Variant report

Variant	nsv469945
Chromosome Location	chr11:24515523-24545353
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:301)
CpG islands
(count:855)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:301 , 50 per page) page: 1 2 3 4 5 6 7

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	chr11:24535771-24536012	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	chr11:24536600-24536828	HepG2	liver:	n/a	n/a
11	CEBPB	chr11:24524696-24525212	MCF-7	breast:	n/a	n/a
12	CEBPB	chr11:24518479-24518656	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD1	chr11:24518674-24518698	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr11:24518563-24518933	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTBP2	chr11:24518245-24518979	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr11:24518689-24518883	LNCaP	prostate:	n/a	n/a
17	CTCF	chr11:24532446-24532497	ProgFib	skin:	n/a	n/a
18	CTCF	chr11:24518700-24518850	HPF	lung:	n/a	n/a
19	CTCF	chr11:24530760-24530910	HAc	cerebellar:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
20	CTCF	chr11:24518660-24518810	NHEK	skin:	n/a	n/a
21	CTCF	chr11:24518760-24518910	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr11:24530785-24530930	GM13977	blood:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
23	CTCF	chr11:24530760-24530910	GM06990	blood:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
24	CTCF	chr11:24529543-24529926	T-47D	breast:	n/a	n/a
25	CTCF	chr11:24530780-24530930	HBMEC	blood vessel:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
26	CTCF	chr11:24529588-24529990	MCF-7	breast:	n/a	n/a
27	CTCF	chr11:24518680-24518830	HEK293	kidney:	n/a	n/a
28	CTCF	chr11:24537300-24537450	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr11:24518648-24518918	Gliobla	brain:	n/a	n/a
30	CTCF	chr11:24518760-24518910	HMEC	breast:	n/a	n/a
31	CTCF	chr11:24529660-24529810	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr11:24530760-24530910	AG04450	lung:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
33	CTCF	chr11:24530800-24530950	AG04450	lung:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
34	CTCF	chr11:24530760-24530910	GM12872	blood:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
35	CTCF	chr11:24518960-24519110	HA-sp	spinal cord:	n/a	n/a
36	CTCF	chr11:24518739-24518790	LNCaP	prostate:	n/a	n/a
37	CTCF	chr11:24537260-24537410	GM12871	blood:	n/a	n/a
38	CTCF	chr11:24518680-24518830	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr11:24530800-24530950	HBMEC	blood vessel:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
40	CTCF	chr11:24530700-24530850	GM12868	blood:	n/a	n/a
41	CTCF	chr11:24518706-24518831	Medullo	brain:	n/a	n/a
42	CTCF	chr11:24537300-24537450	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr11:24537320-24537470	Caco-2	colon:	n/a	n/a
