Variant report

Variant	nsv870962
Chromosome Location	chr1:79755185-79835066
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:571)
CpG islands
(count:122)
Chromatin interactive
region (count:6)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:571 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr1:79761760-79762116	HepG2	liver:	n/a	n/a
2	CEBPB	chr1:79818714-79819083	IMR90	lung:	n/a	n/a
3	CEBPB	chr1:79788426-79789597	IMR90	lung:	n/a	chr1:79789162-79789173
4	CEBPB	chr1:79818740-79819166	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr1:79820840-79821140	IMR90	lung:	n/a	n/a
6	CEBPB	chr1:79789124-79789259	H1-hESC	embryonic stem cell:	n/a	chr1:79789162-79789173
7	CEBPB	chr1:79809139-79809258	A549	lung:	n/a	n/a
8	CEBPB	chr1:79761810-79762112	ECC-1	luminal epithelium:	n/a	n/a
9	CEBPB	chr1:79769847-79770159	IMR90	lung:	n/a	chr1:79769984-79769997 chr1:79769986-79769997 chr1:79769986-79769997
10	CEBPB	chr1:79761787-79762100	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr1:79803932-79804544	HepG2	liver:	n/a	chr1:79804061-79804074 chr1:79804061-79804072 chr1:79804061-79804074 chr1:79804411-79804424 chr1:79804062-79804073 chr1:79804061-79804074
12	CEBPB	chr1:79818713-79819070	A549	lung:	n/a	n/a
13	CEBPB	chr1:79788911-79789418	A549	lung:	n/a	chr1:79789162-79789173
14	CEBPB	chr1:79761748-79762138	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:79788914-79789431	MCF-7	breast:	n/a	chr1:79789162-79789173
16	CEBPB	chr1:79823841-79824095	IMR90	lung:	n/a	chr1:79823979-79823992
17	CEBPB	chr1:79818763-79819079	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr1:79788783-79789533	HCT-116	colon:	n/a	chr1:79789162-79789173
19	CEBPB	chr1:79833950-79834269	HepG2	liver:	n/a	chr1:79834102-79834113
20	CEBPB	chr1:79788903-79789381	HCT-116	colon:	n/a	chr1:79789162-79789173
21	CEBPB	chr1:79788610-79789531	Hela-S3	cervix:	n/a	chr1:79789162-79789173
22	CEBPB	chr1:79788939-79789305	MCF-7	breast:	n/a	chr1:79789162-79789173
23	CEBPB	chr1:79780660-79780860	HepG2	liver:	n/a	chr1:79780750-79780761 chr1:79780809-79780820
24	CEBPB	chr1:79761781-79762112	A549	lung:	n/a	n/a
25	CEBPB	chr1:79788982-79789346	HepG2	liver:	n/a	chr1:79789162-79789173
26	CEBPB	chr1:79818744-79819030	HepG2	liver:	n/a	n/a
27	CEBPB	chr1:79788875-79789455	ECC-1	luminal epithelium:	n/a	chr1:79789162-79789173
28	CEBPB	chr1:79823903-79824108	A549	lung:	n/a	chr1:79823979-79823992
29	CEBPB	chr1:79788813-79789496	A549	lung:	n/a	chr1:79789162-79789173
30	CEBPB	chr1:79803948-79804495	IMR90	lung:	n/a	chr1:79804061-79804074 chr1:79804061-79804072 chr1:79804061-79804074 chr1:79804411-79804424 chr1:79804062-79804073 chr1:79804061-79804074
31	CEBPB	chr1:79761760-79762117	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr1:79788928-79789378	A549	lung:	n/a	chr1:79789162-79789173
33	CEBPB	chr1:79788912-79789364	ECC-1	luminal epithelium:	n/a	chr1:79789162-79789173
34	CTCF	chr1:79819040-79819190	GM12865	blood:	n/a	n/a
35	CTCF	chr1:79819040-79819190	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr1:79819060-79819210	AG04450	lung:	n/a	n/a
37	CTCF	chr1:79819010-79819229	LNCaP	prostate:	n/a	n/a
38	CTCF	chr1:79817060-79817210	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr1:79817160-79817310	HMF	breast:	n/a	n/a
40	CTCF	chr1:79817160-79817310	HPF	lung:	n/a	n/a
41	CTCF	chr1:79819020-79819170	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr1:79819060-79819210	GM12878	blood:	n/a	n/a
43	CTCF	chr1:79819040-79819190	AG10803	skin:	n/a	n/a
44	CTCF	chr1:79818931-79819226	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr1:79817060-79817210	HMF	breast:	n/a	n/a
46	CTCF	chr1:79797480-79797630	GM12871	blood:	n/a	n/a
47	CTCF	chr1:79819020-79819170	GM12878	blood:	n/a	n/a
48	CTCF	chr1:79819080-79819230	GM12871	blood:	n/a	n/a
49	CTCF	chr1:79819080-79819230	MCF-7	breast:	n/a	n/a
50	CTCF	chr1:79819020-79819170	Hela-S3	cervix:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:79801791-79801841	PrEC	prostate:	n/a
