Variant report

Variant	nsv825349
Chromosome Location	chr10:43238099-43265011
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:589)
CpG islands
(count:855)
Chromatin interactive
region (count:14)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:43264291-43264671	K562	blood:	n/a	n/a
2	ATF1	chr10:43264252-43264654	K562	blood:	n/a	n/a
3	ATF1	chr10:43239265-43239373	K562	blood:	n/a	n/a
4	BACH1	chr10:43248608-43248903	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr10:43264879-43264880	K562	blood:	n/a	n/a
6	BHLHE40	chr10:43264256-43264646	K562	blood:	n/a	n/a
7	BHLHE40	chr10:43249101-43249382	K562	blood:	n/a	n/a
8	BRCA1	chr10:43248663-43248943	H1-hESC	embryonic stem cell:	n/a	n/a
9	CCNT2	chr10:43248619-43248819	K562	blood:	n/a	n/a
10	CCNT2	chr10:43264304-43264633	K562	blood:	n/a	n/a
11	CEBPB	chr10:43264321-43264477	K562	blood:	n/a	n/a
12	CEBPB	chr10:43239164-43239414	K562	blood:	n/a	chr10:43239295-43239306
13	CEBPB	chr10:43239156-43239359	HepG2	liver:	n/a	chr10:43239295-43239306
14	CEBPB	chr10:43239152-43239453	K562	blood:	n/a	chr10:43239295-43239306
15	CEBPB	chr10:43264228-43264651	K562	blood:	n/a	n/a
16	CEBPD	chr10:43264121-43264812	K562	blood:	n/a	n/a
17	CEBPD	chr10:43264193-43264757	K562	blood:	n/a	n/a
18	CHD2	chr10:43264433-43264635	K562	blood:	n/a	n/a
19	CHD2	chr10:43254644-43254988	K562	blood:	n/a	n/a
20	CHD2	chr10:43249795-43250076	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr10:43250997-43251011	HepG2	liver:	n/a	n/a
22	CHD2	chr10:43248662-43248941	H1-hESC	embryonic stem cell:	n/a	chr10:43248745-43248752
23	CREB1	chr10:43248635-43249012	A549	lung:	n/a	n/a
24	CREB1	chr10:43248462-43249010	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr10:43248525-43248894	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTBP2	chr10:43248525-43249930	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr10:43248720-43248870	AG04450	lung:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
28	CTCF	chr10:43250740-43250890	AG09319	gingival:	n/a	chr10:43250833-43250842
29	CTCF	chr10:43239740-43239890	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr10:43256633-43256804	HepG2	liver:	n/a	chr10:43256721-43256737 chr10:43256715-43256736 chr10:43256720-43256738
31	CTCF	chr10:43239440-43239590	RPTEC	kidney:	n/a	n/a
32	CTCF	chr10:43248748-43248799	HepG2	liver:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
33	CTCF	chr10:43250720-43250870	HMF	breast:	n/a	chr10:43250833-43250842
34	CTCF	chr10:43248504-43249032	K562	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
35	CTCF	chr10:43248630-43248923	A549	lung:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
36	CTCF	chr10:43250680-43250830	NHEK	skin:	n/a	n/a
37	CTCF	chr10:43250800-43250950	HPAF	blood vessel:	n/a	chr10:43250833-43250842
38	CTCF	chr10:43239740-43239890	GM12864	blood:	n/a	n/a
39	CTCF	chr10:43248720-43248870	HMEC	breast:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
40	CTCF	chr10:43249800-43249950	GM12870	blood:	n/a	chr10:43249860-43249873
41	CTCF	chr10:43239700-43239850	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr10:43248700-43248850	RPTEC	kidney:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
43	CTCF	chr10:43248740-43248890	GM12878	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
44	CTCF	chr10:43250780-43250930	HPAF	blood vessel:	n/a	chr10:43250833-43250842
45	CTCF	chr10:43248700-43248850	GM12874	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
46	CTCF	chr10:43249240-43249390	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr10:43248515-43249001	T-47D	breast:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
48	CTCF	chr10:43248662-43248877	GM12891	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
49	CTCF	chr10:43239720-43239870	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr10:43248596-43248898	SK-N-SH_RA	brain:	n/a	chr10:43248777-43248793 chr10:43248779-43248792

