Variant report

Variant	nsv599293
Chromosome Location	chr5:105757300-105830691
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	CBX3	chr5:105790354-105791158	HCT-116	colon:	n/a	n/a
2	CEBPB	chr5:105799775-105800128	A549	lung:	n/a	chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799959-105799970 chr5:105799959-105799972 chr5:105799961-105799970 chr5:105799960-105799971 chr5:105799862-105799874 chr5:105799959-105799972
3	CEBPB	chr5:105814101-105814422	HepG2	liver:	n/a	chr5:105814270-105814281
4	CEBPB	chr5:105770420-105770643	A549	lung:	n/a	chr5:105770535-105770548 chr5:105770535-105770548 chr5:105770534-105770551 chr5:105770536-105770547
5	CEBPB	chr5:105799818-105800083	H1-hESC	embryonic stem cell:	n/a	chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799959-105799970 chr5:105799959-105799972 chr5:105799961-105799970 chr5:105799960-105799971 chr5:105799862-105799874 chr5:105799959-105799972
6	CEBPB	chr5:105770396-105770623	HepG2	liver:	n/a	chr5:105770535-105770548 chr5:105770535-105770548 chr5:105770534-105770551 chr5:105770536-105770547
7	CEBPB	chr5:105814124-105814357	A549	lung:	n/a	chr5:105814270-105814281
8	CEBPB	chr5:105799793-105800150	HepG2	liver:	n/a	chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799959-105799970 chr5:105799959-105799972 chr5:105799961-105799970 chr5:105799960-105799971 chr5:105799862-105799874 chr5:105799959-105799972
9	CEBPB	chr5:105770388-105770650	IMR90	lung:	n/a	chr5:105770535-105770548 chr5:105770535-105770548 chr5:105770534-105770551 chr5:105770536-105770547
10	CEBPB	chr5:105813435-105813964	MCF-7	breast:	n/a	chr5:105813644-105813656
11	CEBPB	chr5:105813496-105813814	MCF-7	breast:	n/a	chr5:105813644-105813656
12	CEBPB	chr5:105826569-105826777	HepG2	liver:	n/a	chr5:105826713-105826724
13	CEBPB	chr5:105814096-105814440	Hela-S3	cervix:	n/a	chr5:105814270-105814281
14	CEBPB	chr5:105799781-105800144	IMR90	lung:	n/a	chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799961-105799970 chr5:105799959-105799970 chr5:105799959-105799972 chr5:105799961-105799970 chr5:105799960-105799971 chr5:105799862-105799874 chr5:105799959-105799972
15	CTCF	chr5:105790460-105790610	HepG2	liver:	n/a	n/a
16	CTCF	chr5:105790480-105790630	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr5:105790530-105790627	MCF-7	breast:	n/a	n/a
18	CTCF	chr5:105790520-105790670	GM12870	blood:	n/a	n/a
19	CTCF	chr5:105790500-105790650	AG04449	skin:	n/a	n/a
20	CTCF	chr5:105790440-105790590	GM12875	blood:	n/a	n/a
21	CTCF	chr5:105790680-105790830	HAc	cerebellar:	n/a	n/a
22	CTCF	chr5:105790500-105790650	HEK293	kidney:	n/a	n/a
23	CTCF	chr5:105790500-105790650	HPAF	blood vessel:	n/a	n/a
24	CTCF	chr5:105790413-105790707	Medullo	brain:	n/a	n/a
25	CTCF	chr5:105790480-105790630	HMEC	breast:	n/a	n/a
26	CTCF	chr5:105790460-105790610	GM12869	blood:	n/a	n/a
27	CTCF	chr5:105790483-105790655	HepG2	liver:	n/a	n/a
28	CTCF	chr5:105790520-105790670	GM12865	blood:	n/a	n/a
29	CTCF	chr5:105790359-105790823	GM12878	blood:	n/a	n/a
30	CTCF	chr5:105790500-105790650	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr5:105790460-105790610	GM06990	blood:	n/a	n/a
32	CTCF	chr5:105790420-105790570	HFF	foreskin:	n/a	n/a
33	CTCF	chr5:105790460-105790610	Caco-2	colon:	n/a	n/a
34	CTCF	chr5:105790429-105790655	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr5:105790500-105790663	LNCaP	prostate:	n/a	n/a
36	CTCF	chr5:105790480-105790630	A549	lung:	n/a	n/a
37	CTCF	chr5:105790498-105790634	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr5:105790535-105790630	GM19240	blood:	n/a	n/a
39	CTCF	chr5:105790203-105790909	SK-N-SH	brain:	n/a	n/a
40	CTCF	chr5:105790140-105790290	BJ	skin:	n/a	n/a
41	CTCF	chr5:105790520-105790670	BJ	skin:	n/a	n/a
42	CTCF	chr5:105790397-105790614	ECC-1	luminal epithelium:	n/a	n/a
43	CTCF	chr5:105790460-105790610	GM12871	blood:	n/a	n/a
44	CTCF	chr5:105790500-105790650	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr5:105790520-105790670	HMEC	breast:	n/a	n/a
46	CTCF	chr5:105790471-105790615	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr5:105790452-105790671	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr5:105790400-105790550	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr5:105790500-105790650	HPF	lung:	n/a	n/a
50	CTCF	chr5:105790460-105790610	NHDF-neo	bronchial:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:105791135-105791185	AG04449	skin:	fetal
2	chr5:105791135-105791185	Jurkat	blood:	n/a
3	chr5:105791135-105791185	HRPEpiC	eye:	n/a
4	chr5:105791135-105791185	PrEC	prostate:	n/a
5	chr5:105791135-105791185	HCPEpiC	choroid plexus:	n/a
6	chr5:105791135-105791185	HMEC	breast:	n/a
7	chr5:105791135-105791185	CMK	blood:	n/a
8	chr5:105791135-105791185	ProgFib	skin:	n/a
9	chr5:105791135-105791185	MCF-7	breast:	n/a
10	chr5:105791135-105791185	HepG2	liver:	n/a
11	chr5:105791135-105791185	SK-N-MC	brain:	n/a
12	chr5:105791135-105791185	U87	brain:	n/a
13	chr5:105791135-105791185	HCM	heart:	n/a
14	chr5:105791135-105791185	PANC-1	pancreas:	n/a
