Variant report

Variant	nsv871684
Chromosome Location	chr1:58021206-58096379
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:208)
CpG islands
(count:184)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:208 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:58088796-58088953	K562	blood:	n/a	n/a
2	ATF1	chr1:58063178-58063197	K562	blood:	n/a	n/a
3	BACH1	chr1:58088731-58088857	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr1:58088727-58088844	HepG2	liver:	n/a	n/a
5	BHLHE40	chr1:58086631-58086962	HepG2	liver:	n/a	n/a
6	CEBPB	chr1:58058567-58058891	IMR90	lung:	n/a	chr1:58058738-58058749
7	CEBPB	chr1:58082341-58082590	HepG2	liver:	n/a	chr1:58082424-58082435 chr1:58082394-58082407
8	CEBPB	chr1:58057416-58057954	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr1:58058628-58058865	K562	blood:	n/a	chr1:58058738-58058749
10	CEBPB	chr1:58058579-58058899	HepG2	liver:	n/a	chr1:58058738-58058749
11	CEBPB	chr1:58087547-58087831	HepG2	liver:	n/a	chr1:58087680-58087691 chr1:58087679-58087692 chr1:58087678-58087695
12	CEBPB	chr1:58057454-58057785	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:58082349-58082548	A549	lung:	n/a	chr1:58082424-58082435 chr1:58082394-58082407
14	CEBPB	chr1:58058603-58058831	A549	lung:	n/a	chr1:58058738-58058749
15	CEBPB	chr1:58057433-58057791	IMR90	lung:	n/a	n/a
16	CTBP2	chr1:58065752-58066522	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr1:58088800-58089030	HFF	foreskin:	n/a	chr1:58088845-58088858
18	CTCF	chr1:58049651-58049679	GM13977	blood:	n/a	n/a
19	CTCF	chr1:58095315-58095551	GM12878	blood:	n/a	n/a
20	CTCF	chr1:58034861-58034980	GM10248	blood:	n/a	n/a
21	CTCF	chr1:58088760-58088910	HBMEC	blood vessel:	n/a	chr1:58088845-58088858
22	CTCF	chr1:58088820-58088970	HPF	lung:	n/a	chr1:58088845-58088858
23	CTCF	chr1:58095340-58095490	HMF	breast:	n/a	n/a
24	CTCF	chr1:58095340-58095490	SAEC	small airway:	n/a	n/a
25	CTCF	chr1:58089240-58089390	Caco-2	colon:	n/a	n/a
26	CTCF	chr1:58088800-58088950	HEK293	kidney:	n/a	chr1:58088845-58088858
27	CTCF	chr1:58095360-58095510	RPTEC	kidney:	n/a	n/a
28	CTCF	chr1:58088248-58088304	GM20000	blood:	n/a	n/a
29	CTCF	chr1:58086439-58086516	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr1:58028420-58028465	GM13976	blood:	n/a	n/a
31	CTCF	chr1:58088840-58088990	AG09309	skin:	n/a	chr1:58088845-58088858
32	CTCF	chr1:58095429-58095462	LNCaP	prostate:	n/a	n/a
33	CTCF	chr1:58095423-58095463	Medullo	brain:	n/a	n/a
34	CTCF	chr1:58088780-58088930	HCPEpiC	choroid plexus:	n/a	chr1:58088845-58088858
35	CTCF	chr1:58088810-58088852	Fibrobl	skin:	n/a	n/a
36	CTCF	chr1:58089200-58089350	HepG2	liver:	n/a	n/a
37	CTCF	chr1:58026804-58026845	LNCaP	prostate:	n/a	n/a
38	CTCF	chr1:58089400-58089550	HepG2	liver:	n/a	n/a
39	CTCF	chr1:58024340-58024490	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr1:58088800-58088950	HCM	heart:	n/a	chr1:58088845-58088858
41	CTCF	chr1:58089280-58089430	HepG2	liver:	n/a	n/a
42	CTCF	chr1:58034856-58034980	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr1:58039720-58039870	GM12866	blood:	n/a	n/a
