Variant report

Variant	nsv555448
Chromosome Location	chr11:76354115-76383806
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:533)
CpG islands
(count:1590)
Chromatin interactive
region (count:17)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:533 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:76355637-76355872	K562	blood:	n/a	n/a
2	ATF2	chr11:76383568-76384253	GM12878	blood:	n/a	n/a
3	ATF2	chr11:76383508-76384302	GM12878	blood:	n/a	n/a
4	BACH1	chr11:76381231-76382296	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr11:76383752-76384252	GM12878	blood:	n/a	n/a
6	BCL11A	chr11:76383625-76384124	GM12878	blood:	n/a	chr11:76383801-76383810
7	BCL11A	chr11:76383689-76384113	GM12878	blood:	n/a	chr11:76383801-76383810
8	BCL3	chr11:76383570-76384264	GM12878	blood:	n/a	chr11:76383801-76383810
9	BCL3	chr11:76383577-76384052	GM12878	blood:	n/a	chr11:76383801-76383810
10	BCL3	chr11:76381977-76382430	GM12878	blood:	n/a	chr11:76382171-76382184 chr11:76382177-76382186 chr11:76382058-76382071 chr11:76382275-76382284 chr11:76381977-76381986 chr11:76382084-76382097 chr11:76382266-76382275
11	BCLAF1	chr11:76383419-76384152	GM12878	blood:	n/a	chr11:76383801-76383810
12	BCLAF1	chr11:76383520-76384144	GM12878	blood:	n/a	chr11:76383801-76383810
13	BHLHE40	chr11:76382037-76382216	A549	lung:	n/a	chr11:76382168-76382184
14	BHLHE40	chr11:76383575-76384899	GM12878	blood:	n/a	n/a
15	BHLHE40	chr11:76375551-76375902	K562	blood:	n/a	n/a
16	BHLHE40	chr11:76381891-76382431	K562	blood:	n/a	chr11:76382168-76382184 chr11:76382256-76382272 chr11:76381906-76381922
17	BHLHE40	chr11:76381359-76382835	GM12878	blood:	n/a	chr11:76382168-76382184 chr11:76382256-76382272 chr11:76381906-76381922
18	BHLHE40	chr11:76375769-76375994	GM12878	blood:	n/a	n/a
19	BHLHE40	chr11:76377198-76377831	GM12878	blood:	n/a	n/a
20	BRCA1	chr11:76382806-76382829	GM12878	blood:	n/a	n/a
21	CBX3	chr11:76370085-76370536	K562	blood:	n/a	n/a
22	CBX3	chr11:76375519-76375946	K562	blood:	n/a	n/a
23	CCNT2	chr11:76381983-76382233	K562	blood:	n/a	n/a
24	CCNT2	chr11:76375608-76375935	K562	blood:	n/a	chr11:76375737-76375757
25	CEBPB	chr11:76383324-76384193	GM12878	blood:	n/a	n/a
26	CEBPB	chr11:76357123-76357196	A549	lung:	n/a	n/a
27	CEBPB	chr11:76383745-76384040	GM12878	blood:	n/a	n/a
28	CEBPB	chr11:76383408-76383536	K562	blood:	n/a	n/a
29	CEBPB	chr11:76383347-76383610	HepG2	liver:	n/a	n/a
30	CEBPB	chr11:76364486-76365292	IMR90	lung:	n/a	n/a
31	CEBPB	chr11:76355810-76355979	HepG2	liver:	n/a	n/a
32	CEBPB	chr11:76365033-76365118	HepG2	liver:	n/a	n/a
33	CEBPB	chr11:76355695-76356012	Hela-S3	cervix:	n/a	n/a
34	CHD1	chr11:76379287-76379428	GM12878	blood:	n/a	n/a
35	CHD1	chr11:76382307-76382428	GM12878	blood:	n/a	n/a
36	CHD2	chr11:76375957-76376380	GM12878	blood:	n/a	n/a
37	CHD2	chr11:76379559-76379601	GM12878	blood:	n/a	n/a
38	CHD2	chr11:76379236-76379247	GM12878	blood:	n/a	n/a
39	CHD2	chr11:76383495-76385372	GM12878	blood:	n/a	n/a
40	CHD2	chr11:76377394-76377961	GM12878	blood:	n/a	n/a
41	CHD2	chr11:76381844-76382469	GM12878	blood:	n/a	n/a
42	CHD2	chr11:76366487-76366507	GM12878	blood:	n/a	n/a
43	CTCF	chr11:76381559-76381584	GM10248	blood:	n/a	n/a
44	CTCF	chr11:76381480-76381630	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr11:76381500-76381650	SAEC	small airway:	n/a	n/a
46	CTCF	chr11:76378701-76378732	GM19240	blood:	n/a	n/a
47	CTCF	chr11:76382000-76382150	BJ	skin:	n/a	chr11:76382099-76382112
48	CTCF	chr11:76382040-76382209	GM12878	blood:	n/a	chr11:76382099-76382112 chr11:76382167-76382180
49	CTCF	chr11:76382000-76382150	GM12872	blood:	n/a	chr11:76382099-76382112
50	CTCF	chr11:76381940-76382090	GM12868	blood:	n/a	n/a

(count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:76381687-76381737	Hela-S3	cervix:	n/a
2	chr11:76381687-76381737	HRCEpiC	kidney:	n/a
3	chr11:76376064-76376114	HCPEpiC	choroid plexus:	n/a
4	chr11:76382128-76382178	AG10803	skin:	n/a
5	chr11:76381687-76381737	Hela-S3	cervix:	n/a
6	chr11:76381687-76381737	HRCEpiC	kidney:	n/a
7	chr11:76376064-76376114	HCPEpiC	choroid plexus:	n/a
8	chr11:76382128-76382178	AG10803	skin:	n/a
9	chr11:76382794-76382844	GM19239	blood:	n/a
