Variant report

Variant	nsv895379
Chromosome Location	chr10:51022933-51187793
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	ARID3A	chr10:51052979-51053503	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:51044976-51045650	HepG2	liver:	n/a	n/a
3	BACH1	chr10:51035403-51035424	K562	blood:	n/a	n/a
4	BATF	chr10:51042217-51042509	GM12878	blood:	n/a	n/a
5	BATF	chr10:51039759-51040038	GM12878	blood:	n/a	chr10:51039858-51039869
6	BCL3	chr10:51052818-51053497	A549	lung:	n/a	n/a
7	BHLHE40	chr10:51035238-51035619	GM12878	blood:	n/a	n/a
8	CBX3	chr10:51103987-51104280	K562	blood:	n/a	n/a
9	CBX3	chr10:51103941-51104320	K562	blood:	n/a	n/a
10	CEBPB	chr10:51120363-51120697	Hela-S3	cervix:	n/a	chr10:51120380-51120391 chr10:51120380-51120393
11	CEBPB	chr10:51120363-51120417	H1-hESC	embryonic stem cell:	n/a	chr10:51120380-51120391 chr10:51120380-51120393
12	CEBPB	chr10:51052874-51053601	A549	lung:	n/a	chr10:51053042-51053053
13	CEBPB	chr10:51039401-51039732	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr10:51043833-51044157	HepG2	liver:	n/a	n/a
15	CEBPB	chr10:51045007-51045684	A549	lung:	n/a	chr10:51045469-51045480 chr10:51045470-51045481
16	CEBPB	chr10:51052828-51053595	Hela-S3	cervix:	n/a	chr10:51053042-51053053
17	CEBPB	chr10:51108499-51108691	H1-hESC	embryonic stem cell:	n/a	chr10:51108616-51108627 chr10:51108616-51108625 chr10:51108616-51108625 chr10:51108614-51108627 chr10:51108616-51108625 chr10:51108614-51108625 chr10:51108616-51108625
18	CEBPB	chr10:51091883-51092329	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr10:51120223-51120576	HepG2	liver:	n/a	chr10:51120380-51120391 chr10:51120380-51120393
20	CEBPB	chr10:51052790-51053553	IMR90	lung:	n/a	chr10:51053042-51053053
21	CEBPB	chr10:51052841-51053559	A549	lung:	n/a	chr10:51053042-51053053
22	CEBPB	chr10:51046485-51046805	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr10:51108460-51108786	A549	lung:	n/a	chr10:51108616-51108627 chr10:51108616-51108625 chr10:51108616-51108625 chr10:51108614-51108627 chr10:51108616-51108625 chr10:51108614-51108625 chr10:51108616-51108625
24	CEBPB	chr10:51108501-51108786	HepG2	liver:	n/a	chr10:51108616-51108627 chr10:51108616-51108625 chr10:51108616-51108625 chr10:51108614-51108627 chr10:51108616-51108625 chr10:51108614-51108625 chr10:51108616-51108625
25	CEBPB	chr10:51026799-51027095	K562	blood:	n/a	n/a
26	CEBPB	chr10:51045118-51045649	HepG2	liver:	n/a	chr10:51045469-51045480 chr10:51045470-51045481
27	CEBPB	chr10:51052837-51053681	MCF-7	breast:	n/a	chr10:51053042-51053053
28	CEBPB	chr10:51052750-51053623	MCF-7	breast:	n/a	chr10:51053042-51053053
29	CEBPB	chr10:51052922-51053392	K562	blood:	n/a	chr10:51053042-51053053
30	CEBPB	chr10:51052751-51053591	A549	lung:	n/a	chr10:51053042-51053053
31	CEBPB	chr10:51108439-51108789	K562	blood:	n/a	chr10:51108616-51108627 chr10:51108616-51108625 chr10:51108616-51108625 chr10:51108614-51108627 chr10:51108616-51108625 chr10:51108614-51108625 chr10:51108616-51108625
32	CEBPB	chr10:51108511-51108719	Hela-S3	cervix:	n/a	chr10:51108616-51108627 chr10:51108616-51108625 chr10:51108616-51108625 chr10:51108614-51108627 chr10:51108616-51108625 chr10:51108614-51108625 chr10:51108616-51108625
33	CEBPB	chr10:51043820-51044146	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr10:51120227-51120517	K562	blood:	n/a	chr10:51120380-51120391 chr10:51120380-51120393
35	CEBPB	chr10:51120215-51120790	A549	lung:	n/a	chr10:51120380-51120391 chr10:51120380-51120393
36	CEBPB	chr10:51120250-51120795	IMR90	lung:	n/a	chr10:51120380-51120391 chr10:51120380-51120393
37	CEBPB	chr10:51052895-51053556	HepG2	liver:	n/a	chr10:51053042-51053053
38	CEBPB	chr10:51045374-51045567	HepG2	liver:	n/a	chr10:51045469-51045480 chr10:51045470-51045481
39	CEBPB	chr10:51046417-51046852	HCT-116	colon:	n/a	n/a
40	CEBPB	chr10:51125670-51125962	IMR90	lung:	n/a	n/a
41	CEBPB	chr10:51108445-51108786	IMR90	lung:	n/a	chr10:51108616-51108627 chr10:51108616-51108625 chr10:51108616-51108625 chr10:51108614-51108627 chr10:51108616-51108625 chr10:51108614-51108625 chr10:51108616-51108625
42	CEBPB	chr10:51060119-51060498	Hela-S3	cervix:	n/a	chr10:51060224-51060237
43	CHD1	chr10:51037730-51038038	GM12878	blood:	n/a	n/a
44	CTCF	chr10:51098000-51098150	HFF	foreskin:	n/a	n/a
45	CTCF	chr10:51124700-51124850	HMF	breast:	n/a	n/a
46	CTCF	chr10:51098000-51098150	RPTEC	kidney:	n/a	n/a
