Variant report

Variant	nsv897128
Chromosome Location	chr11:25294229-25656452
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	ATF1	chr11:25544434-25544847	K562	blood:	n/a	n/a
2	BACH1	chr11:25623762-25623935	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr11:25630449-25630466	K562	blood:	n/a	n/a
4	CCNT2	chr11:25320905-25321211	K562	blood:	n/a	n/a
5	CEBPB	chr11:25408690-25408973	HepG2	liver:	n/a	chr11:25408812-25408823 chr11:25408812-25408825 chr11:25408738-25408750
6	CEBPB	chr11:25320045-25320349	K562	blood:	n/a	chr11:25320182-25320193
7	CEBPB	chr11:25374297-25374614	HepG2	liver:	n/a	n/a
8	CEBPB	chr11:25320002-25320364	IMR90	lung:	n/a	chr11:25320182-25320193
9	CEBPB	chr11:25414710-25414922	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr11:25322407-25322509	HepG2	liver:	n/a	n/a
11	CEBPB	chr11:25538655-25539020	IMR90	lung:	n/a	n/a
12	CEBPB	chr11:25445309-25445536	HepG2	liver:	n/a	chr11:25445395-25445406
13	CEBPB	chr11:25538674-25539021	HepG2	liver:	n/a	n/a
14	CEBPB	chr11:25654759-25654990	H1-hESC	embryonic stem cell:	n/a	chr11:25654930-25654941
15	CEBPB	chr11:25320902-25320977	HepG2	liver:	n/a	chr11:25320927-25320938
16	CEBPB	chr11:25564061-25564326	HepG2	liver:	n/a	chr11:25564202-25564213
17	CEBPB	chr11:25320004-25320361	HepG2	liver:	n/a	chr11:25320182-25320193
18	CEBPB	chr11:25588146-25588479	HepG2	liver:	n/a	n/a
19	CEBPB	chr11:25316988-25317332	A549	lung:	n/a	chr11:25317135-25317146
20	CEBPB	chr11:25531713-25531942	HepG2	liver:	n/a	chr11:25531815-25531828 chr11:25531835-25531846 chr11:25531834-25531847
21	CEBPB	chr11:25588189-25588366	HepG2	liver:	n/a	n/a
22	CEBPB	chr11:25588263-25588319	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr11:25607889-25608194	HepG2	liver:	n/a	n/a
24	CEBPB	chr11:25418447-25418894	HepG2	liver:	n/a	chr11:25418552-25418563 chr11:25418542-25418555 chr11:25418543-25418554 chr11:25418554-25418563
25	CEBPB	chr11:25431729-25431969	HepG2	liver:	n/a	chr11:25431857-25431868 chr11:25431855-25431872 chr11:25431856-25431869
26	CEBPB	chr11:25559142-25559348	A549	lung:	n/a	chr11:25559275-25559286
27	CEBPB	chr11:25317003-25317327	K562	blood:	n/a	chr11:25317135-25317146
28	CEBPB	chr11:25654767-25655104	IMR90	lung:	n/a	chr11:25654930-25654941
29	CEBPB	chr11:25400561-25400761	HepG2	liver:	n/a	chr11:25400627-25400638
30	CEBPB	chr11:25588119-25588837	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr11:25564104-25564335	H1-hESC	embryonic stem cell:	n/a	chr11:25564202-25564213
32	CEBPB	chr11:25320010-25320354	Hela-S3	cervix:	n/a	chr11:25320182-25320193
33	CEBPB	chr11:25581962-25582274	HepG2	liver:	n/a	chr11:25582118-25582127 chr11:25582118-25582127 chr11:25582118-25582127 chr11:25582118-25582127 chr11:25582116-25582129 chr11:25582116-25582129 chr11:25582116-25582127 chr11:25582117-25582128
34	CEBPB	chr11:25654801-25655170	MCF-7	breast:	n/a	chr11:25654930-25654941
35	CEBPB	chr11:25352386-25352658	HepG2	liver:	n/a	chr11:25352538-25352549 chr11:25352535-25352552
36	CEBPB	chr11:25416211-25416733	Hela-S3	cervix:	n/a	chr11:25416574-25416585 chr11:25416289-25416302
37	CEBPB	chr11:25344243-25344541	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr11:25419380-25419622	HepG2	liver:	n/a	n/a
39	CEBPB	chr11:25320044-25320317	H1-hESC	embryonic stem cell:	n/a	chr11:25320182-25320193
40	CEBPB	chr11:25654846-25655049	MCF-7	breast:	n/a	chr11:25654930-25654941
41	CEBPB	chr11:25317085-25317365	H1-hESC	embryonic stem cell:	n/a	chr11:25317135-25317146
42	CEBPB	chr11:25654764-25655080	HepG2	liver:	n/a	chr11:25654930-25654941
43	CEBPB	chr11:25418371-25418804	Hela-S3	cervix:	n/a	chr11:25418552-25418563 chr11:25418542-25418555 chr11:25418543-25418554 chr11:25418554-25418563
44	CEBPB	chr11:25408737-25408938	Hela-S3	cervix:	n/a	chr11:25408812-25408823 chr11:25408812-25408825 chr11:25408738-25408750
45	CEBPB	chr11:25654797-25655096	A549	lung:	n/a	chr11:25654930-25654941
46	CEBPB	chr11:25557121-25557458	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr11:25400585-25400667	K562	blood:	n/a	chr11:25400627-25400638
