Variant report

Variant	nsv1006323
Chromosome Location	chr2:209228673-209247384
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	ARID3A	chr2:209233745-209234164	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:209235877-209236505	K562	blood:	n/a	n/a
3	ARID3A	chr2:209238174-209238580	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:209238240-209238613	K562	blood:	n/a	n/a
5	ATF1	chr2:209235807-209236248	K562	blood:	n/a	n/a
6	BHLHE40	chr2:209235865-209236444	K562	blood:	n/a	n/a
7	BHLHE40	chr2:209231458-209231762	GM12878	blood:	n/a	n/a
8	CCNT2	chr2:209243607-209243784	K562	blood:	n/a	n/a
9	CCNT2	chr2:209235684-209236200	K562	blood:	n/a	n/a
10	CEBPB	chr2:209233827-209234132	A549	lung:	n/a	chr2:209233922-209233933
11	CEBPB	chr2:209233774-209234153	MCF-7	breast:	n/a	chr2:209233922-209233933
12	CEBPB	chr2:209235790-209236138	K562	blood:	n/a	n/a
13	CEBPB	chr2:209234443-209234834	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:209233800-209234152	MCF-7	breast:	n/a	chr2:209233922-209233933
15	CEBPB	chr2:209233813-209234182	IMR90	lung:	n/a	chr2:209233922-209233933
16	CEBPB	chr2:209235768-209236174	K562	blood:	n/a	n/a
17	CEBPB	chr2:209233870-209234062	HepG2	liver:	n/a	chr2:209233922-209233933
18	CEBPB	chr2:209233818-209234101	HepG2	liver:	n/a	chr2:209233922-209233933
19	CEBPB	chr2:209233734-209234186	Hela-S3	cervix:	n/a	chr2:209233922-209233933
20	CEBPB	chr2:209233720-209234122	A549	lung:	n/a	chr2:209233922-209233933
21	CEBPB	chr2:209233738-209234200	HepG2	liver:	n/a	chr2:209233922-209233933
22	CEBPB	chr2:209238250-209238569	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr2:209233797-209234153	A549	lung:	n/a	chr2:209233922-209233933
24	CEBPD	chr2:209235812-209236227	K562	blood:	n/a	n/a
25	CEBPD	chr2:209235741-209236189	K562	blood:	n/a	n/a
26	CREB1	chr2:209231367-209231831	GM12878	blood:	n/a	n/a
27	CREB1	chr2:209235820-209236371	K562	blood:	n/a	n/a
28	CREB1	chr2:209231397-209231883	GM12878	blood:	n/a	n/a
29	CTCF	chr2:209238340-209238490	GM12875	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
30	CTCF	chr2:209238300-209238450	HMEC	breast:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
31	CTCF	chr2:209238329-209238366	MCF-7	breast:	n/a	n/a
32	CTCF	chr2:209238720-209238870	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr2:209238360-209238510	GM12866	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
34	CTCF	chr2:209238360-209238510	GM06990	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
35	CTCF	chr2:209238300-209238450	HCPEpiC	choroid plexus:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
36	CTCF	chr2:209238280-209238430	HCT-116	colon:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
37	CTCF	chr2:209238082-209238602	HCT-116	colon:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
38	CTCF	chr2:209238760-209238910	GM12873	blood:	n/a	n/a
39	CTCF	chr2:209238248-209238510	Hela-S3	cervix:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
40	CTCF	chr2:209238320-209238470	HA-sp	spinal cord:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
41	CTCF	chr2:209238320-209238470	HMF	breast:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
42	CTCF	chr2:209238129-209238577	HepG2	liver:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
43	CTCF	chr2:209238208-209238541	SK-N-SH_RA	brain:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
44	CTCF	chr2:209238320-209238470	SK-N-SH_RA	brain:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
45	CTCF	chr2:209238340-209238490	NHEK	skin:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
46	CTCF	chr2:209238291-209238460	GM13976	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
47	CTCF	chr2:209238340-209238490	SAEC	small airway:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
48	CTCF	chr2:209238340-209238490	HFF-Myc	foreskin:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
49	CTCF	chr2:209238300-209238450	K562	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
50	CTCF	chr2:209238300-209238450	HRPEpiC	eye:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:209242596-209242646	HRE	kidney:	n/a
2	chr2:209240193-209240243	HEK293	kidney:	embryo
3	chr2:209240193-209240243	AG10803	skin:	n/a
4	chr2:209240193-209240243	GM12892	blood:	n/a
5	chr2:209242596-209242646	GM12878	blood:	n/a
6	chr2:209240193-209240243	ovcar-3	ovarian:	n/a
7	chr2:209240193-209240243	GM12878	blood:	n/a
8	chr2:209240193-209240243	SK-N-SH	brain:	n/a
9	chr2:209242596-209242646	GM12892	blood:	n/a
10	chr2:209240193-209240243	PrEC	prostate:	n/a
11	chr2:209240193-209240243	RPTEC	kidney:	n/a
12	chr2:209242596-209242646	MCF-7	breast:	n/a
13	chr2:209240193-209240243	PANC-1	pancreas:	n/a
14	chr2:209240193-209240243	MCF10A-Er-Src	breast:	n/a
15	chr2:209240193-209240243	IMR90	lung:	fetal
16	chr2:209242596-209242646	AG04450	lung:	fetal
17	chr2:209240193-209240243	LNCaP	prostate:	n/a
18	chr2:209242596-209242646	AG10803	skin:	n/a
19	chr2:209242596-209242646	SK-N-SH_RA	brain:	n/a
