Variant report

Variant	nsv546619
Chromosome Location	chr1:79233493-79614989
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1566)
CpG islands
(count:979)
Chromatin interactive
region (count:19)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1566 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:79305459-79305734	K562	blood:	n/a	n/a
2	ARID3A	chr1:79305438-79305769	HepG2	liver:	n/a	n/a
3	ATF1	chr1:79259668-79259884	K562	blood:	n/a	n/a
4	ATF2	chr1:79506114-79506881	GM12878	blood:	n/a	n/a
5	ATF2	chr1:79507696-79508185	GM12878	blood:	n/a	n/a
6	ATF2	chr1:79507719-79508191	GM12878	blood:	n/a	n/a
7	ATF2	chr1:79505821-79506890	GM12878	blood:	n/a	n/a
8	ATF2	chr1:79350690-79350993	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:79472315-79472519	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr1:79507950-79508076	K562	blood:	n/a	n/a
11	BACH1	chr1:79508075-79508122	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:79545497-79545905	H1-hESC	embryonic stem cell:	n/a	chr1:79545669-79545683
13	BATF	chr1:79506304-79506770	GM12878	blood:	n/a	n/a
14	BATF	chr1:79506383-79506726	GM12878	blood:	n/a	n/a
15	BATF	chr1:79320756-79321223	GM12878	blood:	n/a	chr1:79320825-79320834
16	BATF	chr1:79507758-79508057	GM12878	blood:	n/a	n/a
17	BATF	chr1:79507747-79508138	GM12878	blood:	n/a	n/a
18	BCL11A	chr1:79506346-79506753	GM12878	blood:	n/a	n/a
19	BCL11A	chr1:79300086-79300356	GM12878	blood:	n/a	n/a
20	BCL11A	chr1:79603898-79604245	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL11A	chr1:79507836-79508150	GM12878	blood:	n/a	n/a
22	BCL11A	chr1:79262911-79263285	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL11A	chr1:79507862-79508010	GM12878	blood:	n/a	n/a
24	BCL11A	chr1:79604022-79604167	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCL3	chr1:79507766-79508061	GM12878	blood:	n/a	n/a
26	BCL3	chr1:79506306-79506801	GM12878	blood:	n/a	n/a
27	BCLAF1	chr1:79507869-79508207	GM12878	blood:	n/a	n/a
28	BCLAF1	chr1:79506260-79506789	GM12878	blood:	n/a	n/a
29	BHLHE40	chr1:79320988-79321254	GM12878	blood:	n/a	n/a
30	BHLHE40	chr1:79405513-79405527	GM12878	blood:	n/a	n/a
31	BHLHE40	chr1:79297522-79297765	GM12878	blood:	n/a	n/a
32	BRCA1	chr1:79509475-79509505	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr1:79415111-79415262	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr1:79262865-79262987	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr1:79459804-79459831	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr1:79297275-79297897	HCT-116	colon:	n/a	n/a
37	CBX3	chr1:79299051-79299589	HCT-116	colon:	n/a	n/a
38	CCNT2	chr1:79250632-79250832	K562	blood:	n/a	n/a
39	CEBPB	chr1:79379650-79380020	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr1:79414890-79415047	HepG2	liver:	n/a	chr1:79414944-79414957 chr1:79414973-79414990
41	CEBPB	chr1:79379656-79380004	HepG2	liver:	n/a	n/a
42	CEBPB	chr1:79490048-79490150	H1-hESC	embryonic stem cell:	n/a	chr1:79490066-79490077
43	CEBPB	chr1:79409304-79409537	IMR90	lung:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
44	CEBPB	chr1:79377650-79378354	HepG2	liver:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
45	CEBPB	chr1:79470706-79470922	Hela-S3	cervix:	n/a	chr1:79470789-79470800
46	CEBPB	chr1:79357942-79358268	IMR90	lung:	n/a	n/a
47	CEBPB	chr1:79377749-79377922	H1-hESC	embryonic stem cell:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
48	CEBPB	chr1:79594497-79595010	IMR90	lung:	n/a	chr1:79594917-79594928 chr1:79594917-79594928 chr1:79594917-79594930
49	CEBPB	chr1:79379779-79379879	K562	blood:	n/a	n/a
50	CEBPB	chr1:79507830-79508119	Hela-S3	cervix:	n/a	n/a

