Variant report

Variant	nsv553819
Chromosome Location	chr11:24499370-24545353
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	ATF2	chr11:24518353-24518812	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr11:24518327-24518833	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr11:24518280-24518908	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr11:24537322-24537573	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr11:24535771-24536012	GM12878	blood:	n/a	n/a
6	BATF	chr11:24530777-24530942	GM12878	blood:	n/a	n/a
7	BATF	chr11:24530725-24530946	GM12878	blood:	n/a	n/a
8	BATF	chr11:24535737-24536035	GM12878	blood:	n/a	n/a
9	BHLHE40	chr11:24535932-24535936	GM12878	blood:	n/a	n/a
10	CEBPB	chr11:24499285-24499571	A549	lung:	n/a	chr11:24499435-24499448 chr11:24499435-24499446 chr11:24499436-24499447 chr11:24499437-24499446
11	CEBPB	chr11:24499284-24499616	IMR90	lung:	n/a	chr11:24499435-24499448 chr11:24499435-24499446 chr11:24499436-24499447 chr11:24499437-24499446
12	CEBPB	chr11:24518479-24518656	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr11:24499285-24499610	HepG2	liver:	n/a	chr11:24499435-24499448 chr11:24499435-24499446 chr11:24499436-24499447 chr11:24499437-24499446
14	CEBPB	chr11:24536600-24536828	HepG2	liver:	n/a	n/a
15	CEBPB	chr11:24504498-24504929	MCF-7	breast:	n/a	chr11:24504658-24504667 chr11:24504658-24504667 chr11:24504656-24504669 chr11:24504658-24504667
16	CEBPB	chr11:24502417-24502754	ECC-1	luminal epithelium:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
17	CEBPB	chr11:24500310-24500645	IMR90	lung:	n/a	chr11:24500481-24500492
18	CEBPB	chr11:24502399-24502754	IMR90	lung:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
19	CEBPB	chr11:24502393-24502740	HepG2	liver:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
20	CEBPB	chr11:24502446-24502730	H1-hESC	embryonic stem cell:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
21	CEBPB	chr11:24502444-24502712	A549	lung:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
22	CEBPB	chr11:24504492-24504816	A549	lung:	n/a	chr11:24504658-24504667 chr11:24504658-24504667 chr11:24504656-24504669 chr11:24504658-24504667
23	CEBPB	chr11:24499426-24499477	H1-hESC	embryonic stem cell:	n/a	chr11:24499435-24499448 chr11:24499435-24499446 chr11:24499436-24499447 chr11:24499437-24499446
24	CEBPB	chr11:24502419-24502734	Hela-S3	cervix:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
25	CEBPB	chr11:24504500-24504875	MCF-7	breast:	n/a	chr11:24504658-24504667 chr11:24504658-24504667 chr11:24504656-24504669 chr11:24504658-24504667
26	CEBPB	chr11:24500295-24500561	HepG2	liver:	n/a	chr11:24500481-24500492
27	CEBPB	chr11:24524696-24525212	MCF-7	breast:	n/a	n/a
28	CEBPB	chr11:24500312-24500613	Hela-S3	cervix:	n/a	chr11:24500481-24500492
29	CEBPB	chr11:24499282-24499587	Hela-S3	cervix:	n/a	chr11:24499435-24499448 chr11:24499435-24499446 chr11:24499436-24499447 chr11:24499437-24499446
30	CHD1	chr11:24518674-24518698	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr11:24518563-24518933	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTBP2	chr11:24518245-24518979	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr11:24532446-24532497	ProgFib	skin:	n/a	n/a
34	CTCF	chr11:24537400-24537550	BE2_C	brain:	n/a	n/a
35	CTCF	chr11:24518604-24518946	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr11:24518440-24518516	MCF-7	breast:	n/a	n/a
37	CTCF	chr11:24529543-24529926	T-47D	breast:	n/a	n/a
38	CTCF	chr11:24506653-24506692	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr11:24530760-24530910	HAc	cerebellar:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
40	CTCF	chr11:24518660-24518810	MCF-7	breast:	n/a	n/a
41	CTCF	chr11:24518700-24518850	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr11:24518900-24519050	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr11:24530800-24530950	HA-sp	spinal cord:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
44	CTCF	chr11:24518658-24518954	MCF-7	breast:	n/a	n/a
45	CTCF	chr11:24537340-24537490	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr11:24518780-24518930	HRE	kidney:	n/a	n/a
47	CTCF	chr11:24518680-24518830	NHEK	skin:	n/a	n/a
48	CTCF	chr11:24530660-24530810	HMEC	breast:	n/a	n/a
49	CTCF	chr11:24530730-24530974	HUVEC	blood vessel:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
50	CTCF	chr11:24529660-24529810	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:24518374-24518424	PrEC	prostate:	n/a
2	chr11:24518374-24518424	PrEC	prostate:	n/a
3	chr11:24532473-24532523	Hela-S3	cervix:	n/a
4	chr11:24518737-24518787	MCF-7	breast:	n/a
5	chr11:24518379-24518429	GM12891	blood:	n/a
6	chr11:24518776-24518826	HMEC	breast:	n/a
7	chr11:24518448-24518498	HUVEC	blood vessel:	n/a
8	chr11:24518448-24518498	HCF	heart:	n/a
9	chr11:24518379-24518429	SKMC	muscle:	n/a
10	chr11:24518894-24518944	CMK	blood:	n/a
11	chr11:24532473-24532523	K562	blood:	n/a
12	chr11:24532473-24532523	MCF-7	breast:	n/a
13	chr11:24518414-24518464	U87	brain:	n/a
14	chr11:24518776-24518826	MCF10A-Er-Src	breast:	n/a
15	chr11:24518894-24518944	GM12891	blood:	n/a
16	chr11:24518367-24518417	K562	blood:	n/a
17	chr11:24518894-24518944	SKMC	muscle:	n/a
18	chr11:24518894-24518944	RPTEC	kidney:	n/a
