Variant report

Variant	nsv895484
Chromosome Location	chr10:57323162-57389340
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	BHLHE40	chr10:57359114-57359287	HepG2	liver:	n/a	n/a
2	BRCA1	chr10:57358162-57358227	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr10:57361944-57361962	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr10:57387967-57388151	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr10:57324941-57325103	HepG2	liver:	n/a	n/a
6	CHD1	chr10:57388207-57388403	H1-hESC	embryonic stem cell:	n/a	chr10:57388308-57388318
7	CTCF	chr10:57388040-57388190	SK-N-SH_RA	brain:	n/a	chr10:57388081-57388094 chr10:57388081-57388094
8	CTCF	chr10:57387755-57388826	SK-N-SH	brain:	n/a	chr10:57388081-57388094 chr10:57388081-57388094
9	CTCF	chr10:57388011-57388146	ProgFib	skin:	n/a	chr10:57388081-57388094 chr10:57388081-57388094
10	CTCF	chr10:57388013-57388193	MCF-7	breast:	n/a	chr10:57388081-57388094 chr10:57388081-57388094
11	CTCF	chr10:57388072-57388169	MCF-7	breast:	n/a	chr10:57388081-57388094 chr10:57388081-57388094
12	CTCF	chr10:57388312-57388489	A549	lung:	n/a	n/a
13	CTCF	chr10:57383649-57383745	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr10:57388264-57388490	MCF-7	breast:	n/a	n/a
15	CTCF	chr10:57388398-57388443	NHEK	skin:	n/a	n/a
16	CTCF	chr10:57375308-57375398	GM13977	blood:	n/a	n/a
17	CTCF	chr10:57388327-57388440	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr10:57388362-57388436	ProgFib	skin:	n/a	n/a
19	CTCF	chr10:57361800-57361950	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr10:57383653-57383698	MCF-7	breast:	n/a	n/a
21	CTCF	chr10:57383642-57383730	MCF-7	breast:	n/a	n/a
22	CTCF	chr10:57377306-57377393	GM13976	blood:	n/a	n/a
23	CTCF	chr10:57383574-57383853	A549	lung:	n/a	n/a
24	CTCF	chr10:57359985-57360046	GM10266	blood:	n/a	n/a
25	CTCF	chr10:57388000-57388150	SK-N-SH_RA	brain:	n/a	chr10:57388081-57388094 chr10:57388081-57388094
26	CTCF	chr10:57377009-57377064	GM10248	blood:	n/a	n/a
27	CTCF	chr10:57389220-57389370	GM12872	blood:	n/a	n/a
28	CTCF	chr10:57361772-57361783	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr10:57383597-57383746	A549	lung:	n/a	n/a
30	CTCF	chr10:57361786-57361816	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr10:57388340-57388490	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr10:57388278-57388500	Gliobla	brain:	n/a	n/a
33	CTCF	chr10:57361763-57361846	MCF-7	breast:	n/a	n/a
34	CTCF	chr10:57357723-57357806	GM20000	blood:	n/a	n/a
35	CTCF	chr10:57388000-57388150	HRE	kidney:	n/a	chr10:57388081-57388094 chr10:57388081-57388094
36	CTCF	chr10:57387969-57388253	Gliobla	brain:	n/a	chr10:57388081-57388094 chr10:57388081-57388094
37	CTCF	chr10:57388100-57388250	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr10:57388015-57388201	A549	lung:	n/a	chr10:57388081-57388094 chr10:57388081-57388094
39	CTCF	chr10:57388000-57388150	HBMEC	blood vessel:	n/a	chr10:57388081-57388094 chr10:57388081-57388094
40	CTCF	chr10:57388040-57388190	HRPEpiC	eye:	n/a	chr10:57388081-57388094 chr10:57388081-57388094
41	CTCF	chr10:57388060-57388210	BE2_C	brain:	n/a	chr10:57388081-57388094 chr10:57388081-57388094
42	CTCF	chr10:57389299-57389997	A549	lung:	n/a	chr10:57389621-57389634
43	CTCF	chr10:57389203-57391556	SK-N-SH	brain:	n/a	chr10:57391216-57391229 chr10:57391108-57391121 chr10:57389621-57389634 chr10:57391240-57391248
44	CTCF	chr10:57388370-57388442	GM12891	blood:	n/a	n/a
45	CTCF	chr10:57383570-57383743	A549	lung:	n/a	n/a
46	CTCF	chr10:57388259-57388262	MCF-7	breast:	n/a	n/a
47	CTCF	chr10:57388020-57388170	HAc	cerebellar:	n/a	chr10:57388081-57388094 chr10:57388081-57388094
48	CTCF	chr10:57388072-57388157	MCF-7	breast:	n/a	chr10:57388081-57388094 chr10:57388081-57388094
49	CTCF	chr10:57388220-57388370	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr10:57388001-57388236	H1-hESC	embryonic stem cell:	n/a	chr10:57388081-57388094 chr10:57388081-57388094

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:57388283-57388333	HepG2	liver:	n/a
2	chr10:57387702-57387752	HRE	kidney:	n/a
3	chr10:57388283-57388333	HepG2	liver:	n/a
4	chr10:57387702-57387752	HRE	kidney:	n/a
5	chr10:57387978-57388028	SK-N-SH_RA	brain:	n/a
6	chr10:57388069-57388119	HCT-116	colon:	n/a
7	chr10:57387715-57387765	AG10803	skin:	n/a
8	chr10:57387636-57387686	GM19239	blood:	n/a
9	chr10:57388283-57388333	ECC-1	luminal epithelium:	n/a
10	chr10:57387715-57387765	H1-hESC	embryonic stem cell:	embryo
11	chr10:57387702-57387752	HL-60	blood:	n/a
12	chr10:57388283-57388333	Hela-S3	cervix:	n/a
13	chr10:57388283-57388333	SK-N-MC	brain:	n/a
14	chr10:57389301-57389351	SKMC	muscle:	n/a
15	chr10:57388402-57388452	HMEC	breast:	n/a
16	chr10:57387636-57387686	ovcar-3	ovarian:	n/a
17	chr10:57361794-57361844	MCF-7	breast:	n/a
18	chr10:57387636-57387686	HEK293	kidney:	embryo
19	chr10:57361919-57361969	HepG2	liver:	n/a
20	chr10:57387978-57388028	NB4	blood:	n/a
21	chr10:57388069-57388119	K562	blood:	n/a
22	chr10:57387636-57387686	PANC-1	pancreas:	n/a
23	chr10:57387636-57387686	PFSK-1	brain:	n/a
24	chr10:57389301-57389351	AG09319	gingival:	n/a
