Variant report

Variant	nsv8626
Chromosome Location	chr10:43235537-43263641
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	ATF1	chr10:43239265-43239373	K562	blood:	n/a	n/a
2	BACH1	chr10:43248608-43248903	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr10:43249101-43249382	K562	blood:	n/a	n/a
4	BRCA1	chr10:43248663-43248943	H1-hESC	embryonic stem cell:	n/a	n/a
5	CBX3	chr10:43237046-43237288	K562	blood:	n/a	n/a
6	CBX3	chr10:43236980-43237313	K562	blood:	n/a	n/a
7	CCNT2	chr10:43248619-43248819	K562	blood:	n/a	n/a
8	CEBPB	chr10:43239152-43239453	K562	blood:	n/a	chr10:43239295-43239306
9	CEBPB	chr10:43239156-43239359	HepG2	liver:	n/a	chr10:43239295-43239306
10	CEBPB	chr10:43239164-43239414	K562	blood:	n/a	chr10:43239295-43239306
11	CHD2	chr10:43250997-43251011	HepG2	liver:	n/a	n/a
12	CHD2	chr10:43254644-43254988	K562	blood:	n/a	n/a
13	CHD2	chr10:43248662-43248941	H1-hESC	embryonic stem cell:	n/a	chr10:43248745-43248752
14	CHD2	chr10:43249795-43250076	H1-hESC	embryonic stem cell:	n/a	n/a
15	CREB1	chr10:43248635-43249012	A549	lung:	n/a	n/a
16	CREB1	chr10:43248462-43249010	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr10:43248525-43248894	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTBP2	chr10:43248525-43249930	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr10:43248740-43248890	GM12866	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
20	CTCF	chr10:43248432-43249374	SK-N-SH	brain:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
21	CTCF	chr10:43249740-43249890	AG09319	gingival:	n/a	chr10:43249860-43249873
22	CTCF	chr10:43248700-43248850	GM12875	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
23	CTCF	chr10:43239620-43239770	HCT-116	colon:	n/a	n/a
24	CTCF	chr10:43239660-43239810	HMEC	breast:	n/a	n/a
25	CTCF	chr10:43248596-43248898	SK-N-SH_RA	brain:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
26	CTCF	chr10:43250700-43250850	BJ	skin:	n/a	chr10:43250833-43250842
27	CTCF	chr10:43248665-43248883	SK-N-SH_RA	brain:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
28	CTCF	chr10:43239440-43239590	RPTEC	kidney:	n/a	n/a
29	CTCF	chr10:43250220-43250370	NHEK	skin:	n/a	chr10:43250325-43250338
30	CTCF	chr10:43248680-43248830	HFF	foreskin:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
31	CTCF	chr10:43250680-43250830	NHEK	skin:	n/a	n/a
32	CTCF	chr10:43256680-43256830	GM06990	blood:	n/a	chr10:43256721-43256737 chr10:43256715-43256736 chr10:43256720-43256738
33	CTCF	chr10:43249820-43249970	RPTEC	kidney:	n/a	chr10:43249860-43249873
34	CTCF	chr10:43248700-43248850	GM12873	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
35	CTCF	chr10:43248689-43248843	GM19239	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
36	CTCF	chr10:43249240-43249390	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr10:43249720-43249870	GM12864	blood:	n/a	n/a
38	CTCF	chr10:43248474-43249056	HCT-116	colon:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
39	CTCF	chr10:43256074-43256155	LNCaP	prostate:	n/a	n/a
40	CTCF	chr10:43250800-43250950	HPAF	blood vessel:	n/a	chr10:43250833-43250842
41	CTCF	chr10:43249840-43249990	HVMF	connective:	n/a	chr10:43249860-43249873
42	CTCF	chr10:43256700-43256850	HUVEC	blood vessel:	n/a	chr10:43256721-43256737 chr10:43256715-43256736 chr10:43256720-43256738
43	CTCF	chr10:43248740-43248890	AG09309	skin:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
44	CTCF	chr10:43256658-43256814	HepG2	liver:	n/a	chr10:43256721-43256737 chr10:43256715-43256736 chr10:43256720-43256738
45	CTCF	chr10:43251260-43251410	Caco-2	colon:	n/a	n/a
46	CTCF	chr10:43248638-43248917	GM19238	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
47	CTCF	chr10:43239720-43239870	BE2_C	brain:	n/a	n/a
48	CTCF	chr10:43249860-43250010	HPAF	blood vessel:	n/a	chr10:43249860-43249873
49	CTCF	chr10:43256640-43256783	HepG2	liver:	n/a	chr10:43256721-43256737 chr10:43256715-43256736 chr10:43256720-43256738
50	CTCF	chr10:43249760-43249910	GM12873	blood:	n/a	chr10:43249860-43249873

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43254088-43254138	HIPEpiC	eye:	n/a
2	chr10:43251951-43252001	HEEpiC	esophagus:	n/a
3	chr10:43249924-43249974	K562	blood:	n/a
4	chr10:43247938-43247988	GM12892	blood:	n/a
5	chr10:43250063-43250113	SKMC	muscle:	n/a
6	chr10:43263512-43263562	Hepatocyte	liver:	n/a
7	chr10:43254088-43254138	NHDF-neo	bronchial:	n/a
8	chr10:43252305-43252355	PFSK-1	brain:	n/a
9	chr10:43263580-43263630	HRCEpiC	kidney:	n/a
10	chr10:43249924-43249974	HUVEC	blood vessel:	n/a
11	chr10:43252305-43252355	NHDF-neo	bronchial:	n/a
12	chr10:43249924-43249974	HCT-116	colon:	n/a
13	chr10:43251951-43252001	SK-N-MC	brain:	n/a
14	chr10:43250063-43250113	PFSK-1	brain:	n/a
15	chr10:43251951-43252001	MCF10A-Er-Src	breast:	n/a
16	chr10:43263580-43263630	AG10803	skin:	n/a
17	chr10:43249924-43249974	MCF-7	breast:	n/a
18	chr10:43251951-43252001	T-47D	breast:	n/a
19	chr10:43250800-43250850	U87	brain:	n/a
