Variant report

Variant	nsv1007013
Chromosome Location	chr1:79540957-79619725
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:304)
CpG islands
(count:62)
Chromatin interactive
region (count:2)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:304 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:79545497-79545905	H1-hESC	embryonic stem cell:	n/a	chr1:79545669-79545683
2	BCL11A	chr1:79603898-79604245	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr1:79604022-79604167	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr1:79617796-79617801	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr1:79594497-79595010	IMR90	lung:	n/a	chr1:79594917-79594928 chr1:79594917-79594928 chr1:79594917-79594930
6	CEBPB	chr1:79603920-79604175	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr1:79566107-79566454	IMR90	lung:	n/a	n/a
8	CEBPB	chr1:79587527-79587826	HepG2	liver:	n/a	chr1:79587688-79587699 chr1:79587688-79587701 chr1:79587690-79587701
9	CEBPB	chr1:79560648-79560811	HepG2	liver:	n/a	n/a
10	CEBPB	chr1:79587579-79587715	H1-hESC	embryonic stem cell:	n/a	chr1:79587688-79587699 chr1:79587688-79587701 chr1:79587690-79587701
11	CEBPB	chr1:79583039-79583331	IMR90	lung:	n/a	chr1:79583176-79583189
12	CEBPB	chr1:79571297-79571471	IMR90	lung:	n/a	n/a
13	CEBPB	chr1:79587509-79587865	IMR90	lung:	n/a	chr1:79587688-79587699 chr1:79587688-79587701 chr1:79587690-79587701
14	CEBPD	chr1:79562158-79562660	K562	blood:	n/a	n/a
15	CHD1	chr1:79574652-79574670	GM12878	blood:	n/a	n/a
16	CTCF	chr1:79594580-79594730	HAc	cerebellar:	n/a	n/a
17	CTCF	chr1:79594540-79594690	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr1:79588940-79589090	HPAF	blood vessel:	n/a	n/a
19	CTCF	chr1:79594560-79594710	NHDF-neo	bronchial:	n/a	n/a
20	CTCF	chr1:79594480-79594630	HPAF	blood vessel:	n/a	n/a
21	CTCF	chr1:79545540-79545690	AG10803	skin:	n/a	n/a
22	CTCF	chr1:79594520-79594670	AG04449	skin:	n/a	n/a
23	CTCF	chr1:79588960-79589110	HPAF	blood vessel:	n/a	n/a
24	CTCF	chr1:79590846-79590902	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr1:79594500-79594650	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr1:79588960-79589110	RPTEC	kidney:	n/a	n/a
27	CTCF	chr1:79608940-79609026	Fibrobl	skin:	n/a	n/a
28	CTCF	chr1:79594460-79594610	HCFaa	heart:	n/a	n/a
29	CTCF	chr1:79609060-79609210	HMEC	breast:	n/a	n/a
30	CTCF	chr1:79545620-79545770	AoAF	blood vessel:	n/a	n/a
31	CTCF	chr1:79589060-79589210	NHEK	skin:	n/a	n/a
32	CTCF	chr1:79608525-79608630	GM20000	blood:	n/a	n/a
33	CTCF	chr1:79589080-79589310	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr1:79589024-79589124	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr1:79589000-79589150	HVMF	connective:	n/a	n/a
36	CTCF	chr1:79608992-79609011	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr1:79588940-79589090	HPF	lung:	n/a	n/a
38	CTCF	chr1:79545500-79545650	GM12866	blood:	n/a	n/a
39	CTCF	chr1:79545560-79545710	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr1:79590833-79590962	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:79594520-79594670	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr1:79608985-79608991	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr1:79589000-79589150	HCFaa	heart:	n/a	n/a
