Variant report

Variant	nsv1010441
Chromosome Location	chr1:79320299-79555315
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	chr1:79506114-79506881	GM12878	blood:	n/a	n/a
2	ATF2	chr1:79350690-79350993	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr1:79507696-79508185	GM12878	blood:	n/a	n/a
4	ATF2	chr1:79507719-79508191	GM12878	blood:	n/a	n/a
5	ATF2	chr1:79505821-79506890	GM12878	blood:	n/a	n/a
6	BACH1	chr1:79472315-79472519	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:79507950-79508076	K562	blood:	n/a	n/a
8	BACH1	chr1:79545497-79545905	H1-hESC	embryonic stem cell:	n/a	chr1:79545669-79545683
9	BACH1	chr1:79508075-79508122	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr1:79507758-79508057	GM12878	blood:	n/a	n/a
11	BATF	chr1:79506383-79506726	GM12878	blood:	n/a	n/a
12	BATF	chr1:79320756-79321223	GM12878	blood:	n/a	chr1:79320825-79320834
13	BATF	chr1:79506304-79506770	GM12878	blood:	n/a	n/a
14	BATF	chr1:79507747-79508138	GM12878	blood:	n/a	n/a
15	BCL11A	chr1:79507862-79508010	GM12878	blood:	n/a	n/a
16	BCL11A	chr1:79506346-79506753	GM12878	blood:	n/a	n/a
17	BCL11A	chr1:79507836-79508150	GM12878	blood:	n/a	n/a
18	BCL3	chr1:79506306-79506801	GM12878	blood:	n/a	n/a
19	BCL3	chr1:79507766-79508061	GM12878	blood:	n/a	n/a
20	BCLAF1	chr1:79506260-79506789	GM12878	blood:	n/a	n/a
21	BCLAF1	chr1:79507869-79508207	GM12878	blood:	n/a	n/a
22	BHLHE40	chr1:79405513-79405527	GM12878	blood:	n/a	n/a
23	BHLHE40	chr1:79320988-79321254	GM12878	blood:	n/a	n/a
24	BRCA1	chr1:79415111-79415262	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr1:79509475-79509505	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr1:79459804-79459831	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:79409333-79409445	K562	blood:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
28	CEBPB	chr1:79409304-79409537	IMR90	lung:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
29	CEBPB	chr1:79451152-79451394	A549	lung:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
30	CEBPB	chr1:79451113-79451392	HepG2	liver:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
31	CEBPB	chr1:79489957-79490304	HepG2	liver:	n/a	chr1:79490066-79490077
32	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
33	CEBPB	chr1:79379650-79380020	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr1:79335048-79335094	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr1:79377671-79378334	A549	lung:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
36	CEBPB	chr1:79379745-79379945	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr1:79506115-79506910	GM12878	blood:	n/a	n/a
38	CEBPB	chr1:79409235-79409568	Hela-S3	cervix:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
39	CEBPB	chr1:79453639-79453775	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr1:79379656-79380004	HepG2	liver:	n/a	n/a
41	CEBPB	chr1:79521171-79521337	A549	lung:	n/a	n/a
42	CEBPB	chr1:79334884-79335172	IMR90	lung:	n/a	chr1:79334994-79335005
43	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
44	CEBPB	chr1:79521267-79521303	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr1:79405681-79405919	HepG2	liver:	n/a	n/a
46	CEBPB	chr1:79470706-79470922	Hela-S3	cervix:	n/a	chr1:79470789-79470800
47	CEBPB	chr1:79482686-79482859	HepG2	liver:	n/a	chr1:79482727-79482740 chr1:79482727-79482738 chr1:79482727-79482740
48	CEBPB	chr1:79357252-79357448	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr1:79470712-79470946	A549	lung:	n/a	chr1:79470789-79470800
50	CEBPB	chr1:79357942-79358268	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:79472282-79472332	GM06990	blood:	n/a
2	chr1:79472282-79472332	GM06990	blood:	n/a
3	chr1:79472532-79472582	H1-hESC	embryonic stem cell:	embryo
4	chr1:79474718-79474768	AG09309	skin:	n/a
5	chr1:79472558-79472608	AG09319	gingival:	n/a
6	chr1:79473783-79473833	BJ	skin:	n/a
7	chr1:79472917-79472967	SAEC	small airway:	n/a
8	chr1:79472558-79472608	GM12892	blood:	n/a
9	chr1:79472408-79472458	HEEpiC	esophagus:	n/a
10	chr1:79472532-79472582	AG10803	skin:	n/a
11	chr1:79472408-79472458	GM19239	blood:	n/a
12	chr1:79472558-79472608	AoSMC	blood vessel:	n/a
13	chr1:79473783-79473833	HEK293	kidney:	embryo
14	chr1:79472643-79472693	H1-hESC	embryonic stem cell:	embryo
15	chr1:79472452-79472502	K562	blood:	n/a
16	chr1:79473783-79473833	MCF-7	breast:	n/a
17	chr1:79472917-79472967	Hela-S3	cervix:	n/a
18	chr1:79472532-79472582	GM12891	blood:	n/a
19	chr1:79474718-79474768	MCF-7	breast:	n/a
20	chr1:79473783-79473833	T-47D	breast:	n/a
21	chr1:79473783-79473833	HRCEpiC	kidney:	n/a
22	chr1:79350918-79350968	SKMC	muscle:	n/a
23	chr1:79472532-79472582	HUVEC	blood vessel:	n/a
24	chr1:79472536-79472586	U87	brain:	n/a
25	chr1:79474718-79474768	HMEC	breast:	n/a
26	chr1:79472558-79472608	BE2_C	brain:	n/a
27	chr1:79471984-79472034	ovcar-3	ovarian:	n/a
28	chr1:79472282-79472332	HCM	heart:	n/a
29	chr1:79472408-79472458	Hepatocyte	liver:	n/a
30	chr1:79472917-79472967	SK-N-SH_RA	brain:	n/a
31	chr1:79472536-79472586	GM19239	blood:	n/a
