Variant report

Variant	nsv825305
Chromosome Location	chr10:23698620-23740919
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	chr10:23727699-23728099	K562	blood:	n/a	n/a
2	ARID3A	chr10:23733285-23733343	HepG2	liver:	n/a	n/a
3	ATF1	chr10:23727682-23728115	K562	blood:	n/a	n/a
4	ATF1	chr10:23737809-23738055	K562	blood:	n/a	n/a
5	ATF1	chr10:23734491-23734809	K562	blood:	n/a	n/a
6	ATF2	chr10:23702514-23703106	GM12878	blood:	n/a	n/a
7	ATF2	chr10:23737616-23738178	GM12878	blood:	n/a	n/a
8	ATF2	chr10:23702536-23703127	GM12878	blood:	n/a	n/a
9	ATF3	chr10:23727561-23727818	HepG2	liver:	n/a	chr10:23727728-23727748
10	ATF3	chr10:23727809-23728025	GM12878	blood:	n/a	chr10:23727842-23727862 chr10:23727864-23727873 chr10:23727831-23727851 chr10:23727840-23727853 chr10:23727947-23727967 chr10:23727841-23727852 chr10:23727871-23727880
11	ATF3	chr10:23727825-23728180	GM12878	blood:	n/a	chr10:23727842-23727862 chr10:23728049-23728058 chr10:23727864-23727873 chr10:23727831-23727851 chr10:23727840-23727853 chr10:23727947-23727967 chr10:23728171-23728180 chr10:23727841-23727852 chr10:23728110-23728119 chr10:23727871-23727880
12	ATF3	chr10:23727846-23728076	HepG2	liver:	n/a	chr10:23728049-23728058 chr10:23727864-23727873 chr10:23727947-23727967 chr10:23727871-23727880
13	ATF3	chr10:23727791-23728059	H1-hESC	embryonic stem cell:	n/a	chr10:23727842-23727862 chr10:23728049-23728058 chr10:23727864-23727873 chr10:23727831-23727851 chr10:23727840-23727853 chr10:23727947-23727967 chr10:23727841-23727852 chr10:23727871-23727880
14	ATF3	chr10:23727555-23728054	K562	blood:	n/a	chr10:23727842-23727862 chr10:23727864-23727873 chr10:23727831-23727851 chr10:23727728-23727748 chr10:23727840-23727853 chr10:23727947-23727967 chr10:23727841-23727852 chr10:23727871-23727880
15	BACH1	chr10:23729168-23729332	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr10:23727445-23728096	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr10:23702630-23702959	GM12878	blood:	n/a	n/a
18	BCL11A	chr10:23702589-23702949	GM12878	blood:	n/a	n/a
19	BCLAF1	chr10:23702511-23703028	GM12878	blood:	n/a	n/a
20	BCLAF1	chr10:23727438-23728265	GM12878	blood:	n/a	chr10:23728075-23728088 chr10:23728076-23728089 chr10:23728171-23728184 chr10:23728078-23728091 chr10:23728081-23728094
21	BHLHE40	chr10:23702596-23703036	GM12878	blood:	n/a	n/a
22	BHLHE40	chr10:23727527-23728260	K562	blood:	n/a	chr10:23728075-23728091 chr10:23728078-23728094 chr10:23728103-23728119 chr10:23728076-23728092 chr10:23728100-23728116
23	BHLHE40	chr10:23728711-23728778	K562	blood:	n/a	n/a
24	BHLHE40	chr10:23734589-23734639	K562	blood:	n/a	n/a
25	BHLHE40	chr10:23727520-23728272	GM12878	blood:	n/a	chr10:23728075-23728091 chr10:23728078-23728094 chr10:23728103-23728119 chr10:23728076-23728092 chr10:23728100-23728116
26	BHLHE40	chr10:23727507-23728120	HepG2	liver:	n/a	chr10:23728075-23728091 chr10:23728078-23728094 chr10:23728103-23728119 chr10:23728076-23728092 chr10:23728100-23728116
27	BHLHE40	chr10:23738810-23739128	HepG2	liver:	n/a	chr10:23739004-23739013
28	BHLHE40	chr10:23738836-23739129	K562	blood:	n/a	chr10:23739004-23739013
29	BRCA1	chr10:23727584-23727783	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr10:23727607-23727943	HepG2	liver:	n/a	n/a
31	BRCA1	chr10:23721246-23721792	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr10:23727330-23727803	K562	blood:	n/a	n/a
33	CCNT2	chr10:23727543-23728842	K562	blood:	n/a	chr10:23727864-23727873 chr10:23728171-23728180 chr10:23728307-23728316
34	CCNT2	chr10:23729049-23729330	K562	blood:	n/a	n/a
35	CEBPB	chr10:23705933-23705938	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr10:23701085-23701462	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr10:23710950-23711375	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr10:23702573-23703138	GM12878	blood:	n/a	chr10:23702691-23702702
39	CEBPB	chr10:23702626-23702968	HepG2	liver:	n/a	chr10:23702691-23702702
40	CEBPB	chr10:23715319-23715642	HepG2	liver:	n/a	chr10:23715488-23715497 chr10:23715486-23715497
41	CEBPB	chr10:23715358-23715587	IMR90	lung:	n/a	chr10:23715488-23715497 chr10:23715486-23715497
42	CEBPB	chr10:23737838-23738051	IMR90	lung:	n/a	n/a
43	CEBPB	chr10:23727664-23727698	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr10:23708642-23708831	A549	lung:	n/a	chr10:23708755-23708766
45	CEBPB	chr10:23710012-23710304	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr10:23702560-23702745	IMR90	lung:	n/a	chr10:23702691-23702702
47	CEBPB	chr10:23711736-23711740	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr10:23708653-23708871	HepG2	liver:	n/a	chr10:23708755-23708766
49	CEBPB	chr10:23738390-23738435	K562	blood:	n/a	n/a
50	CEBPB	chr10:23702602-23702811	Hela-S3	cervix:	n/a	chr10:23702691-23702702

