Variant report

Variant	nsv1009859
Chromosome Location	chr1:62435767-62447302
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	BACH1	chr1:62446381-62446560	K562	blood:	n/a	n/a
2	BACH1	chr1:62446282-62446790	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr1:62437864-62437982	K562	blood:	n/a	n/a
4	CEBPB	chr1:62440045-62440218	K562	blood:	n/a	n/a
5	CEBPB	chr1:62446324-62446874	H1-hESC	embryonic stem cell:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
6	CEBPB	chr1:62446355-62446912	IMR90	lung:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
7	CEBPB	chr1:62446583-62446870	HepG2	liver:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
8	CEBPB	chr1:62446313-62446586	K562	blood:	n/a	n/a
9	CEBPB	chr1:62440045-62440224	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr1:62446295-62446907	K562	blood:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
11	CEBPB	chr1:62440023-62440267	HepG2	liver:	n/a	n/a
12	CHD2	chr1:62446418-62446581	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr1:62446374-62446425	Fibrobl	skin:	n/a	n/a
14	CTCF	chr1:62440228-62440270	Kidney_OC	kidney:	n/a	n/a
15	E2F4	chr1:62446465-62446664	MCF10A-Er-Src	breast:	n/a	chr1:62446509-62446518
16	E2F4	chr1:62438634-62439009	MCF10A-Er-Src	breast:	n/a	n/a
17	E2F4	chr1:62440236-62440368	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr1:62446306-62446593	MCF10A-Er-Src	breast:	n/a	chr1:62446463-62446475 chr1:62446464-62446474
19	FOS	chr1:62440074-62440275	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr1:62438816-62439128	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr1:62440032-62440239	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr1:62438813-62439128	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr1:62440055-62440275	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr1:62438769-62439219	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr1:62446306-62446560	MCF10A-Er-Src	breast:	n/a	chr1:62446463-62446475 chr1:62446464-62446474
26	FOS	chr1:62440039-62440275	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr1:62446297-62446593	MCF10A-Er-Src	breast:	n/a	chr1:62446463-62446475 chr1:62446464-62446474
28	FOS	chr1:62446342-62446638	MCF10A-Er-Src	breast:	n/a	chr1:62446463-62446475 chr1:62446464-62446474
29	FOXA1	chr1:62441344-62441639	T-47D	breast:	n/a	n/a
30	FOXA1	chr1:62441400-62441592	T-47D	breast:	n/a	n/a
31	FOXP2	chr1:62446307-62446517	SK-N-MC	brain:	n/a	n/a
32	GATA2	chr1:62445408-62445710	K562	blood:	n/a	n/a
33	GATA3	chr1:62441311-62441758	T-47D	breast:	n/a	n/a
34	GATA3	chr1:62441303-62441694	T-47D	breast:	n/a	n/a
35	KAP1	chr1:62444569-62445769	HEK293	kidney:	n/a	n/a
36	KAP1	chr1:62439821-62440264	HEK293	kidney:	n/a	n/a
37	KAP1	chr1:62444519-62445549	U2OS	brain:	n/a	n/a
38	KAP1	chr1:62439825-62440303	U2OS	brain:	n/a	n/a
39	MAFF	chr1:62442363-62442563	K562	blood:	n/a	chr1:62442431-62442449
40	MAFF	chr1:62440031-62440370	HepG2	liver:	n/a	chr1:62440194-62440212
41	MAFF	chr1:62446277-62446670	K562	blood:	n/a	chr1:62446456-62446474 chr1:62446462-62446476
42	MAFF	chr1:62446295-62446635	HepG2	liver:	n/a	chr1:62446456-62446474 chr1:62446462-62446476
43	MAFF	chr1:62442324-62442575	HepG2	liver:	n/a	chr1:62442431-62442449
44	MAFK	chr1:62446285-62446652	K562	blood:	n/a	chr1:62446458-62446469 chr1:62446461-62446477 chr1:62446459-62446479 chr1:62446458-62446474 chr1:62446462-62446476 chr1:62446458-62446473 chr1:62446463-62446472 chr1:62446465-62446475
45	MAFK	chr1:62440185-62440308	H1-hESC	embryonic stem cell:	n/a	chr1:62440195-62440210
46	MAFK	chr1:62440022-62440335	HepG2	liver:	n/a	chr1:62440195-62440210
47	MAFK	chr1:62446306-62446640	HepG2	liver:	n/a	chr1:62446458-62446469 chr1:62446461-62446477 chr1:62446459-62446479 chr1:62446458-62446474 chr1:62446462-62446476 chr1:62446458-62446473 chr1:62446463-62446472 chr1:62446465-62446475
48	MAFK	chr1:62440013-62440384	HepG2	liver:	n/a	chr1:62440195-62440210
49	MAFK	chr1:62446294-62446660	IMR90	lung:	n/a	chr1:62446458-62446469 chr1:62446461-62446477 chr1:62446459-62446479 chr1:62446458-62446474 chr1:62446462-62446476 chr1:62446458-62446473 chr1:62446463-62446472 chr1:62446465-62446475
50	MAFK	chr1:62442377-62442581	IMR90	lung:	n/a	chr1:62442432-62442447

