Variant report

Variant	nsv556217
Chromosome Location	chr11:104758035-104781313
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:150)
CpG islands
(count:673)
Chromatin interactive
region (count:1)
LncRNA
region (count:54)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:150 , 50 per page) page: 1 2 3

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	BCL3	chr11:104761069-104761606	GM12878	blood:	n/a	n/a
4	BCL3	chr11:104761233-104761516	GM12878	blood:	n/a	n/a
5	CEBPB	chr11:104780576-104780776	HepG2	liver:	n/a	chr11:104780651-104780664 chr11:104780651-104780662
6	CEBPB	chr11:104763488-104764195	IMR90	lung:	n/a	n/a
7	CHD1	chr11:104766544-104766551	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr11:104776140-104776290	Hela-S3	cervix:	n/a	n/a
9	CTCF	chr11:104778804-104778899	GM19240	blood:	n/a	n/a
10	CTCF	chr11:104768760-104768910	GM12871	blood:	n/a	n/a
11	CTCF	chr11:104776040-104776190	HCT-116	colon:	n/a	n/a
12	CTCF	chr11:104776120-104776270	RPTEC	kidney:	n/a	n/a
13	CTCF	chr11:104770111-104770202	GM19238	blood:	n/a	n/a
14	CTCF	chr11:104776149-104776293	Gliobla	brain:	n/a	n/a
15	CTCF	chr11:104776120-104776270	BJ	skin:	n/a	n/a
16	CTCF	chr11:104776760-104776910	HPAF	blood vessel:	n/a	n/a
17	CTCF	chr11:104770177-104770191	GM12891	blood:	n/a	n/a
18	CTCF	chr11:104776080-104776230	Caco-2	colon:	n/a	n/a
19	CTCF	chr11:104778808-104778886	GM19239	blood:	n/a	n/a
20	CTCF	chr11:104778816-104778898	GM12892	blood:	n/a	n/a
21	CTCF	chr11:104778200-104778350	NHDF-neo	bronchial:	n/a	n/a
22	CTCF	chr11:104776140-104776290	HA-sp	spinal cord:	n/a	n/a
23	CTCF	chr11:104776020-104776170	A549	lung:	n/a	n/a
24	CTCF	chr11:104776120-104776270	HPF	lung:	n/a	n/a
25	CTCF	chr11:104776160-104776310	AG09319	gingival:	n/a	n/a
26	CTCF	chr11:104776080-104776230	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr11:104776140-104776290	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr11:104776080-104776230	HCFaa	heart:	n/a	n/a
29	CTCF	chr11:104776128-104776251	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr11:104776060-104776210	NHEK	skin:	n/a	n/a
31	CTCF	chr11:104776100-104776250	RPTEC	kidney:	n/a	n/a
32	CTCF	chr11:104776100-104776250	SAEC	small airway:	n/a	n/a
33	CTCF	chr11:104776160-104776310	AG09309	skin:	n/a	n/a
34	CTCF	chr11:104776140-104776290	Caco-2	colon:	n/a	n/a
35	CTCF	chr11:104776120-104776270	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr11:104778808-104778911	GM19238	blood:	n/a	n/a
37	CTCF	chr11:104770078-104770229	NHEK	skin:	n/a	n/a
38	CTCF	chr11:104776197-104776273	A549	lung:	n/a	n/a
39	CTCF	chr11:104776160-104776310	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr11:104776120-104776270	HEK293	kidney:	n/a	n/a
41	CTCF	chr11:104776178-104776289	ProgFib	skin:	n/a	n/a
42	CTCF	chr11:104776060-104776210	HMF	breast:	n/a	n/a