19	chr11:24518414-24518464	SKMC	muscle:	n/a
20	chr11:24518281-24518331	HUVEC	blood vessel:	n/a
21	chr11:24518367-24518417	HEEpiC	esophagus:	n/a
22	chr11:24518281-24518331	HPAEpiC	pulmonary alveolar:	n/a
23	chr11:24518374-24518424	HEK293	kidney:	embryo
24	chr11:24518149-24518199	HepG2	liver:	n/a
25	chr11:24518149-24518199	Caco-2	colon:	n/a
26	chr11:24518225-24518275	HCM	heart:	n/a
27	chr11:24532473-24532523	AG09309	skin:	n/a
28	chr11:24518379-24518429	IMR90	lung:	fetal
29	chr11:24518414-24518464	HL-60	blood:	n/a
30	chr11:24518281-24518331	NB4	blood:	n/a
31	chr11:24518381-24518431	MCF10A-Er-Src	breast:	n/a
32	chr11:24518381-24518431	AG04449	skin:	fetal
33	chr11:24518381-24518431	PANC-1	pancreas:	n/a
34	chr11:24518379-24518429	NH-A	brain:	n/a
35	chr11:24518367-24518417	NHDF-neo	bronchial:	n/a
36	chr11:24532473-24532523	NHDF-neo	bronchial:	n/a
37	chr11:24518776-24518826	K562	blood:	n/a
38	chr11:24518737-24518787	SK-N-MC	brain:	n/a
39	chr11:24518448-24518498	NHDF-neo	bronchial:	n/a
40	chr11:24518448-24518498	CMK	blood:	n/a
41	chr11:24518894-24518944	AG04450	lung:	fetal
42	chr11:24518448-24518498	HCPEpiC	choroid plexus:	n/a
43	chr11:24518225-24518275	H1-hESC	embryonic stem cell:	embryo
44	chr11:24518281-24518331	HAEpiC	amniotic membrane:	n/a
45	chr11:24518281-24518331	PANC-1	pancreas:	n/a
46	chr11:24518776-24518826	SK-N-SH	brain:	n/a
47	chr11:24535484-24535534	ProgFib	skin:	n/a
48	chr11:24535484-24535534	U87	brain:	n/a
49	chr11:24518737-24518787	HAEpiC	amniotic membrane:	n/a
50	chr11:24518374-24518424	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr11:24534222..24536357-chr11:24537627..24539546,2	MCF-7	breast:
2	chr11:24534222..24536357-chr11:24537627..24539546,2	MCF-7	breast:
3	chr11:24516764..24518659-chr11:24525705..24528388,2	K562	blood:
4	chr10:67189751..67190645-chr11:24504879..24505471,2	MCF-7	breast:

Variant related genes	Relation type
LUZP2	TF binding region
LUZP2	CpG island
ENSG00000187398	chromatin interactions

Extended variants
information (count: 1192 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1192 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7938928	chr11:24499370-24499371	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189484183	chr11:24499371-24499372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552216609	chr11:24499406-24499407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs112476582	chr11:24499422-24499423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531432393	chr11:24499440-24499441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548364349	chr11:24499546-24499547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139157194	chr11:24499552-24499553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs144404946	chr11:24499557-24499558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs372888707	chr11:24499572-24499573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7117588	chr11:24499598-24499599	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs539555321	chr11:24499689-24499690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11027929	chr11:24499698-24499699	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs111819080	chr11:24499709-24499710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs7103320	chr11:24499744-24499745	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs538094765	chr11:24499786-24499787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs377566192	chr11:24499799-24499800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs61611308	chr11:24499812-24499813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs74817540	chr11:24499821-24499822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs59078092	chr11:24499837-24499838	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs11027930	chr11:24499882-24499883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs181488894	chr11:24499921-24499922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs61657718	chr11:24499958-24499959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs59696949	chr11:24499959-24499960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs7942603	chr11:24500047-24500048	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs562885609	chr11:24500048-24500049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185985852	chr11:24500052-24500053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541671045	chr11:24500073-24500074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191978965	chr11:24500078-24500079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs181159625	chr11:24500130-24500131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs368382509	chr11:24500211-24500212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs7942916	chr11:24500213-24500214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs60418514	chr11:24500215-24500216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs536785832	chr11:24500217-24500218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs61569709	chr11:24500253-24500254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs68050348	chr11:24500255-24500256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs58989743	chr11:24500261-24500262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs10767198	