44	CTCF	chr1:79594420-79594570	AoAF	blood vessel:	n/a	n/a
45	E2F4	chr1:79571344-79571489	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr1:79598604-79599050	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr1:79545563-79546075	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr1:79566391-79567068	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr1:79600805-79601005	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr1:79582638-79582936	MCF10A-Er-Src	breast:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:79594960-79595010	IMR90	lung:	fetal
2	chr1:79594960-79595010	IMR90	lung:	fetal
3	chr1:79594960-79595010	GM19239	blood:	n/a
4	chr1:79594960-79595010	SK-N-MC	brain:	n/a
5	chr1:79594960-79595010	ProgFib	skin:	n/a
6	chr1:79594960-79595010	HCF	heart:	n/a
7	chr1:79594960-79595010	NHBE	bronchial:	n/a
8	chr1:79594960-79595010	HEEpiC	esophagus:	n/a
9	chr1:79594960-79595010	HRE	kidney:	n/a
10	chr1:79594960-79595010	PANC-1	pancreas:	n/a
11	chr1:79594960-79595010	GM12892	blood:	n/a
12	chr1:79594960-79595010	GM12878	blood:	n/a
13	chr1:79594960-79595010	HAEpiC	amniotic membrane:	n/a
14	chr1:79594960-79595010	A549	lung:	n/a
15	chr1:79594960-79595010	AG09319	gingival:	n/a
16	chr1:79594960-79595010	HUVEC	blood vessel:	n/a
17	chr1:79594960-79595010	HMEC	breast:	n/a
18	chr1:79594960-79595010	PFSK-1	brain:	n/a
19	chr1:79594960-79595010	BJ	skin:	n/a
20	chr1:79594960-79595010	RPTEC	kidney:	n/a
21	chr1:79594960-79595010	AG09309	skin:	n/a
22	chr1:79594960-79595010	SAEC	small airway:	n/a
23	chr1:79594960-79595010	HNPCEpiC	eye:	n/a
24	chr1:79594960-79595010	Hepatocyte	liver:	n/a
25	chr1:79594960-79595010	HPAEpiC	pulmonary alveolar:	n/a
26	chr1:79594960-79595010	NH-A	brain:	n/a
27	chr1:79594960-79595010	MCF10A-Er-Src	breast:	n/a
28	chr1:79594960-79595010	T-47D	breast:	n/a
29	chr1:79594960-79595010	SK-N-SH	brain:	n/a
30	chr1:79594960-79595010	AG10803	skin:	n/a
31	chr1:79594960-79595010	HEK293	kidney:	embryo
32	chr1:79594960-79595010	H1-hESC	embryonic stem cell:	embryo
33	chr1:79594960-79595010	Jurkat	blood:	n/a
34	chr1:79594960-79595010	K562	blood:	n/a
35	chr1:79594960-79595010	HCPEpiC	choroid plexus:	n/a
36	chr1:79594960-79595010	AG04450	lung:	fetal
37	chr1:79594960-79595010	Caco-2	colon:	n/a
38	chr1:79594960-79595010	SKMC	muscle:	n/a
39	chr1:79594960-79595010	BE2_C	brain:	n/a
40	chr1:79594960-79595010	HCM	heart:	n/a
41	chr1:79594960-79595010	AG04449	skin:	fetal
42	chr1:79594960-79595010	HIPEpiC	eye:	n/a
43	chr1:79594960-79595010	LNCaP	prostate:	n/a
44	chr1:79594960-79595010	ovcar-3	ovarian:	n/a
45	chr1:79594960-79595010	Hela-S3	cervix:	n/a
46	chr1:79594960-79595010	U87	brain:	n/a
47	chr1:79594960-79595010	ECC-1	luminal epithelium:	n/a
48	chr1:79594960-79595010	HCT-116	colon:	n/a
49	chr1:79594960-79595010	HRPEpiC	eye:	n/a
50	chr1:79594960-79595010	NB4	blood:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:79616451..79619205-chr1:79639296..79641396,2	MCF-7	breast:
2	chr1:79536026..79538535-chr1:79539899..79541790,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFI44-7	chr1:79562972-79563122	NONHSAT004086
2	lnc-IFI44-7	chr1:79562042-79562232	NONHSAT004086

