Variant report

Variant	esv3384616
Chromosome Location	chr1:79788134-79814492
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:226)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:226 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr1:79788610-79789531	Hela-S3	cervix:	n/a	chr1:79789162-79789173
2	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
3	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
4	CEBPB	chr1:79788813-79789496	A549	lung:	n/a	chr1:79789162-79789173
5	CEBPB	chr1:79789124-79789259	H1-hESC	embryonic stem cell:	n/a	chr1:79789162-79789173
6	CEBPB	chr1:79788911-79789418	A549	lung:	n/a	chr1:79789162-79789173
7	CEBPB	chr1:79809139-79809258	A549	lung:	n/a	n/a
8	CEBPB	chr1:79788928-79789378	A549	lung:	n/a	chr1:79789162-79789173
9	CEBPB	chr1:79788783-79789533	HCT-116	colon:	n/a	chr1:79789162-79789173
10	CEBPB	chr1:79788875-79789455	ECC-1	luminal epithelium:	n/a	chr1:79789162-79789173
11	CEBPB	chr1:79788982-79789346	HepG2	liver:	n/a	chr1:79789162-79789173
12	CEBPB	chr1:79788426-79789597	IMR90	lung:	n/a	chr1:79789162-79789173
13	CEBPB	chr1:79788903-79789381	HCT-116	colon:	n/a	chr1:79789162-79789173
14	CEBPB	chr1:79788914-79789431	MCF-7	breast:	n/a	chr1:79789162-79789173
15	CEBPB	chr1:79788939-79789305	MCF-7	breast:	n/a	chr1:79789162-79789173
16	CEBPB	chr1:79788912-79789364	ECC-1	luminal epithelium:	n/a	chr1:79789162-79789173
17	CTCF	chr1:79797480-79797630	GM12874	blood:	n/a	n/a
18	CTCF	chr1:79788400-79788550	HMF	breast:	n/a	n/a
19	CTCF	chr1:79797460-79797610	GM12864	blood:	n/a	n/a
20	CTCF	chr1:79788400-79788550	AG04449	skin:	n/a	n/a
21	CTCF	chr1:79797556-79797608	GM19239	blood:	n/a	n/a
22	CTCF	chr1:79788360-79788510	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr1:79788860-79789010	HMF	breast:	n/a	n/a
24	CTCF	chr1:79788220-79788510	AG10803	skin:	n/a	n/a
25	CTCF	chr1:79788480-79788630	NHDF-neo	bronchial:	n/a	n/a
26	CTCF	chr1:79788360-79788510	HCFaa	heart:	n/a	n/a
27	CTCF	chr1:79788420-79788570	GM12875	blood:	n/a	n/a
28	CTCF	chr1:79788340-79788490	HRE	kidney:	n/a	n/a
29	CTCF	chr1:79788340-79788490	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr1:79788140-79788290	RPTEC	kidney:	n/a	n/a
31	CTCF	chr1:79788480-79788630	HCM	heart:	n/a	n/a
32	CTCF	chr1:79788240-79788390	GM12873	blood:	n/a	n/a
33	CTCF	chr1:79788320-79788470	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr1:79796360-79796510	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr1:79788240-79788390	RPTEC	kidney:	n/a	n/a
36	CTCF	chr1:79788460-79788610	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr1:79788180-79788330	HCM	heart:	n/a	n/a
38	CTCF	chr1:79788420-79788570	NHLF	lung:	n/a	n/a
39	CTCF	chr1:79797640-79797790	GM12864	blood:	n/a	n/a
40	CTCF	chr1:79797517-79797648	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:79797513-79797596	A549	lung:	n/a	n/a
42	CTCF	chr1:79788374-79788528	Gliobla	brain:	n/a	n/a
43	CTCF	chr1:79788360-79788510	AG10803	skin:	n/a	n/a
44	CTCF	chr1:79797598-79797601	Medullo	brain:	n/a	n/a
45	CTCF	chr1:79805120-79805270	GM12869	blood:	n/a	n/a
46	CTCF	chr1:79788240-79788390	HFF	foreskin:	n/a	n/a
47	CTCF	chr1:79797489-79797666	MCF-7	breast:	n/a	n/a
48	CTCF	chr1:79788380-79788530	BJ	skin:	n/a	n/a