47	CTCF	chr10:51098224-51098292	Hela-S3	cervix:	n/a	chr10:51098239-51098260 chr10:51098246-51098259 chr10:51098244-51098262
48	CTCF	chr10:51098240-51098390	AG09309	skin:	n/a	chr10:51098246-51098259 chr10:51098244-51098262
49	CTCF	chr10:51124607-51124760	GM13977	blood:	n/a	chr10:51124648-51124669 chr10:51124654-51124670 chr10:51124653-51124671
50	CTCF	chr10:51089520-51089590	Lung_OC	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:51039609-51039659	HPAEpiC	pulmonary alveolar:	n/a
2	chr10:51039609-51039659	HPAEpiC	pulmonary alveolar:	n/a
3	chr10:51039609-51039659	AoSMC	blood vessel:	n/a
4	chr10:51039609-51039659	ProgFib	skin:	n/a
5	chr10:51039609-51039659	LNCaP	prostate:	n/a
6	chr10:51039609-51039659	HNPCEpiC	eye:	n/a
7	chr10:51039609-51039659	K562	blood:	n/a
8	chr10:51039609-51039659	H1-hESC	embryonic stem cell:	embryo
9	chr10:51027379-51027429	MCF-7	breast:	n/a
10	chr10:51039609-51039659	NT2-D1	testis:	n/a
11	chr10:51027379-51027429	SK-N-MC	brain:	n/a
12	chr10:51039609-51039659	PFSK-1	brain:	n/a
13	chr10:51039609-51039659	HEEpiC	esophagus:	n/a
14	chr10:51039609-51039659	T-47D	breast:	n/a
15	chr10:51039609-51039659	PrEC	prostate:	n/a
16	chr10:51039609-51039659	CMK	blood:	n/a
17	chr10:51027379-51027429	SKMC	muscle:	n/a
18	chr10:51027379-51027429	NH-A	brain:	n/a
19	chr10:51027379-51027429	MCF10A-Er-Src	breast:	n/a
20	chr10:51027379-51027429	HAEpiC	amniotic membrane:	n/a
21	chr10:51027379-51027429	HUVEC	blood vessel:	n/a
22	chr10:51039609-51039659	SAEC	small airway:	n/a
23	chr10:51039609-51039659	HAEpiC	amniotic membrane:	n/a
24	chr10:51039609-51039659	RPTEC	kidney:	n/a
25	chr10:51039609-51039659	GM06990	blood:	n/a
26	chr10:51027379-51027429	HRE	kidney:	n/a
27	chr10:51027379-51027429	T-47D	breast:	n/a
28	chr10:51027379-51027429	U87	brain:	n/a
29	chr10:51027379-51027429	ProgFib	skin:	n/a
30	chr10:51027379-51027429	AoSMC	blood vessel:	n/a
31	chr10:51027379-51027429	HEK293	kidney:	embryo
32	chr10:51039609-51039659	GM12892	blood:	n/a
33	chr10:51039609-51039659	Jurkat	blood:	n/a
34	chr10:51027379-51027429	HRCEpiC	kidney:	n/a
35	chr10:51027379-51027429	GM12878	blood:	n/a
36	chr10:51027379-51027429	ovcar-3	ovarian:	n/a
37	chr10:51039609-51039659	BJ	skin:	n/a
38	chr10:51039609-51039659	Hepatocyte	liver:	n/a
39	chr10:51039609-51039659	HRCEpiC	kidney:	n/a
40	chr10:51039609-51039659	NHDF-neo	bronchial:	n/a
41	chr10:51027379-51027429	NT2-D1	testis:	n/a
42	chr10:51027379-51027429	HCT-116	colon:	n/a
43	chr10:51027379-51027429	LNCaP	prostate:	n/a
44	chr10:51027379-51027429	IMR90	lung:	fetal
45	chr10:51039609-51039659	GM12878	blood:	n/a
46	chr10:51039609-51039659	AG04449	skin:	fetal
47	chr10:51027379-51027429	NHDF-neo	bronchial:	n/a
48	chr10:51027379-51027429	Hepatocyte	liver:	n/a
49	chr10:51039609-51039659	AG10803	skin:	n/a
50	chr10:51027379-51027429	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:51041508..51042008-chr5:43483582..43484210,2	Hela-S3	cervix:
2	chr10:51038398..51040460-chr10:51042005..51043947,2	K562	blood:
3	chr10:51022250..51024471-chr10:51024656..51027577,2	K562	blood:
4	chr10:51038398..51040460-chr10:51042005..51043947,2	K562	blood:
5	chr10:51045976..51047972-chr10:51051417..51053268,2	MCF-7	breast:
6	chr10:51041329..51043585-chr10:51045424..51047411,2	K562	blood:
7	chr10:51033722..51037906-chr10:51041660..51043995,3	K562	blood:
8	chr10:51033722..51037906-chr10:51041660..51043995,3	K562	blood:
9	chr10:51028291..51030720-chr10:51030786..51035251,4	K562	blood:
10	chr10:51028291..51030720-chr10:51030786..51035251,4	K562	blood:
11	chr10:51041329..51043585-chr10:51045424..51047411,2	K562	blood:
12	chr10:51045976..51047972-chr10:51051417..51053268,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM21D-1	chr10:51117659-51117988	NONHSAT013322
2	lnc-C10orf53-2	chr10:51023142-51023608	NONHSAT013319

Variant related genes	Relation type
ENSG00000230166	TF binding region
FAM21D	TF binding region
PARG	TF binding region
ENSG00000229870	TF binding region
ENSG00000230166	CpG island
FAM21D	CpG island
PARG	CpG island
ENSG00000229870	CpG island
ENSG00000229870	chromatin interactions
ENSG00000249492	chromatin interactions
ENSG00000151881	chromatin interactions

Extended variants
