Variant report

Variant	nsv1048148
Chromosome Location	chr10:57359414-57498605
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	ATF2	chr10:57401358-57401696	GM12878	blood:	n/a	n/a
2	BACH1	chr10:57390168-57391406	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr10:57401376-57401698	GM12878	blood:	n/a	n/a
4	BCL11A	chr10:57401463-57401688	GM12878	blood:	n/a	chr10:57401610-57401619
5	BRCA1	chr10:57428118-57428215	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr10:57432975-57433057	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr10:57394606-57394927	IMR90	lung:	n/a	chr10:57394769-57394780
8	CEBPB	chr10:57493973-57494246	HepG2	liver:	n/a	chr10:57494109-57494118 chr10:57494109-57494118 chr10:57494107-57494118 chr10:57494109-57494118
9	CEBPB	chr10:57394596-57394911	HepG2	liver:	n/a	chr10:57394769-57394780
10	CEBPB	chr10:57394611-57394911	A549	lung:	n/a	chr10:57394769-57394780
11	CEBPB	chr10:57387967-57388151	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr10:57483591-57483950	A549	lung:	n/a	chr10:57483842-57483853
13	CEBPB	chr10:57361944-57361962	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr10:57483653-57483898	IMR90	lung:	n/a	chr10:57483842-57483853
15	CEBPB	chr10:57483522-57483901	H1-hESC	embryonic stem cell:	n/a	chr10:57483842-57483853
16	CEBPB	chr10:57391045-57391162	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr10:57389489-57389813	H1-hESC	embryonic stem cell:	n/a	chr10:57389598-57389611
18	CEBPB	chr10:57483521-57483980	HepG2	liver:	n/a	chr10:57483842-57483853
19	CEBPB	chr10:57394713-57394811	K562	blood:	n/a	chr10:57394769-57394780
20	CEBPB	chr10:57494052-57494186	H1-hESC	embryonic stem cell:	n/a	chr10:57494109-57494118 chr10:57494109-57494118 chr10:57494107-57494118 chr10:57494109-57494118
21	CEBPB	chr10:57493945-57494290	A549	lung:	n/a	chr10:57494109-57494118 chr10:57494109-57494118 chr10:57494107-57494118 chr10:57494109-57494118
22	CEBPB	chr10:57493950-57494263	IMR90	lung:	n/a	chr10:57494109-57494118 chr10:57494109-57494118 chr10:57494107-57494118 chr10:57494109-57494118
23	CEBPB	chr10:57495562-57495924	HepG2	liver:	n/a	n/a
24	CEBPB	chr10:57400223-57400290	HepG2	liver:	n/a	n/a
25	CEBPZ	chr10:57480976-57481001	HepG2	liver:	n/a	n/a
26	CHD1	chr10:57388207-57388403	H1-hESC	embryonic stem cell:	n/a	chr10:57388308-57388318
27	CHD1	chr10:57390842-57391180	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr10:57390961-57391387	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr10:57390854-57391220	GM12878	blood:	n/a	n/a
30	CREB1	chr10:57390766-57391343	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr10:57390736-57391226	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr10:57390898-57391322	A549	lung:	n/a	n/a
33	CTBP2	chr10:57390282-57391476	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr10:57389580-57389730	HEK293	kidney:	n/a	chr10:57389621-57389634
35	CTCF	chr10:57390976-57391337	A549	lung:	n/a	chr10:57391216-57391229 chr10:57391108-57391121 chr10:57391240-57391248
36	CTCF	chr10:57428160-57428310	SAEC	small airway:	n/a	n/a
37	CTCF	chr10:57388313-57388473	MCF-7	breast:	n/a	n/a
38	CTCF	chr10:57428220-57428370	HMEC	breast:	n/a	n/a
39	CTCF	chr10:57428200-57428350	GM12865	blood:	n/a	n/a
