Variant report

Variant	nsv896916
Chromosome Location	chr11:4712353-4806872
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	chr11:4737623-4737722	K562	blood:	n/a	n/a
2	ATF1	chr11:4793218-4793283	K562	blood:	n/a	n/a
3	ATF1	chr11:4725319-4725444	K562	blood:	n/a	n/a
4	BATF	chr11:4720952-4721308	GM12878	blood:	n/a	chr11:4721121-4721132 chr11:4721122-4721132
5	BATF	chr11:4720966-4721312	GM12878	blood:	n/a	chr11:4721121-4721132 chr11:4721122-4721132
6	BHLHE40	chr11:4735655-4735881	K562	blood:	n/a	chr11:4735729-4735738 chr11:4735728-4735737 chr11:4735726-4735739 chr11:4735728-4735737 chr11:4735722-4735743
7	BHLHE40	chr11:4725569-4725710	K562	blood:	n/a	n/a
8	BHLHE40	chr11:4725424-4725706	GM12878	blood:	n/a	n/a
9	BHLHE40	chr11:4720909-4721365	GM12878	blood:	n/a	n/a
10	CCNT2	chr11:4766868-4767027	K562	blood:	n/a	n/a
11	CEBPB	chr11:4786195-4786260	HepG2	liver:	n/a	chr11:4786226-4786237
12	CEBPB	chr11:4718940-4719281	IMR90	lung:	n/a	chr11:4719120-4719133
13	CEBPB	chr11:4802820-4802858	K562	blood:	n/a	chr11:4802839-4802852 chr11:4802839-4802852 chr11:4802841-4802852
14	CEBPB	chr11:4769720-4769999	K562	blood:	n/a	n/a
15	CEBPB	chr11:4727716-4727917	K562	blood:	n/a	n/a
16	CEBPB	chr11:4769715-4770029	HepG2	liver:	n/a	n/a
17	CEBPB	chr11:4779256-4779493	HepG2	liver:	n/a	chr11:4779363-4779374
18	CEBPB	chr11:4727964-4728051	A549	lung:	n/a	n/a
19	CEBPB	chr11:4769682-4770051	IMR90	lung:	n/a	n/a
20	CEBPB	chr11:4769725-4770036	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr11:4769714-4769970	A549	lung:	n/a	n/a
22	CHD1	chr11:4736940-4736955	GM12878	blood:	n/a	n/a
23	CHD2	chr11:4746213-4746346	K562	blood:	n/a	n/a
24	CHD2	chr11:4725736-4726172	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr11:4804280-4804430	GM12871	blood:	n/a	n/a
26	CTCF	chr11:4744233-4744257	GM10266	blood:	n/a	chr11:4744238-4744254 chr11:4744237-4744255
27	CTCF	chr11:4804260-4804410	GM12872	blood:	n/a	n/a
28	CTCF	chr11:4804220-4804370	GM12866	blood:	n/a	n/a
29	CTCF	chr11:4744126-4744358	K562	blood:	n/a	chr11:4744239-4744260 chr11:4744238-4744254 chr11:4744237-4744255
30	CTCF	chr11:4726264-4726289	Lung_OC	lung:	n/a	n/a
31	CTCF	chr11:4744135-4744413	K562	blood:	n/a	chr11:4744239-4744260 chr11:4744238-4744254 chr11:4744237-4744255
32	CTCF	chr11:4744160-4744310	GM12864	blood:	n/a	chr11:4744239-4744260 chr11:4744238-4744254 chr11:4744237-4744255
33	CTCF	chr11:4744160-4744310	GM12874	blood:	n/a	chr11:4744239-4744260 chr11:4744238-4744254 chr11:4744237-4744255
34	CTCF	chr11:4804260-4804410	AG04450	lung:	n/a	n/a
35	CTCF	chr11:4744118-4744350	HepG2	liver:	n/a	chr11:4744239-4744260 chr11:4744238-4744254 chr11:4744237-4744255
36	CTCF	chr11:4744115-4744359	A549	lung:	n/a	chr11:4744239-4744260 chr11:4744238-4744254 chr11:4744237-4744255
37	CTCF	chr11:4744159-4744323	GM19240	blood:	n/a	chr11:4744239-4744260 chr11:4744238-4744254 chr11:4744237-4744255
38	CTCF	chr11:4804220-4804370	GM12875	blood:	n/a	n/a
39	CTCF	chr11:4744111-4744374	H1-hESC	embryonic stem cell:	n/a	chr11:4744239-4744260 chr11:4744238-4744254 chr11:4744237-4744255
40	CTCF	chr11:4744200-4744350	GM12869	blood:	n/a	chr11:4744239-4744260 chr11:4744238-4744254 chr11:4744237-4744255
41	CTCF	chr11:4744078-4744431	H1-hESC	embryonic stem cell:	n/a	chr11:4744239-4744260 chr11:4744238-4744254 chr11:4744237-4744255
42	CTCF	chr11:4804220-4804370	GM06990	blood:	n/a	n/a
43	CTCF	chr11:4744160-4744310	HEK293	kidney:	n/a	chr11:4744239-4744260 chr11:4744238-4744254 chr11:4744237-4744255
