Variant report

Variant	esv3340677
Chromosome Location	chr2:234580879-234591324
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:110)
CpG islands
(count:305)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:110 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr2:234584648-234585210	A549	lung:	n/a	n/a
2	CEBPB	chr2:234590183-234590481	A549	lung:	n/a	chr2:234590292-234590305 chr2:234590292-234590303
3	CEBPB	chr2:234590254-234590371	HepG2	liver:	n/a	chr2:234590292-234590305 chr2:234590292-234590303
4	CEBPB	chr2:234590167-234590485	Hela-S3	cervix:	n/a	chr2:234590292-234590305 chr2:234590292-234590303
5	CEBPB	chr2:234589336-234589373	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr2:234584626-234585183	A549	lung:	n/a	n/a
7	CEBPB	chr2:234590215-234590473	A549	lung:	n/a	chr2:234590292-234590305 chr2:234590292-234590303
8	CTCF	chr2:234583115-234583216	GM13977	blood:	n/a	n/a
9	CTCF	chr2:234583700-234583850	AG04450	lung:	n/a	n/a
10	CTCF	chr2:234583620-234583770	WERI-Rb-1	eye:	n/a	n/a
11	CTCF	chr2:234583020-234583170	HCT-116	colon:	n/a	n/a
12	CTCF	chr2:234583680-234583830	MCF-7	breast:	n/a	n/a
13	CTCF	chr2:234583400-234583550	RPTEC	kidney:	n/a	n/a
14	CTCF	chr2:234583700-234583850	HPAF	blood vessel:	n/a	n/a
15	CTCF	chr2:234583660-234583810	BE2_C	brain:	n/a	n/a
16	CTCF	chr2:234583640-234583790	WI-38	lung:	n/a	n/a
17	CTCF	chr2:234583640-234583790	HPAF	blood vessel:	n/a	n/a
18	CTCF	chr2:234583700-234583850	RPTEC	kidney:	n/a	n/a
19	CTCF	chr2:234583740-234583890	GM12875	blood:	n/a	n/a
20	CTCF	chr2:234583480-234583630	GM12873	blood:	n/a	n/a
21	CTCF	chr2:234583680-234583830	HVMF	connective:	n/a	n/a
22	CTCF	chr2:234583060-234583210	GM12873	blood:	n/a	n/a
23	CTCF	chr2:234583096-234583222	K562	blood:	n/a	n/a
24	CTCF	chr2:234583620-234583770	HCPEpiC	choroid plexus:	n/a	n/a
25	CTCF	chr2:234583620-234583770	HEK293	kidney:	n/a	n/a
26	CTCF	chr2:234583099-234583181	GM19240	blood:	n/a	n/a
27	CTCF	chr2:234583620-234583770	BE2_C	brain:	n/a	n/a
28	CTCF	chr2:234583640-234583790	NHEK	skin:	n/a	n/a
29	CTCF	chr2:234583099-234583160	GM12892	blood:	n/a	n/a
30	CTCF	chr2:234583600-234583750	HCM	heart:	n/a	n/a
31	CTCF	chr2:234583700-234583850	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr2:234583680-234583830	HCT-116	colon:	n/a	n/a
33	CTCF	chr2:234582987-234583312	GM12878	blood:	n/a	n/a
34	CTCF	chr2:234583640-234583790	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr2:234583060-234583210	HCT-116	colon:	n/a	n/a
36	CTCF	chr2:234591309-234591397	GM13976	blood:	n/a	n/a
37	CTCF	chr2:234583480-234583630	BJ	skin:	n/a	n/a
38	CTCF	chr2:234583101-234583167	GM19238	blood:	n/a	n/a
39	CTCF	chr2:234583640-234583790	GM12873	blood:	n/a	n/a
40	CTCF	chr2:234583680-234583830	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr2:234583360-234583510	GM12875	blood:	n/a	n/a
42	CTCF	chr2:234583740-234583990	HVMF	connective:	n/a	n/a
43	CTCF	chr2:234583680-234583830	HAc	cerebellar:	n/a	n/a
44	CTCF	chr2:234583158-234583182	GM12878	blood:	n/a	n/a