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43248870-43248920	HAEpiC	amniotic membrane:	n/a
2	chr10:43248870-43248920	HAEpiC	amniotic membrane:	n/a
3	chr10:43263649-43263699	PFSK-1	brain:	n/a
4	chr10:43263512-43263562	RPTEC	kidney:	n/a
5	chr10:43263649-43263699	AG09319	gingival:	n/a
6	chr10:43250569-43250619	PFSK-1	brain:	n/a
7	chr10:43252305-43252355	NH-A	brain:	n/a
8	chr10:43250063-43250113	HMEC	breast:	n/a
9	chr10:43263580-43263630	HMEC	breast:	n/a
10	chr10:43249161-43249211	NT2-D1	testis:	n/a
11	chr10:43263512-43263562	GM19239	blood:	n/a
12	chr10:43245080-43245130	HCT-116	colon:	n/a
13	chr10:43249924-43249974	PFSK-1	brain:	n/a
14	chr10:43263580-43263630	HRCEpiC	kidney:	n/a
15	chr10:43245080-43245130	GM12891	blood:	n/a
16	chr10:43251951-43252001	HNPCEpiC	eye:	n/a
17	chr10:43249924-43249974	H1-hESC	embryonic stem cell:	embryo
18	chr10:43251951-43252001	Jurkat	blood:	n/a
19	chr10:43248870-43248920	AG04450	lung:	fetal
20	chr10:43247938-43247988	CMK	blood:	n/a
21	chr10:43247938-43247988	GM06990	blood:	n/a
22	chr10:43263512-43263562	SK-N-MC	brain:	n/a
23	chr10:43250569-43250619	HCM	heart:	n/a
24	chr10:43252305-43252355	ECC-1	luminal epithelium:	n/a
25	chr10:43252305-43252355	Jurkat	blood:	n/a
26	chr10:43250800-43250850	PrEC	prostate:	n/a
27	chr10:43263512-43263562	HIPEpiC	eye:	n/a
28	chr10:43249161-43249211	AG04450	lung:	fetal
29	chr10:43251951-43252001	AG09309	skin:	n/a
30	chr10:43252305-43252355	PrEC	prostate:	n/a
31	chr10:43249161-43249211	HCM	heart:	n/a
32	chr10:43247938-43247988	ovcar-3	ovarian:	n/a
33	chr10:43250569-43250619	NH-A	brain:	n/a
34	chr10:43245080-43245130	HRCEpiC	kidney:	n/a
35	chr10:43263649-43263699	SK-N-SH_RA	brain:	n/a
36	chr10:43252305-43252355	NB4	blood:	n/a
37	chr10:43250063-43250113	HRCEpiC	kidney:	n/a
38	chr10:43250800-43250850	SK-N-SH	brain:	n/a
39	chr10:43250569-43250619	H1-hESC	embryonic stem cell:	embryo
40	chr10:43263649-43263699	H1-hESC	embryonic stem cell:	embryo
41	chr10:43250063-43250113	AG10803	skin:	n/a
42	chr10:43263512-43263562	HNPCEpiC	eye:	n/a
43	chr10:43250569-43250619	MCF-7	breast:	n/a
44	chr10:43263649-43263699	HUVEC	blood vessel:	n/a
45	chr10:43249161-43249211	HRCEpiC	kidney:	n/a
46	chr10:43247938-43247988	AG09319	gingival:	n/a
47	chr10:43250800-43250850	U87	brain:	n/a
48	chr10:43263580-43263630	Caco-2	colon:	n/a
49	chr10:43249924-43249974	GM19239	blood:	n/a
50	chr10:43249924-43249974	HUVEC	blood vessel:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:43263804..43266604-chr10:43268900..43270663,2	MCF-7	breast:
2	chr10:43250283..43253153-chr10:43277432..43279955,3	MCF-7	breast:
3	chr10:43250846..43253793-chr10:43254051..43256963,2	K562	blood:
4	chr10:43258843..43262487-chr10:43264254..43267473,3	K562	blood:
5	chr10:43253135..43254665-chr10:43264247..43266986,2	MCF-7	breast:
6	chr10:43262874..43266209-chr10:43268342..43271637,4	K562	blood:
7	chr10:43245352..43247530-chr10:43276802..43279739,2	K562	blood:
8	chr10:43263552..43268206-chr10:43276275..43279426,5	MCF-7	breast:
9	chr10:43250846..43253793-chr10:43254051..43256963,2	K562	blood:
10	chr10:43261896..43264649-chr10:43275679..43278435,2	MCF-7	breast:
11	chr10:43147543..43150157-chr10:43264028..43266927,2	K562	blood:
12	chr10:43251549..43254175-chr10:43277144..43279429,2	K562	blood:
13	chr10:43258843..43262487-chr10:43264254..43267473,3	K562	blood:
14	chr10:43253135..43254665-chr10:43264247..43266986,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF33B-2	chr10:43246626-43247593	ENSG00000259869.1

No data

Variant related genes	Relation type
ENSG00000259869	TF binding region
DUXAP3	TF binding region
ENSG00000259869	CpG island
DUXAP3	CpG island
ENSG00000165733	chromatin interactions