43	CTCF	chr11:104776149-104776297	NHEK	skin:	n/a	n/a
44	CTCF	chr11:104776160-104776310	HepG2	liver:	n/a	n/a
45	CTCF	chr11:104768740-104768890	GM06990	blood:	n/a	n/a
46	CTCF	chr11:104776100-104776250	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr11:104776120-104776270	HRE	kidney:	n/a	n/a
48	CTCF	chr11:104763260-104763410	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr11:104776100-104776296	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr11:104776092-104776305	HUVEC	blood vessel:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104781259-104781309	K562	blood:	n/a
2	chr11:104769087-104769137	GM12891	blood:	n/a
3	chr11:104781259-104781309	K562	blood:	n/a
4	chr11:104769087-104769137	GM12891	blood:	n/a
5	chr11:104780795-104780845	AG04449	skin:	fetal
6	chr11:104769087-104769137	SK-N-SH	brain:	n/a
7	chr11:104779518-104779568	CMK	blood:	n/a
8	chr11:104769087-104769137	NB4	blood:	n/a
9	chr11:104758259-104758309	HUVEC	blood vessel:	n/a
10	chr11:104758766-104758816	IMR90	lung:	fetal
11	chr11:104758259-104758309	HEK293	kidney:	embryo
12	chr11:104769543-104769593	HCPEpiC	choroid plexus:	n/a
13	chr11:104758259-104758309	HRCEpiC	kidney:	n/a
14	chr11:104762787-104762837	HRE	kidney:	n/a
15	chr11:104778374-104778424	SK-N-SH_RA	brain:	n/a
16	chr11:104758766-104758816	HepG2	liver:	n/a
17	chr11:104778374-104778424	AoSMC	blood vessel:	n/a
18	chr11:104780795-104780845	CMK	blood:	n/a
19	chr11:104779518-104779568	PANC-1	pancreas:	n/a
20	chr11:104780795-104780845	K562	blood:	n/a
21	chr11:104781259-104781309	HRE	kidney:	n/a
22	chr11:104758259-104758309	A549	lung:	n/a
23	chr11:104758766-104758816	SK-N-SH_RA	brain:	n/a
24	chr11:104758766-104758816	AG09319	gingival:	n/a
25	chr11:104758766-104758816	GM19239	blood:	n/a
26	chr11:104780795-104780845	U87	brain:	n/a
27	chr11:104769411-104769461	HEK293	kidney:	embryo
28	chr11:104762787-104762837	GM12892	blood:	n/a
29	chr11:104769543-104769593	NB4	blood:	n/a
30	chr11:104780712-104780762	PFSK-1	brain:	n/a
31	chr11:104779518-104779568	GM06990	blood:	n/a
32	chr11:104758766-104758816	Caco-2	colon:	n/a
33	chr11:104778374-104778424	AG04450	lung:	fetal
34	chr11:104779518-104779568	AG09319	gingival:	n/a
35	chr11:104758766-104758816	PrEC	prostate:	n/a
36	chr11:104780795-104780845	RPTEC	kidney:	n/a
37	chr11:104769087-104769137	HIPEpiC	eye:	n/a
38	chr11:104778374-104778424	NHBE	bronchial:	n/a
39	chr11:104769543-104769593	GM12891	blood:	n/a
40	chr11:104780712-104780762	HCM	heart:	n/a
41	chr11:104758766-104758816	BJ	skin:	n/a
42	chr11:104780712-104780762	NHBE	bronchial:	n/a
43	chr11:104769087-104769137	BJ	skin:	n/a
44	chr11:104758766-104758816	GM06990	blood:	n/a
45	chr11:104758259-104758309	GM12891	blood:	n/a
46	chr11:104769087-104769137	Hepatocyte	liver:	n/a
47	chr11:104769543-104769593	ProgFib	skin:	n/a
48	chr11:104762787-104762837	AG04450	lung:	fetal
