Variant report

Variant	esv2755260
Chromosome Location	chr11:58762747-58854169
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:786)
CpG islands
(count:916)
Chromatin interactive
region (count:4)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:786 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:58792609-58792905	HepG2	liver:	n/a	n/a
2	ATF1	chr11:58779639-58779652	K562	blood:	n/a	n/a
3	ATF2	chr11:58831402-58832419	GM12878	blood:	n/a	n/a
4	ATF2	chr11:58831671-58832143	GM12878	blood:	n/a	n/a
5	ATF2	chr11:58825833-58826405	GM12878	blood:	n/a	n/a
6	BACH1	chr11:58825972-58826213	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr11:58818940-58819193	GM12878	blood:	n/a	n/a
8	BATF	chr11:58826199-58826498	GM12878	blood:	n/a	n/a
9	BATF	chr11:58831786-58832150	GM12878	blood:	n/a	chr11:58831926-58831934
10	BATF	chr11:58831416-58832275	GM12878	blood:	n/a	chr11:58831926-58831934
11	BATF	chr11:58831471-58831776	GM12878	blood:	n/a	n/a
12	BCL11A	chr11:58831483-58831904	GM12878	blood:	n/a	n/a
13	BCL11A	chr11:58831528-58832157	GM12878	blood:	n/a	n/a
14	BCL11A	chr11:58818878-58819275	GM12878	blood:	n/a	chr11:58819091-58819100
15	BCL11A	chr11:58818899-58819262	GM12878	blood:	n/a	chr11:58819091-58819100
16	BCL3	chr11:58831794-58832281	GM12878	blood:	n/a	n/a
17	BHLHE40	chr11:58792570-58792935	HepG2	liver:	n/a	chr11:58792752-58792765 chr11:58792748-58792769
18	BHLHE40	chr11:58826040-58826162	K562	blood:	n/a	n/a
19	BHLHE40	chr11:58820953-58821000	K562	blood:	n/a	n/a
20	BHLHE40	chr11:58825938-58826278	GM12878	blood:	n/a	n/a
21	BRCA1	chr11:58825950-58826184	GM12878	blood:	n/a	n/a
22	CEBPB	chr11:58767565-58767768	HepG2	liver:	n/a	chr11:58767688-58767699 chr11:58767686-58767697
23	CEBPB	chr11:58841369-58841519	IMR90	lung:	n/a	n/a
24	CEBPB	chr11:58825987-58826187	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr11:58779256-58779450	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr11:58780472-58780728	HepG2	liver:	n/a	chr11:58780597-58780608
27	CEBPB	chr11:58767676-58767679	K562	blood:	n/a	n/a
28	CEBPB	chr11:58767586-58767847	H1-hESC	embryonic stem cell:	n/a	chr11:58767688-58767699 chr11:58767686-58767697
29	CEBPB	chr11:58767634-58767824	Hela-S3	cervix:	n/a	chr11:58767688-58767699 chr11:58767686-58767697
30	CEBPB	chr11:58850700-58850889	HepG2	liver:	n/a	n/a
31	CEBPB	chr11:58835714-58835923	HepG2	liver:	n/a	chr11:58835780-58835791
32	CEBPB	chr11:58774084-58774291	HepG2	liver:	n/a	chr11:58774243-58774254
33	CEBPB	chr11:58835627-58835890	IMR90	lung:	n/a	chr11:58835780-58835791
34	CEBPB	chr11:58767588-58767695	A549	lung:	n/a	n/a
35	CEBPB	chr11:58827942-58827984	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr11:58835676-58835875	K562	blood:	n/a	chr11:58835780-58835791
37	CEBPB	chr11:58852160-58852235	HepG2	liver:	n/a	n/a
38	CHD1	chr11:58825963-58826312	GM12878	blood:	n/a	n/a
39	CHD1	chr11:58821218-58821270	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr11:58825822-58826232	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr11:58826018-58826077	K562	blood:	n/a	n/a
42	CHD2	chr11:58825891-58826300	GM12878	blood:	n/a	n/a
43	CREB1	chr11:58845805-58846333	GM12878	blood:	n/a	n/a
44	CREB1	chr11:58845766-58846361	GM12878	blood:	n/a	n/a
45	CTCF	chr11:58820920-58821070	Hela-S3	cervix:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
46	CTCF	chr11:58826000-58826150	HPF	lung:	n/a	n/a
47	CTCF	chr11:58825960-58826197	LNCaP	prostate:	n/a	n/a
48	CTCF	chr11:58825931-58826299	HCT-116	colon:	n/a	n/a
49	CTCF	chr11:58820880-58821030	AG09309	skin:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
50	CTCF	chr11:58820860-58821010	HVMF	connective:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58830191-58830241	AoSMC	blood vessel:	n/a
2	chr11:58830191-58830241	AoSMC	blood vessel:	n/a
3	chr11:58833356-58833406	MCF10A-Er-Src	breast:	n/a
4	chr11:58825870-58825920	AoSMC	blood vessel:	n/a
5	chr11:58830857-58830907	NH-A	brain:	n/a
6	chr11:58826110-58826160	AG04449	skin:	fetal
7	chr11:58806952-58807002	AG09309	skin:	n/a
8	chr11:58830424-58830474	HEEpiC	esophagus:	n/a
9	chr11:58830191-58830241	GM12891	blood:	n/a
10	chr11:58806952-58807002	HRE	kidney:	n/a
11	chr11:58826073-58826123	ovcar-3	ovarian:	n/a
12	chr11:58830424-58830474	NB4	blood:	n/a
13	chr11:58826073-58826123	NT2-D1	testis:	n/a
14	chr11:58826073-58826123	HAEpiC	amniotic membrane:	n/a
15	chr11:58833356-58833406	Hela-S3	cervix:	n/a
16	chr11:58830857-58830907	HCT-116	colon:	n/a
17	chr11:58825870-58825920	SKMC	muscle:	n/a
18	chr11:58828174-58828224	HL-60	blood:	n/a
19	chr11:58826110-58826160	NB4	blood:	n/a
20	chr11:58806952-58807002	GM12891	blood:	n/a
21	chr11:58833356-58833406	BJ	skin:	n/a
22	chr11:58830857-58830907	GM19239	blood:	n/a
23	chr11:58826110-58826160	SK-N-SH	brain:	n/a
24	chr11:58806952-58807002	SK-N-SH_RA	brain:	n/a
25	chr11:58826414-58826464	SKMC	muscle:	n/a
26	chr11:58830191-58830241	HRE	kidney:	n/a
27	chr11:58806952-58807002	SAEC	small airway:	n/a
28	chr11:58833356-58833406	NB4	blood:	n/a
29	chr11:58830610-58830660	ECC-1	luminal epithelium:	n/a
30	chr11:58830424-58830474	AoSMC	blood vessel:	n/a
31	chr11:58810187-58810237	NHBE	bronchial:	n/a