44	CTCF	chr11:4744220-4744370	MCF-7	breast:	n/a	chr11:4744239-4744260 chr11:4744238-4744254 chr11:4744237-4744255
45	CTCF	chr11:4744165-4744348	MCF-7	breast:	n/a	chr11:4744239-4744260 chr11:4744238-4744254 chr11:4744237-4744255
46	CTCF	chr11:4804278-4804347	GM19239	blood:	n/a	n/a
47	CTCF	chr11:4744188-4744313	GM12892	blood:	n/a	chr11:4744239-4744260 chr11:4744238-4744254 chr11:4744237-4744255
48	CTCF	chr11:4718960-4719110	AG04449	skin:	n/a	n/a
49	CTCF	chr11:4804240-4804390	GM12868	blood:	n/a	n/a
50	CTCF	chr11:4743988-4744033	Pancreas_OC	pancreas:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4791012-4791062	MCF10A-Er-Src	breast:	n/a
2	chr11:4716867-4716917	HEK293	kidney:	embryo
3	chr11:4726105-4726155	HIPEpiC	eye:	n/a
4	chr11:4719138-4719188	HNPCEpiC	eye:	n/a
5	chr11:4792272-4792322	HPAEpiC	pulmonary alveolar:	n/a
6	chr11:4792272-4792322	MCF-7	breast:	n/a
7	chr11:4716867-4716917	ovcar-3	ovarian:	n/a
8	chr11:4791012-4791062	A549	lung:	n/a
9	chr11:4716867-4716917	PANC-1	pancreas:	n/a
10	chr11:4792272-4792322	NB4	blood:	n/a
11	chr11:4792272-4792322	Hela-S3	cervix:	n/a
12	chr11:4718962-4719012	NHBE	bronchial:	n/a
13	chr11:4716867-4716917	GM12891	blood:	n/a
14	chr11:4716867-4716917	AG04450	lung:	fetal
15	chr11:4792272-4792322	PrEC	prostate:	n/a
16	chr11:4791012-4791062	ECC-1	luminal epithelium:	n/a
17	chr11:4716867-4716917	IMR90	lung:	fetal
18	chr11:4726105-4726155	LNCaP	prostate:	n/a
19	chr11:4791012-4791062	NB4	blood:	n/a
20	chr11:4716867-4716917	AG10803	skin:	n/a
21	chr11:4720347-4720397	Caco-2	colon:	n/a
22	chr11:4792272-4792322	PFSK-1	brain:	n/a
23	chr11:4718962-4719012	AG10803	skin:	n/a
24	chr11:4716867-4716917	SKMC	muscle:	n/a
25	chr11:4718962-4719012	NB4	blood:	n/a
26	chr11:4792272-4792322	HNPCEpiC	eye:	n/a
27	chr11:4718962-4719012	HCPEpiC	choroid plexus:	n/a
28	chr11:4792272-4792322	LNCaP	prostate:	n/a
29	chr11:4716867-4716917	HCM	heart:	n/a
30	chr11:4726105-4726155	HPAEpiC	pulmonary alveolar:	n/a
31	chr11:4718962-4719012	HCT-116	colon:	n/a
32	chr11:4726105-4726155	HRCEpiC	kidney:	n/a
33	chr11:4791012-4791062	AG10803	skin:	n/a
34	chr11:4792272-4792322	SKMC	muscle:	n/a
35	chr11:4718962-4719012	GM12891	blood:	n/a
36	chr11:4726105-4726155	NH-A	brain:	n/a
37	chr11:4720347-4720397	HCPEpiC	choroid plexus:	n/a
38	chr11:4718962-4719012	ECC-1	luminal epithelium:	n/a
39	chr11:4716867-4716917	HL-60	blood:	n/a
40	chr11:4791012-4791062	MCF-7	breast:	n/a
41	chr11:4791012-4791062	Hela-S3	cervix:	n/a
42	chr11:4720347-4720397	SK-N-SH	brain:	n/a
43	chr11:4719138-4719188	K562	blood:	n/a
44	chr11:4720347-4720397	HIPEpiC	eye:	n/a
45	chr11:4716867-4716917	Jurkat	blood:	n/a
46	chr11:4791012-4791062	HUVEC	blood vessel:	n/a
47	chr11:4716867-4716917	PFSK-1	brain:	n/a
48	chr11:4792272-4792322	HAEpiC	amniotic membrane:	n/a
49	chr11:4716867-4716917	A549	lung:	n/a
50	chr11:4716867-4716917	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:4769802..4772330-chr11:4775914..4778474,2	K562	blood:
2	11:4794705-4799792..11:5721056-5732713	K562	blood:
3	11:4789513-4794705..11:5380014-5384338	H1-hESC	embryonic stem cell:	embryo
4	11:4774420-4775061..11:5714465-5718134	GM12878	blood:
5	11:4789513-4794705..11:4988858-5002113	Hela-S3	cervix:
6	chr11:4780407..4782336-chr11:4786292..4788948,2	K562	blood:
7	11:4794705-4799792..11:5527719-5533869	GM12878	blood:
8	chr11:4778466..4780961-chr11:4783951..4785593,2	K562	blood:
9	11:4794705-4799792..11:5714465-5718134	H1-hESC	embryonic stem cell:	embryo
10	chr11:4783931..4787132-chr11:4790389..4793666,3	K562	blood:
11	11:4794705-4799792..11:5700314-5707362	K562	blood:
12	chr11:4758799..4760631-chr11:4763154..4765476,2	K562	blood:
13	11:4774420-4775061..11:5527719-5533869	GM12878	blood:
14	11:4778081-4789138..11:4988858-5002113	Hela-S3	cervix:
15	chr11:4779685..4780186-chr13:39427810..39428310,2	MCF-7	breast:
16	chr11:4778466..4780961-chr11:4783951..4785593,2	K562	blood:
17	chr11:4758799..4760631-chr11:4763154..4765476,2	K562	blood:
18	11:4778081-4789138..11:5740069-5747001	K562	blood:
19	11:4774420-4775061..11:5250847-5268367	GM12878	blood:
20	11:4789513-4794705..11:5033143-5038367	K562	blood:
21	chr11:4785049..4787150-chr11:4787794..4789663,2	K562	blood:
22	11:4801044-4820112..11:5700314-5707362	H1-hESC	embryonic stem cell:	embryo
23	11:4789513-4794705..11:4799792-4801044	GM12878	blood:
24	11:4778081-4789138..11:5033143-5038367	K562	blood:
25	chr11:4747857..4749971-chr11:4751424..4753265,2	K562	blood:
26	chr11:4716790..4717429-chr5:66479554..66480313,2	MCF-7	breast:
27	chr11:4776926..4782057-chr11:4782402..4785593,4	K562	blood:
28	chr11:4747857..4749971-chr11:4751424..4753265,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MMP26-1	chr11:4726157-4726275	NONHSAT017654
2	lnc-MMP26-1	chr11:4788500-4788571	NONHSAT017654

Variant related genes	Relation type
OR51N1P	TF binding region
ENSG00000201980	TF binding region
OR51F1	TF binding region
OR51C1P	TF binding region
OR51F5P	TF binding region
KRT8P49	TF binding region
OR51C4P	TF binding region
OR51F3P	TF binding region
OR51E2	TF binding region
MMP26	TF binding region
OR51F4P	TF binding region
OR51N1P	CpG island
ENSG00000201980	CpG island
OR51F1	CpG island
OR51C1P	CpG island
OR51F5P	CpG island
KRT8P49	CpG island
OR51C4P	CpG island
OR51F3P	CpG island
OR51E2	CpG island
MMP26	CpG island
OR51F4P	CpG island
ENSG00000132256	chromatin interactions
ENSG00000260629	chromatin interactions
ENSG00000167346	chromatin interactions
ENSG00000224300	chromatin interactions
ENSG00000175520	chromatin interactions
ENSG00000188069	chromatin interactions
ENSG00000225003	chromatin interactions
ENSG00000201980	chromatin interactions
ENSG00000232381	chromatin interactions
ENSG00000229988	chromatin interactions
ENSG00000236248	chromatin interactions
ENSG00000132274	chromatin interactions
ENSG00000223609	chromatin interactions

Extended variants
information (count: 2940 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2940 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11033352	chr11:4712353-4712354	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs556818597	chr11:4712365-4712366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575719668	chr11:4712396-4712397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs117014959	chr11:4712399-4712400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs576925191	chr11:4712403-4712404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148016477	chr11:4712485-4712486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573196270	chr11:4712504-4712505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs540475066	chr11:4712517-4712518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs370478557	chr11:4712547-4712548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs141670434	chr11:4712562-4712563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189672821	