Variant report

Variant	nsv817535
Chromosome Location	chr1:79203834-79473089
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	chr1:79305459-79305734	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	chr1:79350690-79350993	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	chr1:79320988-79321254	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:79405513-79405527	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:79297522-79297765	GM12878	blood:	n/a	n/a
12	BRCA1	chr1:79262865-79262987	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr1:79459804-79459831	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr1:79415111-79415262	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr1:79297275-79297897	HCT-116	colon:	n/a	n/a
16	CBX3	chr1:79299051-79299589	HCT-116	colon:	n/a	n/a
17	CCNT2	chr1:79250632-79250832	K562	blood:	n/a	n/a
18	CEBPB	chr1:79299125-79299471	IMR90	lung:	n/a	n/a
19	CEBPB	chr1:79379656-79380004	HepG2	liver:	n/a	n/a
20	CEBPB	chr1:79334905-79335145	HepG2	liver:	n/a	chr1:79334994-79335005
21	CEBPB	chr1:79226557-79226834	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr1:79350605-79351179	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr1:79409258-79409472	A549	lung:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
24	CEBPB	chr1:79405681-79405919	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:79378071-79378234	K562	blood:	n/a	n/a
26	CEBPB	chr1:79451152-79451394	A549	lung:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
27	CEBPB	chr1:79470706-79470922	Hela-S3	cervix:	n/a	chr1:79470789-79470800
28	CEBPB	chr1:79310676-79310947	HepG2	liver:	n/a	chr1:79310824-79310837 chr1:79310825-79310836
29	CEBPB	chr1:79409304-79409537	IMR90	lung:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
30	CEBPB	chr1:79377650-79378354	IMR90	lung:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
31	CEBPB	chr1:79262914-79263092	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr1:79470712-79470946	A549	lung:	n/a	chr1:79470789-79470800
33	CEBPB	chr1:79297397-79297834	IMR90	lung:	n/a	n/a
34	CEBPB	chr1:79470648-79470928	HepG2	liver:	n/a	chr1:79470789-79470800
35	CEBPB	chr1:79409261-79409575	HepG2	liver:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
36	CEBPB	chr1:79377650-79378354	HepG2	liver:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
37	CEBPB	chr1:79350975-79351035	A549	lung:	n/a	n/a
38	CEBPB	chr1:79265133-79265420	HepG2	liver:	n/a	chr1:79265319-79265330 chr1:79265207-79265220
39	CEBPB	chr1:79379779-79379879	K562	blood:	n/a	n/a
40	CEBPB	chr1:79256120-79256135	Hela-S3	cervix:	n/a	n/a
41	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
42	CEBPB	chr1:79335048-79335094	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr1:79453639-79453775	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr1:79451090-79451446	IMR90	lung:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
45	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
46	CEBPB	chr1:79414781-79415272	Hela-S3	cervix:	n/a	chr1:79414944-79414957 chr1:79414973-79414990
47	CEBPB	chr1:79299089-79299536	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr1:79377613-79378467	Hela-S3	cervix:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
49	CEBPB	chr1:79409235-79409568	Hela-S3	cervix:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
50	CEBPB	chr1:79265892-79266140	HepG2	liver:	n/a	chr1:79265995-79266006 chr1:79265997-79266006

