Variant report

Variant	nsv430231
Chromosome Location	chr10:52119046-52163531
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1044)
CpG islands
(count:244)
Chromatin interactive
region (count:77)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1044 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:52124449-52124686	K562	blood:	n/a	n/a
2	ARID3A	chr10:52153043-52153961	K562	blood:	n/a	n/a
3	ARID3A	chr10:52132787-52132975	K562	blood:	n/a	n/a
4	ARID3A	chr10:52147139-52147416	K562	blood:	n/a	n/a
5	ARID3A	chr10:52156721-52157006	K562	blood:	n/a	n/a
6	ARID3A	chr10:52127535-52127844	K562	blood:	n/a	n/a
7	ARID3A	chr10:52145464-52145662	HepG2	liver:	n/a	n/a
8	ARID3A	chr10:52120334-52120358	K562	blood:	n/a	n/a
9	ARID3A	chr10:52158346-52158930	K562	blood:	n/a	n/a
10	ARID3A	chr10:52154906-52155475	HepG2	liver:	n/a	n/a
11	ARID3A	chr10:52153154-52153949	HepG2	liver:	n/a	n/a
12	ARID3A	chr10:52152230-52152647	HepG2	liver:	n/a	n/a
13	ATF1	chr10:52153039-52153886	K562	blood:	n/a	n/a
14	ATF2	chr10:52134583-52135111	GM12878	blood:	n/a	n/a
15	ATF2	chr10:52156449-52157208	GM12878	blood:	n/a	n/a
16	ATF2	chr10:52156486-52157137	GM12878	blood:	n/a	n/a
17	ATF2	chr10:52122180-52122928	GM12878	blood:	n/a	n/a
18	ATF2	chr10:52122262-52123094	GM12878	blood:	n/a	n/a
19	ATF3	chr10:52163202-52163479	K562	blood:	n/a	n/a
20	ATF3	chr10:52153507-52153922	K562	blood:	n/a	n/a
21	ATF3	chr10:52152945-52153352	K562	blood:	n/a	n/a
22	BACH1	chr10:52125123-52125148	K562	blood:	n/a	n/a
23	BACH1	chr10:52137292-52137448	K562	blood:	n/a	n/a
24	BACH1	chr10:52139666-52139687	K562	blood:	n/a	n/a
25	BATF	chr10:52156516-52157121	GM12878	blood:	n/a	n/a
26	BATF	chr10:52156551-52157040	GM12878	blood:	n/a	n/a
27	BCL11A	chr10:52156618-52157050	GM12878	blood:	n/a	chr10:52156873-52156882
28	BCL3	chr10:52122211-52122788	GM12878	blood:	n/a	chr10:52122692-52122701
29	BCLAF1	chr10:52122244-52123147	GM12878	blood:	n/a	chr10:52122692-52122701
30	BCLAF1	chr10:52156520-52157226	GM12878	blood:	n/a	chr10:52156873-52156882
31	BHLHE40	chr10:52153156-52153821	K562	blood:	n/a	n/a
32	BHLHE40	chr10:52131610-52131907	K562	blood:	n/a	n/a
33	BHLHE40	chr10:52122410-52122772	GM12878	blood:	n/a	n/a
34	BHLHE40	chr10:52156460-52156754	K562	blood:	n/a	n/a
35	BHLHE40	chr10:52157034-52157392	K562	blood:	n/a	n/a
36	BHLHE40	chr10:52153361-52153865	HepG2	liver:	n/a	n/a
37	BRCA1	chr10:52152819-52153936	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr10:52154884-52155413	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr10:52156229-52156417	Hela-S3	cervix:	n/a	n/a
40	CBX3	chr10:52122858-52123308	K562	blood:	n/a	n/a
41	CBX3	chr10:52136699-52137133	K562	blood:	n/a	n/a
42	CCNT2	chr10:52150606-52150745	K562	blood:	n/a	n/a
43	CCNT2	chr10:52161645-52161807	K562	blood:	n/a	n/a
44	CCNT2	chr10:52158746-52158834	K562	blood:	n/a	n/a
45	CCNT2	chr10:52127549-52127843	K562	blood:	n/a	n/a
46	CCNT2	chr10:52153187-52153893	K562	blood:	n/a	n/a
47	CCNT2	chr10:52158337-52158405	K562	blood:	n/a	n/a
48	CCNT2	chr10:52156368-52157018	K562	blood:	n/a	chr10:52156606-52156615 chr10:52156682-52156702 chr10:52156519-52156528
49	CCNT2	chr10:52157302-52157305	K562	blood:	n/a	n/a
50	CCNT2	chr10:52120745-52120879	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:52156632-52156682	AG09319	gingival:	n/a
2	chr10:52120283-52120333	NHBE	bronchial:	n/a
3	chr10:52162583-52162633	AG09319	gingival:	n/a
4	chr10:52145861-52145911	HCM	heart:	n/a
5	chr10:52156632-52156682	LNCaP	prostate:	n/a
6	chr10:52162583-52162633	HRE	kidney:	n/a
7	chr10:52156632-52156682	SKMC	muscle:	n/a
8	chr10:52120283-52120333	LNCaP	prostate:	n/a
9	chr10:52162583-52162633	HUVEC	blood vessel:	n/a
10	chr10:52162583-52162633	HRCEpiC	kidney:	n/a
11	chr10:52145861-52145911	SK-N-SH	brain:	n/a
12	chr10:52120283-52120333	HCT-116	colon:	n/a
13	chr10:52156632-52156682	HEK293	kidney:	embryo
14	chr10:52145861-52145911	AG04449	skin:	fetal
15	chr10:52156632-52156682	HMEC	breast:	n/a
16	chr10:52145861-52145911	HNPCEpiC	eye:	n/a
17	chr10:52120283-52120333	Caco-2	colon:	n/a
18	chr10:52162583-52162633	BJ	skin:	n/a
19	chr10:52156632-52156682	NH-A	brain:	n/a
20	chr10:52120283-52120333	SAEC	small airway:	n/a
21	chr10:52120283-52120333	AG09319	gingival:	n/a
22	chr10:52162583-52162633	SK-N-MC	brain:	n/a
23	chr10:52120283-52120333	BE2_C	brain:	n/a
24	chr10:52120283-52120333	PANC-1	pancreas:	n/a
25	chr10:52162583-52162633	Caco-2	colon:	n/a
