Variant report

Variant	nsv522046
Chromosome Location	chr10:4538492-4570425
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	ATF3	chr10:4562259-4562601	HCT-116	colon:	n/a	n/a
2	BATF	chr10:4564886-4565161	GM12878	blood:	n/a	n/a
3	BATF	chr10:4556707-4556991	GM12878	blood:	n/a	n/a
4	BATF	chr10:4564809-4565232	GM12878	blood:	n/a	n/a
5	BCL11A	chr10:4556668-4557002	GM12878	blood:	n/a	chr10:4556876-4556885
6	BCL11A	chr10:4564853-4565165	GM12878	blood:	n/a	n/a
7	BHLHE40	chr10:4564876-4565159	GM12878	blood:	n/a	n/a
8	CEBPB	chr10:4554806-4555358	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr10:4545289-4545660	H1-hESC	embryonic stem cell:	n/a	chr10:4545473-4545484
10	CEBPB	chr10:4545308-4545619	A549	lung:	n/a	chr10:4545473-4545484
11	CEBPB	chr10:4554851-4555290	IMR90	lung:	n/a	n/a
12	CEBPB	chr10:4562072-4562716	HCT-116	colon:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461
13	CEBPB	chr10:4545363-4545607	Hela-S3	cervix:	n/a	chr10:4545473-4545484
14	CEBPB	chr10:4562195-4562561	HepG2	liver:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461
15	CEBPB	chr10:4550308-4550452	IMR90	lung:	n/a	n/a
16	CEBPB	chr10:4562109-4562666	A549	lung:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461
17	CEBPB	chr10:4562284-4562540	K562	blood:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461
18	CEBPB	chr10:4562162-4562641	Hela-S3	cervix:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461
19	CEBPB	chr10:4545348-4545618	HepG2	liver:	n/a	chr10:4545473-4545484
20	CEBPB	chr10:4545310-4545649	K562	blood:	n/a	chr10:4545473-4545484
21	CEBPB	chr10:4545314-4545642	IMR90	lung:	n/a	chr10:4545473-4545484
22	CEBPB	chr10:4562177-4562613	IMR90	lung:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461
23	CEBPB	chr10:4562180-4562544	K562	blood:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461
24	CEBPB	chr10:4562195-4562596	A549	lung:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461
25	CEBPB	chr10:4555268-4555468	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr10:4562197-4562491	H1-hESC	embryonic stem cell:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461
27	CEBPB	chr10:4562026-4562763	HCT-116	colon:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461 chr10:4562710-4562718
28	CEBPB	chr10:4562211-4562572	A549	lung:	n/a	chr10:4562357-4562370 chr10:4562358-4562369 chr10:4562357-4562370 chr10:4562448-4562461
29	CHD1	chr10:4554749-4555515	IMR90	lung:	n/a	n/a
30	CTCF	chr10:4555115-4555284	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr10:4555100-4555250	K562	blood:	n/a	n/a
32	CTCF	chr10:4555100-4555250	HCM	heart:	n/a	n/a
33	CTCF	chr10:4555160-4555310	NHDF-neo	bronchial:	n/a	n/a
34	CTCF	chr10:4555131-4555294	GM12878	blood:	n/a	n/a
35	CTCF	chr10:4555120-4555270	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr10:4555032-4555523	HCT-116	colon:	n/a	chr10:4555398-4555407
37	CTCF	chr10:4555107-4555338	A549	lung:	n/a	n/a
38	CTCF	chr10:4555140-4555290	HRE	kidney:	n/a	n/a
39	CTCF	chr10:4554926-4555458	A549	lung:	n/a	chr10:4555398-4555407
40	CTCF	chr10:4561935-4561961	GM13976	blood:	n/a	n/a
41	CTCF	chr10:4555120-4555270	MCF-7	breast:	n/a	n/a
42	CTCF	chr10:4555140-4555290	GM06990	blood:	n/a	n/a
43	CTCF	chr10:4541360-4541510	AG10803	skin:	n/a	n/a
44	CTCF	chr10:4555035-4555392	K562	blood:	n/a	n/a
45	CTCF	chr10:4555060-4555210	BE2_C	brain:	n/a	n/a
46	CTCF	chr10:4555120-4555270	HPF	lung:	n/a	n/a
47	CTCF	chr10:4555104-4555311	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr10:4554860-4555010	HAc	cerebellar:	n/a	n/a
49	CTCF	chr10:4555028-4555336	K562	blood:	n/a	n/a
50	CTCF	chr10:4555100-4555250	GM12864	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:4540959-4541009	SKMC	muscle:	n/a
2	chr10:4540959-4541009	HRE	kidney:	n/a
3	chr10:4540959-4541009	AG04450	lung:	fetal
4	chr10:4540959-4541009	MCF-7	breast:	n/a
5	chr10:4540959-4541009	GM19239	blood:	n/a
6	chr10:4540959-4541009	Hepatocyte	liver:	n/a
7	chr10:4540959-4541009	IMR90	lung:	fetal
8	chr10:4540959-4541009	HRPEpiC	eye:	n/a
9	chr10:4540959-4541009	Caco-2	colon:	n/a
10	chr10:4540959-4541009	AG04449	skin:	fetal
11	chr10:4540959-4541009	HMEC	breast:	n/a
12	chr10:4540959-4541009	LNCaP	prostate:	n/a
13	chr10:4540959-4541009	GM12878	blood:	n/a
14	chr10:4540959-4541009	GM12892	blood:	n/a
15	chr10:4540959-4541009	PFSK-1	brain:	n/a
16	chr10:4540959-4541009	SK-N-SH	brain:	n/a
17	chr10:4540959-4541009	AG10803	skin:	n/a
18	chr10:4540959-4541009	NHDF-neo	bronchial:	n/a
19	chr10:4540959-4541009	CMK	blood:	n/a
20	chr10:4540959-4541009	AoSMC	blood vessel:	n/a
21	chr10:4540959-4541009	GM06990	blood:	n/a
22	chr10:4540959-4541009	SK-N-SH_RA	brain:	n/a
23	chr10:4540959-4541009	Hela-S3	cervix:	n/a
24	chr10:4540959-4541009	HPAEpiC	pulmonary alveolar:	n/a
25	chr10:4540959-4541009	BE2_C	brain:	n/a
26	chr10:4540959-4541009	SAEC	small airway:	n/a
27	chr10:4540959-4541009	H1-hESC	embryonic stem cell:	embryo
28	chr10:4540959-4541009	HepG2	liver:	n/a
29	chr10:4540959-4541009	SK-N-MC	brain:	n/a
