Variant report

Variant	esv2759750
Chromosome Location	chr10:52995974-53015583
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	CEBPB	chr10:53010312-53010600	A549	lung:	n/a	chr10:53010468-53010479 chr10:53010467-53010478 chr10:53010467-53010480 chr10:53010467-53010480
2	CEBPB	chr10:53010289-53010617	IMR90	lung:	n/a	chr10:53010468-53010479 chr10:53010467-53010478 chr10:53010467-53010480 chr10:53010467-53010480
3	CEBPB	chr10:53010343-53010615	HepG2	liver:	n/a	chr10:53010468-53010479 chr10:53010467-53010478 chr10:53010467-53010480 chr10:53010467-53010480
4	CEBPB	chr10:53010310-53010619	Hela-S3	cervix:	n/a	chr10:53010468-53010479 chr10:53010467-53010478 chr10:53010467-53010480 chr10:53010467-53010480
5	CEBPB	chr10:53010319-53010589	K562	blood:	n/a	chr10:53010468-53010479 chr10:53010467-53010478 chr10:53010467-53010480 chr10:53010467-53010480
6	CEBPB	chr10:53004743-53004973	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr10:53004681-53004986	IMR90	lung:	n/a	n/a
8	CTCF	chr10:53010200-53010350	GM12872	blood:	n/a	n/a
9	CTCF	chr10:53002269-53002299	Lung_OC	lung:	n/a	n/a
10	E2F4	chr10:53012391-53012525	MCF10A-Er-Src	breast:	n/a	n/a
11	EP300	chr10:53005992-53006328	SK-N-SH_RA	brain:	n/a	chr10:53006023-53006037
12	EP300	chr10:53005801-53007013	SK-N-SH	brain:	n/a	chr10:53006368-53006382 chr10:53006367-53006381 chr10:53006370-53006384 chr10:53006023-53006037
13	EP300	chr10:53006003-53006347	SK-N-SH_RA	brain:	n/a	chr10:53006023-53006037
14	EP300	chr10:53010903-53011223	SK-N-SH_RA	brain:	n/a	chr10:53011147-53011156 chr10:53010928-53010942 chr10:53011067-53011081
15	EP300	chr10:53010808-53011260	SK-N-SH_RA	brain:	n/a	chr10:53011147-53011156 chr10:53010928-53010942 chr10:53011067-53011081
16	EP300	chr10:53010713-53011338	SK-N-SH	brain:	n/a	chr10:53011147-53011156 chr10:53010928-53010942 chr10:53011067-53011081
17	GATA2	chr10:53004535-53005330	SH-SY5Y	brain:	n/a	chr10:53004593-53004609 chr10:53004597-53004606 chr10:53005055-53005066
18	GATA2	chr10:53004453-53004912	HUVEC	blood vessel:	n/a	chr10:53004593-53004609 chr10:53004597-53004606
19	GATA2	chr10:53005821-53006537	SH-SY5Y	brain:	n/a	n/a
20	GATA2	chr10:53005922-53006304	HUVEC	blood vessel:	n/a	n/a
21	GATA3	chr10:53005733-53006728	SK-N-SH	brain:	n/a	n/a
22	GATA3	chr10:53010885-53011413	SK-N-SH	brain:	n/a	n/a
23	GATA3	chr10:53004492-53005101	SH-SY5Y	brain:	n/a	chr10:53004593-53004609 chr10:53004597-53004606 chr10:53005055-53005066
24	GATA3	chr10:53005814-53006540	SK-N-SH	brain:	n/a	n/a
25	GATA3	chr10:53007889-53008078	SH-SY5Y	brain:	n/a	chr10:53008048-53008055 chr10:53008048-53008055 chr10:53008048-53008055 chr10:53008043-53008059 chr10:53008041-53008062
26	GATA3	chr10:53005868-53006414	SH-SY5Y	brain:	n/a	n/a
27	GATA3	chr10:53004322-53005151	SK-N-SH	brain:	n/a	chr10:53004593-53004609 chr10:53004597-53004606 chr10:53005055-53005066
28	GATA3	chr10:53004247-53005184	SK-N-SH	brain:	n/a	chr10:53004593-53004609 chr10:53004597-53004606 chr10:53005055-53005066
29	GATA3	chr10:53010785-53011382	SK-N-SH	brain:	n/a	n/a
30	JUN	chr10:52997315-52997331	K562	blood:	n/a	n/a
31	JUN	chr10:53010815-53011303	HUVEC	blood vessel:	n/a	n/a
32	JUND	chr10:53010837-53011339	SK-N-SH	brain:	n/a	n/a
33	JUND	chr10:53004568-53004949	H1-hESC	embryonic stem cell:	n/a	n/a
34	KAP1	chr10:53004120-53004968	HEK293	kidney:	n/a	n/a
35	KAP1	chr10:53004173-53005045	U2OS	brain:	n/a	n/a
36	MXI1	chr10:53004681-53004911	H1-hESC	embryonic stem cell:	n/a	n/a
37	MYC	chr10:53003091-53003229	H1-hESC	embryonic stem cell:	n/a	n/a
38	NFIC	chr10:53004438-53005040	SK-N-SH	brain:	n/a	n/a
39	NFIC	chr10:53005800-53006506	SK-N-SH	brain:	n/a	n/a
