Variant report

Variant	esv1833248
Chromosome Location	chr1:243044616-243133699
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	BACH1	chr1:243122482-243122506	K562	blood:	n/a	n/a
3	BHLHE40	chr1:243087986-243088483	K562	blood:	n/a	n/a
4	CBX3	chr1:243130209-243130606	K562	blood:	n/a	n/a
5	CBX3	chr1:243100093-243100300	K562	blood:	n/a	n/a
6	CBX3	chr1:243053418-243053739	K562	blood:	n/a	n/a
7	CBX3	chr1:243087941-243088379	K562	blood:	n/a	n/a
8	CCNT2	chr1:243129321-243129526	K562	blood:	n/a	n/a
9	CCNT2	chr1:243087975-243088306	K562	blood:	n/a	n/a
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	CEBPB	chr1:243088005-243088218	K562	blood:	n/a	n/a
18	CEBPB	chr1:243072543-243072743	K562	blood:	n/a	chr1:243072592-243072603
19	CEBPB	chr1:243105260-243105310	HepG2	liver:	n/a	chr1:243105272-243105283
20	CEBPB	chr1:243105243-243105313	A549	lung:	n/a	chr1:243105272-243105283
21	CEBPB	chr1:243072449-243072662	HepG2	liver:	n/a	chr1:243072592-243072603
22	CEBPB	chr1:243072507-243072681	IMR90	lung:	n/a	chr1:243072592-243072603
23	CHD2	chr1:243080927-243080928	K562	blood:	n/a	n/a
24	CHD2	chr1:243087993-243088116	K562	blood:	n/a	n/a
25	CTCF	chr1:243100149-243100353	GM19239	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
26	CTCF	chr1:243046760-243046910	GM12865	blood:	n/a	n/a
27	CTCF	chr1:243100140-243100369	MCF-7	breast:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
28	CTCF	chr1:243100013-243100437	H1-hESC	embryonic stem cell:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
29	CTCF	chr1:243100120-243100270	GM06990	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
30	CTCF	chr1:243095260-243095410	K562	blood:	n/a	chr1:243095371-243095381 chr1:243095368-243095386 chr1:243095363-243095384
31	CTCF	chr1:243100120-243100270	BE2_C	brain:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
32	CTCF	chr1:243100146-243100354	GM19240	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
33	CTCF	chr1:243100117-243100462	T-47D	breast:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
34	CTCF	chr1:243100100-243100250	A549	lung:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
35	CTCF	chr1:243100140-243100290	HMF	breast:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
36	CTCF	chr1:243100200-243100350	GM12873	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
37	CTCF	chr1:243100160-243100310	MCF-7	breast:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
38	CTCF	chr1:243100080-243100230	HL-60	blood:	n/a	n/a
39	CTCF	chr1:243100162-243100338	GM13977	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
40	CTCF	chr1:243124613-243124687	LNCaP	prostate:	n/a	n/a
41	CTCF	chr1:243100120-243100270	GM12864	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
42	CTCF	chr1:243100148-243100365	GM12892	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
43	CTCF	chr1:243100160-243100310	GM12874	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
44	CTCF	chr1:243051220-243051281	LNCaP	prostate:	n/a	n/a
45	CTCF	chr1:243063909-243063983	ProgFib	skin:	n/a	n/a
46	CTCF	chr1:243100180-243100330	WERI-Rb-1	eye:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
47	CTCF	chr1:243109100-243109250	GM12875	blood:	n/a	n/a
48	CTCF	chr1:243110104-243110153	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr1:243100080-243100230	A549	lung:	n/a	n/a
50	CTCF	chr1:243117840-243117990	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:243050875-243050925	HEEpiC	esophagus:	n/a
2	chr1:243057080-243057130	ovcar-3	ovarian:	n/a
3	chr1:243053673-243053723	NB4	blood:	n/a
4	chr1:243053425-243053475	HepG2	liver:	n/a
5	chr1:243053865-243053915	HNPCEpiC	eye:	n/a
6	chr1:243053865-243053915	A549	lung:	n/a
7	chr1:243053934-243053984	PrEC	prostate:	n/a
8	chr1:243057080-243057130	GM12878	blood:	n/a
9	chr1:243054071-243054121	A549	lung:	n/a
10	chr1:243057080-243057130	RPTEC	kidney:	n/a
11	chr1:243053865-243053915	AG10803	skin:	n/a
12	chr1:243053865-243053915	ovcar-3	ovarian:	n/a
13	chr1:243053673-243053723	GM06990	blood:	n/a
14	chr1:243053865-243053915	AG04449	skin:	fetal
15	chr1:243057080-243057130	HCPEpiC	choroid plexus:	n/a
16	chr1:243053934-243053984	U87	brain:	n/a
17	chr1:243050875-243050925	MCF-7	breast:	n/a
18	chr1:243053865-243053915	HEEpiC	esophagus:	n/a
19	chr1:243053425-243053475	NHBE	bronchial:	n/a
20	chr1:243053865-243053915	HPAEpiC	pulmonary alveolar:	n/a
21	chr1:243050875-243050925	ProgFib	skin:	n/a
22	chr1:243053673-243053723	Hepatocyte	liver:	n/a
23	chr1:243050875-243050925	Hepatocyte	liver:	n/a
24	chr1:243053425-243053475	ECC-1	luminal epithelium:	n/a
25	chr1:243057080-243057130	CMK	blood:	n/a
26	chr1:243053425-243053475	HCM	heart:	n/a
27	chr1:243057080-243057130	HIPEpiC	eye:	n/a
28	chr1:243053425-243053475	MCF10A-Er-Src	breast:	n/a
