920	chr1:242974651-242974652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs2780799	chr1:242974655-242974656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs575328329	chr1:242974704-242974705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541421397	chr1:242974731-242974732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564202458	chr1:242974735-242974736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577733453	chr1:242974739-242974740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190738394	chr1:242974742-242974743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs12131878	chr1:242974744-242974745	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs147966208	chr1:242974773-242974774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111912887	chr1:242974774-242974775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540573385	chr1:242974775-242974776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374562048	chr1:242974790-242974791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs60178985	chr1:242974793-242974794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531486252	chr1:242974814-242974815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs369871906	chr1:242974870-242974871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs548226053	chr1:242974881-242974882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs2502326	chr1:242974898-242974899	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs181981496	chr1:242974908-242974909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs2780798	chr1:242975005-242975006	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs2780797	chr1:242975036-242975037	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs186153970	chr1:242975059-242975060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550383137	chr1:242975098-242975099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2809880	chr1:242975099-242975100	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs536142841	chr1:242975156-242975157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549542940	chr1:242976401-242976402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs2780792	chr1:242976421-242976422	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs573982954	chr1:242976425-242976426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555264148	chr1:242976518-242976519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370251451	chr1:242976529-242976530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs2809882	chr1:242976557-242976558	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs534814673	chr1:242976599-242976600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs553413242	chr1:242976602-242976603	Enhancers Flanking Active TSS	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:199 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:242974000-242975000	Enhancers	HMEC	breast
2	chr1:242974600-242975200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr1:242976400-242976600	Enhancers	GM12878-XiMat	blood
4	chr1:242976400-242977000	Enhancers	Primary B cells from cord blood	blood
5	chr1:242976400-242977200	Enhancers	Primary B cells from peripheral blood	blood
6	chr1:242976600-242977200	Flanking Active TSS	GM12878-XiMat	blood
7	chr1:242977200-242977400	Enhancers	GM12878-XiMat	blood
8	chr1:242987200-242988800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr1:242987200-242991000	Enhancers	HMEC	breast
10	chr1:242987400-242988600	Enhancers	A549	lung
11	chr1:242987400-242988800	Enhancers	Muscle Satellite Cultured Cells	--
12	chr1:242987600-242987800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:242987600-242987800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr1:242987600-242988000	Enhancers	HSMMtube	muscle
15	chr1:242987600-242988200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr1:242987600-242988600	Enhancers	Placenta Amnion	Placenta Amnion
17	chr1:242987600-242989000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:242987600-242991800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr1:242987600-242993200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr1:242987800-242988600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr1:242987800-242988600	Enhancers	Hela-S3	cervix
22	chr1:242988000-242990000	Weak transcription	HSMMtube	muscle
23	chr1:242988200-242992000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr1:242988600-242989600	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr1:242988600-242989600	Weak transcription	A549	lung
26	chr1:242988600-242989600	Weak transcription	Hela-S3	cervix
27	chr1:242988600-242991400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr1:242988800-242989200	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr1:242988800-242990000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr1:242989000-242989200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr1:242989000-242989200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr1:242989000-242989400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:242989200-242991800	Enhancers	Muscle Satellite Cultured Cells	--
34	chr1:242989400-242990600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr1:242989600-242990200	Enhancers	Placenta Amnion	Placenta Amnion
36	chr1:242989600-242990400	Enhancers	Hela-S3	cervix
37	chr1:242989600-242991600	Enhancers	A549	lung
38	chr1:242989800-242991600	Enhancers	NH-A	brain
39	chr1:242989800-242991800	Enhancers	Fetal Brain Male	brain
40	chr1:242990000-242990200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr1:242990000-242990200	Enhancers	HSMMtube	muscle
42	chr1:242990200-242991400	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr1:242990800-242993400	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr1:242991400-242991800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr1:242991400-242992000	Enhancers	Brain Anterior Caudate	brain
46	chr1:242991400-242992000	Enhancers	Placenta Amnion	Placenta Amnion
47	chr1:242991400-242992200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr1:242991400-242992600	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr1:242991400-242992800	Enhancers	Brain Cingulate Gyrus	brain
50	chr1:242991400-242992800	Enhancers	Brain Hippocampus Middle	brain

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