Variant report

Variant	nsv894917
Chromosome Location	chr10:19259024-19463367
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	ATF2	chr10:19408000-19408486	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr10:19350592-19350642	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr10:19457572-19457738	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr10:19273641-19273802	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr10:19317627-19317654	K562	blood:	n/a	n/a
6	BCL11A	chr10:19432092-19432361	GM12878	blood:	n/a	n/a
7	BCL11A	chr10:19431852-19432069	GM12878	blood:	n/a	n/a
8	BHLHE40	chr10:19458718-19458920	HepG2	liver:	n/a	n/a
9	BHLHE40	chr10:19436379-19436415	GM12878	blood:	n/a	n/a
10	CCNT2	chr10:19334732-19334932	K562	blood:	n/a	n/a
11	CEBPB	chr10:19406381-19406676	K562	blood:	n/a	chr10:19406538-19406549 chr10:19406537-19406550 chr10:19406537-19406550 chr10:19406539-19406548 chr10:19406539-19406548 chr10:19406539-19406548 chr10:19406537-19406550 chr10:19406539-19406548 chr10:19406537-19406548
12	CEBPB	chr10:19302938-19303346	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr10:19335365-19335448	K562	blood:	n/a	chr10:19335427-19335438
14	CEBPB	chr10:19406369-19406727	HepG2	liver:	n/a	chr10:19406538-19406549 chr10:19406537-19406550 chr10:19406537-19406550 chr10:19406539-19406548 chr10:19406539-19406548 chr10:19406539-19406548 chr10:19406537-19406550 chr10:19406539-19406548 chr10:19406537-19406548
15	CEBPB	chr10:19305115-19305360	A549	lung:	n/a	chr10:19305246-19305257 chr10:19305245-19305258 chr10:19305247-19305256
16	CEBPB	chr10:19406365-19406693	H1-hESC	embryonic stem cell:	n/a	chr10:19406538-19406549 chr10:19406537-19406550 chr10:19406537-19406550 chr10:19406539-19406548 chr10:19406539-19406548 chr10:19406539-19406548 chr10:19406537-19406550 chr10:19406539-19406548 chr10:19406537-19406548
17	CEBPB	chr10:19343269-19343582	HepG2	liver:	n/a	chr10:19343414-19343425 chr10:19343371-19343382
18	CEBPB	chr10:19409445-19409793	A549	lung:	n/a	chr10:19409626-19409637
19	CEBPB	chr10:19400478-19400721	IMR90	lung:	n/a	n/a
20	CEBPB	chr10:19343272-19343589	A549	lung:	n/a	chr10:19343414-19343425 chr10:19343371-19343382
21	CEBPB	chr10:19409404-19409801	MCF-7	breast:	n/a	chr10:19409626-19409637
22	CEBPB	chr10:19312540-19312790	A549	lung:	n/a	chr10:19312657-19312668
23	CEBPB	chr10:19406387-19406727	A549	lung:	n/a	chr10:19406538-19406549 chr10:19406537-19406550 chr10:19406537-19406550 chr10:19406539-19406548 chr10:19406539-19406548 chr10:19406539-19406548 chr10:19406537-19406550 chr10:19406539-19406548 chr10:19406537-19406548
24	CEBPB	chr10:19343290-19343513	Hela-S3	cervix:	n/a	chr10:19343414-19343425 chr10:19343371-19343382
25	CEBPB	chr10:19335311-19335542	IMR90	lung:	n/a	chr10:19335427-19335438
26	CEBPB	chr10:19324305-19324622	A549	lung:	n/a	chr10:19324446-19324457
27	CEBPB	chr10:19270236-19270544	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr10:19324305-19324617	HepG2	liver:	n/a	chr10:19324446-19324457
29	CEBPB	chr10:19406380-19406730	IMR90	lung:	n/a	chr10:19406538-19406549 chr10:19406537-19406550 chr10:19406537-19406550 chr10:19406539-19406548 chr10:19406539-19406548 chr10:19406539-19406548 chr10:19406537-19406550 chr10:19406539-19406548 chr10:19406537-19406548
30	CEBPB	chr10:19312500-19312792	IMR90	lung:	n/a	chr10:19312657-19312668
31	CEBPB	chr10:19409461-19409762	K562	blood:	n/a	chr10:19409626-19409637
32	CEBPB	chr10:19343278-19343480	H1-hESC	embryonic stem cell:	n/a	chr10:19343414-19343425 chr10:19343371-19343382
33	CEBPB	chr10:19315698-19315792	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr10:19335289-19335587	HepG2	liver:	n/a	chr10:19335427-19335438
35	CEBPB	chr10:19343267-19343547	K562	blood:	n/a	chr10:19343414-19343425 chr10:19343371-19343382
36	CEBPB	chr10:19335265-19335609	A549	lung:	n/a	chr10:19335427-19335438
37	CEBPB	chr10:19455086-19455203	HepG2	liver:	n/a	chr10:19455162-19455173
38	CEBPB	chr10:19305128-19305328	HepG2	liver:	n/a	chr10:19305246-19305257 chr10:19305245-19305258 chr10:19305247-19305256
39	CEBPB	chr10:19302924-19303396	IMR90	lung:	n/a	n/a
40	CEBPB	chr10:19312561-19312761	HepG2	liver:	n/a	chr10:19312657-19312668
