Variant report

Variant	nsv1001894
Chromosome Location	chr1:79351364-79542576
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:79507696-79508185	GM12878	blood:	n/a	n/a
2	ATF2	chr1:79506114-79506881	GM12878	blood:	n/a	n/a
3	ATF2	chr1:79505821-79506890	GM12878	blood:	n/a	n/a
4	ATF2	chr1:79507719-79508191	GM12878	blood:	n/a	n/a
5	BACH1	chr1:79508075-79508122	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:79507950-79508076	K562	blood:	n/a	n/a
7	BACH1	chr1:79472315-79472519	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr1:79506304-79506770	GM12878	blood:	n/a	n/a
9	BATF	chr1:79506383-79506726	GM12878	blood:	n/a	n/a
10	BATF	chr1:79507747-79508138	GM12878	blood:	n/a	n/a
11	BATF	chr1:79507758-79508057	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:79507862-79508010	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:79507836-79508150	GM12878	blood:	n/a	n/a
14	BCL11A	chr1:79506346-79506753	GM12878	blood:	n/a	n/a
15	BCL3	chr1:79506306-79506801	GM12878	blood:	n/a	n/a
16	BCL3	chr1:79507766-79508061	GM12878	blood:	n/a	n/a
17	BCLAF1	chr1:79506260-79506789	GM12878	blood:	n/a	n/a
18	BCLAF1	chr1:79507869-79508207	GM12878	blood:	n/a	n/a
19	BHLHE40	chr1:79405513-79405527	GM12878	blood:	n/a	n/a
20	BRCA1	chr1:79415111-79415262	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr1:79509475-79509505	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr1:79459804-79459831	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr1:79490048-79490150	H1-hESC	embryonic stem cell:	n/a	chr1:79490066-79490077
24	CEBPB	chr1:79379656-79380004	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:79506115-79506910	GM12878	blood:	n/a	n/a
26	CEBPB	chr1:79409235-79409568	Hela-S3	cervix:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
27	CEBPB	chr1:79451150-79451399	K562	blood:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
28	CEBPB	chr1:79378071-79378234	K562	blood:	n/a	n/a
29	CEBPB	chr1:79377650-79378354	HepG2	liver:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
30	CEBPB	chr1:79490003-79490203	A549	lung:	n/a	chr1:79490066-79490077
31	CEBPB	chr1:79377641-79378427	ECC-1	luminal epithelium:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
32	CEBPB	chr1:79414890-79415047	HepG2	liver:	n/a	chr1:79414944-79414957 chr1:79414973-79414990
33	CEBPB	chr1:79379712-79379997	A549	lung:	n/a	n/a
34	CEBPB	chr1:79451090-79451446	IMR90	lung:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
35	CEBPB	chr1:79483498-79483817	HepG2	liver:	n/a	chr1:79483669-79483680
36	CEBPB	chr1:79357942-79358268	IMR90	lung:	n/a	n/a
37	CEBPB	chr1:79405681-79405919	HepG2	liver:	n/a	n/a
38	CEBPB	chr1:79482686-79482859	HepG2	liver:	n/a	chr1:79482727-79482740 chr1:79482727-79482738 chr1:79482727-79482740
39	CEBPB	chr1:79357252-79357448	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr1:79470648-79470928	HepG2	liver:	n/a	chr1:79470789-79470800
41	CEBPB	chr1:79379650-79380020	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr1:79377662-79378457	ECC-1	luminal epithelium:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
43	CEBPB	chr1:79377671-79378334	A549	lung:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
44	CEBPB	chr1:79521171-79521337	A549	lung:	n/a	n/a
45	CEBPB	chr1:79521185-79521360	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr1:79414781-79415272	Hela-S3	cervix:	n/a	chr1:79414944-79414957 chr1:79414973-79414990
47	CEBPB	chr1:79470712-79470946	A549	lung:	n/a	chr1:79470789-79470800
48	CEBPB	chr1:79409333-79409445	K562	blood:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
49	CEBPB	chr1:79379779-79379879	K562	blood:	n/a	n/a
50	CEBPB	chr1:79409261-79409575	HepG2	liver:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:79472282-79472332	Caco-2	colon:	n/a
2	chr1:79472282-79472332	Caco-2	colon:	n/a
3	chr1:79472452-79472502	AG09319	gingival:	n/a
4	chr1:79473783-79473833	HL-60	blood:	n/a
5	chr1:79473783-79473833	AG04449	skin:	fetal
6	chr1:79472532-79472582	AG09309	skin:	n/a
7	chr1:79472452-79472502	NB4	blood:	n/a
8	chr1:79472361-79472411	Jurkat	blood:	n/a
9	chr1:79472917-79472967	HMEC	breast:	n/a
10	chr1:79472408-79472458	AG09309	skin:	n/a
11	chr1:79474718-79474768	AoSMC	blood vessel:	n/a
12	chr1:79472361-79472411	NH-A	brain:	n/a
13	chr1:79471984-79472034	AG09309	skin:	n/a
14	chr1:79472643-79472693	HCT-116	colon:	n/a
15	chr1:79472361-79472411	AG04450	lung:	fetal
16	chr1:79472558-79472608	A549	lung:	n/a
17	chr1:79474718-79474768	HCF	heart:	n/a
18	chr1:79471984-79472034	GM12892	blood:	n/a
19	chr1:79472343-79472393	ProgFib	skin:	n/a
20	chr1:79474718-79474768	HEK293	kidney:	embryo
21	chr1:79473783-79473833	AG09309	skin:	n/a
22	chr1:79473783-79473833	PFSK-1	brain:	n/a
23	chr1:79473783-79473833	AoSMC	blood vessel:	n/a
24	chr1:79472536-79472586	PANC-1	pancreas:	n/a
25	chr1:79472361-79472411	HCPEpiC	choroid plexus:	n/a
26	chr1:79473783-79473833	K562	blood:	n/a
27	chr1:79472452-79472502	AG09309	skin:	n/a
28	chr1:79472536-79472586	PrEC	prostate:	n/a
29	chr1:79472917-79472967	AG04449	skin:	fetal
30	chr1:79472917-79472967	AG10803	skin:	n/a
