Variant report

Variant	nsv895429
Chromosome Location	chr10:55564355-55736655
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	chr10:55646406-55646955	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:55724313-55724586	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:55717206-55717861	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:55653961-55654284	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:55710160-55710468	HepG2	liver:	n/a	chr10:55710189-55710205
6	ARID3A	chr10:55699363-55700282	HepG2	liver:	n/a	n/a
7	BACH1	chr10:55701395-55701491	K562	blood:	n/a	n/a
8	BACH1	chr10:55601289-55601329	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr10:55599337-55599400	GM12878	blood:	n/a	n/a
10	BHLHE40	chr10:55593270-55593304	GM12878	blood:	n/a	n/a
11	BRCA1	chr10:55603983-55604027	Hela-S3	cervix:	n/a	n/a
12	CCNT2	chr10:55637294-55637472	K562	blood:	n/a	n/a
13	CCNT2	chr10:55664795-55664881	K562	blood:	n/a	n/a
14	CCNT2	chr10:55587133-55587327	K562	blood:	n/a	n/a
15	CEBPB	chr10:55646421-55646815	HepG2	liver:	n/a	chr10:55646779-55646790 chr10:55646779-55646792
16	CEBPB	chr10:55699503-55699807	HepG2	liver:	n/a	n/a
17	CEBPB	chr10:55717275-55717435	HepG2	liver:	n/a	chr10:55717377-55717388
18	CEBPB	chr10:55717230-55717393	HepG2	liver:	n/a	chr10:55717377-55717388
19	CEBPB	chr10:55654044-55654416	HepG2	liver:	n/a	n/a
20	CEBPB	chr10:55572397-55572600	HepG2	liver:	n/a	chr10:55572521-55572530 chr10:55572521-55572530 chr10:55572519-55572532 chr10:55572521-55572530
21	CEBPB	chr10:55710220-55710433	H1-hESC	embryonic stem cell:	n/a	chr10:55710241-55710252 chr10:55710258-55710269 chr10:55710279-55710290 chr10:55710280-55710291 chr10:55710279-55710292 chr10:55710242-55710253 chr10:55710241-55710252 chr10:55710241-55710254 chr10:55710281-55710290
22	CEBPB	chr10:55659265-55659499	IMR90	lung:	n/a	n/a
23	CEBPB	chr10:55710123-55710465	IMR90	lung:	n/a	chr10:55710241-55710252 chr10:55710258-55710269 chr10:55710279-55710290 chr10:55710280-55710291 chr10:55710279-55710292 chr10:55710242-55710253 chr10:55710241-55710252 chr10:55710241-55710254 chr10:55710281-55710290
24	CEBPB	chr10:55646463-55646995	MCF-7	breast:	n/a	chr10:55646779-55646790 chr10:55646779-55646792
25	CEBPB	chr10:55694537-55694784	HepG2	liver:	n/a	chr10:55694635-55694646
26	CEBPB	chr10:55572413-55572622	H1-hESC	embryonic stem cell:	n/a	chr10:55572521-55572530 chr10:55572521-55572530 chr10:55572519-55572532 chr10:55572521-55572530
27	CEBPB	chr10:55713444-55713755	Hela-S3	cervix:	n/a	chr10:55713605-55713616
28	CEBPB	chr10:55716794-55717575	Hela-S3	cervix:	n/a	chr10:55717377-55717388 chr10:55716937-55716949
29	CEBPB	chr10:55657552-55657619	HepG2	liver:	n/a	n/a
30	CEBPB	chr10:55656136-55656417	A549	lung:	n/a	chr10:55656227-55656238
31	CEBPB	chr10:55601818-55602136	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr10:55710156-55710453	A549	lung:	n/a	chr10:55710241-55710252 chr10:55710258-55710269 chr10:55710279-55710290 chr10:55710280-55710291 chr10:55710279-55710292 chr10:55710242-55710253 chr10:55710241-55710252 chr10:55710241-55710254 chr10:55710281-55710290
33	CEBPB	chr10:55704126-55704331	HepG2	liver:	n/a	chr10:55704166-55704177 chr10:55704168-55704179 chr10:55704166-55704179
34	CEBPB	chr10:55656183-55656384	HepG2	liver:	n/a	chr10:55656227-55656238
35	CEBPB	chr10:55577616-55577876	HepG2	liver:	n/a	n/a
36	CEBPB	chr10:55646576-55646910	A549	lung:	n/a	chr10:55646779-55646790 chr10:55646779-55646792
37	CEBPB	chr10:55646412-55647027	Hela-S3	cervix:	n/a	chr10:55646779-55646790 chr10:55646779-55646792
38	CEBPB	chr10:55646486-55646676	HepG2	liver:	n/a	n/a
39	CEBPB	chr10:55710096-55710489	HepG2	liver:	n/a	chr10:55710241-55710252 chr10:55710258-55710269 chr10:55710279-55710290 chr10:55710280-55710291 chr10:55710279-55710292 chr10:55710242-55710253 chr10:55710241-55710252 chr10:55710241-55710254 chr10:55710281-55710290
40	CEBPB	chr10:55596437-55596799	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr10:55678641-55678961	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr10:55717174-55717552	HepG2	liver:	n/a	chr10:55717377-55717388
43	CEBPB	chr10:55646454-55646819	A549	lung:	n/a	chr10:55646779-55646790 chr10:55646779-55646792
