Variant report

Variant	nsv1014190
Chromosome Location	chr1:152747126-152778861
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:282)
CpG islands
(count:1222)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:282 , 50 per page) page: 1 2 3 4 5 6

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	CEBPB	chr1:152751552-152751774	HepG2	liver:	n/a	chr1:152751690-152751701
4	CTCF	chr1:152750128-152750300	Medullo	brain:	n/a	n/a
5	CTCF	chr1:152750120-152750270	GM12870	blood:	n/a	n/a
6	CTCF	chr1:152750160-152750310	AG04449	skin:	n/a	n/a
7	CTCF	chr1:152747431-152747678	MCF-7	breast:	n/a	chr1:152747561-152747574
8	CTCF	chr1:152750040-152750190	HFF-Myc	foreskin:	n/a	n/a
9	CTCF	chr1:152750162-152750260	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr1:152750140-152750290	SK-N-SH_RA	brain:	n/a	n/a
11	CTCF	chr1:152750120-152750270	A549	lung:	n/a	n/a
12	CTCF	chr1:152750100-152750250	GM12872	blood:	n/a	n/a
13	CTCF	chr1:152750120-152750270	BJ	skin:	n/a	n/a
14	CTCF	chr1:152747500-152747650	Caco-2	colon:	n/a	chr1:152747561-152747574
15	CTCF	chr1:152750100-152750250	GM12870	blood:	n/a	n/a
16	CTCF	chr1:152750124-152750326	ProgFib	skin:	n/a	n/a
17	CTCF	chr1:152747440-152747590	GM06990	blood:	n/a	chr1:152747561-152747574
18	CTCF	chr1:152747444-152747652	MCF-7	breast:	n/a	chr1:152747561-152747574
19	CTCF	chr1:152747480-152747630	NB4	blood:	n/a	chr1:152747561-152747574
20	CTCF	chr1:152747540-152747690	GM12868	blood:	n/a	chr1:152747561-152747574
21	CTCF	chr1:152747520-152747670	GM12865	blood:	n/a	chr1:152747561-152747574
22	CTCF	chr1:152747500-152747650	SAEC	small airway:	n/a	chr1:152747561-152747574
23	CTCF	chr1:152750160-152750310	GM12869	blood:	n/a	n/a
24	CTCF	chr1:152750146-152750296	GM20000	blood:	n/a	n/a
25	CTCF	chr1:152750093-152750348	K562	blood:	n/a	n/a
26	CTCF	chr1:152750140-152750290	NHLF	lung:	n/a	n/a
27	CTCF	chr1:152750060-152750210	GM12801	blood:	n/a	n/a
28	CTCF	chr1:152747460-152747610	HEEpiC	esophagus:	n/a	chr1:152747561-152747574
29	CTCF	chr1:152750120-152750270	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr1:152750223-152750240	LNCaP	prostate:	n/a	n/a
31	CTCF	chr1:152747482-152747647	Fibrobl	skin:	n/a	chr1:152747561-152747574
32	CTCF	chr1:152750120-152750270	HPF	lung:	n/a	n/a
33	CTCF	chr1:152747440-152747590	A549	lung:	n/a	chr1:152747561-152747574
34	CTCF	chr1:152750080-152750230	HMF	breast:	n/a	n/a
35	CTCF	chr1:152758560-152758710	MCF-7	breast:	n/a	n/a
36	CTCF	chr1:152750006-152750406	K562	blood:	n/a	n/a
37	CTCF	chr1:152750160-152750310	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr1:152747460-152747610	GM12866	blood:	n/a	chr1:152747561-152747574
39	CTCF	chr1:152750091-152750340	GM12892	blood:	n/a	n/a
40	CTCF	chr1:152750140-152750290	HMF	breast:	n/a	n/a
41	CTCF	chr1:152747420-152747570	GM12878	blood:	n/a	n/a
42	CTCF	chr1:152750120-152750270	GM12866	blood:	n/a	n/a
43	CTCF	chr1:152750160-152750310	BE2_C	brain:	n/a	n/a
44	CTCF	chr1:152750100-152750250	HRE	kidney:	n/a	n/a
45	CTCF	chr1:152747536-152747583	GM12891	blood:	n/a	chr1:152747561-152747574
46	CTCF	chr1:152750141-152750336	Fibrobl	skin:	n/a	n/a
47	CTCF	chr1:152750131-152750287	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr1:152750140-152750290	GM12867	blood:	n/a	n/a
49	CTCF	chr1:152750144-152750307	GM13977	blood:	n/a	n/a
50	CTCF	chr1:152750120-152750270	HAc	cerebellar:	n/a	n/a

