Variant report

Variant	nsv1043339
Chromosome Location	chr10:118010822-118025492
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:89)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:89 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD2	chr10:118010903-118010923	GM12878	blood:	n/a	n/a
2	CTCF	chr10:118023503-118023672	Fibrobl	skin:	n/a	n/a
3	CTCF	chr10:118016460-118016610	HFF-Myc	foreskin:	n/a	chr10:118016601-118016610
4	CTCF	chr10:118023499-118023632	ProgFib	skin:	n/a	n/a
5	CTCF	chr10:118016500-118016650	WERI-Rb-1	eye:	n/a	chr10:118016601-118016610
6	CTCF	chr10:118023520-118023670	HA-sp	spinal cord:	n/a	n/a
7	CTCF	chr10:118023540-118023690	NHDF-neo	bronchial:	n/a	n/a
8	CTCF	chr10:118023536-118023646	MCF-7	breast:	n/a	n/a
9	CTCF	chr10:118023533-118023652	MCF-7	breast:	n/a	n/a
10	CTCF	chr10:118023596-118023613	LNCaP	prostate:	n/a	n/a
11	CTCF	chr10:118016540-118016690	HepG2	liver:	n/a	chr10:118016601-118016610
12	CTCF	chr10:118023520-118023670	HBMEC	blood vessel:	n/a	n/a
13	CTCF	chr10:118016569-118016649	MCF-7	breast:	n/a	chr10:118016601-118016610
14	CTCF	chr10:118016569-118016640	MCF-7	breast:	n/a	chr10:118016601-118016610
15	CTCF	chr10:118016543-118016625	Fibrobl	skin:	n/a	chr10:118016601-118016610
16	CTCF	chr10:118023440-118023590	AG09309	skin:	n/a	n/a
17	CTCF	chr10:118023480-118023630	NHEK	skin:	n/a	n/a
18	CTCF	chr10:118016480-118016630	AG04449	skin:	n/a	chr10:118016601-118016610
19	CTCF	chr10:118023460-118023610	HA-sp	spinal cord:	n/a	n/a
20	CTCF	chr10:118016480-118016630	WERI-Rb-1	eye:	n/a	chr10:118016601-118016610
21	CTCF	chr10:118023571-118023595	LNCaP	prostate:	n/a	n/a
22	CTCF	chr10:118023520-118023670	MCF-7	breast:	n/a	n/a
23	CTCF	chr10:118023524-118023663	MCF-7	breast:	n/a	n/a
24	CTCF	chr10:118023480-118023630	MCF-7	breast:	n/a	n/a
25	CTCF	chr10:118016556-118016639	MCF-7	breast:	n/a	chr10:118016601-118016610
26	CTCF	chr10:118016560-118016710	A549	lung:	n/a	chr10:118016601-118016610
27	CTCF	chr10:118023471-118023673	MCF-7	breast:	n/a	n/a
28	CTCF	chr10:118023472-118023701	MCF-7	breast:	n/a	n/a
29	CTCF	chr10:118023480-118023630	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr10:118016500-118016650	GM12864	blood:	n/a	chr10:118016601-118016610
31	CTCF	chr10:118023500-118023650	HAc	cerebellar:	n/a	n/a
32	CTCF	chr10:118023335-118023789	MCF-7	breast:	n/a	n/a
33	EBF1	chr10:118012569-118012688	GM12878	blood:	n/a	chr10:118012666-118012677 chr10:118012667-118012677 chr10:118012666-118012679
34	FOS	chr10:118023528-118023755	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr10:118023546-118023723	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr10:118023473-118023667	MCF10A-Er-Src	breast:	n/a	n/a
37	JUND	chr10:118023619-118023779	K562	blood:	n/a	n/a
38	JUND	chr10:118015734-118015898	HepG2	liver:	n/a	n/a
39	KAP1	chr10:118023462-118023826	HEK293	kidney:	n/a	n/a
40	MAFK	chr10:118014933-118015101	HepG2	liver:	n/a	n/a
41	MAX	chr10:118010560-118010914	NB4	blood:	n/a	chr10:118010828-118010838
42	MYC	chr10:118018846-118019234	A549	lung:	n/a	n/a
43	POLR2A	chr10:118011657-118011720	MCF-7	breast:	n/a	n/a
44	POLR2A	chr10:118016416-118016456	ProgFib	skin:	n/a	n/a
45	POLR2A	chr10:118023041-118023044	ProgFib	skin:	n/a	n/a
46	POLR2A	chr10:118014052-118014605	MCF-7	breast:	n/a	n/a
47	POLR2A	chr10:118013503-118013519	MCF-7	breast:	n/a	n/a
48	POLR2A	chr10:118018497-118018506	MCF-7	breast:	n/a	n/a
49	POLR2A	chr10:118017983-118018140	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr10:118022229-118034776	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:118015561-118015611	HCT-116	colon:	n/a
2	chr10:118015561-118015611	GM12878	blood:	n/a
3	chr10:118015561-118015611	MCF-7	breast:	n/a
4	chr10:118015561-118015611	ECC-1	luminal epithelium:	n/a
5	chr10:118015561-118015611	SK-N-SH	brain:	n/a
6	chr10:118015561-118015611	T-47D	breast:	n/a
7	chr10:118015561-118015611	SAEC	small airway:	n/a
8	chr10:118015561-118015611	HRPEpiC	eye:	n/a
9	chr10:118015561-118015611	GM06990	blood:	n/a
10	chr10:118015561-118015611	HUVEC	blood vessel:	n/a
11	chr10:118015561-118015611	HEK293	kidney:	embryo
12	chr10:118015561-118015611	GM19239	blood:	n/a
13	chr10:118015561-118015611	SK-N-MC	brain:	n/a
14	chr10:118015561-118015611	CMK	blood:	n/a
15	chr10:118015561-118015611	A549	lung:	n/a
16	chr10:118015561-118015611	RPTEC	kidney:	n/a
17	chr10:118015561-118015611	LNCaP	prostate:	n/a
18	chr10:118015561-118015611	U87	brain:	n/a
19	chr10:118015561-118015611	HEEpiC	esophagus:	n/a
20	chr10:118015561-118015611	Jurkat	blood:	n/a
21	chr10:118015561-118015611	PrEC	prostate:	n/a
22	chr10:118015561-118015611	IMR90	lung:	fetal
23	chr10:118015561-118015611	AG04450	lung:	fetal
24	chr10:118015561-118015611	ovcar-3	ovarian:	n/a
25	chr10:118015561-118015611	HRCEpiC	kidney:	n/a
26	chr10:118015561-118015611	HCF	heart:	n/a
27	chr10:118015561-118015611	AG10803	skin:	n/a
28	chr10:118015561-118015611	HMEC	breast:	n/a
29	chr10:118015561-118015611	HIPEpiC	eye:	n/a
30	chr10:118015561-118015611	NH-A	brain:	n/a
31	chr10:118015561-118015611	AoSMC	blood vessel:	n/a
32	chr10:118015561-118015611	ProgFib	skin:	n/a
