Variant report

Variant	nsv947200
Chromosome Location	chr1:160870136-160905390
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	ATF1	chr1:160881283-160881568	K562	blood:	n/a	n/a
2	ATF1	chr1:160895577-160895594	K562	blood:	n/a	n/a
3	ATF3	chr1:160895597-160895919	K562	blood:	n/a	n/a
4	ATF3	chr1:160895514-160896112	A549	lung:	n/a	n/a
5	ATF3	chr1:160895552-160896096	A549	lung:	n/a	n/a
6	BHLHE40	chr1:160881275-160881700	K562	blood:	n/a	n/a
7	CEBPB	chr1:160884360-160884367	K562	blood:	n/a	n/a
8	CEBPB	chr1:160881426-160881530	K562	blood:	n/a	n/a
9	CEBPB	chr1:160884312-160884522	HepG2	liver:	n/a	n/a
10	CEBPD	chr1:160881154-160881741	K562	blood:	n/a	n/a
11	CREB1	chr1:160904048-160904272	A549	lung:	n/a	n/a
12	CTCF	chr1:160891809-160891868	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr1:160871738-160871783	GM13977	blood:	n/a	n/a
14	CTCF	chr1:160875500-160875650	GM12871	blood:	n/a	n/a
15	CTCF	chr1:160874238-160874289	GM13976	blood:	n/a	n/a
16	EGR1	chr1:160881057-160881301	K562	blood:	n/a	chr1:160881188-160881202 chr1:160881189-160881202 chr1:160881190-160881200 chr1:160881189-160881202 chr1:160881189-160881202 chr1:160881190-160881200 chr1:160881184-160881206 chr1:160881190-160881201 chr1:160881188-160881203 chr1:160881189-160881202 chr1:160881190-160881201 chr1:160881191-160881200 chr1:160881190-160881199
17	EGR1	chr1:160880997-160881407	K562	blood:	n/a	chr1:160881188-160881202 chr1:160881189-160881202 chr1:160881190-160881200 chr1:160881189-160881202 chr1:160881189-160881202 chr1:160881190-160881200 chr1:160881184-160881206 chr1:160881190-160881201 chr1:160881188-160881203 chr1:160881189-160881202 chr1:160881190-160881201 chr1:160881191-160881200 chr1:160881190-160881199
18	ELF1	chr1:160895677-160895911	K562	blood:	n/a	n/a
19	ELF1	chr1:160895721-160895912	HepG2	liver:	n/a	n/a
20	EP300	chr1:160881297-160881610	K562	blood:	n/a	n/a
21	EP300	chr1:160895760-160895992	GM12878	blood:	n/a	n/a
22	ETS1	chr1:160895662-160895933	A549	lung:	n/a	n/a
23	ETS1	chr1:160895642-160895982	A549	lung:	n/a	n/a
24	FOS	chr1:160887337-160887537	HUVEC	blood vessel:	n/a	n/a
25	FOS	chr1:160895409-160895624	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr1:160895419-160895673	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr1:160895472-160895619	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr1:160904042-160904200	MCF10A-Er-Src	breast:	n/a	n/a
29	GATA1	chr1:160874634-160875095	PBDE	blood:	n/a	n/a
30	GATA1	chr1:160881046-160881824	K562	blood:	n/a	n/a
31	GATA1	chr1:160881004-160881751	PBDE	blood:	n/a	n/a
32	GATA1	chr1:160877653-160878232	PBDE	blood:	n/a	n/a
33	GATA2	chr1:160881307-160881600	K562	blood:	n/a	chr1:160881425-160881439
34	GATA2	chr1:160881222-160881611	K562	blood:	n/a	chr1:160881425-160881439
35	GATA2	chr1:160881317-160881581	HUVEC	blood vessel:	n/a	chr1:160881425-160881439
36	GATA2	chr1:160883067-160883509	K562	blood:	n/a	n/a
37	JUND	chr1:160881323-160881523	K562	blood:	n/a	n/a
38	JUND	chr1:160875593-160875650	K562	blood:	n/a	n/a
39	JUND	chr1:160875435-160875730	H1-hESC	embryonic stem cell:	n/a	chr1:160875566-160875578 chr1:160875565-160875573 chr1:160875568-160875576
40	KAP1	chr1:160881367-160881518	U2OS	brain:	n/a	n/a
41	MYC	chr1:160881291-160881551	K562	blood:	n/a	n/a
42	MYC	chr1:160881299-160881562	K562	blood:	n/a	n/a
43	NANOG	chr1:160883020-160883231	H1-hESC	embryonic stem cell:	n/a	n/a
44	NFYA	chr1:160880012-160880257	K562	blood:	n/a	chr1:160880164-160880182 chr1:160880188-160880206
45	NFYB	chr1:160880022-160880250	Hela-S3	cervix:	n/a	chr1:160880194-160880209 chr1:160880170-160880185
46	NFYB	chr1:160879935-160880373	K562	blood:	n/a	chr1:160880194-160880209 chr1:160880170-160880185
47	NFYB	chr1:160880003-160880376	GM12878	blood:	n/a	chr1:160880194-160880209 chr1:160880170-160880185
48	NR2F2	chr1:160881199-160881658	K562	blood:	n/a	n/a