49	chr11:104758259-104758309	ProgFib	skin:	n/a
50	chr11:104781259-104781309	BE2_C	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:54 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CASP12-2	chr11:104769135-104769397	NR_034066
2	lnc-CASP12-3	chr11:104779562-104779735	NR_034079
3	lnc-CASP12-3	chr11:104772276-104772383	NR_034079
4	lnc-CASP12-3	chr11:104776175-104776284	NONHSAT023943
5	lnc-CASP12-2	chr11:104761097-104761250	NR_034071
6	lnc-CASP12-2	chr11:104761101-104761250	NR_034068
7	lnc-CASP12-2	chr11:104761097-104761250	NR_034061
8	lnc-CASP12-3	chr11:104776175-104776284	NR_034079
9	lnc-CASP12-2	chr11:104763058-104763230	NR_034070
10	lnc-CASP12-2	chr11:104769135-104769397	NR_034070
11	lnc-CASP12-3	chr11:104779562-104779735	NR_034078
12	lnc-CASP12-3	chr11:104774118-104774437	NONHSAT023942
13	lnc-CASP12-3	chr11:104772276-104772386	NR_034078
14	lnc-CASP12-3	chr11:104779415-104779735	NONHSAT023944
15	lnc-CASP12-3	chr11:104772277-104772386	NONHSAT023942
16	lnc-CASP12-2	chr11:104761097-104761250	NR_034066
17	lnc-CASP12-2	chr11:104763058-104763230	NR_034064
18	lnc-CASP12-3	chr11:104779562-104779735	NONHSAT023943
19	lnc-CASP12-2	chr11:104767944-104768195	NR_034071
20	lnc-CASP12-2	chr11:104763058-104763230	NR_034063
21	lnc-CASP12-2	chr11:104763058-104763230	NR_034065
22	lnc-CASP12-2	chr11:104763058-104763230	NR_034071
23	lnc-CASP12-2	chr11:104761101-104761250	NR_034064
24	lnc-CASP12-2	chr11:104767944-104768195	NR_034063
25	lnc-CASP12-2	chr11:104761097-104761250	NR_034065
26	lnc-CASP12-3	chr11:104774118-104774278	NR_034079
27	lnc-CASP12-2	chr11:104761101-104761250	NR_034067
28	lnc-CASP12-2	chr11:104763624-104763718	NR_034070
29	lnc-CASP12-2	chr11:104761925-104762131	NR_034064
30	lnc-CASP12-2	chr11:104769135-104769397	NR_034064
31	lnc-CASP12-2	chr11:104769135-104769397	NR_034071
32	lnc-CASP12-2	chr11:104769135-104769397	NR_034061
33	lnc-CASP12-2	chr11:104761897-104762131	NR_034070
34	lnc-CASP12-3	chr11:104774118-104774278	NR_034078
35	lnc-CASP12-2	chr11:104769135-104769397	NR_034067
36	lnc-CASP12-2	chr11:104767944-104768195	NR_034061
37	lnc-CASP12-2	chr11:104769135-104769397	NR_034068
38	lnc-CASP12-2	chr11:104769135-104769397	NR_034065
39	lnc-CASP12-2	chr11:104769135-104769397	NR_034063
40	lnc-CASP12-2	chr11:104763058-104763230	NR_034068
41	lnc-CASP12-2	chr11:104761897-104762131	NR_034063
42	lnc-CASP12-2	chr11:104763624-104763718	NR_034071
43	lnc-CASP12-2	chr11:104763058-104763230	NR_034067
44	lnc-CASP12-2	chr11:104761101-104761250	NR_034063
45	lnc-CASP12-2	chr11:104767944-104768195	NR_034070
46	lnc-CASP12-2	chr11:104763058-104763230	NR_034066
47	lnc-CASP12-3	chr11:104776175-104776284	NR_034078
48	lnc-CASP12-2	chr11:104767944-104768195	NR_034067
49	lnc-CASP12-2	chr11:104761897-104762131	NR_034061
50	lnc-CASP12-2	chr11:104763058-104763230	NR_034061