15	chr5:105791135-105791185	HAEpiC	amniotic membrane:	n/a
16	chr5:105791135-105791185	ovcar-3	ovarian:	n/a
17	chr5:105791135-105791185	NH-A	brain:	n/a
18	chr5:105791135-105791185	GM12892	blood:	n/a
19	chr5:105791135-105791185	NB4	blood:	n/a
20	chr5:105791135-105791185	Caco-2	colon:	n/a
21	chr5:105791135-105791185	HCF	heart:	n/a
22	chr5:105791135-105791185	BJ	skin:	n/a
23	chr5:105791135-105791185	GM06990	blood:	n/a
24	chr5:105791135-105791185	AG04450	lung:	fetal
25	chr5:105791135-105791185	LNCaP	prostate:	n/a
26	chr5:105791135-105791185	ECC-1	luminal epithelium:	n/a
27	chr5:105791135-105791185	K562	blood:	n/a
28	chr5:105791135-105791185	GM12891	blood:	n/a
29	chr5:105791135-105791185	IMR90	lung:	fetal
30	chr5:105791135-105791185	SK-N-SH_RA	brain:	n/a
31	chr5:105791135-105791185	NT2-D1	testis:	n/a
32	chr5:105791135-105791185	PFSK-1	brain:	n/a
33	chr5:105791135-105791185	HEEpiC	esophagus:	n/a
34	chr5:105791135-105791185	HEK293	kidney:	embryo
35	chr5:105791135-105791185	SKMC	muscle:	n/a
36	chr5:105791135-105791185	T-47D	breast:	n/a
37	chr5:105791135-105791185	HUVEC	blood vessel:	n/a
38	chr5:105791135-105791185	SK-N-SH	brain:	n/a
39	chr5:105791135-105791185	GM12878	blood:	n/a
40	chr5:105791135-105791185	AG10803	skin:	n/a
41	chr5:105791135-105791185	SAEC	small airway:	n/a
42	chr5:105791135-105791185	HNPCEpiC	eye:	n/a
43	chr5:105791135-105791185	HIPEpiC	eye:	n/a
44	chr5:105791135-105791185	HL-60	blood:	n/a
45	chr5:105791135-105791185	NHBE	bronchial:	n/a
46	chr5:105791135-105791185	Hepatocyte	liver:	n/a
47	chr5:105791135-105791185	HCT-116	colon:	n/a
48	chr5:105791135-105791185	HRCEpiC	kidney:	n/a
49	chr5:105791135-105791185	A549	lung:	n/a
50	chr5:105791135-105791185	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:105790013..105791980-chr5:105793268..105795138,2	MCF-7	breast:
2	chr5:105775699..105778002-chr5:105784029..105786359,2	MCF-7	breast:
3	chr5:105807775..105809773-chr5:105811667..105814083,2	MCF-7	breast:
4	chr5:105790013..105791980-chr5:105793268..105795138,2	MCF-7	breast:
5	chr5:105807775..105809773-chr5:105811667..105814083,2	MCF-7	breast:
6	chr5:105775699..105778002-chr5:105784029..105786359,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000251204	TF binding region
ENSG00000251204	CpG island

Extended variants
information (count: 677 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:677 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35641202	chr5:105757300-105757301	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs569741283	chr5:105757305-105757306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373494804	chr5:105757349-105757350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368600467	chr5:105757363-105757364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs139421534	chr5:105757376-105757377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572041254	chr5:105757396-105757397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112254218	chr5:105757418-105757419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs59144361	chr5:105757427-105757428	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs372829020	chr5:105757431-105757432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577173127	chr5:105757440-105757441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs79819046	chr5:105757447-105757448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563041831	chr5:105757567-105757568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs180934556	chr5:105757610-105757611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576560421	chr5:105757622-105757623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs569484872	chr5:105757699-105757700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141069940	chr5:105757823-105757824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs562353971	chr5:105757858-105757859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185341118	chr5:105757888-105757889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs142400321	chr5:105757896-105757897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564029406	chr5:105757951-105757952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532984061	chr5:105757990-105757991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190249975	chr5:105758025-105758026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569761147	chr5:105758035-105758036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529059436	chr5:105758179-105758180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs151290408	chr5:105758205-105758206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140553913	chr5:105758240-105758241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530622696	chr5:105758284-105758285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534558338	chr5:105758331-105758332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs199575302	chr5:105758340-105758341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs557641154	