Variant report

Variant	nsv556379
Chromosome Location	chr11:107627609-107671626
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	chr11:107670016-107670309	K562	blood:	n/a	n/a
2	ARID3A	chr11:107670088-107670292	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:107641785-107642088	K562	blood:	n/a	n/a
4	ARID3A	chr11:107641751-107641928	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:107658025-107658157	K562	blood:	n/a	n/a
6	ATF2	chr11:107656107-107656546	GM12878	blood:	n/a	n/a
7	BACH1	chr11:107649876-107650025	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr11:107658543-107658622	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr11:107669987-107670260	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr11:107656068-107656457	GM12878	blood:	n/a	n/a
11	BATF	chr11:107656116-107656405	GM12878	blood:	n/a	n/a
12	BCL11A	chr11:107656119-107656430	GM12878	blood:	n/a	n/a
13	BCLAF1	chr11:107669922-107670287	GM12878	blood:	n/a	n/a
14	BHLHE40	chr11:107647933-107647974	GM12878	blood:	n/a	n/a
15	CBX3	chr11:107629500-107629773	K562	blood:	n/a	n/a
16	CCNT2	chr11:107651637-107651830	K562	blood:	n/a	n/a
17	CEBPB	chr11:107641274-107641972	IMR90	lung:	n/a	n/a
18	CTCF	chr11:107641600-107641750	HFF-Myc	foreskin:	n/a	n/a
19	CTCF	chr11:107670080-107670230	BE2_C	brain:	n/a	chr11:107670165-107670174
20	CTCF	chr11:107628441-107628753	H1-hESC	embryonic stem cell:	n/a	chr11:107628561-107628582 chr11:107628566-107628584
21	CTCF	chr11:107670080-107670230	GM12866	blood:	n/a	chr11:107670165-107670174
22	CTCF	chr11:107641560-107641710	SAEC	small airway:	n/a	n/a
23	CTCF	chr11:107670100-107670250	HBMEC	blood vessel:	n/a	chr11:107670165-107670174
24	CTCF	chr11:107641800-107641950	GM12875	blood:	n/a	chr11:107641920-107641938 chr11:107641925-107641933 chr11:107641915-107641936 chr11:107641921-107641937
25	CTCF	chr11:107651660-107651810	HMEC	breast:	n/a	chr11:107651689-107651707 chr11:107651684-107651705 chr11:107651690-107651706 chr11:107651696-107651704 chr11:107651691-107651704
26	CTCF	chr11:107670120-107670270	GM12865	blood:	n/a	chr11:107670165-107670174
27	CTCF	chr11:107670001-107670247	ECC-1	luminal epithelium:	n/a	chr11:107670165-107670174
28	CTCF	chr11:107669740-107670572	A549	lung:	n/a	chr11:107670165-107670174
29	CTCF	chr11:107641840-107641990	MCF-7	breast:	n/a	chr11:107641920-107641938 chr11:107641925-107641933 chr11:107641915-107641936 chr11:107641921-107641937
30	CTCF	chr11:107651600-107651750	HBMEC	blood vessel:	n/a	chr11:107651689-107651707 chr11:107651684-107651705 chr11:107651690-107651706 chr11:107651696-107651704 chr11:107651691-107651704
31	CTCF	chr11:107628440-107628590	GM12875	blood:	n/a	chr11:107628561-107628582 chr11:107628566-107628584
32	CTCF	chr11:107641680-107641970	HFF-Myc	foreskin:	n/a	chr11:107641920-107641938 chr11:107641925-107641933 chr11:107641915-107641936 chr11:107641921-107641937
33	CTCF	chr11:107643172-107643308	LNCaP	prostate:	n/a	n/a
34	CTCF	chr11:107670080-107670230	HepG2	liver:	n/a	chr11:107670165-107670174
35	CTCF	chr11:107628507-107628645	Hela-S3	cervix:	n/a	chr11:107628561-107628582 chr11:107628566-107628584
36	CTCF	chr11:107651993-107652017	GM19239	blood:	n/a	n/a
37	CTCF	chr11:107628460-107628610	Hela-S3	cervix:	n/a	chr11:107628561-107628582 chr11:107628566-107628584
38	CTCF	chr11:107670080-107670230	WI-38	lung:	n/a	chr11:107670165-107670174
39	CTCF	chr11:107641920-107642070	HEEpiC	esophagus:	n/a	chr11:107641920-107641938 chr11:107641925-107641933 chr11:107641921-107641937
40	CTCF	chr11:107651800-107651950	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr11:107628540-107628690	HepG2	liver:	n/a	chr11:107628561-107628582 chr11:107628566-107628584
42	CTCF	chr11:107670100-107670250	GM12864	blood:	n/a	chr11:107670165-107670174
43	CTCF	chr11:107670080-107670230	HPF	lung:	n/a	chr11:107670165-107670174
44	CTCF	chr11:107641480-107641630	GM12864	blood:	n/a	n/a
45	CTCF	chr11:107670920-107671070	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr11:107641860-107642010	HCPEpiC	choroid plexus:	n/a	chr11:107641920-107641938 chr11:107641925-107641933 chr11:107641915-107641936 chr11:107641921-107641937
47	CTCF	chr11:107628500-107628650	MCF-7	breast:	n/a	chr11:107628561-107628582 chr11:107628566-107628584
48	CTCF	chr11:107641880-107642030	GM12864	blood:	n/a	chr11:107641920-107641938 chr11:107641925-107641933 chr11:107641915-107641936 chr11:107641921-107641937
49	CTCF	chr11:107651560-107651710	HEK293	kidney:	n/a	chr11:107651689-107651707 chr11:107651684-107651705 chr11:107651690-107651706 chr11:107651696-107651704 chr11:107651691-107651704
50	CTCF	chr11:107670120-107670270	SK-N-SH_RA	brain:	n/a	chr11:107670165-107670174

