Variant report

Variant	nsv550905
Chromosome Location	chr10:54585401-54726056
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1199)
CpG islands
(count:1039)
Chromatin interactive
region (count:8)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1199 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:54643744-54644394	HepG2	liver:	n/a	n/a
2	ATF2	chr10:54725585-54726269	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr10:54668156-54668650	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr10:54668144-54668733	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr10:54725601-54726237	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr10:54725621-54726197	GM12878	blood:	n/a	n/a
7	ATF2	chr10:54643982-54644308	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr10:54725684-54726190	GM12878	blood:	n/a	n/a
9	BACH1	chr10:54671062-54671223	K562	blood:	n/a	n/a
10	BACH1	chr10:54725445-54725479	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr10:54668203-54668557	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr10:54613572-54613777	GM12878	blood:	n/a	chr10:54613640-54613651
13	BATF	chr10:54716730-54716941	GM12878	blood:	n/a	n/a
14	BATF	chr10:54613555-54613782	GM12878	blood:	n/a	chr10:54613640-54613651
15	BATF	chr10:54716683-54716935	GM12878	blood:	n/a	n/a
16	BATF	chr10:54725645-54726140	GM12878	blood:	n/a	n/a
17	BATF	chr10:54724834-54725221	GM12878	blood:	n/a	chr10:54725065-54725076
18	BATF	chr10:54725698-54726077	GM12878	blood:	n/a	n/a
19	BCL11A	chr10:54725573-54726104	GM12878	blood:	n/a	n/a
20	BCL11A	chr10:54683370-54683701	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL11A	chr10:54663343-54663592	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCL11A	chr10:54683273-54683616	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL11A	chr10:54725683-54726105	GM12878	blood:	n/a	n/a
24	BCL11A	chr10:54725865-54726110	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCL11A	chr10:54725832-54726289	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCLAF1	chr10:54725338-54726095	GM12878	blood:	n/a	n/a
27	BCLAF1	chr10:54725611-54726184	GM12878	blood:	n/a	n/a
28	BHLHE40	chr10:54613550-54613793	GM12878	blood:	n/a	n/a
29	BHLHE40	chr10:54725319-54726161	GM12878	blood:	n/a	n/a
30	BHLHE40	chr10:54643727-54644338	HepG2	liver:	n/a	n/a
31	BRCA1	chr10:54725796-54725803	HepG2	liver:	n/a	n/a
32	BRCA1	chr10:54721236-54721259	GM12878	blood:	n/a	n/a
33	CEBPB	chr10:54616811-54617049	A549	lung:	n/a	chr10:54616934-54616947 chr10:54616934-54616947
34	CEBPB	chr10:54643630-54644094	MCF-7	breast:	n/a	n/a
35	CEBPB	chr10:54716151-54716165	HepG2	liver:	n/a	n/a
36	CEBPB	chr10:54643589-54644293	MCF-7	breast:	n/a	n/a
37	CEBPB	chr10:54623984-54624682	IMR90	lung:	n/a	n/a
38	CEBPB	chr10:54722284-54722287	HepG2	liver:	n/a	n/a
39	CEBPB	chr10:54725828-54726384	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr10:54666232-54666453	HepG2	liver:	n/a	n/a
41	CEBPB	chr10:54695377-54695618	A549	lung:	n/a	chr10:54695540-54695549 chr10:54695538-54695549 chr10:54695540-54695551
42	CEBPB	chr10:54624346-54624595	HepG2	liver:	n/a	n/a
43	CEBPB	chr10:54643662-54644094	HepG2	liver:	n/a	n/a
44	CEBPB	chr10:54695358-54695687	HepG2	liver:	n/a	chr10:54695540-54695549 chr10:54695538-54695549 chr10:54695540-54695551
45	CEBPB	chr10:54616827-54617072	Hela-S3	cervix:	n/a	chr10:54616934-54616947 chr10:54616934-54616947
46	CEBPB	chr10:54666161-54666465	IMR90	lung:	n/a	n/a
