Variant report

Variant	nsv482317
Chromosome Location	chr11:56857026-57028631
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1990)
CpG islands
(count:1464)
Chromatin interactive
region (count:71)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1990 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:56917883-56918238	K562	blood:	n/a	n/a
2	ARID3A	chr11:56912157-56912376	K562	blood:	n/a	n/a
3	ARID3A	chr11:57004882-57005146	K562	blood:	n/a	n/a
4	ARID3A	chr11:57017192-57017523	K562	blood:	n/a	n/a
5	ARID3A	chr11:56890656-56890674	K562	blood:	n/a	n/a
6	ARID3A	chr11:57010036-57010311	K562	blood:	n/a	n/a
7	ARID3A	chr11:56894201-56894767	K562	blood:	n/a	n/a
8	ARID3A	chr11:56889946-56890139	K562	blood:	n/a	n/a
9	ATF1	chr11:56917743-56918426	K562	blood:	n/a	n/a
10	ATF1	chr11:57004618-57005088	K562	blood:	n/a	n/a
11	ATF1	chr11:56987408-56987585	K562	blood:	n/a	n/a
12	ATF1	chr11:56981332-56981532	K562	blood:	n/a	n/a
13	ATF1	chr11:56894189-56894605	K562	blood:	n/a	n/a
14	ATF1	chr11:56922978-56923350	K562	blood:	n/a	n/a
15	ATF3	chr11:56983987-56984299	K562	blood:	n/a	n/a
16	BACH1	chr11:56988411-56988430	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr11:56931111-56931311	K562	blood:	n/a	n/a
18	BACH1	chr11:57016624-57016736	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr11:56890713-56890717	K562	blood:	n/a	n/a
20	BACH1	chr11:56946058-56946188	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr11:56920573-56920623	K562	blood:	n/a	n/a
22	BACH1	chr11:56896595-56896600	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr11:57017285-57017488	GM12878	blood:	n/a	n/a
24	BCL3	chr11:56922936-56923196	GM12878	blood:	n/a	chr11:56923176-56923183
25	BHLHE40	chr11:57017178-57017525	GM12878	blood:	n/a	n/a
26	BHLHE40	chr11:57019310-57019539	K562	blood:	n/a	n/a
27	BHLHE40	chr11:56918021-56918351	K562	blood:	n/a	n/a
28	BHLHE40	chr11:56923439-56923443	K562	blood:	n/a	n/a
29	BHLHE40	chr11:56923931-56924113	K562	blood:	n/a	n/a
30	BHLHE40	chr11:56894184-56894803	K562	blood:	n/a	n/a
31	BHLHE40	chr11:56898559-56898942	K562	blood:	n/a	n/a
32	BHLHE40	chr11:57016538-57016765	K562	blood:	n/a	n/a
33	BHLHE40	chr11:56911021-56911385	K562	blood:	n/a	n/a
34	BHLHE40	chr11:56998533-56998685	K562	blood:	n/a	n/a
35	BHLHE40	chr11:56916335-56916673	K562	blood:	n/a	n/a
36	BHLHE40	chr11:57004650-57004671	K562	blood:	n/a	n/a
37	BHLHE40	chr11:56892226-56892423	K562	blood:	n/a	n/a
38	BHLHE40	chr11:57009893-57010264	K562	blood:	n/a	n/a
39	BRCA1	chr11:56940154-56940286	GM12878	blood:	n/a	n/a
40	BRCA1	chr11:56898616-56898964	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr11:57016699-57016724	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr11:57016640-57016787	H1-hESC	embryonic stem cell:	n/a	n/a
43	CBX3	chr11:57004601-57005245	K562	blood:	n/a	n/a
44	CBX3	chr11:56910891-56911311	K562	blood:	n/a	n/a
45	CBX3	chr11:57009767-57010169	K562	blood:	n/a	n/a
46	CBX3	chr11:56894173-56894700	K562	blood:	n/a	n/a
47	CCNT2	chr11:56917710-56918351	K562	blood:	n/a	n/a
48	CCNT2	chr11:57004805-57004979	K562	blood:	n/a	chr11:57004966-57004975
49	CCNT2	chr11:56894158-56894974	K562	blood:	n/a	n/a
50	CCNT2	chr11:57009967-57010256	K562	blood:	n/a	chr11:57010058-57010067 chr11:57010228-57010237

(count:1464 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:56955011-56955061	HCM	heart:	n/a
2	chr11:57005981-57006031	K562	blood:	n/a
3	chr11:57004294-57004344	HIPEpiC	eye:	n/a
4	chr11:56972618-56972668	HepG2	liver:	n/a
5	chr11:57004294-57004344	HRCEpiC	kidney:	n/a
6	chr11:56891858-56891908	NHBE	bronchial:	n/a
7	chr11:57004919-57004969	AoSMC	blood vessel:	n/a
8	chr11:56949074-56949124	HEEpiC	esophagus:	n/a
9	chr11:56956373-56956423	NHDF-neo	bronchial:	n/a
10	chr11:56972618-56972668	HUVEC	blood vessel:	n/a
11	chr11:57005876-57005926	HRCEpiC	kidney:	n/a
12	chr11:57022542-57022592	HRCEpiC	kidney:	n/a
13	chr11:57004919-57004969	HCF	heart:	n/a