31	chr1:79472643-79472693	GM06990	blood:	n/a
32	chr1:79472536-79472586	SK-N-SH	brain:	n/a
33	chr1:79472452-79472502	HMEC	breast:	n/a
34	chr1:79474718-79474768	T-47D	breast:	n/a
35	chr1:79472536-79472586	HAEpiC	amniotic membrane:	n/a
36	chr1:79472452-79472502	HepG2	liver:	n/a
37	chr1:79471984-79472034	H1-hESC	embryonic stem cell:	embryo
38	chr1:79472536-79472586	Caco-2	colon:	n/a
39	chr1:79472361-79472411	HCM	heart:	n/a
40	chr1:79472361-79472411	HRCEpiC	kidney:	n/a
41	chr1:79472558-79472608	HL-60	blood:	n/a
42	chr1:79472343-79472393	HEEpiC	esophagus:	n/a
43	chr1:79471984-79472034	HEK293	kidney:	embryo
44	chr1:79471984-79472034	NB4	blood:	n/a
45	chr1:79472452-79472502	AG04449	skin:	fetal
46	chr1:79472452-79472502	NHDF-neo	bronchial:	n/a
47	chr1:79472643-79472693	ProgFib	skin:	n/a
48	chr1:79472282-79472332	NHBE	bronchial:	n/a
49	chr1:79474718-79474768	HUVEC	blood vessel:	n/a
50	chr1:79472452-79472502	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:79484446..79486654-chr1:79486860..79488839,2	MCF-7	breast:
2	chr1:79356582..79358429-chr1:79361774..79364231,2	MCF-7	breast:
3	chr1:79356582..79358429-chr1:79361774..79364231,2	MCF-7	breast:
4	chr1:79410821..79413576-chr1:79414533..79416679,2	K562	blood:
5	chr1:79411840..79414575-chr1:79858123..79860401,2	K562	blood:
6	chr1:79527063..79529337-chr1:79533334..79535055,2	K562	blood:
7	chr1:79370114..79372345-chr1:79443530..79445892,2	K562	blood:
8	chr1:79536026..79538535-chr1:79539899..79541790,2	K562	blood:
9	chr1:79484446..79486654-chr1:79486860..79488839,2	MCF-7	breast:
10	chr1:79536026..79538535-chr1:79539899..79541790,2	K562	blood:
11	chr1:79527063..79529337-chr1:79533334..79535055,2	K562	blood:
12	chr1:79410821..79413576-chr1:79414533..79416679,2	K562	blood:
13	chr1:79370114..79372345-chr1:79443530..79445892,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ELTD1-1	chr1:79351642-79351681	NONHSAT004083
2	lnc-ELTD1-2	chr1:79490858-79491009	XLOC_000877
3	lnc-ELTD1-2	chr1:79493775-79493876	XLOC_000877

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

Extended variants
information (count: 6352 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:6352 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs151325698	chr1:79351381-79351382	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs78923504	chr1:79351400-79351401	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140739657	chr1:79351401-79351402	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540369286	chr1:79351460-79351461	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs145629686	chr1:79351468-79351469	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs578091998	chr1:79351533-79351534	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181502286	chr1:79351588-79351589	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545276474	chr1:79351601-79351602	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7531816	chr1:79351617-79351618	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs185992021	chr1:79351631-79351632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190799529	chr1:79351687-79351688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs183936891	chr1:79351692-79351693	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569047395	chr1:79351698-79351699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566682737	chr1:79351724-79351725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528577203	chr1:79351736-79351737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187251366	chr1:79351740-79351741	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190872285	chr1:79351741-79351742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555562028	chr1:79351755-79351756	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182586489	chr1:79351766-79351767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187143699	chr1:79351772-79351773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138243035	chr1:79351802-79351803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536166635	chr1:79351804-79351805	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547780004	chr1:79351849-79351850	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191917082	chr1:79351866-79351867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533561178	chr1:79351868-79351869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558574884	chr1:79351873-79351874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115444792	chr1:79351952-79351953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539190185	chr1:79351986-79351987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142785924	chr1:79352014-79352015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182982267	chr1:79352026-79352027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575656995	chr1:79352033-79352034	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372447875	chr1:79352045-79352046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543391837	chr1:79352103-79352104	