Variant report

Variant	nsv828181
Chromosome Location	chr18:12065246-12091392
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:388)
CpG islands
(count:733)
Chromatin interactive
region (count:7)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr18:12076645-12076788	K562	blood:	n/a	n/a
2	CEBPB	chr18:12067926-12068149	K562	blood:	n/a	n/a
3	CEBPB	chr18:12086123-12086565	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr18:12086183-12086554	MCF-7	breast:	n/a	n/a
5	CEBPB	chr18:12069057-12069324	K562	blood:	n/a	n/a
6	CEBPB	chr18:12090640-12090795	HepG2	liver:	n/a	n/a
7	CEBPB	chr18:12069020-12069213	IMR90	lung:	n/a	n/a
8	CEBPB	chr18:12087914-12087930	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr18:12086202-12086530	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr18:12086223-12086412	HepG2	liver:	n/a	n/a
11	CEBPB	chr18:12067920-12068124	HepG2	liver:	n/a	n/a
12	CHD2	chr18:12087795-12087986	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr18:12086349-12086675	Hela-S3	cervix:	n/a	n/a
14	CREB1	chr18:12076434-12076834	A549	lung:	n/a	n/a
15	CTCF	chr18:12074980-12075130	AG04450	lung:	n/a	n/a
16	CTCF	chr18:12074860-12075010	HBMEC	blood vessel:	n/a	n/a
17	CTCF	chr18:12074860-12075010	SAEC	small airway:	n/a	n/a
18	CTCF	chr18:12074860-12075010	HEEpiC	esophagus:	n/a	n/a
19	CTCF	chr18:12074840-12074990	GM12871	blood:	n/a	n/a
20	CTCF	chr18:12068422-12068749	K562	blood:	n/a	n/a
21	CTCF	chr18:12074921-12074935	LNCaP	prostate:	n/a	n/a
22	CTCF	chr18:12074825-12075011	NHEK	skin:	n/a	n/a
23	CTCF	chr18:12086128-12086236	MCF-7	breast:	n/a	chr18:12086159-12086177
24	CTCF	chr18:12068420-12068570	GM12870	blood:	n/a	n/a
25	CTCF	chr18:12074880-12074950	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr18:12074880-12075030	HMF	breast:	n/a	n/a
27	CTCF	chr18:12074860-12075010	GM12869	blood:	n/a	n/a
28	CTCF	chr18:12074840-12074990	GM12865	blood:	n/a	n/a
29	CTCF	chr18:12068261-12068747	K562	blood:	n/a	n/a
30	CTCF	chr18:12074880-12075030	NHEK	skin:	n/a	n/a
31	CTCF	chr18:12074845-12074990	MCF-7	breast:	n/a	n/a
32	CTCF	chr18:12074860-12075010	GM12864	blood:	n/a	n/a
33	CTCF	chr18:12068400-12068550	HVMF	connective:	n/a	n/a
34	CTCF	chr18:12074836-12074994	GM12891	blood:	n/a	n/a
35	CTCF	chr18:12068480-12068630	HCM	heart:	n/a	n/a
36	CTCF	chr18:12068449-12068780	K562	blood:	n/a	n/a
37	CTCF	chr18:12074860-12075010	AG10803	skin:	n/a	n/a
38	CTCF	chr18:12074858-12074993	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr18:12068500-12068650	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr18:12074868-12074952	ProgFib	skin:	n/a	n/a
41	CTCF	chr18:12068460-12068610	GM12867	blood:	n/a	n/a
42	CTCF	chr18:12068500-12068650	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr18:12068520-12068670	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr18:12074920-12075070	NHEK	skin:	n/a	n/a
45	CTCF	chr18:12074832-12074987	GM12878	blood:	n/a	n/a
46	CTCF	chr18:12074861-12075002	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr18:12074880-12075030	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr18:12086706-12086922	K562	blood:	n/a	n/a
49	CTCF	chr18:12076413-12076499	Fibrobl	skin:	n/a	n/a
50	CTCF	chr18:12074877-12074982	MCF-7	breast:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:12076435-12076485	AoSMC	blood vessel:	n/a
2	chr18:12076435-12076485	AoSMC	blood vessel:	n/a
3	chr18:12076365-12076415	GM06990	blood:	n/a
4	chr18:12068099-12068149	RPTEC	kidney:	n/a
5	chr18:12090210-12090260	Caco-2	colon:	n/a
6	chr18:12067067-12067117	HNPCEpiC	eye:	n/a
7	chr18:12068363-12068413	NB4	blood:	n/a
8	chr18:12072395-12072445	AG09309	skin:	n/a
9	chr18:12076476-12076526	K562	blood:	n/a
10	chr18:12072395-12072445	Hela-S3	cervix:	n/a
11	chr18:12077147-12077197	Jurkat	blood:	n/a
12	chr18:12072395-12072445	ECC-1	luminal epithelium:	n/a
13	chr18:12067067-12067117	HCF	heart:	n/a
14	chr18:12076476-12076526	T-47D	breast:	n/a
15	chr18:12068884-12068934	GM12878	blood:	n/a
16	chr18:12076476-12076526	MCF-7	breast:	n/a
17	chr18:12067067-12067117	NHDF-neo	bronchial:	n/a
18	chr18:12068099-12068149	T-47D	breast:	n/a
19	chr18:12076476-12076526	HMEC	breast:	n/a
20	chr18:12068099-12068149	SK-N-SH	brain:	n/a
21	chr18:12073455-12073505	HRE	kidney:	n/a
22	chr18:12076435-12076485	HCT-116	colon:	n/a
23	chr18:12068099-12068149	GM12892	blood:	n/a
24	chr18:12068363-12068413	HepG2	liver:	n/a
25	chr18:12076435-12076485	GM12878	blood:	n/a
26	chr18:12068099-12068149	AG04449	skin:	fetal
27	chr18:12068363-12068413	GM06990	blood:	n/a
28	chr18:12077147-12077197	HL-60	blood:	n/a
29	chr18:12077147-12077197	T-47D	breast:	n/a
30	chr18:12076365-12076415	GM12891	blood:	n/a
31	chr18:12068099-12068149	BJ	skin:	n/a
32	chr18:12068065-12068115	ovcar-3	ovarian:	n/a
33	chr18:12067067-12067117	ovcar-3	ovarian:	n/a
34	chr18:12068363-12068413	NHDF-neo	bronchial:	n/a
35	chr18:12077147-12077197	SAEC	small airway:	n/a
36	chr18:12073455-12073505	SKMC	muscle:	n/a
37	chr18:12077147-12077197	GM12892	blood:	n/a
38	chr18:12067067-12067117	ECC-1	luminal epithelium:	n/a
