Variant report

Variant	nsv875256
Chromosome Location	chr2:142894573-142994328
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	ATF3	chr2:142938814-142939075	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr2:142938828-142938935	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:142927894-142927926	K562	blood:	n/a	n/a
4	BATF	chr2:142943531-142943900	GM12878	blood:	n/a	chr2:142943710-142943721
5	BATF	chr2:142938870-142939091	GM12878	blood:	n/a	chr2:142938978-142938989
6	BCL3	chr2:142923213-142923745	A549	lung:	n/a	chr2:142923513-142923522
7	BCL3	chr2:142923257-142923765	A549	lung:	n/a	chr2:142923513-142923522
8	BHLHE40	chr2:142940546-142940680	GM12878	blood:	n/a	n/a
9	BRCA1	chr2:142938817-142939018	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr2:142897936-142898258	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr2:142943451-142944066	HCT-116	colon:	n/a	n/a
12	CBX3	chr2:142938651-142939222	HCT-116	colon:	n/a	n/a
13	CEBPB	chr2:142990335-142990601	IMR90	lung:	n/a	chr2:142990469-142990480
14	CEBPB	chr2:142910814-142911095	A549	lung:	n/a	chr2:142910933-142910944
15	CEBPB	chr2:142952854-142953168	HepG2	liver:	n/a	chr2:142952985-142952998 chr2:142952986-142952997 chr2:142952992-142953009
16	CEBPB	chr2:142933512-142933939	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr2:142943054-142944070	IMR90	lung:	n/a	n/a
18	CEBPB	chr2:142920808-142921191	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:142920791-142921191	A549	lung:	n/a	n/a
20	CEBPB	chr2:142952846-142953129	IMR90	lung:	n/a	chr2:142952985-142952998 chr2:142952986-142952997 chr2:142952992-142953009
21	CEBPB	chr2:142952879-142953170	A549	lung:	n/a	chr2:142952985-142952998 chr2:142952986-142952997 chr2:142952992-142953009
22	CEBPB	chr2:142943163-142943841	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr2:142945185-142945390	HepG2	liver:	n/a	chr2:142945308-142945319
24	CEBPB	chr2:142910751-142911119	HepG2	liver:	n/a	chr2:142910933-142910944
25	CEBPB	chr2:142957642-142957957	HepG2	liver:	n/a	chr2:142957789-142957800
26	CEBPB	chr2:142952851-142953020	K562	blood:	n/a	chr2:142952985-142952998 chr2:142952986-142952997 chr2:142952992-142953009
27	CEBPB	chr2:142990297-142990622	HepG2	liver:	n/a	chr2:142990469-142990480
28	CEBPB	chr2:142912891-142912981	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr2:142923208-142923246	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:142957660-142957940	A549	lung:	n/a	chr2:142957789-142957800
31	CEBPB	chr2:142926175-142926466	HepG2	liver:	n/a	chr2:142926300-142926311
32	CEBPB	chr2:142972461-142972636	A549	lung:	n/a	n/a
33	CHD1	chr2:142923094-142923933	IMR90	lung:	n/a	n/a
34	CHD2	chr2:142933586-142933907	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr2:142943549-142943902	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr2:142938819-142939058	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr2:142938693-142939146	HepG2	liver:	n/a	n/a
38	CTCF	chr2:142898000-142898150	NHEK	skin:	n/a	chr2:142898102-142898120 chr2:142898097-142898118 chr2:142898067-142898075
39	CTCF	chr2:142943658-142943700	GM10248	blood:	n/a	chr2:142943671-142943680
40	CTCF	chr2:142923258-142923719	MCF-7	breast:	n/a	chr2:142923453-142923471
41	CTCF	chr2:142923320-142923470	HA-sp	spinal cord:	n/a	n/a
42	CTCF	chr2:142923000-142923150	SAEC	small airway:	n/a	n/a
43	CTCF	chr2:142938920-142939070	MCF-7	breast:	n/a	n/a
44	CTCF	chr2:142898016-142898184	LNCaP	prostate:	n/a	chr2:142898102-142898120 chr2:142898097-142898118 chr2:142898067-142898075
45	CTCF	chr2:142923435-142923498	K562	blood:	n/a	chr2:142923453-142923471
46	CTCF	chr2:142923331-142923604	Medullo	brain:	n/a	chr2:142923453-142923471
47	CTCF	chr2:142897940-142898090	NB4	blood:	n/a	chr2:142898067-142898075
48	CTCF	chr2:142898020-142898170	GM12872	blood:	n/a	chr2:142898102-142898120 chr2:142898097-142898118 chr2:142898067-142898075
49	CTCF	chr2:142938900-142939050	GM12871	blood:	n/a	n/a
50	CTCF	chr2:142938820-142938970	NHDF-neo	bronchial:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:142948816-142948866	HCM	heart:	n/a
2	chr2:142948816-142948866	HIPEpiC	eye:	n/a
3	chr2:142948816-142948866	HRE	kidney:	n/a
4	chr2:142948816-142948866	NT2-D1	testis:	n/a
5	chr2:142948816-142948866	NB4	blood:	n/a
6	chr2:142948816-142948866	A549	lung:	n/a
7	chr2:142948816-142948866	NHBE	bronchial:	n/a
8	chr2:142948816-142948866	GM06990	blood:	n/a
9	chr2:142948816-142948866	HNPCEpiC	eye:	n/a
10	chr2:142948816-142948866	HUVEC	blood vessel:	n/a
11	chr2:142948816-142948866	MCF-7	breast:	n/a
12	chr2:142948816-142948866	MCF10A-Er-Src	breast:	n/a
13	chr2:142948816-142948866	Jurkat	blood:	n/a
14	chr2:142948816-142948866	AG09319	gingival:	n/a
15	chr2:142948816-142948866	BE2_C	brain:	n/a
16	chr2:142948816-142948866	RPTEC	kidney:	n/a
17	chr2:142948816-142948866	IMR90	lung:	fetal
18	chr2:142948816-142948866	SKMC	muscle:	n/a
19	chr2:142948816-142948866	AG10803	skin:	n/a
20	chr2:142948816-142948866	Hepatocyte	liver:	n/a
21	chr2:142948816-142948866	Caco-2	colon:	n/a
22	chr2:142948816-142948866	NHDF-neo	bronchial:	n/a
23	chr2:142948816-142948866	AoSMC	blood vessel:	n/a
24	chr2:142948816-142948866	AG09309	skin:	n/a
25	chr2:142948816-142948866	NH-A	brain:	n/a
26	chr2:142948816-142948866	HMEC	breast:	n/a
27	chr2:142948816-142948866	PANC-1	pancreas:	n/a
