Variant report

Variant	nsv894961
Chromosome Location	chr10:23049139-23128475
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:771)
CpG islands
(count:306)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:771 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:23105354-23105554	K562	blood:	n/a	n/a
2	ARID3A	chr10:23111936-23112361	HepG2	liver:	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	chr10:23050539-23050842	K562	blood:	n/a	n/a
6	ATF1	chr10:23105863-23106217	K562	blood:	n/a	n/a
7	ATF1	chr10:23115059-23115131	K562	blood:	n/a	n/a
8	ATF1	chr10:23105202-23105606	K562	blood:	n/a	n/a
9	ATF2	chr10:23105861-23106240	GM12878	blood:	n/a	n/a
10	ATF2	chr10:23054742-23055551	GM12878	blood:	n/a	n/a
11	ATF3	chr10:23105937-23106151	K562	blood:	n/a	n/a
12	ATF3	chr10:23105761-23106291	K562	blood:	n/a	n/a
13	ATF3	chr10:23111828-23112653	HCT-116	colon:	n/a	n/a
14	BACH1	chr10:23099536-23099975	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr10:23111999-23112265	GM12878	blood:	n/a	chr10:23112164-23112175 chr10:23112161-23112171 chr10:23112165-23112175
16	BATF	chr10:23111957-23112328	GM12878	blood:	n/a	chr10:23112164-23112175 chr10:23112161-23112171 chr10:23112165-23112175
17	BATF	chr10:23105876-23106124	GM12878	blood:	n/a	n/a
18	BCLAF1	chr10:23055025-23055595	GM12878	blood:	n/a	chr10:23055268-23055277
19	BHLHE40	chr10:23123428-23123622	K562	blood:	n/a	n/a
20	BHLHE40	chr10:23094220-23094807	K562	blood:	n/a	n/a
21	BHLHE40	chr10:23115061-23115070	K562	blood:	n/a	n/a
22	BHLHE40	chr10:23105216-23106684	K562	blood:	n/a	n/a
23	BHLHE40	chr10:23054747-23055500	GM12878	blood:	n/a	n/a
24	BHLHE40	chr10:23095561-23095655	K562	blood:	n/a	n/a
25	BHLHE40	chr10:23072881-23073064	K562	blood:	n/a	n/a
26	BRCA1	chr10:23105823-23106074	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr10:23106035-23106042	GM12878	blood:	n/a	n/a
28	BRCA1	chr10:23112085-23112534	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr10:23111432-23112684	HCT-116	colon:	n/a	n/a
30	CBX3	chr10:23104991-23106462	HCT-116	colon:	n/a	n/a
31	CBX3	chr10:23111799-23112610	HCT-116	colon:	n/a	n/a
32	CBX3	chr10:23105774-23106703	K562	blood:	n/a	n/a
33	CBX3	chr10:23105716-23106272	K562	blood:	n/a	n/a
34	CCNT2	chr10:23106417-23106674	K562	blood:	n/a	n/a
35	CCNT2	chr10:23105893-23106187	K562	blood:	n/a	n/a
36	CEBPB	chr10:23061017-23061202	HepG2	liver:	n/a	n/a
37	CEBPB	chr10:23122261-23122610	A549	lung:	n/a	chr10:23122434-23122443 chr10:23122485-23122493 chr10:23122434-23122443 chr10:23122432-23122443 chr10:23122434-23122443
38	CEBPB	chr10:23117796-23117816	IMR90	lung:	n/a	n/a
39	CEBPB	chr10:23105944-23106235	HepG2	liver:	n/a	n/a
40	CEBPB	chr10:23104903-23106509	HCT-116	colon:	n/a	chr10:23105065-23105076 chr10:23105063-23105076 chr10:23105063-23105076 chr10:23105063-23105076 chr10:23105065-23105076
41	CEBPB	chr10:23122257-23122625	IMR90	lung:	n/a	chr10:23122434-23122443 chr10:23122485-23122493 chr10:23122434-23122443 chr10:23122432-23122443 chr10:23122434-23122443
42	CEBPB	chr10:23119314-23119612	IMR90	lung:	n/a	chr10:23119488-23119499
43	CEBPB	chr10:23122367-23122504	K562	blood:	n/a	chr10:23122434-23122443 chr10:23122485-23122493 chr10:23122434-23122443 chr10:23122432-23122443 chr10:23122434-23122443
44	CEBPB	chr10:23111809-23112644	HCT-116	colon:	n/a	n/a
45	CEBPB	chr10:23105863-23106159	K562	blood:	n/a	n/a
46	CEBPB	chr10:23105869-23106255	A549	lung:	n/a	n/a
47	CEBPB	chr10:23065385-23065692	IMR90	lung:	n/a	chr10:23065540-23065551 chr10:23065523-23065534
48	CEBPB	chr10:23086814-23087021	IMR90	lung:	n/a	n/a
49	CEBPB	chr10:23105813-23106305	A549	lung:	n/a	n/a
50	CEBPB	chr10:23101641-23101997	K562	blood:	n/a	chr10:23101937-23101950

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:23122421-23122471	AG04449	skin:	fetal
2	chr10:23122421-23122471	AG04449	skin:	fetal
3	chr10:23100186-23100236	NB4	blood:	n/a
4	chr10:23105280-23105330	AG09309	skin:	n/a
5	chr10:23122421-23122471	MCF10A-Er-Src	breast:	n/a
6	chr10:23122421-23122471	AG09309	skin:	n/a
7	chr10:23122421-23122471	HEEpiC	esophagus:	n/a
8	chr10:23122421-23122471	Jurkat	blood:	n/a
9	chr10:23112840-23112890	NHDF-neo	bronchial:	n/a
10	chr10:23100186-23100236	GM06990	blood:	n/a
11	chr10:23122421-23122471	CMK	blood:	n/a
