Variant report

Variant	nsv1045144
Chromosome Location	chr10:43202223-43251692
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	chr10:43234242-43234371	K562	blood:	n/a	n/a
2	ATF1	chr10:43239265-43239373	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	chr10:43236980-43237313	K562	blood:	n/a	n/a
8	CBX3	chr10:43237046-43237288	K562	blood:	n/a	n/a
9	CCNT2	chr10:43248619-43248819	K562	blood:	n/a	n/a
10	CEBPB	chr10:43239164-43239414	K562	blood:	n/a	chr10:43239295-43239306
11	CEBPB	chr10:43204367-43204575	HepG2	liver:	n/a	chr10:43204513-43204524 chr10:43204512-43204525
12	CEBPB	chr10:43239156-43239359	HepG2	liver:	n/a	chr10:43239295-43239306
13	CEBPB	chr10:43230108-43230288	K562	blood:	n/a	n/a
14	CEBPB	chr10:43239152-43239453	K562	blood:	n/a	chr10:43239295-43239306
15	CEBPB	chr10:43230096-43230321	MCF-7	breast:	n/a	n/a
16	CHD2	chr10:43249795-43250076	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr10:43250997-43251011	HepG2	liver:	n/a	n/a
18	CHD2	chr10:43248662-43248941	H1-hESC	embryonic stem cell:	n/a	chr10:43248745-43248752
19	CREB1	chr10:43248635-43249012	A549	lung:	n/a	n/a
20	CREB1	chr10:43248462-43249010	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chr10:43248525-43248894	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTBP2	chr10:43248525-43249930	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr10:43239660-43239810	HMEC	breast:	n/a	n/a
24	CTCF	chr10:43248680-43248830	GM12869	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
25	CTCF	chr10:43250760-43250910	HCT-116	colon:	n/a	chr10:43250833-43250842
26	CTCF	chr10:43248680-43248830	GM12872	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
27	CTCF	chr10:43248720-43248870	Caco-2	colon:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
28	CTCF	chr10:43251298-43251405	K562	blood:	n/a	n/a
29	CTCF	chr10:43248727-43248836	Gliobla	brain:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
30	CTCF	chr10:43250780-43250930	HBMEC	blood vessel:	n/a	chr10:43250833-43250842
31	CTCF	chr10:43249740-43249890	SK-N-SH_RA	brain:	n/a	chr10:43249860-43249873
32	CTCF	chr10:43248409-43249122	HCT-116	colon:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
33	CTCF	chr10:43248660-43248810	HFF-Myc	foreskin:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
34	CTCF	chr10:43248740-43248890	HEEpiC	esophagus:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
35	CTCF	chr10:43249780-43249930	HCFaa	heart:	n/a	chr10:43249860-43249873
36	CTCF	chr10:43250220-43250370	NHEK	skin:	n/a	chr10:43250325-43250338
37	CTCF	chr10:43248680-43248862	GM13976	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
38	CTCF	chr10:43248740-43248890	AG10803	skin:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
39	CTCF	chr10:43239756-43239821	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr10:43248700-43248850	NHDF-neo	bronchial:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
41	CTCF	chr10:43249820-43249970	HBMEC	blood vessel:	n/a	chr10:43249860-43249873
42	CTCF	chr10:43249720-43249870	GM12864	blood:	n/a	n/a
43	CTCF	chr10:43248689-43248843	GM19239	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
44	CTCF	chr10:43248720-43248870	GM12867	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
