Variant report

Variant	nsv540937
Chromosome Location	chr11:4958462-5032685
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:450)
CpG islands
(count:919)
Chromatin interactive
region (count:44)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:450 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:4982222-4982408	K562	blood:	n/a	n/a
2	ATF3	chr11:4982190-4982479	K562	blood:	n/a	n/a
3	CCNT2	chr11:4964325-4964404	K562	blood:	n/a	n/a
4	CEBPB	chr11:4982737-4982970	HepG2	liver:	n/a	chr11:4982850-4982861
5	CEBPB	chr11:4982745-4982919	K562	blood:	n/a	chr11:4982850-4982861
6	CEBPB	chr11:4982771-4982949	A549	lung:	n/a	chr11:4982850-4982861
7	CEBPB	chr11:4979504-4979744	HepG2	liver:	n/a	chr11:4979638-4979649
8	CEBPB	chr11:4994751-4994825	HepG2	liver:	n/a	n/a
9	CEBPB	chr11:5012391-5012630	K562	blood:	n/a	n/a
10	CEBPB	chr11:4959000-4959212	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr11:5028984-5029015	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr11:5025780-5025930	HCPEpiC	choroid plexus:	n/a	n/a
13	CTCF	chr11:4968105-4968165	GM13977	blood:	n/a	n/a
14	CTCF	chr11:5025780-5025930	GM12870	blood:	n/a	n/a
15	CTCF	chr11:5025736-5025984	Medullo	brain:	n/a	n/a
16	CTCF	chr11:5025780-5025930	HRE	kidney:	n/a	n/a
17	CTCF	chr11:5025761-5025924	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr11:5025800-5025950	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr11:5025859-5025886	MCF-7	breast:	n/a	n/a
20	CTCF	chr11:5012440-5012590	NHLF	lung:	n/a	n/a
21	CTCF	chr11:5012428-5012561	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr11:4958741-4958772	Fibrobl	skin:	n/a	n/a
23	CTCF	chr11:5012374-5012566	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr11:5025800-5025949	GM20000	blood:	n/a	n/a
25	CTCF	chr11:5012380-5012530	HCFaa	heart:	n/a	n/a
26	CTCF	chr11:5025820-5025970	GM12874	blood:	n/a	n/a
27	CTCF	chr11:5025740-5025890	NB4	blood:	n/a	n/a
28	CTCF	chr11:5025780-5025930	GM12872	blood:	n/a	n/a
29	CTCF	chr11:4991600-4991750	Caco-2	colon:	n/a	n/a
30	CTCF	chr11:5012380-5012530	HepG2	liver:	n/a	n/a
31	CTCF	chr11:5025800-5025950	GM12870	blood:	n/a	n/a
32	CTCF	chr11:5012440-5012590	GM12874	blood:	n/a	n/a
33	CTCF	chr11:5025800-5025950	GM12872	blood:	n/a	n/a
34	CTCF	chr11:5025725-5025945	A549	lung:	n/a	n/a
35	CTCF	chr11:5025800-5025950	HVMF	connective:	n/a	n/a
36	CTCF	chr11:5012400-5012550	GM12869	blood:	n/a	n/a
37	CTCF	chr11:5025540-5025690	GM12865	blood:	n/a	n/a
38	CTCF	chr11:5012460-5012610	AG04450	lung:	n/a	n/a
39	CTCF	chr11:5025736-5025924	HepG2	liver:	n/a	n/a
40	CTCF	chr11:5025720-5025870	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr11:5025530-5025599	GM19239	blood:	n/a	n/a
42	CTCF	chr11:5012400-5012550	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr11:5025820-5025970	RPTEC	kidney:	n/a	n/a
44	CTCF	chr11:5025800-5025950	GM12865	blood:	n/a	n/a
45	CTCF	chr11:5025676-5026005	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr11:5012420-5012570	MCF-7	breast:	n/a	n/a
47	CTCF	chr11:5025717-5026018	HepG2	liver:	n/a	n/a
48	CTCF	chr11:5012400-5012550	GM12864	blood:	n/a	n/a
49	CTCF	chr11:5025800-5025950	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr11:5025800-5025950	GM06990	blood:	n/a	n/a

(count:919 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4977429-4977479	Jurkat	blood:	n/a
2	chr11:4976263-4976313	H1-hESC	embryonic stem cell:	embryo
3	chr11:5020172-5020222	MCF-7	breast:	n/a
4	chr11:5009311-5009361	GM19239	blood:	n/a
5	chr11:4977429-4977479	Jurkat	blood:	n/a
6	chr11:4976263-4976313	H1-hESC	embryonic stem cell:	embryo
7	chr11:5020172-5020222	MCF-7	breast:	n/a
8	chr11:5009311-5009361	GM19239	blood:	n/a
9	chr11:5010562-5010612	NHBE	bronchial:	n/a
10	chr11:5020582-5020632	HepG2	liver:	n/a
11	chr11:5009201-5009251	AoSMC	blood vessel:	n/a
12	chr11:4976263-4976313	GM12878	blood:	n/a