33	chr10:118015561-118015611	HepG2	liver:	n/a
34	chr10:118015561-118015611	H1-hESC	embryonic stem cell:	embryo
35	chr10:118015561-118015611	PANC-1	pancreas:	n/a
36	chr10:118015561-118015611	BJ	skin:	n/a
37	chr10:118015561-118015611	HRE	kidney:	n/a
38	chr10:118015561-118015611	Caco-2	colon:	n/a
39	chr10:118015561-118015611	NHDF-neo	bronchial:	n/a
40	chr10:118015561-118015611	HCPEpiC	choroid plexus:	n/a
41	chr10:118015561-118015611	SKMC	muscle:	n/a
42	chr10:118015561-118015611	AG09319	gingival:	n/a
43	chr10:118015561-118015611	HNPCEpiC	eye:	n/a
44	chr10:118015561-118015611	NB4	blood:	n/a
45	chr10:118015561-118015611	NT2-D1	testis:	n/a
46	chr10:118015561-118015611	HL-60	blood:	n/a
47	chr10:118015561-118015611	SK-N-SH_RA	brain:	n/a
48	chr10:118015561-118015611	GM12891	blood:	n/a
49	chr10:118015561-118015611	AG09309	skin:	n/a
50	chr10:118015561-118015611	BE2_C	brain:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:118006111..118008440-chr10:118012684..118015165,2	MCF-7	breast:
2	chr10:118011033..118013216-chr10:118027087..118029971,2	MCF-7	breast:
3	chr10:118014146..118017027-chr10:118028962..118031890,3	MCF-7	breast:
4	chr10:117900756..117903776-chr10:118021807..118024348,3	MCF-7	breast:

No data

Variant related genes	Relation type
GFRA1	TF binding region
GFRA1	CpG island
ENSG00000151892	chromatin interactions

Extended variants
information (count: 560 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:560 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12251315	chr10:118010822-118010823	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs74464664	chr10:118010857-118010858	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185798704	chr10:118010911-118010912	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188873111	chr10:118010915-118010916	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs193221877	chr10:118010916-118010917	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546908352	chr10:118010924-118010925	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs112259741	chr10:118010925-118010926	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568661791	chr10:118010961-118010962	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535621854	chr10:118010975-118010976	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs547429712	chr10:118011000-118011001	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566064396	chr10:118011042-118011043	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536292643	chr10:118011051-118011052	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs184392119	chr10:118011086-118011087	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs146471209	chr10:118011135-118011136	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs188095273	chr10:118011145-118011146	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558124799	chr10:118011164-118011165	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573090190	chr10:118011170-118011171	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181421167	chr10:118011207-118011208	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555337586	chr10:118011240-118011241	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548259326	chr10:118011252-118011253	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77854702	chr10:118011299-118011300	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544375421	chr10:118011315-118011316	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184132656	chr10:118011348-118011349	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs75050049	chr10:118011352-118011353	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545054183	chr10:118011368-118011369	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189195438	chr10:118011394-118011395	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527266694	chr10:118011423-118011424	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547290140	chr10:118011454-118011455	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568623127	chr10:118011458-118011459	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529452242	chr10:118011471-118011472	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200081965	chr10:118011475-118011476	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs3032041	chr10:118011476-118011477	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571605735	chr10:118011501-118011502	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs398014872	chr10:118011502-118011503	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs373502089	chr10:118011518-118011519	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537218714	chr10:118011540-118011541	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549374015	chr10:118011550-118011551	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs369201219	chr10:118011562-118011563	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550761443	chr10:118011579-118011580	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558740214	chr10:118011622-118011623	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs569053405	