32	chr1:79472643-79472693	GM12892	blood:	n/a
33	chr1:79472536-79472586	HUVEC	blood vessel:	n/a
34	chr1:79472917-79472967	AG10803	skin:	n/a
35	chr1:79472643-79472693	K562	blood:	n/a
36	chr1:79472532-79472582	HRCEpiC	kidney:	n/a
37	chr1:79473783-79473833	HIPEpiC	eye:	n/a
38	chr1:79472343-79472393	HIPEpiC	eye:	n/a
39	chr1:79472282-79472332	AG09319	gingival:	n/a
40	chr1:79472361-79472411	NHBE	bronchial:	n/a
41	chr1:79472536-79472586	HL-60	blood:	n/a
42	chr1:79472558-79472608	Caco-2	colon:	n/a
43	chr1:79350918-79350968	LNCaP	prostate:	n/a
44	chr1:79472343-79472393	NT2-D1	testis:	n/a
45	chr1:79472536-79472586	HepG2	liver:	n/a
46	chr1:79472282-79472332	AG09309	skin:	n/a
47	chr1:79472343-79472393	CMK	blood:	n/a
48	chr1:79472408-79472458	PFSK-1	brain:	n/a
49	chr1:79472361-79472411	HepG2	liver:	n/a
50	chr1:79350918-79350968	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:79536026..79538535-chr1:79539899..79541790,2	K562	blood:
2	chr1:79410821..79413576-chr1:79414533..79416679,2	K562	blood:
3	chr1:79356582..79358429-chr1:79361774..79364231,2	MCF-7	breast:
4	chr1:79370114..79372345-chr1:79443530..79445892,2	K562	blood:
5	chr1:79536026..79538535-chr1:79539899..79541790,2	K562	blood:
6	chr1:79484446..79486654-chr1:79486860..79488839,2	MCF-7	breast:
7	chr1:79370114..79372345-chr1:79443530..79445892,2	K562	blood:
8	chr1:79527063..79529337-chr1:79533334..79535055,2	K562	blood:
9	chr1:79484446..79486654-chr1:79486860..79488839,2	MCF-7	breast:
10	chr1:79411840..79414575-chr1:79858123..79860401,2	K562	blood:
11	chr1:79410821..79413576-chr1:79414533..79416679,2	K562	blood:
12	chr1:79356582..79358429-chr1:79361774..79364231,2	MCF-7	breast:
13	chr1:79527063..79529337-chr1:79533334..79535055,2	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-ELTD1-1	chr1:79346569-79346750	NONHSAT004083
4	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
IGSF1	miRNA target sites
TCF7L2	miRNA target sites

Extended variants
information (count: 7351 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:7351 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529563345	chr1:79320308-79320309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs111861618	chr1:79320321-79320322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187964825	chr1:79320334-79320335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs143373250	chr1:79320335-79320336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12032722	chr1:79320341-79320342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551459090	chr1:79320348-79320349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs569844229	chr1:79320349-79320350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536834808	chr1:79320350-79320351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs555505715	chr1:79320360-79320361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs548997280	chr1:79320386-79320387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146738044	chr1:79320393-79320394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs199779164	chr1:79320400-79320401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565563576	chr1:79320406-79320407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs1248483	chr1:79320447-79320448	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs545048122	chr1:79320478-79320479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140386842	chr1:79320516-79320517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs201696059	chr1:79320532-79320533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145589348	chr1:79320543-79320544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs542765691	chr1:79320546-79320547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs151015479	chr1:79320547-79320548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529474543	chr1:79320548-79320549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541702404	chr1:79320564-79320565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs115293405	chr1:79320574-79320575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540211676	chr1:79320620-79320621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs192994699	chr1:79320697-79320698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs560211736	chr1:79320712-79320713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs367827060	chr1:79320715-79320716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189181710	chr1:79320731-79320732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs6665405	chr1:79320784-79320785	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs35816862	chr1:79320839-79320840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs530887619	chr1:79320914-79320915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs549216515	chr1:79320931-79320932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567442491	chr1:79320940-79320941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534559687	chr1:79320959-79320960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181671600	