Variant report

Variant	nsv1000988
Chromosome Location	chr1:63061791-63107526
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:380)
CpG islands
(count:183)
Chromatin interactive
region (count:17)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:63087554-63088043	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:63089241-63089296	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:63074554-63075140	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:63079529-63079891	HepG2	liver:	n/a	n/a
5	ATF1	chr1:63087652-63087993	K562	blood:	n/a	n/a
6	ATF2	chr1:63087593-63087996	GM12878	blood:	n/a	n/a
7	ATF2	chr1:63078872-63079532	GM12878	blood:	n/a	n/a
8	ATF2	chr1:63087614-63088085	GM12878	blood:	n/a	n/a
9	ATF3	chr1:63087496-63087981	A549	lung:	n/a	n/a
10	ATF3	chr1:63087530-63087957	A549	lung:	n/a	n/a
11	ATF3	chr1:63087594-63087996	K562	blood:	n/a	n/a
12	BATF	chr1:63064757-63064998	GM12878	blood:	n/a	chr1:63064849-63064860
13	BATF	chr1:63091155-63091470	GM12878	blood:	n/a	n/a
14	BATF	chr1:63087655-63088035	GM12878	blood:	n/a	n/a
15	BATF	chr1:63064713-63065027	GM12878	blood:	n/a	chr1:63064849-63064860
16	BATF	chr1:63087603-63088001	GM12878	blood:	n/a	n/a
17	BCL11A	chr1:63087711-63088043	GM12878	blood:	n/a	n/a
18	BCL11A	chr1:63091142-63091436	GM12878	blood:	n/a	n/a
19	BCL3	chr1:63087446-63088045	A549	lung:	n/a	n/a
20	BCLAF1	chr1:63078822-63079525	GM12878	blood:	n/a	chr1:63079303-63079312
21	BHLHE40	chr1:63078977-63079505	GM12878	blood:	n/a	n/a
22	BHLHE40	chr1:63064805-63064823	GM12878	blood:	n/a	n/a
23	BHLHE40	chr1:63087617-63088019	K562	blood:	n/a	n/a
24	BHLHE40	chr1:63087611-63088010	GM12878	blood:	n/a	n/a
25	BHLHE40	chr1:63099737-63099778	GM12878	blood:	n/a	n/a
26	BHLHE40	chr1:63087555-63087977	HepG2	liver:	n/a	n/a
27	BHLHE40	chr1:63097743-63097749	GM12878	blood:	n/a	n/a
28	BRCA1	chr1:63087609-63087959	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr1:63087587-63087982	K562	blood:	n/a	n/a
30	CEBPB	chr1:63087525-63087960	HepG2	liver:	n/a	n/a
31	CEBPB	chr1:63087515-63087932	MCF-7	breast:	n/a	n/a
32	CEBPB	chr1:63087527-63087965	A549	lung:	n/a	n/a
33	CEBPB	chr1:63087574-63087906	K562	blood:	n/a	n/a
34	CEBPB	chr1:63087591-63087875	HepG2	liver:	n/a	n/a
35	CEBPB	chr1:63087524-63087970	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr1:63087525-63087956	HepG2	liver:	n/a	n/a
37	CEBPB	chr1:63087607-63087903	K562	blood:	n/a	n/a
38	CEBPB	chr1:63087535-63087961	IMR90	lung:	n/a	n/a
39	CEBPB	chr1:63087586-63087872	HepG2	liver:	n/a	n/a
40	CEBPB	chr1:63079623-63080056	A549	lung:	n/a	n/a
41	CEBPB	chr1:63087431-63088083	A549	lung:	n/a	n/a
42	CEBPB	chr1:63074608-63074964	HepG2	liver:	n/a	n/a
43	CEBPB	chr1:63064724-63065042	IMR90	lung:	n/a	n/a
44	CEBPB	chr1:63067238-63067586	IMR90	lung:	n/a	chr1:63067256-63067268
45	CEBPB	chr1:63087542-63087921	A549	lung:	n/a	n/a
46	CEBPD	chr1:63087548-63087810	HepG2	liver:	n/a	n/a
47	CEBPD	chr1:63087604-63087890	HepG2	liver:	n/a	n/a
48	CHD1	chr1:63087700-63087999	GM12878	blood:	n/a	n/a
49	CHD2	chr1:63087575-63087995	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr1:63087695-63087970	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:63062724-63062774	MCF-7	breast:	n/a
2	chr1:63062489-63062539	HNPCEpiC	eye:	n/a
3	chr1:63062724-63062774	HepG2	liver:	n/a
4	chr1:63062212-63062262	A549	lung:	n/a
5	chr1:63062212-63062262	GM19239	blood:	n/a
6	chr1:63062212-63062262	NHDF-neo	bronchial:	n/a
7	chr1:63062489-63062539	AG04449	skin:	fetal
8	chr1:63062489-63062539	IMR90	lung:	fetal
9	chr1:63062212-63062262	HCF	heart:	n/a
10	chr1:63062212-63062262	AG04450	lung:	fetal
11	chr1:63062724-63062774	SK-N-SH_RA	brain:	n/a
12	chr1:63062489-63062539	SK-N-MC	brain:	n/a
13	chr1:63062489-63062539	HL-60	blood:	n/a
14	chr1:63062489-63062539	HEEpiC	esophagus:	n/a
15	chr1:63062212-63062262	AoSMC	blood vessel:	n/a
16	chr1:63062489-63062539	GM12891	blood:	n/a
17	chr1:63062489-63062539	MCF-7	breast:	n/a
18	chr1:63062724-63062774	HCF	heart:	n/a
19	chr1:63062212-63062262	HEEpiC	esophagus:	n/a
20	chr1:63062489-63062539	HCPEpiC	choroid plexus:	n/a
21	chr1:63062212-63062262	ovcar-3	ovarian:	n/a
22	chr1:63062212-63062262	H1-hESC	embryonic stem cell:	embryo
23	chr1:63062724-63062774	Hepatocyte	liver:	n/a
24	chr1:63062724-63062774	HIPEpiC	eye:	n/a
25	chr1:63062212-63062262	MCF10A-Er-Src	breast:	n/a
26	chr1:63062212-63062262	U87	brain:	n/a
27	chr1:63062212-63062262	HPAEpiC	pulmonary alveolar:	n/a
28	chr1:63062724-63062774	GM19239	blood:	n/a
29	chr1:63062724-63062774	Hela-S3	cervix:	n/a
30	chr1:63062212-63062262	GM12878	blood:	n/a
31	chr1:63062724-63062774	ovcar-3	ovarian:	n/a
32	chr1:63062489-63062539	HRPEpiC	eye:	n/a
33	chr1:63062724-63062774	PrEC	prostate:	n/a
34	chr1:63062489-63062539	ovcar-3	ovarian:	n/a
35	chr1:63062212-63062262	SKMC	muscle:	n/a
36	chr1:63062724-63062774	HCT-116	colon:	n/a
37	chr1:63062724-63062774	AG04450	lung:	fetal
38	chr1:63062724-63062774	NT2-D1	testis:	n/a
39	chr1:63062724-63062774	HPAEpiC	pulmonary alveolar:	n/a
40	chr1:63062212-63062262	SK-N-SH	brain:	n/a
41	chr1:63062212-63062262	SK-N-MC	brain:	n/a
42	chr1:63062489-63062539	SAEC	small airway:	n/a
43	chr1:63062489-63062539	BE2_C	brain:	n/a
44	chr1:63062212-63062262	SAEC	small airway:	n/a
45	chr1:63062212-63062262	GM12892	blood:	n/a
46	chr1:63062724-63062774	HL-60	blood:	n/a
47	chr1:63062212-63062262	ECC-1	luminal epithelium:	n/a
48	chr1:63062212-63062262	Caco-2	colon:	n/a
49	chr1:63062724-63062774	RPTEC	kidney:	n/a
50	chr1:63062724-63062774	HEK293	kidney:	embryo