chr11:24500263-24500264	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs7943139	chr11:24500290-24500291	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs7929675	chr11:24500293-24500294	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs564090516	chr11:24500349-24500350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs111678227	chr11:24500400-24500401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs4923190	chr11:24511240-24511241	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs202210905	chr11:24511252-24511253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs77710188	chr11:24511255-24511256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs541027303	chr11:24511259-24511260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs7937325	chr11:24511270-24511271	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs532923710	chr11:24511297-24511298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543139579	chr11:24511300-24511301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs138118923	chr11:24511304-24511305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs531825749	chr11:24511350-24511351	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
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
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Renal cell carcinoma	18194544	CNVD
Myelofibrosis	22110671	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Autism	22102821	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:294 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:24499200-24499800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr11:24499200-24500400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr11:24511200-24511600	Enhancers	HepG2	liver
4	chr11:24517200-24517400	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr11:24517200-24518800	Active TSS	Brain Angular Gyrus	brain
6	chr11:24517200-24519200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
7	chr11:24517200-24519600	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
8	chr11:24517400-24517800	Active TSS	Breast Myoepithelial Primary Cells	Breast
9	chr11:24517400-24518600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
10	chr11:24517400-24520000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
11	chr11:24517600-24517800	Enhancers	Adipose Nuclei	Adipose
12	chr11:24517600-24517800	Enhancers	Brain Hippocampus Middle	brain
13	chr11:24517600-24517800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr11:24517600-24518000	Active TSS	Fetal Brain Female	brain
15	chr11:24517600-24519400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
16	chr11:24517800-24518000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr11:24517800-24518000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
18	chr11:24517800-24518000	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr11:24517800-24518000	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
20	chr11:24517800-24518000	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr11:24517800-24518000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr11:24517800-24518000	Flanking Active TSS	Adipose Nuclei	Adipose
23	chr11:24517800-24518000	Bivalent/Poised TSS	Brain Anterior Caudate	brain
24	chr11:24517800-24518000	Flanking Active TSS	Fetal Brain Male	brain
25	chr11:24517800-24518000	Enhancers	Fetal Heart	heart
26	chr11:24517800-24518000	Bivalent Enhancer	Fetal Intestine Large	intestine
27	chr11:24517800-24518000	Bivalent Enhancer	Fetal Intestine Small	intestine
28	chr11:24517800-24518000	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
29	chr11:24517800-24518000	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
30	chr11:24517800-24518000	Bivalent Enhancer	NHEK	skin
31	chr11:24517800-24518200	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr11:24517800-24518200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
33	chr11:24517800-24518200	Flanking Active TSS	Brain Hippocampus Middle	brain
34	chr11:24517800-24518200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
35	chr11:24517800-24518200	Flanking Bivalent TSS/Enh	Fetal Lung	lung
36	chr11:24517800-24518200	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
37	chr11:24517800-24518200	Active TSS	Fetal Stomach	stomach
38	chr11:24517800-24518200	Bivalent/Poised TSS	NHDF-Ad	bronchial
39	chr11:24517800-24518400	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr11:24517800-24518400	Active TSS	Duodenum Smooth Muscle	Duodenum
41	chr11:24517800-24518400	Flanking Bivalent TSS/Enh	HUVEC	blood vessel
42	chr11:24517800-24518800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr11:24517800-24518800	Bivalent/Poised TSS	Brain Substantia Nigra	brain
44	chr11:24517800-24519000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr11:24517800-24519000	Bivalent/Poised TSS	NHLF	lung
46	chr11:24517800-24519200	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
47	chr11:24517800-24519200	Active TSS	Right Ventricle	heart
48	chr11:24517800-24519400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
49	chr11:24517800-24519400	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr11:24517800-24519400	Active TSS	Brain Cingulate Gyrus	brain

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