chr11:4712640-4712641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs562430394	chr11:4712643-4712644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533090657	chr11:4712646-4712647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182351282	chr11:4712681-4712682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs187546052	chr11:4712695-4712696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527293576	chr11:4712714-4712715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549264872	chr11:4712724-4712725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs563907745	chr11:4712727-4712728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs367662238	chr11:4712734-4712735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs567587608	chr11:4712758-4712759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs193262556	chr11:4712759-4712760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs370141799	chr11:4712775-4712776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs111398163	chr11:4712786-4712787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs117410882	chr11:4712791-4712792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372487401	chr11:4712813-4712814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557830909	chr11:4712898-4712899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566485858	chr11:4712911-4712912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs533955752	chr11:4712931-4712932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs188744135	chr11:4712953-4712954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs114051694	chr11:4712960-4712961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577340398	chr11:4712970-4712971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs192956655	chr11:4712974-4712975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs373184335	chr11:4712978-4712979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184100867	chr11:4712984-4712985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs199694008	chr11:4713040-4713041	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs556764543	chr11:4713106-4713107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs563639755	chr11:4713138-4713139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs578113133	chr11:4713194-4713195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs74052021	chr11:4713196-4713197	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs150890003	chr11:4713197-4713198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532692575	chr11:4713265-4713266	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs369267211	chr11:4713290-4713291	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs552511142	chr11:4713305-4713306	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs565967182	chr11:4713308-4713309	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs180685335	chr11:4713384-4713385	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs77110688	chr11:4713390-4713391	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs201005797	chr11:4713393-4713394	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs139682836	chr11:4713443-4713444	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs142911934	chr11:4713464-4713465	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs549704714	chr11:4713477-4713478	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
