Variant report

Variant	nsv428558
Chromosome Location	chr10:57383256-57524282
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	ATF1	chr10:57507840-57507889	K562	blood:	n/a	n/a
2	ATF2	chr10:57401358-57401696	GM12878	blood:	n/a	n/a
3	BACH1	chr10:57390168-57391406	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr10:57518775-57519069	GM12878	blood:	n/a	chr10:57518959-57518970
5	BATF	chr10:57518771-57519015	GM12878	blood:	n/a	chr10:57518959-57518970
6	BATF	chr10:57401376-57401698	GM12878	blood:	n/a	n/a
7	BCL11A	chr10:57401463-57401688	GM12878	blood:	n/a	chr10:57401610-57401619
8	BCL11A	chr10:57518766-57519117	GM12878	blood:	n/a	n/a
9	BRCA1	chr10:57428118-57428215	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr10:57432975-57433057	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr10:57394713-57394811	K562	blood:	n/a	chr10:57394769-57394780
12	CEBPB	chr10:57483653-57483898	IMR90	lung:	n/a	chr10:57483842-57483853
13	CEBPB	chr10:57394596-57394911	HepG2	liver:	n/a	chr10:57394769-57394780
14	CEBPB	chr10:57394606-57394927	IMR90	lung:	n/a	chr10:57394769-57394780
15	CEBPB	chr10:57493945-57494290	A549	lung:	n/a	chr10:57494109-57494118 chr10:57494109-57494118 chr10:57494107-57494118 chr10:57494109-57494118
16	CEBPB	chr10:57483591-57483950	A549	lung:	n/a	chr10:57483842-57483853
17	CEBPB	chr10:57507027-57507291	HepG2	liver:	n/a	n/a
18	CEBPB	chr10:57512468-57512713	K562	blood:	n/a	n/a
19	CEBPB	chr10:57400223-57400290	HepG2	liver:	n/a	n/a
20	CEBPB	chr10:57506975-57507448	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr10:57494052-57494186	H1-hESC	embryonic stem cell:	n/a	chr10:57494109-57494118 chr10:57494109-57494118 chr10:57494107-57494118 chr10:57494109-57494118
22	CEBPB	chr10:57387967-57388151	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr10:57493973-57494246	HepG2	liver:	n/a	chr10:57494109-57494118 chr10:57494109-57494118 chr10:57494107-57494118 chr10:57494109-57494118
24	CEBPB	chr10:57512602-57512721	A549	lung:	n/a	n/a
25	CEBPB	chr10:57495562-57495924	HepG2	liver:	n/a	n/a
26	CEBPB	chr10:57394611-57394911	A549	lung:	n/a	chr10:57394769-57394780
27	CEBPB	chr10:57391045-57391162	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr10:57389489-57389813	H1-hESC	embryonic stem cell:	n/a	chr10:57389598-57389611
29	CEBPB	chr10:57493950-57494263	IMR90	lung:	n/a	chr10:57494109-57494118 chr10:57494109-57494118 chr10:57494107-57494118 chr10:57494109-57494118
30	CEBPB	chr10:57483521-57483980	HepG2	liver:	n/a	chr10:57483842-57483853
31	CEBPB	chr10:57483522-57483901	H1-hESC	embryonic stem cell:	n/a	chr10:57483842-57483853
32	CEBPZ	chr10:57480976-57481001	HepG2	liver:	n/a	n/a
33	CHD1	chr10:57390842-57391180	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr10:57388207-57388403	H1-hESC	embryonic stem cell:	n/a	chr10:57388308-57388318
35	CHD2	chr10:57390961-57391387	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr10:57390736-57391226	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr10:57390766-57391343	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr10:57390854-57391220	GM12878	blood:	n/a	n/a
39	CREB1	chr10:57390898-57391322	A549	lung:	n/a	n/a
40	CTBP2	chr10:57390282-57391476	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr10:57389360-57389510	GM12878	blood:	n/a	n/a
42	CTCF	chr10:57391100-57391250	HPF	lung:	n/a	chr10:57391216-57391229 chr10:57391108-57391121 chr10:57391240-57391248
43	CTCF	chr10:57388066-57388142	NHEK	skin:	n/a	chr10:57388081-57388094 chr10:57388081-57388094
44	CTCF	chr10:57391080-57391230	SK-N-SH_RA	brain:	n/a	chr10:57391216-57391229 chr10:57391108-57391121
45	CTCF	chr10:57391057-57391280	GM10266	blood:	n/a	chr10:57391216-57391229 chr10:57391108-57391121 chr10:57391240-57391248
46	CTCF	chr10:57428207-57428378	HepG2	liver:	n/a	n/a
47	CTCF	chr10:57500620-57500770	GM12865	blood:	n/a	n/a
48	CTCF	chr10:57391103-57391202	K562	blood:	n/a	chr10:57391108-57391121
49	CTCF	chr10:57390916-57391473	MCF-7	breast:	n/a	chr10:57391216-57391229 chr10:57391108-57391121 chr10:57391240-57391248
50	CTCF	chr10:57391080-57391230	HVMF	connective:	n/a	chr10:57391216-57391229 chr10:57391108-57391121