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:79472343-79472393	A549	lung:	n/a
2	chr1:79472452-79472502	SAEC	small airway:	n/a
3	chr1:79307043-79307093	HUVEC	blood vessel:	n/a
4	chr1:79307043-79307093	GM06990	blood:	n/a
5	chr1:79350918-79350968	HRE	kidney:	n/a
6	chr1:79350918-79350968	HUVEC	blood vessel:	n/a
7	chr1:79472282-79472332	AG04449	skin:	fetal
8	chr1:79350918-79350968	HIPEpiC	eye:	n/a
9	chr1:79307043-79307093	ECC-1	luminal epithelium:	n/a
10	chr1:79472536-79472586	SKMC	muscle:	n/a
11	chr1:79472452-79472502	SKMC	muscle:	n/a
12	chr1:79472558-79472608	K562	blood:	n/a
13	chr1:79472361-79472411	HCM	heart:	n/a
14	chr1:79472536-79472586	MCF10A-Er-Src	breast:	n/a
15	chr1:79472408-79472458	HRCEpiC	kidney:	n/a
16	chr1:79472532-79472582	HUVEC	blood vessel:	n/a
17	chr1:79472343-79472393	AG09319	gingival:	n/a
18	chr1:79350918-79350968	NHDF-neo	bronchial:	n/a
19	chr1:79350918-79350968	ovcar-3	ovarian:	n/a
20	chr1:79472408-79472458	NT2-D1	testis:	n/a
21	chr1:79472408-79472458	GM19239	blood:	n/a
22	chr1:79307043-79307093	HPAEpiC	pulmonary alveolar:	n/a
23	chr1:79472452-79472502	MCF-7	breast:	n/a
24	chr1:79472532-79472582	Caco-2	colon:	n/a
25	chr1:79472452-79472502	K562	blood:	n/a
26	chr1:79350918-79350968	SK-N-SH_RA	brain:	n/a
27	chr1:79472343-79472393	HPAEpiC	pulmonary alveolar:	n/a
28	chr1:79472408-79472458	A549	lung:	n/a
29	chr1:79472343-79472393	AoSMC	blood vessel:	n/a
30	chr1:79472917-79472967	CMK	blood:	n/a
31	chr1:79307043-79307093	SK-N-MC	brain:	n/a
32	chr1:79472558-79472608	GM12891	blood:	n/a
33	chr1:79472532-79472582	U87	brain:	n/a
34	chr1:79472343-79472393	HCT-116	colon:	n/a
35	chr1:79471984-79472034	Caco-2	colon:	n/a
36	chr1:79472532-79472582	HCM	heart:	n/a
37	chr1:79350918-79350968	MCF-7	breast:	n/a
38	chr1:79472408-79472458	HCPEpiC	choroid plexus:	n/a
39	chr1:79472343-79472393	HMEC	breast:	n/a
40	chr1:79472452-79472502	NB4	blood:	n/a
41	chr1:79472452-79472502	BJ	skin:	n/a
42	chr1:79471984-79472034	GM12878	blood:	n/a
43	chr1:79472536-79472586	K562	blood:	n/a
44	chr1:79472536-79472586	GM19239	blood:	n/a
45	chr1:79472917-79472967	AG09319	gingival:	n/a
46	chr1:79472408-79472458	HCF	heart:	n/a
47	chr1:79472917-79472967	SK-N-SH	brain:	n/a
48	chr1:79472282-79472332	HIPEpiC	eye:	n/a
49	chr1:79471984-79472034	AoSMC	blood vessel:	n/a
50	chr1:79472558-79472608	HRE	kidney:	n/a

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

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

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

Extended variants
information (count: 7552 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:7552 , 50 per page) page: 1 2 3 4 5 6 7 ... 152