(count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:79350918-79350968	Jurkat	blood:	n/a
2	chr1:79472343-79472393	SK-N-SH_RA	brain:	n/a
3	chr1:79594960-79595010	GM12892	blood:	n/a
4	chr1:79350918-79350968	Jurkat	blood:	n/a
5	chr1:79472343-79472393	SK-N-SH_RA	brain:	n/a
6	chr1:79594960-79595010	GM12892	blood:	n/a
7	chr1:79594960-79595010	HCPEpiC	choroid plexus:	n/a
8	chr1:79471984-79472034	MCF-7	breast:	n/a
9	chr1:79472452-79472502	Hepatocyte	liver:	n/a
10	chr1:79473783-79473833	PrEC	prostate:	n/a
11	chr1:79473783-79473833	ovcar-3	ovarian:	n/a
12	chr1:79472452-79472502	Hela-S3	cervix:	n/a
13	chr1:79472343-79472393	GM12891	blood:	n/a
14	chr1:79472361-79472411	AG09319	gingival:	n/a
15	chr1:79472343-79472393	IMR90	lung:	fetal
16	chr1:79471984-79472034	SK-N-SH	brain:	n/a
17	chr1:79472452-79472502	NHDF-neo	bronchial:	n/a
18	chr1:79474718-79474768	RPTEC	kidney:	n/a
19	chr1:79473783-79473833	NT2-D1	testis:	n/a
20	chr1:79471984-79472034	GM19239	blood:	n/a
21	chr1:79472343-79472393	U87	brain:	n/a
22	chr1:79473783-79473833	AG09309	skin:	n/a
23	chr1:79472282-79472332	T-47D	breast:	n/a
24	chr1:79472282-79472332	AG09309	skin:	n/a
25	chr1:79471984-79472034	RPTEC	kidney:	n/a
26	chr1:79471984-79472034	Caco-2	colon:	n/a
27	chr1:79471984-79472034	HPAEpiC	pulmonary alveolar:	n/a
28	chr1:79474718-79474768	NHBE	bronchial:	n/a
29	chr1:79474718-79474768	GM06990	blood:	n/a
30	chr1:79474718-79474768	Hela-S3	cervix:	n/a
31	chr1:79473783-79473833	Jurkat	blood:	n/a
32	chr1:79472558-79472608	MCF-7	breast:	n/a
33	chr1:79594960-79595010	Caco-2	colon:	n/a
34	chr1:79307043-79307093	HL-60	blood:	n/a
35	chr1:79472343-79472393	T-47D	breast:	n/a
36	chr1:79472917-79472967	Jurkat	blood:	n/a
37	chr1:79350918-79350968	HRPEpiC	eye:	n/a
38	chr1:79472408-79472458	HRCEpiC	kidney:	n/a
39	chr1:79472452-79472502	AG04449	skin:	fetal
40	chr1:79350918-79350968	HCT-116	colon:	n/a
41	chr1:79474718-79474768	CMK	blood:	n/a
42	chr1:79472917-79472967	HCM	heart:	n/a
43	chr1:79472917-79472967	GM12891	blood:	n/a
44	chr1:79472452-79472502	PANC-1	pancreas:	n/a
45	chr1:79472558-79472608	ProgFib	skin:	n/a
46	chr1:79472536-79472586	NH-A	brain:	n/a
47	chr1:79471984-79472034	HUVEC	blood vessel:	n/a
48	chr1:79472917-79472967	GM12892	blood:	n/a
49	chr1:79472408-79472458	HIPEpiC	eye:	n/a
50	chr1:79472532-79472582	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:79281703..79284146-chr1:79308021..79310225,2	K562	blood:
2	chr1:79536026..79538535-chr1:79539899..79541790,2	K562	blood:
3	chr1:79411840..79414575-chr1:79858123..79860401,2	K562	blood:
4	chr1:79281703..79284146-chr1:79308021..79310225,2	K562	blood:
5	chr1:79370114..79372345-chr1:79443530..79445892,2	K562	blood:
6	chr1:79266346..79267150-chr1:79858034..79858765,3	MCF-7	breast:
7	chr1:79304951..79305958-chr1:79662942..79663752,3	MCF-7	breast:
8	chr1:79299275..79301209-chr1:79305174..79307511,2	K562	blood:
9	chr1:79370114..79372345-chr1:79443530..79445892,2	K562	blood:
10	chr1:79356582..79358429-chr1:79361774..79364231,2	MCF-7	breast:
11	chr1:79527063..79529337-chr1:79533334..79535055,2	K562	blood:
12	chr1:79527063..79529337-chr1:79533334..79535055,2	K562	blood:
13	chr1:79484446..79486654-chr1:79486860..79488839,2	MCF-7	breast:
14	chr1:79299275..79301209-chr1:79305174..79307511,2	K562	blood:
15	chr1:79356582..79358429-chr1:79361774..79364231,2	MCF-7	breast:
16	chr1:79536026..79538535-chr1:79539899..79541790,2	K562	blood:
17	chr1:79410821..79413576-chr1:79414533..79416679,2	K562	blood:
18	chr1:79484446..79486654-chr1:79486860..79488839,2	MCF-7	breast:
19	chr1:79410821..79413576-chr1:79414533..79416679,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFI44-7	chr1:79562042-79562232	NONHSAT004086
2	lnc-ELTD1-1	chr1:79346569-79346750	NONHSAT004083
3	lnc-ELTD1-1	chr1:79351642-79351681	NONHSAT004083
4	lnc-IFI44-7	chr1:79562972-79563122	NONHSAT004086
5	lnc-ELTD1-2	chr1:79490858-79491009	XLOC_000877
6	lnc-ELTD1-2	chr1:79493775-79493876	XLOC_000877