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:57390306-57390356	SK-N-SH	brain:	n/a
2	chr10:57390306-57390356	SK-N-SH	brain:	n/a
3	chr10:57391055-57391105	Caco-2	colon:	n/a
4	chr10:57387978-57388028	AG10803	skin:	n/a
5	chr10:57448681-57448731	HCM	heart:	n/a
6	chr10:57387636-57387686	SK-N-SH_RA	brain:	n/a
7	chr10:57388069-57388119	LNCaP	prostate:	n/a
8	chr10:57389301-57389351	PANC-1	pancreas:	n/a
9	chr10:57448681-57448731	HPAEpiC	pulmonary alveolar:	n/a
10	chr10:57391271-57391321	Hela-S3	cervix:	n/a
11	chr10:57390536-57390586	Caco-2	colon:	n/a
12	chr10:57388341-57388391	U87	brain:	n/a
13	chr10:57391055-57391105	SK-N-SH_RA	brain:	n/a
14	chr10:57391055-57391105	GM19239	blood:	n/a
15	chr10:57394513-57394563	HL-60	blood:	n/a
16	chr10:57390872-57390922	Hepatocyte	liver:	n/a
17	chr10:57390047-57390097	SK-N-SH_RA	brain:	n/a
18	chr10:57387715-57387765	AoSMC	blood vessel:	n/a
19	chr10:57390872-57390922	NHDF-neo	bronchial:	n/a
20	chr10:57388283-57388333	HMEC	breast:	n/a
21	chr10:57390536-57390586	Hela-S3	cervix:	n/a
22	chr10:57394513-57394563	H1-hESC	embryonic stem cell:	embryo
23	chr10:57394513-57394563	HEK293	kidney:	embryo
24	chr10:57390704-57390754	K562	blood:	n/a
25	chr10:57390047-57390097	HCPEpiC	choroid plexus:	n/a
26	chr10:57387511-57387561	HEK293	kidney:	embryo
27	chr10:57388341-57388391	BE2_C	brain:	n/a
28	chr10:57388283-57388333	AG04449	skin:	fetal
29	chr10:57391055-57391105	HNPCEpiC	eye:	n/a
30	chr10:57388283-57388333	GM12891	blood:	n/a
31	chr10:57448681-57448731	HRE	kidney:	n/a
32	chr10:57389906-57389956	A549	lung:	n/a
33	chr10:57390047-57390097	SAEC	small airway:	n/a
34	chr10:57390872-57390922	K562	blood:	n/a
35	chr10:57390536-57390586	BE2_C	brain:	n/a
36	chr10:57387715-57387765	GM12878	blood:	n/a
37	chr10:57388341-57388391	Hepatocyte	liver:	n/a
38	chr10:57391271-57391321	IMR90	lung:	fetal
39	chr10:57390872-57390922	HRPEpiC	eye:	n/a
40	chr10:57390306-57390356	SAEC	small airway:	n/a
41	chr10:57389779-57389829	H1-hESC	embryonic stem cell:	embryo
42	chr10:57387978-57388028	NT2-D1	testis:	n/a
43	chr10:57390704-57390754	ovcar-3	ovarian:	n/a
44	chr10:57390872-57390922	HAEpiC	amniotic membrane:	n/a
45	chr10:57389906-57389956	PANC-1	pancreas:	n/a
46	chr10:57390872-57390922	HNPCEpiC	eye:	n/a
47	chr10:57387511-57387561	HRCEpiC	kidney:	n/a
48	chr10:57448681-57448731	RPTEC	kidney:	n/a
49	chr10:57389301-57389351	AG04450	lung:	fetal
50	chr10:57390047-57390097	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:57047149..57047763-chr10:57389634..57390254,2	MCF-7	breast:
2	chr10:57409945..57412041-chr10:57413337..57415798,2	K562	blood:
3	chr10:57409945..57412041-chr10:57413337..57415798,2	K562	blood:
4	chr10:57475413..57477793-chr10:57482048..57484055,2	K562	blood:
5	chr10:57046815..57047629-chr10:57390561..57391169,3	MCF-7	breast:
6	chr10:57475413..57477793-chr10:57482048..57484055,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTRNR2L5-5	chr10:57506311-57506668	NONHSAT013465