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:152778580-152778630	HCT-116	colon:	n/a
2	chr1:152769896-152769946	HRE	kidney:	n/a
3	chr1:152778580-152778630	HCT-116	colon:	n/a
4	chr1:152769896-152769946	HRE	kidney:	n/a
5	chr1:152747501-152747551	NB4	blood:	n/a
6	chr1:152760341-152760391	HRPEpiC	eye:	n/a
7	chr1:152747472-152747522	PANC-1	pancreas:	n/a
8	chr1:152768267-152768317	IMR90	lung:	fetal
9	chr1:152758632-152758682	HCM	heart:	n/a
10	chr1:152749106-152749156	SAEC	small airway:	n/a
11	chr1:152747501-152747551	PrEC	prostate:	n/a
12	chr1:152747562-152747612	AG09309	skin:	n/a
13	chr1:152770502-152770552	H1-hESC	embryonic stem cell:	embryo
14	chr1:152760341-152760391	HCT-116	colon:	n/a
15	chr1:152747562-152747612	SKMC	muscle:	n/a
16	chr1:152770520-152770570	GM12892	blood:	n/a
17	chr1:152748838-152748888	AoSMC	blood vessel:	n/a
18	chr1:152749106-152749156	Jurkat	blood:	n/a
19	chr1:152770520-152770570	SKMC	muscle:	n/a
20	chr1:152747501-152747551	HRCEpiC	kidney:	n/a
21	chr1:152758632-152758682	AoSMC	blood vessel:	n/a
22	chr1:152769896-152769946	HNPCEpiC	eye:	n/a
23	chr1:152760341-152760391	NHDF-neo	bronchial:	n/a
24	chr1:152759772-152759822	NT2-D1	testis:	n/a
25	chr1:152778580-152778630	Hepatocyte	liver:	n/a
26	chr1:152749106-152749156	SKMC	muscle:	n/a
27	chr1:152759772-152759822	PrEC	prostate:	n/a
28	chr1:152757464-152757514	HCT-116	colon:	n/a
29	chr1:152747562-152747612	AG04450	lung:	fetal
30	chr1:152769246-152769296	PrEC	prostate:	n/a
31	chr1:152770502-152770552	HL-60	blood:	n/a
32	chr1:152777382-152777432	PFSK-1	brain:	n/a
33	chr1:152758755-152758805	SK-N-SH	brain:	n/a
34	chr1:152768476-152768526	HAEpiC	amniotic membrane:	n/a
35	chr1:152747501-152747551	GM12878	blood:	n/a
36	chr1:152770520-152770570	ECC-1	luminal epithelium:	n/a
37	chr1:152758632-152758682	HIPEpiC	eye:	n/a
38	chr1:152749106-152749156	NHDF-neo	bronchial:	n/a
39	chr1:152778580-152778630	AG09319	gingival:	n/a
40	chr1:152769246-152769296	CMK	blood:	n/a
41	chr1:152770502-152770552	HIPEpiC	eye:	n/a
42	chr1:152770502-152770552	AoSMC	blood vessel:	n/a
43	chr1:152758755-152758805	BE2_C	brain:	n/a
44	chr1:152760341-152760391	ProgFib	skin:	n/a
45	chr1:152770520-152770570	PrEC	prostate:	n/a
46	chr1:152758453-152758503	PFSK-1	brain:	n/a
47	chr1:152778580-152778630	ECC-1	luminal epithelium:	n/a
48	chr1:152748838-152748888	AG04450	lung:	fetal
49	chr1:152769896-152769946	Caco-2	colon:	n/a
50	chr1:152768476-152768526	CMK	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:152775301..152777562-chr1:152781297..152783006,2	K562	blood:
2	chr1:152715187..152719235-chr1:152774123..152777725,4	MCF-7	breast:
3	chr1:152758579..152760547-chr1:152770579..152772468,2	MCF-7	breast:
4	chr1:152745990..152747904-chr1:152750482..152752734,2	MCF-7	breast:
5	chr1:152769863..152772434-chr1:152783643..152785689,2	MCF-7	breast:
6	chr1:152626437..152627174-chr1:152749824..152750672,3	MCF-7	breast:
7	chr1:152745990..152747904-chr1:152750482..152752734,2	MCF-7	breast:

No data

Variant related genes	Relation type
LCE1F	TF binding region
LCE1E	TF binding region
LCE1D	TF binding region
LCE1C	TF binding region
LCE1F	CpG island
LCE1E	CpG island
LCE1D	CpG island
LCE1C	CpG island
ENSG00000186226	chromatin interactions
ENSG00000196734	chromatin interactions
ENSG00000233819	chromatin interactions