Extended variants
information (count: 748 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:748 , 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	rs551795167	chr10:43241467-43241468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs191455812	chr10:43241524-43241525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569726500	chr10:43241591-43241592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs537583454	chr10:43241592-43241593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142591166	chr10:43241617-43241618	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs144060664	chr10:43241676-43241677	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs61844763	chr10:43241686-43241687	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs530525913	chr10:43241700-43241701	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs528201401	chr10:43241726-43241727	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs553208936	chr10:43241768-43241769	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs577955894	chr10:43241774-43241775	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs372292165	chr10:43241811-43241812	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs371631581	chr10:43241817-43241818	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs576040957	chr10:43241824-43241825	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs543470003	chr10:43241844-43241845	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs182074860	chr10:43241888-43241889	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs148655130	chr10:43241905-43241906	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs541237583	chr10:43241906-43241907	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs559678461	chr10:43241928-43241929	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs142224714	chr10:43241944-43241945	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs551466520	chr10:43241961-43241962	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs112826707	chr10:43241963-43241964	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs150797631	chr10:43241969-43241970	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs530830339	chr10:43241994-43241995	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs549407438	chr10:43241998-43241999	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs567429103	chr10:43242005-43242006	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs140754831	chr10:43242014-43242015	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs546835601	chr10:43242082-43242083	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs186998749	chr10:43242102-43242103	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs192337935	chr10:43242124-43242125	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs558617029	chr10:43242134-43242135	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs182179174	chr10:43242135-43242136	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs144603497	chr10:43242230-43242231	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs147910998	chr10:43242241-43242242	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs565700569	chr10:43242273-43242274	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs117322654	chr10:43242276-43242277	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs370821001	chr10:43242282-43242283	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs186822638	chr10:43242319-43242320	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs74137935	chr10:43242337-43242338	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs559617782	chr10:43242353-43242354	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs534623718	chr10:43242354-43242355	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs141671885	chr10:43242361-43242362	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs116201372	chr10:43244644-43244645	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs558832083	chr10:43244649-43244650	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs577143667	chr10:43244673-43244674	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs188835647	chr10:43245081-43245082	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs570736069	chr10:43245098-43245099	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs537844989	chr10:43245123-43245124	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs114048584	chr10:43245320-43245321	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs529657307	chr10:43245323-43245324	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
Lung cancer	18438408	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
Mental retardation	21062444	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
Autism	20531469	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:470 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43241400-43241600	Enhancers	K562	blood
2	chr10:43241600-43242400	Active TSS	K562	blood
3	chr10:43248000-43248200	Active TSS	Duodenum Mucosa	Duodenum
4	chr10:43248000-43248800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
5	chr10:43248200-43248400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr10:43248200-43248400	Bivalent/Poised TSS	Primary hematopoietic stem cells short term culture	blood
7	chr10:43248200-43248400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr10:43248200-43248400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr10:43248200-43248400	Enhancers	Adipose Nuclei	Adipose
10	chr10:43248200-43248400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
11	chr10:43248200-43248400	Bivalent Enhancer	Fetal Intestine Small	intestine
12	chr10:43248200-43248400	Enhancers	Pancreas	Pancrea
13	chr10:43248200-43248400	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
14	chr10:43248200-43248400	Bivalent/Poised TSS	Right Ventricle	heart
15	chr10:43248200-43248400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
16	chr10:43248200-43248600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
17	chr10:43248200-43248600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
18	chr10:43248200-43248600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr10:43248200-43248600	Flanking Active TSS	Duodenum Mucosa	Duodenum
20	chr10:43248200-43248600	Flanking Bivalent TSS/Enh	Placenta	Placenta
21	chr10:43248200-43248600	Bivalent/Poised TSS	HUVEC	blood vessel
22	chr10:43248200-43248800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
23	chr10:43248200-43248800	Bivalent Enhancer	Stomach Mucosa	stomach
24	chr10:43248200-43249000	Active TSS	A549	lung
25	chr10:43248200-43249000	Bivalent/Poised TSS	Osteobl	bone
26	chr10:43248200-43250000	Active TSS	Rectal Smooth Muscle	rectum
27	chr10:43248200-43250200	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr10:43248200-43250800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr10:43248200-43251000	Active TSS	Pancreatic Islets	Pancreatic Islet
30	chr10:43248200-43251200	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
31	chr10:43248400-43248600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr10:43248400-43248600	Bivalent Enhancer	Primary hematopoietic stem cells	blood
34	chr10:43248400-43248600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
35	chr10:43248400-43248600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
36	chr10:43248400-43248600	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
37	chr10:43248400-43248600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr10:43248400-43248600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr10:43248400-43248600	Enhancers	Liver	Liver
40	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
41	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
42	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
43	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
44	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
45	chr10:43248400-43248600	Active TSS	Ovary	ovary
46	chr10:43248400-43248600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
47	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
48	chr10:43248400-43248600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
49	chr10:43248400-43248600	Bivalent/Poised TSS	NHEK	skin
50	chr10:43248400-43248800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell

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