Variant report

Variant	esv2759862
Chromosome Location	chr11:104719593-104798545
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:455)
CpG islands
(count:793)
Chromatin interactive
region (count:3)
LncRNA
region (count:72)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:455 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:104768528-104769091	GM12878	blood:	n/a	n/a
2	BATF	chr11:104778610-104778889	GM12878	blood:	n/a	chr11:104778766-104778777
3	BATF	chr11:104753441-104753681	GM12878	blood:	n/a	n/a
4	BCL3	chr11:104761069-104761606	GM12878	blood:	n/a	n/a
5	BCL3	chr11:104761233-104761516	GM12878	blood:	n/a	n/a
6	BHLHE40	chr11:104747879-104748167	GM12878	blood:	n/a	n/a
7	BHLHE40	chr11:104752556-104752567	GM12878	blood:	n/a	n/a
8	CEBPB	chr11:104784953-104785176	HepG2	liver:	n/a	chr11:104785067-104785078
9	CEBPB	chr11:104789758-104789850	A549	lung:	n/a	n/a
10	CEBPB	chr11:104763488-104764195	IMR90	lung:	n/a	n/a
11	CEBPB	chr11:104780576-104780776	HepG2	liver:	n/a	chr11:104780651-104780664 chr11:104780651-104780662
12	CEBPB	chr11:104785033-104785128	Hela-S3	cervix:	n/a	chr11:104785067-104785078
13	CHD1	chr11:104766544-104766551	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr11:104796787-104796814	HepG2	liver:	n/a	n/a
15	CTCF	chr11:104776007-104776406	HCT-116	colon:	n/a	n/a
16	CTCF	chr11:104763260-104763410	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr11:104744007-104744300	GM12878	blood:	n/a	n/a
18	CTCF	chr11:104776140-104776290	HA-sp	spinal cord:	n/a	n/a
19	CTCF	chr11:104776100-104776250	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr11:104776060-104776210	NHEK	skin:	n/a	n/a
21	CTCF	chr11:104744180-104744330	HFF-Myc	foreskin:	n/a	n/a
22	CTCF	chr11:104776140-104776290	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr11:104744120-104744270	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr11:104744180-104744330	HA-sp	spinal cord:	n/a	n/a
25	CTCF	chr11:104776140-104776290	HPAF	blood vessel:	n/a	n/a
26	CTCF	chr11:104744140-104744290	HEK293	kidney:	n/a	n/a
27	CTCF	chr11:104756111-104756146	LNCaP	prostate:	n/a	n/a
28	CTCF	chr11:104743987-104744265	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr11:104750280-104750430	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr11:104776040-104776190	HCT-116	colon:	n/a	n/a
31	CTCF	chr11:104744140-104744290	GM12867	blood:	n/a	n/a
32	CTCF	chr11:104776100-104776250	GM12873	blood:	n/a	n/a
33	CTCF	chr11:104744101-104744257	GM19238	blood:	n/a	n/a
34	CTCF	chr11:104768760-104768910	GM12871	blood:	n/a	n/a
35	CTCF	chr11:104776178-104776289	ProgFib	skin:	n/a	n/a
36	CTCF	chr11:104776120-104776270	BE2_C	brain:	n/a	n/a
37	CTCF	chr11:104744020-104744170	GM06990	blood:	n/a	n/a
38	CTCF	chr11:104776130-104776277	HepG2	liver:	n/a	n/a
39	CTCF	chr11:104778808-104778911	GM19238	blood:	n/a	n/a
40	CTCF	chr11:104770121-104770163	GM12878	blood:	n/a	n/a
41	CTCF	chr11:104776160-104776310	AG04449	skin:	n/a	n/a
42	CTCF	chr11:104776140-104776290	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr11:104756051-104756173	GM12878	blood:	n/a	n/a
