Variant report

Variant	nsv897089
Chromosome Location	chr11:24477706-24545353
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	chr11:24518327-24518833	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr11:24518353-24518812	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr11:24537322-24537573	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr11:24518280-24518908	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr11:24530777-24530942	GM12878	blood:	n/a	n/a
6	BATF	chr11:24530725-24530946	GM12878	blood:	n/a	n/a
7	BATF	chr11:24535737-24536035	GM12878	blood:	n/a	n/a
8	BATF	chr11:24535771-24536012	GM12878	blood:	n/a	n/a
9	BHLHE40	chr11:24535932-24535936	GM12878	blood:	n/a	n/a
10	CEBPB	chr11:24499426-24499477	H1-hESC	embryonic stem cell:	n/a	chr11:24499435-24499448 chr11:24499435-24499446 chr11:24499436-24499447 chr11:24499437-24499446
11	CEBPB	chr11:24536600-24536828	HepG2	liver:	n/a	n/a
12	CEBPB	chr11:24502399-24502754	IMR90	lung:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
13	CEBPB	chr11:24504492-24504816	A549	lung:	n/a	chr11:24504658-24504667 chr11:24504658-24504667 chr11:24504656-24504669 chr11:24504658-24504667
14	CEBPB	chr11:24524696-24525212	MCF-7	breast:	n/a	n/a
15	CEBPB	chr11:24487951-24488156	A549	lung:	n/a	chr11:24488014-24488027
16	CEBPB	chr11:24499284-24499616	IMR90	lung:	n/a	chr11:24499435-24499448 chr11:24499435-24499446 chr11:24499436-24499447 chr11:24499437-24499446
17	CEBPB	chr11:24502419-24502734	Hela-S3	cervix:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
18	CEBPB	chr11:24502417-24502754	ECC-1	luminal epithelium:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
19	CEBPB	chr11:24504500-24504875	MCF-7	breast:	n/a	chr11:24504658-24504667 chr11:24504658-24504667 chr11:24504656-24504669 chr11:24504658-24504667
20	CEBPB	chr11:24499282-24499587	Hela-S3	cervix:	n/a	chr11:24499435-24499448 chr11:24499435-24499446 chr11:24499436-24499447 chr11:24499437-24499446
21	CEBPB	chr11:24502446-24502730	H1-hESC	embryonic stem cell:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
22	CEBPB	chr11:24518479-24518656	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr11:24499285-24499571	A549	lung:	n/a	chr11:24499435-24499448 chr11:24499435-24499446 chr11:24499436-24499447 chr11:24499437-24499446
24	CEBPB	chr11:24504498-24504929	MCF-7	breast:	n/a	chr11:24504658-24504667 chr11:24504658-24504667 chr11:24504656-24504669 chr11:24504658-24504667
25	CEBPB	chr11:24500310-24500645	IMR90	lung:	n/a	chr11:24500481-24500492
26	CEBPB	chr11:24502444-24502712	A549	lung:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
27	CEBPB	chr11:24502393-24502740	HepG2	liver:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
28	CEBPB	chr11:24500312-24500613	Hela-S3	cervix:	n/a	chr11:24500481-24500492
29	CEBPB	chr11:24500295-24500561	HepG2	liver:	n/a	chr11:24500481-24500492
30	CEBPB	chr11:24499285-24499610	HepG2	liver:	n/a	chr11:24499435-24499448 chr11:24499435-24499446 chr11:24499436-24499447 chr11:24499437-24499446
31	CHD1	chr11:24518674-24518698	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr11:24518563-24518933	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTBP2	chr11:24518245-24518979	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr11:24521079-24521142	GM13976	blood:	n/a	n/a
35	CTCF	chr11:24530680-24531037	IMR90	lung:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
36	CTCF	chr11:24518620-24518770	SAEC	small airway:	n/a	n/a
37	CTCF	chr11:24495232-24495281	Pancreas_OC	pancreas:	n/a	n/a
38	CTCF	chr11:24518620-24518770	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr11:24530780-24530930	HCPEpiC	choroid plexus:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
40	CTCF	chr11:24505375-24505420	HepG2	liver:	n/a	n/a
41	CTCF	chr11:24529660-24529810	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr11:24518702-24518846	ProgFib	skin:	n/a	n/a
43	CTCF	chr11:24518700-24518850	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr11:24530820-24530970	AG09319	gingival:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
45	CTCF	chr11:24529727-24529798	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr11:24530700-24530850	GM12868	blood:	n/a	n/a
47	CTCF	chr11:24518680-24518830	HEK293	kidney:	n/a	n/a
48	CTCF	chr11:24530760-24530910	HA-sp	spinal cord:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
49	CTCF	chr11:24530780-24530930	HPAF	blood vessel:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
50	CTCF	chr11:24530576-24531002	SK-N-SH	brain:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:24518737-24518787	HEEpiC	esophagus:	n/a
2	chr11:24518737-24518787	HEEpiC	esophagus:	n/a
3	chr11:24518737-24518787	SK-N-MC	brain:	n/a
4	chr11:24518894-24518944	Hepatocyte	liver:	n/a
5	chr11:24518894-24518944	AG09319	gingival:	n/a
6	chr11:24518414-24518464	SK-N-SH_RA	brain:	n/a
7	chr11:24518737-24518787	HPAEpiC	pulmonary alveolar:	n/a
8	chr11:24518379-24518429	HIPEpiC	eye:	n/a
9	chr11:24518381-24518431	HNPCEpiC	eye:	n/a
10	chr11:24518776-24518826	HCT-116	colon:	n/a
