Variant report

Variant	esv1807726
Chromosome Location	chr1:187445049-187466401
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	chr1:187460152-187460921	HepG2	liver:	n/a	n/a
2	CEBPB	chr1:187460304-187460894	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr1:187460475-187460902	MCF-7	breast:	n/a	n/a
4	CEBPB	chr1:187448517-187448764	IMR90	lung:	n/a	chr1:187448620-187448631
5	CEBPB	chr1:187460418-187461002	MCF-7	breast:	n/a	n/a
6	CEBPB	chr1:187448514-187448722	HepG2	liver:	n/a	chr1:187448620-187448631
7	CEBPB	chr1:187460607-187460877	HepG2	liver:	n/a	n/a
8	CEBPB	chr1:187460064-187461119	IMR90	lung:	n/a	n/a
9	CTCF	chr1:187445940-187446090	HRE	kidney:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
10	CTCF	chr1:187445845-187446156	K562	blood:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
11	CTCF	chr1:187445860-187446010	K562	blood:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
12	CTCF	chr1:187445919-187446036	K562	blood:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
13	CTCF	chr1:187445920-187446070	HPAF	blood vessel:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
14	CTCF	chr1:187445812-187446156	GM12878	blood:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
15	CTCF	chr1:187445900-187446050	AG04449	skin:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
16	CTCF	chr1:187446160-187446310	HUVEC	blood vessel:	n/a	n/a
17	CTCF	chr1:187445835-187446109	HUVEC	blood vessel:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
18	CTCF	chr1:187445840-187445990	NHEK	skin:	n/a	n/a
19	CTCF	chr1:187445980-187446130	NHDF-neo	bronchial:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
20	CTCF	chr1:187445940-187446090	MCF-7	breast:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
21	CTCF	chr1:187445860-187446010	NB4	blood:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
22	CTCF	chr1:187445940-187446090	HCT-116	colon:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
23	CTCF	chr1:187445900-187446050	HCM	heart:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
24	CTCF	chr1:187445940-187446090	HPF	lung:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
25	CTCF	chr1:187445900-187446050	HMF	breast:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
26	CTCF	chr1:187445842-187446016	Gliobla	brain:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
27	CTCF	chr1:187445900-187446050	HCPEpiC	choroid plexus:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
28	CTCF	chr1:187454200-187454350	Caco-2	colon:	n/a	n/a
29	CTCF	chr1:187446020-187446170	HCM	heart:	n/a	n/a
30	CTCF	chr1:187445860-187446010	HMEC	breast:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
31	CTCF	chr1:187445860-187446010	GM12872	blood:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
32	CTCF	chr1:187445920-187446070	RPTEC	kidney:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
33	CTCF	chr1:187446000-187446150	BE2_C	brain:	n/a	n/a
34	CTCF	chr1:187445840-187445990	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr1:187445900-187446050	GM12866	blood:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
36	CTCF	chr1:187445873-187446076	Hela-S3	cervix:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
37	CTCF	chr1:187445883-187446078	H1-hESC	embryonic stem cell:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
38	CTCF	chr1:187445918-187445995	GM10266	blood:	n/a	n/a
39	CTCF	chr1:187445952-187446037	Pancreas_OC	pancreas:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
40	CTCF	chr1:187445791-187446173	IMR90	lung:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
41	CTCF	chr1:187445920-187446070	GM06990	blood:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
42	CTCF	chr1:187445880-187446030	GM12873	blood:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
43	CTCF	chr1:187445940-187446090	Caco-2	colon:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
44	CTCF	chr1:187445920-187446070	HCT-116	colon:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
45	CTCF	chr1:187445880-187446030	HA-sp	spinal cord:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
46	CTCF	chr1:187445731-187446116	MCF-7	breast:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
47	CTCF	chr1:187445920-187446070	HCPEpiC	choroid plexus:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
48	CTCF	chr1:187445880-187446030	NHDF-neo	bronchial:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
49	CTCF	chr1:187445840-187445990	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr1:187445700-187445850	SK-N-SH_RA	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:187445635-187445685	Hela-S3	cervix:	n/a
2	chr1:187460781-187460831	HEK293	kidney:	embryo
3	chr1:187460781-187460831	HUVEC	blood vessel:	n/a
4	chr1:187445635-187445685	T-47D	breast:	n/a
5	chr1:187460781-187460831	AG09319	gingival:	n/a
6	chr1:187445635-187445685	BJ	skin:	n/a
7	chr1:187445635-187445685	HRPEpiC	eye:	n/a
8	chr1:187445635-187445685	Caco-2	colon:	n/a
9	chr1:187460781-187460831	LNCaP	prostate:	n/a
10	chr1:187445635-187445685	PANC-1	pancreas:	n/a
11	chr1:187445635-187445685	ProgFib	skin:	n/a
12	chr1:187445635-187445685	AG04449	skin:	fetal
