Variant report

Variant	nsv540936
Chromosome Location	chr11:4633452-4669343
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	ATF1	chr11:4647476-4647734	K562	blood:	n/a	n/a
2	ATF1	chr11:4640875-4641090	K562	blood:	n/a	n/a
3	BHLHE40	chr11:4658886-4659215	GM12878	blood:	n/a	n/a
4	BHLHE40	chr11:4658172-4658516	K562	blood:	n/a	n/a
5	BHLHE40	chr11:4658189-4658440	GM12878	blood:	n/a	n/a
6	CBX3	chr11:4658108-4658530	K562	blood:	n/a	n/a
7	CEBPB	chr11:4647363-4647690	MCF-7	breast:	n/a	n/a
8	CEBPB	chr11:4661402-4661517	K562	blood:	n/a	n/a
9	CEBPB	chr11:4647421-4647749	K562	blood:	n/a	n/a
10	CEBPB	chr11:4647442-4647716	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr11:4641031-4641091	K562	blood:	n/a	n/a
12	CHD2	chr11:4664571-4664584	K562	blood:	n/a	n/a
13	CHD2	chr11:4665805-4665840	H1-hESC	embryonic stem cell:	n/a	n/a
14	CREB1	chr11:4658091-4658477	A549	lung:	n/a	n/a
15	CTCF	chr11:4647560-4647710	GM12864	blood:	n/a	n/a
16	CTCF	chr11:4647460-4647750	HFF-Myc	foreskin:	n/a	n/a
17	CTCF	chr11:4658119-4658483	GM19238	blood:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316 chr11:4658423-4658431
18	CTCF	chr11:4657760-4657910	GM12864	blood:	n/a	n/a
19	CTCF	chr11:4647493-4647695	GM19238	blood:	n/a	n/a
20	CTCF	chr11:4647540-4647690	AG04449	skin:	n/a	n/a
21	CTCF	chr11:4647520-4647670	HUVEC	blood vessel:	n/a	n/a
22	CTCF	chr11:4659040-4659190	AG09319	gingival:	n/a	n/a
23	CTCF	chr11:4647540-4647690	NHDF-neo	bronchial:	n/a	n/a
24	CTCF	chr11:4647485-4647738	MCF-7	breast:	n/a	n/a
25	CTCF	chr11:4657925-4658636	A549	lung:	n/a	chr11:4658301-4658314 chr11:4658486-4658494 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316 chr11:4658423-4658431
26	CTCF	chr11:4647540-4647690	GM12878	blood:	n/a	n/a
27	CTCF	chr11:4658180-4658330	NHEK	skin:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
28	CTCF	chr11:4647537-4647659	MCF-7	breast:	n/a	n/a
29	CTCF	chr11:4658155-4658455	MCF-7	breast:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316 chr11:4658423-4658431
30	CTCF	chr11:4647460-4647610	GM12866	blood:	n/a	n/a
31	CTCF	chr11:4658162-4658451	MCF-7	breast:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316 chr11:4658423-4658431
32	CTCF	chr11:4658220-4658370	GM12874	blood:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
33	CTCF	chr11:4658200-4658350	GM12871	blood:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
34	CTCF	chr11:4658194-4658383	A549	lung:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
35	CTCF	chr11:4658160-4658310	HFF	foreskin:	n/a	n/a
36	CTCF	chr11:4658220-4658370	AG04450	lung:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
37	CTCF	chr11:4647820-4647970	HVMF	connective:	n/a	n/a
38	CTCF	chr11:4647500-4647766	MCF-7	breast:	n/a	n/a
39	CTCF	chr11:4658150-4658465	GM19239	blood:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316 chr11:4658423-4658431
40	CTCF	chr11:4658133-4658466	Gliobla	brain:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316 chr11:4658423-4658431
41	CTCF	chr11:4658220-4658370	AG04449	skin:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
42	CTCF	chr11:4647486-4647762	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr11:4647540-4647690	K562	blood:	n/a	n/a
44	CTCF	chr11:4647540-4647690	HVMF	connective:	n/a	n/a
45	CTCF	chr11:4647560-4647710	AG09319	gingival:	n/a	n/a
46	CTCF	chr11:4647540-4647690	HPF	lung:	n/a	n/a
47	CTCF	chr11:4647321-4647859	HCT-116	colon:	n/a	n/a
48	CTCF	chr11:4658137-4658474	GM12891	blood:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316 chr11:4658423-4658431
49	CTCF	chr11:4658188-4658440	Lung_OC	lung:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316 chr11:4658423-4658431
50	CTCF	chr11:4647560-4647710	SK-N-SH_RA	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4661207-4661257	HUVEC	blood vessel:	n/a
2	chr11:4661207-4661257	HUVEC	blood vessel:	n/a