28	chr2:142948816-142948866	HCT-116	colon:	n/a
29	chr2:142948816-142948866	CMK	blood:	n/a
30	chr2:142948816-142948866	ovcar-3	ovarian:	n/a
31	chr2:142948816-142948866	HEEpiC	esophagus:	n/a
32	chr2:142948816-142948866	H1-hESC	embryonic stem cell:	embryo
33	chr2:142948816-142948866	HL-60	blood:	n/a
34	chr2:142948816-142948866	GM12878	blood:	n/a
35	chr2:142948816-142948866	U87	brain:	n/a
36	chr2:142948816-142948866	HepG2	liver:	n/a
37	chr2:142948816-142948866	HAEpiC	amniotic membrane:	n/a
38	chr2:142948816-142948866	T-47D	breast:	n/a
39	chr2:142948816-142948866	HCPEpiC	choroid plexus:	n/a
40	chr2:142948816-142948866	PrEC	prostate:	n/a
41	chr2:142948816-142948866	AG04450	lung:	fetal
42	chr2:142948816-142948866	SK-N-MC	brain:	n/a
43	chr2:142948816-142948866	AG04449	skin:	fetal
44	chr2:142948816-142948866	HRCEpiC	kidney:	n/a
45	chr2:142948816-142948866	BJ	skin:	n/a
46	chr2:142948816-142948866	GM12891	blood:	n/a
47	chr2:142948816-142948866	Hela-S3	cervix:	n/a
48	chr2:142948816-142948866	HRPEpiC	eye:	n/a
49	chr2:142948816-142948866	K562	blood:	n/a
50	chr2:142948816-142948866	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:142894381..142895892-chr2:142895976..142898134,2	K562	blood:
2	chr2:142886506..142889089-chr2:142896828..142901902,6	MCF-7	breast:
3	chr2:142923021..142923559-chr2:143339611..143340557,2	MCF-7	breast:
4	chr2:142923038..142923887-chr2:143361151..143361987,2	MCF-7	breast:
5	chr2:142980447..142980950-chr6:143813184..143813684,2	MCF-7	breast:
6	chr2:16997949..16998630-chr2:142992504..142993306,2	MCF-7	breast:
7	chr2:142888202..142889034-chr2:142896341..142897145,2	MCF-7	breast:
8	chr2:142992863..142994705-chr2:142999609..143001458,2	MCF-7	breast:
9	chr2:142938634..142939427-chr2:143044106..143044808,2	MCF-7	breast:
10	chr2:142894220..142896690-chr2:142900528..142902468,2	MCF-7	breast:
11	chr2:142482564..142485203-chr2:142902168..142904224,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRP1B-1	chr2:142895333-142895399	ENSG00000244125.1

Variant related genes	Relation type
ENSG00000244125	TF binding region
ENSG00000244125	CpG island
ENSG00000244125	chromatin interactions
ENSG00000168702	chromatin interactions

Extended variants
information (count: 1483 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1483 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10194564	chr2:142894573-142894574	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542770398	chr2:142894595-142894596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545571115	chr2:142894606-142894607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372459838	chr2:142894648-142894649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565265717	chr2:142894650-142894651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561147408	chr2:142894678-142894679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182012655	chr2:142894697-142894698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs13000211	chr2:142894702-142894703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs13000393	chr2:142894704-142894705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138669396	chr2:142894709-142894710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187055600	chr2:142894743-142894744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111635183	chr2:142894745-142894746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529989979	chr2:142894759-142894760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549704067	chr2:142894807-142894808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531686816	chr2:142894835-142894836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190728420	chr2:142894849-142894850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs9287333	chr2:142894855-142894856	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs115999555	chr2:142894856-142894857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs58439740	chr2:142894910-142894911	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs534722468	chr2:142894911-142894912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181978807	chr2:142894918-142894919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568107280	chr2:142894931-142894932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537036960	chr2:142894935-142894936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10197442	chr2:142894992-142894993	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs10496916	chr2:142894993-142894994	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs538938712	chr2:142895007-142895008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185028692	chr2:142895021-142895022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs75245821	chr2:142895048-142895049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572507400	chr2:142895115-142895116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541519530	chr2:142895129-142895130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149322971	chr2:142895153-142895154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs59529672	chr2:142895174-142895175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555914978	chr2:142895194-142895195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372628294	chr2:142895195-142895196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561044421	