Variant report

Variant	nsv832166
Chromosome Location	chr11:57852031-58006189
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	BACH1	chr11:57963487-57963614	K562	blood:	n/a	n/a
3	CEBPB	chr11:57903675-57903812	K562	blood:	n/a	chr11:57903754-57903767 chr11:57903754-57903765 chr11:57903754-57903767 chr11:57903754-57903767
4	CEBPB	chr11:57903681-57903807	Hela-S3	cervix:	n/a	chr11:57903754-57903767 chr11:57903754-57903765 chr11:57903754-57903767 chr11:57903754-57903767
5	CEBPB	chr11:57903617-57903914	IMR90	lung:	n/a	chr11:57903754-57903767 chr11:57903754-57903765 chr11:57903754-57903767 chr11:57903754-57903767
6	CEBPB	chr11:57941813-57942112	HepG2	liver:	n/a	chr11:57941976-57941987
7	CEBPB	chr11:57959325-57959513	HepG2	liver:	n/a	chr11:57959408-57959419 chr11:57959450-57959462
8	CEBPB	chr11:57918787-57919016	A549	lung:	n/a	chr11:57918888-57918899
9	CEBPB	chr11:57932759-57933412	HepG2	liver:	n/a	chr11:57933335-57933346
10	CEBPB	chr11:57934976-57935084	HepG2	liver:	n/a	chr11:57935022-57935033
11	CEBPB	chr11:57932970-57933434	HepG2	liver:	n/a	chr11:57933335-57933346
12	CEBPB	chr11:57933976-57934113	A549	lung:	n/a	chr11:57934032-57934043
13	CEBPB	chr11:57941847-57942073	A549	lung:	n/a	chr11:57941976-57941987
14	CEBPB	chr11:57933079-57933336	HepG2	liver:	n/a	n/a
15	CEBPB	chr11:57933268-57933270	IMR90	lung:	n/a	n/a
16	CEBPB	chr11:57932980-57933384	HepG2	liver:	n/a	chr11:57933335-57933346
17	CEBPB	chr11:57948145-57948399	HepG2	liver:	n/a	n/a
18	CEBPB	chr11:57918759-57919029	HepG2	liver:	n/a	chr11:57918888-57918899
19	CEBPB	chr11:57933895-57934195	HepG2	liver:	n/a	chr11:57934032-57934043
20	CEBPB	chr11:57903599-57903939	HepG2	liver:	n/a	chr11:57903754-57903767 chr11:57903754-57903765 chr11:57903754-57903767 chr11:57903754-57903767
21	CTCF	chr11:57975011-57975083	GM13976	blood:	n/a	n/a
22	CTCF	chr11:57901360-57901379	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr11:57870800-57870950	K562	blood:	n/a	n/a
24	CTCF	chr11:57870660-57870810	K562	blood:	n/a	n/a
25	CTCF	chr11:57926890-57926936	IMR90	lung:	n/a	n/a
26	CTCF	chr11:57901192-57901562	H1-hESC	embryonic stem cell:	n/a	chr11:57901373-57901391 chr11:57901375-57901396
27	CTCF	chr11:57901338-57901515	K562	blood:	n/a	chr11:57901373-57901391 chr11:57901375-57901396
28	CTCF	chr11:57901740-57901890	GM12872	blood:	n/a	n/a
29	CTCF	chr11:57901785-57901838	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr11:57901660-57901810	GM12873	blood:	n/a	n/a
31	CTCF	chr11:57901720-57901870	GM12865	blood:	n/a	n/a
32	CTCF	chr11:57901700-57901850	HEK293	kidney:	n/a	n/a
33	CTCF	chr11:57995515-57995587	Fibrobl	skin:	n/a	n/a
34	CTCF	chr11:57901378-57901462	Pancreas_OC	pancreas:	n/a	n/a
35	CTCF	chr11:57901810-57901821	GM12892	blood:	n/a	n/a
36	CTCF	chr11:57926720-57926870	RPTEC	kidney:	n/a	n/a
37	CTCF	chr11:57901760-57901910	GM12874	blood:	n/a	n/a
38	CTCF	chr11:57926760-57926910	BJ	skin:	n/a	n/a
39	CTCF	chr11:57995617-57995640	GM19239	blood:	n/a	n/a
40	CTCF	chr11:57901775-57901847	MCF-7	breast:	n/a	n/a
41	CTCF	chr11:57901310-57901485	HepG2	liver:	n/a	chr11:57901373-57901391 chr11:57901375-57901396
