Variant report

Variant	nsv1041633
Chromosome Location	chr11:4639292-4693109
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:599)
CpG islands
(count:796)
Chromatin interactive
region (count:20)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:599 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:4679879-4680384	K562	blood:	n/a	n/a
2	ATF1	chr11:4640875-4641090	K562	blood:	n/a	n/a
3	ATF1	chr11:4647476-4647734	K562	blood:	n/a	n/a
4	ATF1	chr11:4680154-4680354	K562	blood:	n/a	n/a
5	BHLHE40	chr11:4658189-4658440	GM12878	blood:	n/a	n/a
6	BHLHE40	chr11:4679927-4680079	K562	blood:	n/a	n/a
7	BHLHE40	chr11:4658886-4659215	GM12878	blood:	n/a	n/a
8	BHLHE40	chr11:4658172-4658516	K562	blood:	n/a	n/a
9	CBX3	chr11:4658108-4658530	K562	blood:	n/a	n/a
10	CBX3	chr11:4680009-4680493	K562	blood:	n/a	n/a
11	CEBPB	chr11:4641031-4641091	K562	blood:	n/a	n/a
12	CEBPB	chr11:4661402-4661517	K562	blood:	n/a	n/a
13	CEBPB	chr11:4647442-4647716	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr11:4678840-4679165	K562	blood:	n/a	chr11:4678998-4679009
15	CEBPB	chr11:4678853-4679138	HepG2	liver:	n/a	chr11:4678998-4679009
16	CEBPB	chr11:4647363-4647690	MCF-7	breast:	n/a	n/a
17	CEBPB	chr11:4680079-4680430	K562	blood:	n/a	n/a
18	CEBPB	chr11:4680108-4680438	K562	blood:	n/a	n/a
19	CEBPB	chr11:4647421-4647749	K562	blood:	n/a	n/a
20	CEBPD	chr11:4680058-4680601	K562	blood:	n/a	n/a
21	CHD2	chr11:4664571-4664584	K562	blood:	n/a	n/a
22	CHD2	chr11:4665805-4665840	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr11:4680006-4680343	K562	blood:	n/a	n/a
24	CREB1	chr11:4658091-4658477	A549	lung:	n/a	n/a
25	CTCF	chr11:4647501-4647502	GM13977	blood:	n/a	n/a
26	CTCF	chr11:4647500-4647650	GM12870	blood:	n/a	n/a
27	CTCF	chr11:4658156-4658389	HepG2	liver:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
28	CTCF	chr11:4647520-4647670	A549	lung:	n/a	n/a
29	CTCF	chr11:4647434-4647718	MCF-7	breast:	n/a	n/a
30	CTCF	chr11:4658700-4658850	SAEC	small airway:	n/a	n/a
31	CTCF	chr11:4658160-4658310	A549	lung:	n/a	n/a
32	CTCF	chr11:4647540-4647690	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr11:4658093-4658459	A549	lung:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316 chr11:4658423-4658431
34	CTCF	chr11:4658240-4658390	HCT-116	colon:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
35	CTCF	chr11:4658200-4658350	GM12865	blood:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
36	CTCF	chr11:4647540-4647690	HAc	cerebellar:	n/a	n/a
37	CTCF	chr11:4658240-4658390	HBMEC	blood vessel:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
38	CTCF	chr11:4647472-4647752	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr11:4647540-4647690	HCFaa	heart:	n/a	n/a
40	CTCF	chr11:4658153-4658438	H1-hESC	embryonic stem cell:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316 chr11:4658423-4658431
41	CTCF	chr11:4647487-4647733	HepG2	liver:	n/a	n/a
42	CTCF	chr11:4647490-4647771	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr11:4647460-4647610	HFF	foreskin:	n/a	n/a
44	CTCF	chr11:4647560-4647710	GM12864	blood:	n/a	n/a
45	CTCF	chr11:4658180-4658330	WI-38	lung:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
46	CTCF	chr11:4658220-4658370	AG10803	skin:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
47	CTCF	chr11:4658220-4658370	AoAF	blood vessel:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
48	CTCF	chr11:4658200-4658350	BJ	skin:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
49	CTCF	chr11:4647453-4647762	Gliobla	brain:	n/a	n/a
50	CTCF	chr11:4658149-4658451	Medullo	brain:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316 chr11:4658423-4658431