No data

Variant related genes	Relation type
ENSG00000266388	TF binding region
ELTD1	TF binding region
PSAT1P3	TF binding region
ENSG00000266388	CpG island
ELTD1	CpG island
PSAT1P3	CpG island
TCF7L2	miRNA target sites
IGSF1	miRNA target sites

Extended variants
information (count: 10580 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:10580 , 50 per page) page: 1 2 3 4 5 6 7 ... 212

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371098739	chr1:79242660-79242661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs578207854	chr1:79242661-79242662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537848760	chr1:79242724-79242725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs374760991	chr1:79242727-79242728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139110628	chr1:79242736-79242737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182098527	chr1:79242797-79242798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs558171790	chr1:79242856-79242857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187767521	chr1:79242871-79242872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543141539	chr1:79242890-79242891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs150032865	chr1:79242905-79242906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs7540911	chr1:79242937-79242938	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs540085383	chr1:79242993-79242994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs569466593	chr1:79243021-79243022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs72674000	chr1:79243029-79243030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs6690646	chr1:79243077-79243078	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs550468831	chr1:79243086-79243087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562094534	chr1:79243111-79243112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs191376234	chr1:79243121-79243122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547871043	chr1:79243125-79243126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566477867	chr1:79243126-79243127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs74091879	chr1:79243133-79243134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558972601	chr1:79243135-79243136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546850960	chr1:79243157-79243158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs571821519	chr1:79243161-79243162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs539292540	chr1:79243186-79243187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs113026789	chr1:79243195-79243196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs112818609	chr1:79243249-79243250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542823433	chr1:79243307-79243308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs555027303	chr1:79243323-79243324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573231485	chr1:79243324-79243325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561402232	chr1:79243358-79243359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs76765366	chr1:79243399-79243400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs183132744	chr1:79243442-79243443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188562621	chr1:79243467-79243468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs78259942	chr1:79243472-79243473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs199742843	chr1:79243481-79243482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs529139428	chr1:79243482-79243483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs80350896	chr1:79243505-79243506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529625403	chr1:79243620-79243621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs140972535	chr1:79243621-79243622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs560116042	chr1:79243682-79243683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs112797802	chr1:79243692-79243693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs113362051	chr1:79243714-79243715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546836273	chr1:79243715-79243716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs35352586	chr1:79243716-79243717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs375581693	chr1:79243725-79243726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs79301345	chr1:79243741-79243742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs78598987	chr1:79243792-79243793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs529049984	chr1:79243799-79243800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574301667	chr1:79245035-79245036	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Breast cancer	22522925	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:968 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79242600-79243800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:79245000-79246000	Enhancers	Muscle Satellite Cultured Cells	--
3	chr1:79245200-79246000	Enhancers	Osteobl	bone
4	chr1:79245200-79246200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr1:79261200-79261600	Enhancers	Fetal Brain Male	brain
6	chr1:79261600-79263200	Weak transcription	Fetal Brain Male	brain
7	chr1:79262800-79263400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr1:79263200-79265800	Enhancers	Fetal Brain Male	brain
9	chr1:79265200-79265800	Enhancers	Brain Germinal Matrix	brain
10	chr1:79284800-79285200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr1:79285200-79285600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:79285600-79298000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr1:79289800-79291000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr1:79289800-79291600	Enhancers	NHDF-Ad	bronchial
15	chr1:79289800-79291800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr1:79289800-79291800	Enhancers	Osteobl	bone
17	chr1:79290000-79292200	Enhancers	Muscle Satellite Cultured Cells	--
18	chr1:79291000-79296000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr1:79291600-79296000	Weak transcription	NHDF-Ad	bronchial
20	chr1:79291800-79295800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr1:79291800-79296000	Weak transcription	Osteobl	bone
22	chr1:79292200-79295800	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr1:79295000-79295800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr1:79295200-79298400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr1:79295800-79297400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:79295800-79298200	Enhancers	Muscle Satellite Cultured Cells	--
27	chr1:79295800-79300000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr1:79296000-79296200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr1:79296000-79296200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr1:79296000-79296400	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr1:79296000-79299200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr1:79296000-79299800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr1:79296000-79300000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr1:79296000-79300200	Enhancers	NH-A	brain
35	chr1:79296000-79300200	Enhancers	NHDF-Ad	bronchial
36	chr1:79296000-79300200	Enhancers	Osteobl	bone
37	chr1:79296200-79297400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr1:79296200-79297400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr1:79296200-79297600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr1:79296800-79300200	Enhancers	HMEC	breast
41	chr1:79297000-79297400	Enhancers	NHEK	skin
42	chr1:79297000-79299600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr1:79297000-79300400	Enhancers	HSMM	muscle
44	chr1:79297000-79300400	Enhancers	HUVEC	blood vessel
45	chr1:79297200-79299800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr1:79297400-79297600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr1:79297400-79297800	Flanking Active TSS	NHEK	skin
48	chr1:79297400-79299000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr1:79297400-79299400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr1:79297400-79299600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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