Variant report

Variant	nsv832165
Chromosome Location	chr11:57806024-58009076
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	ARID3A	chr11:57932975-57933388	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:57826426-57826764	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:57843315-57843588	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:57828540-57829181	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:57823577-57823798	HepG2	liver:	n/a	n/a
6	ATF1	chr11:57829297-57829610	K562	blood:	n/a	n/a
7	ATF3	chr11:57829338-57829562	K562	blood:	n/a	chr11:57829461-57829476
8	BACH1	chr11:57963487-57963614	K562	blood:	n/a	n/a
9	BATF	chr11:57820385-57820540	GM12878	blood:	n/a	n/a
10	CEBPB	chr11:57826475-57827552	IMR90	lung:	n/a	n/a
11	CEBPB	chr11:57941813-57942112	HepG2	liver:	n/a	chr11:57941976-57941987
12	CEBPB	chr11:57933895-57934195	HepG2	liver:	n/a	chr11:57934032-57934043
13	CEBPB	chr11:57843424-57843525	HepG2	liver:	n/a	n/a
14	CEBPB	chr11:57903617-57903914	IMR90	lung:	n/a	chr11:57903754-57903767 chr11:57903754-57903765 chr11:57903754-57903767 chr11:57903754-57903767
15	CEBPB	chr11:57829149-57829448	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr11:57843315-57843635	HepG2	liver:	n/a	n/a
17	CEBPB	chr11:57841527-57841650	A549	lung:	n/a	chr11:57841555-57841566
18	CEBPB	chr11:57823507-57823852	HepG2	liver:	n/a	chr11:57823696-57823707
19	CEBPB	chr11:57843233-57843677	IMR90	lung:	n/a	n/a
20	CEBPB	chr11:57933079-57933336	HepG2	liver:	n/a	n/a
21	CEBPB	chr11:57959325-57959513	HepG2	liver:	n/a	chr11:57959408-57959419 chr11:57959450-57959462
22	CEBPB	chr11:57934976-57935084	HepG2	liver:	n/a	chr11:57935022-57935033
23	CEBPB	chr11:57932970-57933434	HepG2	liver:	n/a	chr11:57933335-57933346
24	CEBPB	chr11:57948145-57948399	HepG2	liver:	n/a	n/a
25	CEBPB	chr11:57933268-57933270	IMR90	lung:	n/a	n/a
26	CEBPB	chr11:57841532-57841640	HepG2	liver:	n/a	chr11:57841555-57841566
27	CEBPB	chr11:57807051-57807317	HepG2	liver:	n/a	n/a
28	CEBPB	chr11:57827387-57827563	HepG2	liver:	n/a	n/a
29	CEBPB	chr11:57933976-57934113	A549	lung:	n/a	chr11:57934032-57934043
30	CEBPB	chr11:57828885-57829048	HepG2	liver:	n/a	n/a
31	CEBPB	chr11:57825146-57825329	IMR90	lung:	n/a	n/a
32	CEBPB	chr11:57841518-57841732	IMR90	lung:	n/a	chr11:57841555-57841566
33	CEBPB	chr11:57918759-57919029	HepG2	liver:	n/a	chr11:57918888-57918899
34	CEBPB	chr11:57829197-57829840	IMR90	lung:	n/a	n/a
35	CEBPB	chr11:57918787-57919016	A549	lung:	n/a	chr11:57918888-57918899
36	CEBPB	chr11:57828799-57829236	HepG2	liver:	n/a	n/a
37	CEBPB	chr11:57903675-57903812	K562	blood:	n/a	chr11:57903754-57903767 chr11:57903754-57903765 chr11:57903754-57903767 chr11:57903754-57903767
38	CEBPB	chr11:57932980-57933384	HepG2	liver:	n/a	chr11:57933335-57933346
39	CEBPB	chr11:57903599-57903939	HepG2	liver:	n/a	chr11:57903754-57903767 chr11:57903754-57903765 chr11:57903754-57903767 chr11:57903754-57903767
40	CEBPB	chr11:57932759-57933412	HepG2	liver:	n/a	chr11:57933335-57933346
41	CEBPB	chr11:57810992-57811068	HepG2	liver:	n/a	chr11:57811020-57811037 chr11:57811023-57811034
42	CEBPB	chr11:57903681-57903807	Hela-S3	cervix:	n/a	chr11:57903754-57903767 chr11:57903754-57903765 chr11:57903754-57903767 chr11:57903754-57903767
43	CEBPB	chr11:57941847-57942073	A549	lung:	n/a	chr11:57941976-57941987
44	CTCF	chr11:57827400-57827550	RPTEC	kidney:	n/a	n/a
45	CTCF	chr11:57827400-57827550	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr11:57827400-57827550	A549	lung:	n/a	n/a
47	CTCF	chr11:57901737-57901903	K562	blood:	n/a	n/a
48	CTCF	chr11:57836273-57836395	MCF-7	breast:	n/a	chr11:57836325-57836343 chr11:57836340-57836350
49	CTCF	chr11:57827398-57827533	Lung_OC	lung:	n/a	n/a
50	CTCF	chr11:57836299-57836385	HUVEC	blood vessel:	n/a	chr11:57836325-57836343 chr11:57836340-57836350

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:57946199-57946249	HCPEpiC	choroid plexus:	n/a
