Variant report

Variant	nsv894965
Chromosome Location	chr10:23071128-23113841
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:573)
CpG islands
(count:244)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:23111936-23112361	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:23105354-23105554	K562	blood:	n/a	n/a
3	ARID3A	chr10:23105932-23106723	K562	blood:	n/a	n/a
4	ARID3A	chr10:23072818-23073316	K562	blood:	n/a	n/a
5	ATF1	chr10:23105202-23105606	K562	blood:	n/a	n/a
6	ATF1	chr10:23105863-23106217	K562	blood:	n/a	n/a
7	ATF2	chr10:23105861-23106240	GM12878	blood:	n/a	n/a
8	ATF3	chr10:23111828-23112653	HCT-116	colon:	n/a	n/a
9	ATF3	chr10:23105761-23106291	K562	blood:	n/a	n/a
10	ATF3	chr10:23105937-23106151	K562	blood:	n/a	n/a
11	BACH1	chr10:23099536-23099975	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr10:23111957-23112328	GM12878	blood:	n/a	chr10:23112164-23112175 chr10:23112161-23112171 chr10:23112165-23112175
13	BATF	chr10:23105876-23106124	GM12878	blood:	n/a	n/a
14	BATF	chr10:23111999-23112265	GM12878	blood:	n/a	chr10:23112164-23112175 chr10:23112161-23112171 chr10:23112165-23112175
15	BHLHE40	chr10:23105216-23106684	K562	blood:	n/a	n/a
16	BHLHE40	chr10:23094220-23094807	K562	blood:	n/a	n/a
17	BHLHE40	chr10:23095561-23095655	K562	blood:	n/a	n/a
18	BHLHE40	chr10:23072881-23073064	K562	blood:	n/a	n/a
19	BRCA1	chr10:23105823-23106074	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr10:23106035-23106042	GM12878	blood:	n/a	n/a
21	BRCA1	chr10:23112085-23112534	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr10:23105774-23106703	K562	blood:	n/a	n/a
23	CBX3	chr10:23104991-23106462	HCT-116	colon:	n/a	n/a
24	CBX3	chr10:23111432-23112684	HCT-116	colon:	n/a	n/a
25	CBX3	chr10:23111799-23112610	HCT-116	colon:	n/a	n/a
26	CBX3	chr10:23105716-23106272	K562	blood:	n/a	n/a
27	CCNT2	chr10:23105893-23106187	K562	blood:	n/a	n/a
28	CCNT2	chr10:23106417-23106674	K562	blood:	n/a	n/a
29	CEBPB	chr10:23086498-23086573	K562	blood:	n/a	n/a
30	CEBPB	chr10:23105869-23106255	A549	lung:	n/a	n/a
31	CEBPB	chr10:23072761-23073112	K562	blood:	n/a	n/a
32	CEBPB	chr10:23111809-23112644	HCT-116	colon:	n/a	n/a
33	CEBPB	chr10:23105944-23106235	HepG2	liver:	n/a	n/a
34	CEBPB	chr10:23111970-23112308	A549	lung:	n/a	n/a
35	CEBPB	chr10:23105754-23106444	HCT-116	colon:	n/a	n/a
36	CEBPB	chr10:23101707-23102001	HepG2	liver:	n/a	chr10:23101937-23101950
37	CEBPB	chr10:23105863-23106159	K562	blood:	n/a	n/a
38	CEBPB	chr10:23086814-23087021	IMR90	lung:	n/a	n/a
39	CEBPB	chr10:23080302-23080309	K562	blood:	n/a	n/a
40	CEBPB	chr10:23101643-23101990	K562	blood:	n/a	chr10:23101937-23101950
41	CEBPB	chr10:23113187-23113440	MCF-7	breast:	n/a	n/a
42	CEBPB	chr10:23101701-23102013	IMR90	lung:	n/a	chr10:23101937-23101950
43	CEBPB	chr10:23101641-23101997	K562	blood:	n/a	chr10:23101937-23101950
44	CEBPB	chr10:23105833-23106312	K562	blood:	n/a	n/a
45	CEBPB	chr10:23111575-23112673	HCT-116	colon:	n/a	n/a
46	CEBPB	chr10:23105801-23106318	IMR90	lung:	n/a	n/a
47	CEBPB	chr10:23111983-23112293	HepG2	liver:	n/a	n/a
48	CEBPB	chr10:23105851-23106665	K562	blood:	n/a	n/a
49	CEBPB	chr10:23105842-23106280	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr10:23104903-23106509	HCT-116	colon:	n/a	chr10:23105065-23105076 chr10:23105063-23105076 chr10:23105063-23105076 chr10:23105063-23105076 chr10:23105065-23105076

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:23093955-23094005	AG04450	lung:	fetal
2	chr10:23112840-23112890	GM19239	blood:	n/a
3	chr10:23093955-23094005	AG09309	skin:	n/a
4	chr10:23093955-23094005	GM12878	blood:	n/a
5	chr10:23105280-23105330	PFSK-1	brain:	n/a
6	chr10:23100186-23100236	PANC-1	pancreas:	n/a
7	chr10:23100186-23100236	T-47D	breast:	n/a
8	chr10:23112840-23112890	PFSK-1	brain:	n/a
9	chr10:23105280-23105330	ECC-1	luminal epithelium:	n/a
10	chr10:23100186-23100236	Hela-S3	cervix:	n/a
11	chr10:23105280-23105330	CMK	blood:	n/a
12	chr10:23093955-23094005	HCF	heart:	n/a
13	chr10:23093955-23094005	SK-N-MC	brain:	n/a
14	chr10:23105280-23105330	HNPCEpiC	eye:	n/a