47	CEBPB	chr10:54646577-54646781	HepG2	liver:	n/a	chr10:54646696-54646707
48	CHD1	chr10:54683753-54683825	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD1	chr10:54725719-54726390	GM12878	blood:	n/a	n/a
50	CHD2	chr10:54711687-54711945	GM12878	blood:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:54643889-54643939	NHDF-neo	bronchial:	n/a
2	chr10:54669084-54669134	HIPEpiC	eye:	n/a
3	chr10:54643889-54643939	NHDF-neo	bronchial:	n/a
4	chr10:54669084-54669134	HIPEpiC	eye:	n/a
5	chr10:54631212-54631262	SK-N-SH	brain:	n/a
6	chr10:54715153-54715203	SK-N-MC	brain:	n/a
7	chr10:54632322-54632372	Jurkat	blood:	n/a
8	chr10:54714856-54714906	HEEpiC	esophagus:	n/a
9	chr10:54633831-54633881	NHDF-neo	bronchial:	n/a
10	chr10:54676588-54676638	AG10803	skin:	n/a
11	chr10:54629323-54629373	HL-60	blood:	n/a
12	chr10:54633831-54633881	SKMC	muscle:	n/a
13	chr10:54715153-54715203	AG09309	skin:	n/a
14	chr10:54669084-54669134	HEK293	kidney:	embryo
15	chr10:54715153-54715203	Hepatocyte	liver:	n/a
16	chr10:54714816-54714866	SK-N-SH_RA	brain:	n/a
17	chr10:54714764-54714814	HAEpiC	amniotic membrane:	n/a
18	chr10:54632322-54632372	HNPCEpiC	eye:	n/a
19	chr10:54633831-54633881	NB4	blood:	n/a
20	chr10:54643873-54643923	PFSK-1	brain:	n/a
21	chr10:54629323-54629373	AG09319	gingival:	n/a
22	chr10:54631333-54631383	NT2-D1	testis:	n/a
23	chr10:54643873-54643923	PrEC	prostate:	n/a
24	chr10:54631333-54631383	NHDF-neo	bronchial:	n/a
25	chr10:54676588-54676638	HCPEpiC	choroid plexus:	n/a
26	chr10:54631212-54631262	SAEC	small airway:	n/a
27	chr10:54669084-54669134	NH-A	brain:	n/a
28	chr10:54683341-54683391	ECC-1	luminal epithelium:	n/a
29	chr10:54632322-54632372	GM06990	blood:	n/a
30	chr10:54631333-54631383	HCT-116	colon:	n/a
31	chr10:54629323-54629373	SAEC	small airway:	n/a
32	chr10:54643889-54643939	SK-N-SH	brain:	n/a
33	chr10:54715415-54715465	Hepatocyte	liver:	n/a
34	chr10:54714764-54714814	CMK	blood:	n/a
35	chr10:54714856-54714906	NT2-D1	testis:	n/a
36	chr10:54714764-54714814	LNCaP	prostate:	n/a
37	chr10:54669084-54669134	K562	blood:	n/a
38	chr10:54624373-54624423	Jurkat	blood:	n/a
39	chr10:54669084-54669134	GM06990	blood:	n/a
40	chr10:54643873-54643923	HNPCEpiC	eye:	n/a
41	chr10:54714816-54714866	HMEC	breast:	n/a
42	chr10:54643889-54643939	ECC-1	luminal epithelium:	n/a
43	chr10:54633831-54633881	GM12878	blood:	n/a
44	chr10:54715153-54715203	MCF10A-Er-Src	breast:	n/a
45	chr10:54631333-54631383	NB4	blood:	n/a
46	chr10:54643873-54643923	Jurkat	blood:	n/a
47	chr10:54631369-54631419	HRE	kidney:	n/a
48	chr10:54714764-54714814	AoSMC	blood vessel:	n/a
49	chr10:54669084-54669134	HCPEpiC	choroid plexus:	n/a
50	chr10:54715415-54715465	HNPCEpiC	eye:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:54633661..54634164-chr8:33370710..33371662,2	NB4	blood:
2	chr10:54667605..54669824-chr10:54683197..54686169,2	K562	blood:
3	chr10:54667605..54669824-chr10:54683197..54686169,2	K562	blood:
4	chr10:54654118..54656757-chr17:56755700..56758164,2	MCF-7	breast:
5	chr10:54635845..54638328-chr10:54638583..54641520,2	K562	blood:
6	chr10:54577745..54578264-chr10:54643756..54644460,2	MCF-7	breast:
7	chr10:54711771..54712343-chr7:134236733..134237240,2	MCF-7	breast:
8	chr10:54635845..54638328-chr10:54638583..54641520,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MBL2-1	chr10:54698381-54698398	XLOC_008825
2	lnc-MBL2-1	chr10:54703613-54703837	XLOC_008825
3	lnc-MBL2-8	chr10:54720838-54721360	NONHSAT013440

