Variant report

Variant	nsv468863
Chromosome Location	chr11:104875261-104918517
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:423)
CpG islands
(count:1037)
Chromatin interactive
region (count:2)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:423 , 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	ARID3A	chr11:104917801-104918523	HepG2	liver:	n/a	n/a
2	ATF3	chr11:104917796-104918302	A549	lung:	n/a	n/a
3	BATF	chr11:104905695-104905944	GM12878	blood:	n/a	n/a
4	BATF	chr11:104915949-104916196	GM12878	blood:	n/a	n/a
5	BATF	chr11:104905693-104906006	GM12878	blood:	n/a	n/a
6	BCL3	chr11:104917836-104918309	A549	lung:	n/a	chr11:104917968-104917977 chr11:104917969-104917978
7	BCL3	chr11:104917818-104918400	A549	lung:	n/a	chr11:104917968-104917977 chr11:104917969-104917978
8	BHLHE40	chr11:104914225-104914244	GM12878	blood:	n/a	n/a
9	BHLHE40	chr11:104885004-104885054	GM12878	blood:	n/a	n/a
10	BRCA1	chr11:104917502-104918375	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr11:104913608-104913870	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr11:104917592-104918391	A549	lung:	n/a	n/a
13	CEBPB	chr11:104916699-104917013	IMR90	lung:	n/a	chr11:104916858-104916869
14	CEBPB	chr11:104916752-104916931	HepG2	liver:	n/a	chr11:104916858-104916869
15	CEBPB	chr11:104916680-104917050	HepG2	liver:	n/a	chr11:104916858-104916869
16	CEBPB	chr11:104905228-104906180	IMR90	lung:	n/a	chr11:104905915-104905932 chr11:104905600-104905613 chr11:104905919-104905930
17	CEBPB	chr11:104905749-104906194	HepG2	liver:	n/a	chr11:104905915-104905932 chr11:104905919-104905930
18	CEBPB	chr11:104917654-104918310	A549	lung:	n/a	n/a
19	CEBPB	chr11:104917907-104918351	HepG2	liver:	n/a	n/a
20	CEBPB	chr11:104905287-104906325	Hela-S3	cervix:	n/a	chr11:104905915-104905932 chr11:104905600-104905613 chr11:104905919-104905930
21	CEBPB	chr11:104917575-104918420	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr11:104915430-104916328	IMR90	lung:	n/a	chr11:104915784-104915797
23	CEBPB	chr11:104913715-104914022	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr11:104916648-104916931	HepG2	liver:	n/a	chr11:104916858-104916869
25	CEBPB	chr11:104914457-104916305	Hela-S3	cervix:	n/a	chr11:104915784-104915797
26	CEBPB	chr11:104917718-104918298	A549	lung:	n/a	n/a
27	CEBPB	chr11:104917671-104918417	IMR90	lung:	n/a	n/a
28	CEBPB	chr11:104916683-104917034	Hela-S3	cervix:	n/a	chr11:104916858-104916869
29	CEBPB	chr11:104893837-104894118	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr11:104875690-104876153	Hela-S3	cervix:	n/a	n/a
31	CEBPD	chr11:104916761-104916943	HepG2	liver:	n/a	n/a
32	CHD2	chr11:104917679-104918334	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr11:104912156-104912184	HepG2	liver:	n/a	n/a
34	CHD2	chr11:104904637-104904755	GM12878	blood:	n/a	n/a
35	CREB1	chr11:104917957-104918170	A549	lung:	n/a	n/a
36	CREB1	chr11:104917693-104917895	A549	lung:	n/a	chr11:104917785-104917798
37	CTCF	chr11:104917460-104917610	AG10803	skin:	n/a	n/a
38	CTCF	chr11:104905019-104905026	Fibrobl	skin:	n/a	n/a
39	CTCF	chr11:104917320-104917470	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr11:104917320-104917470	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr11:104910741-104910756	GM20000	blood:	n/a	n/a
42	CTCF	chr11:104905277-104905441	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr11:104917440-104917590	AG09319	gingival:	n/a	n/a
44	CTCF	chr11:104915481-104915558	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr11:104904968-104905017	Fibrobl	skin:	n/a	n/a
46	CUX1	chr11:104905825-104905994	GM12878	blood:	n/a	n/a
47	CUX1	chr11:104903977-104904177	GM12878	blood:	n/a	n/a
48	E2F4	chr11:104905789-104906025	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr11:104916685-104916931	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr11:104915974-104916280	MCF10A-Er-Src	breast:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104887371-104887421	AG10803	skin:	n/a
2	chr11:104887307-104887357	A549	lung:	n/a
3	chr11:104894514-104894564	AoSMC	blood vessel:	n/a
4	chr11:104916075-104916125	ECC-1	luminal epithelium:	n/a
5	chr11:104916075-104916125	GM12878	blood:	n/a
6	chr11:104907029-104907079	HIPEpiC	eye:	n/a
7	chr11:104916773-104916823	GM19239	blood:	n/a
8	chr11:104916075-104916125	K562	blood:	n/a
9	chr11:104916773-104916823	HEK293	kidney:	embryo
10	chr11:104896587-104896637	RPTEC	kidney:	n/a
11	chr11:104894514-104894564	Jurkat	blood:	n/a
12	chr11:104907029-104907079	Hela-S3	cervix:	n/a
13	chr11:104916331-104916381	H1-hESC	embryonic stem cell:	embryo
14	chr11:104887307-104887357	SK-N-SH_RA	brain:	n/a
15	chr11:104879683-104879733	AoSMC	blood vessel:	n/a
16	chr11:104916773-104916823	AG04450	lung:	fetal
17	chr11:104915759-104915809	NB4	blood:	n/a
18	chr11:104916018-104916068	AG09309	skin:	n/a
19	chr11:104887307-104887357	NHDF-neo	bronchial:	n/a
20	chr11:104905889-104905939	HCPEpiC	choroid plexus:	n/a
21	chr11:104905889-104905939	HCT-116	colon:	n/a
22	chr11:104916773-104916823	ECC-1	luminal epithelium:	n/a
23	chr11:104887371-104887421	SKMC	muscle:	n/a
24	chr11:104916075-104916125	NHBE	bronchial:	n/a
25	chr11:104916773-104916823	SAEC	small airway:	n/a