20	chr2:209240193-209240243	GM19239	blood:	n/a
21	chr2:209242596-209242646	GM19239	blood:	n/a
22	chr2:209240193-209240243	A549	lung:	n/a
23	chr2:209242596-209242646	HUVEC	blood vessel:	n/a
24	chr2:209240193-209240243	NHBE	bronchial:	n/a
25	chr2:209242596-209242646	NH-A	brain:	n/a
26	chr2:209240193-209240243	Hela-S3	cervix:	n/a
27	chr2:209240193-209240243	AG04449	skin:	fetal
28	chr2:209240193-209240243	CMK	blood:	n/a
29	chr2:209242596-209242646	PANC-1	pancreas:	n/a
30	chr2:209242596-209242646	A549	lung:	n/a
31	chr2:209242596-209242646	GM12891	blood:	n/a
32	chr2:209240193-209240243	HepG2	liver:	n/a
33	chr2:209242596-209242646	HEK293	kidney:	embryo
34	chr2:209240193-209240243	HCF	heart:	n/a
35	chr2:209242596-209242646	NB4	blood:	n/a
36	chr2:209242596-209242646	NT2-D1	testis:	n/a
37	chr2:209240193-209240243	HCM	heart:	n/a
38	chr2:209242596-209242646	PFSK-1	brain:	n/a
39	chr2:209240193-209240243	AoSMC	blood vessel:	n/a
40	chr2:209240193-209240243	NB4	blood:	n/a
41	chr2:209242596-209242646	BE2_C	brain:	n/a
42	chr2:209240193-209240243	PFSK-1	brain:	n/a
43	chr2:209242596-209242646	HCT-116	colon:	n/a
44	chr2:209242596-209242646	U87	brain:	n/a
45	chr2:209242596-209242646	ECC-1	luminal epithelium:	n/a
46	chr2:209240193-209240243	HRPEpiC	eye:	n/a
47	chr2:209242596-209242646	HCF	heart:	n/a
48	chr2:209240193-209240243	K562	blood:	n/a
49	chr2:209242596-209242646	AG09309	skin:	n/a
50	chr2:209240193-209240243	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:209244985..209246550-chr2:209250823..209252697,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000265454	TF binding region
ENSG00000213081	TF binding region
ENSG00000265454	CpG island
ENSG00000213081	CpG island

Extended variants
information (count: 662 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:662 , 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	rs573766700	chr2:209228703-209228704	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs113044678	chr2:209228762-209228763	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs115950954	chr2:209228788-209228789	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs561636641	chr2:209228885-209228886	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs372021049	chr2:209228902-209228903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs543532362	chr2:209228925-209228926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376899091	chr2:209228974-209228975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563418382	chr2:209228992-209228993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138663098	chr2:209229014-209229015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542625640	chr2:209229054-209229055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559771630	chr2:209229055-209229056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528785397	chr2:209229152-209229153	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs551518772	chr2:209229167-209229168	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs57668434	chr2:209229169-209229170	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs13031048	chr2:209229176-209229177	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs571500184	chr2:209229187-209229188	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs531057689	chr2:209229198-209229199	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs186990831	chr2:209229211-209229212	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs567781001	chr2:209229220-209229221	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs536217447	chr2:209229302-209229303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs143585376	chr2:209229366-209229367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565787601	chr2:209229394-209229395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191180676	chr2:209229437-209229438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534921648	chr2:209229461-209229462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6758207	chr2:209229524-209229525	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs577906766	chr2:209229529-209229530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543678453	chr2:209229532-209229533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112866869	chr2:209229544-209229545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183434649	chr2:209229548-209229549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs111351751	chr2:209229553-209229554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112057671	chr2:209229588-209229589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142950906	chr2:209229603-209229604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs377438492	chr2:209229652-209229653	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs528115103	chr2:209229688-209229689	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs185259850	chr2:209229697-209229698	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs111261796	chr2:209229779-209229780	