10	chr11:76381148-76381198	NB4	blood:	n/a
11	chr11:76377572-76377622	SK-N-SH	brain:	n/a
12	chr11:76381937-76381987	GM19239	blood:	n/a
13	chr11:76372128-76372178	GM19239	blood:	n/a
14	chr11:76377572-76377622	BE2_C	brain:	n/a
15	chr11:76371946-76371996	SK-N-MC	brain:	n/a
16	chr11:76381971-76382021	HPAEpiC	pulmonary alveolar:	n/a
17	chr11:76381971-76382021	AG09319	gingival:	n/a
18	chr11:76382149-76382199	HCF	heart:	n/a
19	chr11:76382794-76382844	ECC-1	luminal epithelium:	n/a
20	chr11:76380921-76380971	HCM	heart:	n/a
21	chr11:76381040-76381090	NB4	blood:	n/a
22	chr11:76371932-76371982	SK-N-SH_RA	brain:	n/a
23	chr11:76382149-76382199	GM19239	blood:	n/a
24	chr11:76380605-76380655	NHDF-neo	bronchial:	n/a
25	chr11:76381791-76381841	NHBE	bronchial:	n/a
26	chr11:76381165-76381215	AoSMC	blood vessel:	n/a
27	chr11:76381148-76381198	MCF-7	breast:	n/a
28	chr11:76367177-76367227	GM12878	blood:	n/a
29	chr11:76370510-76370560	NHBE	bronchial:	n/a
30	chr11:76381236-76381286	BE2_C	brain:	n/a
31	chr11:76382149-76382199	AG10803	skin:	n/a
32	chr11:76380921-76380971	SK-N-MC	brain:	n/a
33	chr11:76381971-76382021	SK-N-SH	brain:	n/a
34	chr11:76371932-76371982	NHDF-neo	bronchial:	n/a
35	chr11:76381105-76381155	NH-A	brain:	n/a
36	chr11:76381165-76381215	HCT-116	colon:	n/a
37	chr11:76381687-76381737	ProgFib	skin:	n/a
38	chr11:76381791-76381841	HEEpiC	esophagus:	n/a
39	chr11:76381971-76382021	ovcar-3	ovarian:	n/a
40	chr11:76380921-76380971	K562	blood:	n/a
41	chr11:76381165-76381215	HEK293	kidney:	embryo
42	chr11:76363709-76363759	HNPCEpiC	eye:	n/a
43	chr11:76381081-76381131	HCF	heart:	n/a
44	chr11:76363709-76363759	HUVEC	blood vessel:	n/a
45	chr11:76380605-76380655	ProgFib	skin:	n/a
46	chr11:76381105-76381155	SKMC	muscle:	n/a
47	chr11:76382128-76382178	Hela-S3	cervix:	n/a
48	chr11:76380605-76380655	CMK	blood:	n/a
49	chr11:76381236-76381286	PFSK-1	brain:	n/a
50	chr11:76381081-76381131	CMK	blood:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:76364167..76367346-chr11:76381295..76383595,3	K562	blood:
2	chr11:76377677..76380472-chr11:76382073..76384375,3	K562	blood:
3	chr11:76374882..76378954-chr11:76379483..76384269,6	K562	blood:
4	chr11:76357796..76360555-chr11:76361660..76365376,3	MCF-7	breast:
5	chr11:76377677..76380472-chr11:76382073..76384375,3	K562	blood:
6	chr11:76378581..76382468-chr11:76384470..76388855,6	K562	blood:
7	chr11:76366083..76370493-chr11:76372368..76375402,4	MCF-7	breast:
8	chr11:76374894..76376497-chr11:76377252..76379151,2	K562	blood:
9	chr11:76357796..76360555-chr11:76361660..76365376,3	MCF-7	breast:
10	chr11:76369699..76372480-chr11:76377429..76382603,5	K562	blood:
11	chr11:76341027..76343056-chr11:76363674..76366341,2	K562	blood:
12	chr11:76380390..76383779-chr11:76386028..76388503,4	K562	blood:
13	chr11:76378581..76380312-chr11:76384470..76387173,2	K562	blood:
14	chr11:76374882..76378954-chr11:76379483..76384269,6	K562	blood:
15	chr11:76369874..76374262-chr11:76376488..76382524,6	K562	blood:
16	chr11:76374894..76376497-chr11:76377252..76379151,2	K562	blood:
17	chr11:76372441..76374951-chr11:76384458..76386745,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C11orf30-1	chr11:76370652-76370738	ENSG00000236304.1
2	lnc-PRKRIR-4	chr11:76376915-76377015	NONHSAT023179
3	lnc-C11orf30-1	chr11:76373673-76374910	ENSG00000236304.1
4	lnc-LRRC32-1	chr11:76367493-76367756	ENSG00000254810
5	lnc-LRRC32-1	chr11:76365213-76365599	ENSG00000254810
6	lnc-C11orf30-1	chr11:76368100-76368200	ENSG00000236304.1
7	lnc-PRKRIR-4	chr11:76368614-76369078	NONHSAT023179

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	LRRC32	hsa-miR-335-5p	chr11:76369370-76369393

Variant related genes	Relation type
ENSG00000254975	TF binding region
ENSG00000236304	TF binding region
ENSG00000254810	TF binding region
LRRC32	TF binding region
ENSG00000254975	CpG island
ENSG00000236304	CpG island
ENSG00000254810	CpG island
LRRC32	CpG island
ENSG00000255363	chromatin interactions
ENSG00000254975	chromatin interactions
ENSG00000254810	chromatin interactions
ENSG00000137507	chromatin interactions
ENSG00000236304	chromatin interactions

Extended variants