15	chr10:23112840-23112890	Caco-2	colon:	n/a
16	chr10:23100186-23100236	IMR90	lung:	fetal
17	chr10:23105280-23105330	HCM	heart:	n/a
18	chr10:23100186-23100236	HPAEpiC	pulmonary alveolar:	n/a
19	chr10:23105280-23105330	SK-N-MC	brain:	n/a
20	chr10:23112840-23112890	NH-A	brain:	n/a
21	chr10:23112840-23112890	RPTEC	kidney:	n/a
22	chr10:23100186-23100236	A549	lung:	n/a
23	chr10:23105280-23105330	GM19239	blood:	n/a
24	chr10:23105280-23105330	HMEC	breast:	n/a
25	chr10:23093955-23094005	SK-N-SH	brain:	n/a
26	chr10:23100186-23100236	GM12878	blood:	n/a
27	chr10:23112840-23112890	GM12892	blood:	n/a
28	chr10:23093955-23094005	HCT-116	colon:	n/a
29	chr10:23105280-23105330	AG09319	gingival:	n/a
30	chr10:23112840-23112890	H1-hESC	embryonic stem cell:	embryo
31	chr10:23105280-23105330	HUVEC	blood vessel:	n/a
32	chr10:23112840-23112890	HRPEpiC	eye:	n/a
33	chr10:23105280-23105330	HCPEpiC	choroid plexus:	n/a
34	chr10:23093955-23094005	HAEpiC	amniotic membrane:	n/a
35	chr10:23112840-23112890	HUVEC	blood vessel:	n/a
36	chr10:23112840-23112890	BE2_C	brain:	n/a
37	chr10:23105280-23105330	GM12891	blood:	n/a
38	chr10:23100186-23100236	BJ	skin:	n/a
39	chr10:23105280-23105330	A549	lung:	n/a
40	chr10:23112840-23112890	AG10803	skin:	n/a
41	chr10:23105280-23105330	Hepatocyte	liver:	n/a
42	chr10:23105280-23105330	RPTEC	kidney:	n/a
43	chr10:23100186-23100236	NB4	blood:	n/a
44	chr10:23105280-23105330	BE2_C	brain:	n/a
45	chr10:23100186-23100236	NH-A	brain:	n/a
46	chr10:23100186-23100236	CMK	blood:	n/a
47	chr10:23105280-23105330	HAEpiC	amniotic membrane:	n/a
48	chr10:23112840-23112890	SK-N-SH	brain:	n/a
49	chr10:23100186-23100236	SK-N-SH_RA	brain:	n/a
50	chr10:23112840-23112890	NB4	blood:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:23104132..23107506-chr10:23342632..23345950,5	K562	blood:
2	chr10:22980163..22981684-chr10:23106478..23108245,2	K562	blood:
3	chr10:23098595..23101084-chr2:58865453..58867756,2	MCF-7	breast:
4	chr10:23108350..23110546-chr10:23110740..23113681,3	K562	blood:
5	chr10:23093031..23094566-chr10:23095292..23097801,2	K562	blood:
6	chr10:22918208..22920899-chr10:23105511..23107568,2	K562	blood:
7	chr10:23001422..23003561-chr10:23104622..23106652,2	K562	blood:
8	chr10:23052115..23054835-chr10:23068399..23071194,3	MCF-7	breast:
9	chr10:23103158..23106579-chr10:23341900..23344132,3	K562	blood:
10	chr10:23105492..23108176-chr10:23344426..23345990,3	K562	blood:
11	chr10:23090832..23093813-chr10:23094691..23097138,2	K562	blood:
12	chr10:23089513..23092332-chr10:23095638..23097901,2	K562	blood:
13	chr10:23108350..23110546-chr10:23110740..23113681,3	K562	blood:
14	chr10:23090452..23092008-chr10:23092511..23094369,2	K562	blood:
15	chr10:23090832..23093813-chr10:23094691..23097138,2	K562	blood:
16	chr10:23001483..23003855-chr10:23099770..23102739,2	K562	blood:
17	chr10:23002586..23004698-chr10:23069532..23071170,2	K562	blood:
18	chr10:23093031..23094566-chr10:23095292..23097801,2	K562	blood:
19	chr10:23093887..23094416-chr10:23266755..23267519,2	MCF-7	breast:
20	chr10:23076401..23079823-chr10:23343221..23346091,3	K562	blood:
21	chr10:23080355..23083056-chr10:23096446..23098590,2	K562	blood:
22	chr10:23108350..23110476-chr10:23111720..23113681,2	K562	blood:
23	chr10:23108350..23110476-chr10:23111720..23113681,2	K562	blood:
24	chr10:23080355..23083056-chr10:23096446..23098590,2	K562	blood:
25	chr10:23089513..23092332-chr10:23095638..23097901,2	K562	blood:
26	chr10:23092682..23094839-chr2:187127661..187130019,2	MCF-7	breast:
27	chr10:23108692..23110534-chr10:23308268..23309848,2	K562	blood:
28	chr10:23000874..23003179-chr10:23095051..23097837,2	K562	blood:
29	chr10:23077180..23079268-chr10:23081726..23083280,2	MCF-7	breast:
30	chr10:23077180..23079268-chr10:23081726..23083280,2	MCF-7	breast:
31	chr10:23090452..23092008-chr10:23092511..23094369,2	K562	blood:
32	chr10:23112958..23115115-chr10:23343406..23346225,2	K562	blood:

No data

Variant related genes	Relation type
RNU6-413P	TF binding region
RNU6-413P	CpG island
ENSG00000150867	chromatin interactions

Extended variants
information (count: 1682 )
