Variant report

Variant	nsv540932
Chromosome Location	chr11:4631455-4666157
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	chr11:4658189-4658440	GM12878	blood:	n/a	n/a
4	BHLHE40	chr11:4658172-4658516	K562	blood:	n/a	n/a
5	BHLHE40	chr11:4658886-4659215	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	chr11:4647442-4647716	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr11:4661402-4661517	K562	blood:	n/a	n/a
10	CEBPB	chr11:4647421-4647749	K562	blood:	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	chr11:4647500-4647650	GM12868	blood:	n/a	n/a
16	CTCF	chr11:4658146-4658460	GM12878	blood:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316 chr11:4658423-4658431
17	CTCF	chr11:4647445-4647781	ECC-1	luminal epithelium:	n/a	n/a
18	CTCF	chr11:4658240-4658390	MCF-7	breast:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
19	CTCF	chr11:4658131-4658472	ProgFib	skin:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316 chr11:4658423-4658431
20	CTCF	chr11:4647483-4647732	LNCaP	prostate:	n/a	n/a
21	CTCF	chr11:4658200-4658350	HCT-116	colon:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
22	CTCF	chr11:4658175-4658419	LNCaP	prostate:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
23	CTCF	chr11:4658149-4658444	HUVEC	blood vessel:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316 chr11:4658423-4658431
24	CTCF	chr11:4647520-4647670	HEK293	kidney:	n/a	n/a
25	CTCF	chr11:4647444-4647757	Medullo	brain:	n/a	n/a
26	CTCF	chr11:4647820-4647970	HVMF	connective:	n/a	n/a
27	CTCF	chr11:4658200-4658350	NHDF-neo	bronchial:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
28	CTCF	chr11:4658146-4658464	K562	blood:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316 chr11:4658423-4658431
29	CTCF	chr11:4658180-4658330	NHDF-neo	bronchial:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
30	CTCF	chr11:4658086-4658412	T-47D	breast:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
31	CTCF	chr11:4647520-4647670	BJ	skin:	n/a	n/a
32	CTCF	chr11:4647522-4647726	HepG2	liver:	n/a	n/a
33	CTCF	chr11:4658582-4658626	GM19238	blood:	n/a	n/a
34	CTCF	chr11:4658159-4658440	Hela-S3	cervix:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316 chr11:4658423-4658431
35	CTCF	chr11:4658220-4658370	HMF	breast:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
36	CTCF	chr11:4631560-4631710	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr11:4658240-4658390	HPF	lung:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
38	CTCF	chr11:4647560-4647710	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr11:4647500-4647650	GM12870	blood:	n/a	n/a
40	CTCF	chr11:4658240-4658390	HA-sp	spinal cord:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
41	CTCF	chr11:4658200-4658350	BJ	skin:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
42	CTCF	chr11:4647520-4647670	K562	blood:	n/a	n/a
43	CTCF	chr11:4658165-4658417	A549	lung:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
44	CTCF	chr11:4647540-4647690	GM12873	blood:	n/a	n/a
45	CTCF	chr11:4647520-4647670	A549	lung:	n/a	n/a
46	CTCF	chr11:4647240-4647390	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr11:4647500-4647650	GM12871	blood:	n/a	n/a
48	CTCF	chr11:4647463-4647801	HepG2	liver:	n/a	n/a
49	CTCF	chr11:4647373-4647822	K562	blood:	n/a	n/a
50	CTCF	chr11:4647520-4647670	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4664220-4664270	NH-A	brain:	n/a
2	chr11:4665002-4665052	GM12891	blood:	n/a
3	chr11:4664117-4664167	NHDF-neo	bronchial:	n/a
4	chr11:4664220-4664270	AG10803	skin:	n/a
5	chr11:4631906-4631956	Jurkat	blood:	n/a
6	chr11:4660300-4660350	GM12878	blood:	n/a
7	chr11:4661207-4661257	SK-N-SH	brain:	n/a
8	chr11:4664220-4664270	HRCEpiC	kidney:	n/a
9	chr11:4665165-4665215	SKMC	muscle:	n/a
10	chr11:4665165-4665215	HCPEpiC	choroid plexus:	n/a
11	chr11:4658391-4658441	SK-N-SH_RA	brain:	n/a
12	chr11:4659811-4659861	RPTEC	kidney:	n/a
13	chr11:4665002-4665052	HIPEpiC	eye:	n/a
14	chr11:4664117-4664167	ECC-1	luminal epithelium:	n/a
15	chr11:4665165-4665215	GM12891	blood:	n/a
16	chr11:4661335-4661385	ProgFib	skin:	n/a
17	chr11:4661335-4661385	IMR90	lung:	fetal
18	chr11:4665002-4665052	HL-60	blood:	n/a
19	chr11:4664117-4664167	Caco-2	colon:	n/a
20	chr11:4660300-4660350	AG10803	skin:	n/a
21	chr11:4631906-4631956	HPAEpiC	pulmonary alveolar:	n/a
22	chr11:4665002-4665052	HPAEpiC	pulmonary alveolar:	n/a
23	chr11:4664117-4664167	HRPEpiC	eye:	n/a
24	chr11:4665165-4665215	NHDF-neo	bronchial:	n/a
25	chr11:4664220-4664270	Caco-2	colon:	n/a
26	chr11:4665165-4665215	AG09309	skin:	n/a
27	chr11:4665165-4665215	HEEpiC	esophagus:	n/a
28	chr11:4660300-4660350	HCF	heart:	n/a