44	CEBPB	chr10:55736140-55736317	HepG2	liver:	n/a	n/a
45	CEBPB	chr10:55646415-55646944	HepG2	liver:	n/a	chr10:55646779-55646790 chr10:55646779-55646792
46	CEBPB	chr10:55573444-55573642	HepG2	liver:	n/a	chr10:55573508-55573519
47	CEBPB	chr10:55646449-55646949	MCF-7	breast:	n/a	chr10:55646779-55646790 chr10:55646779-55646792
48	CEBPB	chr10:55699537-55699743	HepG2	liver:	n/a	n/a
49	CEBPB	chr10:55713525-55713758	HepG2	liver:	n/a	chr10:55713605-55713616
50	CEBPB	chr10:55712025-55712195	HepG2	liver:	n/a	chr10:55712071-55712082

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:55651840-55651890	NB4	blood:	n/a
2	chr10:55568997-55569047	SK-N-SH_RA	brain:	n/a
3	chr10:55685173-55685223	GM12891	blood:	n/a
4	chr10:55568997-55569047	NT2-D1	testis:	n/a
5	chr10:55587200-55587250	GM06990	blood:	n/a
6	chr10:55651840-55651890	LNCaP	prostate:	n/a
7	chr10:55685173-55685223	BE2_C	brain:	n/a
8	chr10:55568997-55569047	SK-N-SH	brain:	n/a
9	chr10:55587200-55587250	H1-hESC	embryonic stem cell:	embryo
10	chr10:55651840-55651890	Hepatocyte	liver:	n/a
11	chr10:55568997-55569047	NHDF-neo	bronchial:	n/a
12	chr10:55685173-55685223	HRCEpiC	kidney:	n/a
13	chr10:55685173-55685223	HCPEpiC	choroid plexus:	n/a
14	chr10:55568997-55569047	GM12878	blood:	n/a
15	chr10:55685173-55685223	NHBE	bronchial:	n/a
16	chr10:55651840-55651890	HNPCEpiC	eye:	n/a
17	chr10:55568997-55569047	BJ	skin:	n/a
18	chr10:55587268-55587318	AG04450	lung:	fetal
19	chr10:55587200-55587250	Jurkat	blood:	n/a
20	chr10:55651840-55651890	NHBE	bronchial:	n/a
21	chr10:55587268-55587318	HRE	kidney:	n/a
22	chr10:55587200-55587250	SK-N-SH_RA	brain:	n/a
23	chr10:55587200-55587250	HCF	heart:	n/a
24	chr10:55685173-55685223	K562	blood:	n/a
25	chr10:55651840-55651890	MCF-7	breast:	n/a
26	chr10:55685173-55685223	HepG2	liver:	n/a
27	chr10:55568997-55569047	IMR90	lung:	fetal
28	chr10:55685173-55685223	HUVEC	blood vessel:	n/a
29	chr10:55587268-55587318	SKMC	muscle:	n/a
30	chr10:55568997-55569047	HEK293	kidney:	embryo
31	chr10:55685173-55685223	PFSK-1	brain:	n/a
32	chr10:55651840-55651890	SK-N-MC	brain:	n/a
33	chr10:55587200-55587250	HCT-116	colon:	n/a
34	chr10:55568997-55569047	PrEC	prostate:	n/a
35	chr10:55587200-55587250	SKMC	muscle:	n/a
36	chr10:55587200-55587250	HIPEpiC	eye:	n/a
37	chr10:55651840-55651890	H1-hESC	embryonic stem cell:	embryo
38	chr10:55685173-55685223	Jurkat	blood:	n/a
39	chr10:55651840-55651890	AG09319	gingival:	n/a
40	chr10:55587200-55587250	HRE	kidney:	n/a
41	chr10:55568997-55569047	MCF10A-Er-Src	breast:	n/a
42	chr10:55685173-55685223	RPTEC	kidney:	n/a
43	chr10:55568997-55569047	AG04449	skin:	fetal
44	chr10:55587200-55587250	MCF-7	breast:	n/a
45	chr10:55568997-55569047	HRE	kidney:	n/a
46	chr10:55587200-55587250	NHDF-neo	bronchial:	n/a
47	chr10:55587200-55587250	LNCaP	prostate:	n/a
48	chr10:55587200-55587250	BE2_C	brain:	n/a
49	chr10:55587200-55587250	K562	blood:	n/a
50	chr10:55587268-55587318	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	10:55597627-55602376..10:55892580-55896204	H1-hESC	embryonic stem cell:	embryo
2	10:55597627-55602376..10:55882057-55892580	GM12878	blood:
3	chr10:55658704..55661053-chr10:55661936..55664959,3	K562	blood:
4	chr10:55658704..55661053-chr10:55661936..55664959,3	K562	blood:
5	chr10:55360883..55361625-chr10:55568215..55569121,2	MCF-7	breast:
6	10:55597627-55602376..10:55871238-55872736	GM12878	blood:
7	chr10:55360709..55361787-chr10:55606233..55607054,5	MCF-7	breast:
8	chr10:55595339..55599244-chr10:55601413..55603952,3	K562	blood:
9	10:55597627-55602376..10:55810019-55812112	H1-hESC	embryonic stem cell:	embryo
10	chr10:55057963..55058535-chr10:55568196..55569129,2	MCF-7	breast:
11	chr10:55595339..55599244-chr10:55601413..55603952,3	K562	blood:

Variant related genes	Relation type
PCDH15	TF binding region
PCDH15	CpG island

Extended variants