2	chr11:57828341-57828391	HCT-116	colon:	n/a
3	chr11:57946199-57946249	HCPEpiC	choroid plexus:	n/a
4	chr11:57828341-57828391	HCT-116	colon:	n/a
5	chr11:57981267-57981317	GM19239	blood:	n/a
6	chr11:57957939-57957989	HIPEpiC	eye:	n/a
7	chr11:57996699-57996749	H1-hESC	embryonic stem cell:	embryo
8	chr11:57971290-57971340	Jurkat	blood:	n/a
9	chr11:57995632-57995682	ovcar-3	ovarian:	n/a
10	chr11:57948705-57948755	MCF-7	breast:	n/a
11	chr11:57995632-57995682	SK-N-MC	brain:	n/a
12	chr11:57948705-57948755	SK-N-SH_RA	brain:	n/a
13	chr11:57957939-57957989	K562	blood:	n/a
14	chr11:57995971-57996021	HRCEpiC	kidney:	n/a
15	chr11:57995632-57995682	GM19239	blood:	n/a
16	chr11:57957939-57957989	HPAEpiC	pulmonary alveolar:	n/a
17	chr11:57996557-57996607	PrEC	prostate:	n/a
18	chr11:57996699-57996749	AG09309	skin:	n/a
19	chr11:57995828-57995878	HCF	heart:	n/a
20	chr11:57947030-57947080	HCM	heart:	n/a
21	chr11:57996369-57996419	MCF-7	breast:	n/a
22	chr11:57945730-57945780	LNCaP	prostate:	n/a
23	chr11:57828341-57828391	SAEC	small airway:	n/a
24	chr11:57826364-57826414	GM12892	blood:	n/a
25	chr11:57946199-57946249	PrEC	prostate:	n/a
26	chr11:57945730-57945780	ProgFib	skin:	n/a
27	chr11:57948705-57948755	HCM	heart:	n/a
28	chr11:57945730-57945780	U87	brain:	n/a
29	chr11:57995632-57995682	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:57972167-57972217	SKMC	muscle:	n/a
31	chr11:57957820-57957870	BJ	skin:	n/a
32	chr11:57947030-57947080	HCF	heart:	n/a
33	chr11:57972167-57972217	GM12878	blood:	n/a
34	chr11:57996699-57996749	AoSMC	blood vessel:	n/a
35	chr11:57887499-57887549	K562	blood:	n/a
36	chr11:57972613-57972663	SKMC	muscle:	n/a
37	chr11:57958333-57958383	MCF-7	breast:	n/a
38	chr11:57945730-57945780	SK-N-SH_RA	brain:	n/a
39	chr11:57957939-57957989	PrEC	prostate:	n/a
40	chr11:57887499-57887549	HL-60	blood:	n/a
41	chr11:57995971-57996021	HUVEC	blood vessel:	n/a
42	chr11:57995632-57995682	AoSMC	blood vessel:	n/a
43	chr11:57972613-57972663	HRPEpiC	eye:	n/a
44	chr11:57957575-57957625	HCT-116	colon:	n/a
45	chr11:57958183-57958233	HUVEC	blood vessel:	n/a
46	chr11:57982664-57982714	CMK	blood:	n/a
47	chr11:57948705-57948755	HCT-116	colon:	n/a
48	chr11:57957820-57957870	A549	lung:	n/a
49	chr11:57826364-57826414	AG04450	lung:	fetal
50	chr11:57958183-57958233	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:57594227..57596364-chr11:57829897..57831561,2	K562	blood:
2	chr11:57933220..57935191-chr11:57939017..57941040,2	K562	blood:
3	chr11:57899133..57901340-chr11:57902195..57904014,2	K562	blood:
4	chr11:57893156..57895554-chr11:57899477..57901378,2	K562	blood:
5	chr11:57893156..57895554-chr11:57899477..57901378,2	K562	blood:
6	chr11:57899133..57901340-chr11:57902195..57904014,2	K562	blood:
7	chr11:57900929..57901568-chr9:108114414..108115317,2	MCF-7	breast:
8	chr11:57933220..57935191-chr11:57939017..57941040,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR9I1-1	chr11:57811582-57812814	ENSG00000255146
2	lnc-OR10Q1-1	chr11:58006103-58006146	XLOC_009444
3	lnc-OR9I1-3	chr11:57842874-57842910	NONHSAT021463
4	lnc-OR9I1-3	chr11:57839850-57841101	NONHSAT021463
5	lnc-OR9I1-1	chr11:57825155-57825307	ENSG00000255146
6	lnc-OR9I1-1	chr11:57814729-57815019	ENSG00000255146
7	lnc-OR9I1-1	chr11:57827398-57827610	ENSG00000255146
8	lnc-OR10Q1-1	chr11:58002206-58002441	XLOC_009444

Variant related genes	Relation type
OR5BL1P	TF binding region
OR1S1	TF binding region
OR9I1	TF binding region
ENSG00000255146	TF binding region
OR1S2	TF binding region
OR9Q2	TF binding region
ENSG00000254853	TF binding region
OR9L1P	TF binding region
OR10Q1	TF binding region
VN2R9P	TF binding region
OR9I2P	TF binding region
OR9I3P	TF binding region
OR5BL1P	CpG island
OR1S1	CpG island
OR9I1	CpG island
ENSG00000255146	CpG island
OR1S2	CpG island
OR9Q2	CpG island
ENSG00000254853	CpG island
OR9L1P	CpG island
OR10Q1	CpG island
VN2R9P	CpG island
OR9I2P	CpG island
OR9I3P	CpG island

Extended variants
