Variant report

Variant	esv34111
Chromosome Location	chr11:24802669-25090774
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	chr11:25009070-25009258	K562	blood:	n/a	n/a
2	ATF1	chr11:25081871-25082042	K562	blood:	n/a	n/a
3	BACH1	chr11:24803522-24803562	H1-hESC	embryonic stem cell:	n/a	n/a
4	CBX3	chr11:25021767-25022037	K562	blood:	n/a	n/a
5	CEBPB	chr11:24858194-24858509	A549	lung:	n/a	chr11:24858338-24858349
6	CEBPB	chr11:25086865-25087560	IMR90	lung:	n/a	n/a
7	CEBPB	chr11:24989156-24989385	HepG2	liver:	n/a	chr11:24989268-24989279
8	CEBPB	chr11:25087024-25087563	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr11:24863857-24864208	HepG2	liver:	n/a	chr11:24864031-24864042 chr11:24864031-24864040 chr11:24864029-24864040
10	CEBPB	chr11:24956512-24957036	IMR90	lung:	n/a	chr11:24956840-24956851 chr11:24956839-24956852
11	CEBPB	chr11:24987290-24987705	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr11:25039134-25039334	HepG2	liver:	n/a	chr11:25039206-25039217
13	CEBPB	chr11:24818141-24818434	HepG2	liver:	n/a	chr11:24818286-24818297
14	CEBPB	chr11:24858200-24858510	HepG2	liver:	n/a	chr11:24858338-24858349
15	CEBPB	chr11:24815081-24815946	IMR90	lung:	n/a	chr11:24815782-24815793 chr11:24815782-24815791 chr11:24815782-24815791 chr11:24815782-24815791 chr11:24815780-24815793 chr11:24815782-24815791
16	CEBPB	chr11:24842125-24842480	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr11:24858210-24858508	IMR90	lung:	n/a	chr11:24858338-24858349
18	CEBPB	chr11:25059803-25060143	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr11:24805342-24805483	H1-hESC	embryonic stem cell:	n/a	chr11:24805397-24805409
20	CEBPB	chr11:24842090-24842551	IMR90	lung:	n/a	n/a
21	CEBPB	chr11:24818273-24818408	H1-hESC	embryonic stem cell:	n/a	chr11:24818286-24818297
22	CEBPB	chr11:24858166-24858525	Hela-S3	cervix:	n/a	chr11:24858338-24858349
23	CEBPB	chr11:24956653-24956941	Hela-S3	cervix:	n/a	chr11:24956840-24956851 chr11:24956839-24956852
24	CEBPB	chr11:24956664-24957013	HepG2	liver:	n/a	chr11:24956840-24956851 chr11:24956839-24956852
25	CEBPB	chr11:24985312-24985746	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr11:24956492-24956973	H1-hESC	embryonic stem cell:	n/a	chr11:24956840-24956851 chr11:24956839-24956852
27	CEBPB	chr11:24842234-24842452	A549	lung:	n/a	n/a
28	CEBPB	chr11:24956631-24956949	A549	lung:	n/a	chr11:24956840-24956851 chr11:24956839-24956852
29	CEBPB	chr11:24891643-24891951	Hela-S3	cervix:	n/a	chr11:24891795-24891806 chr11:24891793-24891804
30	CEBPB	chr11:25039084-25039295	Hela-S3	cervix:	n/a	chr11:25039206-25039217
31	CEBPB	chr11:24814640-24815409	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr11:24999430-24999689	HepG2	liver:	n/a	chr11:24999574-24999585 chr11:24999555-24999566 chr11:24999597-24999610
33	CEBPB	chr11:24891615-24891858	HepG2	liver:	n/a	chr11:24891795-24891806 chr11:24891793-24891804
34	CEBPZ	chr11:24883085-24883227	HepG2	liver:	n/a	n/a
35	CTCF	chr11:24866464-24866705	MCF-7	breast:	n/a	n/a
36	CTCF	chr11:24866551-24866565	GM19240	blood:	n/a	n/a
37	CTCF	chr11:24866520-24866670	GM12867	blood:	n/a	n/a
38	CTCF	chr11:24990814-24990848	Medullo	brain:	n/a	n/a
39	CTCF	chr11:24866478-24866688	GM19238	blood:	n/a	n/a
40	CTCF	chr11:24841745-24841839	Pancreas_OC	pancreas:	n/a	n/a
41	CTCF	chr11:24866512-24866650	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr11:24866498-24866673	GM12891	blood:	n/a	n/a
43	CTCF	chr11:24866555-24866640	GM12892	blood:	n/a	n/a
44	CTCF	chr11:24803006-24803108	MCF-7	breast:	n/a	chr11:24803063-24803084 chr11:24803066-24803074 chr11:24803062-24803078
45	CTCF	chr11:24866500-24866689	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr11:24802940-24803090	HPAF	blood vessel:	n/a	chr11:24803063-24803084 chr11:24803066-24803074 chr11:24803062-24803078
47	CTCF	chr11:25077081-25077165	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr11:24803036-24803084	Pancreas_OC	pancreas:	n/a	chr11:24803063-24803084 chr11:24803066-24803074 chr11:24803062-24803078
49	CTCF	chr11:25005740-25005890	AG10803	skin:	n/a	n/a
