Variant report

Variant	esv32551
Chromosome Location	chr11:8457023-8534642
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:140)
CpG islands
(count:122)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:140 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:8463522-8463730	HepG2	liver:	n/a	n/a
2	BACH1	chr11:8463832-8464134	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr11:8499285-8499609	GM12878	blood:	n/a	chr11:8499433-8499441
4	BHLHE40	chr11:8499365-8499582	GM12878	blood:	n/a	n/a
5	CEBPB	chr11:8471506-8471836	A549	lung:	n/a	n/a
6	CEBPB	chr11:8528680-8528768	K562	blood:	n/a	n/a
7	CEBPB	chr11:8483139-8483272	HepG2	liver:	n/a	chr11:8483179-8483192 chr11:8483179-8483190 chr11:8483179-8483190 chr11:8483179-8483192 chr11:8483180-8483191
8	CEBPB	chr11:8471597-8471834	IMR90	lung:	n/a	n/a
9	CEBPB	chr11:8471641-8471792	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr11:8534234-8534335	HepG2	liver:	n/a	n/a
11	CEBPB	chr11:8502526-8502755	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr11:8528642-8528731	A549	lung:	n/a	n/a
13	CEBPB	chr11:8471492-8471848	HepG2	liver:	n/a	n/a
14	CEBPB	chr11:8509924-8510250	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr11:8528637-8528743	HepG2	liver:	n/a	n/a
16	CEBPB	chr11:8525530-8525980	HepG2	liver:	n/a	n/a
17	CEBPB	chr11:8528690-8528693	IMR90	lung:	n/a	n/a
18	CEBPB	chr11:8509961-8510222	ECC-1	luminal epithelium:	n/a	n/a
19	CHD2	chr11:8499393-8499512	GM12878	blood:	n/a	n/a
20	CTCF	chr11:8502630-8502689	GM20000	blood:	n/a	n/a
21	CTCF	chr11:8468235-8468317	GM13976	blood:	n/a	n/a
22	CTCF	chr11:8503160-8503310	AoAF	blood vessel:	n/a	n/a
23	CTCF	chr11:8525740-8525890	GM12864	blood:	n/a	n/a
24	CTCF	chr11:8504520-8504670	GM12869	blood:	n/a	n/a
25	CTCF	chr11:8489187-8489212	GM13977	blood:	n/a	n/a
26	CTCF	chr11:8531672-8531762	Lung_OC	lung:	n/a	n/a
27	CUX1	chr11:8463328-8463656	GM12878	blood:	n/a	n/a
28	E2F4	chr11:8481719-8481748	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr11:8505165-8505167	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr11:8528617-8528636	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr11:8494997-8495110	MCF10A-Er-Src	breast:	n/a	n/a
32	EBF1	chr11:8499357-8499545	GM12878	blood:	n/a	n/a
33	ELK1	chr11:8505700-8505771	K562	blood:	n/a	n/a
34	EP300	chr11:8499122-8499593	GM12878	blood:	n/a	chr11:8499569-8499583 chr11:8499436-8499450
35	EP300	chr11:8499277-8499574	GM12878	blood:	n/a	chr11:8499436-8499450
36	EP300	chr11:8509877-8510460	ECC-1	luminal epithelium:	n/a	n/a
37	FOS	chr11:8534184-8534416	MCF10A-Er-Src	breast:	n/a	chr11:8534262-8534272 chr11:8534262-8534272 chr11:8534262-8534272 chr11:8534262-8534272
38	FOS	chr11:8534156-8534424	MCF10A-Er-Src	breast:	n/a	chr11:8534262-8534272 chr11:8534262-8534272 chr11:8534262-8534272 chr11:8534262-8534272
39	FOS	chr11:8527124-8527229	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr11:8527058-8527306	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr11:8534227-8534421	MCF10A-Er-Src	breast:	n/a	chr11:8534262-8534272 chr11:8534262-8534272 chr11:8534262-8534272 chr11:8534262-8534272
42	FOXA1	chr11:8525571-8526071	HepG2	liver:	n/a	chr11:8525823-8525838
43	FOXA1	chr11:8458502-8458964	HepG2	liver:	n/a	n/a
44	FOXA1	chr11:8525582-8526006	HepG2	liver:	n/a	chr11:8525823-8525838
45	FOXA1	chr11:8458575-8458917	HepG2	liver:	n/a	n/a
46	FOXA1	chr11:8511775-8512073	HepG2	liver:	n/a	n/a
47	FOXA1	chr11:8525578-8525982	HepG2	liver:	n/a	chr11:8525823-8525838
48	FOXA1	chr11:8525587-8525997	HepG2	liver:	n/a	chr11:8525823-8525838
49	FOXA2	chr11:8525645-8525986	HepG2	liver:	n/a	n/a
50	FOXA2	chr11:8525370-8526218	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:8498357-8498407	T-47D	breast:	n/a
2	chr11:8497733-8497783	AG09309	skin:	n/a
3	chr11:8498357-8498407	AoSMC	blood vessel:	n/a
4	chr11:8498357-8498407	RPTEC	kidney:	n/a
5	chr11:8498357-8498407	PFSK-1	brain:	n/a
6	chr11:8498357-8498407	HAEpiC	amniotic membrane:	n/a
7	chr11:8498357-8498407	GM12878	blood:	n/a
8	chr11:8498357-8498407	HL-60	blood:	n/a
9	chr11:8497733-8497783	HCT-116	colon:	n/a
10	chr11:8497733-8497783	K562	blood:	n/a
11	chr11:8498357-8498407	PANC-1	pancreas:	n/a
12	chr11:8497733-8497783	AoSMC	blood vessel:	n/a
13	chr11:8497733-8497783	GM12892	blood:	n/a
14	chr11:8497733-8497783	HRE	kidney:	n/a
15	chr11:8498357-8498407	H1-hESC	embryonic stem cell:	embryo
16	chr11:8497733-8497783	MCF10A-Er-Src	breast:	n/a
17	chr11:8498357-8498407	AG04449	skin:	fetal
18	chr11:8498357-8498407	GM19239	blood:	n/a
19	chr11:8498357-8498407	A549	lung:	n/a
20	chr11:8497733-8497783	PFSK-1	brain:	n/a
21	chr11:8498357-8498407	K562	blood:	n/a
22	chr11:8497733-8497783	Jurkat	blood:	n/a
23	chr11:8498357-8498407	HCT-116	colon:	n/a
24	chr11:8498357-8498407	NHBE	bronchial:	n/a
25	chr11:8497733-8497783	HEK293	kidney:	embryo
26	chr11:8498357-8498407	HRCEpiC	kidney:	n/a
27	chr11:8497733-8497783	LNCaP	prostate:	n/a
28	chr11:8497733-8497783	CMK	blood:	n/a
29	chr11:8497733-8497783	PANC-1	pancreas:	n/a
