Variant report

Variant	esv3465897
Chromosome Location	chr11:104724823-104759731
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:226)
CpG islands
(count:122)
Chromatin interactive
region (count:1)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:226 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr11:104753441-104753681	GM12878	blood:	n/a	n/a
2	BHLHE40	chr11:104747879-104748167	GM12878	blood:	n/a	n/a
3	BHLHE40	chr11:104752556-104752567	GM12878	blood:	n/a	n/a
4	CTCF	chr11:104750320-104750470	GM12873	blood:	n/a	n/a
5	CTCF	chr11:104744180-104744330	HEK293	kidney:	n/a	n/a
6	CTCF	chr11:104756050-104756176	HepG2	liver:	n/a	n/a
7	CTCF	chr11:104744085-104744274	GM19240	blood:	n/a	n/a
8	CTCF	chr11:104750320-104750470	WERI-Rb-1	eye:	n/a	n/a
9	CTCF	chr11:104744121-104744231	NHEK	skin:	n/a	n/a
10	CTCF	chr11:104744120-104744270	HRPEpiC	eye:	n/a	n/a
11	CTCF	chr11:104744180-104744330	HFF-Myc	foreskin:	n/a	n/a
12	CTCF	chr11:104744140-104744290	GM12873	blood:	n/a	n/a
13	CTCF	chr11:104756111-104756146	LNCaP	prostate:	n/a	n/a
14	CTCF	chr11:104744120-104744270	BE2_C	brain:	n/a	n/a
15	CTCF	chr11:104744180-104744330	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr11:104744192-104744217	GM10266	blood:	n/a	n/a
17	CTCF	chr11:104744064-104744234	K562	blood:	n/a	n/a
18	CTCF	chr11:104740760-104740910	Caco-2	colon:	n/a	n/a
19	CTCF	chr11:104744120-104744270	GM12866	blood:	n/a	n/a
20	CTCF	chr11:104744020-104744170	RPTEC	kidney:	n/a	n/a
21	CTCF	chr11:104744100-104744250	HMEC	breast:	n/a	n/a
22	CTCF	chr11:104744125-104744229	GM13977	blood:	n/a	n/a
23	CTCF	chr11:104744200-104744350	GM12867	blood:	n/a	n/a
24	CTCF	chr11:104756065-104756162	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr11:104744140-104744290	GM12864	blood:	n/a	n/a
26	CTCF	chr11:104756000-104756150	GM12868	blood:	n/a	n/a
27	CTCF	chr11:104744040-104744190	RPTEC	kidney:	n/a	n/a
28	CTCF	chr11:104744200-104744350	HFF	foreskin:	n/a	n/a
29	CTCF	chr11:104750398-104750472	NHEK	skin:	n/a	n/a
30	CTCF	chr11:104744160-104744310	HFF-Myc	foreskin:	n/a	n/a
31	CTCF	chr11:104744105-104744230	MCF-7	breast:	n/a	n/a
32	CTCF	chr11:104756060-104756210	HCT-116	colon:	n/a	n/a
33	CTCF	chr11:104744097-104744270	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr11:104750380-104750530	GM12874	blood:	n/a	n/a
35	CTCF	chr11:104744140-104744290	HEK293	kidney:	n/a	n/a
36	CTCF	chr11:104744120-104744270	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr11:104744120-104744270	WI-38	lung:	n/a	n/a
38	CTCF	chr11:104744120-104744270	GM06990	blood:	n/a	n/a
39	CTCF	chr11:104756014-104756230	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr11:104744180-104744330	GM12874	blood:	n/a	n/a
41	CTCF	chr11:104756082-104756179	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr11:104744140-104744290	HPF	lung:	n/a	n/a
43	CTCF	chr11:104750360-104750510	GM12873	blood:	n/a	n/a
44	CTCF	chr11:104744000-104744150	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr11:104755980-104756130	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr11:104744080-104744230	A549	lung:	n/a	n/a
47	CTCF	chr11:104744220-104744370	GM12870	blood:	n/a	n/a
48	CTCF	chr11:104752285-104752418	GM12878	blood:	n/a	n/a
49	CTCF	chr11:104744101-104744257	GM19238	blood:	n/a	n/a
50	CTCF	chr11:104744100-104744250	GM12864	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104758259-104758309	AG04449	skin:	fetal
2	chr11:104758259-104758309	A549	lung:	n/a
3	chr11:104758259-104758309	PrEC	prostate:	n/a
4	chr11:104758766-104758816	AG09309	skin:	n/a
5	chr11:104758259-104758309	RPTEC	kidney:	n/a
6	chr11:104758766-104758816	SAEC	small airway:	n/a
7	chr11:104758259-104758309	GM12878	blood:	n/a
8	chr11:104758259-104758309	HepG2	liver:	n/a
9	chr11:104758259-104758309	HL-60	blood:	n/a
10	chr11:104758766-104758816	ECC-1	luminal epithelium:	n/a
11	chr11:104758766-104758816	H1-hESC	embryonic stem cell:	embryo
12	chr11:104758259-104758309	PANC-1	pancreas:	n/a
13	chr11:104758766-104758816	BE2_C	brain:	n/a
14	chr11:104758259-104758309	Hela-S3	cervix:	n/a
15	chr11:104758766-104758816	NHBE	bronchial:	n/a
16	chr11:104758259-104758309	NH-A	brain:	n/a
17	chr11:104758259-104758309	ovcar-3	ovarian:	n/a
18	chr11:104758259-104758309	HCM	heart:	n/a
19	chr11:104758259-104758309	HRCEpiC	kidney:	n/a
20	chr11:104758766-104758816	NT2-D1	testis:	n/a
21	chr11:104758766-104758816	NHDF-neo	bronchial:	n/a
22	chr11:104758766-104758816	A549	lung:	n/a
23	chr11:104758766-104758816	HCF	heart:	n/a
24	chr11:104758259-104758309	PFSK-1	brain:	n/a
25	chr11:104758766-104758816	BJ	skin:	n/a
26	chr11:104758766-104758816	T-47D	breast:	n/a
27	chr11:104758766-104758816	IMR90	lung:	fetal
28	chr11:104758259-104758309	Jurkat	blood:	n/a
29	chr11:104758766-104758816	Hela-S3	cervix:	n/a
30	chr11:104758259-104758309	K562	blood:	n/a
31	chr11:104758766-104758816	NB4	blood:	n/a
32	chr11:104758259-104758309	SK-N-SH	brain:	n/a
33	chr11:104758259-104758309	HCF	heart:	n/a
34	chr11:104758766-104758816	PrEC	prostate:	n/a
35	chr11:104758766-104758816	SKMC	muscle:	n/a
36	chr11:104758766-104758816	RPTEC	kidney:	n/a
37	chr11:104758259-104758309	HRE	kidney:	n/a