chr5:105758380-105758381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150421766	chr5:105758400-105758401	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs182816376	chr5:105758440-105758441	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs188556442	chr5:105758453-105758454	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs145255677	chr5:105758475-105758476	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs542360323	chr5:105758479-105758480	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs192242165	chr5:105758492-105758493	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs141202929	chr5:105758511-105758512	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs572684951	chr5:105758538-105758539	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs541735576	chr5:105758546-105758547	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs183663594	chr5:105758603-105758604	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs189066316	chr5:105758604-105758605	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs564846349	chr5:105758622-105758623	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs35511362	chr5:105758629-105758630	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs191313123	chr5:105758632-105758633	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs112465285	chr5:105758653-105758654	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs145016903	chr5:105758660-105758661	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs528952800	chr5:105758661-105758662	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs547793190	chr5:105758687-105758688	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs534298538	chr5:105758744-105758745	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs34459153	chr5:105758763-105758764	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:105751800-105758800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:105758400-105759600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr5:105758800-105759600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:105758800-105759600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:105775200-105775600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr5:105779200-105779600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr5:105783600-105784000	Enhancers	Dnd41	blood
8	chr5:105787600-105788000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr5:105787600-105788200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr5:105787800-105788200	Enhancers	Brain Substantia Nigra	brain
11	chr5:105788000-105790000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr5:105789000-105789200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr5:105789000-105791400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr5:105789000-105791400	Enhancers	HMEC	breast
15	chr5:105789400-105790400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr5:105789800-105790000	Enhancers	Brain Cingulate Gyrus	brain
17	chr5:105789800-105791200	Enhancers	Brain Hippocampus Middle	brain
18	chr5:105790000-105790800	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr5:105790000-105791000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr5:105790000-105791200	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr5:105790000-105791400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr5:105790000-105791400	Enhancers	NHEK	skin
23	chr5:105790200-105790600	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr5:105790200-105790800	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr5:105790200-105790800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr5:105790200-105790800	Enhancers	Brain Angular Gyrus	brain
27	chr5:105790200-105791200	Enhancers	Osteobl	bone
28	chr5:105790400-105791000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr5:105790400-105791200	Enhancers	Muscle Satellite Cultured Cells	--
30	chr5:105790400-105791200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr5:105790400-105791200	Enhancers	Brain Anterior Caudate	brain
32	chr5:105790400-105791200	Enhancers	NH-A	brain
33	chr5:105790400-105791400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr5:105790600-105790800	Enhancers	Brain Cingulate Gyrus	brain
35	chr5:105790600-105791200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr5:105791200-105795600	Weak transcription	Osteobl	bone
37	chr5:105795600-105795800	Enhancers	Osteobl	bone
38	chr5:105809400-105810200	Enhancers	Fetal Heart	heart
39	chr5:105809800-105812200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr5:105813000-105814600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr5:105817000-105817800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr5:105817000-105818000	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr5:105817200-105817600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr5:105817200-105817600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr5:105824200-105824800	Enhancers	Osteobl	bone

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