20	chr10:43250800-43250850	Hela-S3	cervix:	n/a
21	chr10:43249924-43249974	HCF	heart:	n/a
22	chr10:43251951-43252001	CMK	blood:	n/a
23	chr10:43263580-43263630	GM12891	blood:	n/a
24	chr10:43251951-43252001	GM06990	blood:	n/a
25	chr10:43252305-43252355	SAEC	small airway:	n/a
26	chr10:43249161-43249211	Caco-2	colon:	n/a
27	chr10:43263512-43263562	HIPEpiC	eye:	n/a
28	chr10:43249161-43249211	HCT-116	colon:	n/a
29	chr10:43263580-43263630	SK-N-MC	brain:	n/a
30	chr10:43249924-43249974	AG04450	lung:	fetal
31	chr10:43250800-43250850	HMEC	breast:	n/a
32	chr10:43248870-43248920	HepG2	liver:	n/a
33	chr10:43263580-43263630	AoSMC	blood vessel:	n/a
34	chr10:43250569-43250619	SK-N-SH_RA	brain:	n/a
35	chr10:43249924-43249974	GM12892	blood:	n/a
36	chr10:43252305-43252355	NHBE	bronchial:	n/a
37	chr10:43250063-43250113	Hela-S3	cervix:	n/a
38	chr10:43248870-43248920	MCF10A-Er-Src	breast:	n/a
39	chr10:43251951-43252001	SK-N-SH_RA	brain:	n/a
40	chr10:43263580-43263630	HMEC	breast:	n/a
41	chr10:43249161-43249211	HEEpiC	esophagus:	n/a
42	chr10:43250800-43250850	PANC-1	pancreas:	n/a
43	chr10:43249924-43249974	PrEC	prostate:	n/a
44	chr10:43251951-43252001	ovcar-3	ovarian:	n/a
45	chr10:43247938-43247988	ProgFib	skin:	n/a
46	chr10:43252305-43252355	HAEpiC	amniotic membrane:	n/a
47	chr10:43248870-43248920	GM12892	blood:	n/a
48	chr10:43263580-43263630	SKMC	muscle:	n/a
49	chr10:43254088-43254138	AG04450	lung:	fetal
50	chr10:43249924-43249974	SK-N-SH_RA	brain:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BMS1-4	chr10:43237124-43237260	NONHSAT012928
2	lnc-BMS1-4	chr10:43236053-43236103	NONHSAT012928
3	lnc-ZNF33B-2	chr10:43246626-43247593	ENSG00000259869.1
4	lnc-BMS1-4	chr10:43236406-43236520	NONHSAT012928

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: 713 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:713 , 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	rs138319506	chr10:43235541-43235542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs186030928	chr10:43235554-43235555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149465851	chr10:43235577-43235578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557246549	chr10:43235592-43235593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190499281	chr10:43235593-43235594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183105338	chr10:43235596-43235597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531926129	chr10:43236078-43236079	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs557183350	chr10:43236084-43236085	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs191900849	chr10:43236417-43236418	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs528492004	chr10:43236508-43236509	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs546660084	chr10:43236515-43236516	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs558772008	chr10:43237129-43237130	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs185997566	chr10:43237154-43237155	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs538769949	chr10:43237195-43237196	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs189309327	chr10:43237200-43237201	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs575367144	chr10:43237203-43237204	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs149737732	chr10:43237218-43237219	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs561194889	chr10:43237228-43237229	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs180967100	chr10:43237238-43237239	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs551795167	chr10:43241467-43241468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191455812	chr10:43241524-43241525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569726500	chr10:43241591-43241592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537583454	chr10:43241592-43241593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs142591166	chr10:43241617-43241618	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs144060664	chr10:43241676-43241677	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs61844763	chr10:43241686-43241687	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs530525913	chr10:43241700-43241701	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs528201401	chr10:43241726-43241727	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs553208936	chr10:43241768-43241769	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs577955894	chr10:43241774-43241775	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs372292165	chr10:43241811-43241812	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs371631581	chr10:43241817-43241818	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs576040957	chr10:43241824-43241825	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs543470003	chr10:43241844-43241845	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs182074860	chr10:43241888-43241889	