48	CEBPB	chr11:25636635-25637011	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr11:25317005-25317377	Hela-S3	cervix:	n/a	chr11:25317135-25317146
50	CEBPB	chr11:25316988-25317320	HepG2	liver:	n/a	chr11:25317135-25317146

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:25537461-25537511	NHBE	bronchial:	n/a
2	chr11:25537461-25537511	NHBE	bronchial:	n/a
3	chr11:25623877-25623927	Hepatocyte	liver:	n/a
4	chr11:25537461-25537511	Hepatocyte	liver:	n/a
5	chr11:25537660-25537710	CMK	blood:	n/a
6	chr11:25623877-25623927	PANC-1	pancreas:	n/a
7	chr11:25623877-25623927	H1-hESC	embryonic stem cell:	embryo
8	chr11:25537461-25537511	MCF-7	breast:	n/a
9	chr11:25537660-25537710	HCM	heart:	n/a
10	chr11:25537461-25537511	PFSK-1	brain:	n/a
11	chr11:25537461-25537511	IMR90	lung:	fetal
12	chr11:25537660-25537710	HepG2	liver:	n/a
13	chr11:25537660-25537710	SK-N-SH_RA	brain:	n/a
14	chr11:25623877-25623927	SK-N-MC	brain:	n/a
15	chr11:25623877-25623927	RPTEC	kidney:	n/a
16	chr11:25537660-25537710	HRPEpiC	eye:	n/a
17	chr11:25623877-25623927	AoSMC	blood vessel:	n/a
18	chr11:25623877-25623927	MCF10A-Er-Src	breast:	n/a
19	chr11:25537461-25537511	HepG2	liver:	n/a
20	chr11:25623877-25623927	HCPEpiC	choroid plexus:	n/a
21	chr11:25537660-25537710	ECC-1	luminal epithelium:	n/a
22	chr11:25537461-25537511	HRCEpiC	kidney:	n/a
23	chr11:25537660-25537710	BJ	skin:	n/a
24	chr11:25537461-25537511	NH-A	brain:	n/a
25	chr11:25537461-25537511	SAEC	small airway:	n/a
26	chr11:25537660-25537710	AG09309	skin:	n/a
27	chr11:25537660-25537710	HEK293	kidney:	embryo
28	chr11:25537461-25537511	CMK	blood:	n/a
29	chr11:25537461-25537511	HAEpiC	amniotic membrane:	n/a
30	chr11:25623877-25623927	HRPEpiC	eye:	n/a
31	chr11:25623877-25623927	SKMC	muscle:	n/a
32	chr11:25623877-25623927	HRE	kidney:	n/a
33	chr11:25537461-25537511	HCF	heart:	n/a
34	chr11:25537461-25537511	HL-60	blood:	n/a
35	chr11:25623877-25623927	SAEC	small airway:	n/a
36	chr11:25537461-25537511	AG04449	skin:	fetal
37	chr11:25537660-25537710	HAEpiC	amniotic membrane:	n/a
38	chr11:25623877-25623927	NHDF-neo	bronchial:	n/a
39	chr11:25537461-25537511	Caco-2	colon:	n/a
40	chr11:25623877-25623927	Caco-2	colon:	n/a
41	chr11:25623877-25623927	U87	brain:	n/a
42	chr11:25537461-25537511	HCT-116	colon:	n/a
43	chr11:25623877-25623927	AG09319	gingival:	n/a
44	chr11:25537660-25537710	PFSK-1	brain:	n/a
45	chr11:25537660-25537710	SAEC	small airway:	n/a
46	chr11:25623877-25623927	T-47D	breast:	n/a
47	chr11:25537660-25537710	AG04449	skin:	fetal
48	chr11:25623877-25623927	SK-N-SH_RA	brain:	n/a
49	chr11:25537660-25537710	K562	blood:	n/a
50	chr11:25537660-25537710	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:25415265..25417629-chr11:25420045..25422355,2	MCF-7	breast:
2	chr11:25383494..25385601-chr11:25405525..25407824,2	K562	blood:
3	chr11:25576575..25578534-chr11:25581809..25585257,3	K562	blood:
4	chr11:25415265..25417629-chr11:25420045..25422355,2	MCF-7	breast:
5	chr11:25619794..25621822-chr11:25698109..25699950,2	K562	blood:
6	chr11:25409717..25412034-chr11:25416145..25417905,2	K562	blood:
7	chr11:25527410..25530094-chr11:25531734..25534138,2	K562	blood:
8	chr11:25409717..25412034-chr11:25416145..25417905,2	K562	blood:
9	chr11:25576575..25578534-chr11:25581809..25585257,3	K562	blood:
10	chr11:25527410..25530094-chr11:25531734..25534138,2	K562	blood:
11	chr11:25383494..25385601-chr11:25405525..25407824,2	K562	blood:
12	chr11:25378401..25379146-chr13:47547550..47548348,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MUC15-3	chr11:25610021-25610341	NONHSAT018448
2	lnc-MUC15-3	chr11:25609916-25610413	NONHSAT018446
3	lnc-LUZP2-2	chr11:25652266-25652587	NONHSAT018449
4	lnc-MUC15-3	chr11:25609802-25609808	NONHSAT018446
5	lnc-MUC15-3	chr11:25610021-25610389	NONHSAT018447

Variant related genes	Relation type
ENSG00000265837	TF binding region
ENSG00000255454	TF binding region
RPL36AP40	TF binding region
ENSG00000265837	CpG island
ENSG00000255454	CpG island
RPL36AP40	CpG island