3	chr11:4660300-4660350	NHBE	bronchial:	n/a
4	chr11:4658391-4658441	HEEpiC	esophagus:	n/a
5	chr11:4665002-4665052	NB4	blood:	n/a
6	chr11:4658391-4658441	K562	blood:	n/a
7	chr11:4665002-4665052	HIPEpiC	eye:	n/a
8	chr11:4658391-4658441	NHBE	bronchial:	n/a
9	chr11:4666412-4666462	HUVEC	blood vessel:	n/a
10	chr11:4665002-4665052	GM12891	blood:	n/a
11	chr11:4666412-4666462	NH-A	brain:	n/a
12	chr11:4665165-4665215	K562	blood:	n/a
13	chr11:4659811-4659861	AG09309	skin:	n/a
14	chr11:4661335-4661385	PANC-1	pancreas:	n/a
15	chr11:4664220-4664270	HNPCEpiC	eye:	n/a
16	chr11:4665002-4665052	IMR90	lung:	fetal
17	chr11:4664117-4664167	PFSK-1	brain:	n/a
18	chr11:4658391-4658441	AG10803	skin:	n/a
19	chr11:4665002-4665052	HRCEpiC	kidney:	n/a
20	chr11:4666412-4666462	A549	lung:	n/a
21	chr11:4664117-4664167	AG09319	gingival:	n/a
22	chr11:4664220-4664270	HCT-116	colon:	n/a
23	chr11:4665002-4665052	HRE	kidney:	n/a
24	chr11:4664220-4664270	AG09319	gingival:	n/a
25	chr11:4659811-4659861	RPTEC	kidney:	n/a
26	chr11:4664117-4664167	HL-60	blood:	n/a
27	chr11:4661207-4661257	HNPCEpiC	eye:	n/a
28	chr11:4658391-4658441	AG09319	gingival:	n/a
29	chr11:4665165-4665215	HAEpiC	amniotic membrane:	n/a
30	chr11:4659811-4659861	SK-N-MC	brain:	n/a
31	chr11:4664117-4664167	Hela-S3	cervix:	n/a
32	chr11:4665165-4665215	AG04450	lung:	fetal
33	chr11:4658391-4658441	HIPEpiC	eye:	n/a
34	chr11:4664117-4664167	HRCEpiC	kidney:	n/a
35	chr11:4661335-4661385	GM12892	blood:	n/a
36	chr11:4666412-4666462	SKMC	muscle:	n/a
37	chr11:4658391-4658441	AoSMC	blood vessel:	n/a
38	chr11:4665002-4665052	HMEC	breast:	n/a
39	chr11:4664117-4664167	HUVEC	blood vessel:	n/a
40	chr11:4665002-4665052	MCF10A-Er-Src	breast:	n/a
41	chr11:4661335-4661385	H1-hESC	embryonic stem cell:	embryo
42	chr11:4661335-4661385	HRE	kidney:	n/a
43	chr11:4661207-4661257	HMEC	breast:	n/a
44	chr11:4664220-4664270	HCM	heart:	n/a
45	chr11:4661207-4661257	NHDF-neo	bronchial:	n/a
46	chr11:4660300-4660350	Hepatocyte	liver:	n/a
47	chr11:4664220-4664270	GM12892	blood:	n/a
48	chr11:4661335-4661385	K562	blood:	n/a
49	chr11:4659811-4659861	U87	brain:	n/a
50	chr11:4664117-4664167	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:4658042..4658694-chr11:4667228..4668066,2	K562	blood:
2	chr11:4657985..4658755-chr11:5391194..5391750,2	MCF-7	breast:
3	chr11:4626393..4630553-chr11:4632444..4636618,6	K562	blood:
4	chr11:4657777..4658387-chr11:5025582..5026377,4	MCF-7	breast:
5	chr11:4667581..4670496-chr11:4674502..4676349,2	K562	blood:
6	chr11:4658042..4658694-chr11:4667228..4668066,2	K562	blood:
7	chr11:4657777..4658777-chr11:5012019..5012933,4	K562	blood:
8	chr11:4658184..4658763-chr11:5145307..5145823,2	MCF-7	breast:
9	chr11:4657872..4658731-chr11:5025387..5026540,3	K562	blood:
10	chr11:4208255..4208841-chr11:4647118..4648091,2	K562	blood:
11	chr11:4658272..4658813-chr11:5025400..5026262,2	MCF-7	breast:
12	chr11:4647527..4648151-chr11:5025801..5026495,2	MCF-7	breast:
13	chr11:4208515..4209433-chr11:4658248..4659042,2	K562	blood:
14	chr11:4647199..4648030-chr11:5025327..5026179,2	K562	blood:
15	chr11:4657833..4658473-chr11:4847439..4848013,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR51D1-1	chr11:4647477-4647663	l_424_chr11:4644432-4650062_testes
2	lnc-OR51D1-1	chr11:4649827-4650062	l_424_chr11:4644432-4650062_testes
3	lnc-OR51D1-1	chr11:4644433-4644768	l_424_chr11:4644432-4650062_testes

Variant related genes	Relation type
OR51E1	TF binding region
TRIM68	TF binding region
OR51D1	TF binding region
OR51E1	CpG island
TRIM68	CpG island
OR51D1	CpG island
ENSG00000167333	chromatin interactions
ENSG00000254480	chromatin interactions
ENSG00000205494	chromatin interactions

Extended variants
