Variant report

Variant	nsv432565
Chromosome Location	chr1:104039979-104156979
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	chr1:104104781-104104969	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:104076441-104076543	K562	blood:	n/a	n/a
3	ARID3A	chr1:104103048-104103509	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:104068425-104069462	K562	blood:	n/a	n/a
5	ARID3A	chr1:104068398-104069159	HepG2	liver:	n/a	n/a
6	ATF2	chr1:104060069-104060653	GM12878	blood:	n/a	n/a
7	ATF2	chr1:104104531-104104991	GM12878	blood:	n/a	n/a
8	ATF2	chr1:104068246-104068748	GM12878	blood:	n/a	n/a
9	ATF2	chr1:104060167-104060706	GM12878	blood:	n/a	n/a
10	ATF2	chr1:104068276-104068823	GM12878	blood:	n/a	n/a
11	BATF	chr1:104068947-104069203	GM12878	blood:	n/a	n/a
12	BATF	chr1:104069989-104070340	GM12878	blood:	n/a	chr1:104070131-104070142
13	BATF	chr1:104059876-104060357	GM12878	blood:	n/a	chr1:104060014-104060024 chr1:104060094-104060103
14	BATF	chr1:104069996-104070255	GM12878	blood:	n/a	chr1:104070131-104070142
15	BCL3	chr1:104081714-104081999	GM12878	blood:	n/a	n/a
16	BCLAF1	chr1:104057548-104057847	GM12878	blood:	n/a	n/a
17	BCLAF1	chr1:104104511-104104987	GM12878	blood:	n/a	n/a
18	BCLAF1	chr1:104068286-104068884	GM12878	blood:	n/a	n/a
19	BHLHE40	chr1:104104614-104104992	GM12878	blood:	n/a	n/a
20	BHLHE40	chr1:104069904-104070362	GM12878	blood:	n/a	n/a
21	BHLHE40	chr1:104067893-104069179	K562	blood:	n/a	n/a
22	BHLHE40	chr1:104068347-104069164	GM12878	blood:	n/a	n/a
23	BRCA1	chr1:104068347-104068826	GM12878	blood:	n/a	chr1:104068541-104068550
24	BRCA1	chr1:104068338-104068741	HepG2	liver:	n/a	chr1:104068541-104068550
25	BRCA1	chr1:104068332-104068755	H1-hESC	embryonic stem cell:	n/a	chr1:104068541-104068550
26	BRCA1	chr1:104068257-104069233	Hela-S3	cervix:	n/a	chr1:104068541-104068550
27	CBX3	chr1:104068335-104068703	K562	blood:	n/a	n/a
28	CBX3	chr1:104068298-104068668	K562	blood:	n/a	n/a
29	CCNT2	chr1:104068442-104069153	K562	blood:	n/a	n/a
30	CEBPB	chr1:104109313-104109613	A549	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
31	CEBPB	chr1:104063491-104063778	IMR90	lung:	n/a	n/a
32	CEBPB	chr1:104069315-104069645	K562	blood:	n/a	chr1:104069437-104069448
33	CEBPB	chr1:104120629-104120899	HepG2	liver:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
34	CEBPB	chr1:104059336-104059587	IMR90	lung:	n/a	n/a
35	CEBPB	chr1:104117700-104117982	IMR90	lung:	n/a	chr1:104117799-104117810
36	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
37	CEBPB	chr1:104103108-104103415	HepG2	liver:	n/a	n/a
38	CEBPB	chr1:104120615-104120913	IMR90	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
39	CEBPB	chr1:104098729-104098994	HepG2	liver:	n/a	n/a
40	CEBPB	chr1:104074143-104074222	HepG2	liver:	n/a	chr1:104074178-104074189
41	CEBPB	chr1:104104662-104104945	Hela-S3	cervix:	n/a	chr1:104104711-104104723
42	CEBPB	chr1:104071533-104071833	HepG2	liver:	n/a	chr1:104071695-104071706
43	CEBPB	chr1:104104635-104104975	HepG2	liver:	n/a	chr1:104104711-104104723
44	CEBPB	chr1:104071591-104071848	IMR90	lung:	n/a	chr1:104071695-104071706
45	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
46	CEBPB	chr1:104117717-104117917	HepG2	liver:	n/a	chr1:104117799-104117810
47	CEBPB	chr1:104120646-104120872	A549	lung:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
48	CEBPB	chr1:104067855-104068146	K562	blood:	n/a	n/a
49	CEBPB	chr1:104128801-104129380	HepG2	liver:	n/a	chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128957-104128970
50	CHD1	chr1:104068464-104069301	GM12878	blood:	n/a	chr1:104068541-104068550

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:104068935-104068985	Hela-S3	cervix:	n/a
2	chr1:104068935-104068985	Hela-S3	cervix:	n/a
3	chr1:104097670-104097720	U87	brain:	n/a
4	chr1:104068567-104068617	H1-hESC	embryonic stem cell:	embryo
5	chr1:104068490-104068540	HRE	kidney:	n/a
6	chr1:104068664-104068714	HEK293	kidney:	embryo
7	chr1:104068301-104068351	U87	brain:	n/a
8	chr1:104068301-104068351	ECC-1	luminal epithelium:	n/a
9	chr1:104068312-104068362	MCF-7	breast:	n/a
10	chr1:104068935-104068985	NB4	blood:	n/a
11	chr1:104068419-104068469	NHBE	bronchial:	n/a
12	chr1:104068488-104068538	IMR90	lung:	fetal
13	chr1:104068490-104068540	SK-N-MC	brain:	n/a
14	chr1:104113061-104113111	HUVEC	blood vessel:	n/a
15	chr1:104068567-104068617	HUVEC	blood vessel:	n/a
16	chr1:104113039-104113089	ProgFib	skin:	n/a
17	chr1:104112143-104112193	ECC-1	luminal epithelium:	n/a
18	chr1:104068312-104068362	SK-N-SH_RA	brain:	n/a
19	chr1:104096621-104096671	T-47D	breast:	n/a
20	chr1:104068704-104068754	BJ	skin:	n/a
21	chr1:104113061-104113111	Hela-S3	cervix:	n/a
22	chr1:104096621-104096671	SKMC	muscle:	n/a
23	chr1:104068312-104068362	SKMC	muscle:	n/a
24	chr1:104112143-104112193	PANC-1	pancreas:	n/a
25	chr1:104113039-104113089	A549	lung:	n/a
26	chr1:104068935-104068985	HCM	heart:	n/a
27	chr1:104096517-104096567	AoSMC	blood vessel:	n/a
28	chr1:104068118-104068168	HIPEpiC	eye:	n/a
29	chr1:104096517-104096567	GM12878	blood:	n/a
30	chr1:104068567-104068617	SK-N-SH	brain:	n/a
