Variant report

Variant	nsv871661
Chromosome Location	chr1:80498496-80563300
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:152)
CpG islands
(count:305)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:152 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:80520012-80520093	K562	blood:	n/a	n/a
2	BACH1	chr1:80549615-80549808	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:80548886-80548916	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:80519821-80520165	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:80515843-80516159	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:80515876-80516018	K562	blood:	n/a	n/a
7	CEBPB	chr1:80555874-80556156	IMR90	lung:	n/a	chr1:80555985-80555998 chr1:80555986-80555997
8	CEBPB	chr1:80548985-80549185	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:80555874-80556123	HepG2	liver:	n/a	chr1:80555985-80555998 chr1:80555986-80555997
10	CTCF	chr1:80525500-80525650	HEK293	kidney:	n/a	n/a
11	CTCF	chr1:80525480-80525630	HEK293	kidney:	n/a	n/a
12	CTCF	chr1:80525500-80525650	HBMEC	blood vessel:	n/a	n/a
13	CTCF	chr1:80548678-80548691	GM20000	blood:	n/a	n/a
14	CTCF	chr1:80525520-80525670	HCFaa	heart:	n/a	n/a
15	CTCF	chr1:80549600-80549750	MCF-7	breast:	n/a	n/a
16	CTCF	chr1:80548693-80548790	GM20000	blood:	n/a	n/a
17	CTCF	chr1:80519998-80520009	NHEK	skin:	n/a	n/a
18	CTCF	chr1:80525580-80525730	HPAF	blood vessel:	n/a	n/a
19	CTCF	chr1:80539526-80539570	GM20000	blood:	n/a	n/a
20	CUX1	chr1:80560706-80560736	GM12878	blood:	n/a	n/a
21	E2F4	chr1:80525847-80526014	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F4	chr1:80522052-80522252	MCF10A-Er-Src	breast:	n/a	n/a
23	EP300	chr1:80519780-80520119	SK-N-SH_RA	brain:	n/a	n/a
24	EP300	chr1:80513554-80513806	SK-N-SH_RA	brain:	n/a	n/a
25	EP300	chr1:80513495-80513754	SK-N-SH_RA	brain:	n/a	n/a
26	FOS	chr1:80530222-80530584	MCF10A-Er-Src	breast:	n/a	chr1:80530401-80530412
27	FOS	chr1:80521965-80522165	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr1:80530263-80530560	HUVEC	blood vessel:	n/a	chr1:80530401-80530412
29	FOS	chr1:80521823-80522209	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr1:80519768-80520308	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr1:80525719-80526027	HUVEC	blood vessel:	n/a	chr1:80525857-80525868
32	FOS	chr1:80530223-80530595	MCF10A-Er-Src	breast:	n/a	chr1:80530401-80530412
33	FOS	chr1:80519809-80520338	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr1:80519823-80520304	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr1:80513513-80513557	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr1:80525743-80526040	MCF10A-Er-Src	breast:	n/a	chr1:80525857-80525868
37	FOS	chr1:80521879-80522152	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr1:80530228-80530609	MCF10A-Er-Src	breast:	n/a	chr1:80530401-80530412
39	FOS	chr1:80525691-80526046	MCF10A-Er-Src	breast:	n/a	chr1:80525857-80525868
