Variant report

Variant	nsv1046458
Chromosome Location	chr10:18629603-18683860
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	BHLHE40	chr10:18657656-18658087	GM12878	blood:	n/a	chr10:18657851-18657860
2	CEBPB	chr10:18683181-18683340	IMR90	lung:	n/a	n/a
3	CEBPB	chr10:18647845-18647989	IMR90	lung:	n/a	chr10:18647884-18647895 chr10:18647883-18647896
4	CEBPB	chr10:18647816-18648016	HepG2	liver:	n/a	chr10:18647884-18647895 chr10:18647883-18647896
5	CEBPB	chr10:18679368-18679983	IMR90	lung:	n/a	n/a
6	CTCF	chr10:18676330-18676353	Pancreas_OC	pancreas:	n/a	n/a
7	CTCF	chr10:18634950-18635025	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr10:18634960-18635110	RPTEC	kidney:	n/a	n/a
9	CTCF	chr10:18634900-18635050	A549	lung:	n/a	n/a
10	CTCF	chr10:18634890-18635068	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr10:18670740-18670890	HEK293	kidney:	n/a	n/a
12	CTCF	chr10:18670700-18670850	HCT-116	colon:	n/a	n/a
13	CTCF	chr10:18634920-18635070	Caco-2	colon:	n/a	n/a
14	CTCF	chr10:18670775-18670898	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr10:18670760-18670910	HMF	breast:	n/a	n/a
16	CTCF	chr10:18670780-18670930	K562	blood:	n/a	n/a
17	CTCF	chr10:18670720-18670870	GM12878	blood:	n/a	n/a
18	CTCF	chr10:18674430-18674479	GM13977	blood:	n/a	n/a
19	CTCF	chr10:18634940-18635090	RPTEC	kidney:	n/a	n/a
20	CTCF	chr10:18634760-18634910	RPTEC	kidney:	n/a	n/a
21	CTCF	chr10:18670780-18670930	GM12872	blood:	n/a	n/a
22	CTCF	chr10:18676235-18676375	GM12878	blood:	n/a	n/a
23	CTCF	chr10:18638020-18638170	NHLF	lung:	n/a	n/a
24	CTCF	chr10:18675458-18675488	GM13977	blood:	n/a	n/a
25	CTCF	chr10:18634933-18635000	Fibrobl	skin:	n/a	n/a
26	EBF1	chr10:18677371-18677479	GM12878	blood:	n/a	chr10:18677391-18677401 chr10:18677392-18677401
27	ELF1	chr10:18637875-18638082	K562	blood:	n/a	chr10:18637968-18637981
28	ELF1	chr10:18653178-18653396	K562	blood:	n/a	chr10:18653315-18653328
29	FOS	chr10:18657663-18658035	MCF10A-Er-Src	breast:	n/a	chr10:18657810-18657819 chr10:18657808-18657815 chr10:18657806-18657817 chr10:18657809-18657820
30	FOS	chr10:18657177-18657450	MCF10A-Er-Src	breast:	n/a	chr10:18657359-18657371
31	FOS	chr10:18679684-18680026	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr10:18657666-18658004	MCF10A-Er-Src	breast:	n/a	chr10:18657810-18657819 chr10:18657808-18657815 chr10:18657806-18657817 chr10:18657809-18657820
33	FOS	chr10:18661857-18661900	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr10:18679667-18680046	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr10:18679682-18680027	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr10:18679669-18680030	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr10:18678250-18678447	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr10:18657663-18658002	MCF10A-Er-Src	breast:	n/a	chr10:18657810-18657819 chr10:18657808-18657815 chr10:18657806-18657817 chr10:18657809-18657820
39	FOS	chr10:18657663-18658003	MCF10A-Er-Src	breast:	n/a	chr10:18657810-18657819 chr10:18657808-18657815 chr10:18657806-18657817 chr10:18657809-18657820