2	chr1:79830414-79830464	BJ	skin:	n/a
3	chr1:79830414-79830464	AG09319	gingival:	n/a
4	chr1:79801791-79801841	AG10803	skin:	n/a
5	chr1:79801791-79801841	ProgFib	skin:	n/a
6	chr1:79830414-79830464	SK-N-MC	brain:	n/a
7	chr1:79830414-79830464	PANC-1	pancreas:	n/a
8	chr1:79830414-79830464	NB4	blood:	n/a
9	chr1:79801791-79801841	Caco-2	colon:	n/a
10	chr1:79830414-79830464	HCT-116	colon:	n/a
11	chr1:79830414-79830464	HIPEpiC	eye:	n/a
12	chr1:79830414-79830464	MCF10A-Er-Src	breast:	n/a
13	chr1:79801791-79801841	Hepatocyte	liver:	n/a
14	chr1:79830414-79830464	HRCEpiC	kidney:	n/a
15	chr1:79801791-79801841	HPAEpiC	pulmonary alveolar:	n/a
16	chr1:79830414-79830464	HL-60	blood:	n/a
17	chr1:79830414-79830464	AG10803	skin:	n/a
18	chr1:79830414-79830464	SKMC	muscle:	n/a
19	chr1:79830414-79830464	SAEC	small airway:	n/a
20	chr1:79830414-79830464	IMR90	lung:	fetal
21	chr1:79830414-79830464	AG04450	lung:	fetal
22	chr1:79801791-79801841	BJ	skin:	n/a
23	chr1:79801791-79801841	AG09319	gingival:	n/a
24	chr1:79801791-79801841	IMR90	lung:	fetal
25	chr1:79801791-79801841	SK-N-MC	brain:	n/a
26	chr1:79801791-79801841	SKMC	muscle:	n/a
27	chr1:79801791-79801841	NH-A	brain:	n/a
28	chr1:79830414-79830464	HUVEC	blood vessel:	n/a
29	chr1:79801791-79801841	HEEpiC	esophagus:	n/a
30	chr1:79801791-79801841	NT2-D1	testis:	n/a
31	chr1:79801791-79801841	ECC-1	luminal epithelium:	n/a
32	chr1:79830414-79830464	CMK	blood:	n/a
33	chr1:79801791-79801841	HRPEpiC	eye:	n/a
34	chr1:79830414-79830464	Caco-2	colon:	n/a
35	chr1:79830414-79830464	NHBE	bronchial:	n/a
36	chr1:79801791-79801841	NHBE	bronchial:	n/a
37	chr1:79830414-79830464	HCM	heart:	n/a
38	chr1:79830414-79830464	ECC-1	luminal epithelium:	n/a
39	chr1:79830414-79830464	HEK293	kidney:	embryo
40	chr1:79830414-79830464	AG09309	skin:	n/a
41	chr1:79830414-79830464	RPTEC	kidney:	n/a
42	chr1:79801791-79801841	MCF-7	breast:	n/a
43	chr1:79830414-79830464	HCF	heart:	n/a
44	chr1:79830414-79830464	PFSK-1	brain:	n/a
45	chr1:79830414-79830464	ProgFib	skin:	n/a
46	chr1:79801791-79801841	HCPEpiC	choroid plexus:	n/a
47	chr1:79801791-79801841	CMK	blood:	n/a
48	chr1:79830414-79830464	A549	lung:	n/a
49	chr1:79830414-79830464	K562	blood:	n/a
50	chr1:79801791-79801841	HNPCEpiC	eye:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:79810637..79813588-chr1:79825621..79828347,3	MCF-7	breast:
2	chr1:79812849..79814988-chr1:79816549..79819262,2	MCF-7	breast:
3	chr1:79810637..79813588-chr1:79825621..79828347,3	MCF-7	breast:
4	chr1:79826260..79828689-chr6:111008268..111010656,2	MCF-7	breast:
5	chr1:79812849..79814988-chr1:79816549..79819262,2	MCF-7	breast:
6	chr1:79725343..79726033-chr1:79818640..79819391,2	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFI44-1	chr1:79790270-79790552	NONHSAT004094
2	lnc-IFI44-1	chr1:79789454-79789644	ENSG00000235011.2
3	lnc-ELTD1-5	chr1:79789429-79789745	NONHSAT004093
4	lnc-IFI44-2	chr1:79775231-79775346	XLOC_000266
5	lnc-ELTD1-5	chr1:79788603-79788631	NONHSAT004093
6	lnc-IFI44-1	chr1:79789454-79789644	XLOC_000267
7	lnc-ELTD1-5	chr1:79789342-79789745	XLOC_000881
8	lnc-IFI44-2	chr1:79775371-79775405	XLOC_000266
9	lnc-IFI44-1	chr1:79790385-79790548	ENSG00000235011.2
10	lnc-ELTD1-5	chr1:79790271-79790552	XLOC_000881
11	lnc-IFI44-1	chr1:79789341-79789745	NONHSAT004094
12	lnc-IFI44-2	chr1:79775231-79775405	XLOC_000266
13	lnc-ELTD1-3	chr1:79775130-79775346	XLOC_000879
14	lnc-IFI44-2	chr1:79775230-79775405	NONHSAT004088
15	lnc-IFI44-1	chr1:79790384-79790534	XLOC_000267
16	lnc-ELTD1-4	chr1:79786813-79786877	XLOC_000880
17	lnc-ELTD1-5	chr1:79790271-79790416	NONHSAT004093
18	lnc-ELTD1-4	chr1:79787090-79787278	XLOC_000880
19	lnc-ELTD1-3	chr1:79778966-79779074	XLOC_000879

No data

Variant related genes	Relation type
ENSG00000235011	TF binding region
ENSG00000235011	CpG island
DYRK2	miRNA target sites
C9orf5	miRNA target sites
ZNF652	miRNA target sites

Extended variants