32	chr11:58830610-58830660	MCF10A-Er-Src	breast:	n/a
33	chr11:58826414-58826464	CMK	blood:	n/a
34	chr11:58826110-58826160	SKMC	muscle:	n/a
35	chr11:58830191-58830241	Caco-2	colon:	n/a
36	chr11:58810187-58810237	AG09309	skin:	n/a
37	chr11:58810187-58810237	HCM	heart:	n/a
38	chr11:58830610-58830660	HPAEpiC	pulmonary alveolar:	n/a
39	chr11:58825870-58825920	GM12891	blood:	n/a
40	chr11:58826475-58826525	Hela-S3	cervix:	n/a
41	chr11:58826475-58826525	PrEC	prostate:	n/a
42	chr11:58806952-58807002	HAEpiC	amniotic membrane:	n/a
43	chr11:58806952-58807002	GM19239	blood:	n/a
44	chr11:58825870-58825920	HCM	heart:	n/a
45	chr11:58830191-58830241	SAEC	small airway:	n/a
46	chr11:58825870-58825920	IMR90	lung:	fetal
47	chr11:58830424-58830474	HUVEC	blood vessel:	n/a
48	chr11:58826073-58826123	HNPCEpiC	eye:	n/a
49	chr11:58826073-58826123	ProgFib	skin:	n/a
50	chr11:58810187-58810237	PrEC	prostate:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:58830364..58831268-chr11:58873992..58874927,2	HCT-116	colon:
2	chr11:58762969..58764487-chr11:58768997..58771127,2	K562	blood:
3	chr11:58762969..58764487-chr11:58768997..58771127,2	K562	blood:
4	chr11:58399679..58402149-chr11:58838160..58840024,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLYATL2-2	chr11:58820930-58821099	NR_033853
2	lnc-GLYATL2-2	chr11:58825845-58825925	NR_033853
3	lnc-GLYATL2-2	chr11:58825845-58825923	ENSG00000255240.1
4	lnc-GLYATL2-2	chr11:58818733-58818781	NR_033853
5	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
6	lnc-GLYATL2-2	chr11:58822768-58822919	ENSG00000255240.1
7	lnc-GLYATL2-2	chr11:58825845-58826132	ENSG00000255240.1
8	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
9	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
10	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1

No data

Variant related genes	Relation type
ENSG00000254786	TF binding region
ENSG00000255240	TF binding region
GLYATL1P3	TF binding region
GLYATL1P4	TF binding region
ENSG00000254786	CpG island
ENSG00000255240	CpG island
GLYATL1P3	CpG island
GLYATL1P4	CpG island
ENSG00000189057	chromatin interactions

Extended variants
information (count: 3512 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:3512 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11229721	chr11:58762747-58762748	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs11229722	chr11:58762849-58762850	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs191816616	chr11:58762893-58762894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs568429408	chr11:58762894-58762895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs367883533	chr11:58762919-58762920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567492862	chr11:58762934-58762935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145344714	chr11:58762953-58762954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375455974	chr11:58762964-58762965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569435448	chr11:58762984-58762985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548239317	chr11:58763089-58763090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528021961	chr11:58763099-58763100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs578012214	chr11:58763103-58763104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369742644	chr11:58763109-58763110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547661009	chr11:58763181-58763182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184010504	chr11:58763253-58763254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553831843	chr11:58763266-58763267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186530139	chr11:58763269-58763270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147675807	chr11:58763281-58763282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189790910	chr11:58763296-58763297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574129088	chr11:58763330-58763331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182358259	chr11:58763376-58763377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544410975	chr11:58763380-58763381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371398423	chr11:58763424-58763425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187071234	chr11:58763425-58763426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192920198	chr11:58763439-58763440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112380036	chr11:58763450-58763451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544977839	chr11:58763527-58763528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149212076	chr11:58763540-58763541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527772648	chr11:58763541-58763542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549413174	chr11:58763572-58763573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183258499	chr11:58763578-58763579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35206731	chr11:58763653-58763654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531502250	chr11:58763664-58763665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535308735	chr11:58763674-58763675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561765766	