11	chr11:24518281-24518331	ECC-1	luminal epithelium:	n/a
12	chr11:24518776-24518826	NH-A	brain:	n/a
13	chr11:24518776-24518826	GM12878	blood:	n/a
14	chr11:24518149-24518199	Jurkat	blood:	n/a
15	chr11:24518381-24518431	CMK	blood:	n/a
16	chr11:24518374-24518424	Hela-S3	cervix:	n/a
17	chr11:24518379-24518429	U87	brain:	n/a
18	chr11:24518379-24518429	GM12878	blood:	n/a
19	chr11:24518448-24518498	NT2-D1	testis:	n/a
20	chr11:24518894-24518944	HMEC	breast:	n/a
21	chr11:24518281-24518331	GM19239	blood:	n/a
22	chr11:24518894-24518944	HPAEpiC	pulmonary alveolar:	n/a
23	chr11:24518281-24518331	AG04449	skin:	fetal
24	chr11:24518149-24518199	HRCEpiC	kidney:	n/a
25	chr11:24518776-24518826	SK-N-MC	brain:	n/a
26	chr11:24518381-24518431	SK-N-MC	brain:	n/a
27	chr11:24518776-24518826	GM12892	blood:	n/a
28	chr11:24518414-24518464	MCF10A-Er-Src	breast:	n/a
29	chr11:24518448-24518498	GM12891	blood:	n/a
30	chr11:24518225-24518275	HNPCEpiC	eye:	n/a
31	chr11:24518281-24518331	AG04450	lung:	fetal
32	chr11:24532473-24532523	T-47D	breast:	n/a
33	chr11:24518367-24518417	RPTEC	kidney:	n/a
34	chr11:24518379-24518429	LNCaP	prostate:	n/a
35	chr11:24518381-24518431	AG10803	skin:	n/a
36	chr11:24518776-24518826	T-47D	breast:	n/a
37	chr11:24518776-24518826	NT2-D1	testis:	n/a
38	chr11:24518225-24518275	Hela-S3	cervix:	n/a
39	chr11:24518367-24518417	SKMC	muscle:	n/a
40	chr11:24518149-24518199	AG09309	skin:	n/a
41	chr11:24518414-24518464	AoSMC	blood vessel:	n/a
42	chr11:24518281-24518331	MCF10A-Er-Src	breast:	n/a
43	chr11:24532473-24532523	GM06990	blood:	n/a
44	chr11:24518894-24518944	CMK	blood:	n/a
45	chr11:24518149-24518199	GM06990	blood:	n/a
46	chr11:24518374-24518424	U87	brain:	n/a
47	chr11:24518379-24518429	Jurkat	blood:	n/a
48	chr11:24518225-24518275	H1-hESC	embryonic stem cell:	embryo
49	chr11:24518225-24518275	NH-A	brain:	n/a
50	chr11:24518381-24518431	HRCEpiC	kidney:	n/a

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: 1354 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1354 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12276835	chr11:24477706-24477707	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188871250	chr11:24477707-24477708	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs141063079	chr11:24477715-24477716	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs180831806	chr11:24477718-24477719	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs372871198	chr11:24477750-24477751	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs186228046	chr11:24477763-24477764	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs542386099	chr11:24477786-24477787	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs565870512	chr11:24477798-24477799	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs534923658	chr11:24477805-24477806	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs78200624	chr11:24477813-24477814	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs144771362	chr11:24477836-24477837	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs11027922	chr11:24477847-24477848	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs556665418	chr11:24477849-24477850	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs552410443	chr11:24477945-24477946	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs375955145	chr11:24479208-24479209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192386225	chr11:24479210-24479211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs545908670	chr11:24479267-24479268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs542173854	chr11:24479331-24479332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561062766	chr11:24479359-24479360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs114353674	chr11:24479368-24479369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546239072	chr11:24479370-24479371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs566124505	chr11:24479468-24479469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183249809	chr11:24479483-24479484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs187908677	chr11:24479487-24479488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs192154763	chr11:24479617-24479618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs184701026	chr11:24479695-24479696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147497307	chr11:24479747-24479748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557511827	chr11:24479809-24479810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574279277	chr11:24479816-24479817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140214070	chr11:24479828-24479829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553442819	chr11:24479831-24479832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs573232630	chr11:24479843-24479844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs75274922	chr11:24479871-24479872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs558749650	chr11:24479891-24479892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575678737	