45	CTCF	chr10:43249700-43249850	HCM	heart:	n/a	n/a
46	CTCF	chr10:43239800-43239950	RPTEC	kidney:	n/a	n/a
47	CTCF	chr10:43248669-43248867	GM20000	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
48	CTCF	chr10:43250700-43250850	HAc	cerebellar:	n/a	chr10:43250833-43250842
49	CTCF	chr10:43249900-43250050	BJ	skin:	n/a	n/a
50	CTCF	chr10:43250860-43251010	AG04449	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43248870-43248920	NB4	blood:	n/a
2	chr10:43248870-43248920	NB4	blood:	n/a
3	chr10:43248870-43248920	HRPEpiC	eye:	n/a
4	chr10:43250063-43250113	GM12878	blood:	n/a
5	chr10:43250800-43250850	ProgFib	skin:	n/a
6	chr10:43245080-43245130	HCPEpiC	choroid plexus:	n/a
7	chr10:43248870-43248920	HAEpiC	amniotic membrane:	n/a
8	chr10:43248870-43248920	HCM	heart:	n/a
9	chr10:43249161-43249211	U87	brain:	n/a
10	chr10:43247938-43247988	SK-N-SH_RA	brain:	n/a
11	chr10:43248870-43248920	HCPEpiC	choroid plexus:	n/a
12	chr10:43216927-43216977	U87	brain:	n/a
13	chr10:43245080-43245130	PFSK-1	brain:	n/a
14	chr10:43250063-43250113	AoSMC	blood vessel:	n/a
15	chr10:43245080-43245130	HRPEpiC	eye:	n/a
16	chr10:43216927-43216977	AG04449	skin:	fetal
17	chr10:43209934-43209984	CMK	blood:	n/a
18	chr10:43248870-43248920	HepG2	liver:	n/a
19	chr10:43216927-43216977	GM12878	blood:	n/a
20	chr10:43250063-43250113	ProgFib	skin:	n/a
21	chr10:43215944-43215994	HRE	kidney:	n/a
22	chr10:43250569-43250619	SKMC	muscle:	n/a
23	chr10:43215944-43215994	A549	lung:	n/a
24	chr10:43250569-43250619	HIPEpiC	eye:	n/a
25	chr10:43247938-43247988	BJ	skin:	n/a
26	chr10:43250063-43250113	A549	lung:	n/a
27	chr10:43250800-43250850	MCF-7	breast:	n/a
28	chr10:43250800-43250850	K562	blood:	n/a
29	chr10:43248870-43248920	NHBE	bronchial:	n/a
30	chr10:43250569-43250619	Hela-S3	cervix:	n/a
31	chr10:43249161-43249211	MCF10A-Er-Src	breast:	n/a
32	chr10:43250063-43250113	HCM	heart:	n/a
33	chr10:43209934-43209984	PrEC	prostate:	n/a
34	chr10:43250569-43250619	K562	blood:	n/a
35	chr10:43249924-43249974	HNPCEpiC	eye:	n/a
36	chr10:43249161-43249211	HCPEpiC	choroid plexus:	n/a
37	chr10:43250800-43250850	PANC-1	pancreas:	n/a
38	chr10:43250800-43250850	AG09309	skin:	n/a
39	chr10:43245080-43245130	SAEC	small airway:	n/a
40	chr10:43250800-43250850	HCM	heart:	n/a
41	chr10:43215944-43215994	HRCEpiC	kidney:	n/a
42	chr10:43215944-43215994	GM19239	blood:	n/a
43	chr10:43245080-43245130	NH-A	brain:	n/a
44	chr10:43249924-43249974	HAEpiC	amniotic membrane:	n/a
45	chr10:43249161-43249211	HIPEpiC	eye:	n/a
46	chr10:43250063-43250113	AG04450	lung:	fetal
47	chr10:43247938-43247988	GM12878	blood:	n/a
48	chr10:43250569-43250619	GM12892	blood:	n/a
49	chr10:43250569-43250619	NH-A	brain:	n/a
50	chr10:43250800-43250850	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:43245352..43247530-chr10:43276802..43279739,2	K562	blood:
2	chr10:43228372..43230638-chr10:43276090..43278496,2	MCF-7	breast:
3	chr10:43250283..43253153-chr10:43277432..43279955,3	MCF-7	breast:
4	chr10:43251549..43254175-chr10:43277144..43279429,2	K562	blood:
5	chr10:43203133..43206798-chr10:43276930..43278950,3	MCF-7	breast:
6	chr10:43250846..43253793-chr10:43254051..43256963,2	K562	blood:

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

Variant related genes	Relation type
ENSG00000259869	TF binding region
RSU1P1	TF binding region
DUXAP3	TF binding region
CUBNP1	TF binding region
ENSG00000259869	CpG island
RSU1P1	CpG island
DUXAP3	CpG island
CUBNP1	CpG island
ENSG00000165733	chromatin interactions

Extended variants
information (count: 1170 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1170 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546250096	chr10:43202605-43202606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs571223778	chr10:43202609-43202610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs190876054	chr10:43202632-43202633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531034494	chr10:43202634-43202635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557056012	chr10:43202668-43202669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs569067857	chr10:43202721-43202722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536476289	chr10:43202799-43202800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs111965806	chr10:43202834-43202835	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs374573435	chr10:43202876-43202877	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs182005801	chr10:43202892-43202893	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs558640229	chr10:43202904-43202905	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs577211044	chr10:43202959-43202960	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs148888894	chr10:43202984-43202985	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs543793611	chr10:43203008-43203009	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs372372757	chr10:43203022-43203023	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs375957570	chr10:43203028-43203029	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs541985743	chr10:43203030-43203031	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs594295	chr10:43203060-43203061	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs185018579	chr10:43203064-43203065	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs552843168	chr10:43203070-43203071	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs564716129	chr10:43203076-43203077	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs595149	chr10:43203245-43203246	Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs199809259	chr10:43203269-43203270	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs568071399	chr10:43203284-43203285	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs116271387	chr10:43203286-43203287	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs374754134	chr10:43203309-43203310	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs569004234	chr10:43203313-43203314	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs1830491	chr10:43203315-43203316	Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs191138987	chr10:43203321-43203322	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs144091768	chr10:43203322-43203323	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs533836726	chr10:43203324-43203325	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs146527889	chr10:43203345-43203346	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs562498790	chr10:43203359-43203360	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs58777155	chr10:43203363-43203364	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs577147723	chr10:43203433-43203434	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs538272512	chr10:43203438-43203439	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs556154373	chr10:43203470-43203471	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs574564604	chr10:43203495-43203496	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs541922563	chr10:43203513-43203514	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs560270793	chr10:43203553-43203554	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs572637860	chr10:43203555-43203556	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs546175026	chr10:43203581-43203582	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs560310534	chr10:43203587-43203588	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs182660969	chr10:43203613-43203614	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs114019410	chr10:43203630-43203631	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs550570145	chr10:43203647-43203648	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs529049200	chr10:43203658-43203659	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs562473562	chr10:43203661-43203662	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs543779	chr10:43203674-43203675	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs188127880	chr10:43203687-43203688	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

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

Chromatin state (count:452 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43202600-43202800	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr10:43202800-43203600	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr10:43212600-43213000	Enhancers	Spleen	Spleen
4	chr10:43212800-43213000	Enhancers	HepG2	liver
5	chr10:43213000-43215800	Weak transcription	Spleen	Spleen
6	chr10:43215800-43216200	ZNF genes & repeats	Spleen	Spleen
7	chr10:43217600-43218000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr10:43227800-43228000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr10:43227800-43228000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr10:43230000-43230400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr10:43232600-43235200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr10:43233200-43235600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr10:43235200-43235400	Enhancers	Gastric	stomach
14	chr10:43241400-43241600	Enhancers	K562	blood
15	chr10:43241600-43242400	Active TSS	K562	blood
16	chr10:43248000-43248200	Active TSS	Duodenum Mucosa	Duodenum
17	chr10:43248000-43248800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr10:43248200-43248400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr10:43248200-43248400	Bivalent/Poised TSS	Primary hematopoietic stem cells short term culture	blood
20	chr10:43248200-43248400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr10:43248200-43248400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr10:43248200-43248400	Enhancers	Adipose Nuclei	Adipose
23	chr10:43248200-43248400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
24	chr10:43248200-43248400	Bivalent Enhancer	Fetal Intestine Small	intestine
25	chr10:43248200-43248400	Enhancers	Pancreas	Pancrea
26	chr10:43248200-43248400	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
27	chr10:43248200-43248400	Bivalent/Poised TSS	Right Ventricle	heart
28	chr10:43248200-43248400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
29	chr10:43248200-43248600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
30	chr10:43248200-43248600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
31	chr10:43248200-43248600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr10:43248200-43248600	Flanking Active TSS	Duodenum Mucosa	Duodenum
33	chr10:43248200-43248600	Flanking Bivalent TSS/Enh	Placenta	Placenta
34	chr10:43248200-43248600	Bivalent/Poised TSS	HUVEC	blood vessel
35	chr10:43248200-43248800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
36	chr10:43248200-43248800	Bivalent Enhancer	Stomach Mucosa	stomach
37	chr10:43248200-43249000	Active TSS	A549	lung
38	chr10:43248200-43249000	Bivalent/Poised TSS	Osteobl	bone
39	chr10:43248200-43250000	Active TSS	Rectal Smooth Muscle	rectum
40	chr10:43248200-43250200	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr10:43248200-43250800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr10:43248200-43251000	Active TSS	Pancreatic Islets	Pancreatic Islet
43	chr10:43248200-43251200	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
44	chr10:43248400-43248600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr10:43248400-43248600	Bivalent Enhancer	Primary hematopoietic stem cells	blood
47	chr10:43248400-43248600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
48	chr10:43248400-43248600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
49	chr10:43248400-43248600	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
50	chr10:43248400-43248600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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