Extended variants
information (count: 914 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:914 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11205102	chr1:152747126-152747127	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs575532433	chr1:152747149-152747150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570899534	chr1:152747160-152747161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537885463	chr1:152747167-152747168	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544276513	chr1:152747181-152747182	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs144232098	chr1:152747206-152747207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549776404	chr1:152747260-152747261	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs533100419	chr1:152747272-152747273	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs61113935	chr1:152747360-152747361	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs560122566	chr1:152747367-152747368	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs528767767	chr1:152747391-152747392	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs568067666	chr1:152747414-152747415	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs535372802	chr1:152747462-152747463	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs76904328	chr1:152747464-152747465	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs370473574	chr1:152747501-152747502	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs531014859	chr1:152747520-152747521	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs550800207	chr1:152747539-152747540	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs570605272	chr1:152747602-152747603	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs72702896	chr1:152747655-152747656	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs553074634	chr1:152747742-152747743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188333620	chr1:152747814-152747815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs4845322	chr1:152747890-152747891	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs539598512	chr1:152748005-152748006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555701924	chr1:152748025-152748026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs193190458	chr1:152748034-152748035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544410804	chr1:152748125-152748126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558033194	chr1:152748170-152748171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564270223	chr1:152748177-152748178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142700326	chr1:152748228-152748229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12239774	chr1:152748253-152748254	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs571725921	chr1:152748319-152748320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559860985	chr1:152748328-152748329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs17669429	chr1:152748369-152748370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113598055	chr1:152748370-152748371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368230175	chr1:152748429-152748430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs150997123	chr1:152748500-152748501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531154069	chr1:152748547-152748548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9724909	chr1:152748636-152748637	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs561668786	chr1:152748679-152748680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534528844	chr1:152748688-152748689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375084658	chr1:152748690-152748691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184668442	chr1:152748714-152748715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547092710	chr1:152748764-152748765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200063389	chr1:152748820-152748821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377484015	chr1:152748839-152748840	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs201066106	chr1:152748844-152748845	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs202145672	chr1:152748845-152748846	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs376202697	chr1:152748847-152748848	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs148988311	chr1:152748870-152748871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115678527	chr1:152748895-152748896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:122)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152743000-152747200	Weak transcription	NHEK	skin
2	chr1:152747000-152747800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:152747200-152747600	Enhancers	NHEK	skin
4	chr1:152747200-152747800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr1:152747200-152747800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr1:152747200-152747800	Enhancers	HMEC	breast
7	chr1:152747800-152755400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr1:152754000-152754200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:152754000-152754200	Enhancers	NHDF-Ad	bronchial
10	chr1:152754200-152755400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr1:152754200-152755400	Weak transcription	NHDF-Ad	bronchial
12	chr1:152754200-152756000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:152755400-152755800	Enhancers	NHDF-Ad	bronchial
14	chr1:152755400-152755800	Enhancers	NHEK	skin
15	chr1:152755400-152756000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr1:152755400-152756000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr1:152755400-152756000	Enhancers	HMEC	breast
18	chr1:152755400-152756000	Enhancers	NHLF	lung
19	chr1:152755600-152755800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr1:152755800-152758200	Weak transcription	NHEK	skin
21	chr1:152755800-152758400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr1:152756000-152758200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr1:152756000-152758200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr1:152756000-152758200	Weak transcription	HMEC	breast
25	chr1:152757200-152757400	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr1:152757400-152758400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr1:152758200-152758400	Enhancers	HMEC	breast
28	chr1:152758200-152758600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr1:152758200-152758600	Enhancers	Fetal Stomach	stomach
30	chr1:152758200-152758800	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr1:152758200-152758800	Enhancers	Ovary	ovary
32	chr1:152758200-152759000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:152758200-152759200	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr1:152758200-152759200	Enhancers	NHEK	skin
35	chr1:152758400-152758600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr1:152758400-152758800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr1:152758400-152759400	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr1:152758400-152759400	Flanking Active TSS	HMEC	breast
39	chr1:152758600-152758800	Bivalent Enhancer	Lung	lung
40	chr1:152758600-152759000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr1:152758600-152759200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr1:152758800-152759200	Enhancers	HepG2	liver
43	chr1:152759000-152759400	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr1:152759000-152759400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr1:152759200-152759800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr1:152759400-152759800	Enhancers	HMEC	breast
47	chr1:152765600-152765800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr1:152765800-152766000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr1:152766000-152767800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr1:152766800-152767800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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