chr10:118011646-118011647	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs181529928	chr10:118011686-118011687	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551555323	chr10:118011758-118011759	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs566872176	chr10:118011776-118011777	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577424265	chr10:118011777-118011778	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533898384	chr10:118011785-118011786	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186855340	chr10:118011829-118011830	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs567854627	chr10:118011851-118011852	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs538077971	chr10:118011877-118011878	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs373614014	chr10:118011889-118011890	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
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
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
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	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
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cornelia de Lange syndrome	24599119	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	16397240	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hepatocellular carcinoma	16750200	CNVD
Barrett''s syndrome	19417022	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neuroticism	17667963	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:165 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:117999800-118011200	Weak transcription	Liver	Liver
2	chr10:118003600-118011200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr10:118007800-118013200	Weak transcription	HSMMtube	muscle
4	chr10:118008000-118014000	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr10:118008600-118012600	Weak transcription	Fetal Muscle Trunk	muscle
6	chr10:118008600-118013400	Weak transcription	HSMM	muscle
7	chr10:118008600-118014000	Weak transcription	Fetal Stomach	stomach
8	chr10:118009000-118013200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr10:118010200-118011200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr10:118010200-118011400	Enhancers	Fetal Muscle Leg	muscle
11	chr10:118010800-118011000	Enhancers	Fetal Lung	lung
12	chr10:118010800-118011400	Enhancers	Brain Anterior Caudate	brain
13	chr10:118011000-118014000	Weak transcription	Fetal Lung	lung
14	chr10:118011200-118011600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr10:118011200-118012000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr10:118011200-118012200	Enhancers	Liver	Liver
17	chr10:118011200-118012200	Enhancers	Gastric	stomach
18	chr10:118011200-118012200	Enhancers	Pancreas	Pancrea
19	chr10:118011200-118015200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr10:118011400-118013000	Weak transcription	Fetal Muscle Leg	muscle
21	chr10:118011400-118014400	Weak transcription	Brain Anterior Caudate	brain
22	chr10:118011600-118012200	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr10:118011800-118012000	Enhancers	Stomach Smooth Muscle	stomach
24	chr10:118011800-118012200	Enhancers	Duodenum Smooth Muscle	Duodenum
25	chr10:118012000-118012200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr10:118012000-118012200	Enhancers	Spleen	Spleen
27	chr10:118012000-118012400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr10:118012000-118013600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr10:118012000-118014400	Weak transcription	Stomach Smooth Muscle	stomach
30	chr10:118012200-118013400	Weak transcription	Liver	Liver
31	chr10:118012200-118015600	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr10:118012200-118016800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr10:118012400-118015000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr10:118012400-118015800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr10:118012600-118012800	Enhancers	Fetal Muscle Trunk	muscle
36	chr10:118012800-118015200	Weak transcription	Fetal Muscle Trunk	muscle
37	chr10:118013000-118017200	Enhancers	Fetal Muscle Leg	muscle
38	chr10:118013200-118014000	Enhancers	HSMMtube	muscle
39	chr10:118013200-118016400	Enhancers	Brain Germinal Matrix	brain
40	chr10:118013200-118017600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr10:118013400-118014800	Enhancers	Liver	Liver
42	chr10:118013400-118016200	Enhancers	HSMM	muscle
43	chr10:118013400-118016400	Enhancers	Ovary	ovary
44	chr10:118013600-118014000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr10:118013800-118014400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr10:118014000-118014200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
47	chr10:118014000-118014400	Flanking Active TSS	HSMMtube	muscle
48	chr10:118014000-118014600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr10:118014000-118014600	Enhancers	Adipose Nuclei	Adipose
50	chr10:118014000-118014800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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