Variant report

Variant	nsv553794
Chromosome Location	chr11:24435202-24537624
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	chr11:24530725-24530946	GM12878	blood:	n/a	n/a
6	BATF	chr11:24535737-24536035	GM12878	blood:	n/a	n/a
7	BATF	chr11:24530777-24530942	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	chr11:24500312-24500613	Hela-S3	cervix:	n/a	chr11:24500481-24500492
11	CEBPB	chr11:24518479-24518656	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr11:24499285-24499610	HepG2	liver:	n/a	chr11:24499435-24499448 chr11:24499435-24499446 chr11:24499436-24499447 chr11:24499437-24499446
13	CEBPB	chr11:24459325-24459347	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr11:24499284-24499616	IMR90	lung:	n/a	chr11:24499435-24499448 chr11:24499435-24499446 chr11:24499436-24499447 chr11:24499437-24499446
15	CEBPB	chr11:24459149-24459440	IMR90	lung:	n/a	chr11:24459283-24459294
16	CEBPB	chr11:24499426-24499477	H1-hESC	embryonic stem cell:	n/a	chr11:24499435-24499448 chr11:24499435-24499446 chr11:24499436-24499447 chr11:24499437-24499446
17	CEBPB	chr11:24504500-24504875	MCF-7	breast:	n/a	chr11:24504658-24504667 chr11:24504658-24504667 chr11:24504656-24504669 chr11:24504658-24504667
18	CEBPB	chr11:24500295-24500561	HepG2	liver:	n/a	chr11:24500481-24500492
19	CEBPB	chr11:24502399-24502754	IMR90	lung:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
20	CEBPB	chr11:24504492-24504816	A549	lung:	n/a	chr11:24504658-24504667 chr11:24504658-24504667 chr11:24504656-24504669 chr11:24504658-24504667
21	CEBPB	chr11:24500310-24500645	IMR90	lung:	n/a	chr11:24500481-24500492
22	CEBPB	chr11:24502444-24502712	A549	lung:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
23	CEBPB	chr11:24459132-24459434	HepG2	liver:	n/a	chr11:24459283-24459294
24	CEBPB	chr11:24524696-24525212	MCF-7	breast:	n/a	n/a
25	CEBPB	chr11:24499285-24499571	A549	lung:	n/a	chr11:24499435-24499448 chr11:24499435-24499446 chr11:24499436-24499447 chr11:24499437-24499446
26	CEBPB	chr11:24536600-24536828	HepG2	liver:	n/a	n/a
27	CEBPB	chr11:24502446-24502730	H1-hESC	embryonic stem cell:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
28	CEBPB	chr11:24502393-24502740	HepG2	liver:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
29	CEBPB	chr11:24487951-24488156	A549	lung:	n/a	chr11:24488014-24488027
30	CEBPB	chr11:24502417-24502754	ECC-1	luminal epithelium:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
31	CEBPB	chr11:24502419-24502734	Hela-S3	cervix:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
32	CEBPB	chr11:24504498-24504929	MCF-7	breast:	n/a	chr11:24504658-24504667 chr11:24504658-24504667 chr11:24504656-24504669 chr11:24504658-24504667
33	CEBPB	chr11:24499282-24499587	Hela-S3	cervix:	n/a	chr11:24499435-24499448 chr11:24499435-24499446 chr11:24499436-24499447 chr11:24499437-24499446
34	CHD1	chr11:24518674-24518698	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr11:24518563-24518933	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTBP2	chr11:24518245-24518979	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr11:24530680-24531037	IMR90	lung:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
38	CTCF	chr11:24518680-24518830	HEK293	kidney:	n/a	n/a
39	CTCF	chr11:24530780-24530930	HCFaa	heart:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
40	CTCF	chr11:24530680-24530830	GM12871	blood:	n/a	n/a
41	CTCF	chr11:24537300-24537450	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr11:24518604-24518946	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr11:24505280-24505430	Caco-2	colon:	n/a	chr11:24505408-24505424
44	CTCF	chr11:24530788-24530893	Medullo	brain:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
45	CTCF	chr11:24530660-24530810	HMEC	breast:	n/a	n/a
46	CTCF	chr11:24537345-24537441	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr11:24472294-24472369	LNCaP	prostate:	n/a	n/a
48	CTCF	chr11:24530760-24530910	HFF	foreskin:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
49	CTCF	chr11:24530730-24530974	HUVEC	blood vessel:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870
50	CTCF	chr11:24530780-24530930	HCPEpiC	choroid plexus:	n/a	chr11:24530853-24530869 chr11:24530854-24530875 chr11:24530852-24530870