13	chr1:187445635-187445685	Hepatocyte	liver:	n/a
14	chr1:187445635-187445685	HNPCEpiC	eye:	n/a
15	chr1:187460781-187460831	PrEC	prostate:	n/a
16	chr1:187445635-187445685	GM12878	blood:	n/a
17	chr1:187445635-187445685	LNCaP	prostate:	n/a
18	chr1:187445635-187445685	HCT-116	colon:	n/a
19	chr1:187445635-187445685	GM06990	blood:	n/a
20	chr1:187460781-187460831	AoSMC	blood vessel:	n/a
21	chr1:187445635-187445685	PFSK-1	brain:	n/a
22	chr1:187445635-187445685	AG04450	lung:	fetal
23	chr1:187460781-187460831	HNPCEpiC	eye:	n/a
24	chr1:187460781-187460831	IMR90	lung:	fetal
25	chr1:187445635-187445685	H1-hESC	embryonic stem cell:	embryo
26	chr1:187460781-187460831	H1-hESC	embryonic stem cell:	embryo
27	chr1:187460781-187460831	HRCEpiC	kidney:	n/a
28	chr1:187460781-187460831	HCF	heart:	n/a
29	chr1:187460781-187460831	SKMC	muscle:	n/a
30	chr1:187445635-187445685	CMK	blood:	n/a
31	chr1:187460781-187460831	BJ	skin:	n/a
32	chr1:187460781-187460831	GM12891	blood:	n/a
33	chr1:187445635-187445685	AoSMC	blood vessel:	n/a
34	chr1:187460781-187460831	GM12878	blood:	n/a
35	chr1:187460781-187460831	ProgFib	skin:	n/a
36	chr1:187460781-187460831	SK-N-SH	brain:	n/a
37	chr1:187460781-187460831	Hepatocyte	liver:	n/a
38	chr1:187445635-187445685	NHDF-neo	bronchial:	n/a
39	chr1:187460781-187460831	NH-A	brain:	n/a
40	chr1:187445635-187445685	HUVEC	blood vessel:	n/a
41	chr1:187445635-187445685	HL-60	blood:	n/a
42	chr1:187445635-187445685	NT2-D1	testis:	n/a
43	chr1:187445635-187445685	GM12892	blood:	n/a
44	chr1:187460781-187460831	AG04449	skin:	fetal
45	chr1:187445635-187445685	HRE	kidney:	n/a
46	chr1:187460781-187460831	U87	brain:	n/a
47	chr1:187445635-187445685	HMEC	breast:	n/a
48	chr1:187445635-187445685	NH-A	brain:	n/a
49	chr1:187445635-187445685	HEK293	kidney:	embryo
50	chr1:187460781-187460831	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:187445527..187446417-chr1:187482131..187482720,2	MCF-7	breast:
2	chr1:187445440..187446428-chr1:187968865..187969402,5	MCF-7	breast:
3	chr1:187460603..187462421-chr1:187469087..187470836,2	MCF-7	breast:
4	chr1:187234168..187234815-chr1:187445615..187446278,2	MCF-7	breast:
5	chr1:187449317..187451017-chr1:187452914..187454633,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLA2G4A-2	chr1:187449425-187449746	ENSG00000272827.1
2	lnc-PLA2G4A-2	chr1:187446152-187446354	XLOC_000498
3	lnc-PLA2G4A-2	chr1:187443288-187449968	NONHSAT008463

Variant related genes	Relation type
ENSG00000272827	TF binding region
ENSG00000272827	CpG island
ENSG00000272827	chromatin interactions
TMEM138	miRNA target sites

Extended variants
information (count: 538 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:538 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4651390	chr1:187445049-187445050	Weak transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs546331322	chr1:187445058-187445059	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs371433280	chr1:187445096-187445097	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs373229919	chr1:187445099-187445100	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs207460784	chr1:187445123-187445124	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs563113420	chr1:187445154-187445155	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs530311781	chr1:187445165-187445166	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs114153531	chr1:187445172-187445173	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs386637672	chr1:187445205-187445206	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs11801693	chr1:187445207-187445208	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs573265099	chr1:187445332-187445333	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs552312378	chr1:187445361-187445362	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs570805733	chr1:187445398-187445399	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs139968128	chr1:187445429-187445430	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs532371928	chr1:187445447-187445448	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs548352321	chr1:187445478-187445479	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs549657007	chr1:187445505-187445506	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs58981203	chr1:187445557-187445558	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs2383623	chr1:187445566-187445567	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs115308773	chr1:187445569-187445570	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs371861136	chr1:187445590-187445591	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs186113096	chr1:187445636-187445637	Weak transcription Enhancers	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs539496449	chr1:187445661-187445662	Weak transcription Enhancers	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs532503215	chr1:187445664-187445665	Weak transcription Enhancers	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs575979593	chr1:187445708-187445709	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs538583734	chr1:187445715-187445716	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs556895936	chr1:187445744-187445745	