information (count: 3115 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:3115 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4838566	chr10:51022933-51022934	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs187115006	chr10:51022948-51022949	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs570541999	chr10:51022962-51022963	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs531502180	chr10:51022985-51022986	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs79938433	chr10:51022986-51022987	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs535384175	chr10:51023033-51023034	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs567770644	chr10:51023067-51023068	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs535092339	chr10:51023071-51023072	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs143860450	chr10:51023130-51023131	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs369487642	chr10:51023216-51023217	Strong transcription Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
11	rs534210219	chr10:51023221-51023222	Strong transcription Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
12	rs559169080	chr10:51023346-51023347	Strong transcription Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
13	rs555346661	chr10:51023359-51023360	Strong transcription Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
14	rs144224037	chr10:51023436-51023437	Strong transcription Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
15	rs544744101	chr10:51023439-51023440	Strong transcription Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
16	rs56040437	chr10:51023607-51023608	Strong transcription Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs574975029	chr10:51023611-51023612	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs199679868	chr10:51023652-51023653	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542287163	chr10:51023661-51023662	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192443693	chr10:51023679-51023680	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs56682916	chr10:51023737-51023738	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148807657	chr10:51023772-51023773	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142454570	chr10:51023782-51023783	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573984645	chr10:51023784-51023785	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544341799	chr10:51023829-51023830	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564379651	chr10:51023847-51023848	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs117850415	chr10:51023864-51023865	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549526201	chr10:51023875-51023876	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs80268480	chr10:51023886-51023887	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs151316142	chr10:51023890-51023891	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547017374	chr10:51023914-51023915	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565554808	chr10:51023931-51023932	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183399688	chr10:51023949-51023950	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs377185934	chr10:51024001-51024002	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571083646	chr10:51024031-51024032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538479010	chr10:51024036-51024037	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187528857	chr10:51024042-51024043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559685675	chr10:51024074-51024075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528783167	chr10:51024112-51024113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575011874	chr10:51024275-51024276	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190512319	chr10:51024344-51024345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182389439	chr10:51024354-51024355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187070075	chr10:51024364-51024365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139367829	chr10:51024382-51024383	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs73312641	chr10:51024428-51024429	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs60022135	chr10:51024439-51024440	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs562127608	chr10:51024479-51024480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200589575	chr10:51024613-51024614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs202194496	chr10:51024629-51024630	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536422818	chr10:51024632-51024633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Cancer	21183584	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