38	chr11:104758766-104758816	HIPEpiC	eye:	n/a
39	chr11:104758766-104758816	HEEpiC	esophagus:	n/a
40	chr11:104758766-104758816	HNPCEpiC	eye:	n/a
41	chr11:104758766-104758816	HMEC	breast:	n/a
42	chr11:104758259-104758309	NHDF-neo	bronchial:	n/a
43	chr11:104758259-104758309	AG09309	skin:	n/a
44	chr11:104758259-104758309	GM12892	blood:	n/a
45	chr11:104758766-104758816	K562	blood:	n/a
46	chr11:104758766-104758816	Hepatocyte	liver:	n/a
47	chr11:104758766-104758816	AG04450	lung:	fetal
48	chr11:104758259-104758309	AG04450	lung:	fetal
49	chr11:104758259-104758309	U87	brain:	n/a
50	chr11:104758766-104758816	U87	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:104747404..104750313-chr11:104761050..104763216,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CASP12-2	chr11:104757418-104757539	NR_034063
2	lnc-CASP12-2	chr11:104757923-104758028	NR_034071
3	lnc-CASP12-2	chr11:104757418-104757539	NR_034064
4	lnc-CASP12-2	chr11:104757923-104758028	NR_034066
5	lnc-CASP12-2	chr11:104757418-104757539	NR_034065
6	lnc-CASP12-2	chr11:104757923-104758028	NR_034070
7	lnc-CASP12-2	chr11:104757418-104757539	NR_034066
8	lnc-CASP12-2	chr11:104757923-104758028	NR_034061
9	lnc-CASP12-2	chr11:104757418-104757539	NR_034068
10	lnc-CASP12-2	chr11:104757418-104757539	NR_034071
11	lnc-CASP12-2	chr11:104757418-104757539	NR_034061
12	lnc-CASP12-2	chr11:104757418-104757539	NR_034067
13	lnc-CASP12-2	chr11:104757418-104757539	NR_034070
14	lnc-CASP12-2	chr11:104757923-104758028	NR_034065

No data

Variant related genes	Relation type
ENSG00000254569	TF binding region
ENSG00000254569	CpG island

Extended variants
information (count: 963 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:963 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543688136	chr11:104724826-104724827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs148626520	chr11:104724850-104724851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574094844	chr11:104724869-104724870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567700871	chr11:104724878-104724879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375681327	chr11:104724898-104724899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181910911	chr11:104724966-104724967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559328428	chr11:104724979-104724980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs377692542	chr11:104725006-104725007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528420458	chr11:104725043-104725044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186930648	chr11:104725073-104725074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369772864	chr11:104725173-104725174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530814370	chr11:104725223-104725224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550551249	chr11:104725233-104725234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs509965	chr11:104725255-104725256	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs529762899	chr11:104725314-104725315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs605555	chr11:104725361-104725362	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs566496190	chr11:104725371-104725372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538604031	chr11:104725379-104725380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558571848	chr11:104725385-104725386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147769560	chr11:104725441-104725442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11226535	chr11:104725501-104725502	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs548968	chr11:104725508-104725509	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs574135075	chr11:104725571-104725572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375657640	chr11:104725660-104725661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542755036	chr11:104725665-104725666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370619974	chr11:104725672-104725673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570556639	chr11:104725684-104725685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190142995	chr11:104725691-104725692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545032379	chr11:104725712-104725713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564936291	chr11:104725714-104725715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569468	chr11:104725820-104725821	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs182382536	chr11:104725833-104725834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78791727	chr11:104725848-104725849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147914482	chr11:104725849-104725850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs57851790	chr11:104725852-104725853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112663620	chr11:104725853-104725854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185168697	chr11:104725876-104725877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370997946	chr11:104725903-104725904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552761	