(count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4676365-4676415	GM19239	blood:	n/a
2	chr11:4664220-4664270	Jurkat	blood:	n/a
3	chr11:4664117-4664167	ECC-1	luminal epithelium:	n/a
4	chr11:4676365-4676415	GM19239	blood:	n/a
5	chr11:4664220-4664270	Jurkat	blood:	n/a
6	chr11:4664117-4664167	ECC-1	luminal epithelium:	n/a
7	chr11:4661335-4661385	HCPEpiC	choroid plexus:	n/a
8	chr11:4661207-4661257	PFSK-1	brain:	n/a
9	chr11:4659811-4659861	GM06990	blood:	n/a
10	chr11:4674353-4674403	Hela-S3	cervix:	n/a
11	chr11:4666412-4666462	HCPEpiC	choroid plexus:	n/a
12	chr11:4658391-4658441	NH-A	brain:	n/a
13	chr11:4664117-4664167	HMEC	breast:	n/a
14	chr11:4674353-4674403	HMEC	breast:	n/a
15	chr11:4661207-4661257	BJ	skin:	n/a
16	chr11:4658391-4658441	CMK	blood:	n/a
17	chr11:4661207-4661257	A549	lung:	n/a
18	chr11:4674353-4674403	AG04449	skin:	fetal
19	chr11:4658391-4658441	PrEC	prostate:	n/a
20	chr11:4661335-4661385	GM12891	blood:	n/a
21	chr11:4661335-4661385	SK-N-SH_RA	brain:	n/a
22	chr11:4666412-4666462	NT2-D1	testis:	n/a
23	chr11:4658391-4658441	MCF-7	breast:	n/a
24	chr11:4676365-4676415	Jurkat	blood:	n/a
25	chr11:4676365-4676415	HAEpiC	amniotic membrane:	n/a
26	chr11:4659811-4659861	SK-N-SH	brain:	n/a
27	chr11:4664220-4664270	PANC-1	pancreas:	n/a
28	chr11:4665002-4665052	AG09319	gingival:	n/a
29	chr11:4661207-4661257	HRCEpiC	kidney:	n/a
30	chr11:4676365-4676415	BE2_C	brain:	n/a
31	chr11:4666412-4666462	HCF	heart:	n/a
32	chr11:4660300-4660350	SKMC	muscle:	n/a
33	chr11:4665165-4665215	HepG2	liver:	n/a
34	chr11:4676365-4676415	AG09319	gingival:	n/a
35	chr11:4664220-4664270	GM06990	blood:	n/a
36	chr11:4676365-4676415	MCF10A-Er-Src	breast:	n/a
37	chr11:4659811-4659861	H1-hESC	embryonic stem cell:	embryo
38	chr11:4664117-4664167	Hepatocyte	liver:	n/a
39	chr11:4665002-4665052	MCF10A-Er-Src	breast:	n/a
40	chr11:4665165-4665215	HCF	heart:	n/a
41	chr11:4666412-4666462	ECC-1	luminal epithelium:	n/a
42	chr11:4660300-4660350	LNCaP	prostate:	n/a
43	chr11:4665165-4665215	BJ	skin:	n/a
44	chr11:4666412-4666462	ovcar-3	ovarian:	n/a
45	chr11:4686966-4687016	HRE	kidney:	n/a
46	chr11:4664117-4664167	HUVEC	blood vessel:	n/a
47	chr11:4674353-4674403	AG09319	gingival:	n/a
48	chr11:4660300-4660350	HRE	kidney:	n/a
49	chr11:4659811-4659861	PFSK-1	brain:	n/a
50	chr11:4686966-4687016	Hepatocyte	liver:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:4677690..4682058-chr11:4682699..4685666,4	K562	blood:
2	chr11:4657833..4658473-chr11:4847439..4848013,2	MCF-7	breast:
3	chr11:4647527..4648151-chr11:5025801..5026495,2	MCF-7	breast:
4	chr11:4658042..4658694-chr11:4667228..4668066,2	K562	blood:
5	chr11:4657872..4658731-chr11:5025387..5026540,3	K562	blood:
6	chr11:4658042..4658694-chr11:4667228..4668066,2	K562	blood:
7	chr11:4658272..4658813-chr11:5025400..5026262,2	MCF-7	breast:
8	chr11:4688697..4691190-chr11:4691672..4693874,2	K562	blood:
9	chr11:4667581..4670496-chr11:4674502..4676349,2	K562	blood:
10	chr11:4657777..4658387-chr11:5025582..5026377,4	MCF-7	breast:
11	chr11:4647199..4648030-chr11:5025327..5026179,2	K562	blood:
12	chr11:4657985..4658755-chr11:5391194..5391750,2	MCF-7	breast:
13	chr11:4657777..4658777-chr11:5012019..5012933,4	K562	blood:
14	chr11:4208515..4209433-chr11:4658248..4659042,2	K562	blood:
15	chr11:4658184..4658763-chr11:5145307..5145823,2	MCF-7	breast:
16	chr11:4676620..4679350-chr11:4683230..4685666,3	K562	blood:
17	chr11:4208255..4208841-chr11:4647118..4648091,2	K562	blood:
18	chr11:4688697..4691190-chr11:4691672..4693874,2	K562	blood:
19	chr11:4676620..4679350-chr11:4683230..4685666,3	K562	blood:
20	chr11:4667581..4670496-chr11:4674502..4676349,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR51E1-1	chr11:4687857-4688192	XLOC_009038
2	lnc-OR51E1-1	chr11:4687857-4688192	XLOC_009038
3	lnc-OR51D1-1	chr11:4644433-4644768	l_424_chr11:4644432-4650062_testes
4	lnc-OR51D1-1	chr11:4647477-4647663	l_424_chr11:4644432-4650062_testes
5	lnc-OR51D1-1	chr11:4649827-4650062	l_424_chr11:4644432-4650062_testes
6	lnc-OR51E1-1	chr11:4690901-4691087	XLOC_009038
7	lnc-OR51E1-1	chr11:4687857-4688192	NONHSAT017652