31	chr1:104068567-104068617	MCF-7	breast:	n/a
32	chr1:104096621-104096671	ECC-1	luminal epithelium:	n/a
33	chr1:104068935-104068985	BE2_C	brain:	n/a
34	chr1:104068490-104068540	AoSMC	blood vessel:	n/a
35	chr1:104068567-104068617	SKMC	muscle:	n/a
36	chr1:104068567-104068617	HL-60	blood:	n/a
37	chr1:104068118-104068168	AG09319	gingival:	n/a
38	chr1:104113039-104113089	GM12891	blood:	n/a
39	chr1:104068121-104068171	ECC-1	luminal epithelium:	n/a
40	chr1:104068603-104068653	MCF-7	breast:	n/a
41	chr1:104068118-104068168	PrEC	prostate:	n/a
42	chr1:104068704-104068754	NB4	blood:	n/a
43	chr1:104068121-104068171	HEK293	kidney:	embryo
44	chr1:104068301-104068351	CMK	blood:	n/a
45	chr1:104111877-104111927	HUVEC	blood vessel:	n/a
46	chr1:104068490-104068540	NB4	blood:	n/a
47	chr1:104068704-104068754	HCT-116	colon:	n/a
48	chr1:104068664-104068714	BJ	skin:	n/a
49	chr1:104065263-104065313	HCPEpiC	choroid plexus:	n/a
50	chr1:104068935-104068985	SK-N-SH	brain:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMY1B-1	chr1:104068018-104068105	XLOC_000945
2	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
3	lnc-AMY1B-1	chr1:104068018-104068115	XLOC_000945
4	lnc-AMY1B-1	chr1:104068018-104068083	ENSG00000224613.2
5	lnc-RNPC3-4	chr1:104066184-104066501	NONHSAT004893
6	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
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
ACTG1P4	TF binding region
ENSG00000224613	TF binding region
RNPC3	TF binding region
AMY2A	TF binding region
RN7SKP285	TF binding region
AMY2B	TF binding region
ACTG1P4	CpG island
ENSG00000224613	CpG island
RNPC3	CpG island
AMY2A	CpG island
RN7SKP285	CpG island
AMY2B	CpG island
ENSG00000017797	chromatin interactions
ENSG00000185946	chromatin interactions
ENSG00000224613	chromatin interactions
ENSG00000240038	chromatin interactions
TOMM34	miRNA target sites

Extended variants
information (count: 3316 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:3316 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556364187	chr1:104040005-104040006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs4244372	chr1:104040027-104040028	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs541553969	chr1:104040040-104040041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549087033	chr1:104040047-104040048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs144868867	chr1:104040241-104040242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546438712	chr1:104040285-104040286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564629492	chr1:104040381-104040382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532076601	chr1:104040419-104040420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148200424	chr1:104040439-104040440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556166809	chr1:104040460-104040461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs11804385	chr1:104040482-104040483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs190820467	chr1:104040485-104040486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529381253	chr1:104040488-104040489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs547933836	chr1:104040502-104040503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566044384	chr1:104040511-104040512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs34073303	chr1:104040512-104040513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs545295403	chr1:104040547-104040548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs539850440	chr1:104040593-104040594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141160693	chr1:104040602-104040603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558767880	chr1:104040611-104040612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs376840755	chr1:104040876-104040877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs570648285	chr1:104040915-104040916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538175869	chr1:104040957-104040958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556063914	chr1:104040964-104040965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183016629	chr1:104040966-104040967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563474761	chr1:104040981-104040982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553462447	chr1:104041031-104041032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs150287606	chr1:104041058-104041059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530729482	chr1:104041101-104041102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545477965	chr1:104041103-104041104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187171840	chr1:104041126-104041127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs59283300	chr1:104041162-104041163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs137986418	chr1:104041173-104041174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191149305	chr1:104041203-104041204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs367674272	chr1:104041341-104041342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs565730344	