Variant report

Variant	nsv526221
Chromosome Location	chr1:79197624-79487080
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	ARID3A	chr1:79305438-79305769	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:79305459-79305734	K562	blood:	n/a	n/a
3	ATF1	chr1:79259668-79259884	K562	blood:	n/a	n/a
4	ATF2	chr1:79350690-79350993	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:79472315-79472519	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr1:79320756-79321223	GM12878	blood:	n/a	chr1:79320825-79320834
7	BCL11A	chr1:79300086-79300356	GM12878	blood:	n/a	n/a
8	BCL11A	chr1:79262911-79263285	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr1:79297522-79297765	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:79405513-79405527	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:79320988-79321254	GM12878	blood:	n/a	n/a
12	BRCA1	chr1:79415111-79415262	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr1:79262865-79262987	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr1:79459804-79459831	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr1:79299051-79299589	HCT-116	colon:	n/a	n/a
16	CBX3	chr1:79297275-79297897	HCT-116	colon:	n/a	n/a
17	CCNT2	chr1:79250632-79250832	K562	blood:	n/a	n/a
18	CEBPB	chr1:79306670-79307003	IMR90	lung:	n/a	n/a
19	CEBPB	chr1:79379678-79379999	IMR90	lung:	n/a	n/a
20	CEBPB	chr1:79451150-79451399	K562	blood:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
21	CEBPB	chr1:79451113-79451392	HepG2	liver:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
22	CEBPB	chr1:79482686-79482859	HepG2	liver:	n/a	chr1:79482727-79482740 chr1:79482727-79482738 chr1:79482727-79482740
23	CEBPB	chr1:79409235-79409568	Hela-S3	cervix:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
24	CEBPB	chr1:79409304-79409537	IMR90	lung:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
25	CEBPB	chr1:79379656-79380004	HepG2	liver:	n/a	n/a
26	CEBPB	chr1:79379779-79379879	K562	blood:	n/a	n/a
27	CEBPB	chr1:79265892-79266140	HepG2	liver:	n/a	chr1:79265995-79266006 chr1:79265997-79266006
28	CEBPB	chr1:79379712-79379997	A549	lung:	n/a	n/a
29	CEBPB	chr1:79262914-79263092	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr1:79197360-79197738	HepG2	liver:	n/a	chr1:79197541-79197552
31	CEBPB	chr1:79470648-79470928	HepG2	liver:	n/a	chr1:79470789-79470800
32	CEBPB	chr1:79350645-79351099	ECC-1	luminal epithelium:	n/a	n/a
33	CEBPB	chr1:79470706-79470922	Hela-S3	cervix:	n/a	chr1:79470789-79470800
34	CEBPB	chr1:79378071-79378234	K562	blood:	n/a	n/a
35	CEBPB	chr1:79291258-79291543	IMR90	lung:	n/a	n/a
36	CEBPB	chr1:79197356-79197735	MCF-7	breast:	n/a	chr1:79197541-79197552
37	CEBPB	chr1:79334884-79335172	IMR90	lung:	n/a	chr1:79334994-79335005
38	CEBPB	chr1:79198927-79198988	K562	blood:	n/a	n/a
39	CEBPB	chr1:79334905-79335145	HepG2	liver:	n/a	chr1:79334994-79335005
40	CEBPB	chr1:79256120-79256135	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr1:79377650-79378354	IMR90	lung:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
42	CEBPB	chr1:79357942-79358268	IMR90	lung:	n/a	n/a
