Variant report

Variant	nsv830915
Chromosome Location	chr1:104024830-104293282
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	chr1:104076441-104076543	K562	blood:	n/a	n/a
2	ARID3A	chr1:104104781-104104969	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:104068398-104069159	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:104103048-104103509	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:104068425-104069462	K562	blood:	n/a	n/a
6	ATF2	chr1:104060167-104060706	GM12878	blood:	n/a	n/a
7	ATF2	chr1:104068246-104068748	GM12878	blood:	n/a	n/a
8	ATF2	chr1:104104531-104104991	GM12878	blood:	n/a	n/a
9	ATF2	chr1:104068276-104068823	GM12878	blood:	n/a	n/a
10	ATF2	chr1:104060069-104060653	GM12878	blood:	n/a	n/a
11	BATF	chr1:104163708-104163856	GM12878	blood:	n/a	n/a
12	BATF	chr1:104069989-104070340	GM12878	blood:	n/a	chr1:104070131-104070142
13	BATF	chr1:104068947-104069203	GM12878	blood:	n/a	n/a
14	BATF	chr1:104059876-104060357	GM12878	blood:	n/a	chr1:104060014-104060024 chr1:104060094-104060103
15	BATF	chr1:104163710-104163876	GM12878	blood:	n/a	n/a
16	BATF	chr1:104069996-104070255	GM12878	blood:	n/a	chr1:104070131-104070142
17	BCL11A	chr1:104163692-104163866	GM12878	blood:	n/a	n/a
18	BCL11A	chr1:104163716-104163847	GM12878	blood:	n/a	n/a
19	BCL3	chr1:104081714-104081999	GM12878	blood:	n/a	n/a
20	BCLAF1	chr1:104068286-104068884	GM12878	blood:	n/a	n/a
21	BCLAF1	chr1:104057548-104057847	GM12878	blood:	n/a	n/a
22	BCLAF1	chr1:104104511-104104987	GM12878	blood:	n/a	n/a
23	BHLHE40	chr1:104069904-104070362	GM12878	blood:	n/a	n/a
24	BHLHE40	chr1:104163686-104163884	HepG2	liver:	n/a	n/a
25	BHLHE40	chr1:104068347-104069164	GM12878	blood:	n/a	n/a
26	BHLHE40	chr1:104104614-104104992	GM12878	blood:	n/a	n/a
27	BHLHE40	chr1:104067893-104069179	K562	blood:	n/a	n/a
28	BRCA1	chr1:104068257-104069233	Hela-S3	cervix:	n/a	chr1:104068541-104068550
29	BRCA1	chr1:104068347-104068826	GM12878	blood:	n/a	chr1:104068541-104068550
30	BRCA1	chr1:104068338-104068741	HepG2	liver:	n/a	chr1:104068541-104068550
31	BRCA1	chr1:104068332-104068755	H1-hESC	embryonic stem cell:	n/a	chr1:104068541-104068550
32	CBX3	chr1:104068335-104068703	K562	blood:	n/a	n/a
33	CBX3	chr1:104068298-104068668	K562	blood:	n/a	n/a
34	CCNT2	chr1:104068442-104069153	K562	blood:	n/a	n/a
35	CEBPB	chr1:104104635-104104975	HepG2	liver:	n/a	chr1:104104711-104104723
36	CEBPB	chr1:104032481-104033124	IMR90	lung:	n/a	chr1:104032645-104032656
37	CEBPB	chr1:104033516-104033806	A549	lung:	n/a	chr1:104033682-104033693
38	CEBPB	chr1:104128801-104129380	HepG2	liver:	n/a	chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128957-104128970
39	CEBPB	chr1:104098729-104098994	HepG2	liver:	n/a	n/a
40	CEBPB	chr1:104109287-104109643	HepG2	liver:	n/a	chr1:104109438-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109515-104109526 chr1:104109440-104109449 chr1:104109438-104109449 chr1:104109440-104109451 chr1:104109440-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109440-104109449
41	CEBPB	chr1:104033532-104033812	H1-hESC	embryonic stem cell:	n/a	chr1:104033682-104033693
42	CEBPB	chr1:104103108-104103415	HepG2	liver:	n/a	n/a
43	CEBPB	chr1:104109284-104109624	IMR90	lung:	n/a	chr1:104109438-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109515-104109526 chr1:104109440-104109449 chr1:104109438-104109449 chr1:104109440-104109451 chr1:104109440-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109440-104109449
44	CEBPB	chr1:104063491-104063778	IMR90	lung:	n/a	n/a
45	CEBPB	chr1:104033511-104033829	K562	blood:	n/a	chr1:104033682-104033693
46	CEBPB	chr1:104033510-104033840	IMR90	lung:	n/a	chr1:104033682-104033693
47	CEBPB	chr1:104120646-104120872	A549	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
48	CEBPB	chr1:104031127-104031327	K562	blood:	n/a	n/a
49	CEBPB	chr1:104059336-104059587	IMR90	lung:	n/a	n/a
50	CEBPB	chr1:104033533-104033826	HepG2	liver:	n/a	chr1:104033682-104033693

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:104068664-104068714	BE2_C	brain:	n/a
2	chr1:104068935-104068985	H1-hESC	embryonic stem cell:	embryo
3	chr1:104068664-104068714	BE2_C	brain:	n/a
4	chr1:104068935-104068985	H1-hESC	embryonic stem cell:	embryo
5	chr1:104239696-104239746	PFSK-1	brain:	n/a
6	chr1:104068704-104068754	PANC-1	pancreas:	n/a
7	chr1:104096621-104096671	H1-hESC	embryonic stem cell:	embryo