Variant related genes	Relation type
PCDH15	TF binding region
ENSG00000270541	TF binding region
GAPDHP21	TF binding region
PCDH15	CpG island
ENSG00000270541	CpG island
GAPDHP21	CpG island

Extended variants
information (count: 1135 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1135 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182998858	chr10:57383267-57383268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs368545282	chr10:57383321-57383322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574566138	chr10:57383331-57383332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540357398	chr10:57383386-57383387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs187334390	chr10:57383396-57383397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576787142	chr10:57383408-57383409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545335859	chr10:57383432-57383433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192686727	chr10:57383469-57383470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374192536	chr10:57383477-57383478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185500090	chr10:57383500-57383501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542643361	chr10:57383564-57383565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574119268	chr10:57383684-57383685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375382829	chr10:57383688-57383689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544392275	chr10:57383707-57383708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541126105	chr10:57383751-57383752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187613508	chr10:57383758-57383759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530115031	chr10:57383763-57383764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs111385032	chr10:57383799-57383800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2463944	chr10:57383801-57383802	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs192579432	chr10:57383813-57383814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552334555	chr10:57383844-57383845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184859287	chr10:57383879-57383880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537781646	chr10:57383896-57383897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554782456	chr10:57383933-57383934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs376407687	chr10:57383948-57383949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568283835	chr10:57383973-57383974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369741376	chr10:57383995-57383996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533837385	chr10:57384005-57384006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs386744058	chr10:57384013-57384014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs2461903	chr10:57384014-57384015	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs545781701	chr10:57384022-57384023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544988990	chr10:57384061-57384062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565060706	chr10:57384116-57384117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112045447	chr10:57384125-57384126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112779047	chr10:57384151-57384152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115298961	chr10:57384171-57384172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs34849218	chr10:57384230-57384231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs386508292	chr10:57384252-57384253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs80325329	chr10:57384322-57384323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs561120781	chr10:57384324-57384325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574709520	chr10:57384363-57384364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540291802	chr10:57384390-57384391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560630780	chr10:57384412-57384413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs117346106	chr10:57384449-57384450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs2257031	chr10:57384496-57384497	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs549841129	chr10:57384514-57384515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2461904	chr10:57384535-57384536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2463945	chr10:57384569-57384570	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs80303122	chr10:57384580-57384581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184720645	chr10:57384628-57384629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Obesity	21956041	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Glioblastoma multiforme	22286061	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	20858243	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
small cell lung cancer	17426248	CNVD

Chromatin state (count:521 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:57374000-57386000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr10:57380000-57387000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr10:57381400-57385400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr10:57381400-57387200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr10:57384200-57387000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr10:57385200-57385400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
7	chr10:57385200-57385600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
8	chr10:57385200-57385800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr10:57385600-57385800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
10	chr10:57385600-57385800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
11	chr10:57385800-57386800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr10:57386000-57386200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr10:57386200-57386600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr10:57386600-57386800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr10:57386800-57387000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr10:57386800-57387000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
17	chr10:57386800-57387000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
18	chr10:57386800-57387200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr10:57386800-57388600	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr10:57386800-57388800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
21	chr10:57386800-57388800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
22	chr10:57387000-57387200	Flanking Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr10:57387000-57387200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr10:57387000-57387200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
25	chr10:57387000-57387200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
26	chr10:57387000-57387200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
27	chr10:57387000-57387200	Active TSS	Fetal Kidney	kidney
28	chr10:57387000-57387600	Active TSS	H9 Cell Line	embryonic stem cell
29	chr10:57387000-57388600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
30	chr10:57387000-57388600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
31	chr10:57387000-57388600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr10:57387000-57388600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr10:57387000-57388800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
34	chr10:57387000-57388800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
35	chr10:57387200-57387400	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr10:57387200-57387400	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr10:57387200-57387400	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr10:57387200-57387400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr10:57387200-57387400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
40	chr10:57387200-57387400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr10:57387200-57387400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr10:57387200-57387400	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
43	chr10:57387200-57387400	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
44	chr10:57387200-57387400	Active TSS	Brain Hippocampus Middle	brain
45	chr10:57387200-57387400	Bivalent Enhancer	Fetal Brain Male	brain
46	chr10:57387200-57387400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
47	chr10:57387200-57387400	Bivalent Enhancer	Fetal Muscle Leg	muscle
48	chr10:57387200-57387600	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr10:57387200-57387600	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
50	chr10:57387200-57387800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast

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