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:63102529..63105125-chr5:46100658..46103318,2	MCF-7	breast:
2	chr1:63081404..63083878-chr1:63086190..63087709,2	K562	blood:
3	chr1:63082239..63084843-chr1:63153676..63156091,2	K562	blood:
4	chr1:63088603..63091388-chr1:63093156..63095465,2	K562	blood:
5	chr1:63081752..63083296-chr1:63090887..63092573,2	MCF-7	breast:
6	chr1:63079121..63081577-chr1:63084088..63085604,2	MCF-7	breast:
7	chr1:63088346..63090747-chr1:63093561..63095201,2	K562	blood:
8	chr1:63088603..63091388-chr1:63093156..63095465,2	K562	blood:
9	chr1:63088346..63090747-chr1:63093561..63095201,2	K562	blood:
10	chr1:63063894..63067391-chr1:63081562..63083857,3	K562	blood:
11	chr1:63063122..63065536-chr1:63066571..63069108,3	K562	blood:
12	chr1:63081752..63083296-chr1:63090887..63092573,2	MCF-7	breast:
13	chr1:63081404..63083878-chr1:63086190..63087709,2	K562	blood:
14	chr1:63079121..63081577-chr1:63084088..63085604,2	MCF-7	breast:
15	chr1:63062723..63066181-chr1:63069299..63072097,3	K562	blood:
16	chr1:63063122..63065536-chr1:63066571..63069108,3	K562	blood:
17	chr1:63065055..63067391-chr1:63081562..63083375,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP1-1	chr1:63066705-63066867	NONHSAT003634
2	lnc-USP1-1	chr1:63067440-63067553	NONHSAT003634
3	lnc-USP1-1	chr1:63067956-63068051	NONHSAT003634

No data

Variant related genes	Relation type
ENSG00000269624	TF binding region
DOCK7	TF binding region
ANGPTL3	TF binding region
ENSG00000213703	TF binding region
ENSG00000269624	CpG island
DOCK7	CpG island
ANGPTL3	CpG island
ENSG00000213703	CpG island
ENSG00000116641	chromatin interactions
ENSG00000235545	chromatin interactions
ENSG00000132855	chromatin interactions