40	CTCF	chr10:57391120-57391270	MCF-7	breast:	n/a	chr10:57391216-57391229 chr10:57391240-57391248
41	CTCF	chr10:57389613-57389647	Hela-S3	cervix:	n/a	chr10:57389621-57389634
42	CTCF	chr10:57389299-57389997	A549	lung:	n/a	chr10:57389621-57389634
43	CTCF	chr10:57428119-57428414	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr10:57391060-57391210	HBMEC	blood vessel:	n/a	chr10:57391108-57391121
45	CTCF	chr10:57391072-57391344	HepG2	liver:	n/a	chr10:57391216-57391229 chr10:57391108-57391121 chr10:57391240-57391248
46	CTCF	chr10:57391080-57391230	HepG2	liver:	n/a	chr10:57391216-57391229 chr10:57391108-57391121
47	CTCF	chr10:57427940-57428090	GM12866	blood:	n/a	n/a
48	CTCF	chr10:57389540-57389690	GM12875	blood:	n/a	chr10:57389621-57389634
49	CTCF	chr10:57389540-57389690	NHDF-neo	bronchial:	n/a	chr10:57389621-57389634
50	CTCF	chr10:57428120-57428270	HPAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:57387636-57387686	PrEC	prostate:	n/a
2	chr10:57387636-57387686	PrEC	prostate:	n/a
3	chr10:57361919-57361969	GM12892	blood:	n/a
4	chr10:57387702-57387752	NHDF-neo	bronchial:	n/a
5	chr10:57387636-57387686	SK-N-SH_RA	brain:	n/a
6	chr10:57448681-57448731	HPAEpiC	pulmonary alveolar:	n/a
7	chr10:57394513-57394563	HEK293	kidney:	embryo
8	chr10:57391271-57391321	Jurkat	blood:	n/a
9	chr10:57387715-57387765	AG10803	skin:	n/a
10	chr10:57387702-57387752	MCF10A-Er-Src	breast:	n/a
11	chr10:57391271-57391321	H1-hESC	embryonic stem cell:	embryo
12	chr10:57361794-57361844	U87	brain:	n/a
13	chr10:57388341-57388391	MCF10A-Er-Src	breast:	n/a
14	chr10:57387702-57387752	GM19239	blood:	n/a
15	chr10:57387702-57387752	AG10803	skin:	n/a
16	chr10:57387715-57387765	GM12891	blood:	n/a
17	chr10:57389676-57389726	U87	brain:	n/a
18	chr10:57361794-57361844	Hela-S3	cervix:	n/a
19	chr10:57387978-57388028	HCPEpiC	choroid plexus:	n/a
20	chr10:57389676-57389726	AG04450	lung:	fetal
21	chr10:57361794-57361844	HMEC	breast:	n/a
22	chr10:57387511-57387561	SAEC	small airway:	n/a
23	chr10:57389676-57389726	SKMC	muscle:	n/a
24	chr10:57388402-57388452	SK-N-SH	brain:	n/a
25	chr10:57361794-57361844	AG04450	lung:	fetal
26	chr10:57387978-57388028	Hepatocyte	liver:	n/a
27	chr10:57387702-57387752	Hela-S3	cervix:	n/a
28	chr10:57390704-57390754	K562	blood:	n/a
29	chr10:57389906-57389956	SK-N-SH	brain:	n/a
30	chr10:57391271-57391321	PANC-1	pancreas:	n/a
31	chr10:57387978-57388028	HMEC	breast:	n/a
32	chr10:57389779-57389829	GM12892	blood:	n/a
33	chr10:57387511-57387561	HEK293	kidney:	embryo
34	chr10:57390536-57390586	NT2-D1	testis:	n/a
35	chr10:57391271-57391321	AG10803	skin:	n/a
36	chr10:57387636-57387686	SK-N-SH	brain:	n/a
37	chr10:57389906-57389956	HPAEpiC	pulmonary alveolar:	n/a
38	chr10:57387715-57387765	GM06990	blood:	n/a
39	chr10:57361919-57361969	HCPEpiC	choroid plexus:	n/a
40	chr10:57361794-57361844	HPAEpiC	pulmonary alveolar:	n/a
41	chr10:57394513-57394563	HCF	heart:	n/a
42	chr10:57389906-57389956	PFSK-1	brain:	n/a
43	chr10:57390536-57390586	BE2_C	brain:	n/a
44	chr10:57387978-57388028	BJ	skin:	n/a
45	chr10:57387702-57387752	HRPEpiC	eye:	n/a
46	chr10:57390047-57390097	RPTEC	kidney:	n/a
47	chr10:57389676-57389726	LNCaP	prostate:	n/a
48	chr10:57390872-57390922	HCF	heart:	n/a
49	chr10:57389676-57389726	NHBE	bronchial:	n/a
50	chr10:57389301-57389351	Hepatocyte	liver:	n/a

