Variant report

Variant	nsv947759
Chromosome Location	chr10:19777703-19779090
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:69)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:69 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr10:19777970-19778068	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD2	chr10:19777819-19778173	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr10:19778080-19778230	HRE	kidney:	n/a	n/a
4	CTCF	chr10:19777840-19777990	AoAF	blood vessel:	n/a	n/a
5	CTCF	chr10:19777900-19778050	HRE	kidney:	n/a	n/a
6	CTCF	chr10:19777880-19778030	HPF	lung:	n/a	n/a
7	CTCF	chr10:19777840-19777990	HPAF	blood vessel:	n/a	n/a
8	CTCF	chr10:19777900-19778050	HepG2	liver:	n/a	n/a
9	CTCF	chr10:19777820-19777970	NHLF	lung:	n/a	n/a
10	CTCF	chr10:19777840-19777990	HAc	cerebellar:	n/a	n/a
11	CTCF	chr10:19777920-19778070	AG09319	gingival:	n/a	n/a
12	CTCF	chr10:19777900-19778050	AG04450	lung:	n/a	n/a
13	CTCF	chr10:19777920-19778070	AG10803	skin:	n/a	n/a
14	CTCF	chr10:19777766-19778130	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr10:19777840-19777990	AG04450	lung:	n/a	n/a
16	CTCF	chr10:19777907-19778037	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr10:19777924-19777992	GM12892	blood:	n/a	n/a
18	CTCF	chr10:19777740-19777890	HFF-Myc	foreskin:	n/a	n/a
19	CTCF	chr10:19777800-19777950	HVMF	connective:	n/a	n/a
20	CTCF	chr10:19777880-19778030	HCPEpiC	choroid plexus:	n/a	n/a
21	CTCF	chr10:19777880-19778030	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr10:19777840-19777990	HVMF	connective:	n/a	n/a
23	CTCF	chr10:19777928-19777965	HepG2	liver:	n/a	n/a
24	CTCF	chr10:19777860-19778010	HCM	heart:	n/a	n/a
25	CTCF	chr10:19777880-19778030	NHDF-neo	bronchial:	n/a	n/a
26	CTCF	chr10:19777900-19778050	HCM	heart:	n/a	n/a
27	CTCF	chr10:19777817-19778134	IMR90	lung:	n/a	n/a
28	CTCF	chr10:19777860-19778010	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr10:19777840-19777990	HRE	kidney:	n/a	n/a
30	CTCF	chr10:19777826-19778050	HepG2	liver:	n/a	n/a
31	CTCF	chr10:19777860-19778010	HMF	breast:	n/a	n/a
32	CTCF	chr10:19777820-19777970	AG09319	gingival:	n/a	n/a
33	CTCF	chr10:19777860-19778010	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr10:19777860-19778010	HCFaa	heart:	n/a	n/a
35	CTCF	chr10:19777903-19778017	Kidney_OC	kidney:	n/a	n/a
36	E2F6	chr10:19777646-19778316	H1-hESC	embryonic stem cell:	n/a	n/a
37	E2F6	chr10:19777318-19778281	H1-hESC	embryonic stem cell:	n/a	n/a
38	EGR1	chr10:19777665-19778131	H1-hESC	embryonic stem cell:	n/a	n/a
39	EGR1	chr10:19777740-19778091	H1-hESC	embryonic stem cell:	n/a	n/a
40	EP300	chr10:19777811-19778139	H1-hESC	embryonic stem cell:	n/a	n/a
41	GABPA	chr10:19777887-19778127	HepG2	liver:	n/a	n/a
42	GTF2F1	chr10:19777803-19778207	H1-hESC	embryonic stem cell:	n/a	n/a
43	JUND	chr10:19777913-19778077	H1-hESC	embryonic stem cell:	n/a	n/a