information (count: 3432 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3432 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557814953	chr11:57806066-57806067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs572973387	chr11:57806131-57806132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190622120	chr11:57806136-57806137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561706437	chr11:57806140-57806141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs573980413	chr11:57806209-57806210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544572308	chr11:57806226-57806227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371378810	chr11:57806231-57806232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141059630	chr11:57806291-57806292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201012066	chr11:57806307-57806308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542935836	chr11:57806316-57806317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533346369	chr11:57806378-57806379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552029686	chr11:57806450-57806451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370124562	chr11:57806453-57806454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560692442	chr11:57806456-57806457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527348901	chr11:57806512-57806513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549111448	chr11:57806522-57806523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567107591	chr11:57806537-57806538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374512334	chr11:57806584-57806585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183487698	chr11:57806606-57806607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537894742	chr11:57806607-57806608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs367605632	chr11:57806633-57806634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553216996	chr11:57806651-57806652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573107599	chr11:57806692-57806693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538425029	chr11:57806838-57806839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs116950157	chr11:57806888-57806889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545534601	chr11:57806920-57806921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571916983	chr11:57806921-57806922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs55653906	chr11:57806939-57806940	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs530667641	chr11:57806981-57806982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs555487468	chr11:57806997-57806998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573940128	chr11:57807014-57807015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs74940263	chr11:57807034-57807035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs368975932	chr11:57807052-57807053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563016334	chr11:57807078-57807079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs578173856	chr11:57807086-57807087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186850632	chr11:57807089-57807090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191186332	chr11:57807125-57807126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183101190	chr11:57807127-57807128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527893991	chr11:57807145-57807146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549097045	chr11:57807184-57807185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186945951	chr11:57807185-57807186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532152494	chr11:57807199-57807200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531194509	chr11:57807203-57807204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79856138	chr11:57807206-57807207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571170542	chr11:57807237-57807238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7126858	chr11:57807254-57807255	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs7113065	chr11:57807283-57807284	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs80122676	chr11:57807285-57807286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536079572	chr11:57807301-57807302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368179180	chr11:57807369-57807370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	17142309	CNVD