30	chr11:8497733-8497783	AG09319	gingival:	n/a
31	chr11:8498357-8498407	ProgFib	skin:	n/a
32	chr11:8498357-8498407	SKMC	muscle:	n/a
33	chr11:8497733-8497783	PrEC	prostate:	n/a
34	chr11:8497733-8497783	ProgFib	skin:	n/a
35	chr11:8498357-8498407	MCF-7	breast:	n/a
36	chr11:8497733-8497783	SKMC	muscle:	n/a
37	chr11:8498357-8498407	IMR90	lung:	fetal
38	chr11:8497733-8497783	A549	lung:	n/a
39	chr11:8498357-8498407	PrEC	prostate:	n/a
40	chr11:8498357-8498407	HRPEpiC	eye:	n/a
41	chr11:8498357-8498407	ovcar-3	ovarian:	n/a
42	chr11:8498357-8498407	AG09319	gingival:	n/a
43	chr11:8498357-8498407	AG09309	skin:	n/a
44	chr11:8498357-8498407	HCF	heart:	n/a
45	chr11:8498357-8498407	U87	brain:	n/a
46	chr11:8498357-8498407	SAEC	small airway:	n/a
47	chr11:8498357-8498407	BE2_C	brain:	n/a
48	chr11:8498357-8498407	HNPCEpiC	eye:	n/a
49	chr11:8497733-8497783	HAEpiC	amniotic membrane:	n/a
50	chr11:8498357-8498407	HepG2	liver:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:8476130..8478449-chr11:8710032..8712204,2	K562	blood:
2	chr11:8506706..8507606-chr4:143536248..143536811,2	MCF-7	breast:
3	chr11:8481047..8482707-chr11:8494545..8496068,2	MCF-7	breast:
4	chr11:8524893..8527404-chr11:8645934..8647701,2	K562	blood:
5	chr11:8481047..8482707-chr11:8494545..8496068,2	MCF-7	breast:
6	chr11:8492298..8495285-chr11:8497970..8500359,2	K562	blood:
7	chr11:8475701..8478486-chr11:8478685..8480466,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIM66-5	chr11:8496195-8496613	NONHSAT017850

No data

Variant related genes	Relation type
STK33	TF binding region
STK33	CpG island
ENSG00000130413	chromatin interactions
ENSG00000166441	chromatin interactions

Extended variants
information (count: 2057 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2057 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138159359	chr11:8457055-8457056	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs199562993	chr11:8457082-8457083	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371270258	chr11:8457137-8457138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147875604	chr11:8457158-8457159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201792701	chr11:8457161-8457162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569860155	chr11:8457166-8457167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538963016	chr11:8457206-8457207	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs10769907	chr11:8457237-8457238	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs571737603	chr11:8457238-8457239	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368617205	chr11:8457243-8457244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370227074	chr11:8457244-8457245	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs540609820	chr11:8457261-8457262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554259878	chr11:8457277-8457278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541906656	chr11:8457295-8457296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543661350	chr11:8457317-8457318	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188977582	chr11:8457330-8457331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577358882	chr11:8457352-8457353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368245074	chr11:8457388-8457389	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs11041922	chr11:8457391-8457392	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs560070480	chr11:8457394-8457395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139807789	chr11:8457466-8457467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs367934535	chr11:8457476-8457477	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550606547	chr11:8457501-8457502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368086378	chr11:8457559-8457560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200387229	chr11:8457560-8457561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371810427	chr11:8457576-8457577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200662514	chr11:8457583-8457584	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375602911	chr11:8457586-8457587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201583070	chr11:8457657-8457658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141134644	chr11:8457681-8457682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550787324	chr11:8457682-8457683	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564012820	chr11:8457758-8457759	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569878003	chr11:8457775-8457776	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532977603	chr11:8457787-8457788	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs11828086	chr11:8457813-8457814	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs145275853	chr11:8457821-8457822	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565605011	