42	CTCF	chr11:57901760-57901910	A549	lung:	n/a	n/a
43	CTCF	chr11:57901339-57901414	GM12878	blood:	n/a	chr11:57901373-57901391 chr11:57901375-57901396
44	CTCF	chr11:57926800-57926950	HMEC	breast:	n/a	n/a
45	CTCF	chr11:57901820-57901970	K562	blood:	n/a	n/a
46	CTCF	chr11:57901640-57901790	AG04450	lung:	n/a	n/a
47	CTCF	chr11:57934260-57934410	NHLF	lung:	n/a	n/a
48	CTCF	chr11:57901700-57901850	GM12873	blood:	n/a	n/a
49	CTCF	chr11:57972688-57972773	GM20000	blood:	n/a	n/a
50	CTCF	chr11:57994708-57994721	ProgFib	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:57995828-57995878	GM06990	blood:	n/a
2	chr11:57957820-57957870	HNPCEpiC	eye:	n/a
3	chr11:57996699-57996749	LNCaP	prostate:	n/a
4	chr11:57887499-57887549	NHBE	bronchial:	n/a
5	chr11:57972167-57972217	LNCaP	prostate:	n/a
6	chr11:57995971-57996021	GM12878	blood:	n/a
7	chr11:57957575-57957625	GM12878	blood:	n/a
8	chr11:57995828-57995878	PANC-1	pancreas:	n/a
9	chr11:57886517-57886567	GM19239	blood:	n/a
10	chr11:57957939-57957989	AG10803	skin:	n/a
11	chr11:57958248-57958298	HMEC	breast:	n/a
12	chr11:57996423-57996473	IMR90	lung:	fetal
13	chr11:57995828-57995878	GM19239	blood:	n/a
14	chr11:57946199-57946249	HEEpiC	esophagus:	n/a
15	chr11:57958248-57958298	HCPEpiC	choroid plexus:	n/a
16	chr11:57887499-57887549	HCPEpiC	choroid plexus:	n/a
17	chr11:57995971-57996021	GM19239	blood:	n/a
18	chr11:57996699-57996749	AG10803	skin:	n/a
19	chr11:57948705-57948755	H1-hESC	embryonic stem cell:	embryo
20	chr11:57886517-57886567	MCF10A-Er-Src	breast:	n/a
21	chr11:57981267-57981317	HMEC	breast:	n/a
22	chr11:57947030-57947080	MCF-7	breast:	n/a
23	chr11:57996699-57996749	HRCEpiC	kidney:	n/a
24	chr11:57948705-57948755	LNCaP	prostate:	n/a
25	chr11:57996699-57996749	HCT-116	colon:	n/a
26	chr11:57971290-57971340	SK-N-MC	brain:	n/a
27	chr11:57996557-57996607	GM12892	blood:	n/a
28	chr11:57995971-57996021	Jurkat	blood:	n/a
29	chr11:57958333-57958383	HUVEC	blood vessel:	n/a
30	chr11:57945730-57945780	ECC-1	luminal epithelium:	n/a
31	chr11:57996557-57996607	HepG2	liver:	n/a
32	chr11:57958248-57958298	HRE	kidney:	n/a
33	chr11:57981245-57981295	BJ	skin:	n/a
34	chr11:57958183-57958233	HUVEC	blood vessel:	n/a
35	chr11:57996557-57996607	SK-N-SH	brain:	n/a
36	chr11:57957939-57957989	SAEC	small airway:	n/a
37	chr11:57958183-57958233	AG10803	skin:	n/a
38	chr11:57958183-57958233	PrEC	prostate:	n/a
39	chr11:57946199-57946249	AoSMC	blood vessel:	n/a
40	chr11:57996371-57996421	ovcar-3	ovarian:	n/a
41	chr11:57996369-57996419	HepG2	liver:	n/a
42	chr11:57995971-57996021	A549	lung:	n/a
43	chr11:57996423-57996473	Jurkat	blood:	n/a
44	chr11:57996557-57996607	AG10803	skin:	n/a
45	chr11:57957102-57957152	HL-60	blood:	n/a
46	chr11:57972613-57972663	HIPEpiC	eye:	n/a
47	chr11:57996423-57996473	ECC-1	luminal epithelium:	n/a
48	chr11:57996369-57996419	NHDF-neo	bronchial:	n/a
49	chr11:57995632-57995682	NH-A	brain:	n/a
50	chr11:57958248-57958298	BE2_C	brain:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR10Q1-1	chr11:58006103-58006146	XLOC_009444
2	lnc-OR10Q1-1	chr11:58002206-58002441	XLOC_009444

