Variant report

Variant	nsv832088
Chromosome Location	chr11:23811591-23945749
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	BACH1	chr11:23878232-23878445	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr11:23895497-23895518	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr11:23924606-23925059	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr11:23878241-23878611	A549	lung:	n/a	chr11:23878381-23878392
5	CEBPB	chr11:23883192-23883491	A549	lung:	n/a	chr11:23883330-23883341 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883329-23883340 chr11:23883331-23883340
6	CEBPB	chr11:23891244-23891619	IMR90	lung:	n/a	n/a
7	CEBPB	chr11:23891235-23891626	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr11:23878231-23878550	A549	lung:	n/a	chr11:23878381-23878392
9	CEBPB	chr11:23820772-23821109	A549	lung:	n/a	n/a
10	CEBPB	chr11:23844303-23844514	HepG2	liver:	n/a	chr11:23844394-23844405
11	CEBPB	chr11:23878304-23878551	ECC-1	luminal epithelium:	n/a	chr11:23878381-23878392
12	CEBPB	chr11:23878204-23878582	Hela-S3	cervix:	n/a	chr11:23878381-23878392
13	CEBPB	chr11:23878236-23878516	MCF-7	breast:	n/a	chr11:23878381-23878392
14	CEBPB	chr11:23924606-23925075	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr11:23921929-23922263	A549	lung:	n/a	chr11:23922112-23922125 chr11:23922112-23922123
16	CEBPB	chr11:23829111-23829319	K562	blood:	n/a	chr11:23829233-23829244
17	CEBPB	chr11:23940961-23941367	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr11:23883174-23883477	IMR90	lung:	n/a	chr11:23883330-23883341 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883329-23883340 chr11:23883331-23883340
19	CEBPB	chr11:23820809-23821124	HepG2	liver:	n/a	chr11:23821104-23821117
20	CEBPB	chr11:23887264-23887584	MCF-7	breast:	n/a	n/a
21	CEBPB	chr11:23883286-23883491	K562	blood:	n/a	chr11:23883330-23883341 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883329-23883340 chr11:23883331-23883340
22	CEBPB	chr11:23878214-23878526	MCF-7	breast:	n/a	chr11:23878381-23878392
23	CEBPB	chr11:23944385-23944494	A549	lung:	n/a	chr11:23944390-23944401
24	CEBPB	chr11:23829064-23829390	IMR90	lung:	n/a	chr11:23829233-23829244
25	CEBPB	chr11:23829094-23829349	A549	lung:	n/a	chr11:23829233-23829244
26	CEBPB	chr11:23921978-23922264	HepG2	liver:	n/a	chr11:23922112-23922125 chr11:23922112-23922123
27	CEBPB	chr11:23829075-23829384	HepG2	liver:	n/a	chr11:23829233-23829244
28	CEBPB	chr11:23878299-23878513	A549	lung:	n/a	chr11:23878381-23878392
29	CEBPB	chr11:23820766-23821130	IMR90	lung:	n/a	chr11:23821104-23821117
30	CEBPB	chr11:23891315-23891609	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr11:23844250-23844479	IMR90	lung:	n/a	chr11:23844394-23844405
32	CEBPB	chr11:23891258-23891626	A549	lung:	n/a	n/a
33	CEBPB	chr11:23921942-23922265	IMR90	lung:	n/a	chr11:23922112-23922125 chr11:23922112-23922123
34	CEBPB	chr11:23924608-23925038	A549	lung:	n/a	n/a
35	CEBPB	chr11:23944263-23944509	HepG2	liver:	n/a	chr11:23944390-23944401
36	CEBPB	chr11:23883263-23883345	H1-hESC	embryonic stem cell:	n/a	chr11:23883330-23883341 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883329-23883340 chr11:23883331-23883340
37	CEBPB	chr11:23876110-23876208	HepG2	liver:	n/a	n/a
38	CEBPB	chr11:23887287-23887522	MCF-7	breast:	n/a	n/a
39	CEBPB	chr11:23878199-23878609	IMR90	lung:	n/a	chr11:23878381-23878392
40	CEBPB	chr11:23944291-23944556	IMR90	lung:	n/a	chr11:23944390-23944401
41	CEBPB	chr11:23924628-23925014	IMR90	lung:	n/a	n/a
42	CEBPB	chr11:23883188-23883494	HepG2	liver:	n/a	chr11:23883330-23883341 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883329-23883340 chr11:23883331-23883340
43	CEBPB	chr11:23918963-23919709	IMR90	lung:	n/a	chr11:23919170-23919181
44	CEBPB	chr11:23891244-23891591	HepG2	liver:	n/a	n/a
45	CEBPB	chr11:23878225-23878534	HepG2	liver:	n/a	chr11:23878381-23878392
46	CEBPB	chr11:23876059-23876251	IMR90	lung:	n/a	n/a
47	CTCF	chr11:23855920-23856070	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr11:23855940-23856090	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr11:23856012-23856107	ProgFib	skin:	n/a	n/a
50	CTCF	chr11:23855920-23856070	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:23926945-23926995	K562	blood:	n/a
2	chr11:23926945-23926995	K562	blood:	n/a
3	chr11:23926945-23926995	PFSK-1	brain:	n/a
4	chr11:23895772-23895822	LNCaP	prostate:	n/a
5	chr11:23926945-23926995	RPTEC	kidney:	n/a
6	chr11:23895772-23895822	Hepatocyte	liver:	n/a
7	chr11:23926945-23926995	AG10803	skin:	n/a
8	chr11:23895772-23895822	HPAEpiC	pulmonary alveolar:	n/a
9	chr11:23926945-23926995	SAEC	small airway:	n/a
10	chr11:23895772-23895822	BJ	skin:	n/a
11	chr11:23919652-23919702	AG04449	skin:	fetal
12	chr11:23895772-23895822	U87	brain:	n/a
13	chr11:23926945-23926995	HCT-116	colon:	n/a
14	chr11:23919652-23919702	Jurkat	blood:	n/a
15	chr11:23926945-23926995	Hela-S3	cervix:	n/a
16	chr11:23926945-23926995	GM12878	blood:	n/a
17	chr11:23919652-23919702	GM12892	blood:	n/a
18	chr11:23926945-23926995	HRPEpiC	eye:	n/a
19	chr11:23919652-23919702	HMEC	breast:	n/a
20	chr11:23926945-23926995	NHDF-neo	bronchial:	n/a
21	chr11:23895772-23895822	MCF-7	breast:	n/a