43	CEBPB	chr1:79451090-79451446	IMR90	lung:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
44	CEBPB	chr1:79226557-79226834	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr1:79297397-79297834	IMR90	lung:	n/a	n/a
46	CEBPB	chr1:79197368-79197731	A549	lung:	n/a	chr1:79197541-79197552
47	CEBPB	chr1:79377703-79378070	A549	lung:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
48	CEBPB	chr1:79265133-79265420	HepG2	liver:	n/a	chr1:79265319-79265330 chr1:79265207-79265220
49	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
50	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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:79472361-79472411	GM19239	blood:	n/a
2	chr1:79472408-79472458	SK-N-MC	brain:	n/a
3	chr1:79474718-79474768	SK-N-MC	brain:	n/a
4	chr1:79474718-79474768	ECC-1	luminal epithelium:	n/a
5	chr1:79472282-79472332	HCF	heart:	n/a
6	chr1:79307043-79307093	MCF10A-Er-Src	breast:	n/a
7	chr1:79472452-79472502	BJ	skin:	n/a
8	chr1:79472536-79472586	SKMC	muscle:	n/a
9	chr1:79472282-79472332	ovcar-3	ovarian:	n/a
10	chr1:79472532-79472582	AG04450	lung:	fetal
11	chr1:79472917-79472967	NT2-D1	testis:	n/a
12	chr1:79472532-79472582	PFSK-1	brain:	n/a
13	chr1:79472532-79472582	MCF-7	breast:	n/a
14	chr1:79472558-79472608	K562	blood:	n/a
15	chr1:79472361-79472411	AG09319	gingival:	n/a
16	chr1:79350918-79350968	A549	lung:	n/a
17	chr1:79472532-79472582	HCPEpiC	choroid plexus:	n/a
18	chr1:79472643-79472693	LNCaP	prostate:	n/a
19	chr1:79307043-79307093	GM12892	blood:	n/a
20	chr1:79307043-79307093	HEEpiC	esophagus:	n/a
21	chr1:79472532-79472582	AG09309	skin:	n/a
22	chr1:79472536-79472586	HEEpiC	esophagus:	n/a
23	chr1:79472917-79472967	T-47D	breast:	n/a
24	chr1:79307043-79307093	HRPEpiC	eye:	n/a
25	chr1:79472282-79472332	BE2_C	brain:	n/a
26	chr1:79474718-79474768	MCF-7	breast:	n/a
27	chr1:79473783-79473833	NB4	blood:	n/a
28	chr1:79472408-79472458	AG04449	skin:	fetal
29	chr1:79472452-79472502	RPTEC	kidney:	n/a
30	chr1:79472452-79472502	GM06990	blood:	n/a
31	chr1:79350918-79350968	Jurkat	blood:	n/a
32	chr1:79307043-79307093	AG04449	skin:	fetal
33	chr1:79350918-79350968	HEEpiC	esophagus:	n/a
34	chr1:79471984-79472034	SK-N-SH	brain:	n/a
35	chr1:79472343-79472393	HEK293	kidney:	embryo
36	chr1:79472361-79472411	SKMC	muscle:	n/a
37	chr1:79472536-79472586	T-47D	breast:	n/a
38	chr1:79471984-79472034	U87	brain:	n/a
39	chr1:79350918-79350968	NHBE	bronchial:	n/a
40	chr1:79472532-79472582	NT2-D1	testis:	n/a
41	chr1:79472643-79472693	GM12892	blood:	n/a
42	chr1:79472408-79472458	NB4	blood:	n/a
43	chr1:79472452-79472502	HCT-116	colon:	n/a
44	chr1:79472282-79472332	PFSK-1	brain:	n/a
45	chr1:79307043-79307093	BJ	skin:	n/a
46	chr1:79471984-79472034	AG04450	lung:	fetal
47	chr1:79472408-79472458	AG10803	skin:	n/a
48	chr1:79307043-79307093	ovcar-3	ovarian:	n/a
49	chr1:79472536-79472586	HL-60	blood:	n/a
50	chr1:79472408-79472458	T-47D	breast:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ELTD1-1	chr1:79351642-79351681	NONHSAT004083
2	lnc-ELTD1-1	chr1:79346569-79346750	NONHSAT004083