44	CTCF	chr11:24529680-24529830	RPTEC	kidney:	n/a	n/a
45	CTCF	chr11:24537351-24537437	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr11:24530839-24530848	LNCaP	prostate:	n/a	n/a
47	CTCF	chr11:24518660-24518810	MCF-7	breast:	n/a	n/a
48	CTCF	chr11:24518660-24518810	HMEC	breast:	n/a	n/a
49	CTCF	chr11:24537300-24537450	HEK293	kidney:	n/a	n/a
50	CTCF	chr11:24537400-24537550	BE2_C	brain:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:24532473-24532523	AoSMC	blood vessel:	n/a
2	chr11:24532473-24532523	AoSMC	blood vessel:	n/a
3	chr11:24518737-24518787	ovcar-3	ovarian:	n/a
4	chr11:24518374-24518424	GM12878	blood:	n/a
5	chr11:24518225-24518275	SK-N-MC	brain:	n/a
6	chr11:24518367-24518417	SK-N-SH_RA	brain:	n/a
7	chr11:24518776-24518826	SAEC	small airway:	n/a
8	chr11:24532473-24532523	NT2-D1	testis:	n/a
9	chr11:24535484-24535534	MCF-7	breast:	n/a
10	chr11:24518379-24518429	HNPCEpiC	eye:	n/a
11	chr11:24518448-24518498	HL-60	blood:	n/a
12	chr11:24518149-24518199	HNPCEpiC	eye:	n/a
13	chr11:24535484-24535534	HRCEpiC	kidney:	n/a
14	chr11:24518379-24518429	PrEC	prostate:	n/a
15	chr11:24518374-24518424	Hela-S3	cervix:	n/a
16	chr11:24518414-24518464	HL-60	blood:	n/a
17	chr11:24518225-24518275	AG04449	skin:	fetal
18	chr11:24518894-24518944	T-47D	breast:	n/a
19	chr11:24518776-24518826	Hepatocyte	liver:	n/a
20	chr11:24535484-24535534	GM12878	blood:	n/a
21	chr11:24518737-24518787	HRCEpiC	kidney:	n/a
22	chr11:24518414-24518464	Caco-2	colon:	n/a
23	chr11:24518149-24518199	K562	blood:	n/a
24	chr11:24518894-24518944	NB4	blood:	n/a
25	chr11:24518894-24518944	CMK	blood:	n/a
26	chr11:24518379-24518429	HAEpiC	amniotic membrane:	n/a
27	chr11:24518894-24518944	H1-hESC	embryonic stem cell:	embryo
28	chr11:24518367-24518417	PANC-1	pancreas:	n/a
29	chr11:24518379-24518429	RPTEC	kidney:	n/a
30	chr11:24518374-24518424	PANC-1	pancreas:	n/a
31	chr11:24518281-24518331	HNPCEpiC	eye:	n/a
32	chr11:24518149-24518199	AG04449	skin:	fetal
33	chr11:24532473-24532523	HCPEpiC	choroid plexus:	n/a
34	chr11:24535484-24535534	NT2-D1	testis:	n/a
35	chr11:24532473-24532523	AG04449	skin:	fetal
36	chr11:24518367-24518417	HRE	kidney:	n/a
37	chr11:24518149-24518199	SKMC	muscle:	n/a
38	chr11:24518776-24518826	HCF	heart:	n/a
39	chr11:24518374-24518424	GM12891	blood:	n/a
40	chr11:24532473-24532523	GM19239	blood:	n/a
41	chr11:24518281-24518331	MCF10A-Er-Src	breast:	n/a
42	chr11:24532473-24532523	ovcar-3	ovarian:	n/a
43	chr11:24518894-24518944	GM12891	blood:	n/a
44	chr11:24518367-24518417	HCF	heart:	n/a
45	chr11:24518379-24518429	GM19239	blood:	n/a
46	chr11:24518776-24518826	PANC-1	pancreas:	n/a
47	chr11:24518367-24518417	AG04449	skin:	fetal
48	chr11:24518894-24518944	BE2_C	brain:	n/a
49	chr11:24518149-24518199	HCT-116	colon:	n/a
50	chr11:24535484-24535534	SK-N-MC	brain:	n/a