12	chr10:23112840-23112890	GM19239	blood:	n/a
13	chr10:23093955-23094005	AoSMC	blood vessel:	n/a
14	chr10:23105280-23105330	H1-hESC	embryonic stem cell:	embryo
15	chr10:23122421-23122471	BJ	skin:	n/a
16	chr10:23100186-23100236	AG04449	skin:	fetal
17	chr10:23122421-23122471	AoSMC	blood vessel:	n/a
18	chr10:23100186-23100236	HCPEpiC	choroid plexus:	n/a
19	chr10:23112840-23112890	HEK293	kidney:	embryo
20	chr10:23112840-23112890	GM12891	blood:	n/a
21	chr10:23122421-23122471	GM12891	blood:	n/a
22	chr10:23105280-23105330	HCM	heart:	n/a
23	chr10:23093955-23094005	GM12892	blood:	n/a
24	chr10:23112840-23112890	HCPEpiC	choroid plexus:	n/a
25	chr10:23105280-23105330	ProgFib	skin:	n/a
26	chr10:23105280-23105330	MCF10A-Er-Src	breast:	n/a
27	chr10:23122421-23122471	HUVEC	blood vessel:	n/a
28	chr10:23093955-23094005	HRPEpiC	eye:	n/a
29	chr10:23100186-23100236	IMR90	lung:	fetal
30	chr10:23112840-23112890	HNPCEpiC	eye:	n/a
31	chr10:23100186-23100236	HRPEpiC	eye:	n/a
32	chr10:23122421-23122471	Hela-S3	cervix:	n/a
33	chr10:23100186-23100236	SK-N-SH_RA	brain:	n/a
34	chr10:23093955-23094005	IMR90	lung:	fetal
35	chr10:23093955-23094005	HNPCEpiC	eye:	n/a
36	chr10:23105280-23105330	SK-N-SH	brain:	n/a
37	chr10:23093955-23094005	SK-N-MC	brain:	n/a
38	chr10:23100186-23100236	Hepatocyte	liver:	n/a
39	chr10:23122421-23122471	PFSK-1	brain:	n/a
40	chr10:23112840-23112890	MCF10A-Er-Src	breast:	n/a
41	chr10:23105280-23105330	HRE	kidney:	n/a
42	chr10:23112840-23112890	SK-N-MC	brain:	n/a
43	chr10:23093955-23094005	HCM	heart:	n/a
44	chr10:23105280-23105330	HepG2	liver:	n/a
45	chr10:23100186-23100236	ECC-1	luminal epithelium:	n/a
46	chr10:23122421-23122471	NHDF-neo	bronchial:	n/a
47	chr10:23105280-23105330	T-47D	breast:	n/a
48	chr10:23122421-23122471	HCM	heart:	n/a
49	chr10:23100186-23100236	HCT-116	colon:	n/a
50	chr10:23105280-23105330	CMK	blood:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:23063472..23065869-chr10:23066281..23069279,2	MCF-7	breast:
2	chr10:23093031..23094566-chr10:23095292..23097801,2	K562	blood:
3	chr10:23090832..23093813-chr10:23094691..23097138,2	K562	blood:
4	chr10:22918208..22920899-chr10:23105511..23107568,2	K562	blood:
5	chr10:23090452..23092008-chr10:23092511..23094369,2	K562	blood:
6	chr10:22989774..22994119-chr10:23044705..23049476,4	K562	blood:
7	chr10:23001422..23003561-chr10:23104622..23106652,2	K562	blood:
8	chr10:23090452..23092008-chr10:23092511..23094369,2	K562	blood:
9	chr10:23077180..23079268-chr10:23081726..23083280,2	MCF-7	breast:
10	chr10:23052115..23054835-chr10:23068399..23071194,3	MCF-7	breast:
11	chr10:23104132..23107506-chr10:23342632..23345950,5	K562	blood:
12	chr10:23108350..23110546-chr10:23110740..23113681,3	K562	blood:
13	chr10:23108350..23110546-chr10:23110740..23113681,3	K562	blood:
14	chr10:23000874..23003179-chr10:23095051..23097837,2	K562	blood:
15	chr10:23108350..23110476-chr10:23111720..23113681,2	K562	blood:
16	chr10:23121025..23123725-chr10:23125978..23128015,2	K562	blood:
17	chr10:23090832..23093813-chr10:23094691..23097138,2	K562	blood:
18	chr10:23076401..23079823-chr10:23343221..23346091,3	K562	blood:
19	chr10:23052115..23054835-chr10:23068399..23071194,3	MCF-7	breast:
20	chr10:23063472..23065869-chr10:23066281..23069279,2	MCF-7	breast:
21	chr10:23108350..23110476-chr10:23111720..23113681,2	K562	blood:
22	chr10:23105492..23108176-chr10:23344426..23345990,3	K562	blood:
23	chr10:23098595..23101084-chr2:58865453..58867756,2	MCF-7	breast:
24	chr10:23092682..23094839-chr2:187127661..187130019,2	MCF-7	breast:
25	chr10:23093031..23094566-chr10:23095292..23097801,2	K562	blood:
26	chr10:23093887..23094416-chr10:23266755..23267519,2	MCF-7	breast:
27	chr10:23080355..23083056-chr10:23096446..23098590,2	K562	blood:
28	chr10:23080355..23083056-chr10:23096446..23098590,2	K562	blood:
29	chr10:23089513..23092332-chr10:23095638..23097901,2	K562	blood:
30	chr10:23108692..23110534-chr10:23308268..23309848,2	K562	blood:
31	chr10:23002586..23004698-chr10:23069532..23071170,2	K562	blood:
32	chr10:22980163..22981684-chr10:23106478..23108245,2	K562	blood:
33	chr10:23077180..23079268-chr10:23081726..23083280,2	MCF-7	breast:
34	chr10:23112958..23115115-chr10:23343406..23346225,2	K562	blood:
35	chr10:23103158..23106579-chr10:23341900..23344132,3	K562	blood:
36	chr10:23121025..23123725-chr10:23125978..23128015,2	K562	blood:
37	chr10:23089513..23092332-chr10:23095638..23097901,2	K562	blood:
38	chr10:23001483..23003855-chr10:23099770..23102739,2	K562	blood:
39	chr10:23124982..23127882-chr10:23130656..23134139,4	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: 2927 )
Associated
traits (count: 38 )

Variant overlapped rSNPs/rCNVs (count:2927 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7922014	chr10:23049139-23049140	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs562697119	chr10:23049153-23049154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs147159717	chr10:23049190-23049191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs140521741	chr10:23049243-23049244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs74121608	chr10:23049322-23049323	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs527997276	chr10:23049349-23049350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185525603	chr10:23049436-23049437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs529125079	chr10:23049440-23049441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570766036	chr10:23049480-23049481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs59315357	chr10:23049493-23049494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550255885	chr10:23049509-23049510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs149715277	chr10:23049521-23049522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189987264	chr10:23049568-23049569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570202752	chr10:23049622-23049623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538020790	chr10:23049644-23049645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554498123	chr10:23049646-23049647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145654201	chr10:23049650-23049651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148902522	chr10:23049651-23049652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs142834268	chr10:23049653-23049654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183172145	chr10:23049667-23049668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374600676	chr10:23049696-23049697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186953020	chr10:23049703-23049704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562235919	chr10:23049720-23049721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575767659	chr10:23049724-23049725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11013120	chr10:23049735-23049736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532871522	chr10:23049739-23049740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542865636	chr10:23049750-23049751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372352320	chr10:23049752-23049753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547775381	chr10:23049756-23049757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs367944621	chr10:23049768-23049769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564844330	chr10:23049805-23049806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533352349	chr10:23049854-23049855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11423438	chr10:23049855-23049856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550232322	chr10:23049871-23049872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375774483	chr10:23049873-23049874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570145120	chr10:23049890-23049891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs76403520	chr10:23049923-23049924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557637567	chr10:23049924-23049925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11340322	chr10:23049940-23049941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201365316	chr10:23049941-23049942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs74890630	chr10:23049953-23049954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372036728	chr10:23049964-23049965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566483391	chr10:23049978-23049979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548333298	chr10:23049994-23049995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568174578	