41	CEBPB	chr10:19343258-19343579	IMR90	lung:	n/a	chr10:19343414-19343425 chr10:19343371-19343382
42	CEBPB	chr10:19273682-19273761	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr10:19409480-19409662	H1-hESC	embryonic stem cell:	n/a	chr10:19409626-19409637
44	CEBPB	chr10:19324306-19324620	IMR90	lung:	n/a	chr10:19324446-19324457
45	CEBPB	chr10:19409450-19409804	IMR90	lung:	n/a	chr10:19409626-19409637
46	CEBPB	chr10:19366278-19366502	IMR90	lung:	n/a	n/a
47	CEBPB	chr10:19310277-19310311	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr10:19409460-19409800	HepG2	liver:	n/a	chr10:19409626-19409637
49	CHD2	chr10:19457614-19457815	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr10:19317648-19317653	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:19400365-19400415	HUVEC	blood vessel:	n/a
2	chr10:19352926-19352976	GM12878	blood:	n/a
3	chr10:19408880-19408930	GM12891	blood:	n/a
4	chr10:19352926-19352976	BJ	skin:	n/a
5	chr10:19352926-19352976	ProgFib	skin:	n/a
6	chr10:19400365-19400415	SK-N-SH	brain:	n/a
7	chr10:19408880-19408930	SK-N-MC	brain:	n/a
8	chr10:19352926-19352976	AG09319	gingival:	n/a
9	chr10:19400365-19400415	HNPCEpiC	eye:	n/a
10	chr10:19352926-19352976	Hepatocyte	liver:	n/a
11	chr10:19408880-19408930	LNCaP	prostate:	n/a
12	chr10:19408880-19408930	HUVEC	blood vessel:	n/a
13	chr10:19400365-19400415	HEK293	kidney:	embryo
14	chr10:19352926-19352976	PrEC	prostate:	n/a
15	chr10:19352926-19352976	SK-N-MC	brain:	n/a
16	chr10:19408880-19408930	MCF-7	breast:	n/a
17	chr10:19408880-19408930	ProgFib	skin:	n/a
18	chr10:19400365-19400415	HAEpiC	amniotic membrane:	n/a
19	chr10:19400365-19400415	AG04449	skin:	fetal
20	chr10:19408880-19408930	HRE	kidney:	n/a
21	chr10:19352926-19352976	HRPEpiC	eye:	n/a
22	chr10:19400365-19400415	HEEpiC	esophagus:	n/a
23	chr10:19400365-19400415	AG09309	skin:	n/a
24	chr10:19400365-19400415	PFSK-1	brain:	n/a
25	chr10:19400365-19400415	GM12891	blood:	n/a
26	chr10:19408880-19408930	SAEC	small airway:	n/a
27	chr10:19408880-19408930	A549	lung:	n/a
28	chr10:19352926-19352976	AG04450	lung:	fetal
29	chr10:19408880-19408930	CMK	blood:	n/a
30	chr10:19400365-19400415	Jurkat	blood:	n/a
31	chr10:19352926-19352976	GM06990	blood:	n/a
32	chr10:19400365-19400415	SK-N-SH_RA	brain:	n/a
33	chr10:19352926-19352976	AG10803	skin:	n/a
34	chr10:19352926-19352976	HIPEpiC	eye:	n/a
35	chr10:19408880-19408930	NB4	blood:	n/a
36	chr10:19408880-19408930	H1-hESC	embryonic stem cell:	embryo
37	chr10:19400365-19400415	HL-60	blood:	n/a
38	chr10:19400365-19400415	NHDF-neo	bronchial:	n/a
39	chr10:19400365-19400415	SKMC	muscle:	n/a
40	chr10:19352926-19352976	U87	brain:	n/a
41	chr10:19352926-19352976	H1-hESC	embryonic stem cell:	embryo
42	chr10:19352926-19352976	SK-N-SH_RA	brain:	n/a
43	chr10:19408880-19408930	PANC-1	pancreas:	n/a
44	chr10:19352926-19352976	HRE	kidney:	n/a
45	chr10:19408880-19408930	NHDF-neo	bronchial:	n/a
46	chr10:19400365-19400415	PrEC	prostate:	n/a
47	chr10:19352926-19352976	HCPEpiC	choroid plexus:	n/a
48	chr10:19352926-19352976	PFSK-1	brain:	n/a
49	chr10:19352926-19352976	HCF	heart:	n/a
50	chr10:19408880-19408930	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr10:19399956..19400936-chr17:59652354..59652900,2	MCF-7	breast:
2	chr10:19419930..19422122-chr10:19424808..19427231,2	K562	blood:
3	chr10:19373201..19375040-chr10:19394247..19396869,2	K562	blood:
4	chr10:19458075..19458575-chr18:36304626..36305400,2	MCF-7	breast:
5	chr10:19419930..19422122-chr10:19424808..19427231,2	K562	blood:
6	chr10:19399936..19400436-chr17:59489681..59490329,3	MCF-7	breast:
7	chr10:19082548..19083519-chr10:19457655..19458211,2	MCF-7	breast:
8	chr10:19369325..19371479-chr10:19375493..19377980,2	K562	blood:
9	chr10:19399936..19400956-chr17:59651934..59652869,4	MCF-7	breast:
10	chr10:19373201..19375040-chr10:19394247..19396869,2	K562	blood:
11	chr10:19424011..19426061-chr10:19435541..19437655,2	K562	blood:
12	chr10:19424011..19426061-chr10:19435541..19437655,2	K562	blood:
13	chr10:19369325..19371479-chr10:19375493..19377980,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf112-2	chr10:19340384-19340566	NONHSAT011658
2	lnc-C10orf112-2	chr10:19340885-19341099	NONHSAT011658

Variant related genes	Relation type