Extended variants
information (count: 4632 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:4632 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6484128	chr11:25302402-25302403	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs568187884	chr11:25302410-25302411	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs533633316	chr11:25302423-25302424	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs553378599	chr11:25302427-25302428	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs186270981	chr11:25302463-25302464	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs539009635	chr11:25302478-25302479	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs11028555	chr11:25302490-25302491	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs575804050	chr11:25302508-25302509	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs553045652	chr11:25302535-25302536	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs544839736	chr11:25302536-25302537	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs11584673	chr11:25302539-25302540	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs577667437	chr11:25302567-25302568	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs561316298	chr11:25302569-25302570	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs574911921	chr11:25302583-25302584	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs370896691	chr11:25302585-25302586	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs148086688	chr11:25302599-25302600	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs113791756	chr11:25302634-25302635	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs532566421	chr11:25302639-25302640	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs552557215	chr11:25302670-25302671	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs111376177	chr11:25302672-25302673	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs531497012	chr11:25302673-25302674	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs2194904	chr11:25302675-25302676	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs2194903	chr11:25302699-25302700	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs72871991	chr11:25302700-25302701	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs547103896	chr11:25302701-25302702	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs369830551	chr11:25302706-25302707	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs570173958	chr11:25302714-25302715	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs539052363	chr11:25302715-25302716	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs186288154	chr11:25302722-25302723	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs113050045	chr11:25302723-25302724	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs183228875	chr11:25302726-25302727	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs555174753	chr11:25302728-25302729	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs371587277	chr11:25302762-25302763	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs113687034	chr11:25302768-25302769	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs2217030	chr11:25302772-25302773	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs35499039	chr11:25302800-25302801	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs554309831	chr11:25302802-25302803	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs545817790	chr11:25302813-25302814	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs577411181	chr11:25302821-25302822	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs546259997	chr11:25302822-25302823	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs186476890	chr11:25302850-25302851	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs189070667	chr11:25302851-25302852	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs190517824	chr11:25302861-25302862	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs541777059	chr11:25302869-25302870	