Variant report

Variant	nsv547930
Chromosome Location	chr1:153672247-153692745
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	chr1:153672136-153672286	K562	blood:	n/a	n/a
2	ARID3A	chr1:153681205-153681214	K562	blood:	n/a	n/a
3	ATF1	chr1:153681171-153681275	K562	blood:	n/a	n/a
4	ATF3	chr1:153688756-153688956	K562	blood:	n/a	n/a
5	BACH1	chr1:153672253-153672378	K562	blood:	n/a	n/a
6	BACH1	chr1:153681860-153681933	K562	blood:	n/a	n/a
7	BATF	chr1:153689854-153690094	GM12878	blood:	n/a	chr1:153689961-153689972
8	BATF	chr1:153689840-153690071	GM12878	blood:	n/a	chr1:153689961-153689972
9	BRCA1	chr1:153680550-153681789	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr1:153681111-153681312	K562	blood:	n/a	chr1:153681117-153681128
11	CEBPB	chr1:153681783-153682028	A549	lung:	n/a	n/a
12	CEBPB	chr1:153681144-153681400	MCF-7	breast:	n/a	n/a
13	CEBPB	chr1:153681177-153681352	K562	blood:	n/a	n/a
14	CEBPB	chr1:153681092-153681520	A549	lung:	n/a	chr1:153681117-153681128
15	CEBPB	chr1:153678046-153678200	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:153673650-153673839	K562	blood:	n/a	chr1:153673657-153673668 chr1:153673656-153673669 chr1:153673656-153673669 chr1:153673656-153673669 chr1:153673656-153673667
17	CEBPB	chr1:153673656-153673846	HepG2	liver:	n/a	chr1:153673657-153673668 chr1:153673656-153673669 chr1:153673656-153673669 chr1:153673656-153673669 chr1:153673656-153673667
18	CEBPB	chr1:153680514-153682077	Hela-S3	cervix:	n/a	chr1:153681117-153681128
19	CEBPB	chr1:153678102-153678322	K562	blood:	n/a	n/a
20	CEBPB	chr1:153681117-153681359	IMR90	lung:	n/a	chr1:153681117-153681128
21	CEBPB	chr1:153673593-153673741	IMR90	lung:	n/a	chr1:153673657-153673668 chr1:153673656-153673669 chr1:153673656-153673669 chr1:153673656-153673669 chr1:153673656-153673667
22	CEBPB	chr1:153673509-153673790	MCF-7	breast:	n/a	chr1:153673657-153673668 chr1:153673656-153673669 chr1:153673656-153673669 chr1:153673656-153673669 chr1:153673656-153673667
23	CEBPB	chr1:153681120-153681425	A549	lung:	n/a	n/a
24	CEBPB	chr1:153681144-153681315	HepG2	liver:	n/a	n/a
25	CHD2	chr1:153681038-153681352	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr1:153680625-153680639	Hela-S3	cervix:	n/a	n/a
27	CREB1	chr1:153681011-153681297	A549	lung:	n/a	n/a
28	CTCF	chr1:153683786-153683875	GM13976	blood:	n/a	n/a
29	CTCF	chr1:153691062-153691140	MCF-7	breast:	n/a	n/a
30	CTCF	chr1:153691035-153691141	MCF-7	breast:	n/a	n/a
31	CTCF	chr1:153675482-153675525	GM13976	blood:	n/a	n/a
32	CTCF	chr1:153690120-153690270	MCF-7	breast:	n/a	n/a
33	CTCF	chr1:153680720-153680870	MCF-7	breast:	n/a	n/a
34	CUX1	chr1:153682413-153682580	K562	blood:	n/a	n/a
35	EBF1	chr1:153678880-153679087	GM12878	blood:	n/a	n/a
36	EGR1	chr1:153672390-153672593	K562	blood:	n/a	n/a
37	EGR1	chr1:153672313-153672585	K562	blood:	n/a	n/a
38	EP300	chr1:153680520-153681426	Hela-S3	cervix:	n/a	n/a
39	FOS	chr1:153688869-153688924	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr1:153681061-153681426	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr1:153678113-153678312	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr1:153691790-153691852	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr1:153688869-153688954	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr1:153678068-153678329	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr1:153678052-153678309	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr1:153681062-153681430	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr1:153691754-153691870	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr1:153681080-153681424	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr1:153688743-153688940	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr1:153681077-153681426	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:153680755..153683313-chr1:153700229..153702126,2	K562	blood:
2	chr1:153649692..153651457-chr1:153668885..153672459,3	K562	blood:
3	chr1:153681393..153682324-chr16:2264390..2265358,2	Hela-S3	cervix:
4	chr1:153642439..153645279-chr1:153680616..153682934,3	MCF-7	breast:
5	chr1:153683195..153686007-chr1:153700603..153703489,3	MCF-7	breast:
6	chr1:153669864..153672115-chr1:153679120..153682442,3	MCF-7	breast:
7	chr1:153679139..153682305-chr1:153689935..153694453,5	MCF-7	breast:
8	chr1:153679572..153681343-chr1:153699326..153701642,2	MCF-7	breast:
9	chr1:153668419..153672342-chr1:153699600..153701905,4	MCF-7	breast:
10	chr1:153643715..153646402-chr1:153669451..153672333,3	K562	blood:
11	chr1:153677967..153682113-chr1:153686591..153688988,3	MCF-7	breast:
12	chr1:153677967..153682113-chr1:153686591..153688988,3	MCF-7	breast:
13	chr1:153679930..153682838-chr1:153699485..153702427,4	MCF-7	breast:
14	chr1:153690798..153692537-chr1:153698848..153701656,2	K562	blood:
15	chr1:153672193..153673896-chr1:153690766..153693363,2	MCF-7	breast:
16	chr1:153676052..153678273-chr1:153679043..153680683,2	MCF-7	breast:
17	chr1:153685180..153687511-chr1:153746756..153749223,2	MCF-7	breast:
18	chr1:153669943..153671545-chr1:153672210..153674806,2	K562	blood:
19	chr1:153679721..153682255-chr1:153699545..153702126,2	K562	blood:
20	chr1:153668994..153671784-chr1:153687110..153689814,2	K562	blood:
21	chr1:153643715..153646402-chr1:153669799..153672333,2	K562	blood:
22	chr1:153679034..153681144-chr1:153743976..153746673,2	MCF-7	breast:
23	chr1:153669010..153673102-chr1:153699484..153702565,5	MCF-7	breast:
24	chr1:153650435..153653664-chr1:153678187..153682235,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ILF2-1	chr1:153689779-153690298	NONHSAT006541
2	lnc-NPR1-1	chr1:153676564-153676859	NONHSAT006540
3	lnc-ILF2-1	chr1:153690592-153690823	NONHSAT006541

Variant related genes	Relation type
ENSG00000235015	TF binding region
RN7SL372P	TF binding region
ENSG00000184207	chromatin interactions
ENSG00000235015	chromatin interactions
ENSG00000169418	chromatin interactions
ENSG00000143621	chromatin interactions
ENSG00000143554	chromatin interactions
ENSG00000242565	chromatin interactions
ENSG00000143624	chromatin interactions

Extended variants
information (count: 770 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:770 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7541193	chr1:153672247-153672248	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs376968503	chr1:153672265-153672266	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs373183614	chr1:153672267-153672268	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs77839209	chr1:153672280-153672281	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs527317698	chr1:153672309-153672310	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs144464734	chr1:153672363-153672364	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs190764309	chr1:153672396-153672397	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs146632842	chr1:153672397-153672398	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs114854186	chr1:153672468-153672469	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs78091222	chr1:153672478-153672479	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs529169064	chr1:153672479-153672480	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs547696384	chr1:153672484-153672485	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs565917285	chr1:153672518-153672519	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs182101360	chr1:153672606-153672607	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs538303638	chr1:153672623-153672624	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs369561727	chr1:153672624-153672625	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs35198082	chr1:153672646-153672647	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs186824575	chr1:153672667-153672668	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs569766708	chr1:153672721-153672722	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs147568097	chr1:153672722-153672723	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs537157400	chr1:153672822-153672823	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs577040008	chr1:153672826-153672827	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs555539047	chr1:153672862-153672863	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs574204758	chr1:153672870-153672871	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs192397685	chr1:153672917-153672918	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs183456843	chr1:153672921-153672922	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs578204882	chr1:153672938-153672939	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs539433781	chr1:153673022-153673023	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs545740603	chr1:153673024-153673025	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs34822599	chr1:153673034-153673035	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs144596402	chr1:153673067-153673068	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs187441220	chr1:153673072-153673073	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs561841519	chr1:153673086-153673087	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs576431507	chr1:153673119-153673120	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs138392037	chr1:153673128-153673129	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs547288758	chr1:153673152-153673153	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs140193974	chr1:153673158-153673159	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs565935096	chr1:153673174-153673175	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs79518383	chr1:153673220-153673221	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs143499847	chr1:153673284-153673285	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs116601425	