49	CTCF	chr1:79797512-79797615	ProgFib	skin:	n/a	n/a
50	CTCF	chr1:79797612-79797614	GM12892	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:79801791-79801841	HNPCEpiC	eye:	n/a
2	chr1:79801791-79801841	HPAEpiC	pulmonary alveolar:	n/a
3	chr1:79801791-79801841	GM06990	blood:	n/a
4	chr1:79801791-79801841	PANC-1	pancreas:	n/a
5	chr1:79801791-79801841	RPTEC	kidney:	n/a
6	chr1:79801791-79801841	HAEpiC	amniotic membrane:	n/a
7	chr1:79801791-79801841	NHBE	bronchial:	n/a
8	chr1:79801791-79801841	T-47D	breast:	n/a
9	chr1:79801791-79801841	SAEC	small airway:	n/a
10	chr1:79801791-79801841	GM12878	blood:	n/a
11	chr1:79801791-79801841	SK-N-MC	brain:	n/a
12	chr1:79801791-79801841	HCT-116	colon:	n/a
13	chr1:79801791-79801841	NH-A	brain:	n/a
14	chr1:79801791-79801841	MCF-7	breast:	n/a
15	chr1:79801791-79801841	HRE	kidney:	n/a
16	chr1:79801791-79801841	AG04449	skin:	fetal
17	chr1:79801791-79801841	SKMC	muscle:	n/a
18	chr1:79801791-79801841	HMEC	breast:	n/a
19	chr1:79801791-79801841	AG10803	skin:	n/a
20	chr1:79801791-79801841	PrEC	prostate:	n/a
21	chr1:79801791-79801841	Caco-2	colon:	n/a
22	chr1:79801791-79801841	ovcar-3	ovarian:	n/a
23	chr1:79801791-79801841	AG09309	skin:	n/a
24	chr1:79801791-79801841	NHDF-neo	bronchial:	n/a
25	chr1:79801791-79801841	BJ	skin:	n/a
26	chr1:79801791-79801841	LNCaP	prostate:	n/a
27	chr1:79801791-79801841	CMK	blood:	n/a
28	chr1:79801791-79801841	GM12891	blood:	n/a
29	chr1:79801791-79801841	AG04450	lung:	fetal
30	chr1:79801791-79801841	AG09319	gingival:	n/a
31	chr1:79801791-79801841	SK-N-SH	brain:	n/a
32	chr1:79801791-79801841	HIPEpiC	eye:	n/a
33	chr1:79801791-79801841	HUVEC	blood vessel:	n/a
34	chr1:79801791-79801841	U87	brain:	n/a
35	chr1:79801791-79801841	Hepatocyte	liver:	n/a
36	chr1:79801791-79801841	NB4	blood:	n/a
37	chr1:79801791-79801841	HCM	heart:	n/a
38	chr1:79801791-79801841	AoSMC	blood vessel:	n/a
39	chr1:79801791-79801841	NT2-D1	testis:	n/a
40	chr1:79801791-79801841	MCF10A-Er-Src	breast:	n/a
41	chr1:79801791-79801841	Hela-S3	cervix:	n/a
42	chr1:79801791-79801841	HCF	heart:	n/a
43	chr1:79801791-79801841	H1-hESC	embryonic stem cell:	embryo
44	chr1:79801791-79801841	GM19239	blood:	n/a
45	chr1:79801791-79801841	K562	blood:	n/a
46	chr1:79801791-79801841	A549	lung:	n/a
47	chr1:79801791-79801841	IMR90	lung:	fetal
48	chr1:79801791-79801841	HEEpiC	esophagus:	n/a
49	chr1:79801791-79801841	HRCEpiC	kidney:	n/a
50	chr1:79801791-79801841	HepG2	liver:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:79812849..79814988-chr1:79816549..79819262,2	MCF-7	breast:
2	chr1:79810637..79813588-chr1:79825621..79828347,3	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ELTD1-5	chr1:79788603-79788631	NONHSAT004093
2	lnc-IFI44-1	chr1:79789454-79789644	ENSG00000235011.2
3	lnc-IFI44-1	chr1:79790384-79790534	XLOC_000267
4	lnc-IFI44-1	chr1:79790385-79790548	ENSG00000235011.2
5	lnc-ELTD1-5	chr1:79789342-79789745	XLOC_000881
6	lnc-ELTD1-5	chr1:79790271-79790552	XLOC_000881
7	lnc-IFI44-1	chr1:79789341-79789745	NONHSAT004094
8	lnc-IFI44-1	chr1:79789454-79789644	XLOC_000267
9	lnc-ELTD1-5	chr1:79789429-79789745	NONHSAT004093
10	lnc-ELTD1-5	chr1:79790271-79790416	NONHSAT004093
11	lnc-IFI44-1	chr1:79790270-79790552	NONHSAT004094