26	chr10:52162583-52162633	NT2-D1	testis:	n/a
27	chr10:52162583-52162633	HRPEpiC	eye:	n/a
28	chr10:52120283-52120333	GM12892	blood:	n/a
29	chr10:52162583-52162633	PFSK-1	brain:	n/a
30	chr10:52120283-52120333	HCPEpiC	choroid plexus:	n/a
31	chr10:52120283-52120333	PFSK-1	brain:	n/a
32	chr10:52162583-52162633	MCF-7	breast:	n/a
33	chr10:52120283-52120333	IMR90	lung:	fetal
34	chr10:52145861-52145911	SAEC	small airway:	n/a
35	chr10:52156632-52156682	HRCEpiC	kidney:	n/a
36	chr10:52162583-52162633	HCM	heart:	n/a
37	chr10:52120283-52120333	GM19239	blood:	n/a
38	chr10:52145861-52145911	MCF10A-Er-Src	breast:	n/a
39	chr10:52145861-52145911	HCT-116	colon:	n/a
40	chr10:52162583-52162633	K562	blood:	n/a
41	chr10:52120283-52120333	NHDF-neo	bronchial:	n/a
42	chr10:52156632-52156682	GM19239	blood:	n/a
43	chr10:52145861-52145911	NT2-D1	testis:	n/a
44	chr10:52145861-52145911	U87	brain:	n/a
45	chr10:52156632-52156682	IMR90	lung:	fetal
46	chr10:52156632-52156682	Caco-2	colon:	n/a
47	chr10:52156632-52156682	ProgFib	skin:	n/a
48	chr10:52156632-52156682	U87	brain:	n/a
49	chr10:52120283-52120333	MCF-7	breast:	n/a
50	chr10:52162583-52162633	RPTEC	kidney:	n/a

(count:77 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:52084925..52086838-chr10:52120229..52123147,2	K562	blood:
2	chr10:52136009..52138905-chr10:52161513..52164062,2	K562	blood:
3	chr10:52149428..52151054-chr10:52153978..52156665,2	K562	blood:
4	chr10:52143975..52146783-chr10:52153265..52157154,4	K562	blood:
5	chr10:52156579..52161749-chr10:52162901..52167145,5	K562	blood:
6	chr10:52127277..52127980-chr10:52180802..52181438,3	MCF-7	breast:
7	chr10:52155995..52158141-chr10:52176386..52179255,3	K562	blood:
8	chr10:52158173..52160799-chr10:52163076..52165080,2	MCF-7	breast:
9	chr10:52097924..52101512-chr10:52122361..52124512,3	K562	blood:
10	chr10:52152624..52157680-chr10:52173844..52179255,6	K562	blood:
11	chr10:52156579..52161749-chr10:52162901..52167145,5	K562	blood:
12	chr10:52125875..52128899-chr10:52129822..52132966,4	K562	blood:
13	chr10:52127262..52128152-chr10:52180974..52181673,2	K562	blood:
14	chr10:52161910..52166825-chr10:52176564..52180969,7	MCF-7	breast:
15	chr10:52139065..52141348-chr10:52143343..52146205,3	K562	blood:
16	chr10:52120816..52123329-chr10:52287278..52290056,2	MCF-7	breast:
17	chr10:52149428..52151054-chr10:52153978..52156665,2	K562	blood:
18	chr10:52131941..52133571-chr10:52135239..52137791,2	MCF-7	breast:
19	chr10:52163174..52165033-chr10:52169624..52171788,2	K562	blood:
20	chr10:52150477..52153075-chr10:52158420..52160955,2	K562	blood:
21	chr10:52152378..52155454-chr10:52174313..52178963,4	MCF-7	breast:
22	chr10:52118184..52120411-chr10:52292971..52295430,2	K562	blood:
23	chr10:52147072..52150928-chr10:52150968..52156665,5	K562	blood:
24	chr10:52144223..52147034-chr10:52152194..52155146,2	MCF-7	breast:
25	chr10:52128591..52131322-chr10:52132559..52135165,2	MCF-7	breast:
26	chr10:52143975..52146783-chr10:52153265..52157154,4	K562	blood:
27	chr10:52131563..52133207-chr10:52144228..52146255,2	K562	blood:
28	chr10:52127857..52130924-chr10:52133934..52136011,3	K562	blood:
29	chr10:52109231..52111670-chr10:52122633..52124290,2	K562	blood:
30	chr10:52131941..52133571-chr10:52135239..52137791,2	MCF-7	breast:
31	chr10:52105040..52107754-chr10:52130504..52132718,2	MCF-7	breast:
32	chr10:52087443..52089388-chr10:52116523..52119614,3	K562	blood:
33	chr10:52154496..52159392-chr10:52160687..52163216,5	K562	blood:
34	chr10:52132102..52134129-chr10:52137496..52139624,2	K562	blood:
35	chr10:52139065..52141348-chr10:52143343..52146205,3	K562	blood:
36	chr10:52132819..52134741-chr10:52135257..52137397,2	K562	blood:
37	chr10:52115339..52118767-chr10:52119079..52123600,6	K562	blood:
38	chr10:52160919..52162899-chr10:52165247..52167938,3	K562	blood:
39	chr10:52139930..52141788-chr10:52152560..52154138,2	MCF-7	breast:
40	chr10:52120330..52124092-chr10:52125493..52129232,4	K562	blood:
41	chr10:52124299..52127180-chr10:52148333..52150881,2	K562	blood:
42	chr10:52133378..52136507-chr10:52147936..52151266,3	MCF-7	breast:
43	chr10:52117604..52119516-chr10:52283791..52286665,2	K562	blood:
44	chr10:52140574..52146052-chr10:52147232..52152526,7	K562	blood:
45	chr10:52153243..52155406-chr10:52158716..52160773,2	K562	blood:
46	chr10:52127520..52128296-chr10:52163800..52164644,2	MCF-7	breast:
47	chr10:52133378..52136507-chr10:52147936..52151266,3	MCF-7	breast:
48	chr10:52124299..52127180-chr10:52148333..52150881,2	K562	blood:
49	chr10:52136009..52138905-chr10:52161513..52164062,2	K562	blood:
50	chr10:52132102..52134129-chr10:52137496..52139624,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000269700	TF binding region
ENSG00000269700	CpG island
ENSG00000238523	chromatin interactions
ENSG00000198964	chromatin interactions
ENSG00000225303	chromatin interactions
ENSG00000269700	chromatin interactions

Extended variants
information (count: 1614 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1614 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2688884	chr10:52119046-52119047	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115671262	chr10:52119100-52119101	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs189986322	chr10:52119166-52119167	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs567524277	chr10:52119184-52119185	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs377749887	chr10:52119190-52119191	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs2574975	chr10:52119297-52119298	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
7	rs566915912	chr10:52119302-52119303	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs568924577	chr10:52119313-52119314	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs199855278	chr10:52119442-52119443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs76105402	chr10:52119443-52119444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34496581	chr10:52119449-52119450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs199779610	chr10:52119455-52119456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539133768	chr10:52119465-52119466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559046951	chr10:52119515-52119516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575657720	chr10:52119519-52119520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs182195066	chr10:52119523-52119524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs10825789	chr10:52119549-52119550	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs575051893	chr10:52119558-52119559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147782947	chr10:52119591-52119592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558913776	chr10:52119602-52119603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572549843	chr10:52119663-52119664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs544606463	chr10:52119669-52119670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11005345	chr10:52119686-52119687	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs116661467	chr10:52119690-52119691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs550731003	chr10:52119799-52119800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs560960379	chr10:52119844-52119845	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs529994973	chr10:52119845-52119846	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546966456	chr10:52119881-52119882	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148846431	chr10:52119977-52119978	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186482952	chr10:52119993-52119994	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575811561	chr10:52120030-52120031	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs572593373	chr10:52120033-52120034	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs539850192	chr10:52120050-52120051	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs552617468	chr10:52120126-52120127	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs371727157	chr10:52120127-52120128	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569304461	chr10:52120137-52120138	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371912428	chr10:52120310-52120311	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs78071707	chr10:52120344-52120345	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190867577	chr10:52120377-52120378	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142578501	chr10:52120386-52120387	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1916568	chr10:52120414-52120415	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs577136312	chr10:52120506-52120507	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs116587818	chr10:52120579-52120580	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs151293255	chr10:52120610-52120611	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs1436206	chr10:52120612-52120613	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs575282789	chr10:52120623-52120624	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs544019214	chr10:52120750-52120751	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs183690394	chr10:52120757-52120758	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531743703	chr10:52120764-52120765	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs10508926	chr10:52120789-52120790	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:59)