Variant related genes	Relation type
ENSG00000235400	TF binding region
ELTD1	TF binding region
ENSG00000235400	CpG island
ELTD1	CpG island

Extended variants
information (count: 7874 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:7874 , 50 per page) page: 1 2 3 4 5 6 7 ... 158

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149069164	chr1:79198013-79198014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs181879636	chr1:79198025-79198026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs4650601	chr1:79198047-79198048	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs527862361	chr1:79198089-79198090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552527624	chr1:79198131-79198132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184629013	chr1:79198135-79198136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571117718	chr1:79198168-79198169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs79516355	chr1:79198169-79198170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550154800	chr1:79198195-79198196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568476151	chr1:79198203-79198204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535920667	chr1:79198259-79198260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs61348701	chr1:79198306-79198307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186524463	chr1:79198391-79198392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528685912	chr1:79198440-79198441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566069578	chr1:79198469-79198470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs374417778	chr1:79198499-79198500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs539604706	chr1:79198539-79198540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs557714950	chr1:79198558-79198559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192361395	chr1:79198563-79198564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs114779101	chr1:79198582-79198583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs112228004	chr1:79198583-79198584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554907091	chr1:79198584-79198585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs115361809	chr1:79198639-79198640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540695856	chr1:79198640-79198641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs1751507	chr1:79198647-79198648	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs577701868	chr1:79198663-79198664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546377621	chr1:79198671-79198672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs182388191	chr1:79198696-79198697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs74094736	chr1:79198755-79198756	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs138988834	chr1:79198758-79198759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562035603	chr1:79198775-79198776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529266323	chr1:79198802-79198803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs142201934	chr1:79198825-79198826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs114365169	chr1:79198930-79198931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs533334227	chr1:79198931-79198932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs116319185	chr1:79198955-79198956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs17102184	chr1:79198987-79198988	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs569529035	chr1:79199017-79199018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs145901078	chr1:79199074-79199075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs148078211	chr1:79199096-79199097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs531750011	chr1:79199116-79199117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534599021	chr1:79199160-79199161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs77769924	chr1:79199188-79199189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs577623122	chr1:79199195-79199196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs544788510	chr1:79199207-79199208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs141851699	chr1:79199232-79199233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370766353	chr1:79199233-79199234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576733496	chr1:79199294-79199295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs150622554	chr1:79199296-79199297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs28582445	chr1:79199313-79199314	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Breast cancer	22522925	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:688 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79198000-79199600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:79199000-79199400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr1:79208200-79210600	Enhancers	Fetal Brain Male	brain
4	chr1:79209200-79209400	Enhancers	HSMM	muscle
5	chr1:79209200-79209600	Enhancers	NHDF-Ad	bronchial
6	chr1:79209200-79209800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:79209200-79210000	Enhancers	Muscle Satellite Cultured Cells	--
8	chr1:79209600-79213400	Weak transcription	NHDF-Ad	bronchial
9	chr1:79210000-79211000	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr1:79211000-79211600	Enhancers	Muscle Satellite Cultured Cells	--
11	chr1:79211200-79211600	Enhancers	HSMM	muscle
12	chr1:79211600-79217200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr1:79217200-79217400	Enhancers	Muscle Satellite Cultured Cells	--
14	chr1:79220200-79220600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr1:79220600-79221400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr1:79221400-79222000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr1:79221400-79222400	Enhancers	HMEC	breast
18	chr1:79221400-79222400	Enhancers	NHEK	skin
19	chr1:79223000-79223200	Enhancers	Fetal Brain Male	brain
20	chr1:79223200-79224400	Weak transcription	Fetal Brain Male	brain
21	chr1:79224400-79224800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr1:79224400-79224800	Enhancers	Fetal Brain Female	brain
23	chr1:79224400-79225200	Enhancers	Fetal Brain Male	brain
24	chr1:79226400-79226800	Enhancers	Muscle Satellite Cultured Cells	--
25	chr1:79226600-79227000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr1:79226600-79227200	Enhancers	Osteobl	bone
27	chr1:79226800-79227200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr1:79226800-79227200	Enhancers	NHDF-Ad	bronchial
29	chr1:79227200-79230600	Weak transcription	Osteobl	bone
30	chr1:79242600-79243800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:79245000-79246000	Enhancers	Muscle Satellite Cultured Cells	--
32	chr1:79245200-79246000	Enhancers	Osteobl	bone
33	chr1:79245200-79246200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr1:79261200-79261600	Enhancers	Fetal Brain Male	brain
35	chr1:79261600-79263200	Weak transcription	Fetal Brain Male	brain
36	chr1:79262800-79263400	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr1:79263200-79265800	Enhancers	Fetal Brain Male	brain
38	chr1:79265200-79265800	Enhancers	Brain Germinal Matrix	brain
39	chr1:79284800-79285200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr1:79285200-79285600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr1:79285600-79298000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr1:79289800-79291000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr1:79289800-79291600	Enhancers	NHDF-Ad	bronchial
44	chr1:79289800-79291800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr1:79289800-79291800	Enhancers	Osteobl	bone
46	chr1:79290000-79292200	Enhancers	Muscle Satellite Cultured Cells	--
47	chr1:79291000-79296000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr1:79291600-79296000	Weak transcription	NHDF-Ad	bronchial
49	chr1:79291800-79295800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr1:79291800-79296000	Weak transcription	Osteobl	bone

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