information (count: 1177 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1177 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116802710	chr11:4633467-4633468	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs117396937	chr11:4633491-4633492	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs542749341	chr11:4633492-4633493	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs186034272	chr11:4633493-4633494	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs576035039	chr11:4633524-4633525	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs74052472	chr11:4633537-4633538	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs558246494	chr11:4633553-4633554	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs576402386	chr11:4633597-4633598	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs541260809	chr11:4633600-4633601	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs540630753	chr11:4633605-4633606	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs371412979	chr11:4633621-4633622	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs191275387	chr11:4633636-4633637	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs117539535	chr11:4633656-4633657	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs541659215	chr11:4633681-4633682	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs563524565	chr11:4633688-4633689	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs115243784	chr11:4633689-4633690	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs550261227	chr11:4633727-4633728	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs565397946	chr11:4633755-4633756	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs78428099	chr11:4633761-4633762	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs373652425	chr11:4633796-4633797	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs547821987	chr11:4633800-4633801	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs566231449	chr11:4633809-4633810	Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs545238111	chr11:4633916-4633917	Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs536999104	chr11:4633948-4633949	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs140524462	chr11:4633949-4633950	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs553740886	chr11:4633956-4633957	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs181343394	chr11:4633976-4633977	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs74052473	chr11:4634012-4634013	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs570224804	chr11:4634060-4634061	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs571283742	chr11:4634092-4634093	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs534311556	chr11:4634112-4634113	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs552981885	chr11:4634125-4634126	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs574625180	chr11:4634226-4634227	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs542139591	chr11:4634230-4634231	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs556988622	chr11:4634253-4634254	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs386750036	chr11:4634265-4634266	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs145622428	chr11:4634267-4634268	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs56113312	chr11:4634286-4634287	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs532694724	chr11:4634298-4634299	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs199551345	chr11:4634310-4634311	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs185938140	chr11:4634351-4634352	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs545305034	chr11:4634370-4634371	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs540217525	chr11:4634383-4634384	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs138321384	chr11:4634408-4634409	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs565867189	chr11:4634496-4634497	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs530055888	chr11:4634514-4634515	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs115253595	chr11:4634539-4634540	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs570257125	chr11:4634608-4634609	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs143152523	chr11:4634735-4634736	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs75603147	chr11:4634742-4634743	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4632000-4633800	Weak transcription	Brain Angular Gyrus	brain