44	JUND	chr10:19777713-19778180	H1-hESC	embryonic stem cell:	n/a	n/a
45	MAX	chr10:19777656-19778286	H1-hESC	embryonic stem cell:	n/a	n/a
46	MAX	chr10:19777859-19778276	HepG2	liver:	n/a	n/a
47	MAX	chr10:19777660-19778270	H1-hESC	embryonic stem cell:	n/a	n/a
48	MAX	chr10:19777585-19778300	H1-hESC	embryonic stem cell:	n/a	n/a
49	MXI1	chr10:19777990-19778164	H1-hESC	embryonic stem cell:	n/a	n/a
50	MYC	chr10:19777867-19778221	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:19778008-19778058	HepG2	liver:	n/a
2	chr10:19778008-19778058	T-47D	breast:	n/a
3	chr10:19778008-19778058	AG10803	skin:	n/a
4	chr10:19778008-19778058	SK-N-MC	brain:	n/a
5	chr10:19778008-19778058	SKMC	muscle:	n/a
6	chr10:19778008-19778058	H1-hESC	embryonic stem cell:	embryo
7	chr10:19778008-19778058	Hela-S3	cervix:	n/a
8	chr10:19778008-19778058	CMK	blood:	n/a
9	chr10:19778008-19778058	BE2_C	brain:	n/a
10	chr10:19778008-19778058	Caco-2	colon:	n/a
11	chr10:19778008-19778058	HMEC	breast:	n/a
12	chr10:19778008-19778058	HAEpiC	amniotic membrane:	n/a
13	chr10:19778008-19778058	HRCEpiC	kidney:	n/a
14	chr10:19778008-19778058	U87	brain:	n/a
15	chr10:19778008-19778058	NHDF-neo	bronchial:	n/a
16	chr10:19778008-19778058	SK-N-SH_RA	brain:	n/a
17	chr10:19778008-19778058	K562	blood:	n/a
18	chr10:19778008-19778058	PrEC	prostate:	n/a
19	chr10:19778008-19778058	RPTEC	kidney:	n/a
20	chr10:19778008-19778058	NH-A	brain:	n/a
21	chr10:19778008-19778058	HL-60	blood:	n/a
22	chr10:19778008-19778058	PFSK-1	brain:	n/a
23	chr10:19778008-19778058	HRPEpiC	eye:	n/a
24	chr10:19778008-19778058	IMR90	lung:	fetal
25	chr10:19778008-19778058	GM12892	blood:	n/a
26	chr10:19778008-19778058	HCT-116	colon:	n/a
27	chr10:19778008-19778058	NB4	blood:	n/a
28	chr10:19778008-19778058	GM06990	blood:	n/a
29	chr10:19778008-19778058	ECC-1	luminal epithelium:	n/a
30	chr10:19778008-19778058	HRE	kidney:	n/a
31	chr10:19778008-19778058	GM12878	blood:	n/a
32	chr10:19778008-19778058	GM12891	blood:	n/a
33	chr10:19778008-19778058	AoSMC	blood vessel:	n/a
34	chr10:19778008-19778058	Jurkat	blood:	n/a
35	chr10:19778008-19778058	ovcar-3	ovarian:	n/a
36	chr10:19778008-19778058	SK-N-SH	brain:	n/a
37	chr10:19778008-19778058	AG04449	skin:	fetal
38	chr10:19778008-19778058	SAEC	small airway:	n/a
39	chr10:19778008-19778058	PANC-1	pancreas:	n/a
40	chr10:19778008-19778058	HNPCEpiC	eye:	n/a
41	chr10:19778008-19778058	MCF-7	breast:	n/a
42	chr10:19778008-19778058	HEEpiC	esophagus:	n/a
43	chr10:19778008-19778058	GM19239	blood:	n/a
44	chr10:19778008-19778058	AG09319	gingival:	n/a
45	chr10:19778008-19778058	HCM	heart:	n/a
46	chr10:19778008-19778058	AG04450	lung:	fetal
47	chr10:19778008-19778058	LNCaP	prostate:	n/a
48	chr10:19778008-19778058	A549	lung:	n/a
49	chr10:19778008-19778058	HCPEpiC	choroid plexus:	n/a
50	chr10:19778008-19778058	HIPEpiC	eye:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLXDC2-6	chr10:19778030-19778329	NONHSAT011661