49	NR2F2	chr1:160903518-160903925	K562	blood:	n/a	n/a
50	NR2F2	chr1:160881165-160881608	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:160903135-160903185	GM12892	blood:	n/a
2	chr1:160903135-160903185	U87	brain:	n/a
3	chr1:160903135-160903185	HRE	kidney:	n/a
4	chr1:160903135-160903185	GM12878	blood:	n/a
5	chr1:160903135-160903185	SK-N-SH	brain:	n/a
6	chr1:160903135-160903185	NT2-D1	testis:	n/a
7	chr1:160903135-160903185	NH-A	brain:	n/a
8	chr1:160903135-160903185	HPAEpiC	pulmonary alveolar:	n/a
9	chr1:160903135-160903185	AG09309	skin:	n/a
10	chr1:160903135-160903185	MCF-7	breast:	n/a
11	chr1:160903135-160903185	Jurkat	blood:	n/a
12	chr1:160903135-160903185	IMR90	lung:	fetal
13	chr1:160903135-160903185	CMK	blood:	n/a
14	chr1:160903135-160903185	T-47D	breast:	n/a
15	chr1:160903135-160903185	AG09319	gingival:	n/a
16	chr1:160903135-160903185	ECC-1	luminal epithelium:	n/a
17	chr1:160903135-160903185	HCM	heart:	n/a
18	chr1:160903135-160903185	PFSK-1	brain:	n/a
19	chr1:160903135-160903185	Hepatocyte	liver:	n/a
20	chr1:160903135-160903185	ovcar-3	ovarian:	n/a
21	chr1:160903135-160903185	NB4	blood:	n/a
22	chr1:160903135-160903185	BE2_C	brain:	n/a
23	chr1:160903135-160903185	ProgFib	skin:	n/a
24	chr1:160903135-160903185	AG04450	lung:	fetal
25	chr1:160903135-160903185	HAEpiC	amniotic membrane:	n/a
26	chr1:160903135-160903185	GM12891	blood:	n/a
27	chr1:160903135-160903185	HNPCEpiC	eye:	n/a
28	chr1:160903135-160903185	LNCaP	prostate:	n/a
29	chr1:160903135-160903185	HepG2	liver:	n/a
30	chr1:160903135-160903185	SK-N-MC	brain:	n/a
31	chr1:160903135-160903185	K562	blood:	n/a
32	chr1:160903135-160903185	PANC-1	pancreas:	n/a
33	chr1:160903135-160903185	NHDF-neo	bronchial:	n/a
34	chr1:160903135-160903185	RPTEC	kidney:	n/a
35	chr1:160903135-160903185	SK-N-SH_RA	brain:	n/a
36	chr1:160903135-160903185	GM06990	blood:	n/a
37	chr1:160903135-160903185	AoSMC	blood vessel:	n/a
38	chr1:160903135-160903185	A549	lung:	n/a
39	chr1:160903135-160903185	HMEC	breast:	n/a
40	chr1:160903135-160903185	HCPEpiC	choroid plexus:	n/a
41	chr1:160903135-160903185	MCF10A-Er-Src	breast:	n/a
42	chr1:160903135-160903185	Caco-2	colon:	n/a
43	chr1:160903135-160903185	PrEC	prostate:	n/a
44	chr1:160903135-160903185	HUVEC	blood vessel:	n/a
45	chr1:160903135-160903185	AG04449	skin:	fetal
46	chr1:160903135-160903185	HRPEpiC	eye:	n/a
47	chr1:160903135-160903185	HRCEpiC	kidney:	n/a
48	chr1:160903135-160903185	HCT-116	colon:	n/a
49	chr1:160903135-160903185	SKMC	muscle:	n/a
50	chr1:160903135-160903185	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:160869759..160871916-chr1:160873094..160874895,2	K562	blood:
2	chr1:160869759..160871916-chr1:160873094..160874895,2	K562	blood:
3	chr1:160874204..160876595-chr1:160877694..160880011,2	MCF-7	breast:
4	chr1:160850486..160853249-chr1:160886390..160887944,2	K562	blood:
5	chr1:160872347..160875327-chr1:160877154..160879416,3	K562	blood:
6	chr1:160874204..160876595-chr1:160877694..160880011,2	MCF-7	breast:
7	chr1:160872347..160875327-chr1:160877154..160879416,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ITLN2-1	chr1:160904035-160904170	XLOC_001064
2	lnc-ITLN2-1	chr1:160901529-160901967	XLOC_001064

Variant related genes	Relation type
ENSG00000198358	TF binding region
ENSG00000233691	TF binding region
ENSG00000232188	TF binding region
ENSG00000198358	CpG island
ENSG00000233691	CpG island
ENSG00000232188	CpG island
ENSG00000179914	chromatin interactions

Extended variants