40	FOSL2	chr10:18657587-18658039	SK-N-SH	brain:	n/a	chr10:18657810-18657819 chr10:18657808-18657815 chr10:18657806-18657817 chr10:18657809-18657820
41	GATA3	chr10:18632311-18632423	SH-SY5Y	brain:	n/a	n/a
42	JUN	chr10:18661935-18661970	K562	blood:	n/a	n/a
43	JUND	chr10:18647357-18647578	H1-hESC	embryonic stem cell:	n/a	n/a
44	KAP1	chr10:18665253-18665581	HEK293	kidney:	n/a	n/a
45	MAFF	chr10:18635406-18635550	HepG2	liver:	n/a	n/a
46	MAFF	chr10:18647873-18647973	HepG2	liver:	n/a	chr10:18647923-18647941
47	MAFK	chr10:18647821-18648054	HepG2	liver:	n/a	n/a
48	MAFK	chr10:18649748-18650027	HepG2	liver:	n/a	n/a
49	MAFK	chr10:18637089-18637204	HepG2	liver:	n/a	n/a
50	MAFK	chr10:18649732-18650034	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:18629568-18629618	HPAEpiC	pulmonary alveolar:	n/a
2	chr10:18629568-18629618	HIPEpiC	eye:	n/a
3	chr10:18629602-18629652	HRCEpiC	kidney:	n/a
4	chr10:18629677-18629727	AG09309	skin:	n/a
5	chr10:18679429-18679479	A549	lung:	n/a
6	chr10:18679429-18679479	SK-N-MC	brain:	n/a
7	chr10:18679429-18679479	PFSK-1	brain:	n/a
8	chr10:18629677-18629727	SK-N-SH	brain:	n/a
9	chr10:18679429-18679479	GM12891	blood:	n/a
10	chr10:18679429-18679479	SK-N-SH_RA	brain:	n/a
11	chr10:18629677-18629727	U87	brain:	n/a
12	chr10:18629602-18629652	GM12892	blood:	n/a
13	chr10:18629674-18629724	HMEC	breast:	n/a
14	chr10:18629602-18629652	HNPCEpiC	eye:	n/a
15	chr10:18629674-18629724	GM12892	blood:	n/a
16	chr10:18629602-18629652	HL-60	blood:	n/a
17	chr10:18679429-18679479	NT2-D1	testis:	n/a
18	chr10:18629674-18629724	IMR90	lung:	fetal
19	chr10:18629602-18629652	IMR90	lung:	fetal
20	chr10:18629602-18629652	NB4	blood:	n/a
21	chr10:18629677-18629727	SAEC	small airway:	n/a
22	chr10:18629568-18629618	SK-N-MC	brain:	n/a
23	chr10:18629677-18629727	Caco-2	colon:	n/a
24	chr10:18629674-18629724	GM12878	blood:	n/a
25	chr10:18629677-18629727	NHBE	bronchial:	n/a
26	chr10:18629568-18629618	SK-N-SH_RA	brain:	n/a
27	chr10:18629677-18629727	HCM	heart:	n/a
28	chr10:18629674-18629724	HCF	heart:	n/a
29	chr10:18629568-18629618	NB4	blood:	n/a
30	chr10:18679429-18679479	HAEpiC	amniotic membrane:	n/a
31	chr10:18629674-18629724	CMK	blood:	n/a
32	chr10:18629674-18629724	HCPEpiC	choroid plexus:	n/a
33	chr10:18679429-18679479	LNCaP	prostate:	n/a
34	chr10:18629674-18629724	ProgFib	skin:	n/a
35	chr10:18629674-18629724	GM19239	blood:	n/a
36	chr10:18629568-18629618	ECC-1	luminal epithelium:	n/a
37	chr10:18679429-18679479	ProgFib	skin:	n/a
38	chr10:18629568-18629618	AoSMC	blood vessel:	n/a
39	chr10:18629677-18629727	IMR90	lung:	fetal
40	chr10:18629602-18629652	Caco-2	colon:	n/a
41	chr10:18629602-18629652	A549	lung:	n/a
42	chr10:18679429-18679479	AG10803	skin:	n/a
43	chr10:18629568-18629618	SKMC	muscle:	n/a
44	chr10:18629674-18629724	HRE	kidney:	n/a
45	chr10:18629674-18629724	PFSK-1	brain:	n/a
46	chr10:18629568-18629618	HEEpiC	esophagus:	n/a
47	chr10:18629602-18629652	HIPEpiC	eye:	n/a
48	chr10:18629677-18629727	BJ	skin:	n/a
49	chr10:18629677-18629727	HEK293	kidney:	embryo
50	chr10:18629568-18629618	GM12891	blood:	n/a