information (count: 2848 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:2848 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7896093	chr10:55564355-55564356	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs190538843	chr10:55564373-55564374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372529228	chr10:55564413-55564414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554951771	chr10:55564451-55564452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574421499	chr10:55564492-55564493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs76899590	chr10:55564501-55564502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182925594	chr10:55564507-55564508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs114857010	chr10:55564509-55564510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs193019997	chr10:55564549-55564550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545617092	chr10:55564580-55564581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562732916	chr10:55564660-55564661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531391217	chr10:55564674-55564675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542043598	chr10:55564677-55564678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574918191	chr10:55564686-55564687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs142988507	chr10:55564687-55564688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548505256	chr10:55564690-55564691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560165497	chr10:55564694-55564695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184058149	chr10:55564720-55564721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187582471	chr10:55564723-55564724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192798236	chr10:55564827-55564828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566989050	chr10:55564832-55564833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539162063	chr10:55564841-55564842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11003862	chr10:55564846-55564847	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs569471842	chr10:55564891-55564892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538052241	chr10:55564907-55564908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555246420	chr10:55564908-55564909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138876893	chr10:55564917-55564918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545750189	chr10:55564919-55564920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533557906	chr10:55564966-55564967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528890298	chr10:55565053-55565054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374008376	chr10:55565057-55565058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs184690950	chr10:55565078-55565079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533047629	chr10:55565107-55565108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370460765	chr10:55565188-55565189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576408631	chr10:55565197-55565198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74134790	chr10:55565227-55565228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs139265171	chr10:55565234-55565235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564143196	chr10:55565238-55565239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562434578	chr10:55565270-55565271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576236721	chr10:55565316-55565317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201049227	chr10:55565331-55565332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541615966	chr10:55565363-55565364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114133702	chr10:55565364-55565365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527549957	chr10:55565419-55565420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547691243	chr10:55565421-55565422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560504011	chr10:55565457-55565458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs74134791	chr10:55565506-55565507	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs552683305	chr10:55565542-55565543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569208331	chr10:55565548-55565549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538441794	chr10:55565556-55565557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
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