information (count: 1031 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:1031 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550570186	chr1:160870220-160870221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs560965118	chr1:160870222-160870223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529750778	chr1:160870242-160870243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114992350	chr1:160870257-160870258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35879014	chr1:160870261-160870262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566654216	chr1:160870283-160870284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538582804	chr1:160870309-160870310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs6694185	chr1:160870319-160870320	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs568776369	chr1:160870359-160870360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs60719109	chr1:160870366-160870367	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs554502921	chr1:160870393-160870394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574877867	chr1:160870399-160870400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534297628	chr1:160870401-160870402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554101531	chr1:160870453-160870454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575590399	chr1:160870456-160870457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181103133	chr1:160870473-160870474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs6669353	chr1:160870479-160870480	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs539588315	chr1:160870505-160870506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563199690	chr1:160870550-160870551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147665959	chr1:160870590-160870591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544233030	chr1:160870620-160870621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560926898	chr1:160870642-160870643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs117706112	chr1:160870701-160870702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571941032	chr1:160870711-160870712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201958453	chr1:160870744-160870745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537764189	chr1:160870760-160870761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs11265512	chr1:160870841-160870842	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs556087861	chr1:160870848-160870849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370817718	chr1:160870903-160870904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373883932	chr1:160870921-160870922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532350721	chr1:160870935-160870936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551924947	chr1:160870940-160870941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs117408543	chr1:160870956-160870957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537739226	chr1:160870974-160870975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548225304	chr1:160870976-160870977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78727645	chr1:160870977-160870978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573980333	chr1:160870997-160870998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs186968584	chr1:160871033-160871034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190602791	chr1:160871089-160871090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570831558	chr1:160871090-160871091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs74617414	chr1:160871119-160871120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183524992	chr1:160871134-160871135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540044626	chr1:160871157-160871158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556751004	chr1:160871163-160871164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576846843	chr1:160871180-160871181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536343120	chr1:160871182-160871183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79749222	chr1:160871271-160871272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554294130	chr1:160871280-160871281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544578825	chr1:160871283-160871284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561058313	chr1:160871303-160871304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	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