8	chr1:104068121-104068171	BE2_C	brain:	n/a
9	chr1:104113061-104113111	GM19239	blood:	n/a
10	chr1:104113061-104113111	HPAEpiC	pulmonary alveolar:	n/a
11	chr1:104068419-104068469	CMK	blood:	n/a
12	chr1:104097670-104097720	GM12878	blood:	n/a
13	chr1:104068567-104068617	GM12891	blood:	n/a
14	chr1:104096517-104096567	Jurkat	blood:	n/a
15	chr1:104068704-104068754	U87	brain:	n/a
16	chr1:104113061-104113111	IMR90	lung:	fetal
17	chr1:104113061-104113111	MCF10A-Er-Src	breast:	n/a
18	chr1:104113039-104113089	AG09309	skin:	n/a
19	chr1:104112143-104112193	ECC-1	luminal epithelium:	n/a
20	chr1:104112143-104112193	NH-A	brain:	n/a
21	chr1:104068664-104068714	T-47D	breast:	n/a
22	chr1:104160257-104160307	RPTEC	kidney:	n/a
23	chr1:104068488-104068538	ovcar-3	ovarian:	n/a
24	chr1:104068490-104068540	SK-N-MC	brain:	n/a
25	chr1:104068301-104068351	SK-N-SH	brain:	n/a
26	chr1:104068488-104068538	HCF	heart:	n/a
27	chr1:104068603-104068653	HRE	kidney:	n/a
28	chr1:104068121-104068171	HCM	heart:	n/a
29	chr1:104068419-104068469	HCF	heart:	n/a
30	chr1:104068419-104068469	GM12878	blood:	n/a
31	chr1:104068419-104068469	ovcar-3	ovarian:	n/a
32	chr1:104068935-104068985	ovcar-3	ovarian:	n/a
33	chr1:104068488-104068538	HIPEpiC	eye:	n/a
34	chr1:104068301-104068351	NHDF-neo	bronchial:	n/a
35	chr1:104068488-104068538	SKMC	muscle:	n/a
36	chr1:104113039-104113089	HRPEpiC	eye:	n/a
37	chr1:104068567-104068617	K562	blood:	n/a
38	chr1:104113039-104113089	U87	brain:	n/a
39	chr1:104068664-104068714	AG04450	lung:	fetal
40	chr1:104068301-104068351	U87	brain:	n/a
41	chr1:104160257-104160307	GM06990	blood:	n/a
42	chr1:104068935-104068985	HEEpiC	esophagus:	n/a
43	chr1:104113061-104113111	AG04449	skin:	fetal
44	chr1:104239696-104239746	HepG2	liver:	n/a
45	chr1:104068490-104068540	SAEC	small airway:	n/a
46	chr1:104068121-104068171	MCF10A-Er-Src	breast:	n/a
47	chr1:104112143-104112193	GM12878	blood:	n/a
48	chr1:104068419-104068469	SK-N-SH	brain:	n/a
49	chr1:104068419-104068469	Hepatocyte	liver:	n/a
50	chr1:104068603-104068653	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:104067350..104071361-chr1:104071688..104074634,4	K562	blood:
2	chr1:104068373..104071907-chr1:104081557..104086760,7	K562	blood:
3	chr1:104068373..104071907-chr1:104081557..104086760,7	K562	blood:
4	chr1:104087556..104090106-chr1:104096002..104097509,2	K562	blood:
5	chr1:104084688..104087612-chr1:104092885..104095420,2	K562	blood:
6	chr1:104067956..104068800-chr18:9474823..9475445,2	Hela-S3	cervix:
7	chr1:104075755..104077597-chr1:104090154..104091919,2	K562	blood:
8	chr1:104120354..104123298-chr1:104128850..104131166,2	K562	blood:
9	chr1:104067752..104069863-chr1:104085885..104087467,2	MCF-7	breast:
10	chr1:104087556..104090106-chr1:104096002..104097509,2	K562	blood:
11	chr1:104068563..104070409-chr1:104091369..104094625,4	MCF-7	breast:
12	chr1:104067221..104069850-chr1:104074751..104077723,3	MCF-7	breast:
13	chr1:104067350..104070075-chr1:104070516..104073483,5	K562	blood:
14	chr1:104068563..104070409-chr1:104091369..104094625,4	MCF-7	breast:
15	chr1:104075755..104077597-chr1:104090154..104091919,2	K562	blood:
16	chr1:104120354..104123298-chr1:104128850..104131166,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMY1B-1	chr1:104068018-104068083	ENSG00000224613.2
2	lnc-AMY1B-1	chr1:104068018-104068105	XLOC_000945
3	lnc-AMY1B-1	chr1:104068018-104068115	XLOC_000945
4	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
5	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
6	lnc-RNPC3-4	chr1:104066184-104066501	NONHSAT004893
7	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RNPC3	hsa-miR-192-5p	chr1:104096163-104096184

Variant related genes	Relation type
RNPC3	TF binding region
AMY1B	TF binding region
ENSG00000234441	TF binding region
AMY2A	TF binding region
AMY1C	TF binding region
ACTG1P4	TF binding region
AMYP1	TF binding region
AMY1A	TF binding region
RN7SKP285	TF binding region
AMY2B	TF binding region
ENSG00000224613	TF binding region
RNPC3	CpG island
AMY1B	CpG island
ENSG00000234441	CpG island
AMY2A	CpG island
AMY1C	CpG island
ACTG1P4	CpG island
AMYP1	CpG island
AMY1A	CpG island
RN7SKP285	CpG island
AMY2B	CpG island
ENSG00000224613	CpG island
ENSG00000185946	chromatin interactions
ENSG00000017797	chromatin interactions
ENSG00000240038	chromatin interactions