Obesity	21956041	CNVD
Developmental delay	21948486	CNVD
Intellectual disability	21948486	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
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Glioblastoma multiforme	22286061	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
Colorectal cancer	16774939	CNVD
Autism	20858243	CNVD
Melanoma	17363583	CNVD
Breast cancer	22522925	CNVD
Usher type I cohort	17277737	CNVD
Usher type I cohort	21436283	CNVD
Leukemia	21357790	CNVD
Medulloblastoma	22832581	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:155 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:55562400-55568600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr10:55566400-55566800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr10:55566400-55566800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr10:55566400-55567000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr10:55568400-55568600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr10:55568400-55569000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr10:55568600-55568800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr10:55590400-55590800	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr10:55590600-55590800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr10:55590600-55591000	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr10:55590600-55591200	Enhancers	H1 Cell Line	embryonic stem cell
12	chr10:55590600-55591200	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr10:55590600-55591200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr10:55591600-55592800	Enhancers	HUVEC	blood vessel
15	chr10:55595800-55596400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr10:55596000-55596400	Enhancers	Placenta Amnion	Placenta Amnion
17	chr10:55596000-55596600	Enhancers	HMEC	breast
18	chr10:55596000-55596600	Enhancers	NHEK	skin
19	chr10:55596200-55597000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr10:55596200-55597000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr10:55596400-55596600	Enhancers	Fetal Lung	lung
22	chr10:55596800-55599800	Weak transcription	Fetal Lung	lung
23	chr10:55599600-55599800	Enhancers	Brain Hippocampus Middle	brain
24	chr10:55599600-55600000	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr10:55599600-55600200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr10:55599600-55600200	Enhancers	Fetal Stomach	stomach
27	chr10:55599800-55600000	Enhancers	Fetal Lung	lung
28	chr10:55599800-55603600	Weak transcription	Brain Hippocampus Middle	brain
29	chr10:55600000-55603800	Weak transcription	Fetal Lung	lung
30	chr10:55600000-55604000	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr10:55601200-55601400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr10:55601400-55602000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr10:55602000-55602600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr10:55602600-55603000	Enhancers	Brain Substantia Nigra	brain
35	chr10:55602600-55603600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr10:55603000-55603400	Weak transcription	Brain Substantia Nigra	brain
37	chr10:55603400-55604200	Enhancers	Brain Substantia Nigra	brain
38	chr10:55603600-55603800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr10:55603600-55604000	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr10:55603600-55604000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr10:55603600-55604000	Enhancers	Brain Cingulate Gyrus	brain
42	chr10:55603600-55604000	Enhancers	Dnd41	blood
43	chr10:55603600-55604200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr10:55603600-55604200	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr10:55603600-55604200	Enhancers	Brain Angular Gyrus	brain
46	chr10:55603600-55604200	Enhancers	Colon Smooth Muscle	Colon
47	chr10:55603600-55604400	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr10:55603600-55604400	Enhancers	Brain Hippocampus Middle	brain
49	chr10:55603800-55604200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr10:55603800-55604200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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