No data

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

Extended variants
information (count: 633 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:633 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114554770	chr1:79788135-79788136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs542991424	chr1:79788136-79788137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191391756	chr1:79788137-79788138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs11162689	chr1:79788169-79788170	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs544312884	chr1:79788170-79788171	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs113887565	chr1:79788180-79788181	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs549938421	chr1:79788183-79788184	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs183758878	chr1:79788187-79788188	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs375181646	chr1:79788195-79788196	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs569797279	chr1:79788215-79788216	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs116302438	chr1:79788286-79788287	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs538839598	chr1:79788305-79788306	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs561641385	chr1:79788354-79788355	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs187704052	chr1:79788357-79788358	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs139980665	chr1:79788359-79788360	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs141866459	chr1:79788373-79788374	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs192621166	chr1:79788379-79788380	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs550659025	chr1:79788402-79788403	Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs182198236	chr1:79788411-79788412	Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs536052859	chr1:79788443-79788444	Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs554435109	chr1:79788486-79788487	Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs72945074	chr1:79788513-79788514	Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs533828223	chr1:79788516-79788517	Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs186802051	chr1:79788544-79788545	Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs576901690	chr1:79788595-79788596	Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs115507379	chr1:79788598-79788599	Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs1929622	chr1:79788600-79788601	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs574548628	chr1:79788636-79788637	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs372010421	chr1:79788678-79788679	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs543225909	chr1:79788717-79788718	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs79385564	chr1:79788724-79788725	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs528817771	chr1:79788734-79788735	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs534989861	chr1:79788794-79788795	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs192737761	chr1:79788858-79788859	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs184569815	chr1:79788859-79788860	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs550524109	chr1:79788917-79788918	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs116114629	chr1:79788927-79788928	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs531182104	chr1:79788948-79788949	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs114889027	chr1:79789075-79789076	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs548396162	chr1:79789080-79789081	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs554695837	chr1:79789083-79789084	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs566536190	chr1:79789104-79789105	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs534141251	chr1:79789114-79789115	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs192840412	chr1:79789144-79789145	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs147871773	chr1:79789150-79789151	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs139831390	chr1:79789160-79789161	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs77009546	chr1:79789189-79789190	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs563220916	chr1:79789196-79789197	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs574611918	chr1:79789222-79789223	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs17600871	chr1:79789226-79789227	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:100)

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

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79788000-79788400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr1:79788000-79788600	Enhancers	Muscle Satellite Cultured Cells	--
3	chr1:79788000-79789800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:79788000-79789800	Enhancers	NHDF-Ad	bronchial
5	chr1:79788200-79788600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr1:79788200-79789600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr1:79788200-79789600	Enhancers	Hela-S3	cervix
8	chr1:79788200-79790000	Enhancers	NHLF	lung
9	chr1:79788400-79788600	Enhancers	NH-A	brain
10	chr1:79788400-79788800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr1:79788400-79789600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr1:79788400-79789600	Enhancers	Osteobl	bone
13	chr1:79788400-79789800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr1:79788400-79789800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:79788400-79789800	Enhancers	HMEC	breast
16	chr1:79788600-79789000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr1:79788600-79789000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:79788600-79789000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
19	chr1:79788600-79789000	Enhancers	HUVEC	blood vessel
20	chr1:79788600-79789000	Flanking Active TSS	NH-A	brain
21	chr1:79788600-79789600	Enhancers	NHEK	skin
22	chr1:79788600-79789800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr1:79788600-79789800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr1:79788800-79789400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr1:79788800-79789400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr1:79788800-79789600	Active TSS	A549	lung
27	chr1:79788800-79789800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr1:79788800-79789800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:79788800-79789800	Enhancers	Placenta	Placenta
30	chr1:79789000-79789200	Enhancers	NH-A	brain
31	chr1:79789000-79789600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr1:79789000-79789800	Enhancers	Muscle Satellite Cultured Cells	--
33	chr1:79789200-79789400	Flanking Active TSS	NH-A	brain
34	chr1:79789400-79789800	Enhancers	NH-A	brain
35	chr1:79789800-79790000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr1:79789800-79790600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr1:79789800-79790600	Weak transcription	NHDF-Ad	bronchial
38	chr1:79790000-79790800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr1:79790600-79790800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr1:79790600-79790800	ZNF genes & repeats	NHDF-Ad	bronchial
41	chr1:79790800-79792800	Weak transcription	NHDF-Ad	bronchial
42	chr1:79792400-79795800	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr1:79793400-79794200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr1:79793600-79794000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr1:79794000-79798400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr1:79795200-79795600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr1:79795200-79795800	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr1:79795400-79795600	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr1:79795600-79797400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr1:79795600-79797600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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