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:107640397-107640447	MCF10A-Er-Src	breast:	n/a
2	chr11:107640397-107640447	MCF10A-Er-Src	breast:	n/a
3	chr11:107662133-107662183	BE2_C	brain:	n/a
4	chr11:107662133-107662183	AG10803	skin:	n/a
5	chr11:107662133-107662183	HNPCEpiC	eye:	n/a
6	chr11:107640397-107640447	HCT-116	colon:	n/a
7	chr11:107640397-107640447	Caco-2	colon:	n/a
8	chr11:107662133-107662183	T-47D	breast:	n/a
9	chr11:107640397-107640447	GM12891	blood:	n/a
10	chr11:107640397-107640447	MCF-7	breast:	n/a
11	chr11:107662133-107662183	CMK	blood:	n/a
12	chr11:107640397-107640447	HEK293	kidney:	embryo
13	chr11:107662133-107662183	GM06990	blood:	n/a
14	chr11:107662133-107662183	MCF-7	breast:	n/a
15	chr11:107662133-107662183	Jurkat	blood:	n/a
16	chr11:107640397-107640447	A549	lung:	n/a
17	chr11:107640397-107640447	AG04449	skin:	fetal
18	chr11:107640397-107640447	AG04450	lung:	fetal
19	chr11:107662133-107662183	HAEpiC	amniotic membrane:	n/a
20	chr11:107640397-107640447	HEEpiC	esophagus:	n/a
21	chr11:107640397-107640447	AG09319	gingival:	n/a
22	chr11:107662133-107662183	A549	lung:	n/a
23	chr11:107662133-107662183	HepG2	liver:	n/a
24	chr11:107662133-107662183	HRPEpiC	eye:	n/a
25	chr11:107640397-107640447	GM19239	blood:	n/a
26	chr11:107662133-107662183	NB4	blood:	n/a
27	chr11:107640397-107640447	HepG2	liver:	n/a
28	chr11:107662133-107662183	MCF10A-Er-Src	breast:	n/a
29	chr11:107662133-107662183	H1-hESC	embryonic stem cell:	embryo
30	chr11:107662133-107662183	AG04449	skin:	fetal
31	chr11:107662133-107662183	GM19239	blood:	n/a
32	chr11:107640397-107640447	Hela-S3	cervix:	n/a
33	chr11:107640397-107640447	NHBE	bronchial:	n/a
34	chr11:107662133-107662183	NH-A	brain:	n/a
35	chr11:107640397-107640447	BE2_C	brain:	n/a
36	chr11:107662133-107662183	HIPEpiC	eye:	n/a
37	chr11:107640397-107640447	HCF	heart:	n/a
38	chr11:107640397-107640447	SAEC	small airway:	n/a
39	chr11:107640397-107640447	SK-N-MC	brain:	n/a
40	chr11:107640397-107640447	HNPCEpiC	eye:	n/a
41	chr11:107662133-107662183	HCF	heart:	n/a
42	chr11:107640397-107640447	SKMC	muscle:	n/a
43	chr11:107662133-107662183	HCPEpiC	choroid plexus:	n/a
44	chr11:107640397-107640447	NT2-D1	testis:	n/a
45	chr11:107662133-107662183	U87	brain:	n/a
46	chr11:107662133-107662183	PrEC	prostate:	n/a
47	chr11:107662133-107662183	AG09309	skin:	n/a
48	chr11:107662133-107662183	ECC-1	luminal epithelium:	n/a
49	chr11:107640397-107640447	SK-N-SH	brain:	n/a
50	chr11:107662133-107662183	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:107636795..107638295-chr11:107651566..107653122,2	K562	blood:
2	chr11:107623853..107625487-chr11:107628696..107631031,2	K562	blood:
3	chr11:107663159..107665072-chr11:107667163..107669875,2	MCF-7	breast:
4	chr11:107447313..107447854-chr11:107640968..107641965,2	K562	blood:
5	chr1:201191728..201192238-chr11:107650401..107650990,2	MCF-7	breast:
6	chr11:107611768..107612356-chr11:107641576..107642546,2	MCF-7	breast:
7	chr11:107670081..107670628-chr11:107695151..107695710,2	K562	blood:
8	chr11:107560069..107560995-chr11:107641497..107642096,3	MCF-7	breast:
9	chr11:107636795..107638295-chr11:107651566..107653122,2	K562	blood:
10	chr11:107614634..107615702-chr11:107641448..107642000,3	MCF-7	breast:
11	chr11:107641920..107642539-chr11:107651250..107651774,2	K562	blood:
12	chr11:107611439..107612355-chr11:107641879..107642586,3	K562	blood:
13	chr11:107646046..107648383-chr11:107654593..107656210,2	MCF-7	breast:
14	chr11:107646046..107648383-chr11:107654593..107656210,2	MCF-7	breast:
15	chr11:107663159..107665072-chr11:107667163..107669875,2	MCF-7	breast:
16	chr11:107670116..107670647-chr11:107768751..107769447,2	MCF-7	breast:
17	chr11:107641920..107642539-chr11:107651250..107651774,2	K562	blood:

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SLC35F2	hsa-miR-155-5p	chr11:107662756-107662777

Variant related genes	Relation type
ENSG00000214306	TF binding region
ENSG00000214305	TF binding region
ENSG00000214306	CpG island
ENSG00000214305	CpG island

Extended variants
information (count: 1362 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1362 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs67991834	chr11:107627609-107627610	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552343033	chr11:107627617-107627618	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149860572	chr11:107627631-107627632	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534847121	chr11:107627635-107627636	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186315968	chr11:107627712-107627713	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192027891	chr11:107627720-107627721	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144673112	chr11:107627729-107627730	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148520474	chr11:107627738-107627739	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12802831	chr11:107627745-107627746	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs543604225	chr11:107627781-107627782	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182491035	chr11:107627782-107627783	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576858313	chr11:107627798-107627799	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112278171	chr11:107627805-107627806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs112720406	chr11:107627845-107627846	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs145401982	chr11:107627846-107627847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529657273	chr11:107627851-107627852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs11212348	chr11:107627852-107627853	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs185899022	chr11:107627861-107627862	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs7937429	chr11:107627862-107627863	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs552728212	chr11:107627903-107627904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs574902	chr11:107627954-107627955	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs377627259	chr11:107627964-107627965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552789642	chr11:107627967-107627968	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369970866	chr11:107627991-107627992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572993530	chr11:107628005-107628006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147696048	chr11:107628011-107628012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200880519	chr11:107628016-107628017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs34451171	chr11:107628018-107628019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7937362	chr11:107628022-107628023	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs373375307	chr11:107628035-107628036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561420238	chr11:107628084-107628085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554854181	chr11:107628090-107628091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569927718	chr11:107628141-107628142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145258152	chr11:107628144-107628145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558698246	chr11:107628167-107628168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576988076	chr11:107628245-107628246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540692666	chr11:107628264-107628265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552661229	chr11:107628271-107628272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574049099	chr11:107628305-107628306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs368053816	chr11:107628312-107628313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574758787	chr11:107628336-107628337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563178028	chr11:107628354-107628355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs4754248	chr11:107628383-107628384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112435389	chr11:107628411-107628412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377045085	chr11:107628438-107628439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12224163	chr11:107628519-107628520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563978547	chr11:107628604-107628605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532893374	chr11:107628612-107628613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552899255	chr11:107628655-107628656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370192290	chr11:107628683-107628684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	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
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Obesity	19966786	CNVD
Renal cell carcinoma	21668985	CNVD
Cancer	20164920	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD

Chromatin state (count:325 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107624600-107630000	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr11:107625800-107629600	Weak transcription	Fetal Muscle Leg	muscle
3	chr11:107627000-107627800	Enhancers	Brain Cingulate Gyrus	brain
4	chr11:107627000-107627800	Enhancers	Brain Inferior Temporal Lobe	brain
5	chr11:107627000-107627800	Enhancers	Brain Substantia Nigra	brain
6	chr11:107627200-107628000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr11:107627600-107627800	Flanking Active TSS	Brain Hippocampus Middle	brain
8	chr11:107628000-107629800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr11:107628800-107629000	Enhancers	H9 Cell Line	embryonic stem cell
10	chr11:107628800-107630000	Enhancers	K562	blood
11	chr11:107629000-107630200	Enhancers	Duodenum Mucosa	Duodenum
12	chr11:107629200-107630000	Enhancers	Rectal Mucosa Donor 29	rectum
13	chr11:107629200-107630200	Enhancers	Stomach Mucosa	stomach
14	chr11:107629600-107630400	Enhancers	Fetal Muscle Leg	muscle
15	chr11:107630000-107630200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr11:107630000-107630200	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr11:107638600-107642000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr11:107638800-107639000	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr11:107638800-107641800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr11:107639000-107641200	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr11:107639400-107640200	Enhancers	K562	blood
22	chr11:107639400-107641800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr11:107639400-107641800	Enhancers	HSMMtube	muscle
24	chr11:107639600-107640000	Enhancers	Fetal Brain Male	brain
25	chr11:107639600-107640600	Enhancers	Fetal Muscle Trunk	muscle
26	chr11:107639600-107642000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr11:107639800-107640000	Flanking Active TSS	Osteobl	bone
28	chr11:107639800-107640200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr11:107639800-107640200	Enhancers	NHLF	lung
30	chr11:107639800-107640600	Enhancers	Muscle Satellite Cultured Cells	--
31	chr11:107639800-107641400	Enhancers	NH-A	brain
32	chr11:107639800-107641800	Enhancers	HSMM	muscle
33	chr11:107639800-107641800	Enhancers	NHDF-Ad	bronchial
34	chr11:107640000-107640200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr11:107640000-107640200	Enhancers	Fetal Muscle Leg	muscle
36	chr11:107640000-107640200	Enhancers	Placenta Amnion	Placenta Amnion
37	chr11:107640000-107640400	Weak transcription	Fetal Brain Male	brain
38	chr11:107640000-107640800	Enhancers	Psoas Muscle	Psoas
39	chr11:107640000-107641400	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr11:107640000-107641400	Enhancers	Osteobl	bone
41	chr11:107640000-107641800	Enhancers	GM12878-XiMat	blood
42	chr11:107640000-107642200	Enhancers	Fetal Brain Female	brain
43	chr11:107640200-107641200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr11:107640200-107641200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr11:107640200-107641200	Weak transcription	Fetal Muscle Leg	muscle
46	chr11:107640200-107641200	Weak transcription	NHLF	lung
47	chr11:107640400-107641400	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr11:107640400-107642400	Enhancers	Fetal Brain Male	brain
49	chr11:107640600-107641000	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr11:107640600-107642000	Weak transcription	Fetal Muscle Trunk	muscle

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