Variant report

Variant	nsv831983
Chromosome Location	chr10:110267919-110467318
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	chr10:110456347-110457342	GM12878	blood:	n/a	n/a
2	ATF2	chr10:110456533-110457197	GM12878	blood:	n/a	n/a
3	BACH1	chr10:110411257-110411297	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr10:110456463-110456881	GM12878	blood:	n/a	n/a
5	BATF	chr10:110304346-110304543	GM12878	blood:	n/a	n/a
6	BATF	chr10:110448126-110448316	GM12878	blood:	n/a	n/a
7	BATF	chr10:110456889-110457181	GM12878	blood:	n/a	n/a
8	BATF	chr10:110456553-110457223	GM12878	blood:	n/a	n/a
9	BCL11A	chr10:110456486-110457262	GM12878	blood:	n/a	chr10:110457059-110457066
10	BCL11A	chr10:110358060-110358473	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr10:110304396-110304505	K562	blood:	n/a	n/a
12	BHLHE40	chr10:110456557-110457157	GM12878	blood:	n/a	n/a
13	BHLHE40	chr10:110304371-110304548	GM12878	blood:	n/a	n/a
14	CEBPB	chr10:110389561-110389919	MCF-7	breast:	n/a	n/a
15	CEBPB	chr10:110277538-110277700	HepG2	liver:	n/a	chr10:110277668-110277679 chr10:110277669-110277680 chr10:110277668-110277681 chr10:110277668-110277681 chr10:110277668-110277681
16	CEBPB	chr10:110283153-110283335	HepG2	liver:	n/a	chr10:110283268-110283279 chr10:110283319-110283330 chr10:110283268-110283281
17	CEBPB	chr10:110429006-110429640	H1-hESC	embryonic stem cell:	n/a	chr10:110429079-110429092 chr10:110429079-110429090 chr10:110429081-110429090 chr10:110429108-110429119 chr10:110429081-110429090 chr10:110429108-110429121 chr10:110429081-110429092 chr10:110429079-110429092 chr10:110429081-110429090 chr10:110429081-110429090
18	CEBPB	chr10:110389708-110389933	IMR90	lung:	n/a	n/a
19	CEBPB	chr10:110410053-110410294	HepG2	liver:	n/a	chr10:110410134-110410145
20	CEBPB	chr10:110428935-110429593	IMR90	lung:	n/a	chr10:110429079-110429092 chr10:110429079-110429090 chr10:110429081-110429090 chr10:110429108-110429119 chr10:110429081-110429090 chr10:110429108-110429121 chr10:110429081-110429092 chr10:110429079-110429092 chr10:110429081-110429090 chr10:110429081-110429090
21	CEBPB	chr10:110314833-110315005	A549	lung:	n/a	n/a
22	CEBPB	chr10:110358649-110358910	MCF-7	breast:	n/a	n/a
23	CEBPB	chr10:110306946-110307156	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr10:110389649-110390002	MCF-7	breast:	n/a	n/a
25	CEBPB	chr10:110389598-110389968	HepG2	liver:	n/a	n/a
26	CEBPB	chr10:110389642-110389953	A549	lung:	n/a	n/a
27	CEBPB	chr10:110429355-110429628	A549	lung:	n/a	n/a
28	CEBPB	chr10:110428957-110429637	HepG2	liver:	n/a	chr10:110429079-110429092 chr10:110429079-110429090 chr10:110429081-110429090 chr10:110429108-110429119 chr10:110429081-110429090 chr10:110429108-110429121 chr10:110429081-110429092 chr10:110429079-110429092 chr10:110429081-110429090 chr10:110429081-110429090
29	CHD1	chr10:110456602-110456729	GM12878	blood:	n/a	n/a
30	CHD2	chr10:110354117-110354343	GM12878	blood:	n/a	n/a
31	CHD2	chr10:110456518-110457160	GM12878	blood:	n/a	n/a
32	CTCF	chr10:110347492-110347527	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr10:110304420-110304570	GM12872	blood:	n/a	n/a
34	CTCF	chr10:110304365-110304581	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr10:110304400-110304550	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr10:110304349-110304592	K562	blood:	n/a	n/a
37	CTCF	chr10:110304400-110304550	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr10:110304148-110304228	GM10248	blood:	n/a	n/a
39	CTCF	chr10:110450980-110451130	GM12873	blood:	n/a	n/a
40	CTCF	chr10:110454140-110454290	GM12871	blood:	n/a	n/a
41	CTCF	chr10:110304340-110304602	GM10248	blood:	n/a	n/a
42	CTCF	chr10:110304318-110304525	K562	blood:	n/a	n/a
43	CTCF	chr10:110304420-110304570	GM12864	blood:	n/a	n/a
44	CTCF	chr10:110304400-110304550	GM06990	blood:	n/a	n/a
45	CTCF	chr10:110304380-110304530	HCT-116	colon:	n/a	n/a
46	CTCF	chr10:110304352-110304550	Lung_OC	lung:	n/a	n/a
47	CTCF	chr10:110304344-110304595	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr10:110304400-110304550	HMF	breast:	n/a	n/a
49	CTCF	chr10:110311460-110311610	GM12878	blood:	n/a	n/a
50	CTCF	chr10:110304730-110304816	GM13977	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:110282010-110282060	HepG2	liver:	n/a
2	chr10:110282010-110282060	HepG2	liver:	n/a
3	chr10:110326660-110326710	HUVEC	blood vessel:	n/a
4	chr10:110326440-110326490	NHDF-neo	bronchial:	n/a
5	chr10:110282010-110282060	NH-A	brain:	n/a
6	chr10:110326562-110326612	ECC-1	luminal epithelium:	n/a
7	chr10:110326562-110326612	ProgFib	skin:	n/a
8	chr10:110326440-110326490	SKMC	muscle:	n/a
9	chr10:110326325-110326375	PFSK-1	brain:	n/a
10	chr10:110326562-110326612	AG04449	skin:	fetal
11	chr10:110326562-110326612	AG09309	skin:	n/a
12	chr10:110282010-110282060	K562	blood:	n/a
13	chr10:110326562-110326612	SAEC	small airway:	n/a
14	chr10:110282010-110282060	Hepatocyte	liver:	n/a
15	chr10:110326325-110326375	IMR90	lung:	fetal
16	chr10:110326562-110326612	T-47D	breast:	n/a
17	chr10:110326748-110326798	HNPCEpiC	eye:	n/a
18	chr10:110326660-110326710	HCPEpiC	choroid plexus:	n/a
19	chr10:110326325-110326375	HIPEpiC	eye:	n/a
20	chr10:110326748-110326798	HAEpiC	amniotic membrane:	n/a
21	chr10:110282010-110282060	PrEC	prostate:	n/a
22	chr10:110326325-110326375	Hepatocyte	liver:	n/a
23	chr10:110326325-110326375	AG10803	skin:	n/a
24	chr10:110326440-110326490	HEK293	kidney:	embryo
25	chr10:110326748-110326798	PANC-1	pancreas:	n/a
26	chr10:110282010-110282060	AG10803	skin:	n/a
27	chr10:110326440-110326490	PANC-1	pancreas:	n/a
28	chr10:110326440-110326490	GM19239	blood:	n/a
29	chr10:110326562-110326612	HEK293	kidney:	embryo
30	chr10:110326748-110326798	CMK	blood:	n/a