22	chr11:23895772-23895822	HUVEC	blood vessel:	n/a
23	chr11:23926945-23926995	BJ	skin:	n/a
24	chr11:23919652-23919702	GM19239	blood:	n/a
25	chr11:23895772-23895822	BE2_C	brain:	n/a
26	chr11:23926945-23926995	CMK	blood:	n/a
27	chr11:23919652-23919702	HPAEpiC	pulmonary alveolar:	n/a
28	chr11:23926945-23926995	U87	brain:	n/a
29	chr11:23919652-23919702	LNCaP	prostate:	n/a
30	chr11:23919652-23919702	BE2_C	brain:	n/a
31	chr11:23895772-23895822	SK-N-SH	brain:	n/a
32	chr11:23895772-23895822	SAEC	small airway:	n/a
33	chr11:23895772-23895822	HCT-116	colon:	n/a
34	chr11:23919652-23919702	SAEC	small airway:	n/a
35	chr11:23926945-23926995	HMEC	breast:	n/a
36	chr11:23919652-23919702	HUVEC	blood vessel:	n/a
37	chr11:23926945-23926995	HL-60	blood:	n/a
38	chr11:23919652-23919702	U87	brain:	n/a
39	chr11:23919652-23919702	ovcar-3	ovarian:	n/a
40	chr11:23919652-23919702	SK-N-SH_RA	brain:	n/a
41	chr11:23919652-23919702	PFSK-1	brain:	n/a
42	chr11:23926945-23926995	HEEpiC	esophagus:	n/a
43	chr11:23919652-23919702	A549	lung:	n/a
44	chr11:23919652-23919702	IMR90	lung:	fetal
45	chr11:23926945-23926995	PrEC	prostate:	n/a
46	chr11:23919652-23919702	SK-N-SH	brain:	n/a
47	chr11:23895772-23895822	ovcar-3	ovarian:	n/a
48	chr11:23919652-23919702	NB4	blood:	n/a
49	chr11:23895772-23895822	GM06990	blood:	n/a
50	chr11:23919652-23919702	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:23822728..23824994-chr11:23830826..23833587,2	K562	blood:
2	chr11:23822728..23824994-chr11:23830826..23833587,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-17A1.2.1-2	chr11:23826000-23826222	XLOC_009395
2	lnc-RP11-17A1.2.1-2	chr11:23829736-23829778	XLOC_009395
3	lnc-LUZP2-3	chr11:23911055-23911129	NONHSAT018434
4	lnc-RP11-17A1.2.1-2	chr11:23826025-23826144	ENSG00000254861
5	lnc-LUZP2-1	chr11:23818254-23818516	ENSG00000255193
6	lnc-RP11-17A1.2.1-5	chr11:23817463-23817487	NONHSAT018430
7	lnc-RP11-17A1.2.1-6	chr11:23874839-23875216	NONHSAT018433
8	lnc-RP11-17A1.2.1-5	chr11:23818256-23819005	NONHSAT018430
9	lnc-RP11-17A1.2.1-6	chr11:23877391-23877541	NONHSAT018433
10	lnc-LUZP2-3	chr11:23908634-23908905	NONHSAT018434
11	lnc-LUZP2-1	chr11:23816369-23816430	ENSG00000255193

Variant related genes	Relation type
RNU6-783P	TF binding region
ENSG00000254861	TF binding region
RNU6-783P	CpG island
ENSG00000254861	CpG island

Extended variants
information (count: 2852 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2852 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs151261222	chr11:23811597-23811598	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs376496967	chr11:23811622-23811623	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530951884	chr11:23811670-23811671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559522509	chr11:23811671-23811672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs73423747	chr11:23811702-23811703	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs7947028	chr11:23811715-23811716	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs547303618	chr11:23811737-23811738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs4131591	chr11:23811770-23811771	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs75141445	chr11:23811773-23811774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs116513914	chr11:23811784-23811785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs116067228	chr11:23811798-23811799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537927421	chr11:23811804-23811805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554304307	chr11:23811832-23811833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs4131590	chr11:23811851-23811852	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs540186046	chr11:23811856-23811857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183932632	chr11:23811916-23811917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs139972525	chr11:23811929-23811930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545647248	chr11:23811958-23811959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs555305645	chr11:23811987-23811988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs79113695	chr11:23812047-23812048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530935317	chr11:23812053-23812054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs551038186	chr11:23812054-23812055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188775046	chr11:23812058-23812059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs530112132	chr11:23812062-23812063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs111341113	chr11:23812065-23812066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567127619	chr11:23812069-23812070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528202925	chr11:23812075-23812076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376340729	chr11:23812148-23812149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569420522	chr11:23812153-23812154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs537587158	chr11:23812193-23812194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs193025438	chr11:23812214-23812215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574098254	