chr10:23050008-23050009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs534045795	chr10:23050055-23050056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553779482	chr10:23050059-23050060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs151038760	chr10:23050174-23050175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs539032106	chr10:23050180-23050181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs555760606	chr10:23050191-23050192	Weak transcription Enhancers	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:592 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23043400-23050200	Weak transcription	Brain Anterior Caudate	brain
2	chr10:23046000-23050000	Weak transcription	Brain Angular Gyrus	brain
3	chr10:23047400-23050000	Weak transcription	Brain Substantia Nigra	brain
4	chr10:23047600-23050000	Weak transcription	Brain Cingulate Gyrus	brain
5	chr10:23048000-23050000	Weak transcription	Brain Hippocampus Middle	brain
6	chr10:23048600-23049600	Enhancers	HepG2	liver
7	chr10:23049000-23051800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr10:23050000-23050400	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr10:23050000-23050400	Enhancers	Brain Cingulate Gyrus	brain
10	chr10:23050000-23051200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr10:23050000-23051200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr10:23050000-23051200	Enhancers	K562	blood
13	chr10:23050000-23051600	Enhancers	Brain Angular Gyrus	brain
14	chr10:23050000-23051600	Enhancers	Brain Substantia Nigra	brain
15	chr10:23050000-23052400	Enhancers	Brain Hippocampus Middle	brain
16	chr10:23050200-23051200	Enhancers	H1 Cell Line	embryonic stem cell
17	chr10:23050200-23051400	Enhancers	Brain Anterior Caudate	brain
18	chr10:23050200-23051800	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr10:23050400-23051400	Weak transcription	Brain Cingulate Gyrus	brain
20	chr10:23050600-23051000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr10:23050600-23051200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr10:23050600-23051200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr10:23050800-23051200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr10:23050800-23051400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr10:23051200-23053200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr10:23051400-23052400	Enhancers	Brain Cingulate Gyrus	brain
27	chr10:23051400-23053200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr10:23051400-23053200	Weak transcription	Brain Anterior Caudate	brain
29	chr10:23051600-23052000	Weak transcription	Brain Substantia Nigra	brain
30	chr10:23051800-23052200	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr10:23051800-23052400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr10:23052000-23057600	Enhancers	Brain Substantia Nigra	brain
33	chr10:23052200-23052400	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr10:23052200-23052600	Enhancers	Primary B cells from peripheral blood	blood
35	chr10:23052400-23053200	Weak transcription	Brain Hippocampus Middle	brain
36	chr10:23052400-23053400	Weak transcription	Brain Cingulate Gyrus	brain
37	chr10:23052400-23053400	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr10:23052600-23053000	Weak transcription	Primary B cells from peripheral blood	blood
39	chr10:23053000-23053600	Enhancers	Right Atrium	heart
40	chr10:23053000-23054000	Enhancers	Aorta	Aorta
41	chr10:23053000-23057000	Enhancers	Primary B cells from peripheral blood	blood
42	chr10:23053200-23053400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr10:23053200-23053800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr10:23053200-23054000	Enhancers	Brain Anterior Caudate	brain
45	chr10:23053200-23054000	Enhancers	Brain Hippocampus Middle	brain
46	chr10:23053200-23054200	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr10:23053400-23054000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr10:23053400-23054000	Enhancers	Brain Cingulate Gyrus	brain
49	chr10:23053400-23054200	Enhancers	Adipose Nuclei	Adipose
50	chr10:23053400-23054200	Enhancers	Brain Inferior Temporal Lobe	brain

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