Variant report

Variant	nsv550694
Chromosome Location	chr10:43218552-43253587
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	ATF1	chr10:43234242-43234371	K562	blood:	n/a	n/a
3	BACH1	chr10:43248608-43248903	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr10:43218973-43219261	GM12878	blood:	n/a	n/a
5	BHLHE40	chr10:43249101-43249382	K562	blood:	n/a	n/a
6	BRCA1	chr10:43248663-43248943	H1-hESC	embryonic stem cell:	n/a	n/a
7	CBX3	chr10:43237046-43237288	K562	blood:	n/a	n/a
8	CBX3	chr10:43236980-43237313	K562	blood:	n/a	n/a
9	CCNT2	chr10:43248619-43248819	K562	blood:	n/a	n/a
10	CEBPB	chr10:43230096-43230321	MCF-7	breast:	n/a	n/a
11	CEBPB	chr10:43230108-43230288	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	CHD2	chr10:43249795-43250076	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr10:43248662-43248941	H1-hESC	embryonic stem cell:	n/a	chr10:43248745-43248752
17	CHD2	chr10:43250997-43251011	HepG2	liver:	n/a	n/a
18	CREB1	chr10:43248462-43249010	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr10:43248635-43249012	A549	lung:	n/a	n/a
20	CREB1	chr10:43248525-43248894	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTBP2	chr10:43248525-43249930	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr10:43250680-43250830	GM12870	blood:	n/a	n/a
23	CTCF	chr10:43239700-43239850	GM12870	blood:	n/a	n/a
24	CTCF	chr10:43250680-43250830	NHEK	skin:	n/a	n/a
25	CTCF	chr10:43248700-43248850	GM12868	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
26	CTCF	chr10:43248700-43248850	GM12874	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
27	CTCF	chr10:43248720-43248870	GM12867	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
28	CTCF	chr10:43248680-43248830	HCT-116	colon:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
29	CTCF	chr10:43250720-43250870	AG04449	skin:	n/a	chr10:43250833-43250842
30	CTCF	chr10:43248643-43248932	Medullo	brain:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
31	CTCF	chr10:43239720-43239870	MCF-7	breast:	n/a	n/a
32	CTCF	chr10:43249720-43249870	GM12864	blood:	n/a	n/a
33	CTCF	chr10:43250760-43250910	GM12873	blood:	n/a	chr10:43250833-43250842
34	CTCF	chr10:43249820-43249970	HPF	lung:	n/a	chr10:43249860-43249873
35	CTCF	chr10:43239756-43239821	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr10:43248624-43248912	Fibrobl	skin:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
37	CTCF	chr10:43249760-43249910	AG09319	gingival:	n/a	chr10:43249860-43249873
38	CTCF	chr10:43249760-43249910	GM12873	blood:	n/a	chr10:43249860-43249873
39	CTCF	chr10:43228363-43228436	GM13976	blood:	n/a	n/a
40	CTCF	chr10:43248674-43248901	HUVEC	blood vessel:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
41	CTCF	chr10:43250740-43250890	AG04450	lung:	n/a	chr10:43250833-43250842
42	CTCF	chr10:43239713-43239845	K562	blood:	n/a	n/a
43	CTCF	chr10:43248740-43248890	HUVEC	blood vessel:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
44	CTCF	chr10:43239740-43239890	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr10:43248727-43248836	Gliobla	brain:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
46	CTCF	chr10:43251240-43251390	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr10:43248700-43248850	GM06990	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
48	CTCF	chr10:43239760-43239910	K562	blood:	n/a	n/a
49	CTCF	chr10:43248740-43248890	AG10803	skin:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
50	CTCF	chr10:43248474-43249056	HCT-116	colon:	n/a	chr10:43248777-43248793 chr10:43248779-43248792