No data

Variant related genes	Relation type
ENSG00000201196	TF binding region
ENSG00000201196	CpG island
ENSG00000200997	chromatin interactions
ENSG00000129696	chromatin interactions
ENSG00000239039	chromatin interactions
FGFR1	miRNA target sites
CDC14A	miRNA target sites

Extended variants
information (count: 4502 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:4502 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10824813	chr10:54595602-54595603	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184836376	chr10:54595650-54595651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571699790	chr10:54595680-54595681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs56141225	chr10:54595681-54595682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565140521	chr10:54595693-54595694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs555826873	chr10:54595721-54595722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572403013	chr10:54595723-54595724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs34990659	chr10:54595789-54595790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs551117799	chr10:54595798-54595799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs372733946	chr10:54595801-54595802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189147376	chr10:54595809-54595810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541523402	chr10:54595822-54595823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534213549	chr10:54595840-54595841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564288091	chr10:54595852-54595853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533184122	chr10:54595853-54595854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545678497	chr10:54595866-54595867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs554205691	chr10:54595890-54595891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562482909	chr10:54595900-54595901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs145156541	chr10:54595928-54595929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548035264	chr10:54595960-54595961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567609438	chr10:54595963-54595964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568258510	chr10:54595969-54595970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs527364152	chr10:54596001-54596002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs369562795	chr10:54596004-54596005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs547493600	chr10:54596008-54596009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs10824814	chr10:54596025-54596026	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs539473203	chr10:54596034-54596035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs147580472	chr10:54596052-54596053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556329106	chr10:54596058-54596059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570406442	chr10:54596075-54596076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576120251	chr10:54596081-54596082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536148921	chr10:54596128-54596129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs545170598	chr10:54596238-54596239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs192771228	chr10:54596310-54596311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572614852	chr10:54596335-54596336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541138005	chr10:54596337-54596338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs557865821	chr10:54596372-54596373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs577607591	chr10:54596376-54596377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs35114420	chr10:54596383-54596384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184682705	chr10:54596401-54596402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs543458711	chr10:54596404-54596405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563346242	chr10:54596424-54596425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs148983530	chr10:54596443-54596444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12254163	chr10:54596462-54596463	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs561706802	chr10:54596466-54596467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527511434	chr10:54596476-54596477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139069089	chr10:54596507-54596508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375951750	chr10:54596509-54596510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189902918	chr10:54596525-54596526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540665943	chr10:54596538-54596539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Chronic lymphocytic leukemia	21546498	CNVD
Obesity	21956041	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:715 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:54595600-54596400	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr10:54596400-54597600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr10:54597600-54598000	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr10:54610200-54612400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr10:54610800-54611000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
6	chr10:54611000-54612600	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr10:54611400-54611600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr10:54611600-54612400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr10:54612000-54613000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr10:54612400-54612600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr10:54612400-54612800	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr10:54612400-54613000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr10:54612400-54613000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr10:54612400-54613000	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr10:54614200-54614600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr10:54616400-54617200	Enhancers	Fetal Intestine Large	intestine
17	chr10:54617200-54618400	Weak transcription	Fetal Intestine Large	intestine
18	chr10:54617800-54619000	Enhancers	Fetal Heart	heart
19	chr10:54618400-54618800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr10:54618400-54618800	Enhancers	Fetal Intestine Large	intestine
21	chr10:54618400-54618800	Enhancers	HMEC	breast
22	chr10:54618600-54619000	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr10:54618800-54621200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr10:54618800-54622600	Weak transcription	HMEC	breast
25	chr10:54618800-54623600	Weak transcription	Fetal Intestine Large	intestine
26	chr10:54619000-54619400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr10:54619000-54623800	Weak transcription	Fetal Heart	heart
28	chr10:54619400-54619600	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr10:54619400-54620000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr10:54619600-54622600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr10:54621200-54621800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr10:54621800-54622600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr10:54622600-54625200	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr10:54622600-54625200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr10:54622600-54625400	Enhancers	HMEC	breast
36	chr10:54623000-54625400	Enhancers	NHEK	skin
37	chr10:54623000-54626000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr10:54623200-54626000	Enhancers	NHLF	lung
39	chr10:54623400-54624600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr10:54623400-54625000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr10:54623400-54625200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr10:54623400-54625200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr10:54623400-54625400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr10:54623400-54625400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr10:54623600-54624600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr10:54623600-54624600	Enhancers	H9 Cell Line	embryonic stem cell
47	chr10:54623600-54625000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr10:54623600-54625000	Enhancers	Fetal Intestine Large	intestine
49	chr10:54623600-54625200	Enhancers	NH-A	brain
50	chr10:54623800-54624000	Enhancers	HSMM	muscle

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