26	chr11:104876060-104876110	HepG2	liver:	n/a
27	chr11:104894216-104894266	ovcar-3	ovarian:	n/a
28	chr11:104905834-104905884	HCPEpiC	choroid plexus:	n/a
29	chr11:104907029-104907079	AoSMC	blood vessel:	n/a
30	chr11:104896587-104896637	Jurkat	blood:	n/a
31	chr11:104887307-104887357	HCT-116	colon:	n/a
32	chr11:104916331-104916381	GM19239	blood:	n/a
33	chr11:104879683-104879733	AG04450	lung:	fetal
34	chr11:104887371-104887421	ECC-1	luminal epithelium:	n/a
35	chr11:104916331-104916381	A549	lung:	n/a
36	chr11:104915759-104915809	GM06990	blood:	n/a
37	chr11:104896587-104896637	GM06990	blood:	n/a
38	chr11:104887371-104887421	Caco-2	colon:	n/a
39	chr11:104896587-104896637	AG10803	skin:	n/a
40	chr11:104905889-104905939	SAEC	small airway:	n/a
41	chr11:104916075-104916125	SAEC	small airway:	n/a
42	chr11:104916018-104916068	HCPEpiC	choroid plexus:	n/a
43	chr11:104906381-104906431	Hepatocyte	liver:	n/a
44	chr11:104905889-104905939	AG04449	skin:	fetal
45	chr11:104894514-104894564	Hela-S3	cervix:	n/a
46	chr11:104906381-104906431	PFSK-1	brain:	n/a
47	chr11:104894514-104894564	AG10803	skin:	n/a
48	chr11:104905889-104905939	HEK293	kidney:	embryo
49	chr11:104887371-104887421	NB4	blood:	n/a
50	chr11:104896587-104896637	GM19239	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:104894289..104896311-chr11:104901290..104902903,2	K562	blood:
2	chr11:104894289..104896311-chr11:104901290..104902903,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CASP5-2	chr11:104896235-104896327	NONHSAT023949
2	lnc-CASP5-2	chr11:104897569-104897899	NONHSAT023949
3	lnc-CARD16-1	chr11:104904935-104905085	NONHSAT023950
4	lnc-CARD16-1	chr11:104901581-104902007	NONHSAT023950

No data

Variant related genes	Relation type
CASP5	TF binding region
CASP1	TF binding region
CARD16	TF binding region
CASP5	CpG island
CASP1	CpG island
CARD16	CpG island

Extended variants
information (count: 1946 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1946 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3181175	chr11:104875261-104875262	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575074804	chr11:104875271-104875272	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540775420	chr11:104875282-104875283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560610338	chr11:104875421-104875422	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs377632756	chr11:104875477-104875478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs17103510	chr11:104875526-104875527	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs375961564	chr11:104875532-104875533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562696567	chr11:104875539-104875540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531513357	chr11:104875598-104875599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548072197	chr11:104875604-104875605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567962113	chr11:104875673-104875674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs540798064	chr11:104875731-104875732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs45581634	chr11:104875747-104875748	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs555396068	chr11:104875802-104875803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547124690	chr11:104875803-104875804	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181966586	chr11:104875832-104875833	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375917324	chr11:104875853-104875854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186643563	chr11:104875883-104875884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370565535	chr11:104875954-104875955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191492048	chr11:104875971-104875972	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569509228	chr11:104875985-104875986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538577790	chr11:104875998-104875999	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574230877	chr11:104876075-104876076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149812631	chr11:104876080-104876081	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78145568	chr11:104876081-104876082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76900659	chr11:104876083-104876084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs66790604	chr11:104876084-104876085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150350364	chr11:104876085-104876086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs71037292	chr11:104876121-104876122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs59169404	chr11:104876124-104876125	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs61537972	chr11:104876241-104876242	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs114038433	chr11:104876297-104876298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11226574	chr11:104876380-104876381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554035933	chr11:104876442-104876443	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542306717	chr11:104876443-104876444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577272784	