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43252305-43252355	GM06990	blood:	n/a
2	chr10:43249924-43249974	AG09319	gingival:	n/a
3	chr10:43252305-43252355	GM06990	blood:	n/a
4	chr10:43249924-43249974	AG09319	gingival:	n/a
5	chr10:43250800-43250850	AG04449	skin:	fetal
6	chr10:43251951-43252001	HEK293	kidney:	embryo
7	chr10:43251951-43252001	AG10803	skin:	n/a
8	chr10:43245080-43245130	HPAEpiC	pulmonary alveolar:	n/a
9	chr10:43250063-43250113	GM12892	blood:	n/a
10	chr10:43247938-43247988	HCPEpiC	choroid plexus:	n/a
11	chr10:43249161-43249211	NHDF-neo	bronchial:	n/a
12	chr10:43245080-43245130	AoSMC	blood vessel:	n/a
13	chr10:43250800-43250850	ECC-1	luminal epithelium:	n/a
14	chr10:43252305-43252355	MCF-7	breast:	n/a
15	chr10:43250800-43250850	HAEpiC	amniotic membrane:	n/a
16	chr10:43252305-43252355	HIPEpiC	eye:	n/a
17	chr10:43250569-43250619	HEK293	kidney:	embryo
18	chr10:43250569-43250619	HMEC	breast:	n/a
19	chr10:43252305-43252355	AG04449	skin:	fetal
20	chr10:43250800-43250850	HIPEpiC	eye:	n/a
21	chr10:43252305-43252355	HPAEpiC	pulmonary alveolar:	n/a
22	chr10:43249161-43249211	HMEC	breast:	n/a
23	chr10:43250063-43250113	MCF-7	breast:	n/a
24	chr10:43250800-43250850	PFSK-1	brain:	n/a
25	chr10:43247938-43247988	Hela-S3	cervix:	n/a
26	chr10:43250569-43250619	GM12878	blood:	n/a
27	chr10:43247938-43247988	Jurkat	blood:	n/a
28	chr10:43250569-43250619	PFSK-1	brain:	n/a
29	chr10:43250063-43250113	CMK	blood:	n/a
30	chr10:43250569-43250619	ProgFib	skin:	n/a
31	chr10:43252305-43252355	SAEC	small airway:	n/a
32	chr10:43251951-43252001	NHDF-neo	bronchial:	n/a
33	chr10:43249924-43249974	HCT-116	colon:	n/a
34	chr10:43250800-43250850	CMK	blood:	n/a
35	chr10:43249924-43249974	U87	brain:	n/a
36	chr10:43252305-43252355	H1-hESC	embryonic stem cell:	embryo
37	chr10:43249924-43249974	MCF-7	breast:	n/a
38	chr10:43250063-43250113	MCF10A-Er-Src	breast:	n/a
39	chr10:43252305-43252355	NHBE	bronchial:	n/a
40	chr10:43248870-43248920	Hepatocyte	liver:	n/a
41	chr10:43247938-43247988	GM06990	blood:	n/a
42	chr10:43248870-43248920	A549	lung:	n/a
43	chr10:43245080-43245130	ovcar-3	ovarian:	n/a
44	chr10:43249161-43249211	HRCEpiC	kidney:	n/a
45	chr10:43249161-43249211	PrEC	prostate:	n/a
46	chr10:43251951-43252001	AG09319	gingival:	n/a
47	chr10:43248870-43248920	HUVEC	blood vessel:	n/a
48	chr10:43250800-43250850	HepG2	liver:	n/a
49	chr10:43250063-43250113	GM12878	blood:	n/a
50	chr10:43252305-43252355	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr10:43228372..43230638-chr10:43276090..43278496,2	MCF-7	breast:
2	chr10:43245352..43247530-chr10:43276802..43279739,2	K562	blood:
3	chr10:43251549..43254175-chr10:43277144..43279429,2	K562	blood:
4	chr10:43250283..43253153-chr10:43277432..43279955,3	MCF-7	breast:
5	chr10:43253135..43254665-chr10:43264247..43266986,2	MCF-7	breast:
6	chr10:43250846..43253793-chr10:43254051..43256963,2	K562	blood:

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

Variant related genes	Relation type
ENSG00000259869	TF binding region
RSU1P1	TF binding region
DUXAP3	TF binding region
ENSG00000259869	CpG island
RSU1P1	CpG island
DUXAP3	CpG island
ENSG00000165733	chromatin interactions