Variant related genes	Relation type
CACNB2	TF binding region
CACNB2	CpG island

Extended variants
information (count: 2396 )
Associated
traits (count: 40 )

Variant overlapped rSNPs/rCNVs (count:2396 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10828545	chr10:18629603-18629604	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs541145429	chr10:18629663-18629664	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs182634399	chr10:18629672-18629673	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs556131650	chr10:18629682-18629683	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs551335125	chr10:18629692-18629693	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs557805225	chr10:18629695-18629696	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs186962230	chr10:18629707-18629708	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs114519689	chr10:18629778-18629779	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs550258909	chr10:18629836-18629837	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs369696287	chr10:18629852-18629853	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs374233500	chr10:18629885-18629886	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs12266692	chr10:18629886-18629887	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs377533233	chr10:18629915-18629916	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs530723634	chr10:18629928-18629929	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs191227810	chr10:18629940-18629941	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs146042014	chr10:18629941-18629942	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs201816240	chr10:18629946-18629947	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs547845807	chr10:18629999-18630000	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs184120039	chr10:18630003-18630004	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs540011648	chr10:18630149-18630150	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs527849410	chr10:18630154-18630155	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs146363841	chr10:18630162-18630163	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138372212	chr10:18630176-18630177	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs550509179	chr10:18630201-18630202	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs142860244	chr10:18630210-18630211	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576177959	chr10:18630243-18630244	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538588827	chr10:18630285-18630286	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs144267613	chr10:18630351-18630352	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540699894	chr10:18630391-18630392	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs188673689	chr10:18630423-18630424	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs577705892	chr10:18630424-18630425	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs545149887	chr10:18630434-18630435	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs193233995	chr10:18630435-18630436	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs78794602	chr10:18630481-18630482	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs185311761	chr10:18630497-18630498	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs12573736	chr10:18630649-18630650	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs529246083	chr10:18630657-18630658	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547513592	chr10:18630678-18630679	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs566123335	chr10:18630684-18630685	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188907024	chr10:18630734-18630735	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374109979	chr10:18630764-18630765	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs558791735	chr10:18630784-18630785	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs537678360	chr10:18630802-18630803	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556077572	chr10:18630846-18630847	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs574434426	chr10:18630869-18630870	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs539256700	chr10:18630872-18630873	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs10458703	chr10:18630884-18630885	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs552704764	chr10:18630900-18630901	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376631221	chr10:18630948-18630949	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs191871490	chr10:18631002-18631003	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:40)

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
Esophageal cancer	21851588	CNVD
Intracranial aneurysm	16715129	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16616336	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	22083797	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:284 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18629200-18629800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr10:18629200-18629800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr10:18629200-18630200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr10:18629200-18630200	Active TSS	Colon Smooth Muscle	Colon
5	chr10:18629200-18630400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr10:18629200-18630400	Active TSS	Aorta	Aorta
7	chr10:18629400-18629800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr10:18629400-18629800	Active TSS	Brain Hippocampus Middle	brain
9	chr10:18629400-18629800	Flanking Active TSS	Fetal Brain Male	brain
10	chr10:18629400-18629800	Active TSS	Fetal Intestine Small	intestine
11	chr10:18629400-18629800	Active TSS	Pancreatic Islets	Pancreatic Islet
12	chr10:18629400-18629800	Active TSS	Lung	lung
13	chr10:18629400-18629800	Active TSS	Skeletal Muscle Female	skeletal muscle
14	chr10:18629400-18629800	Flanking Active TSS	NHLF	lung
15	chr10:18629400-18629800	Flanking Active TSS	Osteobl	bone
16	chr10:18629400-18630000	Active TSS	Breast Myoepithelial Primary Cells	Breast
17	chr10:18629400-18630000	Bivalent/Poised TSS	Muscle Satellite Cultured Cells	--
18	chr10:18629400-18630000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr10:18629400-18630000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr10:18629400-18630000	Active TSS	Colonic Mucosa	Colon
21	chr10:18629400-18630000	Flanking Active TSS	Fetal Brain Female	brain
22	chr10:18629400-18630000	Flanking Active TSS	Fetal Lung	lung
23	chr10:18629400-18630000	Active TSS	Fetal Muscle Trunk	muscle
24	chr10:18629400-18630000	Flanking Active TSS	Ovary	ovary
25	chr10:18629400-18630000	Active TSS	Pancreas	Pancrea
26	chr10:18629400-18630000	Active TSS	Psoas Muscle	Psoas
27	chr10:18629400-18630000	Active TSS	Rectal Mucosa Donor 31	rectum
28	chr10:18629400-18630000	Active TSS	Skeletal Muscle Male	skeletal muscle
29	chr10:18629400-18630200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr10:18629400-18630200	Active TSS	Brain Angular Gyrus	brain
31	chr10:18629400-18630200	Active TSS	Duodenum Mucosa	Duodenum
32	chr10:18629400-18630200	Active TSS	Duodenum Smooth Muscle	Duodenum
33	chr10:18629400-18630200	Active TSS	Fetal Kidney	kidney
34	chr10:18629400-18630200	Active TSS	Fetal Stomach	stomach
35	chr10:18629400-18630200	Active TSS	Rectal Smooth Muscle	rectum
36	chr10:18629400-18630200	Flanking Active TSS	NH-A	brain
37	chr10:18629400-18630200	Active TSS	NHDF-Ad	bronchial
38	chr10:18629400-18630400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr10:18629400-18630400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
40	chr10:18629400-18630400	Active TSS	Brain Inferior Temporal Lobe	brain
41	chr10:18629400-18630400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
42	chr10:18629400-18630400	Active TSS	Rectal Mucosa Donor 29	rectum
43	chr10:18629400-18630400	Active TSS	Stomach Smooth Muscle	stomach
44	chr10:18629400-18631600	Active TSS	Left Ventricle	heart
45	chr10:18629400-18632600	Active TSS	Right Atrium	heart
46	chr10:18629400-18632800	Active TSS	Right Ventricle	heart
47	chr10:18629600-18629800	Active TSS	Brain Germinal Matrix	brain
48	chr10:18629600-18629800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
49	chr10:18629600-18630000	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr10:18629600-18630000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin

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