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs34918094	chr2:209229791-209229792	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs113436715	chr2:209229792-209229793	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs565266278	chr2:209229863-209229864	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs527885458	chr2:209229866-209229867	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs530992202	chr2:209229928-209229929	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs62195333	chr2:209229940-209229941	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs561518181	chr2:209230007-209230008	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs13395035	chr2:209230011-209230012	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs546634471	chr2:209230012-209230013	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs528902557	chr2:209230028-209230029	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs1898436	chr2:209230052-209230053	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs539080772	chr2:209230054-209230055	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs549786231	chr2:209230070-209230071	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs1898437	chr2:209230087-209230088	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	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
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209220200-209229800	Weak transcription	Colon Smooth Muscle	Colon
2	chr2:209220200-209235200	Weak transcription	K562	blood
3	chr2:209221800-209231200	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr2:209224800-209234200	Weak transcription	Placenta	Placenta
5	chr2:209226000-209230200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr2:209226000-209230800	Weak transcription	Spleen	Spleen
7	chr2:209226000-209234200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr2:209227400-209229200	Enhancers	NHDF-Ad	bronchial
9	chr2:209227600-209229200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr2:209227600-209229200	Enhancers	Muscle Satellite Cultured Cells	--
11	chr2:209227800-209228800	Enhancers	HSMMtube	muscle
12	chr2:209227800-209229000	Enhancers	HMEC	breast
13	chr2:209227800-209229200	Enhancers	NHLF	lung
14	chr2:209228000-209228800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr2:209228000-209228800	Enhancers	GM12878-XiMat	blood
16	chr2:209228000-209228800	Enhancers	NHEK	skin
17	chr2:209228000-209228800	Enhancers	Osteobl	bone
18	chr2:209228000-209229000	Enhancers	Hela-S3	cervix
19	chr2:209228200-209231200	Weak transcription	Primary hematopoietic stem cells	blood
20	chr2:209228400-209229000	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr2:209228400-209229200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr2:209228800-209234000	Weak transcription	Osteobl	bone
23	chr2:209229200-209229400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr2:209229200-209234600	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr2:209229400-209229600	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr2:209229800-209230000	ZNF genes & repeats	Colon Smooth Muscle	Colon
27	chr2:209230800-209231200	Enhancers	Primary B cells from peripheral blood	blood
28	chr2:209231000-209231200	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr2:209231000-209231200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr2:209231000-209231200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr2:209231000-209231200	Enhancers	GM12878-XiMat	blood
32	chr2:209231000-209231400	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr2:209231200-209231400	Flanking Active TSS	Primary B cells from cord blood	blood
34	chr2:209231200-209231400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
35	chr2:209231200-209231400	Enhancers	Spleen	Spleen
36	chr2:209231200-209231600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr2:209231200-209231600	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr2:209231200-209231600	Flanking Active TSS	GM12878-XiMat	blood
39	chr2:209231200-209231800	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr2:209231200-209231800	Flanking Active TSS	Primary B cells from peripheral blood	blood
41	chr2:209231200-209231800	Enhancers	Primary hematopoietic stem cells	blood
42	chr2:209231200-209231800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr2:209231200-209231800	Active TSS	Monocytes-CD14+_RO01746	blood
44	chr2:209231400-209231800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
45	chr2:209231400-209231800	Active TSS	Primary B cells from cord blood	blood
46	chr2:209231400-209232000	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr2:209231600-209231800	Active TSS	GM12878-XiMat	blood
48	chr2:209231600-209232200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr2:209231800-209232000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr2:209231800-209232200	Enhancers	Primary B cells from peripheral blood	blood

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