45	CTCF	chr2:234583620-234583770	HepG2	liver:	n/a	n/a
46	CTCF	chr2:234583600-234583750	HMEC	breast:	n/a	n/a
47	CTCF	chr2:234583080-234583230	GM12875	blood:	n/a	n/a
48	CTCF	chr2:234583660-234583810	GM12872	blood:	n/a	n/a
49	CTCF	chr2:234583760-234583910	BJ	skin:	n/a	n/a
50	CTCF	chr2:234583620-234583770	A549	lung:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:234589374-234589424	HMEC	breast:	n/a
2	chr2:234590590-234590640	GM19239	blood:	n/a
3	chr2:234589810-234589860	NT2-D1	testis:	n/a
4	chr2:234589374-234589424	GM19239	blood:	n/a
5	chr2:234580842-234580892	MCF10A-Er-Src	breast:	n/a
6	chr2:234580842-234580892	NT2-D1	testis:	n/a
7	chr2:234589374-234589424	GM12892	blood:	n/a
8	chr2:234590590-234590640	CMK	blood:	n/a
9	chr2:234589374-234589424	HCT-116	colon:	n/a
10	chr2:234589810-234589860	Hepatocyte	liver:	n/a
11	chr2:234590865-234590915	RPTEC	kidney:	n/a
12	chr2:234590865-234590915	BE2_C	brain:	n/a
13	chr2:234589374-234589424	SKMC	muscle:	n/a
14	chr2:234589374-234589424	Caco-2	colon:	n/a
15	chr2:234590590-234590640	Caco-2	colon:	n/a
16	chr2:234590590-234590640	HIPEpiC	eye:	n/a
17	chr2:234589374-234589424	SK-N-SH_RA	brain:	n/a
18	chr2:234589374-234589424	NH-A	brain:	n/a
19	chr2:234580842-234580892	HPAEpiC	pulmonary alveolar:	n/a
20	chr2:234590865-234590915	GM06990	blood:	n/a
21	chr2:234580842-234580892	HAEpiC	amniotic membrane:	n/a
22	chr2:234590590-234590640	IMR90	lung:	fetal
23	chr2:234590865-234590915	K562	blood:	n/a
24	chr2:234589374-234589424	ovcar-3	ovarian:	n/a
25	chr2:234589374-234589424	HRE	kidney:	n/a
26	chr2:234590590-234590640	HRPEpiC	eye:	n/a
27	chr2:234589810-234589860	GM12878	blood:	n/a
28	chr2:234589810-234589860	NHDF-neo	bronchial:	n/a
29	chr2:234590590-234590640	NT2-D1	testis:	n/a
30	chr2:234590865-234590915	PrEC	prostate:	n/a
31	chr2:234590865-234590915	HAEpiC	amniotic membrane:	n/a
32	chr2:234589374-234589424	SAEC	small airway:	n/a
33	chr2:234580842-234580892	NHDF-neo	bronchial:	n/a
34	chr2:234590865-234590915	HCF	heart:	n/a
35	chr2:234589810-234589860	Jurkat	blood:	n/a
36	chr2:234589374-234589424	BE2_C	brain:	n/a
37	chr2:234590590-234590640	ProgFib	skin:	n/a
38	chr2:234590865-234590915	HUVEC	blood vessel:	n/a
39	chr2:234580842-234580892	GM19239	blood:	n/a
40	chr2:234590590-234590640	Hepatocyte	liver:	n/a
41	chr2:234589810-234589860	CMK	blood:	n/a
42	chr2:234589374-234589424	AG09319	gingival:	n/a
43	chr2:234589810-234589860	ECC-1	luminal epithelium:	n/a
44	chr2:234590865-234590915	AG10803	skin:	n/a
45	chr2:234580842-234580892	Caco-2	colon:	n/a
46	chr2:234590590-234590640	Jurkat	blood:	n/a
47	chr2:234590590-234590640	HCM	heart:	n/a
48	chr2:234589374-234589424	GM12891	blood:	n/a
49	chr2:234590590-234590640	GM06990	blood:	n/a
50	chr2:234589374-234589424	ProgFib	skin:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:234578802..234581575-chr2:234598668..234600515,2	MCF-7	breast:
2	chr2:234585462..234589750-chr2:234597767..234600526,3	MCF-7	breast:
3	chr2:234577799..234579592-chr2:234583305..234585773,2	K562	blood:

No data

Variant related genes	Relation type
UGT1A7	TF binding region
UGT1A7	CpG island
ENSG00000167165	chromatin interactions

Extended variants
information (count: 490 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555995846	chr2:234580888-234580889	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs574626292	chr2:234580901-234580902	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs377398548	chr2:234580911-234580912	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs576749742	chr2:234580915-234580916	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs370692027	chr2:234580917-234580918	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs374589183	chr2:234580949-234580950	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs148880087	chr2:234580966-234580967	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs28946876	chr2:234580967-234580968	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
9	rs376368364	chr2:234580968-234580969	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs370181544	chr2:234580984-234580985	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs374130776	chr2:234580986-234580987	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs76167146	chr2:234581002-234581003	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs138301590	chr2:234581003-234581004	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs113101046	chr2:234581012-234581013	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs200266032	chr2:234581021-234581022	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs148513688	chr2:234581025-234581026	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs367716901	chr2:234581042-234581043	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs149398312	chr2:234581064-234581065	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs151238339	chr2:234581080-234581081	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs145923738	chr2:234581083-234581084	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs576793496	chr2:234581084-234581085	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs372244167	chr2:234581085-234581086	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs141811044	chr2:234581106-234581107	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs201310933	chr2:234581125-234581126	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs145038612	chr2:234581127-234581128	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs545447386	chr2:234581131-234581132	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs373933295	chr2:234581147-234581148	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs368611098	chr2:234581163-234581164	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs151216459	chr2:234581168-234581169	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs148522431	chr2:234581195-234581196	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs377261531	chr2:234581196-234581197	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs201242485	chr2:234581200-234581201	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs111861762	chr2:234581202-234581203	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs369779434	chr2:234581221-234581222	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs146422336	chr2:234581264-234581265	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs200362930	chr2:234581267-234581268	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs199518861	chr2:234581289-234581290	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs371652390	chr2:234581296-234581297	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs561534651	chr2:234581299-234581300	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs66915469	chr2:234581306-234581307	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs201422390	chr2:234581313-234581314	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs17863776	chr2:234581336-234581337	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs375970481	chr2:234581341-234581342	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs368960201	chr2:234581344-234581345	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs58597806	chr2:234581346-234581347	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs200148096	chr2:234581360-234581361	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs150454866	chr2:234581361-234581362	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs142414435	chr2:234581373-234581374	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs4663870	chr2:234581374-234581375	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs376424202	chr2:234581382-234581383	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	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
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
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	22429812	CNVD
Bladder cancer	21909424	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
prenatal diagnosis	22389664	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mental retardation	20152051	CNVD
Cancer	21183584	CNVD
Albright''s disease	22277900	CNVD
Brachydactyly-Mental Retardation Syndrome	22470819	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Colorectal cancer	19359472	CNVD
Autism	18414403	CNVD
Chronic myeloid leukemia	21384125	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234554600-234587800	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr2:234559800-234592800	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr2:234580400-234582200	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr2:234580600-234582400	Active TSS	Liver	Liver
5	chr2:234580600-234582400	Weak transcription	A549	lung
6	chr2:234581400-234582000	Enhancers	Primary B cells from cord blood	blood
7	chr2:234582400-234582600	Flanking Active TSS	Liver	Liver
8	chr2:234582400-234582600	Flanking Active TSS	A549	lung
9	chr2:234582600-234582800	Active TSS	Liver	Liver
10	chr2:234582600-234582800	Enhancers	A549	lung
11	chr2:234582800-234583000	Flanking Active TSS	A549	lung
12	chr2:234582800-234584000	Flanking Active TSS	Liver	Liver
13	chr2:234583000-234585400	Enhancers	A549	lung
14	chr2:234583400-234584200	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr2:234583800-234584200	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr2:234584000-234585600	Enhancers	Liver	Liver
17	chr2:234584600-234585400	Enhancers	NH-A	brain
18	chr2:234585400-234588000	Weak transcription	A549	lung
19	chr2:234585600-234589000	Weak transcription	Liver	Liver
20	chr2:234587800-234588000	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr2:234587800-234588200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr2:234588000-234589800	Enhancers	A549	lung
23	chr2:234588000-234593000	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr2:234588600-234597000	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr2:234589000-234590800	Enhancers	Liver	Liver
26	chr2:234589200-234589400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr2:234589200-234589400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr2:234589200-234589400	Enhancers	Esophagus	oesophagus
29	chr2:234589200-234589800	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr2:234589400-234589600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr2:234589400-234590600	Weak transcription	Esophagus	oesophagus
32	chr2:234589400-234590800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr2:234589800-234590200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr2:234589800-234593000	Weak transcription	A549	lung
35	chr2:234590000-234597800	Weak transcription	Colonic Mucosa	Colon
36	chr2:234590200-234591800	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr2:234590600-234590800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr2:234590600-234590800	Enhancers	Esophagus	oesophagus
39	chr2:234590800-234591600	Enhancers	Primary hematopoietic stem cells	blood
40	chr2:234590800-234592600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr2:234590800-234597400	Weak transcription	Liver	Liver
42	chr2:234590800-234599800	Weak transcription	Esophagus	oesophagus
43	chr2:234591000-234592600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr2:234591200-234591600	Enhancers	Primary B cells from cord blood	blood

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