chr11:23812217-23812218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533504589	chr11:23812218-23812219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200418929	chr11:23812257-23812258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553667332	chr11:23812278-23812279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs144453875	chr11:23812314-23812315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546055133	chr11:23812317-23812318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556119005	chr11:23812318-23812319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576175969	chr11:23812320-23812321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571821975	chr11:23812340-23812341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544426861	chr11:23812341-23812342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561315745	chr11:23812346-23812347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184505852	chr11:23812348-23812349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540596343	chr11:23812349-23812350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187677717	chr11:23812358-23812359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7481201	chr11:23812362-23812363	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs34442919	chr11:23812383-23812384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs141466500	chr11:23812407-23812408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569399578	chr11:23812413-23812414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531889650	chr11:23812497-23812498	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
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:224 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:23810400-23812200	Enhancers	Rectal Mucosa Donor 31	rectum
2	chr11:23810600-23811800	Enhancers	Pancreas	Pancrea
3	chr11:23810600-23811800	Enhancers	Dnd41	blood
4	chr11:23810600-23811800	Enhancers	HepG2	liver
5	chr11:23810600-23812000	Enhancers	Stomach Mucosa	stomach
6	chr11:23810600-23812200	Enhancers	Fetal Intestine Large	intestine
7	chr11:23810600-23812200	Enhancers	Fetal Intestine Small	intestine
8	chr11:23810600-23812200	Enhancers	Sigmoid Colon	Sigmoid Colon
9	chr11:23810800-23811800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr11:23811000-23811800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr11:23811000-23811800	Enhancers	HSMM	muscle
12	chr11:23811000-23812200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr11:23811000-23812200	Enhancers	NH-A	brain
14	chr11:23811200-23811600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:23811200-23811600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr11:23811200-23811800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr11:23811200-23811800	Enhancers	Muscle Satellite Cultured Cells	--
18	chr11:23811200-23811800	Enhancers	Osteobl	bone
19	chr11:23811200-23812000	Enhancers	Placenta Amnion	Placenta Amnion
20	chr11:23811400-23811800	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr11:23811600-23812000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr11:23811600-23812000	Enhancers	Hela-S3	cervix
23	chr11:23812000-23812200	Enhancers	Rectal Mucosa Donor 29	rectum
24	chr11:23812200-23818600	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr11:23815000-23815400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr11:23815000-23815600	ZNF genes & repeats	Aorta	Aorta
27	chr11:23818600-23819400	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr11:23818600-23820800	Enhancers	Colon Smooth Muscle	Colon
29	chr11:23819400-23819800	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr11:23819600-23820000	Enhancers	Stomach Mucosa	stomach
31	chr11:23819800-23820600	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr11:23819800-23821000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr11:23820200-23820600	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr11:23820400-23820800	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr11:23820400-23821000	Enhancers	Rectal Smooth Muscle	rectum
36	chr11:23820800-23828200	Weak transcription	Colon Smooth Muscle	Colon
37	chr11:23821000-23822600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr11:23822600-23823400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr11:23823600-23824200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr11:23826200-23826800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr11:23828200-23828600	Enhancers	Colon Smooth Muscle	Colon
42	chr11:23829600-23834800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr11:23848000-23848800	Enhancers	Fetal Lung	lung
44	chr11:23868000-23869200	Enhancers	HUVEC	blood vessel
45	chr11:23868800-23869000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr11:23877800-23878200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr11:23878000-23878400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr11:23878000-23878600	Enhancers	Muscle Satellite Cultured Cells	--
49	chr11:23878200-23878600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr11:23878200-23878600	Enhancers	Fetal Lung	lung

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