Melanoma	17363583	CNVD

Chromatin state (count:352 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:57792000-57811400	Weak transcription	Right Atrium	heart
2	chr11:57799200-57808200	Weak transcription	Pancreas	Pancrea
3	chr11:57799400-57808400	Weak transcription	Lung	lung
4	chr11:57806800-57807000	Enhancers	HepG2	liver
5	chr11:57808200-57809000	Enhancers	Pancreas	Pancrea
6	chr11:57808400-57809000	ZNF genes & repeats	Lung	lung
7	chr11:57808600-57809000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr11:57813000-57813600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr11:57813200-57814200	Enhancers	NHEK	skin
10	chr11:57813400-57813800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr11:57813600-57825000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr11:57814400-57815200	Enhancers	HepG2	liver
13	chr11:57821400-57821600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr11:57821600-57826000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr11:57821800-57825000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr11:57823600-57828400	Enhancers	HepG2	liver
17	chr11:57824600-57826400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr11:57824600-57830000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr11:57824600-57830600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr11:57824800-57825800	Enhancers	HSMM	muscle
21	chr11:57824800-57826000	Enhancers	HSMMtube	muscle
22	chr11:57824800-57826800	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr11:57824800-57830000	Enhancers	Placenta Amnion	Placenta Amnion
24	chr11:57824800-57830200	Enhancers	NHLF	lung
25	chr11:57825000-57825200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr11:57825000-57826400	Enhancers	Pancreas	Pancrea
27	chr11:57825000-57826800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr11:57825000-57826800	Enhancers	Placenta	Placenta
29	chr11:57825000-57830200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr11:57825000-57830600	Enhancers	HMEC	breast
31	chr11:57825200-57825800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr11:57825200-57826800	Enhancers	H1 Cell Line	embryonic stem cell
33	chr11:57825200-57830600	Enhancers	NHEK	skin
34	chr11:57825400-57826800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr11:57825400-57828800	Enhancers	Fetal Heart	heart
36	chr11:57825400-57830000	Enhancers	Muscle Satellite Cultured Cells	--
37	chr11:57825600-57826000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr11:57825600-57826200	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr11:57825600-57826200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr11:57825600-57826200	Enhancers	Aorta	Aorta
41	chr11:57825600-57826400	Enhancers	Gastric	stomach
42	chr11:57825600-57826400	Enhancers	Lung	lung
43	chr11:57825600-57826400	Enhancers	Right Atrium	heart
44	chr11:57825600-57826400	Enhancers	Right Ventricle	heart
45	chr11:57825600-57826600	Enhancers	Stomach Smooth Muscle	stomach
46	chr11:57825600-57826800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr11:57825600-57826800	Enhancers	Left Ventricle	heart
48	chr11:57825600-57826800	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr11:57825600-57826800	Enhancers	NH-A	brain
50	chr11:57825600-57827000	Enhancers	Fetal Muscle Trunk	muscle

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