Variant report

Variant	nsv897012
Chromosome Location	chr11:16189326-16283644
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:670)
CpG islands
(count:0)
Chromatin interactive
region (count:68)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:670 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:16261422-16261856	K562	blood:	n/a	n/a
2	ARID3A	chr11:16207874-16207901	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:16274129-16274292	K562	blood:	n/a	n/a
4	ARID3A	chr11:16205814-16206820	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:16274051-16274250	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:16213058-16213194	K562	blood:	n/a	n/a
7	ARID3A	chr11:16225893-16226444	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:16247839-16248178	HepG2	liver:	n/a	n/a
9	ARID3A	chr11:16215594-16215968	K562	blood:	n/a	n/a
10	ARID3A	chr11:16191230-16191468	HepG2	liver:	n/a	n/a
11	ATF1	chr11:16235644-16235823	K562	blood:	n/a	n/a
12	ATF1	chr11:16215396-16215970	K562	blood:	n/a	n/a
13	ATF1	chr11:16220369-16220662	K562	blood:	n/a	n/a
14	BACH1	chr11:16261791-16261801	K562	blood:	n/a	n/a
15	BACH1	chr11:16273238-16273356	K562	blood:	n/a	n/a
16	BHLHE40	chr11:16215449-16216034	K562	blood:	n/a	n/a
17	BHLHE40	chr11:16199289-16199544	K562	blood:	n/a	n/a
18	BHLHE40	chr11:16213195-16213262	K562	blood:	n/a	n/a
19	BHLHE40	chr11:16220419-16220582	K562	blood:	n/a	n/a
20	BHLHE40	chr11:16261173-16261323	K562	blood:	n/a	n/a
21	BHLHE40	chr11:16248034-16248148	K562	blood:	n/a	n/a
22	BHLHE40	chr11:16262212-16262324	K562	blood:	n/a	n/a
23	BRCA1	chr11:16202510-16202654	H1-hESC	embryonic stem cell:	n/a	n/a
24	CBX3	chr11:16269564-16270388	K562	blood:	n/a	n/a
25	CBX3	chr11:16224012-16224364	K562	blood:	n/a	n/a
26	CCNT2	chr11:16199326-16199738	K562	blood:	n/a	n/a
27	CCNT2	chr11:16212965-16213273	K562	blood:	n/a	n/a
28	CCNT2	chr11:16215570-16215985	K562	blood:	n/a	n/a
29	CEBPB	chr11:16255090-16255143	IMR90	lung:	n/a	n/a
30	CEBPB	chr11:16199202-16199767	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr11:16243293-16243394	A549	lung:	n/a	n/a
32	CEBPB	chr11:16199144-16199636	IMR90	lung:	n/a	n/a
33	CEBPB	chr11:16235572-16235891	K562	blood:	n/a	chr11:16235739-16235750
34	CEBPB	chr11:16212815-16213144	K562	blood:	n/a	chr11:16212957-16212968
35	CEBPB	chr11:16235689-16235763	HepG2	liver:	n/a	chr11:16235739-16235750
36	CEBPB	chr11:16212810-16213094	IMR90	lung:	n/a	chr11:16212957-16212968
37	CEBPB	chr11:16212797-16213130	K562	blood:	n/a	chr11:16212957-16212968
38	CEBPB	chr11:16236683-16236798	H1-hESC	embryonic stem cell:	n/a	chr11:16236707-16236718
39	CEBPB	chr11:16205822-16206014	A549	lung:	n/a	chr11:16205894-16205905 chr11:16205894-16205907
40	CEBPB	chr11:16215587-16215962	K562	blood:	n/a	n/a
41	CEBPB	chr11:16199260-16199498	A549	lung:	n/a	n/a
42	CEBPB	chr11:16199142-16199524	K562	blood:	n/a	n/a
43	CEBPB	chr11:16212861-16213052	H1-hESC	embryonic stem cell:	n/a	chr11:16212957-16212968
44	CEBPB	chr11:16236628-16236796	A549	lung:	n/a	chr11:16236707-16236718
45	CEBPB	chr11:16236561-16236882	HepG2	liver:	n/a	chr11:16236707-16236718
46	CEBPB	chr11:16205661-16206551	A549	lung:	n/a	chr11:16205894-16205905 chr11:16205894-16205907
47	CEBPB	chr11:16205734-16206077	HepG2	liver:	n/a	chr11:16205894-16205905 chr11:16205894-16205907
48	CEBPB	chr11:16212816-16213029	HepG2	liver:	n/a	chr11:16212957-16212968
49	CEBPB	chr11:16236581-16236894	IMR90	lung:	n/a	chr11:16236707-16236718
50	CEBPB	chr11:16215546-16215947	K562	blood:	n/a	n/a