39	chr18:12068884-12068934	SK-N-SH	brain:	n/a
40	chr18:12073455-12073505	GM06990	blood:	n/a
41	chr18:12067067-12067117	HRE	kidney:	n/a
42	chr18:12068065-12068115	ECC-1	luminal epithelium:	n/a
43	chr18:12077147-12077197	ovcar-3	ovarian:	n/a
44	chr18:12090210-12090260	MCF-7	breast:	n/a
45	chr18:12072395-12072445	MCF-7	breast:	n/a
46	chr18:12068363-12068413	HCPEpiC	choroid plexus:	n/a
47	chr18:12073455-12073505	MCF-7	breast:	n/a
48	chr18:12068065-12068115	NB4	blood:	n/a
49	chr18:12067067-12067117	HCM	heart:	n/a
50	chr18:12068099-12068149	SK-N-SH_RA	brain:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:12076450..12076959-chr4:22517248..22517778,2	HCT-116	colon:
2	chr18:12084453..12086286-chr18:12088021..12090033,2	K562	blood:
3	chr18:12067124..12068644-chr19:18543710..18545856,2	K562	blood:
4	chr18:12088519..12091150-chr18:12096385..12097943,2	K562	blood:
5	chr18:12067124..12068647-chr19:18543710..18545740,2	K562	blood:
6	chr18:12084453..12086286-chr18:12088021..12090033,2	K562	blood:
7	chr18:12063010..12065990-chr19:13351067..13352603,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD62-1	chr18:12073319-12073537	XLOC_012628
2	lnc-ANKRD62-2	chr18:12081539-12081657	ENSG00000267722.1
3	lnc-ANKRD62-1	chr18:12074792-12075074	XLOC_012628
4	lnc-ANKRD62-2	chr18:12081796-12081838	ENSG00000267722.1
5	lnc-ANKRD62-2	chr18:12085171-12085266	ENSG00000267722.1

No data

Variant related genes	Relation type
ENSG00000267722	TF binding region
ANKRD62	TF binding region
ENSG00000256616	TF binding region
ENSG00000267533	TF binding region
ENSG00000267722	CpG island
ANKRD62	CpG island
ENSG00000256616	CpG island
ENSG00000267533	CpG island
ENSG00000152990	chromatin interactions
ENSG00000130511	chromatin interactions

Extended variants
information (count: 1085 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1085 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528674402	chr18:12065269-12065270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs528310238	chr18:12065278-12065279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185089500	chr18:12065302-12065303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113373002	chr18:12065308-12065309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190377031	chr18:12065316-12065317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550591152	chr18:12065330-12065331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182073864	chr18:12065331-12065332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187676464	chr18:12065376-12065377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551720552	chr18:12065378-12065379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs78033763	chr18:12065379-12065380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533988707	chr18:12065382-12065383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553456972	chr18:12065402-12065403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144666439	chr18:12065404-12065405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535475166	chr18:12065413-12065414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373829494	chr18:12065443-12065444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535570758	chr18:12065501-12065502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188109494	chr18:12065535-12065536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575828422	chr18:12065538-12065539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546061941	chr18:12065545-12065546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs117275867	chr18:12065552-12065553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs550665592	chr18:12065594-12065595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555637883	chr18:12065647-12065648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573051983	chr18:12065651-12065652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs180916816	chr18:12065653-12065654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569253556	chr18:12065666-12065667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73947248	chr18:12065710-12065711	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs185584784	chr18:12065717-12065718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543839706	chr18:12065729-12065730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372271599	chr18:12065742-12065743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562476882	chr18:12065781-12065782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532972454	chr18:12065784-12065785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs79254630	chr18:12065810-12065811	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs111717198	chr18:12065822-12065823	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575808337	chr18:12065824-12065825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190151563	chr18:12065829-12065830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs77684286	