Variant report

Variant	esv1810004
Chromosome Location	chr1:62436942-62451029
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	chr1:62446355-62446912	IMR90	lung:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
6	CEBPB	chr1:62446313-62446586	K562	blood:	n/a	n/a
7	CEBPB	chr1:62446583-62446870	HepG2	liver:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
8	CEBPB	chr1:62440023-62440267	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:62446295-62446907	K562	blood:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
10	CEBPB	chr1:62440045-62440224	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr1:62446324-62446874	H1-hESC	embryonic stem cell:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
12	CHD2	chr1:62448125-62448179	GM12878	blood:	n/a	n/a
13	CHD2	chr1:62446418-62446581	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr1:62446374-62446425	Fibrobl	skin:	n/a	n/a
15	CTCF	chr1:62440228-62440270	Kidney_OC	kidney:	n/a	n/a
16	E2F4	chr1:62446465-62446664	MCF10A-Er-Src	breast:	n/a	chr1:62446509-62446518
17	E2F4	chr1:62438634-62439009	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F4	chr1:62440236-62440368	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr1:62438813-62439128	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr1:62440032-62440239	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr1:62440055-62440275	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr1:62446297-62446593	MCF10A-Er-Src	breast:	n/a	chr1:62446463-62446475 chr1:62446464-62446474
23	FOS	chr1:62440074-62440275	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr1:62438816-62439128	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr1:62446342-62446638	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	chr1:62446306-62446593	MCF10A-Er-Src	breast:	n/a	chr1:62446463-62446475 chr1:62446464-62446474
28	FOS	chr1:62446306-62446560	MCF10A-Er-Src	breast:	n/a	chr1:62446463-62446475 chr1:62446464-62446474
29	FOS	chr1:62438769-62439219	MCF10A-Er-Src	breast:	n/a	n/a
30	FOXA1	chr1:62441400-62441592	T-47D	breast:	n/a	n/a
31	FOXA1	chr1:62441344-62441639	T-47D	breast:	n/a	n/a
32	FOXP2	chr1:62446307-62446517	SK-N-MC	brain:	n/a	n/a
33	GATA2	chr1:62445408-62445710	K562	blood:	n/a	n/a
34	GATA3	chr1:62441303-62441694	T-47D	breast:	n/a	n/a
35	GATA3	chr1:62448112-62448183	SH-SY5Y	brain:	n/a	n/a
36	GATA3	chr1:62441311-62441758	T-47D	breast:	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	KAP1	chr1:62439821-62440264	HEK293	kidney:	n/a	n/a
40	KAP1	chr1:62444569-62445769	HEK293	kidney:	n/a	n/a
41	MAFF	chr1:62446277-62446670	K562	blood:	n/a	chr1:62446456-62446474 chr1:62446462-62446476
42	MAFF	chr1:62440031-62440370	HepG2	liver:	n/a	chr1:62440194-62440212
43	MAFF	chr1:62442363-62442563	K562	blood:	n/a	chr1:62442431-62442449
44	MAFF	chr1:62442324-62442575	HepG2	liver:	n/a	chr1:62442431-62442449
45	MAFF	chr1:62446295-62446635	HepG2	liver:	n/a	chr1:62446456-62446474 chr1:62446462-62446476
46	MAFK	chr1:62440185-62440308	H1-hESC	embryonic stem cell:	n/a	chr1:62440195-62440210
47	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
48	MAFK	chr1:62440022-62440335	HepG2	liver:	n/a	chr1:62440195-62440210
49	MAFK	chr1:62442377-62442581	IMR90	lung:	n/a	chr1:62442432-62442447
50	MAFK	chr1:62442272-62442620	HepG2	liver:	n/a	chr1:62442432-62442447

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:62445916-62445966	SK-N-SH	brain:	n/a
2	chr1:62445916-62445966	GM12878	blood:	n/a
3	chr1:62445916-62445966	ovcar-3	ovarian:	n/a
4	chr1:62445916-62445966	NHBE	bronchial:	n/a
5	chr1:62445916-62445966	HepG2	liver:	n/a
6	chr1:62445916-62445966	HRPEpiC	eye:	n/a
7	chr1:62445916-62445966	BJ	skin:	n/a
8	chr1:62445916-62445966	GM12891	blood:	n/a
9	chr1:62445916-62445966	ProgFib	skin:	n/a
10	chr1:62445916-62445966	AoSMC	blood vessel:	n/a
11	chr1:62445916-62445966	ECC-1	luminal epithelium:	n/a
12	chr1:62445916-62445966	AG09309	skin:	n/a
13	chr1:62445916-62445966	GM06990	blood:	n/a
14	chr1:62445916-62445966	NH-A	brain:	n/a
15	chr1:62445916-62445966	H1-hESC	embryonic stem cell:	embryo
16	chr1:62445916-62445966	SK-N-SH_RA	brain:	n/a
17	chr1:62445916-62445966	GM12892	blood:	n/a
18	chr1:62445916-62445966	T-47D	breast:	n/a
19	chr1:62445916-62445966	SKMC	muscle:	n/a
20	chr1:62445916-62445966	NB4	blood:	n/a
21	chr1:62445916-62445966	AG04450	lung:	fetal
22	chr1:62445916-62445966	HRCEpiC	kidney:	n/a
23	chr1:62445916-62445966	Jurkat	blood:	n/a
24	chr1:62445916-62445966	RPTEC	kidney:	n/a
25	chr1:62445916-62445966	HEK293	kidney:	embryo
26	chr1:62445916-62445966	A549	lung:	n/a
27	chr1:62445916-62445966	SK-N-MC	brain:	n/a
28	chr1:62445916-62445966	MCF10A-Er-Src	breast:	n/a