Associated
traits (count: 38 )

Variant overlapped rSNPs/rCNVs (count:1682 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10828334	chr10:23071128-23071129	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
2	rs373269385	chr10:23071140-23071141	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs139790983	chr10:23071194-23071195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187857951	chr10:23071195-23071196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572127736	chr10:23071232-23071233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555590750	chr10:23071235-23071236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138534767	chr10:23071247-23071248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs66874110	chr10:23071251-23071252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12249328	chr10:23071253-23071254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373250923	chr10:23071269-23071270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557736094	chr10:23071278-23071279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541541456	chr10:23071326-23071327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs35330560	chr10:23071342-23071343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs578016343	chr10:23071383-23071384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543397765	chr10:23071552-23071553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563282663	chr10:23071553-23071554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573719520	chr10:23071562-23071563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149078736	chr10:23071567-23071568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs193178136	chr10:23071570-23071571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143192559	chr10:23071581-23071582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374092144	chr10:23071599-23071600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112501165	chr10:23071621-23071622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140960229	chr10:23071622-23071623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531509809	chr10:23071624-23071625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372780257	chr10:23071639-23071640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376279042	chr10:23071641-23071642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551965152	chr10:23071656-23071657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565207354	chr10:23071714-23071715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115260978	chr10:23071732-23071733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11592137	chr10:23071768-23071769	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs567320526	chr10:23071822-23071823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571629243	chr10:23071833-23071834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185289812	chr10:23071866-23071867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370916631	chr10:23071883-23071884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs138910774	chr10:23071884-23071885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563534499	chr10:23071904-23071905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs73600518	chr10:23071973-23071974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201662284	chr10:23072039-23072040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557936159	chr10:23072047-23072048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530842606	chr10:23072079-23072080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552060617	chr10:23072086-23072087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571527084	chr10:23072126-23072127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370282032	chr10:23072147-23072148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199914938	chr10:23072148-23072149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200612172	chr10:23072151-23072152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201663711	chr10:23072152-23072153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs78877721	chr10:23072154-23072155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138387763	chr10:23072184-23072185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374425800	chr10:23072203-23072204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375073408	chr10:23072207-23072208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:38)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23069800-23080600	Weak transcription	Brain Hippocampus Middle	brain