29	chr11:4631906-4631956	ECC-1	luminal epithelium:	n/a
30	chr11:4631906-4631956	NT2-D1	testis:	n/a
31	chr11:4665002-4665052	HCT-116	colon:	n/a
32	chr11:4664117-4664167	HAEpiC	amniotic membrane:	n/a
33	chr11:4661207-4661257	AG04449	skin:	fetal
34	chr11:4665165-4665215	PANC-1	pancreas:	n/a
35	chr11:4660300-4660350	AoSMC	blood vessel:	n/a
36	chr11:4661207-4661257	HMEC	breast:	n/a
37	chr11:4661207-4661257	Caco-2	colon:	n/a
38	chr11:4665165-4665215	AG09319	gingival:	n/a
39	chr11:4664117-4664167	NB4	blood:	n/a
40	chr11:4659811-4659861	GM06990	blood:	n/a
41	chr11:4664220-4664270	AG04449	skin:	fetal
42	chr11:4661335-4661385	MCF10A-Er-Src	breast:	n/a
43	chr11:4659811-4659861	SK-N-MC	brain:	n/a
44	chr11:4664220-4664270	Hepatocyte	liver:	n/a
45	chr11:4664220-4664270	HCPEpiC	choroid plexus:	n/a
46	chr11:4631906-4631956	LNCaP	prostate:	n/a
47	chr11:4659811-4659861	SAEC	small airway:	n/a
48	chr11:4661335-4661385	NHDF-neo	bronchial:	n/a
49	chr11:4659811-4659861	GM19239	blood:	n/a
50	chr11:4660300-4660350	U87	brain:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR51D1-1	chr11:4649827-4650062	l_424_chr11:4644432-4650062_testes
2	lnc-OR51D1-1	chr11:4647477-4647663	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
ENSG00000205494	chromatin interactions
ENSG00000254480	chromatin interactions

Extended variants
information (count: 1114 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1114 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545623551	chr11:4631463-4631464	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs560251552	chr11:4631473-4631474	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs117266981	chr11:4631475-4631476	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs542603230	chr11:4631476-4631477	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs73399640	chr11:4631526-4631527	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs531615295	chr11:4631561-4631562	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs79553555	chr11:4631578-4631579	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs34568660	chr11:4631605-4631606	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs571230291	chr11:4631614-4631615	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs532127589	chr11:4631615-4631616	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs188223104	chr11:4631718-4631719	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs566622939	chr11:4631723-4631724	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs565771068	chr11:4631815-4631816	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs74052467	chr11:4631863-4631864	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs201595522	chr11:4631881-4631882	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs5789334	chr11:4631882-4631883	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs74649702	chr11:4631883-4631884	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs3064145	chr11:4631886-4631887	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs543933495	chr11:4631887-4631888	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs370357588	chr11:4631888-4631889	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs373708122	chr11:4631890-4631891	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs151079395	chr11:4631906-4631907	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs141120607	chr11:4631921-4631922	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs192728678	chr11:4631934-4631935	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs556852769	chr11:4631984-4631985	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs200319102	chr11:4631990-4631991	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs578252868	chr11:4631992-4631993	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs202190163	chr11:4631993-4631994	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs201183694	chr11:4632014-4632015	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs545507868	chr11:4632020-4632021	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs74052468	chr11:4632065-4632066	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs531934953	chr11:4632088-4632089	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554451035	chr11:4632113-4632114	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs74052470	chr11:4632159-4632160	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs542390451	chr11:4632184-4632185	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs368628319	chr11:4632261-4632262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs547003598	chr11:4632283-4632284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375490780	