UBE2V2P1	TF binding region
UBE2V2P1	CpG island

Extended variants
information (count: 7083 )
Associated
traits (count: 44 )

Variant overlapped rSNPs/rCNVs (count:7083 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531437891	chr10:19264434-19264435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs548517420	chr10:19264448-19264449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566744719	chr10:19264462-19264463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376043027	chr10:19264505-19264506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs550037853	chr10:19264564-19264565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185158426	chr10:19264703-19264704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531942774	chr10:19264713-19264714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558804388	chr10:19264717-19264718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570844408	chr10:19264727-19264728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs35308475	chr10:19264748-19264749	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs77983654	chr10:19264787-19264788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs574429944	chr10:19264796-19264797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1339055	chr10:19264802-19264803	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs12263833	chr10:19264850-19264851	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs74121135	chr10:19264928-19264929	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs147212168	chr10:19264930-19264931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs112819944	chr10:19264934-19264935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564355815	chr10:19265013-19265014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531653086	chr10:19265030-19265031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140625970	chr10:19265036-19265037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561736182	chr10:19265037-19265038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530167651	chr10:19265071-19265072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368863956	chr10:19265075-19265076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs548390418	chr10:19265091-19265092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115232108	chr10:19265097-19265098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs1339054	chr10:19265130-19265131	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs369363907	chr10:19265136-19265137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs552171618	chr10:19265142-19265143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs144552365	chr10:19265155-19265156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538154699	chr10:19265158-19265159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs376943538	chr10:19265192-19265193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs538103128	chr10:19265194-19265195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550310802	chr10:19265232-19265233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs556770846	chr10:19265237-19265238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374824465	chr10:19265248-19265249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs578193926	chr10:19265279-19265280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs568548882	chr10:19265306-19265307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs536090894	chr10:19265545-19265546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs7070237	chr10:19265552-19265553	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs572204291	chr10:19265553-19265554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs117923701	chr10:19265560-19265561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557807906	chr10:19265593-19265594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs7085754	chr10:19265594-19265595	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs7085755	chr10:19265598-19265599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs151242653	chr10:19265622-19265623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs112173677	chr10:19265635-19265636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541256535	chr10:19265666-19265667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560350392	chr10:19265675-19265676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs527803789	chr10:19265692-19265693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552108249	chr10:19265693-19265694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:44)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