Extended variants
information (count: 709 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:709 , 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	rs1807366	chr10:43218552-43218553	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553340931	chr10:43218567-43218568	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs375515849	chr10:43218647-43218648	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs185015893	chr10:43218702-43218703	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs557077925	chr10:43218720-43218721	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs575650877	chr10:43218724-43218725	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs542792040	chr10:43218726-43218727	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs554738123	chr10:43218774-43218775	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs371454534	chr10:43218775-43218776	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs573127442	chr10:43218806-43218807	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs187974990	chr10:43218828-43218829	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs2506102	chr10:43218840-43218841	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs532697742	chr10:43218882-43218883	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs141753456	chr10:43218883-43218884	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs568047017	chr10:43218897-43218898	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs563178200	chr10:43218906-43218907	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs147186688	chr10:43218945-43218946	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs548834950	chr10:43218983-43218984	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs567997450	chr10:43219019-43219020	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs556811008	chr10:43219043-43219044	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs372883671	chr10:43219058-43219059	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs9730806	chr10:43219070-43219071	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs538983431	chr10:43219120-43219121	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs546835900	chr10:43219204-43219205	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs571516795	chr10:43219243-43219244	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs538564688	chr10:43219246-43219247	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs557312741	chr10:43219248-43219249	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs569201371	chr10:43219353-43219354	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs148703054	chr10:43219428-43219429	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs553171908	chr10:43219458-43219459	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs11594734	chr10:43219479-43219480	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs536727184	chr10:43219495-43219496	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs554676841	chr10:43219545-43219546	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs573015519	chr10:43219549-43219550	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs534080696	chr10:43219573-43219574	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs192191231	chr10:43219579-43219580	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs386743144	chr10:43219600-43219601	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs7903713	chr10:43219601-43219602	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs544627147	chr10:43219641-43219642	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs572501909	chr10:43219661-43219662	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs563275177	chr10:43219662-43219663	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs369866770	chr10:43219679-43219680	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs542663535	chr10:43219684-43219685	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs370192221	chr10:43219688-43219689	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs560940383	chr10:43219732-43219733	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs373098703	chr10:43219800-43219801	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs138797438	chr10:43219827-43219828	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs546774447	chr10:43219920-43219921	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs200701127	chr10:43220024-43220025	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs10900264	chr10:43220025-43220026	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:56)

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
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:455 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43227800-43228000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:43227800-43228000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr10:43230000-43230400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr10:43232600-43235200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr10:43233200-43235600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr10:43235200-43235400	Enhancers	Gastric	stomach
7	chr10:43241400-43241600	Enhancers	K562	blood
8	chr10:43241600-43242400	Active TSS	K562	blood
9	chr10:43248000-43248200	Active TSS	Duodenum Mucosa	Duodenum
10	chr10:43248000-43248800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
11	chr10:43248200-43248400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr10:43248200-43248400	Bivalent/Poised TSS	Primary hematopoietic stem cells short term culture	blood
13	chr10:43248200-43248400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr10:43248200-43248400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr10:43248200-43248400	Enhancers	Adipose Nuclei	Adipose
16	chr10:43248200-43248400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
17	chr10:43248200-43248400	Bivalent Enhancer	Fetal Intestine Small	intestine
18	chr10:43248200-43248400	Enhancers	Pancreas	Pancrea
19	chr10:43248200-43248400	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
20	chr10:43248200-43248400	Bivalent/Poised TSS	Right Ventricle	heart
21	chr10:43248200-43248400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
22	chr10:43248200-43248600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
23	chr10:43248200-43248600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
24	chr10:43248200-43248600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr10:43248200-43248600	Flanking Active TSS	Duodenum Mucosa	Duodenum
26	chr10:43248200-43248600	Flanking Bivalent TSS/Enh	Placenta	Placenta
27	chr10:43248200-43248600	Bivalent/Poised TSS	HUVEC	blood vessel
28	chr10:43248200-43248800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
29	chr10:43248200-43248800	Bivalent Enhancer	Stomach Mucosa	stomach
30	chr10:43248200-43249000	Active TSS	A549	lung
31	chr10:43248200-43249000	Bivalent/Poised TSS	Osteobl	bone
32	chr10:43248200-43250000	Active TSS	Rectal Smooth Muscle	rectum
33	chr10:43248200-43250200	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr10:43248200-43250800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr10:43248200-43251000	Active TSS	Pancreatic Islets	Pancreatic Islet
36	chr10:43248200-43251200	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
37	chr10:43248400-43248600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr10:43248400-43248600	Bivalent Enhancer	Primary hematopoietic stem cells	blood
40	chr10:43248400-43248600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
41	chr10:43248400-43248600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
42	chr10:43248400-43248600	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
43	chr10:43248400-43248600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr10:43248400-43248600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr10:43248400-43248600	Enhancers	Liver	Liver
46	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
47	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
48	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
49	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
50	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle

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