44	CTCF	chr11:104744180-104744330	A549	lung:	n/a	n/a
45	CTCF	chr11:104778200-104778350	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr11:104744200-104744350	GM12867	blood:	n/a	n/a
47	CTCF	chr11:104756014-104756230	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr11:104776092-104776305	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr11:104756065-104756171	GM19240	blood:	n/a	n/a
50	CTCF	chr11:104776020-104776170	A549	lung:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104789052-104789102	GM19239	blood:	n/a
2	chr11:104780795-104780845	AG04449	skin:	fetal
3	chr11:104789337-104789387	NT2-D1	testis:	n/a
4	chr11:104789052-104789102	HRCEpiC	kidney:	n/a
5	chr11:104769087-104769137	HCF	heart:	n/a
6	chr11:104789052-104789102	NT2-D1	testis:	n/a
7	chr11:104781259-104781309	NHBE	bronchial:	n/a
8	chr11:104778374-104778424	K562	blood:	n/a
9	chr11:104769543-104769593	NH-A	brain:	n/a
10	chr11:104758259-104758309	GM19239	blood:	n/a
11	chr11:104789052-104789102	H1-hESC	embryonic stem cell:	embryo
12	chr11:104769087-104769137	AoSMC	blood vessel:	n/a
13	chr11:104780795-104780845	AG10803	skin:	n/a
14	chr11:104789337-104789387	GM19239	blood:	n/a
15	chr11:104779518-104779568	PANC-1	pancreas:	n/a
16	chr11:104779518-104779568	HAEpiC	amniotic membrane:	n/a
17	chr11:104780712-104780762	BE2_C	brain:	n/a
18	chr11:104789337-104789387	Caco-2	colon:	n/a
19	chr11:104780712-104780762	BJ	skin:	n/a
20	chr11:104762787-104762837	HPAEpiC	pulmonary alveolar:	n/a
21	chr11:104762787-104762837	GM19239	blood:	n/a
22	chr11:104769411-104769461	SKMC	muscle:	n/a
23	chr11:104762787-104762837	CMK	blood:	n/a
24	chr11:104769411-104769461	ProgFib	skin:	n/a
25	chr11:104780795-104780845	GM12891	blood:	n/a
26	chr11:104780712-104780762	SAEC	small airway:	n/a
27	chr11:104762787-104762837	LNCaP	prostate:	n/a
28	chr11:104769411-104769461	A549	lung:	n/a
29	chr11:104780712-104780762	SK-N-SH_RA	brain:	n/a
30	chr11:104780795-104780845	AG09319	gingival:	n/a
31	chr11:104781259-104781309	GM12892	blood:	n/a
32	chr11:104778374-104778424	HRPEpiC	eye:	n/a
33	chr11:104780712-104780762	IMR90	lung:	fetal
34	chr11:104758259-104758309	GM12891	blood:	n/a
35	chr11:104780712-104780762	AG09309	skin:	n/a
36	chr11:104769411-104769461	SK-N-SH	brain:	n/a
37	chr11:104769543-104769593	SK-N-SH	brain:	n/a
38	chr11:104780712-104780762	Caco-2	colon:	n/a
39	chr11:104758766-104758816	Hepatocyte	liver:	n/a
40	chr11:104780712-104780762	HIPEpiC	eye:	n/a
41	chr11:104780795-104780845	SK-N-SH	brain:	n/a
42	chr11:104762787-104762837	PANC-1	pancreas:	n/a
43	chr11:104769411-104769461	HRE	kidney:	n/a
44	chr11:104778374-104778424	GM19239	blood:	n/a
45	chr11:104778374-104778424	SK-N-SH_RA	brain:	n/a
46	chr11:104780795-104780845	RPTEC	kidney:	n/a
47	chr11:104758766-104758816	MCF10A-Er-Src	breast:	n/a
48	chr11:104769087-104769137	Hepatocyte	liver:	n/a
49	chr11:104769543-104769593	AoSMC	blood vessel:	n/a
50	chr11:104779518-104779568	H1-hESC	embryonic stem cell:	embryo

