Variant report

Variant	esv18442
Chromosome Location	chr2:114167656-114267309
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1072)
CpG islands
(count:1834)
Chromatin interactive
region (count:0)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1072 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:114181075-114181226	HepG2	liver:	n/a	n/a
2	ATF1	chr2:114195252-114195468	K562	blood:	n/a	n/a
3	ATF3	chr2:114195215-114195323	K562	blood:	n/a	n/a
4	BATF	chr2:114196999-114197200	GM12878	blood:	n/a	n/a
5	BATF	chr2:114173977-114174745	GM12878	blood:	n/a	n/a
6	BATF	chr2:114188935-114190118	GM12878	blood:	n/a	chr2:114189910-114189918
7	BATF	chr2:114196004-114196344	GM12878	blood:	n/a	n/a
8	BATF	chr2:114189261-114190171	GM12878	blood:	n/a	chr2:114189910-114189918
9	BATF	chr2:114188569-114188750	GM12878	blood:	n/a	n/a
10	BATF	chr2:114209720-114209940	GM12878	blood:	n/a	n/a
11	BATF	chr2:114206782-114207175	GM12878	blood:	n/a	n/a
12	BATF	chr2:114206835-114207033	GM12878	blood:	n/a	n/a
13	BATF	chr2:114194968-114195790	GM12878	blood:	n/a	chr2:114195333-114195346
14	BATF	chr2:114251658-114251933	GM12878	blood:	n/a	n/a
15	BATF	chr2:114174348-114174775	GM12878	blood:	n/a	n/a
16	BATF	chr2:114179478-114179679	GM12878	blood:	n/a	n/a
17	BATF	chr2:114221639-114221843	GM12878	blood:	n/a	n/a
18	BATF	chr2:114253690-114253875	GM12878	blood:	n/a	n/a
19	BATF	chr2:114190291-114190748	GM12878	blood:	n/a	n/a
20	BATF	chr2:114175312-114175602	GM12878	blood:	n/a	chr2:114175554-114175563
21	BATF	chr2:114188216-114188558	GM12878	blood:	n/a	n/a
22	BATF	chr2:114217280-114217821	GM12878	blood:	n/a	n/a
23	BATF	chr2:114188894-114189247	GM12878	blood:	n/a	n/a
24	BATF	chr2:114194949-114195748	GM12878	blood:	n/a	chr2:114195333-114195346
25	BATF	chr2:114196059-114196346	GM12878	blood:	n/a	n/a
26	BATF	chr2:114241890-114242082	GM12878	blood:	n/a	n/a
27	BATF	chr2:114217254-114217816	GM12878	blood:	n/a	n/a
28	BATF	chr2:114190256-114190764	GM12878	blood:	n/a	n/a
29	BATF	chr2:114217887-114218111	GM12878	blood:	n/a	n/a
30	BATF	chr2:114214368-114214841	GM12878	blood:	n/a	n/a
31	BATF	chr2:114216587-114216848	GM12878	blood:	n/a	n/a
32	BATF	chr2:114242853-114243066	GM12878	blood:	n/a	n/a
33	BATF	chr2:114188181-114188552	GM12878	blood:	n/a	n/a
34	BCL11A	chr2:114217254-114217924	GM12878	blood:	n/a	n/a
35	BCL11A	chr2:114221142-114221444	GM12878	blood:	n/a	n/a
36	BCL11A	chr2:114206565-114206813	GM12878	blood:	n/a	n/a
37	BCL11A	chr2:114214598-114214952	GM12878	blood:	n/a	n/a
38	BCL11A	chr2:114257159-114257329	GM12878	blood:	n/a	n/a
39	BCL11A	chr2:114174457-114174846	GM12878	blood:	n/a	n/a
40	BCL11A	chr2:114206875-114207274	GM12878	blood:	n/a	n/a
41	BCL11A	chr2:114194982-114195839	GM12878	blood:	n/a	n/a
42	BCL11A	chr2:114217288-114217875	GM12878	blood:	n/a	n/a
43	BCL11A	chr2:114221827-114222010	GM12878	blood:	n/a	n/a
44	BCL11A	chr2:114238925-114239211	GM12878	blood:	n/a	n/a
45	BCL11A	chr2:114216516-114216944	GM12878	blood:	n/a	n/a
46	BCL11A	chr2:114190281-114190590	GM12878	blood:	n/a	n/a
47	BCL11A	chr2:114173796-114174016	GM12878	blood:	n/a	n/a
48	BCL11A	chr2:114208376-114208816	GM12878	blood:	n/a	n/a
49	BCL11A	chr2:114194953-114196275	GM12878	blood:	n/a	n/a
50	BCL11A	chr2:114214317-114214657	GM12878	blood:	n/a	n/a