44	CTCF	chr1:58095400-58095550	HMEC	breast:	n/a	n/a
45	CTCF	chr1:58095420-58095570	RPTEC	kidney:	n/a	n/a
46	CTCF	chr1:58073500-58073650	GM12865	blood:	n/a	n/a
47	CTCF	chr1:58088920-58089070	HRE	kidney:	n/a	n/a
48	CTCF	chr1:58088800-58088950	BJ	skin:	n/a	chr1:58088845-58088858
49	CTCF	chr1:58086360-58086510	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr1:58079120-58079270	WERI-Rb-1	eye:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:58063953-58064003	HCM	heart:	n/a
2	chr1:58063953-58064003	HCM	heart:	n/a
3	chr1:58089001-58089051	HCF	heart:	n/a
4	chr1:58089001-58089051	HNPCEpiC	eye:	n/a
5	chr1:58089001-58089051	HCT-116	colon:	n/a
6	chr1:58089001-58089051	MCF10A-Er-Src	breast:	n/a
7	chr1:58063953-58064003	IMR90	lung:	fetal
8	chr1:58089001-58089051	NH-A	brain:	n/a
9	chr1:58063953-58064003	PFSK-1	brain:	n/a
10	chr1:58063953-58064003	PANC-1	pancreas:	n/a
11	chr1:58089357-58089407	Caco-2	colon:	n/a
12	chr1:58089357-58089407	RPTEC	kidney:	n/a
13	chr1:58089001-58089051	IMR90	lung:	fetal
14	chr1:58089357-58089407	Hepatocyte	liver:	n/a
15	chr1:58089357-58089407	AoSMC	blood vessel:	n/a
16	chr1:58089357-58089407	HNPCEpiC	eye:	n/a
17	chr1:58063953-58064003	HNPCEpiC	eye:	n/a
18	chr1:58089001-58089051	A549	lung:	n/a
19	chr1:58089001-58089051	H1-hESC	embryonic stem cell:	embryo
20	chr1:58089001-58089051	AG09319	gingival:	n/a
21	chr1:58089001-58089051	GM12892	blood:	n/a
22	chr1:58089357-58089407	U87	brain:	n/a
23	chr1:58063953-58064003	A549	lung:	n/a
24	chr1:58063953-58064003	H1-hESC	embryonic stem cell:	embryo
25	chr1:58063953-58064003	HPAEpiC	pulmonary alveolar:	n/a
26	chr1:58089001-58089051	SK-N-MC	brain:	n/a
27	chr1:58089001-58089051	PANC-1	pancreas:	n/a
28	chr1:58063953-58064003	MCF10A-Er-Src	breast:	n/a
29	chr1:58089001-58089051	SK-N-SH_RA	brain:	n/a
30	chr1:58063953-58064003	HAEpiC	amniotic membrane:	n/a
31	chr1:58063953-58064003	HCPEpiC	choroid plexus:	n/a
32	chr1:58063953-58064003	SK-N-SH_RA	brain:	n/a
33	chr1:58063953-58064003	GM12892	blood:	n/a
34	chr1:58089357-58089407	BJ	skin:	n/a
35	chr1:58063953-58064003	HRCEpiC	kidney:	n/a
36	chr1:58063953-58064003	NHBE	bronchial:	n/a
37	chr1:58089001-58089051	HEEpiC	esophagus:	n/a
38	chr1:58089001-58089051	NHDF-neo	bronchial:	n/a
39	chr1:58089001-58089051	PFSK-1	brain:	n/a
40	chr1:58063953-58064003	HRPEpiC	eye:	n/a
41	chr1:58089001-58089051	CMK	blood:	n/a
42	chr1:58089001-58089051	HepG2	liver:	n/a
43	chr1:58063953-58064003	SK-N-SH	brain:	n/a
44	chr1:58089001-58089051	AG09309	skin:	n/a
45	chr1:58063953-58064003	SKMC	muscle:	n/a
46	chr1:58089001-58089051	Hepatocyte	liver:	n/a
47	chr1:58063953-58064003	ovcar-3	ovarian:	n/a
48	chr1:58089357-58089407	NB4	blood:	n/a
49	chr1:58089357-58089407	ProgFib	skin:	n/a
50	chr1:58089357-58089407	GM12892	blood:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:57972252..57973978-chr1:58083473..58085053,2	K562	blood:
2	chr1:58083604..58085124-chr19:54704799..54707163,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8B-3	chr1:58071519-58071878	NONHSAT003477