chr11:8457850-8457851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534338980	chr11:8457873-8457874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532945466	chr11:8457893-8457894	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182094168	chr11:8457906-8457907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574461347	chr11:8458001-8458002	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377565037	chr11:8458050-8458051	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186689554	chr11:8458062-8458063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566325345	chr11:8458063-8458064	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565339687	chr11:8458114-8458115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111314120	chr11:8458119-8458120	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368053553	chr11:8458178-8458179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537193268	chr11:8458183-8458184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191495049	chr11:8458185-8458186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577397602	chr11:8458189-8458190	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Dysmorphic features	22052655	CNVD
Intellectual disability	22052655	CNVD
Obesity	22052655	CNVD
Prostate cancer	18632612	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21785460	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:148 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8446400-8464000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:8447800-8464200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr11:8448000-8461000	Weak transcription	Ovary	ovary
4	chr11:8451600-8463600	Weak transcription	Fetal Heart	heart
5	chr11:8451600-8464000	Weak transcription	Left Ventricle	heart
6	chr11:8453800-8464000	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr11:8454400-8458200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:8456400-8458200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr11:8456400-8463800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr11:8456600-8463200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr11:8456800-8463400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr11:8457000-8458800	Weak transcription	Stomach Smooth Muscle	stomach
13	chr11:8457000-8463400	Weak transcription	Primary hematopoietic stem cells	blood
14	chr11:8458200-8463200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr11:8458200-8463400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr11:8460000-8460200	Enhancers	Fetal Lung	lung
17	chr11:8460200-8463600	Weak transcription	Fetal Lung	lung
18	chr11:8460200-8481200	Weak transcription	Fetal Kidney	kidney
19	chr11:8461000-8462000	Strong transcription	Ovary	ovary
20	chr11:8462000-8484600	Weak transcription	Ovary	ovary
21	chr11:8463200-8463600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr11:8463200-8465000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr11:8463400-8464400	Enhancers	Primary hematopoietic stem cells	blood
24	chr11:8463400-8464600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr11:8463400-8465000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr11:8463600-8464400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr11:8463600-8464600	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr11:8463600-8464600	Enhancers	Fetal Heart	heart
29	chr11:8463600-8464600	Enhancers	Fetal Lung	lung
30	chr11:8463800-8464000	Enhancers	Brain Germinal Matrix	brain
31	chr11:8463800-8464400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr11:8463800-8464400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr11:8463800-8464600	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr11:8463800-8464600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr11:8464000-8464200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr11:8464000-8464200	Enhancers	Left Ventricle	heart
37	chr11:8464000-8464400	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr11:8464000-8464400	Enhancers	Fetal Brain Female	brain
39	chr11:8464000-8464600	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr11:8464200-8464400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr11:8464200-8464400	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr11:8464400-8464600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr11:8464400-8483400	Weak transcription	Primary hematopoietic stem cells	blood
44	chr11:8464400-8488200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr11:8464600-8484800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr11:8464600-8485800	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr11:8464600-8488200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr11:8464600-8489000	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr11:8464600-8495800	Weak transcription	Fetal Heart	heart
50	chr11:8471800-8482600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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