chr11:4632300-4632301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561053904	chr11:4632365-4632366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs531180235	chr11:4632371-4632372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550724215	chr11:4632411-4632412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs11295440	chr11:4632415-4632416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs77325532	chr11:4632422-4632423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201533016	chr11:4632424-4632425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs190003200	chr11:4632425-4632426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs11033015	chr11:4632460-4632461	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs184259834	chr11:4632504-4632505	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs11033016	chr11:4632552-4632553	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs11033017	chr11:4632583-4632584	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs4910640	chr11:4632588-4632589	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:310 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4629800-4631600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr11:4630000-4631600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr11:4630000-4631600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr11:4630000-4631600	Weak transcription	Primary B cells from cord blood	blood
5	chr11:4630000-4631600	Weak transcription	Ovary	ovary
6	chr11:4630000-4631600	Weak transcription	Thymus	Thymus
7	chr11:4630000-4631600	Weak transcription	NHEK	skin
8	chr11:4630000-4631600	Weak transcription	Osteobl	bone
9	chr11:4630000-4633200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr11:4630200-4631600	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr11:4630200-4631600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr11:4630200-4631600	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr11:4630200-4631600	Weak transcription	HUVEC	blood vessel
14	chr11:4631000-4631600	Enhancers	Left Ventricle	heart
15	chr11:4631000-4632000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
16	chr11:4631000-4632000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
17	chr11:4631200-4631600	Weak transcription	Lung	lung
18	chr11:4631200-4631800	Enhancers	Small Intestine	intestine
19	chr11:4631200-4632000	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr11:4631200-4632000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
21	chr11:4631200-4632000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
22	chr11:4631200-4632000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr11:4631200-4632000	Active TSS	Right Atrium	heart
24	chr11:4631200-4632000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr11:4631400-4631600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
26	chr11:4631400-4631600	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr11:4631400-4631600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr11:4631400-4631600	Flanking Active TSS	Adipose Nuclei	Adipose
29	chr11:4631400-4631600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr11:4631400-4631600	Enhancers	Fetal Intestine Small	intestine
31	chr11:4631400-4631600	Enhancers	Placenta	Placenta
32	chr11:4631400-4631600	Enhancers	Fetal Thymus	thymus
33	chr11:4631400-4631600	Enhancers	Spleen	Spleen
34	chr11:4631400-4631800	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr11:4631400-4631800	Flanking Active TSS	Primary B cells from peripheral blood	blood
36	chr11:4631400-4631800	Active TSS	Primary T cells from cord blood	blood
37	chr11:4631400-4631800	Flanking Active TSS	Primary hematopoietic stem cells	blood
38	chr11:4631400-4631800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
39	chr11:4631400-4631800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
40	chr11:4631400-4631800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
41	chr11:4631400-4631800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
42	chr11:4631400-4631800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr11:4631400-4631800	Enhancers	Liver	Liver
44	chr11:4631400-4631800	Active TSS	Brain Hippocampus Middle	brain
45	chr11:4631400-4631800	Active TSS	Rectal Smooth Muscle	rectum
46	chr11:4631400-4631800	Active TSS	NHDF-Ad	bronchial
47	chr11:4631400-4632000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
48	chr11:4631400-4632000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
49	chr11:4631400-4632000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr11:4631400-4632000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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