40	NFIC	chr10:53010801-53011437	SK-N-SH	brain:	n/a	n/a
41	PBX3	chr10:53005931-53006726	SK-N-SH	brain:	n/a	n/a
42	PBX3	chr10:53010807-53011287	SK-N-SH	brain:	n/a	n/a
43	PBX3	chr10:53010792-53011416	SK-N-SH	brain:	n/a	n/a
44	POLR2A	chr10:52996331-52996388	ProgFib	skin:	n/a	n/a
45	POLR2A	chr10:53010819-53011267	SK-N-SH	brain:	n/a	n/a
46	POLR2A	chr10:53014569-53014760	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr10:53005979-53006221	SK-N-SH	brain:	n/a	n/a
48	POLR2A	chr10:53009905-53010605	H1-neurons	neurons:	n/a	n/a
49	POLR2A	chr10:53013343-53013375	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr10:53004652-53004854	HUVEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:53004308-53004358	HMEC	breast:	n/a
2	chr10:53011793-53011843	MCF-7	breast:	n/a
3	chr10:53004308-53004358	AoSMC	blood vessel:	n/a
4	chr10:53004308-53004358	A549	lung:	n/a
5	chr10:53004308-53004358	HAEpiC	amniotic membrane:	n/a
6	chr10:53011793-53011843	AG09319	gingival:	n/a
7	chr10:53004308-53004358	H1-hESC	embryonic stem cell:	embryo
8	chr10:53004308-53004358	ProgFib	skin:	n/a
9	chr10:53004308-53004358	BJ	skin:	n/a
10	chr10:53011793-53011843	H1-hESC	embryonic stem cell:	embryo
11	chr10:53004308-53004358	HIPEpiC	eye:	n/a
12	chr10:53004308-53004358	SK-N-MC	brain:	n/a
13	chr10:53004308-53004358	HCM	heart:	n/a
14	chr10:53004308-53004358	GM12892	blood:	n/a
15	chr10:53004308-53004358	SK-N-SH	brain:	n/a
16	chr10:53011793-53011843	NHBE	bronchial:	n/a
17	chr10:53004308-53004358	HEEpiC	esophagus:	n/a
18	chr10:53011793-53011843	AG09309	skin:	n/a
19	chr10:53004308-53004358	HCF	heart:	n/a
20	chr10:53011793-53011843	SK-N-MC	brain:	n/a
21	chr10:53004308-53004358	MCF-7	breast:	n/a
22	chr10:53011793-53011843	T-47D	breast:	n/a
23	chr10:53004308-53004358	SK-N-SH_RA	brain:	n/a
24	chr10:53011793-53011843	BE2_C	brain:	n/a
25	chr10:53011793-53011843	BJ	skin:	n/a
26	chr10:53004308-53004358	SKMC	muscle:	n/a
27	chr10:53011793-53011843	PANC-1	pancreas:	n/a
28	chr10:53011793-53011843	ProgFib	skin:	n/a
29	chr10:53004308-53004358	AG09319	gingival:	n/a
30	chr10:53011793-53011843	IMR90	lung:	fetal
31	chr10:53011793-53011843	HAEpiC	amniotic membrane:	n/a
32	chr10:53011793-53011843	GM19239	blood:	n/a
33	chr10:53011793-53011843	SK-N-SH_RA	brain:	n/a
34	chr10:53011793-53011843	HRCEpiC	kidney:	n/a
35	chr10:53011793-53011843	GM12892	blood:	n/a
36	chr10:53004308-53004358	HRE	kidney:	n/a
37	chr10:53011793-53011843	NHDF-neo	bronchial:	n/a
38	chr10:53004308-53004358	HPAEpiC	pulmonary alveolar:	n/a
39	chr10:53011793-53011843	AG04449	skin:	fetal
40	chr10:53004308-53004358	IMR90	lung:	fetal
41	chr10:53004308-53004358	PFSK-1	brain:	n/a
42	chr10:53011793-53011843	HCM	heart:	n/a
43	chr10:53004308-53004358	Caco-2	colon:	n/a
44	chr10:53011793-53011843	SK-N-SH	brain:	n/a
45	chr10:53011793-53011843	AoSMC	blood vessel:	n/a
46	chr10:53004308-53004358	NHDF-neo	bronchial:	n/a
47	chr10:53011793-53011843	Hepatocyte	liver:	n/a
48	chr10:53011793-53011843	HUVEC	blood vessel:	n/a
49	chr10:53004308-53004358	NH-A	brain:	n/a
50	chr10:53011793-53011843	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:53008618..53010640-chr10:53013381..53015189,2	K562	blood:
2	chr10:53008618..53010801-chr10:53013381..53015189,3	K562	blood:
3	chr10:53000277..53002226-chr10:53004321..53006404,2	K562	blood:
4	chr10:53008618..53010801-chr10:53013381..53015189,3	K562	blood:
5	chr10:53008618..53010640-chr10:53013381..53015189,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-A1CF-3	chr10:53004654-53004895	ENSG00000231132.1
2	lnc-A1CF-3	chr10:53005481-53005566	ENSG00000231132.1
3	lnc-A1CF-3	chr10:53005249-53005366	ENSG00000231132.1