chr11:24479930-24479931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs200843124	chr11:24479972-24479973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138368131	chr11:24479975-24479976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373693982	chr11:24479976-24479977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10834345	chr11:24480040-24480041	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs189516945	chr11:24480102-24480103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529979545	chr11:24480107-24480108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs368060544	chr11:24480146-24480147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs559722355	chr11:24480148-24480149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs117127589	chr11:24480164-24480165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs552262340	chr11:24480178-24480179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs17306915	chr11:24480232-24480233	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs561976642	chr11:24480255-24480256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs192972303	chr11:24480294-24480295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs144059714	chr11:24480326-24480327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs61877499	chr11:24480344-24480345	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:24477400-24478000	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
2	chr11:24479200-24479600	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr11:24479200-24480800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:24482200-24483200	Enhancers	Brain Substantia Nigra	brain
5	chr11:24482600-24482800	Enhancers	Brain Hippocampus Middle	brain
6	chr11:24482600-24483000	Enhancers	Brain Cingulate Gyrus	brain
7	chr11:24483200-24483600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr11:24485400-24485800	Enhancers	Adipose Nuclei	Adipose
9	chr11:24485600-24486400	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr11:24485600-24486400	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr11:24486000-24486400	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr11:24499200-24499800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr11:24499200-24500400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr11:24511200-24511600	Enhancers	HepG2	liver
15	chr11:24517200-24517400	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr11:24517200-24518800	Active TSS	Brain Angular Gyrus	brain
17	chr11:24517200-24519200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
18	chr11:24517200-24519600	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
19	chr11:24517400-24517800	Active TSS	Breast Myoepithelial Primary Cells	Breast
20	chr11:24517400-24518600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
21	chr11:24517400-24520000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
22	chr11:24517600-24517800	Enhancers	Adipose Nuclei	Adipose
23	chr11:24517600-24517800	Enhancers	Brain Hippocampus Middle	brain
24	chr11:24517600-24517800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr11:24517600-24518000	Active TSS	Fetal Brain Female	brain
26	chr11:24517600-24519400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
27	chr11:24517800-24518000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr11:24517800-24518000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
29	chr11:24517800-24518000	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr11:24517800-24518000	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
31	chr11:24517800-24518000	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr11:24517800-24518000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr11:24517800-24518000	Flanking Active TSS	Adipose Nuclei	Adipose
34	chr11:24517800-24518000	Bivalent/Poised TSS	Brain Anterior Caudate	brain
35	chr11:24517800-24518000	Flanking Active TSS	Fetal Brain Male	brain
36	chr11:24517800-24518000	Enhancers	Fetal Heart	heart
37	chr11:24517800-24518000	Bivalent Enhancer	Fetal Intestine Large	intestine
38	chr11:24517800-24518000	Bivalent Enhancer	Fetal Intestine Small	intestine
39	chr11:24517800-24518000	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
40	chr11:24517800-24518000	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
41	chr11:24517800-24518000	Bivalent Enhancer	NHEK	skin
42	chr11:24517800-24518200	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr11:24517800-24518200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
44	chr11:24517800-24518200	Flanking Active TSS	Brain Hippocampus Middle	brain
45	chr11:24517800-24518200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
46	chr11:24517800-24518200	Flanking Bivalent TSS/Enh	Fetal Lung	lung
47	chr11:24517800-24518200	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
48	chr11:24517800-24518200	Active TSS	Fetal Stomach	stomach
49	chr11:24517800-24518200	Bivalent/Poised TSS	NHDF-Ad	bronchial
50	chr11:24517800-24518400	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived

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