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

Variant related genes	Relation type
ENSG00000236744	TF binding region
GAPDHP21	TF binding region
PCDH15	TF binding region
ENSG00000236744	CpG island
GAPDHP21	CpG island
PCDH15	CpG island

Extended variants
information (count: 1120 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1120 , 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	rs188662396	chr10:57360020-57360021	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs554535697	chr10:57361208-57361209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574529321	chr10:57361218-57361219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115040609	chr10:57361261-57361262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181387647	chr10:57361286-57361287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576931395	chr10:57361293-57361294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114185810	chr10:57361385-57361386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs146886117	chr10:57361401-57361402	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs531429210	chr10:57361473-57361474	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs541985185	chr10:57361475-57361476	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs560681490	chr10:57361503-57361504	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs140647916	chr10:57361506-57361507	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs544110407	chr10:57361603-57361604	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs547237765	chr10:57361689-57361690	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs142930122	chr10:57361690-57361691	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs184589040	chr10:57361698-57361699	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs552494498	chr10:57361699-57361700	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs569151201	chr10:57361707-57361708	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs189130325	chr10:57361708-57361709	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs554674512	chr10:57361776-57361777	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs568087951	chr10:57361790-57361791	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs181508057	chr10:57361804-57361805	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs116345005	chr10:57361816-57361817	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs545122422	chr10:57361818-57361819	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs377733450	chr10:57361821-57361822	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs556383312	chr10:57361835-57361836	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs10430549	chr10:57361844-57361845	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs375958398	chr10:57361879-57361880	Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs76215526	chr10:57361889-57361890	Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs75032509	chr10:57361890-57361891	Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs541925477	chr10:57361891-57361892	Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs79676999	chr10:57361894-57361895	Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs561786960	chr10:57361905-57361906	Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs186006782	chr10:57361929-57361930	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs540673415	chr10:57361936-57361937	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs75677554	chr10:57361937-57361938	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs4304667	chr10:57361944-57361945	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs532687112	chr10:57361962-57361963	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs77309758	chr10:57361975-57361976	Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs76649901	chr10:57361980-57361981	Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs79441661	chr10:57361986-57361987	Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs182048139	chr10:57361992-57361993	Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs80136087	chr10:57361995-57361996	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs76649263	chr10:57361999-57362000	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs74863948	chr10:57362004-57362005	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs79318827	chr10:57362008-57362009	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs186267409	chr10:57362010-57362011	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs75621583	chr10:57362013-57362014	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs368899998	chr10:57362038-57362039	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs4551668	chr10:57362083-57362084	Active TSS	n/a	n/a	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
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
small cell lung cancer	17426248	CNVD

Chromatin state (count:548 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:57361200-57361400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr10:57361400-57362000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr10:57361400-57362200	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr10:57361400-57362200	Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr10:57361400-57362200	Active TSS	HUES64 Cell Line	embryonic stem cell
6	chr10:57361400-57362200	Active TSS	iPS-20b Cell Line	embryonic stem cell
7	chr10:57361400-57362200	Active TSS	Fetal Brain Female	brain
8	chr10:57361600-57361800	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
9	chr10:57361600-57362000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr10:57361600-57362000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr10:57361600-57362000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr10:57361600-57362000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr10:57361600-57362000	Active TSS	Brain Inferior Temporal Lobe	brain
14	chr10:57361600-57362000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
15	chr10:57361600-57362000	Enhancers	Lung	lung
16	chr10:57361600-57362000	Enhancers	Pancreas	Pancrea
17	chr10:57361600-57362000	Active TSS	HMEC	breast
18	chr10:57361600-57362200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
19	chr10:57361600-57362200	Active TSS	H1 Cell Line	embryonic stem cell
20	chr10:57361600-57362200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr10:57361600-57362200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr10:57361600-57362200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr10:57361600-57362200	Active TSS	H9 Cell Line	embryonic stem cell
24	chr10:57361600-57362200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr10:57361600-57362200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr10:57361600-57362200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr10:57361600-57362200	Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr10:57361600-57362200	Active TSS	iPS-15b Cell Line	embryonic stem cell
29	chr10:57361600-57362200	Active TSS	iPS-18 Cell Line	embryonic stem cell
30	chr10:57361600-57362200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr10:57361600-57362200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr10:57361600-57362200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
33	chr10:57361600-57362200	Active TSS	Breast Myoepithelial Primary Cells	Breast
34	chr10:57361600-57362200	Active TSS	Primary hematopoietic stem cells	blood
35	chr10:57361600-57362200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr10:57361600-57362200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr10:57361600-57362200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr10:57361600-57362200	Active TSS	Brain Anterior Caudate	brain
39	chr10:57361600-57362200	Active TSS	Brain Germinal Matrix	brain
40	chr10:57361600-57362200	Active TSS	Brain Hippocampus Middle	brain
41	chr10:57361600-57362200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
42	chr10:57361600-57362200	Active TSS	Fetal Kidney	kidney
43	chr10:57361600-57362200	Active TSS	Fetal Stomach	stomach
44	chr10:57361600-57362200	Active TSS	Gastric	stomach
45	chr10:57361800-57362200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr10:57361800-57362200	Active TSS	Cortex derived primary cultured neurospheres	brain
47	chr10:57362000-57362200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr10:57374000-57386000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr10:57380000-57387000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr10:57381200-57381400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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