29	chr1:243053934-243053984	SAEC	small airway:	n/a
30	chr1:243053934-243053984	HepG2	liver:	n/a
31	chr1:243050875-243050925	SK-N-SH	brain:	n/a
32	chr1:243053865-243053915	SK-N-SH_RA	brain:	n/a
33	chr1:243054071-243054121	HL-60	blood:	n/a
34	chr1:243053934-243053984	GM12878	blood:	n/a
35	chr1:243057080-243057130	SK-N-MC	brain:	n/a
36	chr1:243053865-243053915	BE2_C	brain:	n/a
37	chr1:243057080-243057130	Hepatocyte	liver:	n/a
38	chr1:243053425-243053475	IMR90	lung:	fetal
39	chr1:243050875-243050925	GM12878	blood:	n/a
40	chr1:243053865-243053915	HL-60	blood:	n/a
41	chr1:243053934-243053984	MCF-7	breast:	n/a
42	chr1:243053673-243053723	ovcar-3	ovarian:	n/a
43	chr1:243053865-243053915	NH-A	brain:	n/a
44	chr1:243050875-243050925	IMR90	lung:	fetal
45	chr1:243057080-243057130	H1-hESC	embryonic stem cell:	embryo
46	chr1:243053673-243053723	HCF	heart:	n/a
47	chr1:243053934-243053984	LNCaP	prostate:	n/a
48	chr1:243053425-243053475	Caco-2	colon:	n/a
49	chr1:243053673-243053723	BE2_C	brain:	n/a
50	chr1:243053673-243053723	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:
2	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:
3	chr1:242991254..242992220-chr1:243099841..243100636,3	MCF-7	breast:

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-CEP170-9	chr1:243076529-243076866	refGeneNc_994_NR_026778
4	lnc-CEP170-8	chr1:243077153-243077520	expReg_chr1_22679_-
5	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

Extended variants
information (count: 1163 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1163 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563478024	chr1:243044618-243044619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs562804398	chr1:243044620-243044621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573876222	chr1:243044760-243044761	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542873197	chr1:243044786-243044787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372583723	chr1:243044789-243044790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs138258809	chr1:243044823-243044824	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs114791184	chr1:243044853-243044854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189639198	chr1:243044867-243044868	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551395984	chr1:243044889-243044890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs77944505	chr1:243044951-243044952	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs35105770	chr1:243044962-243044963	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs550914097	chr1:243044966-243044967	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs35705897	chr1:243044998-243044999	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567811661	chr1:243045000-243045001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs36084319	chr1:243045002-243045003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536550690	chr1:243045027-243045028	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141838361	chr1:243045029-243045030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561942844	chr1:243045067-243045068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566821345	chr1:243045074-243045075	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs3003549	chr1:243045081-243045082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs35261722	chr1:243045106-243045107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558511382	chr1:243045120-243045121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34863369	chr1:243045128-243045129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575360052	chr1:243045164-243045165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs34176754	chr1:243045169-243045170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs35923705	chr1:243045224-243045225	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs544429900	chr1:243045258-243045259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185876773	chr1:243045275-243045276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566555629	chr1:243045294-243045295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs35083058	chr1:243045314-243045315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35864981	chr1:243045318-243045319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs34567501	chr1:243045368-243045369	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529047346	chr1:243045418-243045419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10926902	chr1:243045431-243045432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542563123	chr1:243045469-243045470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190684206	chr1:243045479-243045480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575110392	