30	chr10:4540959-4541009	HEK293	kidney:	embryo
31	chr10:4540959-4541009	A549	lung:	n/a
32	chr10:4540959-4541009	AG09309	skin:	n/a
33	chr10:4540959-4541009	NT2-D1	testis:	n/a
34	chr10:4540959-4541009	HCM	heart:	n/a
35	chr10:4540959-4541009	HL-60	blood:	n/a
36	chr10:4540959-4541009	K562	blood:	n/a
37	chr10:4540959-4541009	RPTEC	kidney:	n/a
38	chr10:4540959-4541009	HUVEC	blood vessel:	n/a
39	chr10:4540959-4541009	HEEpiC	esophagus:	n/a
40	chr10:4540959-4541009	GM12891	blood:	n/a
41	chr10:4540959-4541009	ECC-1	luminal epithelium:	n/a
42	chr10:4540959-4541009	ovcar-3	ovarian:	n/a
43	chr10:4540959-4541009	HAEpiC	amniotic membrane:	n/a
44	chr10:4540959-4541009	HIPEpiC	eye:	n/a
45	chr10:4540959-4541009	PrEC	prostate:	n/a
46	chr10:4540959-4541009	T-47D	breast:	n/a
47	chr10:4540959-4541009	HCPEpiC	choroid plexus:	n/a
48	chr10:4540959-4541009	NH-A	brain:	n/a
49	chr10:4540959-4541009	BJ	skin:	n/a
50	chr10:4540959-4541009	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:4554890..4555444-chr10:4808771..4809867,3	MCF-7	breast:
2	chr10:4544404..4547324-chr10:4547868..4549793,2	K562	blood:
3	chr10:4566048..4568244-chr10:4578718..4581032,2	MCF-7	breast:
4	chr10:4569855..4572321-chr10:4573462..4575585,2	K562	blood:
5	chr10:4554767..4555670-chr10:4691719..4692590,2	MCF-7	breast:
6	chr10:3827049..3829866-chr10:4557123..4559023,2	MCF-7	breast:
7	chr10:4544404..4547324-chr10:4547868..4549793,2	K562	blood:
8	chr10:4554517..4555692-chr10:4698473..4699407,4	MCF-7	breast:
9	chr10:4554774..4555300-chr10:4623885..4624517,2	MCF-7	breast:
10	chr10:4554964..4555693-chr10:4698445..4699397,2	MCF-7	breast:
11	chr10:4554314..4555272-chr10:4813439..4814001,3	MCF-7	breast:
12	chr10:4554841..4555595-chr10:4693003..4693874,4	MCF-7	breast:
13	chr10:4216515..4217122-chr10:4555119..4555688,2	MCF-7	breast:
14	chr10:4553609..4555147-chr10:4560263..4562993,2	K562	blood:
15	chr10:4553609..4555147-chr10:4560263..4562993,2	K562	blood:
16	chr10:4555087..4556892-chr10:4807552..4809332,2	MCF-7	breast:

Variant related genes	Relation type
RNU6-163P	TF binding region
RNU6-163P	CpG island
ENSG00000231298	chromatin interactions
ENSG00000067082	chromatin interactions

Extended variants
information (count: 1384 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1384 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4551658	chr10:4538492-4538493	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs375629527	chr10:4538498-4538499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540459109	chr10:4538544-4538545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577508358	chr10:4538551-4538552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188090896	chr10:4538564-4538565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181339645	chr10:4538630-4538631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544168283	chr10:4538644-4538645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562566562	chr10:4538669-4538670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533185988	chr10:4538670-4538671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545364672	chr10:4538688-4538689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560881724	chr10:4538698-4538699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs184734290	chr10:4538721-4538722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549558576	chr10:4538736-4538737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76501464	chr10:4538765-4538766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189500145	chr10:4538776-4538777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs4278426	chr10:4538795-4538796	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs568847877	chr10:4538864-4538865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539450796	chr10:4538867-4538868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140143845	chr10:4538885-4538886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs4457647	chr10:4538940-4538941	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs182097707	chr10:4538943-4538944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555554621	chr10:4538947-4538948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10795178	chr10:4538975-4538976	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs137860976	chr10:4538999-4539000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142473589	chr10:4539000-4539001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34024505	chr10:4539018-4539019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs398114003	chr10:4539026-4539027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs76893436	chr10:4539041-4539042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs77442045	chr10:4539042-4539043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549454757	chr10:4539065-4539066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10795179	chr10:4539077-4539078	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs186752790	