29	chr1:62445916-62445966	Hepatocyte	liver:	n/a
30	chr1:62445916-62445966	PFSK-1	brain:	n/a
31	chr1:62445916-62445966	IMR90	lung:	fetal
32	chr1:62445916-62445966	GM19239	blood:	n/a
33	chr1:62445916-62445966	HIPEpiC	eye:	n/a
34	chr1:62445916-62445966	PANC-1	pancreas:	n/a
35	chr1:62445916-62445966	HRE	kidney:	n/a
36	chr1:62445916-62445966	Hela-S3	cervix:	n/a
37	chr1:62445916-62445966	HCPEpiC	choroid plexus:	n/a
38	chr1:62445916-62445966	BE2_C	brain:	n/a
39	chr1:62445916-62445966	NHDF-neo	bronchial:	n/a
40	chr1:62445916-62445966	AG10803	skin:	n/a
41	chr1:62445916-62445966	NT2-D1	testis:	n/a
42	chr1:62445916-62445966	SAEC	small airway:	n/a
43	chr1:62445916-62445966	HPAEpiC	pulmonary alveolar:	n/a
44	chr1:62445916-62445966	MCF-7	breast:	n/a
45	chr1:62445916-62445966	HL-60	blood:	n/a
46	chr1:62445916-62445966	CMK	blood:	n/a
47	chr1:62445916-62445966	PrEC	prostate:	n/a
48	chr1:62445916-62445966	HCT-116	colon:	n/a
49	chr1:62445916-62445966	HAEpiC	amniotic membrane:	n/a
50	chr1:62445916-62445966	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:62444307..62446951-chr1:62447722..62450460,2	K562	blood:
2	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: 563 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:563 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534745869	chr1:62437007-62437008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552667999	chr1:62437021-62437022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs556592236	chr1:62437036-62437037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182056294	chr1:62437058-62437059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149878501	chr1:62437070-62437071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557681566	chr1:62437194-62437195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184530069	chr1:62437219-62437220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577522769	chr1:62437254-62437255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189189084	chr1:62437298-62437299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558358291	chr1:62437312-62437313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115244251	chr1:62437385-62437386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs540735083	chr1:62437444-62437445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs5774579	chr1:62437500-62437501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561892517	chr1:62437501-62437502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs34076700	chr1:62437508-62437509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs397794743	chr1:62437514-62437515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs72676289	chr1:62437524-62437525	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs550540240	chr1:62437525-62437526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542823035	chr1:62437541-62437542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181213003	chr1:62437558-62437559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544245827	chr1:62437590-62437591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs145843988	chr1:62437688-62437689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530751384	chr1:62437854-62437855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149010718	chr1:62437862-62437863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2482894	chr1:62437872-62437873	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs528143358	chr1:62437886-62437887	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs2498969	chr1:62437927-62437928	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs200373554	chr1:62437931-62437932	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs138400397	chr1:62437932-62437933	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs185772079	chr1:62437937-62437938	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs141368976	chr1:62437945-62437946	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs569548932	chr1:62437980-62437981	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs576319643	chr1:62438049-62438050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145051465	chr1:62438080-62438081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190587816	chr1:62438160-62438161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533991357	chr1:62438182-62438183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555828847	chr1:62438209-62438210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs573836693	chr1:62438243-62438244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544184936	