(count:1834 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:114260096-114260146	MCF10A-Er-Src	breast:	n/a
2	chr2:114261793-114261843	HUVEC	blood vessel:	n/a
3	chr2:114194541-114194591	HL-60	blood:	n/a
4	chr2:114194645-114194695	HRE	kidney:	n/a
5	chr2:114260096-114260146	MCF10A-Er-Src	breast:	n/a
6	chr2:114261793-114261843	HUVEC	blood vessel:	n/a
7	chr2:114194541-114194591	HL-60	blood:	n/a
8	chr2:114194645-114194695	HRE	kidney:	n/a
9	chr2:114206313-114206363	HRE	kidney:	n/a
10	chr2:114252811-114252861	Jurkat	blood:	n/a
11	chr2:114261270-114261320	CMK	blood:	n/a
12	chr2:114256454-114256504	Caco-2	colon:	n/a
13	chr2:114261793-114261843	NH-A	brain:	n/a
14	chr2:114262013-114262063	NH-A	brain:	n/a
15	chr2:114260766-114260816	HCT-116	colon:	n/a
16	chr2:114252811-114252861	SK-N-SH_RA	brain:	n/a
17	chr2:114260766-114260816	NB4	blood:	n/a
18	chr2:114259669-114259719	AG04450	lung:	fetal
19	chr2:114261270-114261320	AoSMC	blood vessel:	n/a
20	chr2:114260766-114260816	HCM	heart:	n/a
21	chr2:114252811-114252861	HCPEpiC	choroid plexus:	n/a
22	chr2:114260096-114260146	HEEpiC	esophagus:	n/a
23	chr2:114195528-114195578	AG09319	gingival:	n/a
24	chr2:114260096-114260146	AG09319	gingival:	n/a
25	chr2:114265743-114265793	HPAEpiC	pulmonary alveolar:	n/a
26	chr2:114260142-114260192	BJ	skin:	n/a
27	chr2:114256673-114256723	NB4	blood:	n/a
28	chr2:114196091-114196141	HUVEC	blood vessel:	n/a
29	chr2:114194541-114194591	LNCaP	prostate:	n/a
30	chr2:114265743-114265793	HMEC	breast:	n/a
31	chr2:114256454-114256504	AG10803	skin:	n/a
32	chr2:114194645-114194695	HUVEC	blood vessel:	n/a
33	chr2:114259296-114259346	MCF-7	breast:	n/a
34	chr2:114261793-114261843	PrEC	prostate:	n/a
35	chr2:114197839-114197889	AG04449	skin:	fetal
36	chr2:114261369-114261419	PFSK-1	brain:	n/a
37	chr2:114260766-114260816	H1-hESC	embryonic stem cell:	embryo
38	chr2:114194645-114194695	HepG2	liver:	n/a
39	chr2:114256673-114256723	AG10803	skin:	n/a
40	chr2:114196091-114196141	GM06990	blood:	n/a
41	chr2:114256673-114256723	PANC-1	pancreas:	n/a
42	chr2:114256406-114256456	RPTEC	kidney:	n/a
43	chr2:114194645-114194695	HMEC	breast:	n/a
44	chr2:114261369-114261419	GM06990	blood:	n/a
45	chr2:114197839-114197889	NB4	blood:	n/a
46	chr2:114194645-114194695	AG04450	lung:	fetal
47	chr2:114259296-114259346	GM06990	blood:	n/a
48	chr2:114256392-114256442	HNPCEpiC	eye:	n/a
49	chr2:114256421-114256471	ProgFib	skin:	n/a
50	chr2:114197839-114197889	Jurkat	blood:	n/a

No data

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXD4L1-1	chr2:114261556-114261635	XLOC_001631
2	lnc-FOXD4L1-1	chr2:114265430-114265581	XLOC_001631
3	lnc-FOXD4L1-1	chr2:114265429-114265842	NONHSAT073783
4	lnc-FOXD4L1-1	chr2:114261182-114261242	XLOC_001631
5	lnc-FOXD4L1-1	chr2:114265430-114265842	XLOC_001631
6	lnc-AC016745.1-3	chr2:114189481-114189719	expReg_chr2_8632_-
7	lnc-FOXD4L1-1	chr2:114261181-114261242	NONHSAT073783
8	lnc-CBWD2-2	chr2:114190177-114193619	ENSG00000272563.1
9	lnc-FOXD4L1-1	chr2:114261833-114261941	XLOC_001631
10	lnc-AC016745.1-5	chr2:114184831-114185141	expReg_chr2_8625_-
11	lnc-FOXD4L1-1	chr2:114261833-114262184	XLOC_001631
12	lnc-FOXD4L1-1	chr2:114261620-114262184	NONHSAT073783
13	lnc-AC016745.1-4	chr2:114186646-114186941	expReg_chr2_8628_-
14	lnc-FOXD4L1-1	chr2:114261680-114261941	XLOC_001631
15	lnc-CBWD2-1	chr2:114182072-114182152	ENSG00000234997.1
16	lnc-CBWD2-1	chr2:114182475-114182901	ENSG00000234997.1