50	CTCF	chr11:24802840-24802990	HEEpiC	esophagus:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:25070714-25070764	AG04449	skin:	fetal
2	chr11:25070714-25070764	A549	lung:	n/a
3	chr11:25001602-25001652	SAEC	small airway:	n/a
4	chr11:25001602-25001652	GM12891	blood:	n/a
5	chr11:25070714-25070764	Caco-2	colon:	n/a
6	chr11:24849257-24849307	ECC-1	luminal epithelium:	n/a
7	chr11:25001602-25001652	HRPEpiC	eye:	n/a
8	chr11:25001602-25001652	PFSK-1	brain:	n/a
9	chr11:25070714-25070764	HMEC	breast:	n/a
10	chr11:24849257-24849307	PrEC	prostate:	n/a
11	chr11:24849257-24849307	IMR90	lung:	fetal
12	chr11:24849257-24849307	HIPEpiC	eye:	n/a
13	chr11:25070714-25070764	HEK293	kidney:	embryo
14	chr11:24849257-24849307	BE2_C	brain:	n/a
15	chr11:25070714-25070764	GM19239	blood:	n/a
16	chr11:24849257-24849307	HL-60	blood:	n/a
17	chr11:25001602-25001652	AG09309	skin:	n/a
18	chr11:25070714-25070764	ProgFib	skin:	n/a
19	chr11:24849257-24849307	MCF-7	breast:	n/a
20	chr11:25001602-25001652	HPAEpiC	pulmonary alveolar:	n/a
21	chr11:24849257-24849307	GM12878	blood:	n/a
22	chr11:25001602-25001652	AG09319	gingival:	n/a
23	chr11:25001602-25001652	LNCaP	prostate:	n/a
24	chr11:24849257-24849307	K562	blood:	n/a
25	chr11:24849257-24849307	HCT-116	colon:	n/a
26	chr11:25001602-25001652	SKMC	muscle:	n/a
27	chr11:25001602-25001652	T-47D	breast:	n/a
28	chr11:25001602-25001652	MCF-7	breast:	n/a
29	chr11:25001602-25001652	HCM	heart:	n/a
30	chr11:25001602-25001652	HAEpiC	amniotic membrane:	n/a
31	chr11:24849257-24849307	U87	brain:	n/a
32	chr11:24849257-24849307	GM19239	blood:	n/a
33	chr11:25070714-25070764	HCT-116	colon:	n/a
34	chr11:25001602-25001652	SK-N-SH	brain:	n/a
35	chr11:25070714-25070764	AoSMC	blood vessel:	n/a
36	chr11:25070714-25070764	AG09309	skin:	n/a
37	chr11:25070714-25070764	GM12892	blood:	n/a
38	chr11:25001602-25001652	HEK293	kidney:	embryo
39	chr11:25001602-25001652	HRCEpiC	kidney:	n/a
40	chr11:25070714-25070764	Hepatocyte	liver:	n/a
41	chr11:25001602-25001652	ProgFib	skin:	n/a
42	chr11:25001602-25001652	Caco-2	colon:	n/a
43	chr11:25070714-25070764	HRPEpiC	eye:	n/a
44	chr11:25070714-25070764	BJ	skin:	n/a
45	chr11:24849257-24849307	Caco-2	colon:	n/a
46	chr11:25070714-25070764	SAEC	small airway:	n/a
47	chr11:25070714-25070764	AG10803	skin:	n/a
48	chr11:25001602-25001652	RPTEC	kidney:	n/a
49	chr11:25001602-25001652	NH-A	brain:	n/a
50	chr11:25001602-25001652	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:22849480..22851377-chr11:25062549..25065391,2	K562	blood:
2	chr11:24903396..24905343-chr11:24907051..24909322,2	MCF-7	breast:
3	chr11:24581046..24581849-chr11:24814221..24814913,2	MCF-7	breast:
4	chr11:24849820..24852040-chr11:24856564..24859378,2	MCF-7	breast:
5	chr11:24884268..24885897-chr11:24886910..24889026,2	K562	blood:
6	chr11:24996714..24999047-chr11:25009138..25011539,2	K562	blood:
7	chr11:24809134..24811557-chr11:24813025..24815138,2	MCF-7	breast:
8	chr11:24963255..24966039-chr11:24972736..24975455,2	MCF-7	breast:
9	chr11:24946469..24947067-chr5:172264421..172265010,2	MCF-7	breast:
10	chr11:25033492..25034324-chr14:24994179..24994819,2	MCF-7	breast:
11	chr11:24849820..24852040-chr11:24856564..24859378,2	MCF-7	breast:
12	chr11:24996714..24999047-chr11:25009138..25011539,2	K562	blood:
13	chr11:24884268..24885897-chr11:24886910..24889026,2	K562	blood:
14	chr11:24802835..24803539-chr11:25755478..25755981,2	MCF-7	breast:
15	chr11:24802681..24803507-chr11:25755699..25756641,3	MCF-7	breast:
16	chr11:24903396..24905343-chr11:24907051..24909322,2	MCF-7	breast:
17	chr11:24963255..24966039-chr11:24972736..24975455,2	MCF-7	breast:
18	chr11:24809134..24811557-chr11:24813025..24815138,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANO3-5	chr11:24913311-24913474	NONHSAT018440
2	lnc-ANO3-5	chr11:24913775-24914067	NONHSAT018440

Variant related genes	Relation type
LUZP2	TF binding region
LUZP2	CpG island
ENSG00000254456	chromatin interactions
ENSG00000246225	chromatin interactions
ENSG00000198168	chromatin interactions

Extended variants