31	chr10:110326562-110326612	K562	blood:	n/a
32	chr10:110326440-110326490	AG09309	skin:	n/a
33	chr10:110326660-110326710	Jurkat	blood:	n/a
34	chr10:110326562-110326612	SKMC	muscle:	n/a
35	chr10:110326660-110326710	A549	lung:	n/a
36	chr10:110326562-110326612	NHDF-neo	bronchial:	n/a
37	chr10:110282010-110282060	HIPEpiC	eye:	n/a
38	chr10:110326660-110326710	IMR90	lung:	fetal
39	chr10:110326325-110326375	GM12891	blood:	n/a
40	chr10:110282010-110282060	ProgFib	skin:	n/a
41	chr10:110326440-110326490	BE2_C	brain:	n/a
42	chr10:110282010-110282060	ovcar-3	ovarian:	n/a
43	chr10:110282010-110282060	AoSMC	blood vessel:	n/a
44	chr10:110326562-110326612	PANC-1	pancreas:	n/a
45	chr10:110326562-110326612	HNPCEpiC	eye:	n/a
46	chr10:110326440-110326490	BJ	skin:	n/a
47	chr10:110326660-110326710	HRCEpiC	kidney:	n/a
48	chr10:110326660-110326710	HIPEpiC	eye:	n/a
49	chr10:110326325-110326375	HEK293	kidney:	embryo
50	chr10:110326325-110326375	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:110379538..110381981-chr10:110384603..110386733,2	MCF-7	breast:
2	chr10:110333027..110334929-chr10:110351219..110353665,2	K562	blood:
3	chr10:110333027..110334929-chr10:110351219..110353665,2	K562	blood:
4	chr10:110341253..110342207-chr10:110358545..110359102,2	MCF-7	breast:
5	chr10:110367562..110370011-chr10:110375438..110378123,2	K562	blood:
6	chr10:110194574..110195178-chr10:110303726..110304524,2	MCF-7	breast:
7	chr10:110379538..110381981-chr10:110384603..110386733,2	MCF-7	breast:
8	chr10:110367562..110370011-chr10:110375438..110378123,2	K562	blood:
9	chr10:110341253..110342207-chr10:110358545..110359102,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-XPNPEP1-1	chr10:110307733-110308115	XLOC_008945
2	lnc-XPNPEP1-3	chr10:110299653-110299705	NONHSAT016304
3	lnc-XPNPEP1-3	chr10:110311425-110311563	NONHSAT016304
4	lnc-XPNPEP1-1	chr10:110309663-110309715	XLOC_008945
5	lnc-XPNPEP1-1	chr10:110321435-110321573	XLOC_008945
6	lnc-ADD3-12	chr10:110460266-110460283	NONHSAT016306
7	lnc-XPNPEP1-3	chr10:110297723-110298105	NONHSAT016304

Variant related genes	Relation type
ENSG00000203434	TF binding region
ENSG00000223381	TF binding region
ENSG00000203434	CpG island
ENSG00000223381	CpG island

Extended variants
information (count: 4891 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:4891 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528245348	chr10:110271495-110271496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs551552510	chr10:110271500-110271501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564976362	chr10:110271501-110271502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs530820627	chr10:110271514-110271515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557270786	chr10:110271515-110271516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs550630893	chr10:110271528-110271529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs566896180	chr10:110271529-110271530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532904138	chr10:110271538-110271539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535861486	chr10:110271541-110271542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546249300	chr10:110271567-110271568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566226674	chr10:110271577-110271578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs180715945	chr10:110271594-110271595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs184253174	chr10:110271598-110271599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566135048	chr10:110271605-110271606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575514621	chr10:110271638-110271639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539669302	chr10:110271639-110271640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs111479180	chr10:110271675-110271676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537719221	chr10:110271693-110271694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146400374	chr10:110271699-110271700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558302672	chr10:110271703-110271704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs557701560	chr10:110271769-110271770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs369752261	chr10:110271781-110271782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs34635249	chr10:110271788-110271789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs201902302	chr10:110271794-110271795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs574040332	chr10:110271807-110271808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs34243527	chr10:110271814-110271815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543043894	chr10:110271830-110271831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs112831218	chr10:110271834-110271835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs576879709	chr10:110271845-110271846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545208619	chr10:110271857-110271858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs35851237	chr10:110271895-110271896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs189566592	chr10:110271898-110271899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs11194139	chr10:110271908-110271909	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs182090175	chr10:110271914-110271915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs552696355	chr10:110271917-110271918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187643046	chr10:110271919-110271920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs148577623	chr10:110272004-110272005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs537640562	