No data

Variant related genes	Relation type
OR51E1	TF binding region
OR51A9P	TF binding region
OR51D1	TF binding region
OR51E1	CpG island
OR51A9P	CpG island
OR51D1	CpG island
ENSG00000180723	chromatin interactions
ENSG00000254480	chromatin interactions
ENSG00000205494	chromatin interactions

Extended variants
information (count: 2000 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2000 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11600417	chr11:4639292-4639293	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559534879	chr11:4639345-4639346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529865999	chr11:4639377-4639378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs11033044	chr11:4639416-4639417	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs561373034	chr11:4639422-4639423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373209107	chr11:4639435-4639436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs77901736	chr11:4639436-4639437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138609883	chr11:4639461-4639462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182099828	chr11:4639499-4639500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572190809	chr11:4639522-4639523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs113918908	chr11:4639638-4639639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113617099	chr11:4639640-4639641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs146976364	chr11:4639676-4639677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186302725	chr11:4639677-4639678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554441445	chr11:4639690-4639691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574432880	chr11:4639729-4639730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs114026524	chr11:4639773-4639774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569452773	chr11:4639780-4639781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372758020	chr11:4639783-4639784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35953640	chr11:4639788-4639789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs79392023	chr11:4639798-4639799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs398015232	chr11:4639799-4639800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200358608	chr11:4639800-4639801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191591695	chr11:4639805-4639806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377164715	chr11:4639824-4639825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs180873822	chr11:4639836-4639837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577047934	chr11:4639837-4639838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143692542	chr11:4639856-4639857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112891848	chr11:4639866-4639867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574530587	chr11:4639968-4639969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs115751867	chr11:4640008-4640009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561356318	chr11:4640016-4640017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11033047	chr11:4640062-4640063	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs562546373	chr11:4640098-4640099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs148193405	chr11:4640189-4640190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565313601	chr11:4640207-4640208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs545497671	chr11:4640208-4640209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs59463394	chr11:4640226-4640227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs7104893	chr11:4640229-4640230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs532415184	chr11:4640254-4640255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs548041152	chr11:4640261-4640262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566246525	chr11:4640266-4640267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs565267699	chr11:4640267-4640268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185327602	chr11:4640275-4640276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs548421427	chr11:4640346-4640347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs7104070	chr11:4640381-4640382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs141221277	chr11:4640391-4640392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552629245	chr11:4640392-4640393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558244518	chr11:4640406-4640407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs75653677	chr11:4640461-4640462	Weak transcription Enhancers	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	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
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD

Chromatin state (count:285 , 50 per page) page: 1 2 3 4 5 6

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

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