information (count: 4648 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:4648 , 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	rs559918529	chr11:24802723-24802724	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs565426719	chr11:24802742-24802743	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs531284487	chr11:24802754-24802755	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs145565015	chr11:24802755-24802756	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs148903038	chr11:24802827-24802828	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs190954176	chr11:24802832-24802833	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs74517460	chr11:24802950-24802951	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs562803989	chr11:24802964-24802965	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs371869202	chr11:24803003-24803004	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs538638143	chr11:24803004-24803005	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs76276745	chr11:24803032-24803033	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs1386248	chr11:24803061-24803062	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs538176099	chr11:24803074-24803075	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs79744194	chr11:24803095-24803096	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs574595261	chr11:24803099-24803100	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs540282713	chr11:24803105-24803106	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs10525419	chr11:24803133-24803134	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs5790438	chr11:24803134-24803135	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs553911654	chr11:24803144-24803145	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs577050807	chr11:24803157-24803158	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs545811818	chr11:24803186-24803187	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs375412962	chr11:24803194-24803195	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs1386247	chr11:24803201-24803202	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs2129358	chr11:24803203-24803204	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs376043271	chr11:24803217-24803218	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs544903868	chr11:24803258-24803259	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs376323307	chr11:24803261-24803262	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs530241757	chr11:24803269-24803270	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs76779952	chr11:24803331-24803332	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs137921631	chr11:24803332-24803333	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs532499949	chr11:24803348-24803349	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs143388722	chr11:24803360-24803361	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs184047491	chr11:24803364-24803365	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs1386246	chr11:24803380-24803381	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs189130086	chr11:24803426-24803427	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs1386245	chr11:24803438-24803439	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs11028172	chr11:24803458-24803459	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs145743029	chr11:24803469-24803470	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs138757811	chr11:24803545-24803546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142746801	chr11:24803553-24803554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2631398	chr11:24803571-24803572	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs12270328	chr11:24803577-24803578	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs192842067	chr11:24803591-24803592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs561617091	chr11:24803606-24803607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs530360832	