chr10:4539080-4539081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542818349	chr10:4539107-4539108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561487756	chr10:4539122-4539123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10795180	chr10:4539126-4539127	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs10795181	chr10:4539130-4539131	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs569010405	chr10:4539153-4539154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10795182	chr10:4539155-4539156	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs568888442	chr10:4539157-4539158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10795183	chr10:4539161-4539162	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs566608257	chr10:4539172-4539173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534118549	chr10:4539175-4539176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs61831294	chr10:4539185-4539186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs368280011	chr10:4539197-4539198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145271744	chr10:4539198-4539199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs61831295	chr10:4539201-4539202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557081078	chr10:4539202-4539203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs367576030	chr10:4539214-4539215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs61831296	chr10:4539238-4539239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192483170	chr10:4539242-4539243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
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
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:364 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4537200-4539400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr10:4539400-4540600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr10:4539600-4540400	Enhancers	NHDF-Ad	bronchial
4	chr10:4539600-4540600	Enhancers	Fetal Lung	lung
5	chr10:4539800-4540400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr10:4539800-4540800	Enhancers	Right Ventricle	heart
7	chr10:4539800-4541600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr10:4540000-4541600	Enhancers	Fetal Brain Female	brain
9	chr10:4540200-4540400	Enhancers	Fetal Heart	heart
10	chr10:4540200-4540600	Enhancers	Muscle Satellite Cultured Cells	--
11	chr10:4540200-4540600	Enhancers	Stomach Smooth Muscle	stomach
12	chr10:4540200-4540600	Enhancers	Osteobl	bone
13	chr10:4540200-4541200	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr10:4540200-4541600	Enhancers	Fetal Stomach	stomach
15	chr10:4540200-4541800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr10:4540200-4542200	Enhancers	Colon Smooth Muscle	Colon
17	chr10:4540400-4540600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr10:4540400-4540600	Enhancers	Aorta	Aorta
19	chr10:4540400-4541000	Enhancers	Brain Angular Gyrus	brain
20	chr10:4540400-4541000	Enhancers	Ovary	ovary
21	chr10:4540400-4541000	Flanking Active TSS	NHDF-Ad	bronchial
22	chr10:4540400-4541200	Flanking Active TSS	Fetal Heart	heart
23	chr10:4540400-4541400	Enhancers	Adipose Nuclei	Adipose
24	chr10:4540400-4541400	Enhancers	Fetal Muscle Leg	muscle
25	chr10:4540400-4541600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr10:4540400-4541600	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr10:4540400-4541600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr10:4540400-4541600	Enhancers	HSMMtube	muscle
29	chr10:4540400-4541600	Enhancers	NH-A	brain
30	chr10:4540400-4541600	Enhancers	NHLF	lung
31	chr10:4540400-4541800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr10:4540400-4542200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr10:4540400-4542200	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr10:4540400-4542200	Enhancers	Rectal Smooth Muscle	rectum
35	chr10:4540400-4542200	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr10:4540400-4542200	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr10:4540400-4542200	Enhancers	HMEC	breast
38	chr10:4540400-4542200	Enhancers	HSMM	muscle
39	chr10:4540600-4540800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr10:4540600-4540800	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr10:4540600-4540800	Enhancers	Gastric	stomach
42	chr10:4540600-4540800	Enhancers	Left Ventricle	heart
43	chr10:4540600-4541000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
44	chr10:4540600-4541000	Flanking Active TSS	Fetal Lung	lung
45	chr10:4540600-4541000	Flanking Active TSS	Stomach Smooth Muscle	stomach
46	chr10:4540600-4541000	Flanking Active TSS	Osteobl	bone
47	chr10:4540600-4541400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr10:4540600-4541600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr10:4540600-4541600	Enhancers	Brain Hippocampus Middle	brain
50	chr10:4540600-4541600	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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