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561259013	chr1:79352122-79352123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554594750	chr1:79352165-79352166	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187615164	chr1:79352176-79352177	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7532212	chr1:79352227-79352228	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs6424614	chr1:79352231-79352232	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs192950200	chr1:79352235-79352236	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs115735533	chr1:79352242-79352243	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1968952	chr1:79352249-79352250	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs1968953	chr1:79352253-79352254	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs185559870	chr1:79352284-79352285	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548040158	chr1:79352295-79352296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1968954	chr1:79352296-79352297	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs533754484	chr1:79352309-79352310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2635119	chr1:79352340-79352341	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs570511720	chr1:79352348-79352349	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113481384	chr1:79352380-79352381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190436158	chr1:79352384-79352385	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:540 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79348600-79405600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:79350200-79351400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr1:79350200-79351400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr1:79350400-79351400	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr1:79350400-79351400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr1:79350400-79351600	Enhancers	Muscle Satellite Cultured Cells	--
7	chr1:79350600-79351600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr1:79350800-79358600	Strong transcription	HUVEC	blood vessel
9	chr1:79351000-79360800	Weak transcription	Left Ventricle	heart
10	chr1:79351000-79365600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr1:79351000-79367600	Weak transcription	Adipose Nuclei	Adipose
12	chr1:79351200-79351600	Enhancers	Hela-S3	cervix
13	chr1:79351200-79355800	Weak transcription	NH-A	brain
14	chr1:79351200-79356400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:79351200-79356400	Weak transcription	NHDF-Ad	bronchial
16	chr1:79351200-79357400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr1:79351200-79357600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:79351200-79358000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr1:79351600-79354800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr1:79356400-79358200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr1:79356400-79358200	Enhancers	NHDF-Ad	bronchial
22	chr1:79357400-79357600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:79357600-79358000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:79357600-79358400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr1:79357600-79358400	Enhancers	Muscle Satellite Cultured Cells	--
26	chr1:79357600-79358600	Enhancers	Osteobl	bone
27	chr1:79357800-79358200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr1:79358000-79358200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr1:79358000-79358400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr1:79358200-79358400	Flanking Active TSS	NHDF-Ad	bronchial
31	chr1:79358200-79358600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr1:79358400-79358600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr1:79358400-79358600	Active TSS	NHDF-Ad	bronchial
34	chr1:79358600-79367200	Weak transcription	HUVEC	blood vessel
35	chr1:79365600-79366600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr1:79366600-79380400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr1:79367200-79368000	Strong transcription	HUVEC	blood vessel
38	chr1:79367200-79377600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr1:79368000-79368200	Weak transcription	HUVEC	blood vessel
40	chr1:79368200-79369200	Strong transcription	HUVEC	blood vessel
41	chr1:79369200-79375000	Weak transcription	HUVEC	blood vessel
42	chr1:79371600-79404200	Weak transcription	Left Ventricle	heart
43	chr1:79374000-79383600	Weak transcription	NH-A	brain
44	chr1:79375000-79383600	Strong transcription	HUVEC	blood vessel
45	chr1:79376000-79376400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr1:79376000-79376400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr1:79376000-79376800	Enhancers	Muscle Satellite Cultured Cells	--
48	chr1:79376400-79377600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr1:79376800-79382800	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr1:79377400-79378200	Enhancers	Adipose Nuclei	Adipose

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