chr11:24803618-24803619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150890401	chr11:24803656-24803657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs2631397	chr11:24803665-24803666	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs12277395	chr11:24803678-24803679	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs2631396	chr11:24803726-24803727	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs11820007	chr11:24803738-24803739	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:55)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:243 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:24803000-24804200	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr11:24803000-24805600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr11:24803200-24804000	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr11:24803200-24804600	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr11:24803400-24803800	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr11:24803400-24804000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr11:24803400-24804200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr11:24803400-24804200	Enhancers	Fetal Intestine Large	intestine
9	chr11:24803600-24805200	Enhancers	Fetal Heart	heart
10	chr11:24803800-24804200	Enhancers	H1 Cell Line	embryonic stem cell
11	chr11:24803800-24804400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr11:24804000-24805200	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr11:24804200-24805200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr11:24804200-24805200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr11:24804200-24805400	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr11:24805200-24805400	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr11:24805200-24805600	Enhancers	H9 Cell Line	embryonic stem cell
18	chr11:24805200-24805600	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr11:24805200-24805600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr11:24805400-24805600	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr11:24805600-24805800	Enhancers	H1 Cell Line	embryonic stem cell
22	chr11:24814200-24814600	Enhancers	Fetal Intestine Large	intestine
23	chr11:24814200-24816200	Enhancers	Fetal Heart	heart
24	chr11:24814400-24814800	Enhancers	Adipose Nuclei	Adipose
25	chr11:24814400-24815000	Enhancers	Hela-S3	cervix
26	chr11:24814800-24816200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr11:24815000-24818400	Weak transcription	Hela-S3	cervix
28	chr11:24816200-24816600	Weak transcription	Fetal Heart	heart
29	chr11:24816200-24818400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr11:24816600-24819400	Enhancers	Fetal Heart	heart
31	chr11:24818400-24818600	Enhancers	Hela-S3	cervix
32	chr11:24818400-24819200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr11:24818400-24819400	Enhancers	Fetal Lung	lung
34	chr11:24819400-24820600	Weak transcription	Fetal Heart	heart
35	chr11:24820600-24820800	Enhancers	Fetal Heart	heart
36	chr11:24820800-24821200	Weak transcription	Fetal Heart	heart
37	chr11:24821200-24823000	Enhancers	Fetal Heart	heart
38	chr11:24823000-24823400	Weak transcription	Fetal Heart	heart
39	chr11:24823400-24825000	Enhancers	Fetal Heart	heart
40	chr11:24829200-24830400	Enhancers	Liver	Liver
41	chr11:24832000-24832600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr11:24832600-24834600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr11:24832800-24833200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr11:24832800-24833200	Enhancers	Adipose Nuclei	Adipose
45	chr11:24832800-24833400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr11:24841600-24842400	Enhancers	Stomach Mucosa	stomach
47	chr11:24843800-24844800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr11:24844800-24850000	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr11:24848000-24848200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr11:24848200-24849400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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