25	chr10:57388283-57388333	GM06990	blood:	n/a
26	chr10:57388069-57388119	PFSK-1	brain:	n/a
27	chr10:57387702-57387752	GM12892	blood:	n/a
28	chr10:57388069-57388119	HAEpiC	amniotic membrane:	n/a
29	chr10:57389301-57389351	GM12891	blood:	n/a
30	chr10:57388341-57388391	ECC-1	luminal epithelium:	n/a
31	chr10:57388283-57388333	ProgFib	skin:	n/a
32	chr10:57387702-57387752	MCF-7	breast:	n/a
33	chr10:57387511-57387561	AG04450	lung:	fetal
34	chr10:57361919-57361969	AG04450	lung:	fetal
35	chr10:57387702-57387752	U87	brain:	n/a
36	chr10:57387511-57387561	MCF10A-Er-Src	breast:	n/a
37	chr10:57361794-57361844	HepG2	liver:	n/a
38	chr10:57388402-57388452	AoSMC	blood vessel:	n/a
39	chr10:57387702-57387752	RPTEC	kidney:	n/a
40	chr10:57387702-57387752	T-47D	breast:	n/a
41	chr10:57387636-57387686	ProgFib	skin:	n/a
42	chr10:57388069-57388119	PrEC	prostate:	n/a
43	chr10:57388341-57388391	GM12891	blood:	n/a
44	chr10:57388283-57388333	NB4	blood:	n/a
45	chr10:57361919-57361969	AoSMC	blood vessel:	n/a
46	chr10:57387511-57387561	HL-60	blood:	n/a
47	chr10:57388283-57388333	A549	lung:	n/a
48	chr10:57361794-57361844	HPAEpiC	pulmonary alveolar:	n/a
49	chr10:57361794-57361844	HNPCEpiC	eye:	n/a
50	chr10:57387715-57387765	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:57342122..57342664-chr13:103425291..103426132,2	HCT-116	colon:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZWINT-4	chr10:57356873-57356993	ENSG00000236744.2
2	lnc-ZWINT-4	chr10:57335410-57335471	ENSG00000236744.2
3	lnc-ZWINT-4	chr10:57335410-57335471	ENSG00000236744.1
4	lnc-ZWINT-4	chr10:57356873-57356993	ENSG00000236744.1

Variant related genes	Relation type
ENSG00000238355	TF binding region
ENSG00000236744	TF binding region
PCDH15	TF binding region
MTRNR2L5	TF binding region
ENSG00000238355	CpG island
ENSG00000236744	CpG island
PCDH15	CpG island
MTRNR2L5	CpG island
ENSG00000151287	chromatin interactions

Extended variants
information (count: 771 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:771 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12264767	chr10:57323162-57323163	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs551369549	chr10:57323200-57323201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573627932	chr10:57323201-57323202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs61851706	chr10:57323228-57323229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs374665465	chr10:57323237-57323238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143195362	chr10:57323273-57323274	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs189099990	chr10:57323340-57323341	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs372187236	chr10:57323341-57323342	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs571290755	chr10:57323348-57323349	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs536626538	chr10:57323404-57323405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs181484025	chr10:57323422-57323423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs369706614	chr10:57323430-57323431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs567244112	chr10:57323493-57323494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs541575666	chr10:57323509-57323510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs536295918	chr10:57323530-57323531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555549204	chr10:57323539-57323540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571772659	chr10:57324946-57324947	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs374684773	chr10:57325013-57325014	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs115738852	chr10:57325017-57325018	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs557609373	chr10:57325032-57325033	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs567586213	chr10:57325038-57325039	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs148570590	chr10:57325040-57325041	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs190586838	chr10:57325053-57325054	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs553550969	chr10:57325063-57325064	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs145434171	chr10:57325099-57325100	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs538037929	chr10:57325685-57325686	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs4275525	chr10:57325716-57325717	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs574397788	chr10:57325737-57325738	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs540099267	chr10:57325745-57325746	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs192163471	chr10:57325761-57325762	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs559735324	chr10:57325774-57325775	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs78286984	chr10:57325797-57325798	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs545612682	chr10:57325814-57325815	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs184224248	chr10:57325843-57325844	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs151211883	