chr18:12065906-12065907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182791294	chr18:12065921-12065922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs377291479	chr18:12065941-12065942	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369842323	chr18:12065960-12065961	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142956293	chr18:12065989-12065990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567070811	chr18:12066035-12066036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs11873137	chr18:12066039-12066040	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs117565449	chr18:12066040-12066041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34592004	chr18:12066063-12066064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375764633	chr18:12066091-12066092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371533981	chr18:12066134-12066135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7237502	chr18:12066145-12066146	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs555954203	chr18:12066161-12066162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574173399	chr18:12066210-12066211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544261282	chr18:12066215-12066216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	20531469	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:212 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12055600-12076400	Weak transcription	Right Atrium	heart
2	chr18:12064600-12067000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr18:12064800-12065400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr18:12065800-12066000	Enhancers	H9 Cell Line	embryonic stem cell
5	chr18:12066000-12076400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr18:12067000-12068600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr18:12067400-12068400	Enhancers	Fetal Muscle Trunk	muscle
8	chr18:12068000-12068600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr18:12068200-12068600	Active TSS	Pancreas	Pancrea
10	chr18:12068200-12068800	Active TSS	HUVEC	blood vessel
11	chr18:12068200-12069000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr18:12068600-12069200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr18:12068600-12076400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr18:12068800-12069000	Bivalent/Poised TSS	Osteobl	bone
15	chr18:12068800-12069200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr18:12068800-12069200	Enhancers	Fetal Lung	lung
17	chr18:12068800-12069200	Flanking Active TSS	HUVEC	blood vessel
18	chr18:12069000-12069200	Active TSS	Osteobl	bone
19	chr18:12069200-12069400	Enhancers	HUVEC	blood vessel
20	chr18:12069200-12071000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr18:12069400-12070600	Weak transcription	HUVEC	blood vessel
22	chr18:12070600-12072200	Enhancers	HUVEC	blood vessel
23	chr18:12071000-12071400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr18:12072200-12076400	Weak transcription	HUVEC	blood vessel
25	chr18:12074600-12077000	Active TSS	Fetal Brain Female	brain
26	chr18:12075000-12075400	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr18:12075400-12076600	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr18:12076000-12076200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
29	chr18:12076200-12076400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
30	chr18:12076200-12076400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
31	chr18:12076200-12076400	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr18:12076200-12076400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr18:12076200-12076400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
34	chr18:12076200-12076400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
35	chr18:12076200-12076400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
36	chr18:12076200-12076400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
37	chr18:12076200-12076400	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr18:12076200-12076400	Bivalent/Poised TSS	Primary hematopoietic stem cells short term culture	blood
39	chr18:12076200-12076400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
40	chr18:12076200-12076400	Flanking Bivalent TSS/Enh	HepG2	liver
41	chr18:12076200-12076600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr18:12076200-12076600	Bivalent Enhancer	K562	blood
43	chr18:12076200-12076600	Enhancers	NH-A	brain
44	chr18:12076200-12076800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr18:12076200-12076800	Active TSS	Adipose Nuclei	Adipose
46	chr18:12076200-12076800	Active TSS	Pancreatic Islets	Pancreatic Islet
47	chr18:12076200-12077000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr18:12076200-12077000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr18:12076200-12077000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr18:12076200-12077000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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