information (count: 1265 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1265 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10899245	chr11:76354115-76354116	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs555705536	chr11:76354137-76354138	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs151021332	chr11:76354149-76354150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs7126722	chr11:76354161-76354162	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs12360650	chr11:76354165-76354166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
6	rs140443685	chr11:76354179-76354180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571419947	chr11:76354195-76354196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145652632	chr11:76354197-76354198	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550792447	chr11:76354206-76354207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183528616	chr11:76354250-76354251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs79345570	chr11:76354256-76354257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138300529	chr11:76354327-76354328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188179766	chr11:76354372-76354373	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34208519	chr11:76354393-76354394	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534755052	chr11:76354400-76354401	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557835224	chr11:76354403-76354404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs367965243	chr11:76354417-76354418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs7483624	chr11:76354434-76354435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191893497	chr11:76354445-76354446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs116487028	chr11:76354461-76354462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs557556370	chr11:76354462-76354463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574221244	chr11:76354489-76354490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145065948	chr11:76354602-76354603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10899246	chr11:76354652-76354653	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs199980808	chr11:76354664-76354665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528095453	chr11:76354670-76354671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7949577	chr11:76354700-76354701	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs568342545	chr11:76354734-76354735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182269583	chr11:76354739-76354740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138918248	chr11:76354749-76354750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534029396	chr11:76354757-76354758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535506288	chr11:76354788-76354789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547445042	chr11:76354836-76354837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs9651764	chr11:76354842-76354843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567476570	chr11:76354858-76354859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186976725	chr11:76354911-76354912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs144834369	chr11:76354912-76354913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs148174767	chr11:76354916-76354917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575573750	chr11:76354935-76354936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575943981	chr11:76354948-76354949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557773945	chr11:76355045-76355046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536803518	chr11:76355054-76355055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191449212	chr11:76355073-76355074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141621766	chr11:76355083-76355084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558494724	chr11:76355101-76355102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376104287	chr11:76355112-76355113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557247454	chr11:76355123-76355124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574182102	chr11:76355163-76355164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543304371	chr11:76355171-76355172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371167425	chr11:76355179-76355180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	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