2	chr10:23070000-23075200	Weak transcription	Brain Angular Gyrus	brain
3	chr10:23075200-23076000	Enhancers	Brain Angular Gyrus	brain
4	chr10:23080600-23081200	Enhancers	Brain Hippocampus Middle	brain
5	chr10:23080800-23081200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr10:23080800-23081200	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr10:23081000-23081400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr10:23081000-23081800	Enhancers	NHEK	skin
9	chr10:23081200-23092000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr10:23081200-23093000	Weak transcription	Brain Hippocampus Middle	brain
11	chr10:23089400-23089600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr10:23090000-23090800	Enhancers	Rectal Smooth Muscle	rectum
13	chr10:23090000-23093000	Enhancers	Fetal Stomach	stomach
14	chr10:23090200-23090800	Enhancers	Primary hematopoietic stem cells	blood
15	chr10:23090200-23091400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr10:23090400-23090600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr10:23090400-23092000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr10:23090600-23090800	Enhancers	Brain Cingulate Gyrus	brain
19	chr10:23090600-23091000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr10:23090600-23091000	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr10:23090600-23091000	Enhancers	Fetal Lung	lung
22	chr10:23090600-23091200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr10:23090600-23091800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr10:23090800-23091600	Weak transcription	Brain Cingulate Gyrus	brain
25	chr10:23090800-23091800	Weak transcription	Primary hematopoietic stem cells	blood
26	chr10:23090800-23091800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr10:23090800-23094400	Weak transcription	Rectal Smooth Muscle	rectum
28	chr10:23090800-23095000	Enhancers	NHDF-Ad	bronchial
29	chr10:23091000-23091400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr10:23091000-23093600	Weak transcription	Fetal Lung	lung
31	chr10:23091000-23093800	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr10:23091200-23091600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr10:23091600-23092400	Enhancers	Brain Cingulate Gyrus	brain
34	chr10:23091600-23095800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr10:23091600-23096000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr10:23091800-23092000	Enhancers	Muscle Satellite Cultured Cells	--
37	chr10:23091800-23092200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr10:23091800-23092200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr10:23091800-23093000	Enhancers	NH-A	brain
40	chr10:23091800-23093200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr10:23091800-23094800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr10:23091800-23094800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr10:23091800-23095000	Enhancers	HSMMtube	muscle
44	chr10:23092000-23092200	Enhancers	Primary hematopoietic stem cells	blood
45	chr10:23092000-23092400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
46	chr10:23092000-23092400	Enhancers	Brain Germinal Matrix	brain
47	chr10:23092000-23093000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr10:23092000-23093000	Enhancers	HMEC	breast
49	chr10:23092000-23093400	Enhancers	Stomach Smooth Muscle	stomach
50	chr10:23092000-23094200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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