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

No.	Distal block	Cell Line	Cell type
1	chr11:104747404..104750313-chr11:104761050..104763216,2	K562	blood:
2	chr11:104715402..104717976-chr11:104720645..104722717,2	K562	blood:
3	chr11:104747404..104750313-chr11:104761050..104763216,2	K562	blood:

(count:72 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CASP12-2	chr11:104769135-104769397	NR_034063
2	lnc-CASP12-3	chr11:104776175-104776284	NONHSAT023943
3	lnc-CASP12-2	chr11:104769135-104769397	NR_034065
4	lnc-CASP12-2	chr11:104767944-104768195	NR_034061
5	lnc-CASP12-2	chr11:104761101-104761250	NR_034067
6	lnc-CASP12-2	chr11:104761897-104762131	NR_034070
7	lnc-CASP12-2	chr11:104757418-104757539	NR_034064
8	lnc-CASP12-3	chr11:104779415-104779735	NONHSAT023944
9	lnc-CASP12-2	chr11:104767944-104768195	NR_034063
10	lnc-CASP12-2	chr11:104761097-104761250	NR_034070
11	lnc-CASP12-2	chr11:104763058-104763230	NR_034061
12	lnc-CASP12-2	chr11:104763058-104763230	NR_034067
13	lnc-CASP12-2	chr11:104757418-104757539	NR_034070
14	lnc-CASP12-2	chr11:104757418-104757539	NR_034065
15	lnc-CASP12-3	chr11:104774118-104774437	NONHSAT023942
16	lnc-CASP12-2	chr11:104769135-104769397	NR_034061
17	lnc-CASP12-2	chr11:104761925-104762131	NR_034064
18	lnc-CASP12-3	chr11:104774118-104774278	NONHSAT023943
19	lnc-CASP12-3	chr11:104788840-104788902	NR_034078
20	lnc-CASP12-3	chr11:104772276-104772386	NR_034078
21	lnc-CASP12-2	chr11:104769135-104769397	NR_034064
22	lnc-CASP12-2	chr11:104769135-104769397	NR_034071
23	lnc-CASP12-3	chr11:104788840-104788870	NONHSAT023944
24	lnc-CASP12-3	chr11:104788840-104788902	NR_034079
25	lnc-CASP12-2	chr11:104761101-104761250	NR_034063
26	lnc-CASP12-3	chr11:104776175-104776284	NR_034078
27	lnc-CASP12-2	chr11:104757923-104758028	NR_034061
28	lnc-CASP12-2	chr11:104767944-104768195	NR_034065
29	lnc-CASP12-2	chr11:104761101-104761250	NR_034068
30	lnc-CASP12-2	chr11:104757418-104757539	NR_034063
31	lnc-CASP12-2	chr11:104763624-104763718	NR_034071
32	lnc-CASP12-2	chr11:104761097-104761250	NR_034066
33	lnc-CASP12-2	chr11:104757923-104758028	NR_034066
34	lnc-CASP12-3	chr11:104772277-104772386	NONHSAT023942
35	lnc-CASP12-2	chr11:104763058-104763230	NR_034071
36	lnc-CASP12-3	chr11:104774118-104774278	NR_034078
37	lnc-CASP12-3	chr11:104779562-104779735	NONHSAT023943
38	lnc-CASP12-2	chr11:104757418-104757539	NR_034071
39	lnc-CASP12-2	chr11:104763058-104763230	NR_034063
40	lnc-CASP12-2	chr11:104769135-104769397	NR_034066
41	lnc-CASP12-2	chr11:104763058-104763230	NR_034068
42	lnc-CASP12-2	chr11:104757418-104757539	NR_034066
43	lnc-CASP12-2	chr11:104763058-104763230	NR_034066
44	lnc-CASP12-2	chr11:104763058-104763230	NR_034064
45	lnc-CASP12-3	chr11:104776175-104776284	NR_034079
46	lnc-CASP12-3	chr11:104779562-104779735	NR_034079
47	lnc-CASP12-2	chr11:104763058-104763230	NR_034065
48	lnc-CASP12-3	chr11:104789658-104789800	NONHSAT023943
49	lnc-CASP12-2	chr11:104757923-104758028	NR_034070
50	lnc-CASP12-3	chr11:104779562-104779735	NR_034078

No data

Variant related genes	Relation type
ENSG00000235505	TF binding region
CASP12	TF binding region
ENSG00000254569	TF binding region
ENSG00000235505	CpG island
CASP12	CpG island
ENSG00000254569	CpG island