Variant related genes	Relation type
ENSG00000231132	TF binding region
ENSG00000231132	CpG island
ENSG00000231132	chromatin interactions

Extended variants
information (count: 707 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:707 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1915672	chr10:52995974-52995975	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs549657442	chr10:52995985-52995986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563374538	chr10:52996032-52996033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs139691901	chr10:52996038-52996039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182258389	chr10:52996071-52996072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565949998	chr10:52996089-52996090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113062167	chr10:52996100-52996101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548331499	chr10:52996162-52996163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186567104	chr10:52996204-52996205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs10996250	chr10:52996213-52996214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1915673	chr10:52996214-52996215	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs191214935	chr10:52996220-52996221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114182204	chr10:52996246-52996247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200767015	chr10:52996269-52996270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs397944642	chr10:52996282-52996283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145287293	chr10:52996301-52996302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185844846	chr10:52996302-52996303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188760765	chr10:52996316-52996317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542985862	chr10:52996322-52996323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs61295989	chr10:52996323-52996324	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs573462812	chr10:52996411-52996412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148599732	chr10:52996420-52996421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs193157541	chr10:52996462-52996463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs111288353	chr10:52996467-52996468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544828275	chr10:52996486-52996487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184997677	chr10:52996489-52996490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375448393	chr10:52996555-52996556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188729110	chr10:52996563-52996564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529018317	chr10:52996592-52996593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548976260	chr10:52996595-52996596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559423640	chr10:52996606-52996607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs561617631	chr10:52996609-52996610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528375783	chr10:52996703-52996704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551437181	chr10:52996755-52996756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs151160402	chr10:52996766-52996767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs149817621	chr10:52996768-52996769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs536808299	chr10:52996775-52996776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550378610	chr10:52996846-52996847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs577145725	chr10:52996900-52996901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536375442	chr10:52996932-52996933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552934947	chr10:52996954-52996955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs573197014	chr10:52997045-52997046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74885225	chr10:52997062-52997063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181156457	chr10:52997069-52997070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558944907	chr10:52997074-52997075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575908322	chr10:52997100-52997101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115790131	chr10:52997110-52997111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376290100	chr10:52997112-52997113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561493695	chr10:52997126-52997127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372560577	chr10:52997195-52997196	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
Cancer	21183584	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
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Intellectual disability	22045946	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
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Cancer	20164920	CNVD
Ollier disease	21235737	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	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

Chromatin state (count:243 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52991200-53003000	Weak transcription	Left Ventricle	heart
2	chr10:52991400-52996600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr10:52992000-53006200	Weak transcription	Aorta	Aorta
4	chr10:52992200-53003600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr10:52992200-53009600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr10:52992800-53002200	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr10:52993000-52998000	Weak transcription	Psoas Muscle	Psoas
8	chr10:52993000-52998200	Weak transcription	Right Atrium	heart
9	chr10:52993000-53003200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr10:52994000-53003200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr10:52996600-52997000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr10:52998000-52998400	Enhancers	Psoas Muscle	Psoas
13	chr10:52998200-52999800	Enhancers	Right Atrium	heart
14	chr10:52998400-52999400	Weak transcription	Psoas Muscle	Psoas
15	chr10:52999400-52999800	Enhancers	Psoas Muscle	Psoas
16	chr10:52999800-53001800	Weak transcription	Psoas Muscle	Psoas
17	chr10:52999800-53004600	Weak transcription	Right Atrium	heart
18	chr10:53000000-53004400	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr10:53000400-53002000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr10:53000400-53004200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr10:53000600-53004000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr10:53000800-53001000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr10:53001000-53001200	Enhancers	Colon Smooth Muscle	Colon
24	chr10:53001000-53001400	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr10:53001000-53001800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr10:53001000-53001800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr10:53001000-53001800	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr10:53001200-53001600	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr10:53001200-53002000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr10:53001200-53005800	Weak transcription	Colon Smooth Muscle	Colon
31	chr10:53001400-53003200	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr10:53001600-53001800	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr10:53001600-53002200	Enhancers	Brain Germinal Matrix	brain
34	chr10:53001600-53002800	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr10:53001800-53003400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr10:53001800-53004200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr10:53001800-53004800	Enhancers	Psoas Muscle	Psoas
38	chr10:53001800-53005800	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr10:53002000-53003000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr10:53002000-53003600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr10:53002200-53002400	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr10:53002400-53002800	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr10:53002400-53003800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr10:53002800-53003600	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr10:53002800-53003600	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr10:53003000-53003200	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr10:53003000-53003200	Enhancers	Fetal Brain Male	brain
48	chr10:53003000-53003200	Enhancers	Left Ventricle	heart
49	chr10:53003000-53004400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr10:53003200-53003600	Enhancers	H9 Cell Line	embryonic stem cell

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