chr1:79320995-79320996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs571601810	chr1:79320998-79320999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140667879	chr1:79321023-79321024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs6667376	chr1:79321034-79321035	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs534411586	chr1:79321049-79321050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs75282893	chr1:79321050-79321051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564649037	chr1:79321074-79321075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536304354	chr1:79321096-79321097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs113236991	chr1:79321141-79321142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574175792	chr1:79321167-79321168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs72675825	chr1:79321215-79321216	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs17411195	chr1:79321255-79321256	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs189514361	chr1:79321289-79321290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs555436791	chr1:79321317-79321318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs180692307	chr1:79321328-79321329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs545318669	chr1:79321351-79321352	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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

Chromatin state (count:637 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79319800-79321200	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr1:79320600-79321400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr1:79320600-79321400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr1:79320800-79321400	Enhancers	Primary hematopoietic stem cells	blood
5	chr1:79332400-79332600	Enhancers	Fetal Stomach	stomach
6	chr1:79332600-79336400	Weak transcription	Fetal Stomach	stomach
7	chr1:79334200-79335000	Enhancers	Fetal Lung	lung
8	chr1:79335000-79335400	Weak transcription	Fetal Lung	lung
9	chr1:79335400-79336200	Enhancers	Fetal Lung	lung
10	chr1:79336400-79336800	Enhancers	Fetal Stomach	stomach
11	chr1:79336800-79337400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr1:79336800-79337600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
13	chr1:79338200-79339200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr1:79338200-79339200	Enhancers	Muscle Satellite Cultured Cells	--
15	chr1:79338200-79339200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr1:79338800-79339200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr1:79346400-79350800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr1:79346600-79350800	Weak transcription	HUVEC	blood vessel
19	chr1:79348400-79348600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr1:79348600-79405600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr1:79350200-79350400	Enhancers	Hela-S3	cervix
22	chr1:79350200-79350600	Enhancers	Colon Smooth Muscle	Colon
23	chr1:79350200-79351000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr1:79350200-79351000	Enhancers	Rectal Smooth Muscle	rectum
25	chr1:79350200-79351200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr1:79350200-79351200	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr1:79350200-79351400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr1:79350200-79351400	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr1:79350400-79350800	Enhancers	Fetal Kidney	kidney
30	chr1:79350400-79351000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr1:79350400-79351000	Enhancers	Fetal Stomach	stomach
32	chr1:79350400-79351200	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr1:79350400-79351200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr1:79350400-79351200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:79350400-79351200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr1:79350400-79351200	Flanking Active TSS	Hela-S3	cervix
37	chr1:79350400-79351200	Enhancers	NH-A	brain
38	chr1:79350400-79351400	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr1:79350400-79351400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr1:79350400-79351600	Enhancers	Muscle Satellite Cultured Cells	--
41	chr1:79350600-79351000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr1:79350600-79351000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr1:79350600-79351000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr1:79350600-79351000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr1:79350600-79351000	Enhancers	Adipose Nuclei	Adipose
46	chr1:79350600-79351000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr1:79350600-79351000	Enhancers	Fetal Lung	lung
48	chr1:79350600-79351000	Enhancers	Psoas Muscle	Psoas
49	chr1:79350600-79351200	Enhancers	H1 Cell Line	embryonic stem cell
50	chr1:79350600-79351200	Enhancers	HUES6 Cell Line	embryonic stem cell

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