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs148655130	chr10:43241905-43241906	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs541237583	chr10:43241906-43241907	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs559678461	chr10:43241928-43241929	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs142224714	chr10:43241944-43241945	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs551466520	chr10:43241961-43241962	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs112826707	chr10:43241963-43241964	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs150797631	chr10:43241969-43241970	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs530830339	chr10:43241994-43241995	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs549407438	chr10:43241998-43241999	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs567429103	chr10:43242005-43242006	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs140754831	chr10:43242014-43242015	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs546835601	chr10:43242082-43242083	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs186998749	chr10:43242102-43242103	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs192337935	chr10:43242124-43242125	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs558617029	chr10:43242134-43242135	Active TSS	n/a	n/a	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:459 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43233200-43235600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr10:43241400-43241600	Enhancers	K562	blood
3	chr10:43241600-43242400	Active TSS	K562	blood
4	chr10:43248000-43248200	Active TSS	Duodenum Mucosa	Duodenum
5	chr10:43248000-43248800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
6	chr10:43248200-43248400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr10:43248200-43248400	Bivalent/Poised TSS	Primary hematopoietic stem cells short term culture	blood
8	chr10:43248200-43248400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr10:43248200-43248400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr10:43248200-43248400	Enhancers	Adipose Nuclei	Adipose
11	chr10:43248200-43248400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
12	chr10:43248200-43248400	Bivalent Enhancer	Fetal Intestine Small	intestine
13	chr10:43248200-43248400	Enhancers	Pancreas	Pancrea
14	chr10:43248200-43248400	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
15	chr10:43248200-43248400	Bivalent/Poised TSS	Right Ventricle	heart
16	chr10:43248200-43248400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
17	chr10:43248200-43248600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
18	chr10:43248200-43248600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
19	chr10:43248200-43248600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr10:43248200-43248600	Flanking Active TSS	Duodenum Mucosa	Duodenum
21	chr10:43248200-43248600	Flanking Bivalent TSS/Enh	Placenta	Placenta
22	chr10:43248200-43248600	Bivalent/Poised TSS	HUVEC	blood vessel
23	chr10:43248200-43248800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
24	chr10:43248200-43248800	Bivalent Enhancer	Stomach Mucosa	stomach
25	chr10:43248200-43249000	Active TSS	A549	lung
26	chr10:43248200-43249000	Bivalent/Poised TSS	Osteobl	bone
27	chr10:43248200-43250000	Active TSS	Rectal Smooth Muscle	rectum
28	chr10:43248200-43250200	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr10:43248200-43250800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr10:43248200-43251000	Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr10:43248200-43251200	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
32	chr10:43248400-43248600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr10:43248400-43248600	Bivalent Enhancer	Primary hematopoietic stem cells	blood
35	chr10:43248400-43248600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
36	chr10:43248400-43248600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
37	chr10:43248400-43248600	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
38	chr10:43248400-43248600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr10:43248400-43248600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr10:43248400-43248600	Enhancers	Liver	Liver
41	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
42	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
43	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
44	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
45	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
46	chr10:43248400-43248600	Active TSS	Ovary	ovary
47	chr10:43248400-43248600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
48	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
49	chr10:43248400-43248600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
50	chr10:43248400-43248600	Bivalent/Poised TSS	NHEK	skin

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