No data

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

Extended variants
information (count: 937 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:937 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs484438	chr11:104758035-104758036	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563371877	chr11:104758049-104758050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147819564	chr11:104758078-104758079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs200757065	chr11:104758097-104758098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147443677	chr11:104758111-104758112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs56670368	chr11:104758118-104758119	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs12276274	chr11:104758161-104758162	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs190492754	chr11:104758194-104758195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548034856	chr11:104758260-104758261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570925421	chr11:104758263-104758264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs113334746	chr11:104758264-104758265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148869736	chr11:104758267-104758268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs528005206	chr11:104758390-104758391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565774849	chr11:104758395-104758396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs77997163	chr11:104758396-104758397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs376167970	chr11:104758403-104758404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs77784259	chr11:104758420-104758421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12790476	chr11:104758435-104758436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376183099	chr11:104758480-104758481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs572029290	chr11:104758485-104758486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12807286	chr11:104758490-104758491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376482442	chr11:104758497-104758498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs114432171	chr11:104758505-104758506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs148103469	chr11:104758531-104758532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs577787071	chr11:104758537-104758538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554422754	chr11:104758585-104758586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183592826	chr11:104758595-104758596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186474932	chr11:104758705-104758706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191405031	chr11:104758745-104758746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542649309	chr11:104758754-104758755	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559366916	chr11:104758766-104758767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182726596	chr11:104758847-104758848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547810870	chr11:104758868-104758869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186493627	chr11:104758892-104758893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533408256	chr11:104758911-104758912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560339	chr11:104758974-104758975	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs141841601	chr11:104758975-104758976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573237143	chr11:104759055-104759056	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs548980938	chr11:104759176-104759177	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7929558	chr11:104759191-104759192	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs71464742	chr11:104759248-104759249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150192515	chr11:104759262-104759263	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs489229	chr11:104759288-104759289	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs78494517	chr11:104759317-104759318	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192592312	chr11:104759318-104759319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139038291	chr11:104759328-104759329	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542712696	chr11:104759346-104759347	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142232208	chr11:104759387-104759388	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs78555624	chr11:104759407-104759408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs146372273	chr11:104759479-104759480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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

Chromatin state (count:339 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104744200-104761000	Weak transcription	Aorta	Aorta
2	chr11:104745600-104768600	Weak transcription	Left Ventricle	heart
3	chr11:104752800-104766200	Weak transcription	Stomach Smooth Muscle	stomach
4	chr11:104754400-104768600	Weak transcription	Pancreas	Pancrea
5	chr11:104757400-104765000	Weak transcription	Colon Smooth Muscle	Colon
6	chr11:104757600-104763400	Weak transcription	Adipose Nuclei	Adipose
7	chr11:104757800-104758600	Weak transcription	Ovary	ovary
8	chr11:104758600-104759600	Strong transcription	Ovary	ovary
9	chr11:104759600-104761800	Weak transcription	Ovary	ovary
10	chr11:104759800-104768600	Weak transcription	Lung	lung
11	chr11:104760000-104760200	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr11:104760200-104765000	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr11:104760400-104760800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr11:104760800-104765200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr11:104760800-104765200	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr11:104761000-104762200	Strong transcription	Aorta	Aorta
17	chr11:104761400-104761600	ZNF genes & repeats	Fetal Kidney	kidney
18	chr11:104761400-104763800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr11:104761400-104764400	Enhancers	NHDF-Ad	bronchial
20	chr11:104761400-104765800	Enhancers	HUVEC	blood vessel
21	chr11:104761800-104762000	Enhancers	NHLF	lung
22	chr11:104761800-104762200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr11:104761800-104762200	Genic enhancers	Ovary	ovary
24	chr11:104761800-104762400	Enhancers	NH-A	brain
25	chr11:104762000-104762200	Enhancers	Psoas Muscle	Psoas
26	chr11:104762000-104762400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr11:104762000-104762400	Enhancers	Muscle Satellite Cultured Cells	--
28	chr11:104762000-104762600	Weak transcription	NHLF	lung
29	chr11:104762200-104762800	Weak transcription	Ovary	ovary
30	chr11:104762200-104763200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr11:104762200-104763600	Weak transcription	Aorta	Aorta
32	chr11:104762200-104768600	Weak transcription	Psoas Muscle	Psoas
33	chr11:104762400-104762800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr11:104762400-104762800	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr11:104762400-104762800	Weak transcription	NH-A	brain
36	chr11:104762600-104764200	Enhancers	NHLF	lung
37	chr11:104762800-104763600	Enhancers	Muscle Satellite Cultured Cells	--
38	chr11:104762800-104764000	Enhancers	Ovary	ovary
39	chr11:104762800-104764000	Enhancers	NH-A	brain
40	chr11:104762800-104764400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr11:104763000-104763200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr11:104763000-104763600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr11:104763000-104764400	Enhancers	Osteobl	bone
44	chr11:104763200-104763400	Enhancers	H9 Cell Line	embryonic stem cell
45	chr11:104763200-104764000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr11:104763200-104764000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr11:104763200-104764200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr11:104763200-104764400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr11:104763400-104763800	Active TSS	Fetal Brain Male	brain
50	chr11:104763400-104764000	Enhancers	Adipose Nuclei	Adipose

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