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs561981427	chr11:25302880-25302881	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs527490502	chr11:25302881-25302882	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs183774528	chr11:25302893-25302894	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs570261449	chr11:25302895-25302896	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs181238416	chr11:25302899-25302900	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs532857028	chr11:25302901-25302902	Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:25302400-25303000	Active TSS	HUES6 Cell Line	embryonic stem cell
2	chr11:25312400-25314800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr11:25313600-25313800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:25313800-25322800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr11:25315000-25316400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr11:25321200-25321400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr11:25339400-25340000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr11:25339400-25340600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr11:25340000-25340400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr11:25340400-25340800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr11:25372400-25373000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr11:25377200-25378400	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr11:25378200-25380200	Enhancers	Fetal Heart	heart
14	chr11:25380200-25381600	Weak transcription	Fetal Heart	heart
15	chr11:25381600-25382800	Enhancers	Fetal Heart	heart
16	chr11:25404200-25404400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr11:25405400-25410000	Weak transcription	Right Atrium	heart
18	chr11:25424000-25424200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
19	chr11:25444800-25445600	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr11:25445000-25445400	Enhancers	H1 Cell Line	embryonic stem cell
21	chr11:25445000-25445400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr11:25445000-25445400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr11:25445000-25445400	Enhancers	Small Intestine	intestine
24	chr11:25445200-25445800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr11:25445200-25446000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr11:25446800-25447400	Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr11:25456000-25456800	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr11:25456400-25457800	Enhancers	HepG2	liver
29	chr11:25456600-25457400	Enhancers	Liver	Liver
30	chr11:25460000-25460200	Enhancers	Fetal Kidney	kidney
31	chr11:25462400-25463000	Enhancers	Brain Germinal Matrix	brain
32	chr11:25462400-25463200	Enhancers	Fetal Lung	lung
33	chr11:25462400-25464400	Enhancers	Fetal Stomach	stomach
34	chr11:25462600-25463400	Enhancers	Fetal Kidney	kidney
35	chr11:25462600-25464200	Enhancers	Adipose Nuclei	Adipose
36	chr11:25462800-25464200	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr11:25463000-25464200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr11:25463000-25464400	Enhancers	Colon Smooth Muscle	Colon
39	chr11:25463200-25463400	Enhancers	Liver	Liver
40	chr11:25463200-25464000	Weak transcription	Fetal Lung	lung
41	chr11:25464000-25464400	Enhancers	Fetal Lung	lung
42	chr11:25464200-25464400	Enhancers	Liver	Liver
43	chr11:25464400-25464800	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr11:25470600-25471000	Enhancers	Fetal Brain Male	brain
45	chr11:25470600-25471200	Enhancers	Fetal Lung	lung
46	chr11:25475200-25475600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr11:25478400-25479400	Enhancers	Brain Germinal Matrix	brain
48	chr11:25498800-25499600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr11:25503400-25503600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr11:25503600-25507400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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