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:24518414-24518464	HMEC	breast:	n/a
2	chr11:24518737-24518787	AG10803	skin:	n/a
3	chr11:24469509-24469559	HRE	kidney:	n/a
4	chr11:24518414-24518464	HIPEpiC	eye:	n/a
5	chr11:24518894-24518944	T-47D	breast:	n/a
6	chr11:24469509-24469559	MCF-7	breast:	n/a
7	chr11:24518737-24518787	HRPEpiC	eye:	n/a
8	chr11:24518281-24518331	NB4	blood:	n/a
9	chr11:24518374-24518424	HNPCEpiC	eye:	n/a
10	chr11:24518374-24518424	SK-N-SH	brain:	n/a
11	chr11:24532473-24532523	IMR90	lung:	fetal
12	chr11:24535484-24535534	AG09319	gingival:	n/a
13	chr11:24518776-24518826	MCF-7	breast:	n/a
14	chr11:24436937-24436987	MCF10A-Er-Src	breast:	n/a
15	chr11:24436937-24436987	SK-N-MC	brain:	n/a
16	chr11:24518225-24518275	NHDF-neo	bronchial:	n/a
17	chr11:24518281-24518331	SAEC	small airway:	n/a
18	chr11:24518379-24518429	Jurkat	blood:	n/a
19	chr11:24436937-24436987	AG10803	skin:	n/a
20	chr11:24518448-24518498	Hela-S3	cervix:	n/a
21	chr11:24469509-24469559	Jurkat	blood:	n/a
22	chr11:24518414-24518464	LNCaP	prostate:	n/a
23	chr11:24518225-24518275	Hepatocyte	liver:	n/a
24	chr11:24518448-24518498	HEK293	kidney:	embryo
25	chr11:24535484-24535534	U87	brain:	n/a
26	chr11:24518894-24518944	A549	lung:	n/a
27	chr11:24532473-24532523	HRCEpiC	kidney:	n/a
28	chr11:24518737-24518787	HRE	kidney:	n/a
29	chr11:24518737-24518787	Hepatocyte	liver:	n/a
30	chr11:24518414-24518464	HCPEpiC	choroid plexus:	n/a
31	chr11:24518737-24518787	HL-60	blood:	n/a
32	chr11:24518894-24518944	MCF-7	breast:	n/a
33	chr11:24518225-24518275	AG10803	skin:	n/a
34	chr11:24469509-24469559	GM06990	blood:	n/a
35	chr11:24518381-24518431	AoSMC	blood vessel:	n/a
36	chr11:24518381-24518431	SK-N-SH_RA	brain:	n/a
37	chr11:24518448-24518498	NHBE	bronchial:	n/a
38	chr11:24518367-24518417	GM19239	blood:	n/a
39	chr11:24518149-24518199	GM12878	blood:	n/a
40	chr11:24518737-24518787	HCF	heart:	n/a
41	chr11:24518225-24518275	NB4	blood:	n/a
42	chr11:24518381-24518431	PrEC	prostate:	n/a
43	chr11:24518367-24518417	MCF-7	breast:	n/a
44	chr11:24518281-24518331	HCM	heart:	n/a
45	chr11:24518414-24518464	H1-hESC	embryonic stem cell:	embryo
46	chr11:24532473-24532523	NB4	blood:	n/a
47	chr11:24518414-24518464	HCT-116	colon:	n/a
48	chr11:24518414-24518464	Caco-2	colon:	n/a
49	chr11:24518374-24518424	RPTEC	kidney:	n/a
50	chr11:24518776-24518826	AG09319	gingival:	n/a

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	chr10:67189751..67190645-chr11:24504879..24505471,2	MCF-7	breast:

Variant related genes	Relation type
LUZP2	TF binding region
ENSG00000207252	TF binding region
LUZP2	CpG island
ENSG00000207252	CpG island
ENSG00000187398	chromatin interactions

Extended variants
information (count: 1881 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1881 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4307720	chr11:24435202-24435203	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs150141887	chr11:24435226-24435227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528283661	chr11:24435288-24435289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539910756	chr11:24435308-24435309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs191977780	chr11:24435318-24435319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185357094	chr11:24435324-24435325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189808254	chr11:24435331-24435332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532091778	chr11:24435352-24435353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548768519	chr11:24435357-24435358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201035337	chr11:24435396-24435397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs565580326	chr11:24435399-24435400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112751610	chr11:24435428-24435429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375123743	chr11:24435544-24435545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369224687	chr11:24435568-24435569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571436043	chr11:24435593-24435594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537068156	chr11:24435607-24435608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138647659	chr11:24435611-24435612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200744110	chr11:24435626-24435627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2403929	chr11:24435629-24435630	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs548915320	chr11:24435688-24435689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368581967	chr11:24435711-24435712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537204370	chr11:24435749-24435750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372172059	chr11:24435779-24435780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184365107	chr11:24435793-24435794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs16912548	chr11:24435797-24435798	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs140419391	chr11:24435818-24435819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564801699	chr11:24435840-24435841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145595092	chr11:24435881-24435882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188035483	chr11:24435891-24435892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371088681	chr11:24435914-24435915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555551715	chr11:24435932-24435933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570851631	chr11:24435934-24435935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563487203	chr11:24435947-24435948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138105590	chr11:24435951-24435952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549113973	chr11:24435968-24435969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565815515	chr11:24435990-24435991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538384961	chr11:24436012-24436013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551127357	chr11:24436014-24436015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11027885	chr11:24436022-24436023	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs536903817	chr11:24436037-24436038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs59296326	chr11:24436041-24436042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374622753	chr11:24436057-24436058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576475765	chr11:24436058-24436059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200555016	chr11:24436059-24436060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563039498	chr11:24436060-24436061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs60679769	chr11:24436062-24436063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs61875434	chr11:24436063-24436064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34727201	chr11:24436064-24436065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556928048	chr11:24436073-24436074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149469940	chr11:24436098-24436099	Weak transcription	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:330 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:24431400-24440200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:24437000-24437200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:24437200-24437400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:24437400-24437800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr11:24439600-24440200	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr11:24440200-24442800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr11:24442800-24443400	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr11:24443000-24444200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr11:24443200-24443600	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr11:24443200-24443600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr11:24443200-24443600	Enhancers	HMEC	breast
12	chr11:24443200-24444000	Enhancers	NHEK	skin
13	chr11:24449600-24450000	Enhancers	Fetal Intestine Large	intestine
14	chr11:24449800-24450200	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr11:24464600-24467600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
16	chr11:24465400-24466800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr11:24465800-24466200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr11:24465800-24467000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
19	chr11:24465800-24467200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
20	chr11:24465800-24467800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
21	chr11:24466000-24467600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
22	chr11:24466400-24467600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
23	chr11:24467200-24469200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr11:24467400-24471200	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr11:24467600-24468600	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr11:24467600-24468600	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr11:24467600-24469000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr11:24467800-24470600	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr11:24468600-24471600	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr11:24468600-24471600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr11:24469000-24471000	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr11:24469200-24470000	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr11:24469200-24470600	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr11:24469400-24470200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr11:24470000-24470800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr11:24470600-24471000	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr11:24470800-24471200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr11:24474800-24475600	Enhancers	Hela-S3	cervix
39	chr11:24477400-24478000	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
40	chr11:24479200-24479600	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr11:24479200-24480800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:24482200-24483200	Enhancers	Brain Substantia Nigra	brain
43	chr11:24482600-24482800	Enhancers	Brain Hippocampus Middle	brain
44	chr11:24482600-24483000	Enhancers	Brain Cingulate Gyrus	brain
45	chr11:24483200-24483600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr11:24485400-24485800	Enhancers	Adipose Nuclei	Adipose
47	chr11:24485600-24486400	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr11:24485600-24486400	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr11:24486000-24486400	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr11:24499200-24499800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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