chr1:243045620-243045621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545058167	chr1:243045624-243045625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564844996	chr1:243045695-243045696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149368500	chr1:243045712-243045713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544253041	chr1:243045727-243045728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs147510698	chr1:243045732-243045733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12029605	chr1:243045760-243045761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182857111	chr1:243045774-243045775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546869364	chr1:243045820-243045821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187357580	chr1:243045876-243045877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533449361	chr1:243045907-243045908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561332476	chr1:243045926-243045927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192201498	chr1:243045968-243045969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559715158	chr1:243046042-243046043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:243041000-243046600	Weak transcription	Pancreas	Pancrea
2	chr1:243044400-243045400	Enhancers	Fetal Heart	heart
3	chr1:243046600-243046800	Enhancers	Pancreas	Pancrea
4	chr1:243046800-243053600	Weak transcription	Pancreas	Pancrea
5	chr1:243047200-243049000	Weak transcription	A549	lung
6	chr1:243049000-243049200	Enhancers	A549	lung
7	chr1:243049200-243049800	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr1:243049200-243049800	Enhancers	Liver	Liver
9	chr1:243049200-243049800	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr1:243049200-243049800	Enhancers	Sigmoid Colon	Sigmoid Colon
11	chr1:243049200-243049800	Flanking Active TSS	A549	lung
12	chr1:243049200-243049800	Enhancers	HepG2	liver
13	chr1:243049600-243049800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:243049800-243050600	Enhancers	A549	lung
15	chr1:243049800-243053600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr1:243049800-243053600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr1:243050600-243051800	Weak transcription	A549	lung
18	chr1:243053400-243053600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr1:243053600-243053800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr1:243053600-243054000	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr1:243053600-243054000	Active TSS	H1 Cell Line	embryonic stem cell
22	chr1:243053600-243054000	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr1:243053600-243054000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr1:243053600-243054000	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr1:243053600-243054000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr1:243053600-243054000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr1:243053600-243054000	Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr1:243053600-243054000	Active TSS	iPS-18 Cell Line	embryonic stem cell
29	chr1:243053600-243054000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr1:243053600-243054000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr1:243053600-243054000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
32	chr1:243053600-243054000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr1:243053600-243054000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr1:243053600-243054000	Bivalent Enhancer	Brain Hippocampus Middle	brain
35	chr1:243053600-243054000	Enhancers	Fetal Brain Male	brain
36	chr1:243053600-243054000	Bivalent/Poised TSS	Fetal Brain Female	brain
37	chr1:243053600-243054000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr1:243053600-243054000	Enhancers	Pancreas	Pancrea
39	chr1:243053600-243054000	Enhancers	Placenta Amnion	Placenta Amnion
40	chr1:243053600-243054000	Bivalent Enhancer	HMEC	breast
41	chr1:243053600-243054200	Active TSS	HUES48 Cell Line	embryonic stem cell
42	chr1:243053600-243054200	Active TSS	HUES64 Cell Line	embryonic stem cell
43	chr1:243053600-243054200	Active TSS	iPS-15b Cell Line	embryonic stem cell
44	chr1:243053600-243054200	Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr1:243053600-243054200	Active TSS	Brain Germinal Matrix	brain
46	chr1:243053600-243054200	Active TSS	HSMM	muscle
47	chr1:243053800-243054000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr1:243053800-243054000	Bivalent Enhancer	Colonic Mucosa	Colon
49	chr1:243053800-243054200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
50	chr1:243053800-243054600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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