14	chr11:56948015-56948065	MCF-7	breast:	n/a
15	chr11:56955011-56955061	AG10803	skin:	n/a
16	chr11:57004919-57004969	GM06990	blood:	n/a
17	chr11:56972618-56972668	GM06990	blood:	n/a
18	chr11:57004934-57004984	A549	lung:	n/a
19	chr11:57004294-57004344	SKMC	muscle:	n/a
20	chr11:57004007-57004057	PANC-1	pancreas:	n/a
21	chr11:56956428-56956478	HAEpiC	amniotic membrane:	n/a
22	chr11:56952128-56952178	Jurkat	blood:	n/a
23	chr11:57001479-57001529	HEEpiC	esophagus:	n/a
24	chr11:56948018-56948068	BE2_C	brain:	n/a
25	chr11:57005981-57006031	GM12892	blood:	n/a
26	chr11:57003857-57003907	AG04449	skin:	fetal
27	chr11:57022542-57022592	HUVEC	blood vessel:	n/a
28	chr11:56955011-56955061	BJ	skin:	n/a
29	chr11:56948015-56948065	BE2_C	brain:	n/a
30	chr11:56923527-56923577	SK-N-MC	brain:	n/a
31	chr11:57004919-57004969	BJ	skin:	n/a
32	chr11:57005876-57005926	NB4	blood:	n/a
33	chr11:56948018-56948068	U87	brain:	n/a
34	chr11:56949074-56949124	HRE	kidney:	n/a
35	chr11:56945579-56945629	A549	lung:	n/a
36	chr11:56956373-56956423	ProgFib	skin:	n/a
37	chr11:56955011-56955061	LNCaP	prostate:	n/a
38	chr11:57022542-57022592	HCF	heart:	n/a
39	chr11:56948015-56948065	Hela-S3	cervix:	n/a
40	chr11:56956373-56956423	H1-hESC	embryonic stem cell:	embryo
41	chr11:57022542-57022592	NH-A	brain:	n/a
42	chr11:57004294-57004344	MCF-7	breast:	n/a
43	chr11:56947754-56947804	GM19239	blood:	n/a
44	chr11:57004294-57004344	AG04449	skin:	fetal
45	chr11:56891858-56891908	GM06990	blood:	n/a
46	chr11:56949288-56949338	HIPEpiC	eye:	n/a
47	chr11:56945579-56945629	AG04449	skin:	fetal
48	chr11:56956428-56956478	NHDF-neo	bronchial:	n/a
49	chr11:56972618-56972668	NT2-D1	testis:	n/a
50	chr11:56955011-56955061	AG09319	gingival:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:56923234..56925283-chr11:57012223..57015017,2	K562	blood:
2	chr11:56897171..56899424-chr11:57016274..57018526,19	MCF-7	breast:
3	chr11:56855527..56859007-chr11:56860909..56863428,3	K562	blood:
4	chr11:56945716..56947687-chr11:56952025..56954655,2	K562	blood:
5	chr11:56949100..56951767-chr11:56952168..56954744,3	MCF-7	breast:
6	chr11:56885086..56888597-chr11:56892497..56898874,6	K562	blood:
7	chr11:56952647..56955298-chr11:56956349..56958322,2	K562	blood:
8	chr11:56769288..56770290-chr11:57016463..57017822,3	K562	blood:
9	chr11:56929121..56930915-chr11:56933459..56936245,2	K562	blood:
10	chr11:57011184..57013387-chr11:57014609..57016452,2	K562	blood:
11	chr11:56923234..56925283-chr11:57012223..57015017,2	K562	blood:
12	chr11:56608365..56609372-chr11:57017133..57018075,3	MCF-7	breast:
13	chr11:56883857..56884825-chr11:57016233..57017822,10	MCF-7	breast:
14	chr11:56982364..56984084-chr11:56987113..56988700,2	K562	blood:
15	chr11:56608400..56609354-chr11:57016455..57017401,5	MCF-7	breast:
16	chr11:56912064..56913723-chr11:57003459..57006074,2	K562	blood:
17	chr11:56989037..56991877-chr11:56993430..56996007,2	K562	blood:
18	chr11:56894402..56895909-chr11:57012164..57014326,2	K562	blood:
19	chr11:56885086..56888597-chr11:56892497..56898874,6	K562	blood:
20	chr11:56950383..56952572-chr11:56977333..56980182,2	K562	blood:
21	chr11:56992305..56993973-chr11:56996074..56998381,2	K562	blood:
22	chr11:56916772..56919758-chr11:56922805..56925674,2	K562	blood:
23	chr11:57011184..57013387-chr11:57014609..57016452,2	K562	blood:
24	chr11:56855527..56859007-chr11:56860909..56863428,3	K562	blood:
25	chr11:56999799..57002436-chr11:57003214..57005140,3	K562	blood:
26	chr11:56898268..56899163-chr11:57016603..57017757,8	K562	blood:
27	chr11:56917823..56920526-chr11:57190278..57193048,2	K562	blood:
28	chr11:56883739..56884861-chr11:57016166..57017852,7	K562	blood:
29	chr11:56907060..56908951-chr11:56910842..56913533,2	K562	blood:
30	chr11:56982363..56983864-chr11:56987113..56989576,2	K562	blood:
31	chr11:56897171..56899424-chr11:57016274..57018526,19	MCF-7	breast:
32	chr11:56946370..56948285-chr11:56958607..56960284,2	MCF-7	breast:
33	chr11:56891684..56895187-chr11:57015179..57019419,3	K562	blood:
34	chr11:56912031..56914480-chr11:56915685..56918667,3	K562	blood:
35	chr11:56888220..56889882-chr11:57010746..57012751,2	K562	blood:
36	chr11:56894402..56895909-chr11:57012164..57014326,2	K562	blood:
37	chr11:56898304..56899186-chr11:57016267..57017234,5	MCF-7	breast:
38	chr11:56982363..56983864-chr11:56987113..56989576,2	K562	blood:
39	chr11:56982364..56984084-chr11:56987113..56988700,2	K562	blood:
40	chr11:56992305..56993973-chr11:56996074..56998381,2	K562	blood:
41	chr11:57010853..57012684-chr11:57014374..57016452,2	K562	blood:
42	chr11:56989037..56991877-chr11:56993430..56996007,2	K562	blood:
43	chr11:57010853..57012684-chr11:57014374..57016452,2	K562	blood:
44	chr11:57016610..57017236-chr11:57045093..57045790,2	K562	blood:
45	chr11:56946187..56949626-chr11:56951175..56954538,4	K562	blood:
46	chr11:57000179..57002436-chr11:57003214..57005510,2	K562	blood:
47	chr11:56945716..56947687-chr11:56952025..56954655,2	K562	blood:
48	chr11:56912031..56914480-chr11:56915685..56918667,3	K562	blood:
49	chr11:56996267..56998926-chr11:57000187..57002136,2	K562	blood:
50	chr11:56608383..56609306-chr11:57016176..57017128,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-P2RX3-4	chr11:56956461-56959187	NONHSAT021403
2	lnc-APLNR-2	chr11:56936197-56936267	NONHSAT021401
3	lnc-LRRC55-1	chr11:56948622-56948750	NONHSAT021402
4	lnc-APLNR-2	chr11:56929314-56929882	NONHSAT021401
5	lnc-LRRC55-1	chr11:56947536-56947757	NONHSAT021402

No data

Variant related genes	Relation type
APLNR	TF binding region
LRRC55	TF binding region
APLNR	CpG island
LRRC55	CpG island
ENSG00000254979	chromatin interactions
ENSG00000214872	chromatin interactions
ENSG00000183908	chromatin interactions
ENSG00000254662	chromatin interactions
ENSG00000149115	chromatin interactions
ENSG00000134817	chromatin interactions

Extended variants
information (count: 5953 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:5953 , 50 per page) page: 1 2 3 4 5 6 7 ... 120

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189004397	chr11:56857029-56857030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs570130413	chr11:56857089-56857090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553806829	chr11:56857093-56857094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs11228901	chr11:56857099-56857100	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs668370	chr11:56857116-56857117	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs539408496	chr11:56857176-56857177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs35128983	chr11:56857264-56857265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs727575	chr11:56857310-56857311	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs575885090	chr11:56857418-56857419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs77587071	chr11:56857425-56857426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181956525	chr11:56857426-56857427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs494932	chr11:56857443-56857444	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs535075806	chr11:56857476-56857477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186387115	chr11:56857523-56857524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190841545	chr11:56857646-56857647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs77015944	chr11:56857650-56857651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564273389	chr11:56857756-56857757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183038199	chr11:56857816-56857817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541730484	chr11:56857881-56857882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376964861	chr11:56857931-56857932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369845460	chr11:56857932-56857933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs199779548	