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

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

No data

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

Extended variants
information (count: 1123 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1123 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115694374	chr11:24516142-24516143	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs58494204	chr11:24516171-24516172	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs201082683	chr11:24516184-24516185	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs117374293	chr11:24517211-24517212	Bivalent/Poised TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs191850364	chr11:24517226-24517227	Bivalent/Poised TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs11027951	chr11:24517243-24517244	Bivalent/Poised TSS Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs576607352	chr11:24517244-24517245	Bivalent/Poised TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs542363735	chr11:24517275-24517276	Bivalent/Poised TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs375487416	chr11:24517311-24517312	Bivalent/Poised TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs183615388	chr11:24517350-24517351	Bivalent/Poised TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs527956747	chr11:24517377-24517378	Bivalent/Poised TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs147532356	chr11:24517383-24517384	Bivalent/Poised TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs567342279	chr11:24517386-24517387	Bivalent/Poised TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs374339790	chr11:24517413-24517414	Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs372125024	chr11:24517432-24517433	Bivalent/Poised TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs117325253	chr11:24517437-24517438	Bivalent/Poised TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs570130188	chr11:24517470-24517471	Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs117133012	chr11:24517479-24517480	Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs117489455	chr11:24517480-24517481	Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs565848777	chr11:24517516-24517517	Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs534632143	chr11:24517517-24517518	Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs138857846	chr11:24517543-24517544	Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs398015592	chr11:24517565-24517566	Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs57895694	chr11:24517566-24517567	Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs201386472	chr11:24517570-24517571	Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs58329610	chr11:24517572-24517573	Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs557618429	chr11:24517574-24517575	Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs147027316	chr11:24517575-24517576	Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs67705729	chr11:24517576-24517577	Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs61875584	chr11:24517578-24517579	Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs60419515	chr11:24517580-24517581	Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs61875586	chr11:24517584-24517585	Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs58990881	chr11:24517590-24517591	Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs570953542	chr11:24517594-24517595	Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs35396469	chr11:24517609-24517610	Bivalent/Poised TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs531330856	chr11:24517617-24517618	Bivalent/Poised TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs549393359	chr11:24517699-24517700	Bivalent/Poised TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs182597971	chr11:24517710-24517711	Bivalent/Poised TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556783968	chr11:24517763-24517764	Bivalent/Poised TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs141553193	chr11:24517776-24517777	Bivalent/Poised TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542075225	chr11:24517833-24517834	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs117790082	chr11:24517837-24517838	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs113377895	chr11:24517852-24517853	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs572653291	chr11:24517853-24517854	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs4147349	chr11:24517929-24517930	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs186528146	chr11:24517938-24517939	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs567720589	chr11:24517992-24517993	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs565938338	chr11:24518052-24518053	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs533409564	chr11:24518079-24518080	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs80015235	chr11:24518123-24518124	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	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:291 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:24517200-24517400	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr11:24517200-24518800	Active TSS	Brain Angular Gyrus	brain
3	chr11:24517200-24519200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
4	chr11:24517200-24519600	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
5	chr11:24517400-24517800	Active TSS	Breast Myoepithelial Primary Cells	Breast
6	chr11:24517400-24518600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
7	chr11:24517400-24520000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
8	chr11:24517600-24517800	Enhancers	Adipose Nuclei	Adipose
9	chr11:24517600-24517800	Enhancers	Brain Hippocampus Middle	brain
10	chr11:24517600-24517800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr11:24517600-24518000	Active TSS	Fetal Brain Female	brain
12	chr11:24517600-24519400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
13	chr11:24517800-24518000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr11:24517800-24518000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
15	chr11:24517800-24518000	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr11:24517800-24518000	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
17	chr11:24517800-24518000	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr11:24517800-24518000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr11:24517800-24518000	Flanking Active TSS	Adipose Nuclei	Adipose
20	chr11:24517800-24518000	Bivalent/Poised TSS	Brain Anterior Caudate	brain
21	chr11:24517800-24518000	Flanking Active TSS	Fetal Brain Male	brain
22	chr11:24517800-24518000	Enhancers	Fetal Heart	heart
23	chr11:24517800-24518000	Bivalent Enhancer	Fetal Intestine Large	intestine
24	chr11:24517800-24518000	Bivalent Enhancer	Fetal Intestine Small	intestine
25	chr11:24517800-24518000	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
26	chr11:24517800-24518000	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
27	chr11:24517800-24518000	Bivalent Enhancer	NHEK	skin
28	chr11:24517800-24518200	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr11:24517800-24518200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
30	chr11:24517800-24518200	Flanking Active TSS	Brain Hippocampus Middle	brain
31	chr11:24517800-24518200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
32	chr11:24517800-24518200	Flanking Bivalent TSS/Enh	Fetal Lung	lung
33	chr11:24517800-24518200	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
34	chr11:24517800-24518200	Active TSS	Fetal Stomach	stomach
35	chr11:24517800-24518200	Bivalent/Poised TSS	NHDF-Ad	bronchial
36	chr11:24517800-24518400	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr11:24517800-24518400	Active TSS	Duodenum Smooth Muscle	Duodenum
38	chr11:24517800-24518400	Flanking Bivalent TSS/Enh	HUVEC	blood vessel
39	chr11:24517800-24518800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr11:24517800-24518800	Bivalent/Poised TSS	Brain Substantia Nigra	brain
41	chr11:24517800-24519000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr11:24517800-24519000	Bivalent/Poised TSS	NHLF	lung
43	chr11:24517800-24519200	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
44	chr11:24517800-24519200	Active TSS	Right Ventricle	heart
45	chr11:24517800-24519400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
46	chr11:24517800-24519400	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr11:24517800-24519400	Active TSS	Brain Cingulate Gyrus	brain
48	chr11:24517800-24519400	Bivalent/Poised TSS	NH-A	brain
49	chr11:24517800-24519600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
50	chr11:24517800-24519600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell

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