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
Intellectual disability	22045946	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
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1195 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52096400-52123000	Weak transcription	Small Intestine	intestine
2	chr10:52103000-52122400	Weak transcription	HUVEC	blood vessel
3	chr10:52104000-52123200	Weak transcription	Aorta	Aorta
4	chr10:52104000-52134000	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr10:52104000-52141400	Weak transcription	Pancreas	Pancrea
6	chr10:52104200-52133600	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr10:52104200-52134200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr10:52104200-52157000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr10:52108000-52120400	Weak transcription	Ovary	ovary
10	chr10:52108000-52125400	Weak transcription	Right Ventricle	heart
11	chr10:52109400-52134400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr10:52109800-52120000	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr10:52110400-52120600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr10:52111800-52123000	Weak transcription	Primary T cells from cord blood	blood
15	chr10:52113600-52120200	Weak transcription	Fetal Stomach	stomach
16	chr10:52115800-52120800	Weak transcription	Fetal Muscle Leg	muscle
17	chr10:52115800-52121000	Weak transcription	Lung	lung
18	chr10:52115800-52142200	Weak transcription	Fetal Intestine Small	intestine
19	chr10:52117200-52119200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr10:52117200-52119400	Enhancers	Brain Substantia Nigra	brain
21	chr10:52117400-52133400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr10:52117600-52121800	Enhancers	Brain Cingulate Gyrus	brain
23	chr10:52117600-52122200	Enhancers	Fetal Lung	lung
24	chr10:52118000-52119400	Flanking Active TSS	K562	blood
25	chr10:52118000-52119800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr10:52118000-52119800	Enhancers	Brain Anterior Caudate	brain
27	chr10:52118200-52119200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
28	chr10:52118200-52119400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr10:52118200-52119400	Enhancers	Brain Angular Gyrus	brain
30	chr10:52118200-52119400	Enhancers	Hela-S3	cervix
31	chr10:52118200-52119800	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr10:52118200-52120200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr10:52118200-52121600	Enhancers	Brain Hippocampus Middle	brain
34	chr10:52118200-52121800	Enhancers	Adipose Nuclei	Adipose
35	chr10:52118400-52119600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr10:52118400-52120200	Weak transcription	HSMMtube	muscle
37	chr10:52118400-52120600	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr10:52118600-52119200	Enhancers	Rectal Mucosa Donor 29	rectum
39	chr10:52118600-52120000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr10:52118600-52120200	Weak transcription	Primary B cells from cord blood	blood
41	chr10:52118600-52120600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr10:52118800-52119200	Enhancers	NHLF	lung
43	chr10:52118800-52121800	Enhancers	Liver	Liver
44	chr10:52119000-52119200	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr10:52119000-52120000	Weak transcription	NHDF-Ad	bronchial
46	chr10:52119000-52120200	Weak transcription	Right Atrium	heart
47	chr10:52119000-52120400	Weak transcription	Psoas Muscle	Psoas
48	chr10:52119000-52121000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
49	chr10:52119000-52121000	Weak transcription	Left Ventricle	heart
50	chr10:52119000-52121600	Weak transcription	NHEK	skin

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