No data

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:16187549..16190511-chr11:16315345..16317594,2	K562	blood:
2	chr11:16212721..16213531-chr11:16627544..16628402,2	K562	blood:
3	chr11:16273658..16274622-chr11:16627404..16628365,5	MCF-7	breast:
4	chr11:16277289..16281774-chr11:16284462..16288431,5	K562	blood:
5	chr11:16254762..16258115-chr11:16260794..16264082,4	K562	blood:
6	chr11:16187914..16189713-chr11:16626672..16629483,2	K562	blood:
7	chr11:16223882..16226263-chr11:16229633..16231626,2	K562	blood:
8	chr11:16213881..16214546-chr11:16634890..16635879,2	K562	blood:
9	chr11:16209269..16212267-chr11:16243598..16245269,2	K562	blood:
10	chr11:16219560..16222671-chr11:16224548..16227962,3	K562	blood:
11	chr11:16192356..16194022-chr11:16198076..16200331,2	K562	blood:
12	chr11:16272523..16274102-chr11:16278731..16281096,3	K562	blood:
13	chr11:16226649..16230230-chr11:16231608..16235450,4	K562	blood:
14	chr11:16213165..16216422-chr11:16216965..16220387,3	K562	blood:
15	chr11:16258646..16260759-chr11:16262336..16265198,2	K562	blood:
16	chr11:16192356..16194022-chr11:16198076..16200331,2	K562	blood:
17	chr11:16212554..16213580-chr11:16627486..16628319,3	MCF-7	breast:
18	chr11:16251614..16253946-chr11:16259376..16260960,2	K562	blood:
19	chr11:16248287..16249803-chr11:16256816..16258558,2	K562	blood:
20	chr11:16252253..16255458-chr11:16256326..16259202,3	K562	blood:
21	chr11:16198617..16200800-chr11:16214986..16217270,2	K562	blood:
22	chr11:16191988..16194982-chr11:16195738..16200331,5	K562	blood:
23	chr11:16215320..16217059-chr11:16240927..16242475,2	K562	blood:
24	chr11:16191988..16194982-chr11:16195738..16200331,5	K562	blood:
25	chr11:16253958..16256004-chr11:16256326..16259109,2	K562	blood:
26	chr11:16252253..16255458-chr11:16256326..16259202,3	K562	blood:
27	chr11:16215320..16217059-chr11:16240927..16242475,2	K562	blood:
28	chr11:16245998..16247921-chr11:16262395..16264566,2	K562	blood:
29	chr11:16213165..16216422-chr11:16216965..16220387,3	K562	blood:
30	chr11:16226649..16230230-chr11:16231608..16235450,4	K562	blood:
31	chr11:16258646..16260759-chr11:16262336..16265198,2	K562	blood:
32	chr11:16253250..16255469-chr11:16319154..16321553,2	K562	blood:
33	chr11:16215659..16217331-chr11:16627513..16629554,2	K562	blood:
34	chr11:16263238..16264748-chr11:16273911..16275537,2	K562	blood:
35	chr11:16245998..16247921-chr11:16262395..16264566,2	K562	blood:
36	chr11:16262539..16264266-chr11:16264896..16266667,2	K562	blood:
37	chr11:16212664..16213531-chr11:16634934..16635871,3	K562	blood:
38	chr11:16192988..16195969-chr11:16626575..16628656,2	K562	blood:
39	chr11:16209269..16212267-chr11:16243598..16245269,2	K562	blood:
40	chr11:16240077..16244324-chr11:16251034..16255034,5	K562	blood:
41	chr11:16254286..16256657-chr11:16264384..16267054,2	K562	blood:
42	chr11:16199096..16201886-chr11:16205151..16207192,2	MCF-7	breast:
43	chr11:16254762..16258115-chr11:16260794..16264082,4	K562	blood:
44	chr11:16265440..16267766-chr11:16271349..16273913,2	K562	blood:
45	chr11:16223882..16226263-chr11:16229633..16231626,2	K562	blood:
46	chr11:16262539..16264266-chr11:16264896..16266667,2	K562	blood:
47	chr11:16253958..16256004-chr11:16256326..16259109,2	K562	blood:
48	chr11:16235541..16237281-chr11:16252412..16254092,2	K562	blood:
49	chr11:16218926..16220596-chr11:16221268..16223735,2	K562	blood:
50	chr11:16215831..16218271-chr11:16626703..16629554,2	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLEKHA7-5	chr11:16221974-16222435	NONHSAT018173

No data

Variant related genes	Relation type
SOX6	TF binding region
ENSG00000110693	chromatin interactions