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
Intracranial aneurysm	16715129	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16616336	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	22083797	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:299 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:19264400-19265400	Enhancers	Fetal Intestine Small	intestine
2	chr10:19264400-19268400	Enhancers	Fetal Intestine Large	intestine
3	chr10:19264600-19265400	Enhancers	Duodenum Mucosa	Duodenum
4	chr10:19265400-19266200	Weak transcription	Duodenum Mucosa	Duodenum
5	chr10:19265400-19266200	Weak transcription	Fetal Intestine Small	intestine
6	chr10:19266200-19266400	Enhancers	Duodenum Mucosa	Duodenum
7	chr10:19266200-19267800	Enhancers	Fetal Intestine Small	intestine
8	chr10:19266400-19267000	Weak transcription	Duodenum Mucosa	Duodenum
9	chr10:19267000-19267200	Enhancers	Duodenum Mucosa	Duodenum
10	chr10:19267800-19273200	Weak transcription	Fetal Intestine Small	intestine
11	chr10:19268400-19268800	Weak transcription	Fetal Intestine Large	intestine
12	chr10:19268800-19269000	Enhancers	Fetal Intestine Large	intestine
13	chr10:19268800-19269200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr10:19268800-19269200	Enhancers	Fetal Lung	lung
15	chr10:19269000-19273200	Weak transcription	Fetal Intestine Large	intestine
16	chr10:19269200-19273400	Weak transcription	Fetal Lung	lung
17	chr10:19273200-19273600	Enhancers	Fetal Intestine Large	intestine
18	chr10:19273200-19273800	Enhancers	Fetal Intestine Small	intestine
19	chr10:19273400-19273600	Enhancers	Fetal Lung	lung
20	chr10:19273400-19273800	Enhancers	Hela-S3	cervix
21	chr10:19273600-19274000	Weak transcription	Fetal Lung	lung
22	chr10:19274000-19274400	Enhancers	Fetal Lung	lung
23	chr10:19290400-19290800	Enhancers	Hela-S3	cervix
24	chr10:19296000-19296400	Enhancers	Placenta	Placenta
25	chr10:19302600-19303000	Enhancers	Muscle Satellite Cultured Cells	--
26	chr10:19302800-19303400	Enhancers	NH-A	brain
27	chr10:19303800-19304000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr10:19303800-19304000	Enhancers	Placenta	Placenta
29	chr10:19304000-19309400	Weak transcription	Placenta	Placenta
30	chr10:19306400-19306600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr10:19306600-19307400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr10:19306600-19307400	Enhancers	Fetal Intestine Large	intestine
33	chr10:19306600-19307600	Enhancers	Fetal Intestine Small	intestine
34	chr10:19307600-19308000	Weak transcription	Fetal Intestine Small	intestine
35	chr10:19308000-19308400	Enhancers	Fetal Intestine Small	intestine
36	chr10:19309400-19310200	Enhancers	Placenta	Placenta
37	chr10:19309600-19310400	Enhancers	HepG2	liver
38	chr10:19309800-19310000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr10:19311400-19312000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr10:19311600-19312000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr10:19311600-19312000	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr10:19311800-19312000	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr10:19312200-19313200	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr10:19313200-19313600	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr10:19313600-19313800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr10:19317800-19318200	Enhancers	Fetal Heart	heart
47	chr10:19318200-19319800	Weak transcription	Fetal Heart	heart
48	chr10:19319200-19319600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr10:19319800-19321200	Enhancers	Fetal Heart	heart
50	chr10:19320200-19321200	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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