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Melanoma	18172304	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21482786	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	16608533	CNVD
Usher syndrome	18421352	CNVD
Ovarian cancer	21240255	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	22355333	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1129 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76350800-76356200	Weak transcription	Adipose Nuclei	Adipose
2	chr11:76350800-76365000	Weak transcription	Lung	lung
3	chr11:76351600-76356000	Weak transcription	Placenta	Placenta
4	chr11:76352400-76354200	Enhancers	Primary B cells from cord blood	blood
5	chr11:76353000-76354400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
6	chr11:76354400-76354600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr11:76354400-76354600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr11:76354400-76354600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr11:76354600-76355600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr11:76354600-76355600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr11:76355200-76356400	Enhancers	NHEK	skin
12	chr11:76355600-76355800	Enhancers	Primary T cells from cord blood	blood
13	chr11:76355600-76355800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
14	chr11:76355600-76356000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr11:76355600-76356400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr11:76355600-76356600	Enhancers	K562	blood
17	chr11:76355800-76356000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr11:76355800-76356200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr11:76355800-76356200	Enhancers	Placenta Amnion	Placenta Amnion
20	chr11:76355800-76356400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr11:76356000-76356200	Enhancers	Placenta	Placenta
22	chr11:76356200-76356400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr11:76356200-76356400	Weak transcription	Placenta	Placenta
24	chr11:76356200-76356600	Enhancers	Adipose Nuclei	Adipose
25	chr11:76356400-76357200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr11:76357600-76358000	Active TSS	Fetal Heart	heart
27	chr11:76359000-76359200	Enhancers	Right Atrium	heart
28	chr11:76359200-76359600	Enhancers	Fetal Muscle Trunk	muscle
29	chr11:76359200-76364800	Weak transcription	Right Atrium	heart
30	chr11:76359400-76359600	Enhancers	Aorta	Aorta
31	chr11:76359400-76359600	Enhancers	Left Ventricle	heart
32	chr11:76359400-76361600	Enhancers	Fetal Muscle Leg	muscle
33	chr11:76359600-76360800	Weak transcription	Aorta	Aorta
34	chr11:76359600-76360800	Weak transcription	Fetal Muscle Trunk	muscle
35	chr11:76359600-76360800	Weak transcription	Left Ventricle	heart
36	chr11:76359800-76360600	Enhancers	Fetal Stomach	stomach
37	chr11:76360000-76362400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr11:76360200-76360400	Bivalent Enhancer	HSMMtube	muscle
39	chr11:76360200-76361400	Enhancers	Fetal Lung	lung
40	chr11:76360200-76361800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr11:76360200-76361800	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr11:76360400-76361600	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr11:76360400-76362400	Enhancers	Adipose Nuclei	Adipose
44	chr11:76360600-76361200	Weak transcription	Fetal Stomach	stomach
45	chr11:76360800-76361000	Enhancers	Colonic Mucosa	Colon
46	chr11:76360800-76361400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr11:76360800-76361400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr11:76360800-76361400	Enhancers	Aorta	Aorta
49	chr11:76360800-76361400	Enhancers	Fetal Kidney	kidney
50	chr11:76360800-76361400	Enhancers	Fetal Muscle Trunk	muscle

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