chr1:153673298-153673299	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs75375629	chr1:153673325-153673326	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs77437324	chr1:153673326-153673327	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs537126787	chr1:153673332-153673333	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs555477294	chr1:153673348-153673349	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs375296596	chr1:153673402-153673403	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs535369545	chr1:153673449-153673450	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs550315565	chr1:153673459-153673460	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs567670884	chr1:153673483-153673484	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs535194111	chr1:153673508-153673509	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

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
Ewing''s sarcoma	21437220	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
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	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
Esophageal squamous carcinoma	18350619	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
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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	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
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
Follicular lymphoma	20505157	CNVD
Liver carcinoma	19366792	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:153669200-153672400	Enhancers	A549	lung
2	chr1:153669600-153672600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:153670000-153672400	Enhancers	NHDF-Ad	bronchial
4	chr1:153670800-153672400	Enhancers	GM12878-XiMat	blood
5	chr1:153671000-153672600	Enhancers	Adipose Nuclei	Adipose
6	chr1:153671000-153672600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr1:153671200-153672600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr1:153671200-153672600	Enhancers	K562	blood
9	chr1:153671200-153672800	Weak transcription	Primary B cells from cord blood	blood
10	chr1:153671400-153672400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr1:153671600-153678200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr1:153671800-153672400	Enhancers	HUVEC	blood vessel
13	chr1:153672000-153674800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:153672000-153675200	Weak transcription	Right Atrium	heart
15	chr1:153672200-153673200	Enhancers	Hela-S3	cervix
16	chr1:153672200-153673800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr1:153672600-153674600	Weak transcription	K562	blood
18	chr1:153674600-153675200	Enhancers	K562	blood
19	chr1:153674800-153675000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr1:153675000-153679400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr1:153675200-153680600	Weak transcription	K562	blood
22	chr1:153678000-153678200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr1:153678200-153680600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr1:153679200-153679800	Enhancers	Hela-S3	cervix
25	chr1:153679800-153680200	Weak transcription	Hela-S3	cervix
26	chr1:153680200-153680600	Enhancers	Hela-S3	cervix
27	chr1:153680400-153681000	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr1:153680400-153681600	Enhancers	Placenta	Placenta
29	chr1:153680600-153681000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr1:153680600-153681000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr1:153680600-153681000	Enhancers	Adipose Nuclei	Adipose
32	chr1:153680600-153681000	Flanking Active TSS	Hela-S3	cervix
33	chr1:153680600-153681200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr1:153680600-153681200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:153680600-153681200	Enhancers	HepG2	liver
36	chr1:153680600-153682000	Enhancers	A549	lung
37	chr1:153680600-153682000	Enhancers	K562	blood
38	chr1:153681000-153681200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr1:153681000-153681200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr1:153681000-153681800	Active TSS	Hela-S3	cervix
41	chr1:153681000-153683200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr1:153681600-153682000	Flanking Active TSS	Placenta	Placenta
43	chr1:153681800-153682000	Flanking Active TSS	Hela-S3	cervix
44	chr1:153682000-153682400	Enhancers	Hela-S3	cervix
45	chr1:153682000-153683400	Weak transcription	A549	lung
46	chr1:153682400-153683200	Weak transcription	Hela-S3	cervix
47	chr1:153683200-153683400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr1:153683200-153683600	Enhancers	Hela-S3	cervix
49	chr1:153683400-153683800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr1:153683400-153683800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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