chr11:104725921-104725922	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs546733731	chr11:104725938-104725939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs17103215	chr11:104725945-104725946	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs532221936	chr11:104725989-104725990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189591548	chr11:104726006-104726007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200523511	chr11:104726017-104726018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368037094	chr11:104726033-104726034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553015156	chr11:104726034-104726035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568824124	chr11:104726068-104726069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537351799	chr11:104726184-104726185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs619515	chr11:104726216-104726217	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs201638158	chr11:104726258-104726259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Tetralogy of Fallot	22912587	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:168 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104715600-104730000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr11:104726400-104726600	Enhancers	Brain Inferior Temporal Lobe	brain
3	chr11:104727000-104728400	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr11:104727200-104728000	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr11:104727200-104728800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr11:104727400-104727800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr11:104727400-104728000	Enhancers	NHEK	skin
8	chr11:104727400-104728600	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr11:104727400-104728600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr11:104727600-104727800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr11:104727600-104728200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr11:104727600-104728600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:104727600-104728600	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr11:104727800-104728200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr11:104727800-104728200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr11:104728000-104731000	Enhancers	Dnd41	blood
17	chr11:104728200-104729800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr11:104728200-104730200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr11:104728400-104728800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr11:104728400-104729800	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr11:104728400-104729800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
22	chr11:104728600-104730000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr11:104728600-104730200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr11:104728800-104729800	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr11:104728800-104730600	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr11:104729000-104729400	Enhancers	Primary T killer memory cells from peripheral blood	blood
27	chr11:104729000-104730200	Enhancers	Primary B cells from cord blood	blood
28	chr11:104729000-104730400	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr11:104729000-104730600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr11:104729000-104730800	Enhancers	Primary B cells from peripheral blood	blood
31	chr11:104729200-104730200	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr11:104729400-104730400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr11:104729400-104730400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr11:104729400-104730600	Enhancers	Primary T cells from cord blood	blood
35	chr11:104729800-104730000	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr11:104729800-104730000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
37	chr11:104729800-104730200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr11:104729800-104730400	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr11:104729800-104730400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr11:104730000-104730200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr11:104730000-104730400	Enhancers	H9 Cell Line	embryonic stem cell
42	chr11:104730000-104730600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr11:104730000-104730600	Enhancers	Fetal Thymus	thymus
44	chr11:104730000-104730800	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr11:104730000-104731200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr11:104730200-104730400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr11:104730200-104730400	Flanking Active TSS	Primary B cells from cord blood	blood
48	chr11:104730200-104730400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
49	chr11:104730200-104730600	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr11:104730200-104730600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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