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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21045282	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Idiopathic thrombocytopenic purpura	17827395	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:145 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:160870200-160875600	Weak transcription	Spleen	Spleen
2	chr1:160871400-160871600	Enhancers	Right Atrium	heart
3	chr1:160871600-160872000	Enhancers	Ovary	ovary
4	chr1:160871600-160874200	Weak transcription	Right Atrium	heart
5	chr1:160872000-160873600	Weak transcription	Ovary	ovary
6	chr1:160872200-160872800	Enhancers	Gastric	stomach
7	chr1:160872800-160875200	Weak transcription	Gastric	stomach
8	chr1:160873600-160877200	Enhancers	Ovary	ovary
9	chr1:160873800-160875000	Enhancers	Fetal Heart	heart
10	chr1:160874200-160875400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr1:160874200-160875800	Enhancers	Right Atrium	heart
12	chr1:160874400-160875000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:160874400-160875400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr1:160874400-160875600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr1:160874400-160875800	Enhancers	Fetal Intestine Large	intestine
16	chr1:160874400-160876000	Enhancers	Stomach Mucosa	stomach
17	chr1:160874600-160875400	Enhancers	Fetal Intestine Small	intestine
18	chr1:160874600-160875600	Enhancers	Pancreas	Pancrea
19	chr1:160874600-160875800	Enhancers	Right Ventricle	heart
20	chr1:160875000-160875400	Enhancers	Left Ventricle	heart
21	chr1:160875000-160875800	Flanking Active TSS	Fetal Heart	heart
22	chr1:160875000-160876000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr1:160875200-160875400	Enhancers	Gastric	stomach
24	chr1:160875400-160875800	Weak transcription	Gastric	stomach
25	chr1:160875400-160875800	Weak transcription	Left Ventricle	heart
26	chr1:160875400-160876000	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr1:160875400-160880600	Weak transcription	Fetal Intestine Small	intestine
28	chr1:160875600-160875800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr1:160875600-160880600	Weak transcription	Pancreas	Pancrea
30	chr1:160875800-160876000	Enhancers	Gastric	stomach
31	chr1:160875800-160876000	Enhancers	Left Ventricle	heart
32	chr1:160875800-160878400	Weak transcription	Right Atrium	heart
33	chr1:160875800-160879200	Enhancers	Fetal Heart	heart
34	chr1:160875800-160879800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr1:160875800-160880600	Weak transcription	Right Ventricle	heart
36	chr1:160876000-160876400	Weak transcription	Stomach Mucosa	stomach
37	chr1:160876000-160877800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr1:160876000-160878400	Weak transcription	Gastric	stomach
39	chr1:160876000-160878400	Weak transcription	Left Ventricle	heart
40	chr1:160876400-160876600	Enhancers	Stomach Mucosa	stomach
41	chr1:160876600-160881200	Weak transcription	Stomach Mucosa	stomach
42	chr1:160877200-160877600	Weak transcription	Ovary	ovary
43	chr1:160877600-160878600	Enhancers	Ovary	ovary
44	chr1:160877800-160878800	Enhancers	Aorta	Aorta
45	chr1:160877800-160880200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr1:160878400-160879200	Enhancers	Right Atrium	heart
47	chr1:160878400-160880000	Enhancers	Gastric	stomach
48	chr1:160878400-160880000	Enhancers	Left Ventricle	heart
49	chr1:160878600-160879000	Weak transcription	Ovary	ovary
50	chr1:160879000-160879200	ZNF genes & repeats	Ovary	ovary

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