No data

Variant related genes	Relation type
RPS20P5	TF binding region
RPS20P5	CpG island
ENSG00000170889	chromatin interactions

Extended variants
information (count: 2288 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2288 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6687355	chr1:58021206-58021207	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs557637609	chr1:58021249-58021250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577282611	chr1:58021293-58021294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545935588	chr1:58021327-58021328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572138808	chr1:58021440-58021441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192748932	chr1:58021505-58021506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184591099	chr1:58021612-58021613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542585842	chr1:58021632-58021633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562353933	chr1:58021662-58021663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs72914836	chr1:58021673-58021674	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs369895122	chr1:58021703-58021704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138473329	chr1:58021717-58021718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114799894	chr1:58021743-58021744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549567548	chr1:58021773-58021774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368820720	chr1:58021785-58021786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544854470	chr1:58021817-58021818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs72676951	chr1:58021821-58021822	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs947236	chr1:58021836-58021837	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs947237	chr1:58021882-58021883	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs534577972	chr1:58021902-58021903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563062516	chr1:58021909-58021910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557940351	chr1:58021917-58021918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12564935	chr1:58021931-58021932	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs142564260	chr1:58021932-58021933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377341952	chr1:58021934-58021935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146899825	chr1:58021936-58021937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs368444430	chr1:58021953-58021954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189851869	chr1:58021959-58021960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572716828	chr1:58022019-58022020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs2805855	chr1:58022073-58022074	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs564708599	chr1:58022093-58022094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192078396	chr1:58022104-58022105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549879451	chr1:58022109-58022110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532542369	chr1:58022113-58022114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563020633	chr1:58022123-58022124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114376391	chr1:58022124-58022125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547435877	chr1:58022151-58022152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184474866	chr1:58022157-58022158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565294830	chr1:58022246-58022247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148367101	chr1:58022250-58022251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2204377	chr1:58022264-58022265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565851047	chr1:58022304-58022305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141586114	chr1:58022309-58022310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189261895	chr1:58022340-58022341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530104756	chr1:58022382-58022383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556723984	chr1:58022421-58022422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377356711	chr1:58022434-58022435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370226828	chr1:58022530-58022531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs386631494	chr1:58022533-58022534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535919041	chr1:58022535-58022536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
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
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
Meckel-Gruber syndrome	21572526	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	16616336	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	19490664	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Developmental delay	21147756	CNVD

Chromatin state (count:437 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:58020200-58024000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:58024000-58024200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:58037000-58039200	Weak transcription	Stomach Mucosa	stomach
4	chr1:58037400-58038200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr1:58038200-58042000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr1:58039200-58046800	Enhancers	Stomach Mucosa	stomach
7	chr1:58040600-58040800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr1:58041000-58042000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr1:58041400-58041600	Enhancers	Small Intestine	intestine
10	chr1:58041600-58042600	Weak transcription	Small Intestine	intestine
11	chr1:58042000-58042800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr1:58042000-58043000	Enhancers	Fetal Intestine Small	intestine
13	chr1:58042000-58044200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr1:58042000-58044800	Enhancers	Duodenum Mucosa	Duodenum
15	chr1:58042200-58042600	Enhancers	Fetal Intestine Large	intestine
16	chr1:58042600-58043400	Enhancers	Small Intestine	intestine
17	chr1:58042600-58043600	Weak transcription	Fetal Intestine Large	intestine
18	chr1:58042800-58051600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr1:58043000-58043800	Weak transcription	Fetal Intestine Small	intestine
20	chr1:58043800-58044000	Enhancers	Fetal Intestine Large	intestine
21	chr1:58043800-58044200	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr1:58043800-58044800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr1:58044000-58044200	Enhancers	Fetal Intestine Small	intestine
24	chr1:58044200-58045000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr1:58044400-58044800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr1:58044400-58045200	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr1:58046800-58049200	Weak transcription	Stomach Mucosa	stomach
28	chr1:58048400-58048600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr1:58048400-58049000	Enhancers	H9 Cell Line	embryonic stem cell
30	chr1:58048600-58051800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:58049000-58049600	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr1:58049600-58049800	Enhancers	H9 Cell Line	embryonic stem cell
33	chr1:58051200-58052200	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr1:58051600-58054000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr1:58051800-58053000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr1:58052000-58061200	Weak transcription	Stomach Mucosa	stomach
37	chr1:58052200-58052600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr1:58052600-58053400	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr1:58052600-58053600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr1:58053000-58058000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr1:58053400-58057200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr1:58053600-58062200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr1:58054000-58056800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr1:58056400-58058200	Enhancers	NHEK	skin
45	chr1:58056400-58058400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr1:58056400-58062200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr1:58056600-58058600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr1:58056800-58057600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr1:58056800-58058200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr1:58056800-58058200	Enhancers	HMEC	breast

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