13	chr11:5019849-5019899	LNCaP	prostate:	n/a
14	chr11:5009489-5009539	HCM	heart:	n/a
15	chr11:5008936-5008986	NH-A	brain:	n/a
16	chr11:5008936-5008986	HCT-116	colon:	n/a
17	chr11:5013610-5013660	ovcar-3	ovarian:	n/a
18	chr11:5010562-5010612	AG04449	skin:	fetal
19	chr11:5019849-5019899	BE2_C	brain:	n/a
20	chr11:5019849-5019899	HRPEpiC	eye:	n/a
21	chr11:5008936-5008986	AG09309	skin:	n/a
22	chr11:5013610-5013660	HRPEpiC	eye:	n/a
23	chr11:5009489-5009539	IMR90	lung:	fetal
24	chr11:5008411-5008461	RPTEC	kidney:	n/a
25	chr11:4977924-4977974	K562	blood:	n/a
26	chr11:5020172-5020222	HRE	kidney:	n/a
27	chr11:5008936-5008986	SKMC	muscle:	n/a
28	chr11:5020582-5020632	PFSK-1	brain:	n/a
29	chr11:5020582-5020632	Jurkat	blood:	n/a
30	chr11:5008411-5008461	NHDF-neo	bronchial:	n/a
31	chr11:4977001-4977051	HCM	heart:	n/a
32	chr11:5013610-5013660	HAEpiC	amniotic membrane:	n/a
33	chr11:5019849-5019899	NT2-D1	testis:	n/a
34	chr11:5019849-5019899	HL-60	blood:	n/a
35	chr11:5008411-5008461	NHBE	bronchial:	n/a
36	chr11:5019849-5019899	AG09319	gingival:	n/a
37	chr11:5008411-5008461	Caco-2	colon:	n/a
38	chr11:5009311-5009361	HMEC	breast:	n/a
39	chr11:4976263-4976313	AoSMC	blood vessel:	n/a
40	chr11:4977001-4977051	CMK	blood:	n/a
41	chr11:4977924-4977974	AG09319	gingival:	n/a
42	chr11:4977540-4977590	H1-hESC	embryonic stem cell:	embryo
43	chr11:5008936-5008986	MCF10A-Er-Src	breast:	n/a
44	chr11:5010562-5010612	BJ	skin:	n/a
45	chr11:4977429-4977479	Caco-2	colon:	n/a
46	chr11:5013610-5013660	AG10803	skin:	n/a
47	chr11:4977924-4977974	HRE	kidney:	n/a
48	chr11:5008411-5008461	GM19239	blood:	n/a
49	chr11:5020582-5020632	HEEpiC	esophagus:	n/a
50	chr11:5020582-5020632	AG04450	lung:	fetal

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	11:5020673-5032983..11:5700314-5707362	K562	blood:
2	11:4988858-5002113..11:5714465-5718134	Hela-S3	cervix:
3	11:4789513-4794705..11:5020673-5032983	K562	blood:
4	11:4988858-5002113..11:5243048-5250847	Hela-S3	cervix:
5	11:4988858-5002113..11:5469844-5475173	Hela-S3	cervix:
6	chr11:5016770..5019630-chr11:5023396..5025327,2	K562	blood:
7	11:4778081-4789138..11:5020673-5032983	K562	blood:
8	11:4778081-4789138..11:4988858-5002113	Hela-S3	cervix:
9	11:4957178-4961904..11:5721056-5732713	H1-hESC	embryonic stem cell:	embryo
10	11:4988858-5002113..11:5527719-5533869	Hela-S3	cervix:
11	11:4988858-5002113..11:5707362-5712027	Hela-S3	cervix:
12	chr11:4987860..4989604-chr11:4992698..4994558,2	K562	blood:
13	11:4869840-4870943..11:5020673-5032983	K562	blood:
14	11:4988858-5002113..11:5505728-5514500	Hela-S3	cervix:
15	chr11:4998734..5001673-chr11:5002692..5004874,2	MCF-7	breast:
16	chr11:4658272..4658813-chr11:5025400..5026262,2	MCF-7	breast:
17	chr11:4657872..4658731-chr11:5025387..5026540,3	K562	blood:
18	chr11:4208282..4208943-chr11:5025361..5026418,3	K562	blood:
19	chr11:4647199..4648030-chr11:5025327..5026179,2	K562	blood:
20	11:4988858-5002113..11:5250847-5268367	Hela-S3	cervix:
21	chr11:5002701..5004789-chr11:5011037..5012979,2	K562	blood:
22	11:5020673-5032983..11:5721056-5732713	K562	blood:
23	chr11:4657777..4658777-chr11:5012019..5012933,4	K562	blood:
24	chr11:4987860..4989604-chr11:4992698..4994558,2	K562	blood:
25	chr11:4990355..4993246-chr11:4998122..4999862,2	K562	blood:
26	11:4778081-4789138..11:4979189-4988077	K562	blood:
27	11:5020673-5032983..11:5566274-5571131	K562	blood:
28	11:4988858-5002113..11:5721056-5732713	Hela-S3	cervix:
29	11:4940074-4947279..11:4988858-5002113	Hela-S3	cervix:
30	chr11:4647527..4648151-chr11:5025801..5026495,2	MCF-7	breast:
31	11:5020673-5032983..11:5527719-5533869	K562	blood:
32	11:4988858-5002113..11:5600743-5604452	Hela-S3	cervix:
33	11:4988858-5002113..11:5566274-5571131	Hela-S3	cervix:
34	chr11:4990355..4993246-chr11:4998122..4999862,2	K562	blood:
35	11:4789513-4794705..11:4988858-5002113	Hela-S3	cervix:
36	chr11:5016770..5019630-chr11:5023396..5025327,2	K562	blood:
37	11:4789513-4794705..11:4979189-4988077	K562	blood:
38	chr11:5002701..5004789-chr11:5011037..5012979,2	K562	blood:
39	chr11:4657777..4658387-chr11:5025582..5026377,4	MCF-7	breast:
40	11:4988858-5002113..11:5700314-5707362	Hela-S3	cervix:
41	chr11:4208337..4209114-chr11:5025486..5026266,2	MCF-7	breast:
42	11:5018576-5020673..11:5033143-5038367	GM12878	blood:
43	chr11:4998734..5001673-chr11:5002692..5004874,2	MCF-7	breast:
44	11:4900708-4903421..11:5020673-5032983	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MMP26-1	chr11:5009500-5009540	NONHSAT017654
2	lnc-MMP26-1	chr11:5010878-5011060	NONHSAT017654

No data

Variant related genes	Relation type
OR51L1	TF binding region
OR51A4	TF binding region
OR51P1P	TF binding region
OR51A5P	TF binding region
OR51A2	TF binding region
MMP26	TF binding region
OR51A3P	TF binding region
OR51L1	CpG island
OR51A4	CpG island
OR51P1P	CpG island
OR51A5P	CpG island
OR51A2	CpG island
MMP26	CpG island
OR51A3P	CpG island
ENSG00000176900	chromatin interactions
ENSG00000181609	chromatin interactions
ENSG00000175520	chromatin interactions
ENSG00000187747	chromatin interactions
ENSG00000244734	chromatin interactions
ENSG00000254480	chromatin interactions
ENSG00000224300	chromatin interactions
ENSG00000223609	chromatin interactions
ENSG00000176922	chromatin interactions
ENSG00000188069	chromatin interactions
ENSG00000132274	chromatin interactions
ENSG00000229988	chromatin interactions
ENSG00000221031	chromatin interactions
ENSG00000176879	chromatin interactions
ENSG00000167346	chromatin interactions
ENSG00000181616	chromatin interactions
ENSG00000187918	chromatin interactions
ENSG00000260629	chromatin interactions
ENSG00000132256	chromatin interactions

Extended variants
information (count: 2017 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2017 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527938241	chr11:4958466-4958467	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs113586569	chr11:4958470-4958471	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs567514488	chr11:4958476-4958477	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs145981823	chr11:4958479-4958480	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs112971772	chr11:4958484-4958485	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs571185236	chr11:4958492-4958493	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs191007202	chr11:4958533-4958534	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs373665620	chr11:4958547-4958548	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs550982337	chr11:4958561-4958562	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs565976556	chr11:4958573-4958574	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs536504954	chr11:4958598-4958599	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs183281985	chr11:4958610-4958611	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs187578778	chr11:4958614-4958615	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs113680032	chr11:4958631-4958632	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs578175058	chr11:4958645-4958646	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs11034732	chr11:4958647-4958648	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs578007088	chr11:4958668-4958669	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs545394845	chr11:4958684-4958685	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs141589345	chr11:4958699-4958700	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs16907558	chr11:4958702-4958703	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs542901250	chr11:4958703-4958704	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs189992692	