chr10:57325862-57325863	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs531057015	chr10:57325876-57325877	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs551154798	chr10:57325904-57325905	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs539414618	chr10:57325916-57325917	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs561284012	chr10:57326010-57326011	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs530433049	chr10:57326022-57326023	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs375299081	chr10:57326024-57326025	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs188556030	chr10:57326036-57326037	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs564272936	chr10:57326037-57326038	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs539311706	chr10:57327068-57327069	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs556140432	chr10:57327092-57327093	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs575919411	chr10:57327179-57327180	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs567268602	chr10:57327194-57327195	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs4642984	chr10:57327227-57327228	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs555485868	chr10:57327237-57327238	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs575127578	chr10:57327251-57327252	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:57322200-57323600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr10:57341600-57342000	Enhancers	Gastric	stomach
3	chr10:57352000-57352400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr10:57361200-57361400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr10:57361400-57362000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr10:57361400-57362200	Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr10:57361400-57362200	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr10:57361400-57362200	Active TSS	HUES64 Cell Line	embryonic stem cell
9	chr10:57361400-57362200	Active TSS	iPS-20b Cell Line	embryonic stem cell
10	chr10:57361400-57362200	Active TSS	Fetal Brain Female	brain
11	chr10:57361600-57361800	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
12	chr10:57361600-57362000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr10:57361600-57362000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr10:57361600-57362000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr10:57361600-57362000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr10:57361600-57362000	Active TSS	Brain Inferior Temporal Lobe	brain
17	chr10:57361600-57362000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
18	chr10:57361600-57362000	Enhancers	Lung	lung
19	chr10:57361600-57362000	Enhancers	Pancreas	Pancrea
20	chr10:57361600-57362000	Active TSS	HMEC	breast
21	chr10:57361600-57362200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
22	chr10:57361600-57362200	Active TSS	H1 Cell Line	embryonic stem cell
23	chr10:57361600-57362200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr10:57361600-57362200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr10:57361600-57362200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr10:57361600-57362200	Active TSS	H9 Cell Line	embryonic stem cell
27	chr10:57361600-57362200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr10:57361600-57362200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr10:57361600-57362200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr10:57361600-57362200	Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr10:57361600-57362200	Active TSS	iPS-15b Cell Line	embryonic stem cell
32	chr10:57361600-57362200	Active TSS	iPS-18 Cell Line	embryonic stem cell
33	chr10:57361600-57362200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr10:57361600-57362200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr10:57361600-57362200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
36	chr10:57361600-57362200	Active TSS	Breast Myoepithelial Primary Cells	Breast
37	chr10:57361600-57362200	Active TSS	Primary hematopoietic stem cells	blood
38	chr10:57361600-57362200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr10:57361600-57362200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr10:57361600-57362200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr10:57361600-57362200	Active TSS	Brain Anterior Caudate	brain
42	chr10:57361600-57362200	Active TSS	Brain Germinal Matrix	brain
43	chr10:57361600-57362200	Active TSS	Brain Hippocampus Middle	brain
44	chr10:57361600-57362200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
45	chr10:57361600-57362200	Active TSS	Fetal Kidney	kidney
46	chr10:57361600-57362200	Active TSS	Fetal Stomach	stomach
47	chr10:57361600-57362200	Active TSS	Gastric	stomach
48	chr10:57361800-57362200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr10:57361800-57362200	Active TSS	Cortex derived primary cultured neurospheres	brain
50	chr10:57362000-57362200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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