No data

Variant related genes	Relation type
ENSG00000266388	TF binding region
ENSG00000266388	CpG island

Extended variants
information (count: 2371 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2371 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs71643223	chr1:79544809-79544810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs114381297	chr1:79544833-79544834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553555466	chr1:79544835-79544836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563946924	chr1:79544871-79544872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531358331	chr1:79544936-79544937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs550072488	chr1:79544937-79544938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs116072673	chr1:79544943-79544944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs61769010	chr1:79545012-79545013	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs547108710	chr1:79545035-79545036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188002885	chr1:79545042-79545043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs145335857	chr1:79545072-79545073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556242751	chr1:79545097-79545098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs17102729	chr1:79545125-79545126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190967358	chr1:79545154-79545155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs571076657	chr1:79545214-79545215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs182409286	chr1:79545226-79545227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556699264	chr1:79545234-79545235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146148505	chr1:79545275-79545276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs377177400	chr1:79545371-79545372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs542506469	chr1:79545410-79545411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187942720	chr1:79545411-79545412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368803415	chr1:79545423-79545424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572066199	chr1:79545495-79545496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545897561	chr1:79545543-79545544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs192529006	chr1:79545622-79545623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371627080	chr1:79545656-79545657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542874929	chr1:79545671-79545672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs78611038	chr1:79545705-79545706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs11162615	chr1:79545732-79545733	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs369246647	chr1:79545749-79545750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs529223097	chr1:79545761-79545762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs111845264	chr1:79545770-79545771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs545283800	chr1:79545830-79545831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369133061	chr1:79545864-79545865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs74456743	chr1:79545866-79545867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs11162616	chr1:79545911-79545912	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs532926540	chr1:79545913-79545914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs116629022	chr1:79545940-79545941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs577357723	chr1:79545963-79545964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184016122	chr1:79545979-79545980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs533086902	chr1:79545985-79545986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs187344127	chr1:79546008-79546009	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs140197466	chr1:79546040-79546041	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76179596	chr1:79546055-79546056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572130518	chr1:79546064-79546065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192292430	chr1:79546067-79546068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572112340	chr1:79546138-79546139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143926788	chr1:79546144-79546145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146292685	chr1:79546146-79546147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs114481401	chr1:79546209-79546210	Enhancers Weak transcription	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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79544800-79548600	Enhancers	HUVEC	blood vessel
2	chr1:79545000-79546000	Enhancers	Adipose Nuclei	Adipose
3	chr1:79545200-79546000	Enhancers	HMEC	breast
4	chr1:79545200-79546000	Enhancers	NH-A	brain
5	chr1:79545200-79546000	Enhancers	NHDF-Ad	bronchial
6	chr1:79545200-79546200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr1:79545200-79546200	Enhancers	Muscle Satellite Cultured Cells	--
8	chr1:79545200-79546600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr1:79545200-79546600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr1:79545200-79546600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:79545400-79545800	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr1:79545400-79545800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr1:79545400-79545800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr1:79545400-79545800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr1:79545400-79546000	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr1:79545400-79546000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr1:79545400-79546000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr1:79545400-79546000	Enhancers	H9 Cell Line	embryonic stem cell
19	chr1:79545400-79546000	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr1:79545400-79546000	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr1:79545400-79546000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr1:79545400-79546000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr1:79545400-79546000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr1:79545400-79546000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr1:79545400-79546000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:79545400-79546000	Enhancers	Hela-S3	cervix
27	chr1:79545400-79546000	Enhancers	HSMM	muscle
28	chr1:79545400-79546000	Enhancers	HSMMtube	muscle
29	chr1:79545400-79546000	Enhancers	NHLF	lung
30	chr1:79545400-79546000	Enhancers	Osteobl	bone
31	chr1:79545600-79545800	Enhancers	GM12878-XiMat	blood
32	chr1:79545600-79546000	Enhancers	H1 Cell Line	embryonic stem cell
33	chr1:79545600-79546000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr1:79545600-79546000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:79545600-79546000	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr1:79545600-79546000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:79545600-79546000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr1:79545600-79546000	Enhancers	Spleen	Spleen
39	chr1:79546000-79555000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr1:79546600-79547800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr1:79547800-79548400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr1:79554200-79555400	Enhancers	HMEC	breast
43	chr1:79554800-79555200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr1:79555000-79557200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr1:79555200-79556200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr1:79555400-79555800	Weak transcription	HMEC	breast
47	chr1:79555800-79557200	Enhancers	HMEC	breast
48	chr1:79556200-79556400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr1:79556400-79557000	Enhancers	HUVEC	blood vessel
50	chr1:79556400-79557400	Enhancers	Muscle Satellite Cultured Cells	--

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