Extended variants
information (count: 2567 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2567 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10895740	chr11:104719593-104719594	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs138701659	chr11:104719604-104719605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530339854	chr11:104719624-104719625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547926848	chr11:104719682-104719683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568030121	chr11:104719686-104719687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs11226534	chr11:104719708-104719709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs609552	chr11:104719725-104719726	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs149343212	chr11:104719734-104719735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs180966074	chr11:104719777-104719778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185289303	chr11:104719784-104719785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112731865	chr11:104719818-104719819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs74496837	chr11:104719903-104719904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs35524338	chr11:104719939-104719940	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs544278663	chr11:104720003-104720004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146398107	chr11:104720021-104720022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144157649	chr11:104720033-104720034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs68154774	chr11:104720034-104720035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149962155	chr11:104720036-104720037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574742938	chr11:104720051-104720052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs71303264	chr11:104720056-104720057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540181402	chr11:104720138-104720139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560350646	chr11:104720161-104720162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34726750	chr11:104720190-104720191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189615810	chr11:104720201-104720202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546062963	chr11:104720286-104720287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs115657975	chr11:104720300-104720301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139736899	chr11:104720309-104720310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548231121	chr11:104720337-104720338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567983929	chr11:104720344-104720345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527236531	chr11:104720380-104720381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181798493	chr11:104720415-104720416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144402887	chr11:104720429-104720430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146121996	chr11:104720451-104720452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552382121	chr11:104720467-104720468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569093949	chr11:104720475-104720476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368786467	chr11:104720497-104720498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534567415	chr11:104720525-104720526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555020901	chr11:104720528-104720529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561253731	chr11:104720560-104720561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140566401	chr11:104720599-104720600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115482806	chr11:104720610-104720611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554201441	chr11:104720616-104720617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554257732	chr11:104720676-104720677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150937898	chr11:104720701-104720702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186106350	chr11:104720707-104720708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34651252	chr11:104720785-104720786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576259922	chr11:104720838-104720839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541583496	chr11:104720869-104720870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550933937	chr11:104720874-104720875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373915349	chr11:104720877-104720878	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:801 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104715600-104730000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr11:104723400-104724200	Enhancers	NHDF-Ad	bronchial
3	chr11:104726400-104726600	Enhancers	Brain Inferior Temporal Lobe	brain
4	chr11:104727000-104728400	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr11:104727200-104728000	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr11:104727200-104728800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr11:104727400-104727800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr11:104727400-104728000	Enhancers	NHEK	skin
9	chr11:104727400-104728600	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr11:104727400-104728600	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr11:104727600-104727800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
12	chr11:104727600-104728200	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr11:104727600-104728600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr11:104727600-104728600	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr11:104727800-104728200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr11:104727800-104728200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr11:104728000-104731000	Enhancers	Dnd41	blood
18	chr11:104728200-104729800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr11:104728200-104730200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr11:104728400-104728800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr11:104728400-104729800	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr11:104728400-104729800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
23	chr11:104728600-104730000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr11:104728600-104730200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr11:104728800-104729800	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr11:104728800-104730600	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr11:104729000-104729400	Enhancers	Primary T killer memory cells from peripheral blood	blood
28	chr11:104729000-104730200	Enhancers	Primary B cells from cord blood	blood
29	chr11:104729000-104730400	Enhancers	Primary T helper cells fromperipheralblood	blood
30	chr11:104729000-104730600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr11:104729000-104730800	Enhancers	Primary B cells from peripheral blood	blood
32	chr11:104729200-104730200	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr11:104729400-104730400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr11:104729400-104730400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr11:104729400-104730600	Enhancers	Primary T cells from cord blood	blood
36	chr11:104729800-104730000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr11:104729800-104730000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
38	chr11:104729800-104730200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr11:104729800-104730400	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr11:104729800-104730400	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr11:104730000-104730200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
42	chr11:104730000-104730400	Enhancers	H9 Cell Line	embryonic stem cell
43	chr11:104730000-104730600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr11:104730000-104730600	Enhancers	Fetal Thymus	thymus
45	chr11:104730000-104730800	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr11:104730000-104731200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr11:104730200-104730400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr11:104730200-104730400	Flanking Active TSS	Primary B cells from cord blood	blood
49	chr11:104730200-104730400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
50	chr11:104730200-104730600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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