No data

Variant related genes	Relation type
ENSG00000238091	TF binding region
CBWD2	TF binding region
ENSG00000272563	TF binding region
FOXD4L1	TF binding region
ENSG00000234997	TF binding region
ENSG00000234148	TF binding region
ENSG00000238091	CpG island
CBWD2	CpG island
ENSG00000272563	CpG island
FOXD4L1	CpG island
ENSG00000234997	CpG island
ENSG00000234148	CpG island
H2AFX	miRNA target sites
GZF1	miRNA target sites

Extended variants
information (count: 2301 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2301 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7355765	chr2:114167663-114167664	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs10185940	chr2:114167667-114167668	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs373125063	chr2:114167673-114167674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546005144	chr2:114167692-114167693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559855083	chr2:114167742-114167743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573357279	chr2:114167749-114167750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191616613	chr2:114167766-114167767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562408446	chr2:114167768-114167769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542651041	chr2:114167771-114167772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200412662	chr2:114167778-114167779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9646922	chr2:114167782-114167783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4849214	chr2:114167783-114167784	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs114077438	chr2:114167898-114167899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546387280	chr2:114167905-114167906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4849215	chr2:114167937-114167938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566615807	chr2:114167955-114167956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565500678	chr2:114167990-114167991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529124400	chr2:114168033-114168034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs142023933	chr2:114168058-114168059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549252094	chr2:114168059-114168060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184209139	chr2:114168072-114168073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187484131	chr2:114168083-114168084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556911242	chr2:114168118-114168119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570518728	chr2:114168175-114168176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539872005	chr2:114168290-114168291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553236239	chr2:114168309-114168310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573373243	chr2:114168353-114168354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114252737	chr2:114168382-114168383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556073499	chr2:114168470-114168471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs199550975	chr2:114168511-114168512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201640380	chr2:114168553-114168554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575980588	chr2:114168649-114168650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544935721	chr2:114168665-114168666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564031427	chr2:114168666-114168667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532793500	chr2:114168670-114168671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370857277	chr2:114168698-114168699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540322026	chr2:114168716-114168717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560031112	chr2:114168744-114168745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531029224	chr2:114168747-114168748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529072446	chr2:114168894-114168895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548935284	chr2:114168907-114168908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568737150	chr2:114168914-114168915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs62159974	chr2:114168972-114168973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114711703	chr2:114168975-114168976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551262632	chr2:114168985-114168986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570506915	chr2:114168986-114168987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539486851	chr2:114169009-114169010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372363201	chr2:114169018-114169019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553414862	chr2:114169061-114169062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566880640	chr2:114169119-114169120	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
Prostate cancer	18632612	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
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:771 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:114164800-114170400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr2:114165400-114170200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr2:114165400-114173400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:114167200-114173400	Weak transcription	GM12878-XiMat	blood
5	chr2:114167400-114173800	Weak transcription	Lung	lung
6	chr2:114170200-114170600	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr2:114170400-114170600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr2:114173200-114173800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:114173400-114174200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr2:114173400-114174200	ZNF genes & repeats	GM12878-XiMat	blood
11	chr2:114173600-114173800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
12	chr2:114173800-114174000	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr2:114173800-114174000	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr2:114173800-114174000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr2:114173800-114174000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr2:114173800-114174000	Flanking Bivalent TSS/Enh	Lung	lung
17	chr2:114173800-114174000	Enhancers	Pancreas	Pancrea
18	chr2:114174200-114175800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr2:114181000-114181400	Enhancers	HepG2	liver
20	chr2:114187000-114191400	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr2:114187400-114187600	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr2:114187400-114187800	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr2:114187800-114188200	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr2:114188200-114189800	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr2:114188400-114188800	Enhancers	Primary B cells from peripheral blood	blood
26	chr2:114188400-114189800	Active TSS	Monocytes-CD14+_RO01746	blood
27	chr2:114188600-114189000	Active TSS	GM12878-XiMat	blood
28	chr2:114188800-114189000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr2:114188800-114189800	Weak transcription	Primary B cells from peripheral blood	blood
30	chr2:114188800-114191200	Enhancers	Primary B cells from cord blood	blood
31	chr2:114189000-114189600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr2:114189000-114189800	Weak transcription	GM12878-XiMat	blood
33	chr2:114189400-114190200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr2:114189600-114190200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr2:114189800-114190000	Active TSS	GM12878-XiMat	blood
36	chr2:114189800-114190200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
37	chr2:114189800-114190200	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr2:114189800-114190200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
39	chr2:114189800-114191400	Enhancers	Primary B cells from peripheral blood	blood
40	chr2:114190000-114190200	Flanking Active TSS	GM12878-XiMat	blood
41	chr2:114190200-114190400	Active TSS	Primary neutrophils fromperipheralblood	blood
42	chr2:114190200-114190400	Enhancers	GM12878-XiMat	blood
43	chr2:114190200-114191000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr2:114190200-114191200	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr2:114190200-114194600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr2:114190200-114194600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr2:114190400-114190800	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr2:114190400-114190800	Weak transcription	GM12878-XiMat	blood
49	chr2:114190800-114191400	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr2:114190800-114191400	Enhancers	GM12878-XiMat	blood

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