information (count: 1612 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1612 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182970141	chr1:79758843-79758844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs536832266	chr1:79758941-79758942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555351225	chr1:79758946-79758947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs573583290	chr1:79758951-79758952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs80153120	chr1:79758970-79758971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs368690590	chr1:79758984-79758985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540533130	chr1:79758996-79758997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs540555188	chr1:79759067-79759068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565297305	chr1:79759072-79759073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs187623796	chr1:79759085-79759086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs540100203	chr1:79759089-79759090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557558779	chr1:79759105-79759106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs79619167	chr1:79759122-79759123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528844466	chr1:79759124-79759125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142325244	chr1:79759131-79759132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192647852	chr1:79759158-79759159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs150089376	chr1:79759172-79759173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559867962	chr1:79759216-79759217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7515632	chr1:79759232-79759233	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs182135447	chr1:79759263-79759264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs138420129	chr1:79759284-79759285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573547448	chr1:79759321-79759322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs187761208	chr1:79759340-79759341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149281384	chr1:79759376-79759377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542418202	chr1:79759412-79759413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs75255963	chr1:79759439-79759440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs12064196	chr1:79759457-79759458	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs548708522	chr1:79759459-79759460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs535497263	chr1:79759594-79759595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs144076287	chr1:79759595-79759596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567040055	chr1:79759631-79759632	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs1331717	chr1:79759634-79759635	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs192890586	chr1:79759668-79759669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs114940352	chr1:79759693-79759694	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371950928	chr1:79759720-79759721	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184572951	chr1:79759744-79759745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376538508	chr1:79759755-79759756	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556283371	chr1:79759763-79759764	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147316425	chr1:79759773-79759774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565315503	chr1:79759779-79759780	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs527966271	chr1:79759784-79759785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541877673	chr1:79759835-79759836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189845945	chr1:79759855-79759856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192846190	chr1:79759893-79759894	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546106101	chr1:79759907-79759908	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564207928	chr1:79759976-79759977	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184593963	chr1:79759990-79759991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142248140	chr1:79760004-79760005	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568020227	chr1:79760009-79760010	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529014114	chr1:79760020-79760021	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