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:23732088-23732138	PANC-1	pancreas:	n/a
2	chr10:23728376-23728426	HL-60	blood:	n/a
3	chr10:23732088-23732138	NB4	blood:	n/a
4	chr10:23728250-23728300	NB4	blood:	n/a
5	chr10:23727984-23728034	ProgFib	skin:	n/a
6	chr10:23729247-23729297	NHBE	bronchial:	n/a
7	chr10:23728250-23728300	NH-A	brain:	n/a
8	chr10:23707382-23707432	NH-A	brain:	n/a
9	chr10:23732088-23732138	AoSMC	blood vessel:	n/a
10	chr10:23727984-23728034	SKMC	muscle:	n/a
11	chr10:23727572-23727622	HEK293	kidney:	embryo
12	chr10:23729247-23729297	HCT-116	colon:	n/a
13	chr10:23728250-23728300	PFSK-1	brain:	n/a
14	chr10:23727984-23728034	HMEC	breast:	n/a
15	chr10:23728250-23728300	SAEC	small airway:	n/a
16	chr10:23727931-23727981	AG09319	gingival:	n/a
17	chr10:23729522-23729572	SKMC	muscle:	n/a
18	chr10:23727572-23727622	HUVEC	blood vessel:	n/a
19	chr10:23727931-23727981	NT2-D1	testis:	n/a
20	chr10:23727572-23727622	HRPEpiC	eye:	n/a
21	chr10:23707382-23707432	HEK293	kidney:	embryo
22	chr10:23729247-23729297	Hepatocyte	liver:	n/a
23	chr10:23729247-23729297	SKMC	muscle:	n/a
24	chr10:23732088-23732138	GM06990	blood:	n/a
25	chr10:23729522-23729572	T-47D	breast:	n/a
26	chr10:23729522-23729572	HNPCEpiC	eye:	n/a
27	chr10:23727572-23727622	AG09319	gingival:	n/a
28	chr10:23732088-23732138	AG04450	lung:	fetal
29	chr10:23732088-23732138	GM12878	blood:	n/a
30	chr10:23727572-23727622	IMR90	lung:	fetal
31	chr10:23707382-23707432	HMEC	breast:	n/a
32	chr10:23728376-23728426	SKMC	muscle:	n/a
33	chr10:23728250-23728300	HIPEpiC	eye:	n/a
34	chr10:23728376-23728426	U87	brain:	n/a
35	chr10:23729247-23729297	Jurkat	blood:	n/a
36	chr10:23728376-23728426	NB4	blood:	n/a
37	chr10:23729247-23729297	HAEpiC	amniotic membrane:	n/a
38	chr10:23707382-23707432	HPAEpiC	pulmonary alveolar:	n/a
39	chr10:23728376-23728426	HMEC	breast:	n/a
40	chr10:23707382-23707432	HCM	heart:	n/a
41	chr10:23707382-23707432	GM12878	blood:	n/a
42	chr10:23732088-23732138	MCF10A-Er-Src	breast:	n/a
43	chr10:23732088-23732138	HRCEpiC	kidney:	n/a
44	chr10:23727931-23727981	MCF10A-Er-Src	breast:	n/a
45	chr10:23728376-23728426	AG09309	skin:	n/a
46	chr10:23728376-23728426	HCM	heart:	n/a
47	chr10:23728376-23728426	ECC-1	luminal epithelium:	n/a
48	chr10:23728376-23728426	K562	blood:	n/a
49	chr10:23727984-23728034	HepG2	liver:	n/a
50	chr10:23729522-23729572	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:23727668..23728613-chr16:56965645..56966488,2	Hela-S3	cervix:
2	chr10:23707659..23710608-chr10:23712696..23714287,2	MCF-7	breast:
3	chr10:23715110..23718111-chr10:23726420..23729994,4	MCF-7	breast:
4	chr10:23707659..23710608-chr10:23712696..23714287,2	MCF-7	breast:
5	chr10:23718207..23720291-chr10:23725300..23726968,2	K562	blood:
6	chr10:23707420..23709381-chr10:23709579..23712222,2	MCF-7	breast:
7	chr10:23718339..23720291-chr10:23725094..23726968,2	K562	blood:
8	chr10:23729334..23732028-chr10:23747440..23749180,2	MCF-7	breast:
9	chr10:23732769..23734965-chr10:23736236..23739152,2	K562	blood:
10	chr10:23698540..23700935-chr10:23715186..23717309,2	MCF-7	breast:
11	chr10:23732386..23735333-chr10:23736238..23738738,2	MCF-7	breast:
12	chr10:23727770..23728754-chr6:170125045..170126039,2	Hela-S3	cervix:
13	chr10:23732769..23734965-chr10:23736236..23739152,2	K562	blood:
14	chr10:23698540..23700935-chr10:23715186..23717309,2	MCF-7	breast:
15	chr10:23726848..23728712-chr10:23736442..23738987,2	K562	blood:
16	chr10:23735979..23737585-chr10:23742563..23744622,2	MCF-7	breast:
17	chr10:23616493..23618340-chr10:23698443..23701341,2	MCF-7	breast:
18	chr10:23732386..23735333-chr10:23736238..23738738,2	MCF-7	breast:
19	chr10:23726971..23730687-chr10:23732679..23735165,3	MCF-7	breast:
20	chr10:23732163..23734973-chr10:23736467..23739152,3	K562	blood:
21	chr10:23737577..23740196-chr10:23740591..23742744,2	K562	blood:
22	chr10:23718207..23720291-chr10:23725300..23726968,2	K562	blood:
23	chr10:23718339..23720291-chr10:23725094..23726968,2	K562	blood:
24	chr10:23728096..23730469-chr10:23730500..23732412,3	MCF-7	breast:
25	chr10:23737577..23740196-chr10:23740591..23742744,2	K562	blood:
26	chr10:23707420..23709381-chr10:23709579..23712222,2	MCF-7	breast:
27	chr10:23710434..23711949-chr10:23726274..23728400,2	MCF-7	breast:
28	chr10:23719313..23724177-chr10:23725494..23728219,5	MCF-7	breast:
29	chr10:23732163..23734973-chr10:23736467..23739152,3	K562	blood:
30	chr10:23720439..23723434-chr10:23726111..23729992,4	MCF-7	breast:
31	chr10:23731583..23733567-chr10:23742543..23744623,2	MCF-7	breast:
32	chr10:23631888..23635089-chr10:23727661..23730060,4	MCF-7	breast:
33	chr10:23710737..23713285-chr10:23727540..23729458,2	MCF-7	breast:
34	chr10:23727536..23729786-chr10:23733356..23736222,2	MCF-7	breast:
35	chr10:23734822..23737617-chr10:23738406..23741055,2	MCF-7	breast:
36	chr10:23734822..23737617-chr10:23738406..23741055,2	MCF-7	breast:

No.	miRNA target gene	miRNA name	Chromosome Location
1	OTUD1	hsa-miR-320a	chr10:23730200-23730223
2	OTUD1	hsa-miR-181a-5p	chr10:23729959-23729981
3	OTUD1	hsa-miR-340-5p	chr10:23730231-23730252
4	OTUD1	hsa-miR-19b-3p	chr10:23730642-23730665
5	OTUD1	hsa-miR-340-5p	chr10:23730709-23730729
6	OTUD1	hsa-miR-19b-3p	chr10:23730155-23730162
7	OTUD1	hsa-miR-181a-5p	chr10:23731061-23731082
8	OTUD1	hsa-miR-19b-3p	chr10:23730142-23730162

Variant related genes	Relation type
OTUD1	TF binding region
OTUD1	CpG island
ENSG00000227704	chromatin interactions
ENSG00000224215	chromatin interactions
ENSG00000179133	chromatin interactions
ENSG00000165312	chromatin interactions
ENSG00000232640	chromatin interactions
ENSG00000051108	chromatin interactions

Extended variants
information (count: 1865 )
Associated
traits (count: 39 )

Variant overlapped rSNPs/rCNVs (count:1865 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543038555	chr10:23698641-23698642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs553078667	chr10:23698677-23698678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573158430	chr10:23698760-23698761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531684102	chr10:23698780-23698781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545120183	chr10:23698796-23698797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550087878	chr10:23698799-23698800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564991420	chr10:23698831-23698832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532969591	chr10:23698852-23698853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139511270	chr10:23698903-23698904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185786079	chr10:23698972-23698973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529159292	chr10:23698980-23698981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73602544	chr10:23698987-23698988	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs531686225	chr10:23698999-23699000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549504460	chr10:23699093-23699094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190060442	chr10:23699132-23699133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539834901	chr10:23699134-23699135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551508016	chr10:23699165-23699166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs367647881	chr10:23699224-23699225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368999891	chr10:23699241-23699242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571352281	chr10:23699283-23699284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571473301	chr10:23699306-23699307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557253696	chr10:23699310-23699311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567985316	chr10:23699359-23699360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536562076	chr10:23699366-23699367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10828451	chr10:23699379-23699380	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs572906112	chr10:23699410-23699411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183070337	chr10:23699431-23699432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187493271	chr10:23699438-23699439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs193298310	chr10:23699439-23699440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183781714	chr10:23699444-23699445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543636263	chr10:23699452-23699453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376630061	chr10:23699455-23699456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547194706	chr10:23699456-23699457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565804555	chr10:23699510-23699511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529055523	chr10:23699528-23699529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547432586	chr10:23699549-23699550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374986654	chr10:23699552-23699553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376121664	chr10:23699569-23699570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535946007	chr10:23699578-23699579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554599435	chr10:23699581-23699582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200994415	chr10:23699594-23699595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7100504	chr10:23699610-23699611	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs551396094	chr10:23699646-23699647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571396631	chr10:23699647-23699648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147599991	chr10:23699698-23699699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs115143740	chr10:23699733-23699734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567785902	chr10:23699749-23699750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536807999	chr10:23699792-23699793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs116719588	chr10:23699804-23699805	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
50	rs149029592	chr10:23699811-23699812	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:39)

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
Breast cancer	22522925	CNVD

Chromatin state (count:1033 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23689400-23701000	Weak transcription	Osteobl	bone
2	chr10:23693800-23706400	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr10:23693800-23706400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr10:23694000-23701000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr10:23694600-23701400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr10:23694600-23707800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr10:23696000-23700600	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr10:23697000-23706400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr10:23697600-23701000	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr10:23698400-23701200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr10:23699800-23700000	Enhancers	Primary B cells from cord blood	blood
12	chr10:23699800-23700000	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr10:23699800-23700000	Bivalent/Poised TSS	Primary T helper memory cells from peripheral blood 1	blood
14	chr10:23699800-23700000	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr10:23699800-23700000	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
16	chr10:23699800-23700000	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr10:23699800-23700000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr10:23700000-23702800	Weak transcription	Primary B cells from cord blood	blood
19	chr10:23700600-23703800	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr10:23701000-23701200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
21	chr10:23701000-23701400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr10:23701000-23701600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr10:23701000-23701600	Enhancers	HSMM	muscle
24	chr10:23701000-23701600	Enhancers	HSMMtube	muscle
25	chr10:23701000-23701600	Enhancers	Osteobl	bone
26	chr10:23701000-23701800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr10:23701000-23703400	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr10:23701200-23701400	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr10:23701200-23701600	Enhancers	Primary B cells from peripheral blood	blood
30	chr10:23701200-23701600	Enhancers	Hela-S3	cervix
31	chr10:23701200-23707800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr10:23701400-23701600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr10:23701400-23701600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr10:23701400-23701600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
35	chr10:23701400-23704200	Enhancers	GM12878-XiMat	blood
36	chr10:23701400-23706200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr10:23701600-23702000	Weak transcription	Primary B cells from peripheral blood	blood
38	chr10:23701600-23702000	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr10:23701600-23707400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr10:23701600-23709600	Weak transcription	Hela-S3	cervix
41	chr10:23702000-23702400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
42	chr10:23702000-23703600	Enhancers	Primary B cells from peripheral blood	blood
43	chr10:23702200-23703400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr10:23702400-23703000	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr10:23702800-23703400	Enhancers	Primary B cells from cord blood	blood
46	chr10:23703000-23703400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
47	chr10:23703400-23703800	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr10:23704000-23704200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr10:23704200-23704400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr10:23704200-23705800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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