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

Extended variants
information (count: 1962 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1962 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529849650	chr11:57876619-57876620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs147812088	chr11:57876663-57876664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs61738000	chr11:57876682-57876683	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs141462561	chr11:57876691-57876692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs34718541	chr11:57876765-57876766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150390009	chr11:57876767-57876768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs200097330	chr11:57876769-57876770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs543435749	chr11:57879983-57879984	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs558876245	chr11:57880031-57880032	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs79617807	chr11:57880067-57880068	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs78628229	chr11:57880094-57880095	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs144279253	chr11:57880191-57880192	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs573019618	chr11:57880192-57880193	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs542491116	chr11:57880194-57880195	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs562674613	chr11:57881882-57881883	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs533126475	chr11:57881886-57881887	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs562193498	chr11:57881911-57881912	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs551332942	chr11:57881960-57881961	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs151008913	chr11:57881968-57881969	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs535077181	chr11:57881989-57881990	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs148010035	chr11:57887189-57887190	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs544076557	chr11:57887197-57887198	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs575282273	chr11:57887211-57887212	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs545500390	chr11:57887225-57887226	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs191748228	chr11:57887241-57887242	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs141657148	chr11:57887246-57887247	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs372570282	chr11:57887499-57887500	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs116192459	chr11:57887500-57887501	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs548436537	chr11:57887510-57887511	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs376098892	chr11:57887514-57887515	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs367864127	chr11:57887516-57887517	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs182301889	chr11:57887540-57887541	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs7934149	chr11:57888566-57888567	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs562836084	chr11:57888623-57888624	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs35639120	chr11:57888636-57888637	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs577159624	chr11:57888640-57888641	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs139560454	chr11:57888695-57888696	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs545267700	chr11:57888755-57888756	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs570412116	chr11:57888759-57888760	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs544458494	chr11:57894415-57894416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs73480801	chr11:57894423-57894424	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs376360587	chr11:57894429-57894430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs7130381	chr11:57894443-57894444	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs552723615	chr11:57894450-57894451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112217986	chr11:57894461-57894462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs528520654	chr11:57894482-57894483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs184139147	chr11:57894504-57894505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs368659914	chr11:57894509-57894510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs535756428	chr11:57894514-57894515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs550716442	chr11:57894517-57894518	Enhancers	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	17142309	CNVD
Melanoma	17363583	CNVD

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:57876600-57876800	Enhancers	Gastric	stomach
2	chr11:57894400-57895400	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr11:57894800-57895200	Enhancers	HSMMtube	muscle
4	chr11:57895000-57895400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr11:57900000-57901800	Enhancers	NHEK	skin
6	chr11:57900200-57901600	Enhancers	Fetal Intestine Large	intestine
7	chr11:57900400-57900800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr11:57900400-57901600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr11:57900800-57901200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr11:57901000-57901400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr11:57901000-57901400	Enhancers	HepG2	liver
12	chr11:57901000-57901600	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr11:57901000-57901600	Enhancers	H9 Cell Line	embryonic stem cell
14	chr11:57901200-57901400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr11:57901400-57903600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr11:57903600-57904200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr11:57904200-57909400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:57909200-57909400	Enhancers	Fetal Lung	lung
19	chr11:57909400-57909600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr11:57909400-57910400	Weak transcription	Fetal Lung	lung
21	chr11:57909600-57910800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr11:57910400-57910800	Enhancers	Fetal Lung	lung
23	chr11:57910800-57911200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr11:57911200-57912800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr11:57912800-57913000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr11:57912800-57913800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr11:57919000-57919400	Enhancers	HepG2	liver
28	chr11:57920200-57920600	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr11:57921200-57922000	Enhancers	Fetal Intestine Small	intestine
30	chr11:57921600-57921800	Enhancers	Duodenum Mucosa	Duodenum
31	chr11:57922400-57922600	Enhancers	Duodenum Mucosa	Duodenum
32	chr11:57930200-57933600	Enhancers	Fetal Intestine Small	intestine
33	chr11:57930800-57931000	Enhancers	Small Intestine	intestine
34	chr11:57930800-57933200	Enhancers	Duodenum Mucosa	Duodenum
35	chr11:57930800-57935400	Enhancers	HepG2	liver
36	chr11:57931000-57931400	Enhancers	Brain Germinal Matrix	brain
37	chr11:57931000-57932200	Enhancers	Pancreas	Pancrea
38	chr11:57931000-57932600	Weak transcription	Small Intestine	intestine
39	chr11:57931000-57934400	Enhancers	Fetal Intestine Large	intestine
40	chr11:57931200-57931600	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr11:57931400-57932200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr11:57931400-57932600	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr11:57931600-57932400	Enhancers	Esophagus	oesophagus
44	chr11:57931800-57932600	Enhancers	Stomach Mucosa	stomach
45	chr11:57932000-57933400	Enhancers	Rectal Mucosa Donor 29	rectum
46	chr11:57932600-57934200	Enhancers	Small Intestine	intestine
47	chr11:57934400-57939200	Weak transcription	Fetal Intestine Large	intestine
48	chr11:57938800-57939200	Enhancers	Pancreas	Pancrea
49	chr11:57938800-57939400	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr11:57939200-57939800	Enhancers	Fetal Intestine Large	intestine

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