Breast cancer	22522925	CNVD

Chromatin state (count:174 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79758800-79761000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr1:79759000-79760200	Enhancers	Muscle Satellite Cultured Cells	--
3	chr1:79759200-79759600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr1:79759200-79760200	Enhancers	HUVEC	blood vessel
5	chr1:79759200-79761200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr1:79759200-79761200	Enhancers	NHDF-Ad	bronchial
7	chr1:79759400-79759800	Enhancers	HMEC	breast
8	chr1:79759400-79760200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr1:79759600-79759800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr1:79759600-79761000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr1:79760000-79760200	Enhancers	Aorta	Aorta
12	chr1:79760000-79761000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr1:79760200-79760800	Weak transcription	Aorta	Aorta
14	chr1:79760200-79761400	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr1:79760800-79761000	Enhancers	Aorta	Aorta
16	chr1:79761000-79761400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr1:79761000-79761600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr1:79761000-79762200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr1:79761200-79761600	Flanking Active TSS	NHDF-Ad	bronchial
20	chr1:79761200-79761600	Enhancers	Osteobl	bone
21	chr1:79761200-79762400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr1:79761400-79761600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr1:79761400-79762200	Enhancers	Muscle Satellite Cultured Cells	--
24	chr1:79761600-79762000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr1:79761600-79762000	Enhancers	Adipose Nuclei	Adipose
26	chr1:79761600-79762000	Enhancers	NHDF-Ad	bronchial
27	chr1:79761600-79762000	Flanking Active TSS	Osteobl	bone
28	chr1:79761600-79762200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr1:79762000-79762200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr1:79762000-79762600	Enhancers	Osteobl	bone
31	chr1:79762200-79762800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr1:79762400-79762800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr1:79762800-79769800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr1:79767200-79770800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr1:79768200-79768800	Enhancers	Fetal Kidney	kidney
36	chr1:79768600-79769000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr1:79768600-79769000	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr1:79768600-79769000	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr1:79768600-79769200	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr1:79768600-79769200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr1:79768600-79769200	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr1:79768600-79770000	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr1:79768800-79769200	Enhancers	Brain Germinal Matrix	brain
44	chr1:79769200-79769600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr1:79769600-79770200	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr1:79769800-79770400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:79772400-79772600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr1:79778000-79781600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr1:79779000-79779400	Enhancers	Osteobl	bone
50	chr1:79779000-79779600	Enhancers	Muscle Satellite Cultured Cells	--

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