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:62445916-62445966	PrEC	prostate:	n/a
2	chr1:62445916-62445966	ProgFib	skin:	n/a
3	chr1:62445916-62445966	NHDF-neo	bronchial:	n/a
4	chr1:62445916-62445966	Hepatocyte	liver:	n/a
5	chr1:62445916-62445966	Caco-2	colon:	n/a
6	chr1:62445916-62445966	IMR90	lung:	fetal
7	chr1:62445916-62445966	RPTEC	kidney:	n/a
8	chr1:62445916-62445966	GM12892	blood:	n/a
9	chr1:62445916-62445966	H1-hESC	embryonic stem cell:	embryo
10	chr1:62445916-62445966	HAEpiC	amniotic membrane:	n/a
11	chr1:62445916-62445966	PFSK-1	brain:	n/a
12	chr1:62445916-62445966	HMEC	breast:	n/a
13	chr1:62445916-62445966	AoSMC	blood vessel:	n/a
14	chr1:62445916-62445966	GM06990	blood:	n/a
15	chr1:62445916-62445966	GM12878	blood:	n/a
16	chr1:62445916-62445966	SKMC	muscle:	n/a
17	chr1:62445916-62445966	HIPEpiC	eye:	n/a
18	chr1:62445916-62445966	HEEpiC	esophagus:	n/a
19	chr1:62445916-62445966	AG10803	skin:	n/a
20	chr1:62445916-62445966	Hela-S3	cervix:	n/a
21	chr1:62445916-62445966	SAEC	small airway:	n/a
22	chr1:62445916-62445966	ECC-1	luminal epithelium:	n/a
23	chr1:62445916-62445966	BE2_C	brain:	n/a
24	chr1:62445916-62445966	SK-N-SH	brain:	n/a
25	chr1:62445916-62445966	GM12891	blood:	n/a
26	chr1:62445916-62445966	NH-A	brain:	n/a
27	chr1:62445916-62445966	HEK293	kidney:	embryo
28	chr1:62445916-62445966	U87	brain:	n/a
29	chr1:62445916-62445966	NT2-D1	testis:	n/a
30	chr1:62445916-62445966	HRCEpiC	kidney:	n/a
31	chr1:62445916-62445966	HCF	heart:	n/a
32	chr1:62445916-62445966	HPAEpiC	pulmonary alveolar:	n/a
33	chr1:62445916-62445966	BJ	skin:	n/a
34	chr1:62445916-62445966	NHBE	bronchial:	n/a
35	chr1:62445916-62445966	CMK	blood:	n/a
36	chr1:62445916-62445966	SK-N-SH_RA	brain:	n/a
37	chr1:62445916-62445966	MCF-7	breast:	n/a
38	chr1:62445916-62445966	A549	lung:	n/a
39	chr1:62445916-62445966	AG04449	skin:	fetal
40	chr1:62445916-62445966	AG09319	gingival:	n/a
41	chr1:62445916-62445966	HCPEpiC	choroid plexus:	n/a
42	chr1:62445916-62445966	HCM	heart:	n/a
43	chr1:62445916-62445966	HRPEpiC	eye:	n/a
44	chr1:62445916-62445966	HUVEC	blood vessel:	n/a
45	chr1:62445916-62445966	HepG2	liver:	n/a
46	chr1:62445916-62445966	K562	blood:	n/a
47	chr1:62445916-62445966	Jurkat	blood:	n/a
48	chr1:62445916-62445966	HRE	kidney:	n/a
49	chr1:62445916-62445966	AG04450	lung:	fetal
50	chr1:62445916-62445966	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:62444307..62446951-chr1:62447722..62450460,2	K562	blood:

Variant related genes	Relation type
INADL	TF binding region
INADL	CpG island

Extended variants
information (count: 420 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:420 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548327745	chr1:62435797-62435798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs375699186	chr1:62435807-62435808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182847285	chr1:62435837-62435838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187527323	chr1:62435838-62435839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375939024	chr1:62435883-62435884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564456588	chr1:62435930-62435931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs72676286	chr1:62435960-62435961	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs149756660	chr1:62435963-62435964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547009647	chr1:62435968-62435969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368536917	chr1:62435969-62435970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78002816	chr1:62435972-62435973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374537221	chr1:62435980-62435981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs11801215	chr1:62435982-62435983	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs140534052	chr1:62435991-62435992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184112408	chr1:62436002-62436003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs371994376	chr1:62436031-62436032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs545388728	chr1:62436042-62436043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558234189	chr1:62436044-62436045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187484436	chr1:62436051-62436052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563592485	chr1:62436097-62436098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192760297	chr1:62436098-62436099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs531027575	chr1:62436172-62436173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144289693	chr1:62436223-62436224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs61775622	chr1:62436225-62436226	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs147808526	chr1:62436380-62436381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2482892	chr1:62436407-62436408	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs557546651	chr1:62436408-62436409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575909925	chr1:62436419-62436420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147697116	chr1:62436450-62436451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377355448	chr1:62436451-62436452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546464288	chr1:62436455-62436456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564411380	chr1:62436464-62436465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140807617	chr1:62436556-62436557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200365428	chr1:62436557-62436558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs373656120	chr1:62436558-62436559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368886720	chr1:62436580-62436581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528620639	chr1:62436583-62436584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370203287	chr1:62436598-62436599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs114094828	chr1:62436650-62436651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185380493	chr1:62436661-62436662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529903207	chr1:62436687-62436688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190678663	chr1:62436732-62436733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567594909	chr1:62436758-62436759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140088115	chr1:62436784-62436785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530616764	chr1:62436867-62436868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551994318	chr1:62436904-62436905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2482893	chr1:62436929-62436930	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs534745869	chr1:62437007-62437008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552667999	chr1:62437021-62437022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556592236	chr1:62437036-62437037	Weak transcription	n/a	n/a	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
Medullary thyroid carcinoma	18765511	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62385000-62494200	Weak transcription	Aorta	Aorta
2	chr1:62409000-62436800	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr1:62409200-62456000	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr1:62409200-62456800	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr1:62409200-62457000	Weak transcription	Fetal Intestine Large	intestine
6	chr1:62409200-62518600	Weak transcription	Pancreas	Pancrea
7	chr1:62409400-62458400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr1:62418200-62446400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:62418400-62441400	Weak transcription	Fetal Kidney	kidney
10	chr1:62419600-62445800	Weak transcription	Left Ventricle	heart
11	chr1:62424200-62436600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr1:62424200-62494200	Weak transcription	Esophagus	oesophagus
13	chr1:62424800-62438200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr1:62425000-62441400	Weak transcription	Stomach Mucosa	stomach
15	chr1:62430600-62442200	Weak transcription	Fetal Intestine Small	intestine
16	chr1:62432200-62439000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr1:62433400-62439200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:62433600-62456800	Weak transcription	NHEK	skin
19	chr1:62433800-62438600	Weak transcription	HMEC	breast
20	chr1:62433800-62444800	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr1:62433800-62445400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr1:62434000-62457000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr1:62434800-62444800	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr1:62435400-62435800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr1:62435800-62436000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr1:62436000-62436400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr1:62438200-62438600	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr1:62438400-62439000	Enhancers	Liver	Liver
29	chr1:62438400-62439200	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr1:62438600-62439600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr1:62438600-62439600	Enhancers	Placenta Amnion	Placenta Amnion
32	chr1:62438600-62445000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr1:62438800-62439000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr1:62439000-62439200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr1:62439000-62439400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr1:62439000-62439800	Enhancers	Psoas Muscle	Psoas
37	chr1:62439000-62439800	Active TSS	Skeletal Muscle Female	skeletal muscle
38	chr1:62439000-62440000	Flanking Active TSS	Liver	Liver
39	chr1:62439000-62440000	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr1:62439200-62439600	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr1:62439200-62440200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr1:62439200-62441200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr1:62439400-62441200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr1:62439600-62439800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr1:62439600-62439800	Enhancers	Skeletal Muscle Male	skeletal muscle
46	chr1:62439800-62440000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
47	chr1:62439800-62440400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr1:62439800-62440800	Weak transcription	Psoas Muscle	Psoas
49	chr1:62439800-62440800	Enhancers	HepG2	liver
50	chr1:62439800-62441000	Weak transcription	Skeletal Muscle Male	skeletal muscle

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