Variant report

Variant	nsv895377
Chromosome Location	chr10:50588990-50678212
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1147)
CpG islands
(count:1772)
Chromatin interactive
region (count:67)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1147 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:50643335-50643526	HepG2	liver:	n/a	n/a
2	ATF1	chr10:50599901-50599921	K562	blood:	n/a	n/a
3	ATF1	chr10:50655062-50655184	K562	blood:	n/a	n/a
4	ATF2	chr10:50627041-50627474	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr10:50615570-50615967	GM12878	blood:	n/a	n/a
6	ATF3	chr10:50616559-50616803	K562	blood:	n/a	n/a
7	ATF3	chr10:50654112-50654389	K562	blood:	n/a	n/a
8	BACH1	chr10:50627142-50627453	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr10:50604737-50604776	K562	blood:	n/a	n/a
10	BACH1	chr10:50603297-50603382	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr10:50605962-50606039	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr10:50627149-50627339	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr10:50615618-50615953	K562	blood:	n/a	n/a
14	BHLHE40	chr10:50616566-50616729	K562	blood:	n/a	n/a
15	BRCA1	chr10:50595150-50595448	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr10:50615592-50615892	HepG2	liver:	n/a	n/a
17	CBX3	chr10:50671643-50672016	K562	blood:	n/a	n/a
18	CCNT2	chr10:50605949-50606794	K562	blood:	n/a	chr10:50606753-50606762
19	CEBPB	chr10:50634643-50635007	MCF-7	breast:	n/a	n/a
20	CEBPB	chr10:50594980-50595652	Hela-S3	cervix:	n/a	chr10:50595197-50595208
21	CEBPB	chr10:50615622-50615950	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr10:50595111-50595329	HepG2	liver:	n/a	chr10:50595197-50595208
23	CEBPB	chr10:50634731-50635026	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr10:50638345-50638543	HepG2	liver:	n/a	chr10:50638445-50638456
25	CEBPB	chr10:50597585-50597882	HepG2	liver:	n/a	chr10:50597749-50597760 chr10:50597748-50597761
26	CEBPB	chr10:50626975-50627525	MCF-7	breast:	n/a	n/a
27	CEBPB	chr10:50652452-50652808	IMR90	lung:	n/a	chr10:50652615-50652626
28	CEBPB	chr10:50595002-50595575	IMR90	lung:	n/a	chr10:50595197-50595208
29	CEBPB	chr10:50597593-50597913	K562	blood:	n/a	chr10:50597749-50597760 chr10:50597748-50597761
30	CEBPB	chr10:50652441-50652866	HepG2	liver:	n/a	chr10:50652615-50652626
31	CEBPB	chr10:50634825-50634942	HepG2	liver:	n/a	n/a
32	CEBPB	chr10:50616524-50616825	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr10:50635852-50635969	K562	blood:	n/a	n/a
34	CEBPB	chr10:50616495-50616811	K562	blood:	n/a	n/a
35	CEBPB	chr10:50634703-50635043	HepG2	liver:	n/a	n/a
36	CEBPB	chr10:50597614-50597791	K562	blood:	n/a	chr10:50597749-50597760 chr10:50597748-50597761
37	CHD1	chr10:50604671-50604736	GM12878	blood:	n/a	n/a
38	CHD1	chr10:50615415-50616082	IMR90	lung:	n/a	n/a
39	CHD2	chr10:50615707-50615958	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr10:50603620-50603731	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr10:50667511-50667518	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr10:50603130-50603326	H1-hESC	embryonic stem cell:	n/a	chr10:50603266-50603276
43	CHD2	chr10:50673895-50674095	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr10:50606098-50606294	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr10:50648390-50648425	K562	blood:	n/a	n/a
46	CHD2	chr10:50595038-50595513	Hela-S3	cervix:	n/a	n/a
47	CREB1	chr10:50616522-50616818	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr10:50616459-50616912	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTBP2	chr10:50602676-50604541	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTBP2	chr10:50605205-50606680	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1772 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:50604569-50604619	HMEC	breast:	n/a
2	chr10:50600265-50600315	RPTEC	kidney:	n/a
3	chr10:50599620-50599670	NB4	blood:	n/a
4	chr10:50604569-50604619	HMEC	breast:	n/a
5	chr10:50600265-50600315	RPTEC	kidney:	n/a
6	chr10:50599620-50599670	NB4	blood:	n/a
7	chr10:50603612-50603662	HCF	heart:	n/a
8	chr10:50604569-50604619	NH-A	brain:	n/a
9	chr10:50602990-50603040	Hepatocyte	liver:	n/a
10	chr10:50606043-50606093	Jurkat	blood:	n/a
11	chr10:50602664-50602714	H1-hESC	embryonic stem cell:	embryo
12	chr10:50606043-50606093	SKMC	muscle:	n/a
13	chr10:50604499-50604549	HNPCEpiC	eye:	n/a
14	chr10:50649795-50649845	AG04450	lung:	fetal
15	chr10:50606683-50606733	AG09319	gingival:	n/a
16	chr10:50649723-50649773	HNPCEpiC	eye:	n/a
17	chr10:50605707-50605757	HRE	kidney:	n/a
18	chr10:50649666-50649716	NHDF-neo	bronchial:	n/a
19	chr10:50604518-50604568	NHDF-neo	bronchial:	n/a