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs191066026	chr1:187445868-187445869	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs143533041	chr1:187445874-187445875	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs74135624	chr1:187445879-187445880	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs572477460	chr1:187445978-187445979	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs529688089	chr1:187445989-187445990	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs146659522	chr1:187446022-187446023	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs564365620	chr1:187446023-187446024	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs531729381	chr1:187446076-187446077	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs547825392	chr1:187446084-187446085	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs148412487	chr1:187446089-187446090	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs529124012	chr1:187446147-187446148	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs547216815	chr1:187446170-187446171	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs565851524	chr1:187446187-187446188	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs182345780	chr1:187446198-187446199	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs530487390	chr1:187446240-187446241	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs551450458	chr1:187446258-187446259	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs551097977	chr1:187446285-187446286	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs569601574	chr1:187446306-187446307	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs72724256	chr1:187446318-187446319	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs555365384	chr1:187446343-187446344	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs551874485	chr1:187446383-187446384	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs74135625	chr1:187446386-187446387	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs115978864	chr1:187446459-187446460	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Urothelial carcinoma	21177765	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	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
Myelofibrosis	22110671	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Schizophrenia	19197363	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17899364	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:187439400-187446200	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr1:187439400-187446400	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr1:187441000-187446200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr1:187441600-187445400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:187444000-187446200	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr1:187444000-187446200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr1:187444200-187445800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr1:187444200-187446200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr1:187445400-187450600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr1:187445800-187447200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr1:187446200-187446600	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr1:187446200-187447000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr1:187446200-187447000	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr1:187446200-187447000	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr1:187446200-187447000	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr1:187446200-187447000	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr1:187448000-187448200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr1:187449600-187450200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr1:187450600-187450800	Enhancers	Brain Substantia Nigra	brain
20	chr1:187450600-187451200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr1:187450800-187451200	Active TSS	Brain Substantia Nigra	brain
22	chr1:187451200-187451800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr1:187451800-187455400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr1:187455400-187457200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:187459800-187461600	Enhancers	Hela-S3	cervix
26	chr1:187460000-187460200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr1:187460000-187460200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr1:187460000-187460200	Enhancers	Placenta	Placenta
29	chr1:187460000-187461400	Enhancers	A549	lung
30	chr1:187460000-187461800	Enhancers	HepG2	liver
31	chr1:187460200-187461200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr1:187460200-187461200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr1:187460200-187461200	Weak transcription	Placenta	Placenta
34	chr1:187461200-187461600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr1:187461200-187461600	Enhancers	Placenta	Placenta
36	chr1:187461200-187461800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr1:187461400-187461600	ZNF genes & repeats	Right Atrium	heart

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