Variant report

Variant	esv1799962
Chromosome Location	chr1:152751946-152778711
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	CEBPB	chr1:152752164-152752209	K562	blood:	n/a	chr1:152752194-152752205
2	CEBPB	chr1:152752036-152752272	HepG2	liver:	n/a	chr1:152752194-152752205
3	CTCF	chr1:152758532-152758657	NHEK	skin:	n/a	n/a
4	CTCF	chr1:152758560-152758710	HEEpiC	esophagus:	n/a	n/a
5	CTCF	chr1:152758640-152758790	SAEC	small airway:	n/a	n/a
6	CTCF	chr1:152758500-152758650	GM12874	blood:	n/a	n/a
7	CTCF	chr1:152758620-152758770	SAEC	small airway:	n/a	n/a
8	CTCF	chr1:152758480-152758630	HEEpiC	esophagus:	n/a	n/a
9	CTCF	chr1:152769087-152769143	Fibrobl	skin:	n/a	n/a
10	CTCF	chr1:152772992-152773083	GM10266	blood:	n/a	n/a
11	CTCF	chr1:152758560-152758710	MCF-7	breast:	n/a	n/a
12	CTCF	chr1:152758480-152758630	HMEC	breast:	n/a	n/a
13	CTCF	chr1:152769160-152769310	GM12869	blood:	n/a	n/a
14	CTCF	chr1:152758560-152758710	NHEK	skin:	n/a	n/a
15	CTCF	chr1:152758560-152758710	HMEC	breast:	n/a	n/a
16	CUX1	chr1:152752718-152752744	K562	blood:	n/a	n/a
17	EBF1	chr1:152757069-152757071	GM12878	blood:	n/a	n/a
18	FOS	chr1:152755680-152755881	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr1:152758570-152758718	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr1:152773916-152774024	MCF10A-Er-Src	breast:	n/a	chr1:152774008-152774016 chr1:152774007-152774017 chr1:152774006-152774018
21	FOS	chr1:152758506-152758818	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr1:152755681-152755857	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr1:152773965-152774021	MCF10A-Er-Src	breast:	n/a	chr1:152774008-152774016 chr1:152774007-152774017 chr1:152774006-152774018
24	FOS	chr1:152758540-152758758	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr1:152773870-152774066	MCF10A-Er-Src	breast:	n/a	chr1:152774008-152774016 chr1:152774007-152774017 chr1:152774006-152774018
26	FOS	chr1:152773863-152774161	MCF10A-Er-Src	breast:	n/a	chr1:152774008-152774016 chr1:152774007-152774017 chr1:152774006-152774018
27	FOS	chr1:152758533-152758807	MCF10A-Er-Src	breast:	n/a	n/a
28	GATA2	chr1:152755392-152756056	HUVEC	blood vessel:	n/a	chr1:152755525-152755534 chr1:152755915-152755924
29	GATA2	chr1:152755508-152755735	SH-SY5Y	brain:	n/a	chr1:152755525-152755534
30	GATA3	chr1:152755295-152755433	SH-SY5Y	brain:	n/a	n/a
31	IRF1	chr1:152752999-152753013	K562	blood:	n/a	n/a
32	IRF1	chr1:152771838-152771869	K562	blood:	n/a	n/a
33	MAFF	chr1:152773839-152774176	HepG2	liver:	n/a	chr1:152773999-152774017 chr1:152774005-152774019
34	MAFF	chr1:152773860-152774158	K562	blood:	n/a	chr1:152773999-152774017 chr1:152774005-152774019
35	MAFK	chr1:152776161-152776261	HepG2	liver:	n/a	n/a
36	MAFK	chr1:152773842-152774192	HepG2	liver:	n/a	chr1:152774009-152774018 chr1:152774008-152774018 chr1:152774006-152774015 chr1:152774002-152774022 chr1:152774005-152774019 chr1:152774004-152774020 chr1:152774001-152774017 chr1:152774001-152774016
37	MAFK	chr1:152773827-152774195	HepG2	liver:	n/a	chr1:152774009-152774018 chr1:152774008-152774018 chr1:152774006-152774015 chr1:152774002-152774022 chr1:152774005-152774019 chr1:152774004-152774020 chr1:152774001-152774017 chr1:152774001-152774016
38	MAFK	chr1:152773863-152774181	K562	blood:	n/a	chr1:152774009-152774018 chr1:152774008-152774018 chr1:152774006-152774015 chr1:152774002-152774022 chr1:152774005-152774019 chr1:152774004-152774020 chr1:152774001-152774017 chr1:152774001-152774016
39	MAFK	chr1:152766742-152766841	HepG2	liver:	n/a	chr1:152766787-152766803 chr1:152766788-152766802 chr1:152766791-152766801 chr1:152766785-152766805 chr1:152766792-152766801 chr1:152766789-152766798 chr1:152766784-152766800
40	MAFK	chr1:152773942-152774072	Hela-S3	cervix:	n/a	chr1:152774009-152774018 chr1:152774008-152774018 chr1:152774006-152774015 chr1:152774002-152774022 chr1:152774005-152774019 chr1:152774004-152774020 chr1:152774001-152774017 chr1:152774001-152774016