20	chr10:50603359-50603409	NHDF-neo	bronchial:	n/a
21	chr10:50616478-50616528	HCT-116	colon:	n/a
22	chr10:50595181-50595231	BJ	skin:	n/a
23	chr10:50606683-50606733	AG10803	skin:	n/a
24	chr10:50649723-50649773	NH-A	brain:	n/a
25	chr10:50626838-50626888	U87	brain:	n/a
26	chr10:50608262-50608312	Jurkat	blood:	n/a
27	chr10:50603612-50603662	HRPEpiC	eye:	n/a
28	chr10:50603925-50603975	NHDF-neo	bronchial:	n/a
29	chr10:50606683-50606733	Hepatocyte	liver:	n/a
30	chr10:50605613-50605663	MCF10A-Er-Src	breast:	n/a
31	chr10:50608262-50608312	HRCEpiC	kidney:	n/a
32	chr10:50606043-50606093	HCM	heart:	n/a
33	chr10:50649795-50649845	T-47D	breast:	n/a
34	chr10:50609364-50609414	SAEC	small airway:	n/a
35	chr10:50600744-50600794	MCF10A-Er-Src	breast:	n/a
36	chr10:50599882-50599932	HCPEpiC	choroid plexus:	n/a
37	chr10:50605158-50605208	HCF	heart:	n/a
38	chr10:50602664-50602714	HNPCEpiC	eye:	n/a
39	chr10:50609364-50609414	PrEC	prostate:	n/a
40	chr10:50599882-50599932	HCM	heart:	n/a
41	chr10:50616478-50616528	HRE	kidney:	n/a
42	chr10:50606043-50606093	HCPEpiC	choroid plexus:	n/a
43	chr10:50650021-50650071	AG04450	lung:	fetal
44	chr10:50650021-50650071	K562	blood:	n/a
45	chr10:50595181-50595231	HRCEpiC	kidney:	n/a
46	chr10:50616478-50616528	AG10803	skin:	n/a
47	chr10:50649666-50649716	SK-N-MC	brain:	n/a
48	chr10:50599620-50599670	LNCaP	prostate:	n/a
49	chr10:50595181-50595231	PFSK-1	brain:	n/a
50	chr10:50604499-50604549	IMR90	lung:	fetal

(count:67 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:50617316..50619314-chr10:50731416..50733517,2	K562	blood:
2	chr10:50189056..50189642-chr10:50626103..50626925,2	K562	blood:
3	chr10:50660820..50663158-chr10:50667419..50669518,2	K562	blood:
4	chr10:50590808..50592740-chr10:50594264..50595933,2	K562	blood:
5	chr10:50660820..50663158-chr10:50667419..50669518,2	K562	blood:
6	chr10:50589316..50590909-chr10:50591054..50594050,2	K562	blood:
7	chr10:50634343..50637099-chr10:50638662..50640604,2	K562	blood:
8	chr10:50589316..50590909-chr10:50591054..50594050,2	K562	blood:
9	chr10:50615325..50616246-chr10:50688939..50689617,2	MCF-7	breast:
10	chr10:50615306..50616280-chr10:50726775..50727751,7	MCF-7	breast:
11	chr10:50634343..50637099-chr10:50638662..50640604,2	K562	blood:
12	chr10:50615329..50616281-chr10:50719977..50720927,6	K562	blood:
13	chr10:50604685..50607956-chr10:50611021..50613887,3	K562	blood:
14	chr10:50634883..50637223-chr10:50637702..50640162,3	K562	blood:
15	chr10:50582554..50584087-chr10:50604119..50606052,2	K562	blood:
16	chr10:50598458..50600419-chr10:50603443..50605608,2	MCF-7	breast:
17	chr10:50619418..50623241-chr10:50624041..50628384,4	K562	blood:
18	chr10:50617513..50618069-chr10:50720162..50720944,3	MCF-7	breast:
19	chr10:50656731..50658500-chr10:50666252..50669153,2	MCF-7	breast:
20	chr10:50634883..50637223-chr10:50637702..50640162,3	K562	blood:
21	chr10:50635267..50636982-chr10:50640291..50641806,2	K562	blood:
22	chr10:50615493..50616931-chr10:50720236..50720959,5	MCF-7	breast:
23	chr10:50648534..50651045-chr10:50651718..50653272,2	MCF-7	breast:
24	chr10:50586997..50589481-chr10:50594678..50597355,2	MCF-7	breast:
25	chr10:50600535..50602330-chr10:50610420..50612748,2	MCF-7	breast:
26	chr10:50593199..50596011-chr10:50596938..50598821,2	K562	blood:
27	chr10:50599197..50602326-chr10:50603771..50607673,3	K562	blood:
28	chr10:50590808..50592740-chr10:50594264..50595933,2	K562	blood:
29	chr10:50532499..50533452-chr10:50615439..50616339,3	MCF-7	breast:
30	chr10:50601157..50603668-chr10:50610918..50613730,3	K562	blood:
31	chr10:50593199..50596011-chr10:50596938..50598821,2	K562	blood:
32	chr10:50376986..50378609-chr10:50649744..50651324,2	K562	blood:
33	chr10:50661658..50664065-chr10:50667787..50669518,2	K562	blood:
34	chr10:50661658..50664065-chr10:50667787..50669518,2	K562	blood:
35	chr10:50598458..50600419-chr10:50603443..50605608,2	MCF-7	breast:
36	chr10:50625768..50626670-chr10:50720019..50720792,2	MCF-7	breast:
37	chr10:50615564..50616150-chr10:50626091..50626641,2	MCF-7	breast:
38	chr10:50587898..50588680-chr10:50601547..50602465,2	K562	blood:
39	chr10:50648888..50650860-chr10:50652961..50655311,2	K562	blood:
40	chr10:50604685..50607956-chr10:50611021..50613887,3	K562	blood:
41	chr10:50663321..50665073-chr10:50668527..50670258,2	K562	blood:
42	chr10:50641718..50643509-chr10:50649347..50652073,2	MCF-7	breast:
43	chr10:50586997..50589481-chr10:50594678..50597355,2	MCF-7	breast:
44	chr10:50599562..50602600-chr10:50603375..50606319,3	MCF-7	breast:
45	chr10:50641718..50643509-chr10:50649347..50652073,2	MCF-7	breast:
46	chr10:50599562..50602600-chr10:50603375..50606319,3	MCF-7	breast:
47	chr10:50656731..50658500-chr10:50666252..50669153,2	MCF-7	breast:
48	chr10:50648534..50651045-chr10:50651718..50653272,2	MCF-7	breast:
49	chr10:50614876..50616264-chr10:50720008..50720823,3	MCF-7	breast:
50	chr10:50191545..50194244-chr10:50619440..50622301,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf71-1	chr10:50627323-50627556	ENSG00000235939.1
2	lnc-C10orf71-3	chr10:50639184-50639919	NONHSAT013305
3	lnc-ERCC6-1	chr10:50641879-50655452	NONHSAT013306

No data

Variant related genes	Relation type
ENSG00000235939	TF binding region
DRGX	TF binding region
ENSG00000235939	CpG island
DRGX	CpG island
ENSG00000243251	chromatin interactions
ENSG00000226576	chromatin interactions
ENSG00000225830	chromatin interactions
ENSG00000264800	chromatin interactions
ENSG00000235939	chromatin interactions
ENSG00000258838	chromatin interactions
ENSG00000165606	chromatin interactions

Extended variants
information (count: 3357 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:3357 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7903692	chr10:50588990-50588991	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530352944	chr10:50589006-50589007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548492059	chr10:50589009-50589010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560444166	chr10:50589018-50589019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs527893511	chr10:50589040-50589041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs7915692	chr10:50589050-50589051	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs192634354	chr10:50589075-50589076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538236030	chr10:50589076-50589077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550234749	chr10:50589119-50589120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568341697	chr10:50589125-50589126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs74659683	chr10:50589201-50589202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117463916	chr10:50589206-50589207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572105460	chr10:50589235-50589236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539666419	chr10:50589257-50589258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557557873	chr10:50589277-50589278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576119456	chr10:50589295-50589296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375220628	chr10:50589310-50589311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369286007	chr10:50589312-50589313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554911457	chr10:50589355-50589356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7916121	chr10:50589372-50589373	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs376092595	chr10:50589394-50589395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs34320929	chr10:50589405-50589406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542075689	chr10:50589444-50589445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560845132	chr10:50589446-50589447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184974612	chr10:50589462-50589463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546420186	chr10:50589467-50589468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564411125	chr10:50589492-50589493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531872089	chr10:50589504-50589505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188963010	chr10:50589518-50589519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568429896	chr10:50589520-50589521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149468934	chr10:50589549-50589550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547371860	chr10:50589555-50589556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566005107	chr10:50589559-50589560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144604045	chr10:50589606-50589607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557959054	chr10:50589683-50589684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs77321095	chr10:50589721-50589722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs912471	chr10:50589743-50589744	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs555049803	chr10:50589752-50589753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138776827	chr10:50589753-50589754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192171731	chr10:50589771-50589772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554163194	chr10:50589834-50589835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560451804	chr10:50589854-50589855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546060363	