No data

Variant related genes	Relation type
MALRD1	TF binding region
HMGN1P20	TF binding region
MALRD1	CpG island
HMGN1P20	CpG island

Extended variants
information (count: 59 )
Associated
traits (count: 41 )

Variant overlapped rSNPs/rCNVs (count:59 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150590886	chr10:19777784-19777785	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs575658794	chr10:19777801-19777802	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs558028754	chr10:19777812-19777813	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs182221105	chr10:19777894-19777895	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs112165212	chr10:19777907-19777908	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	mRNA abundance
6	rs562620700	chr10:19777921-19777922	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs574423191	chr10:19777927-19777928	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs541810782	chr10:19777935-19777936	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs140676971	chr10:19777949-19777950	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs552047496	chr10:19777950-19777951	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs144638852	chr10:19777969-19777970	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs114167223	chr10:19777981-19777982	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs72788548	chr10:19777982-19777983	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs569354999	chr10:19777984-19777985	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs2151234	chr10:19778056-19778057	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs2184035	chr10:19778072-19778073	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs566869157	chr10:19778079-19778080	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
18	rs10827496	chr10:19778158-19778159	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs531113616	chr10:19778194-19778195	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
20	rs559282092	chr10:19778225-19778226	Flanking Active TSS Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
21	rs186186689	chr10:19778303-19778304	Flanking Active TSS Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
22	rs552543765	chr10:19778311-19778312	Flanking Active TSS Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
23	rs571152291	chr10:19778317-19778318	Flanking Active TSS Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
24	rs190669678	chr10:19778319-19778320	Flanking Active TSS Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
25	rs538457832	chr10:19778336-19778337	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs375824167	chr10:19778337-19778338	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs182886567	chr10:19778351-19778352	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs187220204	chr10:19778353-19778354	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs541548685	chr10:19778361-19778362	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs369554904	chr10:19778497-19778498	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs191230629	chr10:19778590-19778591	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs16906129	chr10:19778596-19778597	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs2884448	chr10:19778614-19778615	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs546789447	chr10:19778616-19778617	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs571635769	chr10:19778640-19778641	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs16918856	chr10:19778651-19778652	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs561725752	chr10:19778692-19778693	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs74317226	chr10:19778700-19778701	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs183139846	chr10:19778767-19778768	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs371443907	chr10:19778778-19778779	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs116690927	chr10:19778793-19778794	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs73595818	chr10:19778828-19778829	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs552579391	chr10:19778832-19778833	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs571166180	chr10:19778851-19778852	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs538113294	chr10:19778858-19778859	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs117375459	chr10:19778883-19778884	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs568555019	chr10:19778890-19778891	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs75936873	chr10:19778893-19778894	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs139960063	chr10:19778913-19778914	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs572701416	chr10:19778922-19778923	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:41)

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
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:19740000-19781200	Weak transcription	Duodenum Mucosa	Duodenum
2	chr10:19777200-19778000	Enhancers	Fetal Thymus	thymus
3	chr10:19777200-19778400	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr10:19777400-19777800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr10:19777400-19777800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr10:19777400-19777800	Enhancers	Muscle Satellite Cultured Cells	--
7	chr10:19777400-19778200	Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr10:19777400-19778200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr10:19777400-19778400	Active TSS	Breast Myoepithelial Primary Cells	Breast
10	chr10:19777400-19778400	Active TSS	Thymus	Thymus
11	chr10:19777400-19778600	Active TSS	Primary hematopoietic stem cells	blood
12	chr10:19777400-19778800	Enhancers	H1 Cell Line	embryonic stem cell
13	chr10:19777400-19778800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr10:19777600-19777800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr10:19777600-19777800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
16	chr10:19777600-19777800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr10:19777600-19777800	Active TSS	Fetal Intestine Small	intestine
18	chr10:19777600-19778200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr10:19777600-19778200	Active TSS	Brain Anterior Caudate	brain
20	chr10:19777600-19778200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
21	chr10:19777600-19778200	Active TSS	Fetal Brain Female	brain
22	chr10:19777600-19778200	Active TSS	Fetal Heart	heart
23	chr10:19777600-19778200	Active TSS	Fetal Lung	lung
24	chr10:19777600-19778200	Active TSS	NHLF	lung
25	chr10:19777600-19778200	Active TSS	Osteobl	bone
26	chr10:19777600-19778400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr10:19777600-19778400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr10:19777600-19778400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr10:19777600-19778400	Active TSS	Adipose Nuclei	Adipose
30	chr10:19777600-19778400	Active TSS	Colon Smooth Muscle	Colon
31	chr10:19777600-19778400	Active TSS	Fetal Intestine Large	intestine
32	chr10:19777600-19778400	Active TSS	Fetal Kidney	kidney
33	chr10:19777600-19778400	Active TSS	Pancreatic Islets	Pancreatic Islet
34	chr10:19777600-19778400	Active TSS	Monocytes-CD14+_RO01746	blood
35	chr10:19777600-19778600	Active TSS	Aorta	Aorta
36	chr10:19777600-19778600	Active TSS	Duodenum Smooth Muscle	Duodenum
37	chr10:19777600-19778600	Active TSS	Fetal Stomach	stomach
38	chr10:19777600-19778600	Active TSS	Right Atrium	heart
39	chr10:19777600-19778800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr10:19777600-19778800	Active TSS	Brain Hippocampus Middle	brain
41	chr10:19777600-19778800	Active TSS	Ovary	ovary
42	chr10:19777600-19779000	Active TSS	Skeletal Muscle Female	skeletal muscle
43	chr10:19777600-19779200	Active TSS	Stomach Smooth Muscle	stomach
44	chr10:19777800-19778000	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr10:19777800-19778000	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr10:19777800-19778000	Active TSS	iPS-15b Cell Line	embryonic stem cell
47	chr10:19777800-19778000	Active TSS	Primary monocytes fromperipheralblood	blood
48	chr10:19777800-19778000	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr10:19777800-19778000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
50	chr10:19777800-19778000	Enhancers	Fetal Brain Male	brain

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