chr11:58763724-58763725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374798035	chr11:58763730-58763731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368952878	chr11:58763743-58763744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142467741	chr11:58763769-58763770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571544750	chr11:58763809-58763810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373466208	chr11:58763815-58763816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553795059	chr11:58763819-58763820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7941415	chr11:58763854-58763855	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs188627292	chr11:58763886-58763887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369805721	chr11:58763916-58763917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192997512	chr11:58763954-58763955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs151290741	chr11:58763958-58763959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140556969	chr11:58763960-58763961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs499729	chr11:58763971-58763972	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs571097190	chr11:58763983-58763984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577898189	chr11:58763984-58763985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:503 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58754000-58765800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr11:58757400-58766600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr11:58758600-58766400	Weak transcription	Primary B cells from cord blood	blood
4	chr11:58760400-58767000	Weak transcription	GM12878-XiMat	blood
5	chr11:58760600-58764400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr11:58761000-58769200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr11:58761400-58765600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr11:58762400-58766400	Weak transcription	Primary B cells from peripheral blood	blood
9	chr11:58764400-58764800	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr11:58764800-58775200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr11:58765600-58766400	Enhancers	Liver	Liver
12	chr11:58765600-58767800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr11:58765800-58766200	Strong transcription	Primary hematopoietic stem cells	blood
14	chr11:58766200-58769000	Weak transcription	Primary hematopoietic stem cells	blood
15	chr11:58766400-58766600	Enhancers	Stomach Mucosa	stomach
16	chr11:58766400-58766800	Flanking Active TSS	Liver	Liver
17	chr11:58766400-58767600	Enhancers	Primary B cells from cord blood	blood
18	chr11:58766400-58767600	Enhancers	Primary B cells from peripheral blood	blood
19	chr11:58766600-58767200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
20	chr11:58766600-58767400	Enhancers	Sigmoid Colon	Sigmoid Colon
21	chr11:58766600-58768000	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr11:58766600-58768000	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr11:58766800-58767200	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr11:58766800-58767800	Enhancers	Liver	Liver
25	chr11:58767000-58767400	Enhancers	GM12878-XiMat	blood
26	chr11:58767200-58767400	Enhancers	Stomach Mucosa	stomach
27	chr11:58767200-58774000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr11:58767600-58770000	Weak transcription	Primary B cells from cord blood	blood
29	chr11:58767600-58776400	Weak transcription	Primary B cells from peripheral blood	blood
30	chr11:58767800-58769200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr11:58767800-58771200	Weak transcription	Liver	Liver
32	chr11:58769000-58770600	Enhancers	Primary hematopoietic stem cells	blood
33	chr11:58769200-58770400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr11:58769200-58770400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr11:58770000-58771600	Strong transcription	Primary B cells from cord blood	blood
36	chr11:58770400-58773600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr11:58770400-58774400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr11:58770600-58775200	Weak transcription	Primary hematopoietic stem cells	blood
39	chr11:58771200-58772200	Enhancers	Liver	Liver
40	chr11:58771600-58776600	Weak transcription	Primary B cells from cord blood	blood
41	chr11:58772200-58772600	Weak transcription	Liver	Liver
42	chr11:58772600-58773600	Enhancers	Liver	Liver
43	chr11:58773600-58776000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr11:58773600-58776000	Weak transcription	Liver	Liver
45	chr11:58774000-58774200	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr11:58774200-58774600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr11:58774400-58775200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr11:58774600-58774800	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr11:58774800-58775800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr11:58775200-58778600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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