chr10:50589858-50589859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564675378	chr10:50589861-50589862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141866327	chr10:50589862-50589863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377575179	chr10:50589885-50589886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543897403	chr10:50590016-50590017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562167094	chr10:50590073-50590074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs115279433	chr10:50590109-50590110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115327532	chr10:50590133-50590134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Developmental delay	21147756	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
Hypotonia	21948486	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1349 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50588000-50591000	Weak transcription	Right Atrium	heart
2	chr10:50588200-50591600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr10:50591600-50594800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:50593600-50596200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr10:50594000-50594400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr10:50594200-50594600	Enhancers	Esophagus	oesophagus
7	chr10:50594400-50594800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr10:50594400-50595400	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr10:50594400-50595400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr10:50594400-50595600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr10:50594600-50595400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr10:50594600-50595600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr10:50594600-50595800	Enhancers	Hela-S3	cervix
14	chr10:50594800-50595200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr10:50594800-50595200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
16	chr10:50594800-50595200	Enhancers	NHLF	lung
17	chr10:50594800-50595400	Enhancers	Osteobl	bone
18	chr10:50594800-50595800	Enhancers	HSMM	muscle
19	chr10:50594800-50598000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr10:50595200-50595800	Enhancers	Muscle Satellite Cultured Cells	--
21	chr10:50595800-50596000	Bivalent Enhancer	HSMM	muscle
22	chr10:50598200-50598800	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr10:50599000-50600000	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr10:50600000-50600600	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr10:50600200-50600400	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr10:50600800-50603000	Weak transcription	Right Atrium	heart
27	chr10:50601800-50602000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr10:50602200-50604200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
29	chr10:50602600-50602800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
30	chr10:50602600-50602800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
31	chr10:50602600-50602800	Bivalent Enhancer	Left Ventricle	heart
32	chr10:50602600-50603000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr10:50602600-50604200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
34	chr10:50602600-50604200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
35	chr10:50602600-50604200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr10:50602600-50604400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
37	chr10:50602800-50603000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
38	chr10:50602800-50603000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
39	chr10:50602800-50603000	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
40	chr10:50602800-50603200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr10:50602800-50603200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
42	chr10:50602800-50603400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr10:50602800-50603600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
44	chr10:50602800-50604000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr10:50602800-50604000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
46	chr10:50602800-50604200	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr10:50602800-50604200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr10:50602800-50604200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
49	chr10:50602800-50604200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
50	chr10:50602800-50604200	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell

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