chr1:104041574-104041575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs182977962	chr1:104041656-104041657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529527063	chr1:104041680-104041681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187560790	chr1:104041722-104041723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191677469	chr1:104041724-104041725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533509173	chr1:104041725-104041726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35872386	chr1:104041798-104041799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs34067685	chr1:104041854-104041855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144201022	chr1:104041907-104041908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551470127	chr1:104041953-104041954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs74905560	chr1:104041971-104041972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548934936	chr1:104041980-104041981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183005176	chr1:104042041-104042042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567876276	chr1:104042044-104042045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76010878	chr1:104042127-104042128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
Ovarian clear cell carcinoma	21343371	CNVD
Autism	19287141	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1580 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:104035200-104040000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr1:104038000-104040600	Enhancers	Muscle Satellite Cultured Cells	--
3	chr1:104038600-104040600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:104039000-104040000	Weak transcription	Osteobl	bone
5	chr1:104039000-104041400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr1:104039200-104040600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr1:104039400-104040000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr1:104039400-104041200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:104039400-104041400	Enhancers	HMEC	breast
10	chr1:104039600-104040600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr1:104040000-104040400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:104040000-104040400	Enhancers	Osteobl	bone
13	chr1:104040000-104040800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr1:104040000-104041200	Enhancers	NHEK	skin
15	chr1:104040200-104040600	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr1:104040600-104043600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr1:104040600-104044000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr1:104040800-104041400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr1:104041400-104041600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr1:104043000-104043200	Enhancers	Aorta	Aorta
21	chr1:104043200-104046400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr1:104043200-104067400	Weak transcription	Aorta	Aorta
23	chr1:104043600-104044600	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr1:104044000-104044600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr1:104046000-104047200	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr1:104046200-104046800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr1:104046200-104047000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr1:104046200-104047200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr1:104046400-104046800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr1:104046400-104046800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr1:104046400-104047000	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr1:104050000-104067400	Weak transcription	Left Ventricle	heart
33	chr1:104051800-104052400	Enhancers	HUVEC	blood vessel
34	chr1:104052000-104052600	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr1:104052200-104052600	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr1:104054400-104066200	Weak transcription	Psoas Muscle	Psoas
37	chr1:104054800-104062600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr1:104056200-104060600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr1:104056400-104056600	Enhancers	HMEC	breast
40	chr1:104056400-104056800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr1:104056400-104057600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr1:104056400-104059800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr1:104056600-104056800	Enhancers	Muscle Satellite Cultured Cells	--
44	chr1:104056600-104056800	Enhancers	Osteobl	bone
45	chr1:104056800-104058400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr1:104056800-104058400	Weak transcription	Osteobl	bone
47	chr1:104057200-104058200	Weak transcription	HMEC	breast
48	chr1:104057600-104059000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr1:104057800-104058600	Enhancers	Primary T helper cells PMA-I stimulated	--
50	chr1:104058200-104060400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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