ENSG00000224613	chromatin interactions
TOMM34	miRNA target sites

Extended variants
information (count: 3800 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:3800 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555187204	chr1:104024838-104024839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs573357032	chr1:104024866-104024867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540777826	chr1:104024944-104024945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371409648	chr1:104025030-104025031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs147885228	chr1:104025031-104025032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs544225178	chr1:104025047-104025048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs181546135	chr1:104025055-104025056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562526114	chr1:104025166-104025167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs530173033	chr1:104025172-104025173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs548273085	chr1:104025200-104025201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113206295	chr1:104025213-104025214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs12758921	chr1:104025242-104025243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373249340	chr1:104025248-104025249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185971279	chr1:104025304-104025305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs114490087	chr1:104025337-104025338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs114448287	chr1:104025413-104025414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs538915179	chr1:104025471-104025472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550632067	chr1:104025510-104025511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs566274474	chr1:104025541-104025542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368810156	chr1:104025668-104025669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs560699296	chr1:104025713-104025714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568863811	chr1:104025757-104025758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536400482	chr1:104025762-104025763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs370640363	chr1:104025772-104025773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188477848	chr1:104025784-104025785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540473214	chr1:104032418-104032419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs186462304	chr1:104032436-104032437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570815323	chr1:104032489-104032490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs10881166	chr1:104032552-104032553	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs528885589	chr1:104032588-104032589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537031931	chr1:104032643-104032644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs74938237	chr1:104032653-104032654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs568593400	chr1:104032671-104032672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs79491928	chr1:104032705-104032706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs553995170	chr1:104032768-104032769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539472573	chr1:104032789-104032790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs115462499	chr1:104032798-104032799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539848459	chr1:104032814-104032815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558840843	chr1:104032821-104032822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs577205399	chr1:104032832-104032833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs79947807	chr1:104032854-104032855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544217278	chr1:104032871-104032872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs556105554	chr1:104032888-104032889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs79848992	chr1:104032916-104032917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs541877936	chr1:104032960-104032961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs370424468	chr1:104032988-104032989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs201891558	chr1:104033034-104033035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373553120	chr1:104033054-104033055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182322359	chr1:104033066-104033067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551753817	chr1:104033090-104033091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