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Schizophrenia	23813976	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
XY gonadal dysgenesis	20685758	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	21645411	CNVD
Lung adenocarcinoma	21935476	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1704 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:51018600-51023200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr10:51019800-51023400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr10:51019800-51053400	Weak transcription	Small Intestine	intestine
4	chr10:51020000-51025200	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr10:51020200-51023000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr10:51020400-51049600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr10:51020600-51023000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr10:51020600-51023000	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr10:51020800-51025400	Weak transcription	Primary hematopoietic stem cells	blood
10	chr10:51021000-51023000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr10:51021000-51023000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr10:51021000-51023000	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr10:51021000-51023200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr10:51021200-51023000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr10:51021200-51023000	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr10:51021200-51023000	Weak transcription	Primary B cells from cord blood	blood
17	chr10:51021200-51023000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr10:51021200-51023000	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr10:51021200-51023000	Weak transcription	NHDF-Ad	bronchial
20	chr10:51021200-51023200	Weak transcription	Primary T cells from cord blood	blood
21	chr10:51021200-51025400	Weak transcription	Aorta	Aorta
22	chr10:51021200-51025800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr10:51021200-51026800	Weak transcription	Gastric	stomach
24	chr10:51021400-51023000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr10:51021400-51023000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr10:51021400-51023000	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr10:51021400-51023000	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr10:51021400-51023000	Weak transcription	HSMM	muscle
29	chr10:51021400-51023200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr10:51021400-51023200	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr10:51021400-51023200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr10:51021400-51023200	Weak transcription	Brain Germinal Matrix	brain
33	chr10:51021400-51023200	Weak transcription	Placenta	Placenta
34	chr10:51021400-51023200	Weak transcription	Dnd41	blood
35	chr10:51021400-51023200	Weak transcription	NH-A	brain
36	chr10:51021400-51023400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr10:51021400-51025000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr10:51021400-51025200	Weak transcription	Brain Anterior Caudate	brain
39	chr10:51021400-51025400	Weak transcription	Brain Cingulate Gyrus	brain
40	chr10:51021400-51025400	Weak transcription	Brain Hippocampus Middle	brain
41	chr10:51021400-51025600	Weak transcription	GM12878-XiMat	blood
42	chr10:51021600-51023000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr10:51021600-51023200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr10:51021600-51023200	Weak transcription	Adipose Nuclei	Adipose
45	chr10:51021600-51023200	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr10:51021600-51023400	Weak transcription	Primary B cells from peripheral blood	blood
47	chr10:51021600-51023400	Weak transcription	Left Ventricle	heart
48	chr10:51021600-51023600	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr10:51021600-51023600	Weak transcription	A549	lung
50	chr10:51021600-51025000	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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