40	FOS	chr1:80513575-80513703	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr1:80519809-80520284	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr1:80530268-80530557	MCF10A-Er-Src	breast:	n/a	chr1:80530401-80530412
43	FOSL2	chr1:80519832-80520165	MCF-7	breast:	n/a	n/a
44	FOXA1	chr1:80549609-80549832	HepG2	liver:	n/a	n/a
45	FOXA1	chr1:80549567-80549835	HepG2	liver:	n/a	n/a
46	FOXA1	chr1:80549610-80549839	HepG2	liver:	n/a	n/a
47	FOXA1	chr1:80549561-80549820	T-47D	breast:	n/a	n/a
48	FOXA1	chr1:80549477-80549916	T-47D	breast:	n/a	n/a
49	FOXA2	chr1:80549610-80549881	A549	lung:	n/a	n/a
50	FOXA2	chr1:80549639-80549810	HepG2	liver:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:80516486-80516536	HL-60	blood:	n/a
2	chr1:80517098-80517148	CMK	blood:	n/a
3	chr1:80517010-80517060	HRPEpiC	eye:	n/a
4	chr1:80516486-80516536	PrEC	prostate:	n/a
5	chr1:80516138-80516188	NB4	blood:	n/a
6	chr1:80516486-80516536	H1-hESC	embryonic stem cell:	embryo
7	chr1:80516591-80516641	CMK	blood:	n/a
8	chr1:80516138-80516188	AG09309	skin:	n/a
9	chr1:80516138-80516188	SK-N-SH	brain:	n/a
10	chr1:80516138-80516188	BE2_C	brain:	n/a
11	chr1:80517098-80517148	T-47D	breast:	n/a
12	chr1:80517010-80517060	AG10803	skin:	n/a
13	chr1:80517010-80517060	Jurkat	blood:	n/a
14	chr1:80517098-80517148	Hepatocyte	liver:	n/a
15	chr1:80516138-80516188	K562	blood:	n/a
16	chr1:80516591-80516641	HRPEpiC	eye:	n/a
17	chr1:80516591-80516641	BJ	skin:	n/a
18	chr1:80516138-80516188	HMEC	breast:	n/a
19	chr1:80516591-80516641	SKMC	muscle:	n/a
20	chr1:80517010-80517060	MCF10A-Er-Src	breast:	n/a
21	chr1:80517098-80517148	BE2_C	brain:	n/a
22	chr1:80517010-80517060	HUVEC	blood vessel:	n/a
23	chr1:80516591-80516641	SK-N-SH_RA	brain:	n/a
24	chr1:80517010-80517060	AG04450	lung:	fetal
25	chr1:80516591-80516641	HCF	heart:	n/a
26	chr1:80516138-80516188	HEEpiC	esophagus:	n/a
27	chr1:80516486-80516536	HepG2	liver:	n/a
28	chr1:80517010-80517060	H1-hESC	embryonic stem cell:	embryo
29	chr1:80516138-80516188	SK-N-SH_RA	brain:	n/a
30	chr1:80517098-80517148	PFSK-1	brain:	n/a
31	chr1:80517098-80517148	Jurkat	blood:	n/a
32	chr1:80517010-80517060	SK-N-MC	brain:	n/a
33	chr1:80516486-80516536	HCM	heart:	n/a
34	chr1:80516591-80516641	HCM	heart:	n/a
35	chr1:80516591-80516641	NHBE	bronchial:	n/a
36	chr1:80517098-80517148	GM12878	blood:	n/a
37	chr1:80516486-80516536	NB4	blood:	n/a
38	chr1:80516138-80516188	AG04450	lung:	fetal
39	chr1:80517010-80517060	PrEC	prostate:	n/a
40	chr1:80516138-80516188	NH-A	brain:	n/a
41	chr1:80516486-80516536	AG04450	lung:	fetal
42	chr1:80516591-80516641	SAEC	small airway:	n/a
43	chr1:80516591-80516641	GM12878	blood:	n/a
44	chr1:80517098-80517148	GM19239	blood:	n/a
45	chr1:80517010-80517060	IMR90	lung:	fetal
46	chr1:80516486-80516536	CMK	blood:	n/a
47	chr1:80516591-80516641	AG09309	skin:	n/a
48	chr1:80516486-80516536	HEK293	kidney:	embryo
49	chr1:80516486-80516536	HIPEpiC	eye:	n/a
50	chr1:80517010-80517060	NT2-D1	testis:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ELTD1-11	chr1:80557788-80558922	NONHSAT004104