chr11:104876493-104876494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528431104	chr11:104876494-104876495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs199963576	chr11:104876518-104876519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372871703	chr11:104876548-104876549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182769650	chr11:104876554-104876555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187138374	chr11:104876566-104876567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs45524138	chr11:104876637-104876638	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs144474202	chr11:104876674-104876675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs45556734	chr11:104876689-104876690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs3181174	chr11:104876724-104876725	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs527549098	chr11:104876729-104876730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs546900862	chr11:104876762-104876763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs189998453	chr11:104876861-104876862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182113644	chr11:104876865-104876866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189066143	chr11:104876897-104876898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Melanoma	17363583	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Obesity	19966786	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:1319 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104864000-104877800	Weak transcription	Fetal Intestine Small	intestine
2	chr11:104872800-104876000	Weak transcription	Hela-S3	cervix
3	chr11:104872800-104876200	Weak transcription	Placenta	Placenta
4	chr11:104874000-104875400	Enhancers	HepG2	liver
5	chr11:104875000-104876400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr11:104875000-104876600	Enhancers	HUVEC	blood vessel
7	chr11:104875200-104875600	Enhancers	NHDF-Ad	bronchial
8	chr11:104875400-104875800	Weak transcription	HepG2	liver
9	chr11:104875800-104876400	Enhancers	HepG2	liver
10	chr11:104876000-104876400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr11:104876000-104876800	Enhancers	Hela-S3	cervix
12	chr11:104876200-104876600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr11:104876200-104876600	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr11:104876200-104876600	Enhancers	Placenta	Placenta
15	chr11:104876400-104877800	Weak transcription	HepG2	liver
16	chr11:104876600-104879800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr11:104877800-104878200	Enhancers	HepG2	liver
18	chr11:104878200-104881600	Weak transcription	HepG2	liver
19	chr11:104879800-104880200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr11:104880200-104881400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr11:104881400-104881800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr11:104881600-104882200	Enhancers	HepG2	liver
23	chr11:104881800-104883000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr11:104883000-104883200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr11:104885200-104893000	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr11:104886800-104887200	Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr11:104887200-104887600	Active TSS	Placenta	Placenta
28	chr11:104887600-104896800	Weak transcription	Placenta	Placenta
29	chr11:104891800-104893600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr11:104892600-104896400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr11:104892800-104894400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr11:104892800-104896400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr11:104893000-104893200	Active TSS	Primary neutrophils fromperipheralblood	blood
34	chr11:104893000-104893200	Enhancers	Fetal Intestine Large	intestine
35	chr11:104893000-104893200	Active TSS	Sigmoid Colon	Sigmoid Colon
36	chr11:104893000-104893200	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr11:104893000-104893600	Active TSS	Rectal Mucosa Donor 31	rectum
38	chr11:104893200-104893400	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr11:104893200-104893400	Active TSS	Primary B cells from cord blood	blood
40	chr11:104893200-104893400	Active TSS	Rectal Mucosa Donor 29	rectum
41	chr11:104893200-104893400	Flanking Active TSS	Sigmoid Colon	Sigmoid Colon
42	chr11:104893200-104893600	Flanking Active TSS	Fetal Intestine Large	intestine
43	chr11:104893200-104893800	Active TSS	Colonic Mucosa	Colon
44	chr11:104893200-104893800	Enhancers	Duodenum Mucosa	Duodenum
45	chr11:104893200-104894400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
46	chr11:104893200-104894400	Enhancers	Primary T helper cells fromperipheralblood	blood
47	chr11:104893200-104894600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
48	chr11:104893200-104894800	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr11:104893200-104894800	Enhancers	Primary hematopoietic stem cells	blood
50	chr11:104893200-104894800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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