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
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:156 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4712200-4712400	Enhancers	Gastric	stomach
2	chr11:4712400-4712800	Enhancers	Left Ventricle	heart
3	chr11:4712400-4713200	Enhancers	Fetal Heart	heart
4	chr11:4713200-4713600	Flanking Active TSS	Fetal Heart	heart
5	chr11:4713200-4714000	Enhancers	Colon Smooth Muscle	Colon
6	chr11:4713600-4714000	Enhancers	Fetal Heart	heart
7	chr11:4714000-4715200	Weak transcription	Colon Smooth Muscle	Colon
8	chr11:4714000-4715200	Weak transcription	Fetal Heart	heart
9	chr11:4715000-4715200	Enhancers	Rectal Smooth Muscle	rectum
10	chr11:4715200-4715400	Enhancers	Colon Smooth Muscle	Colon
11	chr11:4715200-4716000	Weak transcription	Rectal Smooth Muscle	rectum
12	chr11:4715200-4717200	Enhancers	Fetal Heart	heart
13	chr11:4715400-4715600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr11:4715400-4715800	Weak transcription	Colon Smooth Muscle	Colon
15	chr11:4715800-4716000	Enhancers	Colon Smooth Muscle	Colon
16	chr11:4716000-4716200	Flanking Active TSS	Colon Smooth Muscle	Colon
17	chr11:4716000-4716400	Enhancers	Rectal Smooth Muscle	rectum
18	chr11:4716000-4717000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr11:4716200-4716400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr11:4716200-4716400	Enhancers	Ovary	ovary
21	chr11:4716200-4719000	Active TSS	Colon Smooth Muscle	Colon
22	chr11:4716400-4717400	Weak transcription	Rectal Smooth Muscle	rectum
23	chr11:4717200-4717800	Active TSS	Ovary	ovary
24	chr11:4717400-4718600	Active TSS	Rectal Smooth Muscle	rectum
25	chr11:4717800-4718800	Weak transcription	Ovary	ovary
26	chr11:4718600-4718800	Flanking Active TSS	Rectal Smooth Muscle	rectum
27	chr11:4718800-4719000	Enhancers	Ovary	ovary
28	chr11:4718800-4719000	Active TSS	Rectal Smooth Muscle	rectum
29	chr11:4718800-4719600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr11:4719000-4719400	Enhancers	Rectal Smooth Muscle	rectum
31	chr11:4719000-4720200	Enhancers	Colon Smooth Muscle	Colon
32	chr11:4719200-4725200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr11:4719400-4723200	Weak transcription	Rectal Smooth Muscle	rectum
34	chr11:4720200-4721200	Weak transcription	Colon Smooth Muscle	Colon
35	chr11:4720600-4721200	Enhancers	GM12878-XiMat	blood
36	chr11:4721200-4721400	Flanking Active TSS	GM12878-XiMat	blood
37	chr11:4721200-4722000	Enhancers	Colon Smooth Muscle	Colon
38	chr11:4722000-4723000	Weak transcription	Colon Smooth Muscle	Colon
39	chr11:4723000-4723600	Enhancers	Colon Smooth Muscle	Colon
40	chr11:4723200-4723800	Enhancers	Rectal Smooth Muscle	rectum
41	chr11:4723400-4723600	Enhancers	Fetal Muscle Leg	muscle
42	chr11:4723600-4724600	Weak transcription	Colon Smooth Muscle	Colon
43	chr11:4723600-4724600	Weak transcription	Fetal Muscle Leg	muscle
44	chr11:4723800-4724200	Weak transcription	Rectal Smooth Muscle	rectum
45	chr11:4723800-4725200	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr11:4724200-4726200	Enhancers	Rectal Smooth Muscle	rectum
47	chr11:4724400-4726200	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr11:4724600-4725400	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr11:4724600-4725400	Enhancers	Fetal Kidney	kidney
50	chr11:4724600-4726200	Enhancers	Colon Smooth Muscle	Colon

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