chr10:110272062-110272063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs371655775	chr10:110272067-110272068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574533906	chr10:110272089-110272090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs566165332	chr10:110272152-110272153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs112343501	chr10:110272191-110272192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs76643492	chr10:110272214-110272215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552007618	chr10:110272230-110272231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs571776563	chr10:110272254-110272255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs537255962	chr10:110272258-110272259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs1332281	chr10:110272296-110272297	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs574382630	chr10:110272334-110272335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141640925	chr10:110272360-110272361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs536989216	chr10:110272362-110272363	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
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
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
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	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
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
renal hypoplasia	20603712	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Cornelia de Lange syndrome	24599119	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	16397240	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	16616336	CNVD
Chronic lymphocytic leukemia	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Barrett''s syndrome	19417022	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:110271400-110272600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr10:110271600-110272600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr10:110272400-110273200	Enhancers	Primary hematopoietic stem cells	blood
4	chr10:110272600-110274000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr10:110272600-110274600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr10:110273200-110275200	Weak transcription	Primary hematopoietic stem cells	blood
7	chr10:110274000-110276200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr10:110274600-110275800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr10:110275200-110275800	Enhancers	Primary hematopoietic stem cells	blood
10	chr10:110275200-110275800	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr10:110275800-110281000	Weak transcription	Primary hematopoietic stem cells	blood
12	chr10:110275800-110281200	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr10:110276000-110276200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr10:110277800-110279000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr10:110279400-110282200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr10:110279800-110280000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr10:110280000-110281000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr10:110281000-110282000	Enhancers	Primary hematopoietic stem cells	blood
19	chr10:110281000-110282600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr10:110281200-110282200	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr10:110281200-110284000	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr10:110281400-110282200	Enhancers	Fetal Kidney	kidney
23	chr10:110281600-110282200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr10:110281600-110282200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr10:110281800-110283000	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr10:110282000-110282600	Enhancers	H9 Cell Line	embryonic stem cell
27	chr10:110282000-110282800	Enhancers	H1 Cell Line	embryonic stem cell
28	chr10:110282000-110283000	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr10:110282400-110282800	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr10:110282600-110283000	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr10:110283000-110285600	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr10:110285600-110286400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr10:110292400-110293000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
34	chr10:110302200-110302600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr10:110302600-110305600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr10:110304200-110304400	Enhancers	Primary B cells from peripheral blood	blood
37	chr10:110304200-110304400	Enhancers	Brain Cingulate Gyrus	brain
38	chr10:110304200-110304600	Active TSS	Spleen	Spleen
39	chr10:110304600-110305600	Weak transcription	Primary B cells from peripheral blood	blood
40	chr10:110304600-110309400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr10:110305200-110306200	Enhancers	GM12878-XiMat	blood
42	chr10:110305600-110306000	Enhancers	Primary B cells from peripheral blood	blood
43	chr10:110305600-110306000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr10:110309400-110309600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr10:110309600-110310000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr10:110310000-110310200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr10:110310000-110310600	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr10:110310200-110311400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr10:110311400-110312200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr10:110311600-110312200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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