chr2:142895197-142895198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527587700	chr2:142895207-142895208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189885684	chr2:142895230-142895231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543389099	chr2:142895249-142895250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201769083	chr2:142895269-142895270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182366163	chr2:142895293-142895294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563315375	chr2:142895307-142895308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs13417943	chr2:142895328-142895329	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs375488116	chr2:142895329-142895330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs4143778	chr2:142895344-142895345	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs375801604	chr2:142895349-142895350	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs528268659	chr2:142895406-142895407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185495694	chr2:142895414-142895415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568147673	chr2:142895467-142895468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs72998331	chr2:142895478-142895479	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs374614583	chr2:142895479-142895480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma	21080181	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Autism	22543975	CNVD
Cancer	20164920	CNVD
Hypertension	22686481	CNVD
Hypospadia	22686481	CNVD
Intellectual disability	22686481	CNVD
Omphalocele	22686481	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:147 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:142889200-142900800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:142892800-142897000	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr2:142892800-142897200	Weak transcription	Brain Anterior Caudate	brain
4	chr2:142896800-142898000	Enhancers	Dnd41	blood
5	chr2:142897000-142897400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr2:142897000-142897400	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr2:142897200-142897600	Enhancers	Brain Anterior Caudate	brain
8	chr2:142897400-142898000	Active TSS	Brain Inferior Temporal Lobe	brain
9	chr2:142897600-142898000	Active TSS	Brain Anterior Caudate	brain
10	chr2:142897800-142898000	Enhancers	Brain Hippocampus Middle	brain
11	chr2:142900200-142900600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr2:142900200-142900600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr2:142905400-142905600	Enhancers	Fetal Heart	heart
14	chr2:142923400-142923800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr2:142923400-142923800	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr2:142923400-142923800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr2:142923400-142923800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr2:142923400-142923800	Enhancers	Right Atrium	heart
19	chr2:142923600-142923800	Enhancers	GM12878-XiMat	blood
20	chr2:142933600-142935600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr2:142933800-142934600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr2:142934200-142935200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr2:142934200-142935200	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr2:142934600-142935200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr2:142934600-142943200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr2:142935200-142943200	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr2:142938400-142938800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr2:142938400-142939000	Active TSS	iPS-15b Cell Line	embryonic stem cell
29	chr2:142938400-142939200	Active TSS	HepG2	liver
30	chr2:142938600-142938800	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr2:142938600-142938800	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr2:142938600-142939000	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr2:142938600-142939000	Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr2:142938600-142939000	Active TSS	Brain Hippocampus Middle	brain
35	chr2:142938600-142939000	Enhancers	Pancreas	Pancrea
36	chr2:142938600-142939200	Active TSS	Brain Substantia Nigra	brain
37	chr2:142938800-142943000	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr2:142938800-142943400	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr2:142939000-142939200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr2:142939000-142939200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr2:142939000-142943000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr2:142939200-142943000	Weak transcription	HepG2	liver
43	chr2:142940200-142948200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr2:142942200-142943000	Enhancers	HUVEC	blood vessel
45	chr2:142942600-142942800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr2:142942600-142943400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr2:142942600-142944000	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr2:142942600-142944600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr2:142942600-142944600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr2:142942600-142944600	Enhancers	Dnd41	blood

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