Extended variants
information (count: 1561 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1561 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77354949	chr1:63061814-63061815	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs573300763	chr1:63061825-63061826	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs35123493	chr1:63061840-63061841	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs72649570	chr1:63061844-63061845	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs149364366	chr1:63061850-63061851	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547368927	chr1:63061869-63061870	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs141794880	chr1:63061885-63061886	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs11207997	chr1:63061906-63061907	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs181471655	chr1:63061924-63061925	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs150428533	chr1:63061940-63061941	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564966056	chr1:63061960-63061961	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563860868	chr1:63061971-63061972	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186011618	chr1:63061984-63061985	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs72649572	chr1:63062018-63062019	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530517180	chr1:63062036-63062037	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546991207	chr1:63062075-63062076	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs565874988	chr1:63062131-63062132	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs568326118	chr1:63062202-63062203	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191145608	chr1:63062216-63062217	Weak transcription Strong transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs554860249	chr1:63062242-63062243	Weak transcription Strong transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs532426120	chr1:63062258-63062259	Weak transcription Strong transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs537236179	chr1:63062281-63062282	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs558720437	chr1:63062305-63062306	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs576851908	chr1:63062307-63062308	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540741675	chr1:63062314-63062315	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552949139	chr1:63062320-63062321	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs138234803	chr1:63062376-63062377	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs551840638	chr1:63062401-63062402	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs536340521	chr1:63062439-63062440	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs181596788	chr1:63062490-63062491	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs116514612	chr1:63062529-63062530	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs531043366	chr1:63062533-63062534	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs554752701	chr1:63062550-63062551	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs545963584	chr1:63062591-63062592	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs564309721	chr1:63062627-63062628	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs569711057	chr1:63062635-63062636	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs528598005	chr1:63062637-63062638	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs546735134	chr1:63062645-63062646	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs568447559	chr1:63062667-63062668	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529271399	chr1:63062724-63062725	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs185773146	chr1:63062737-63062738	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs191086880	chr1:63062811-63062812	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs149558895	chr1:63062822-63062823	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs528161173	chr1:63062859-63062860	Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs183279674	chr1:63062946-63062947	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs187806040	chr1:63062971-63062972	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191171206	chr1:63062986-63062987	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs546741644	chr1:63063031-63063032	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs570519859	chr1:63063099-63063100	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs568241193	chr1:63063163-63063164	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Breast cancer	16620391	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:865 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:63007200-63096200	Weak transcription	HUVEC	blood vessel
2	chr1:63010800-63078400	Weak transcription	A549	lung
3	chr1:63036800-63113600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr1:63038400-63087600	Weak transcription	NHEK	skin
5	chr1:63038400-63095600	Weak transcription	Brain Germinal Matrix	brain
6	chr1:63038600-63083000	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr1:63039000-63063400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr1:63039200-63095200	Weak transcription	Ovary	ovary
9	chr1:63041000-63095200	Weak transcription	Fetal Muscle Leg	muscle
10	chr1:63041000-63095600	Weak transcription	Fetal Stomach	stomach
11	chr1:63042200-63083600	Weak transcription	Fetal Muscle Trunk	muscle
12	chr1:63044000-63076000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr1:63047600-63077000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr1:63050600-63083800	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr1:63051000-63066400	Weak transcription	NHLF	lung
16	chr1:63051400-63062800	Weak transcription	Psoas Muscle	Psoas
17	chr1:63051800-63075800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr1:63051800-63077000	Weak transcription	Primary hematopoietic stem cells	blood
19	chr1:63051800-63083400	Weak transcription	Fetal Lung	lung
20	chr1:63051800-63096000	Weak transcription	Left Ventricle	heart
21	chr1:63052000-63062200	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr1:63052400-63062400	Weak transcription	Fetal Intestine Small	intestine
23	chr1:63052400-63083800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr1:63052600-63077200	Weak transcription	HSMM	muscle
25	chr1:63052600-63084400	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr1:63052800-63062400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr1:63052800-63067000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr1:63053000-63068000	Weak transcription	NHDF-Ad	bronchial
29	chr1:63054600-63064800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr1:63054800-63079800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr1:63054800-63087600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr1:63055200-63063000	Weak transcription	NH-A	brain
33	chr1:63057000-63082800	Weak transcription	Brain Anterior Caudate	brain
34	chr1:63057000-63083800	Weak transcription	Adipose Nuclei	Adipose
35	chr1:63057600-63061800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr1:63058400-63062400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr1:63059400-63065200	Enhancers	HepG2	liver
38	chr1:63060200-63062400	Enhancers	Liver	Liver
39	chr1:63060600-63061800	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr1:63060600-63062400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr1:63060600-63063400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr1:63060600-63066200	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr1:63060600-63076600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr1:63061200-63062800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr1:63061200-63064400	Weak transcription	Osteobl	bone
46	chr1:63061400-63062600	Enhancers	Fetal Intestine Large	intestine
47	chr1:63061600-63063600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr1:63061800-63063000	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr1:63061800-63063200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:63062200-63063200	Strong transcription	Cortex derived primary cultured neurospheres	brain

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