41	MAFK	chr1:152773121-152773159	HepG2	liver:	n/a	n/a
42	MAFK	chr1:152773841-152774182	IMR90	lung:	n/a	chr1:152774009-152774018 chr1:152774008-152774018 chr1:152774006-152774015 chr1:152774002-152774022 chr1:152774005-152774019 chr1:152774004-152774020 chr1:152774001-152774017 chr1:152774001-152774016
43	MAZ	chr1:152758779-152758852	HepG2	liver:	n/a	n/a
44	MYC	chr1:152758505-152758819	MCF10A-Er-Src	breast:	n/a	chr1:152758627-152758637 chr1:152758628-152758638
45	MYC	chr1:152758504-152758818	MCF10A-Er-Src	breast:	n/a	chr1:152758627-152758637 chr1:152758628-152758638
46	MYC	chr1:152769224-152769300	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr1:152760407-152760482	Gliobla	brain:	n/a	n/a
48	POLR2A	chr1:152758556-152758687	A549	lung:	n/a	n/a
49	POLR2A	chr1:152770872-152770963	Gliobla	brain:	n/a	n/a
50	POLR2A	chr1:152760649-152760777	Gliobla	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:152770520-152770570	NHDF-neo	bronchial:	n/a
2	chr1:152770520-152770570	NHDF-neo	bronchial:	n/a
3	chr1:152758632-152758682	HEK293	kidney:	embryo
4	chr1:152758755-152758805	PrEC	prostate:	n/a
5	chr1:152757464-152757514	BE2_C	brain:	n/a
6	chr1:152769896-152769946	HEEpiC	esophagus:	n/a
7	chr1:152769246-152769296	AG09309	skin:	n/a
8	chr1:152757464-152757514	AoSMC	blood vessel:	n/a
9	chr1:152769896-152769946	SKMC	muscle:	n/a
10	chr1:152770520-152770570	HMEC	breast:	n/a
11	chr1:152760341-152760391	GM19239	blood:	n/a
12	chr1:152760341-152760391	H1-hESC	embryonic stem cell:	embryo
13	chr1:152778580-152778630	HRCEpiC	kidney:	n/a
14	chr1:152760341-152760391	MCF10A-Er-Src	breast:	n/a
15	chr1:152758632-152758682	SK-N-SH_RA	brain:	n/a
16	chr1:152757464-152757514	HMEC	breast:	n/a
17	chr1:152759772-152759822	NH-A	brain:	n/a
18	chr1:152769246-152769296	HAEpiC	amniotic membrane:	n/a
19	chr1:152778580-152778630	SK-N-MC	brain:	n/a
20	chr1:152758453-152758503	CMK	blood:	n/a
21	chr1:152760341-152760391	HCF	heart:	n/a
22	chr1:152759772-152759822	HMEC	breast:	n/a
23	chr1:152768267-152768317	GM06990	blood:	n/a
24	chr1:152768476-152768526	PrEC	prostate:	n/a
25	chr1:152769896-152769946	HRE	kidney:	n/a
26	chr1:152768476-152768526	K562	blood:	n/a
27	chr1:152757464-152757514	IMR90	lung:	fetal
28	chr1:152758755-152758805	MCF10A-Er-Src	breast:	n/a
29	chr1:152758453-152758503	K562	blood:	n/a
30	chr1:152777382-152777432	ECC-1	luminal epithelium:	n/a
31	chr1:152769896-152769946	PrEC	prostate:	n/a
32	chr1:152770502-152770552	HPAEpiC	pulmonary alveolar:	n/a
33	chr1:152770502-152770552	SK-N-SH_RA	brain:	n/a
34	chr1:152758453-152758503	NH-A	brain:	n/a
35	chr1:152769896-152769946	AG09319	gingival:	n/a
36	chr1:152758755-152758805	CMK	blood:	n/a
37	chr1:152768267-152768317	HCT-116	colon:	n/a
38	chr1:152760341-152760391	HCPEpiC	choroid plexus:	n/a
39	chr1:152768476-152768526	HAEpiC	amniotic membrane:	n/a
40	chr1:152768727-152768777	HepG2	liver:	n/a
41	chr1:152757464-152757514	HRCEpiC	kidney:	n/a
42	chr1:152760341-152760391	MCF-7	breast:	n/a
43	chr1:152759772-152759822	NT2-D1	testis:	n/a
44	chr1:152768727-152768777	MCF10A-Er-Src	breast:	n/a
45	chr1:152760341-152760391	PANC-1	pancreas:	n/a
46	chr1:152769246-152769296	HEEpiC	esophagus:	n/a
47	chr1:152777382-152777432	AG04449	skin:	fetal
48	chr1:152758755-152758805	HAEpiC	amniotic membrane:	n/a
49	chr1:152768727-152768777	Hela-S3	cervix:	n/a
50	chr1:152768267-152768317	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:152758579..152760547-chr1:152770579..152772468,2	MCF-7	breast:
2	chr1:152715187..152719235-chr1:152774123..152777725,4	MCF-7	breast:
3	chr1:152745990..152747904-chr1:152750482..152752734,2	MCF-7	breast:
4	chr1:152775301..152777562-chr1:152781297..152783006,2	K562	blood:
5	chr1:152769863..152772434-chr1:152783643..152785689,2	MCF-7	breast:

Variant related genes	Relation type
LCE1E	TF binding region
LCE1D	TF binding region
LCE1C	TF binding region
LCE1E	CpG island
LCE1D	CpG island
LCE1C	CpG island
ENSG00000196734	chromatin interactions
ENSG00000186226	chromatin interactions
ENSG00000233819	chromatin interactions

Extended variants
information (count: 704 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:704 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535153341	chr1:152751999-152752000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs114011911	chr1:152752016-152752017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191492936	chr1:152752053-152752054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543267261	chr1:152752058-152752059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2010006	chr1:152752066-152752067	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs577110916	chr1:152752094-152752095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184154384	chr1:152752132-152752133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143431039	chr1:152752188-152752189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575225822	chr1:152752232-152752233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186626175	chr1:152752242-152752243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191387004	chr1:152752270-152752271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548324066	chr1:152752275-152752276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561618257	chr1:152752290-152752291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184429446	chr1:152752297-152752298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190495454	chr1:152752298-152752299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570248932	chr1:152752315-152752316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568855793	chr1:152752323-152752324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529283527	chr1:152752324-152752325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539346981	chr1:152752332-152752333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552480246	chr1:152752373-152752374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs75630595	chr1:152752398-152752399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557810228	chr1:152752412-152752413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182160533	chr1:152752424-152752425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375191705	chr1:152752425-152752426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116001673	chr1:152752443-152752444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568073767	chr1:152752454-152752455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537040460	chr1:152752472-152752473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146724136	chr1:152752530-152752531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368506250	chr1:152752588-152752589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145413148	chr1:152752599-152752600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546116343	chr1:152752614-152752615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552861927	chr1:152752626-152752627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572995388	chr1:152752638-152752639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541903441	chr1:152752683-152752684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185083910	chr1:152752711-152752712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530668507	chr1:152752724-152752725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1888962	chr1:152752796-152752797	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs564142533	chr1:152752810-152752811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139264898	chr1:152752926-152752927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs367926221	chr1:152752959-152752960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541330767	chr1:152753019-152753020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566095799	chr1:152753021-152753022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551345281	chr1:152753036-152753037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528676221	chr1:152753041-152753042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189245623	chr1:152753144-152753145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs35930169	chr1:152753195-152753196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs150950393	chr1:152753219-152753220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181217879	chr1:152753323-152753324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557065757	chr1:152753350-152753351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570830616	chr1:152753371-152753372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

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
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	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
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
Breast cancer	21611746	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
Follicular lymphoma	18703704	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
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	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
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152747800-152755400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr1:152754000-152754200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:152754000-152754200	Enhancers	NHDF-Ad	bronchial
4	chr1:152754200-152755400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:152754200-152755400	Weak transcription	NHDF-Ad	bronchial
6	chr1:152754200-152756000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:152755400-152755800	Enhancers	NHDF-Ad	bronchial
8	chr1:152755400-152755800	Enhancers	NHEK	skin
9	chr1:152755400-152756000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:152755400-152756000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr1:152755400-152756000	Enhancers	HMEC	breast
12	chr1:152755400-152756000	Enhancers	NHLF	lung
13	chr1:152755600-152755800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr1:152755800-152758200	Weak transcription	NHEK	skin
15	chr1:152755800-152758400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr1:152756000-152758200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr1:152756000-152758200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr1:152756000-152758200	Weak transcription	HMEC	breast
19	chr1:152757200-152757400	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr1:152757400-152758400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr1:152758200-152758400	Enhancers	HMEC	breast
22	chr1:152758200-152758600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr1:152758200-152758600	Enhancers	Fetal Stomach	stomach
24	chr1:152758200-152758800	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr1:152758200-152758800	Enhancers	Ovary	ovary
26	chr1:152758200-152759000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr1:152758200-152759200	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr1:152758200-152759200	Enhancers	NHEK	skin
29	chr1:152758400-152758600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr1:152758400-152758800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr1:152758400-152759400	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr1:152758400-152759400	Flanking Active TSS	HMEC	breast
33	chr1:152758600-152758800	Bivalent Enhancer	Lung	lung
34	chr1:152758600-152759000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr1:152758600-152759200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr1:152758800-152759200	Enhancers	HepG2	liver
37	chr1:152759000-152759400	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr1:152759000-152759400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr1:152759200-152759800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr1:152759400-152759800	Enhancers	HMEC	breast
41	chr1:152765600-152765800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr1:152765800-152766000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr1:152766000-152767800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr1:152766800-152767800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr1:152767600-152769600	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr1:152767800-152769000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr1:152768000-152769000	Enhancers	Brain Hippocampus Middle	brain
48	chr1:152769400-152769800	Enhancers	Spleen	Spleen
49	chr1:152769600-152770200	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr1:152770200-152770400	Enhancers	Cortex derived primary cultured neurospheres	brain

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