2	chr11:4633200-4634000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:4633200-4634000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr11:4636600-4643400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr11:4640200-4640800	Enhancers	Fetal Intestine Small	intestine
6	chr11:4640600-4641000	Enhancers	K562	blood
7	chr11:4644800-4647000	Weak transcription	Psoas Muscle	Psoas
8	chr11:4647400-4647800	Enhancers	K562	blood
9	chr11:4647600-4648000	Enhancers	Colon Smooth Muscle	Colon
10	chr11:4647600-4648200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr11:4647800-4649800	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr11:4647800-4650000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr11:4647800-4650000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr11:4648000-4649600	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr11:4648200-4648600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr11:4648600-4649600	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr11:4648800-4649600	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr11:4649200-4649400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr11:4657400-4658000	Enhancers	Ovary	ovary
20	chr11:4657800-4658000	Enhancers	Adipose Nuclei	Adipose
21	chr11:4658000-4658200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr11:4658000-4658200	Bivalent Enhancer	Brain Cingulate Gyrus	brain
23	chr11:4658000-4658200	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr11:4658000-4658200	Enhancers	Brain Substantia Nigra	brain
25	chr11:4658000-4658200	Bivalent Enhancer	Duodenum Mucosa	Duodenum
26	chr11:4658000-4658200	Flanking Active TSS	Ovary	ovary
27	chr11:4658000-4658200	Weak transcription	Right Atrium	heart
28	chr11:4658000-4658200	Flanking Bivalent TSS/Enh	K562	blood
29	chr11:4658000-4658400	Enhancers	Primary T helper naive cells from peripheral blood	blood
30	chr11:4658000-4658400	Enhancers	Right Ventricle	heart
31	chr11:4658000-4658600	Enhancers	Primary B cells from peripheral blood	blood
32	chr11:4658000-4658600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
33	chr11:4658000-4658600	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr11:4658000-4658600	Active TSS	Stomach Smooth Muscle	stomach
35	chr11:4658000-4658800	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr11:4658000-4658800	Flanking Active TSS	Adipose Nuclei	Adipose
37	chr11:4658200-4658400	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr11:4658200-4658400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr11:4658200-4658400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr11:4658200-4658400	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr11:4658200-4658400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
42	chr11:4658200-4658400	Active TSS	Gastric	stomach
43	chr11:4658200-4658400	Enhancers	Ovary	ovary
44	chr11:4658200-4658400	Active TSS	Rectal Mucosa Donor 29	rectum
45	chr11:4658200-4658400	Active TSS	Rectal Mucosa Donor 31	rectum
46	chr11:4658200-4658400	Active TSS	Skeletal Muscle Male	skeletal muscle
47	chr11:4658200-4658400	Active TSS	Skeletal Muscle Female	skeletal muscle
48	chr11:4658200-4658400	Enhancers	K562	blood
49	chr11:4658200-4658600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
50	chr11:4658200-4658600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood

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