No data

Variant related genes	Relation type
ENSG00000235756	TF binding region
ENSG00000235756	CpG island

Extended variants
information (count: 1716 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1716 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572540786	chr1:80502420-80502421	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs183736337	chr1:80502441-80502442	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs116565863	chr1:80502442-80502443	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs527921785	chr1:80502457-80502458	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs561335103	chr1:80502465-80502466	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs189366848	chr1:80502515-80502516	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs529999623	chr1:80502527-80502528	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs76814880	chr1:80502538-80502539	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs550510898	chr1:80502589-80502590	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs78270866	chr1:80502611-80502612	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs560677230	chr1:80502629-80502630	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs549829219	chr1:80502672-80502673	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs150741978	chr1:80502743-80502744	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181350547	chr1:80502757-80502758	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547421264	chr1:80502800-80502801	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs374785954	chr1:80502865-80502866	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563943683	chr1:80502879-80502880	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139117267	chr1:80502953-80502954	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs557985680	chr1:80503057-80503058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs576273997	chr1:80503059-80503060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs186359976	chr1:80503117-80503118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs145134058	chr1:80503127-80503128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs147708870	chr1:80503155-80503156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs190019733	chr1:80503163-80503164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540786267	chr1:80503203-80503204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181448521	chr1:80503206-80503207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs572702808	chr1:80503222-80503223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532831517	chr1:80503223-80503224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546152711	chr1:80503296-80503297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186086551	chr1:80503299-80503300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs116242532	chr1:80503310-80503311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs140936826	chr1:80503319-80503320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs369545382	chr1:80503338-80503339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs555358962	chr1:80503410-80503411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374691074	chr1:80503411-80503412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs144896448	chr1:80503417-80503418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561842102	chr1:80503421-80503422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs529309281	chr1:80503476-80503477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs2184613	chr1:80503523-80503524	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs565886454	chr1:80503557-80503558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs145881084	chr1:80503558-80503559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs569897269	chr1:80503559-80503560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs111922815	chr1:80503597-80503598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs555544613	chr1:80503631-80503632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567366725	chr1:80503632-80503633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566133414	chr1:80503645-80503646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs148925225	chr1:80503739-80503740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191197039	chr1:80503780-80503781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs533936227	chr1:80503796-80503797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs201453507	chr1:80503839-80503840	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	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
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:80502400-80502800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr1:80502400-80503000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:80502600-80503000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr1:80502600-80503000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr1:80503000-80503400	Enhancers	Fetal Heart	heart
6	chr1:80503200-80504000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr1:80504000-80507600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr1:80507600-80508200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr1:80508200-80508600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr1:80508600-80508800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr1:80511400-80519600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:80512600-80512800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr1:80512800-80516000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr1:80516000-80516200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr1:80516200-80516600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:80516200-80519400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr1:80517000-80519000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr1:80519000-80519600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr1:80519400-80519800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr1:80519400-80520800	Enhancers	HMEC	breast
21	chr1:80519600-80520000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr1:80519600-80520000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr1:80519600-80520000	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr1:80519600-80520200	Enhancers	Left Ventricle	heart
25	chr1:80519600-80520400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr1:80519600-80520400	Enhancers	NH-A	brain
27	chr1:80519600-80520800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr1:80519800-80520200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr1:80519800-80520200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr1:80519800-80520200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr1:80519800-80520200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr1:80519800-80520200	Enhancers	Hela-S3	cervix
33	chr1:80519800-80520400	Enhancers	A549	lung
34	chr1:80519800-80520800	Enhancers	NHEK	skin
35	chr1:80520800-80521800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr1:80520800-80530000	Weak transcription	NHEK	skin
37	chr1:80521800-80522400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr1:80522400-80525400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:80525400-80525800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr1:80525800-80529800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr1:80526000-80529800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr1:80529400-80530800	Enhancers	HMEC	breast
43	chr1:80529800-80530200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr1:80529800-80530200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr1:80530000-80530400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr1:80530000-80530400	Enhancers	NHEK	skin
47	chr1:80530000-80532400	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr1:80530200-80531400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr1:80530200-80531800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr1:80530400-80531600	Weak transcription	NHEK	skin

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