Extended variants
information (count: 3019 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:3019 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12360975	chr11:16189326-16189327	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs376334343	chr11:16189350-16189351	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs534670496	chr11:16189364-16189365	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs75041314	chr11:16189365-16189366	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs551654228	chr11:16189375-16189376	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs183484231	chr11:16189377-16189378	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs144419342	chr11:16189380-16189381	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs570241013	chr11:16189414-16189415	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs531161285	chr11:16189553-16189554	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs575771097	chr11:16189566-16189567	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs553877351	chr11:16189590-16189591	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs542883799	chr11:16189640-16189641	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs561528253	chr11:16189747-16189748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147416064	chr11:16189769-16189770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573882899	chr11:16189774-16189775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs16932664	chr11:16189807-16189808	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs77535014	chr11:16189834-16189835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532060146	chr11:16189895-16189896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550629621	chr11:16189970-16189971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568894441	chr11:16189987-16189988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs139976381	chr11:16190069-16190070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548108100	chr11:16190084-16190085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566382110	chr11:16190103-16190104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs77529913	chr11:16190116-16190117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189327904	chr11:16190142-16190143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577611625	chr11:16190151-16190152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562357491	chr11:16190191-16190192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575802971	chr11:16190193-16190194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565613413	chr11:16190198-16190199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192684844	chr11:16190286-16190287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539500165	chr11:16190342-16190343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371472006	chr11:16190385-16190386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557409610	chr11:16190399-16190400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575661961	chr11:16190428-16190429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs544781165	chr11:16190465-16190466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs145481192	chr11:16190472-16190473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs555214028	chr11:16190507-16190508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs145184014	chr11:16190541-16190542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs565608003	chr11:16190553-16190554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149142646	chr11:16190641-16190642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543882601	chr11:16190743-16190744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562576181	chr11:16190808-16190809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs79650972	chr11:16190855-16190856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs554302409	chr11:16190889-16190890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs142442620	chr11:16190908-16190909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs151327175	chr11:16190956-16190957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs527529334	chr11:16190985-16190986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552029145	chr11:16190989-16190990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs566773829	chr11:16191036-16191037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538987504	chr11:16191045-16191046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
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
small cell lung cancer	20016488	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
Ovine squamous-cell carcinoma	17599052	CNVD
Neuroblastoma	19435921	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21785460	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:608 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:16172400-16191400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr11:16172600-16191400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr11:16174200-16191200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr11:16182000-16191600	Weak transcription	Psoas Muscle	Psoas
5	chr11:16182800-16190800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr11:16183400-16192000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr11:16185800-16205600	Weak transcription	Fetal Intestine Large	intestine
8	chr11:16188000-16189400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr11:16188400-16191200	Weak transcription	NHDF-Ad	bronchial
10	chr11:16188800-16191600	Weak transcription	Osteobl	bone
11	chr11:16189000-16189600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr11:16189200-16189400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr11:16189200-16189600	Enhancers	Fetal Lung	lung
14	chr11:16189200-16190000	Enhancers	Fetal Heart	heart
15	chr11:16189400-16191000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr11:16189400-16199200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr11:16189600-16191000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr11:16189600-16191000	Weak transcription	Fetal Lung	lung
19	chr11:16190000-16196400	Weak transcription	Fetal Heart	heart
20	chr11:16190400-16192400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr11:16190800-16191600	Enhancers	Muscle Satellite Cultured Cells	--
22	chr11:16190800-16191800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr11:16190800-16192200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr11:16190800-16194200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr11:16190800-16194200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr11:16190800-16194400	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr11:16190800-16194600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr11:16191000-16191800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr11:16191000-16192000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr11:16191000-16192800	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr11:16191000-16193000	Enhancers	Fetal Lung	lung
32	chr11:16191000-16193000	Enhancers	A549	lung
33	chr11:16191000-16194200	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr11:16191000-16194800	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr11:16191200-16191800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr11:16191200-16191800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr11:16191200-16191800	Enhancers	NHDF-Ad	bronchial
38	chr11:16191200-16192200	Enhancers	H1 Cell Line	embryonic stem cell
39	chr11:16191200-16192800	Enhancers	Brain Germinal Matrix	brain
40	chr11:16191200-16194200	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr11:16191400-16192000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:16191400-16192200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr11:16191400-16193000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr11:16191400-16194000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr11:16191400-16194800	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr11:16191600-16191800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr11:16191600-16191800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr11:16191600-16191800	Enhancers	Psoas Muscle	Psoas
49	chr11:16191600-16192200	Enhancers	Fetal Muscle Leg	muscle
50	chr11:16191600-16192400	Enhancers	H9 Cell Line	embryonic stem cell

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