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565594520	chr1:79208213-79208214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs192450182	chr1:79208289-79208290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs1613137	chr1:79208296-79208297	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs569527600	chr1:79208297-79208298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184815810	chr1:79208352-79208353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs188061404	chr1:79208363-79208364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139529586	chr1:79208378-79208379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542395199	chr1:79208379-79208380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554415817	chr1:79208387-79208388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1612254	chr1:79208400-79208401	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs546542277	chr1:79208403-79208404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564830727	chr1:79208417-79208418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576344014	chr1:79208433-79208434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs543840680	chr1:79208455-79208456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544976170	chr1:79208456-79208457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529353298	chr1:79208472-79208473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs547151246	chr1:79208487-79208488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559140168	chr1:79208494-79208495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs61768666	chr1:79208519-79208520	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs180760847	chr1:79208539-79208540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569971506	chr1:79208543-79208544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs2801037	chr1:79208678-79208679	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs541345092	chr1:79208683-79208684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs548965465	chr1:79208735-79208736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561048662	chr1:79208750-79208751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs12131016	chr1:79208790-79208791	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs1475401	chr1:79208816-79208817	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs184409661	chr1:79208842-79208843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs147940386	chr1:79208848-79208849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563392004	chr1:79208922-79208923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs367746406	chr1:79208958-79208959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs189688233	chr1:79208961-79208962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371659805	chr1:79208962-79208963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs576719821	chr1:79208979-79208980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543408975	chr1:79208992-79208993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs374039521	chr1:79209000-79209001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs532514291	chr1:79209008-79209009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575590988	chr1:79209021-79209022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573765544	chr1:79209029-79209030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs10571367	chr1:79209033-79209034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541151043	chr1:79209035-79209036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201027296	chr1:79209037-79209038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs398053148	chr1:79209038-79209039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs559453434	chr1:79209098-79209099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs1780734	chr1:79209102-79209103	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs1967821	chr1:79209105-79209106	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs376886571	chr1:79209165-79209166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs112867270	chr1:79209213-79209214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs181456388	chr1:79209223-79209224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530843411	chr1:79209272-79209273	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
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:683 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79208200-79210600	Enhancers	Fetal Brain Male	brain
2	chr1:79209200-79209400	Enhancers	HSMM	muscle
3	chr1:79209200-79209600	Enhancers	NHDF-Ad	bronchial
4	chr1:79209200-79209800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr1:79209200-79210000	Enhancers	Muscle Satellite Cultured Cells	--
6	chr1:79209600-79213400	Weak transcription	NHDF-Ad	bronchial
7	chr1:79210000-79211000	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr1:79211000-79211600	Enhancers	Muscle Satellite Cultured Cells	--
9	chr1:79211200-79211600	Enhancers	HSMM	muscle
10	chr1:79211600-79217200	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr1:79217200-79217400	Enhancers	Muscle Satellite Cultured Cells	--
12	chr1:79220200-79220600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr1:79220600-79221400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr1:79221400-79222000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr1:79221400-79222400	Enhancers	HMEC	breast
16	chr1:79221400-79222400	Enhancers	NHEK	skin
17	chr1:79223000-79223200	Enhancers	Fetal Brain Male	brain
18	chr1:79223200-79224400	Weak transcription	Fetal Brain Male	brain
19	chr1:79224400-79224800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr1:79224400-79224800	Enhancers	Fetal Brain Female	brain
21	chr1:79224400-79225200	Enhancers	Fetal Brain Male	brain
22	chr1:79226400-79226800	Enhancers	Muscle Satellite Cultured Cells	--
23	chr1:79226600-79227000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr1:79226600-79227200	Enhancers	Osteobl	bone
25	chr1:79226800-79227200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr1:79226800-79227200	Enhancers	NHDF-Ad	bronchial
27	chr1:79227200-79230600	Weak transcription	Osteobl	bone
28	chr1:79242600-79243800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr1:79245000-79246000	Enhancers	Muscle Satellite Cultured Cells	--
30	chr1:79245200-79246000	Enhancers	Osteobl	bone
31	chr1:79245200-79246200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr1:79261200-79261600	Enhancers	Fetal Brain Male	brain
33	chr1:79261600-79263200	Weak transcription	Fetal Brain Male	brain
34	chr1:79262800-79263400	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr1:79263200-79265800	Enhancers	Fetal Brain Male	brain
36	chr1:79265200-79265800	Enhancers	Brain Germinal Matrix	brain
37	chr1:79284800-79285200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr1:79285200-79285600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:79285600-79298000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr1:79289800-79291000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr1:79289800-79291600	Enhancers	NHDF-Ad	bronchial
42	chr1:79289800-79291800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr1:79289800-79291800	Enhancers	Osteobl	bone
44	chr1:79290000-79292200	Enhancers	Muscle Satellite Cultured Cells	--
45	chr1:79291000-79296000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr1:79291600-79296000	Weak transcription	NHDF-Ad	bronchial
47	chr1:79291800-79295800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr1:79291800-79296000	Weak transcription	Osteobl	bone
49	chr1:79292200-79295800	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr1:79295000-79295800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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