chr1:62438255-62438256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562572811	chr1:62438296-62438297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs180926028	chr1:62438308-62438309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546095912	chr1:62438350-62438351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs564087327	chr1:62438385-62438386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536322444	chr1:62438427-62438428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs528283963	chr1:62438442-62438443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs543701660	chr1:62438517-62438518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149772077	chr1:62438538-62438539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs71050186	chr1:62438539-62438540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs397980339	chr1:62438541-62438542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs67832271	chr1:62438546-62438547	Weak transcription Enhancers	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:133 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62385000-62494200	Weak transcription	Aorta	Aorta
2	chr1:62409200-62456000	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr1:62409200-62456800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr1:62409200-62457000	Weak transcription	Fetal Intestine Large	intestine
5	chr1:62409200-62518600	Weak transcription	Pancreas	Pancrea
6	chr1:62409400-62458400	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr1:62418200-62446400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr1:62418400-62441400	Weak transcription	Fetal Kidney	kidney
9	chr1:62419600-62445800	Weak transcription	Left Ventricle	heart
10	chr1:62424200-62494200	Weak transcription	Esophagus	oesophagus
11	chr1:62424800-62438200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr1:62425000-62441400	Weak transcription	Stomach Mucosa	stomach
13	chr1:62430600-62442200	Weak transcription	Fetal Intestine Small	intestine
14	chr1:62432200-62439000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr1:62433400-62439200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr1:62433600-62456800	Weak transcription	NHEK	skin
17	chr1:62433800-62438600	Weak transcription	HMEC	breast
18	chr1:62433800-62444800	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr1:62433800-62445400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr1:62434000-62457000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr1:62434800-62444800	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr1:62438200-62438600	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr1:62438400-62439000	Enhancers	Liver	Liver
24	chr1:62438400-62439200	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr1:62438600-62439600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr1:62438600-62439600	Enhancers	Placenta Amnion	Placenta Amnion
27	chr1:62438600-62445000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr1:62438800-62439000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr1:62439000-62439200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr1:62439000-62439400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr1:62439000-62439800	Enhancers	Psoas Muscle	Psoas
32	chr1:62439000-62439800	Active TSS	Skeletal Muscle Female	skeletal muscle
33	chr1:62439000-62440000	Flanking Active TSS	Liver	Liver
34	chr1:62439000-62440000	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr1:62439200-62439600	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr1:62439200-62440200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr1:62439200-62441200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr1:62439400-62441200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr1:62439600-62439800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr1:62439600-62439800	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr1:62439800-62440000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
42	chr1:62439800-62440400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr1:62439800-62440800	Weak transcription	Psoas Muscle	Psoas
44	chr1:62439800-62440800	Enhancers	HepG2	liver
45	chr1:62439800-62441000	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr1:62440000-62440800	Enhancers	Liver	Liver
47	chr1:62440000-62441200	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr1:62440200-62440400	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr1:62440200-62440800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr1:62440400-62441600	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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