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
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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Cancer	22429812	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Multiple myeloma	17550852	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	19287141	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1600 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:104021600-104025800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:104032400-104032800	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr1:104032400-104033000	Enhancers	Muscle Satellite Cultured Cells	--
4	chr1:104032400-104033000	Enhancers	Hela-S3	cervix
5	chr1:104032600-104033000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr1:104032800-104033000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:104033000-104034800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr1:104033000-104038000	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr1:104034400-104038600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr1:104034800-104035000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr1:104034800-104035200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:104035200-104040000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr1:104037200-104039400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr1:104038000-104040600	Enhancers	Muscle Satellite Cultured Cells	--
15	chr1:104038600-104040600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr1:104038800-104039000	Enhancers	Osteobl	bone
17	chr1:104038800-104039600	Enhancers	NHLF	lung
18	chr1:104039000-104039400	Enhancers	NH-A	brain
19	chr1:104039000-104040000	Weak transcription	Osteobl	bone
20	chr1:104039000-104041400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr1:104039200-104039400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr1:104039200-104040600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr1:104039400-104040000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr1:104039400-104041200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr1:104039400-104041400	Enhancers	HMEC	breast
26	chr1:104039600-104040600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr1:104040000-104040400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr1:104040000-104040400	Enhancers	Osteobl	bone
29	chr1:104040000-104040800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr1:104040000-104041200	Enhancers	NHEK	skin
31	chr1:104040200-104040600	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr1:104040600-104043600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr1:104040600-104044000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr1:104040800-104041400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr1:104041400-104041600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr1:104043000-104043200	Enhancers	Aorta	Aorta
37	chr1:104043200-104046400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr1:104043200-104067400	Weak transcription	Aorta	Aorta
39	chr1:104043600-104044600	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr1:104044000-104044600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr1:104046000-104047200	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr1:104046200-104046800	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr1:104046200-104047000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr1:104046200-104047200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr1:104046400-104046800	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr1:104046400-104046800	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr1:104046400-104047000	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr1:104050000-104067400	Weak transcription	Left Ventricle	heart
49	chr1:104051800-104052400	Enhancers	HUVEC	blood vessel
50	chr1:104052000-104052600	Enhancers	Monocytes-CD14+_RO01746	blood

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