chr11:4958710-4958711	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs2596005	chr11:4958758-4958759	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs549935793	chr11:4958762-4958763	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs571336816	chr11:4958764-4958765	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs375718323	chr11:4958773-4958774	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs528929443	chr11:4958802-4958803	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs368224907	chr11:4958803-4958804	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs549090834	chr11:4958822-4958823	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs183304917	chr11:4958823-4958824	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs34522077	chr11:4958829-4958830	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs565536625	chr11:4958861-4958862	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs536591110	chr11:4958862-4958863	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs112640060	chr11:4958868-4958869	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs569895216	chr11:4958917-4958918	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs537258545	chr11:4958924-4958925	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs146130616	chr11:4958925-4958926	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs187795250	chr11:4958926-4958927	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs367950388	chr11:4958928-4958929	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs570572952	chr11:4958935-4958936	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs554176266	chr11:4958948-4958949	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs17339000	chr11:4958961-4958962	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
43	rs376932196	chr11:4959002-4959003	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs546587440	chr11:4959021-4959022	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs542940031	chr11:4959035-4959036	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs547376095	chr11:4959053-4959054	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs113461373	chr11:4959080-4959081	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs576296404	chr11:4959107-4959108	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs543621562	chr11:4959115-4959116	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs565292167	chr11:4959116-4959117	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4983800-4984200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr11:4986800-4987200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr11:4987200-4988200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:4988200-4988400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:5000200-5001000	Enhancers	Fetal Lung	lung
6	chr11:5000400-5001400	Enhancers	Fetal Muscle Leg	muscle
7	chr11:5001000-5004000	Weak transcription	Fetal Lung	lung
8	chr11:5002600-5005400	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr11:5004000-5005800	Enhancers	Fetal Lung	lung
10	chr11:5005400-5005600	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr11:5009200-5009400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr11:5010800-5011200	Active TSS	Spleen	Spleen
13	chr11:5020400-5020800	Active TSS	Brain Substantia Nigra	brain
14	chr11:5025800-5026400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr11:5026000-5026800	Enhancers	NHEK	skin
16	chr11:5026200-5026800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr11:5026200-5026800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr11:5026200-5026800	Enhancers	HMEC	breast
19	chr11:5026400-5026800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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