chr11:56857937-56857938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200368964	chr11:56857938-56857939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs397781338	chr11:56857940-56857941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371029949	chr11:56857941-56857942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530758618	chr11:56857977-56857978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140174962	chr11:56858080-56858081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561954168	chr11:56858095-56858096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529251604	chr11:56858097-56858098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548554949	chr11:56858108-56858109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186745833	chr11:56858115-56858116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563541395	chr11:56858122-56858123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs3017561	chr11:56858161-56858162	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs552410409	chr11:56858163-56858164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576794250	chr11:56858216-56858217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182810715	chr11:56858259-56858260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372759711	chr11:56858262-56858263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs3017563	chr11:56858305-56858306	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs532540509	chr11:56858310-56858311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546833362	chr11:56858333-56858334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552541047	chr11:56858342-56858343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562876191	chr11:56858365-56858366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549345679	chr11:56858371-56858372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544145252	chr11:56858391-56858392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368634276	chr11:56858392-56858393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556877174	chr11:56858422-56858423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187933722	chr11:56858435-56858436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs539492256	chr11:56858452-56858453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557547836	chr11:56858478-56858479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10501362	chr11:56858483-56858484	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	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
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1928 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:56855000-56857200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr11:56855200-56857400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:56856000-56861400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr11:56856000-56864800	Weak transcription	Fetal Lung	lung
5	chr11:56857000-56857200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr11:56861000-56861200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr11:56861000-56862400	Enhancers	Fetal Kidney	kidney
8	chr11:56861000-56863600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr11:56861200-56861800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr11:56861400-56862000	Enhancers	HSMMtube	muscle
11	chr11:56861400-56862600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr11:56861400-56864000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr11:56861600-56861800	Enhancers	Fetal Stomach	stomach
14	chr11:56861600-56862200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr11:56861600-56862400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr11:56861600-56862800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr11:56861800-56862000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr11:56861800-56862000	Enhancers	Fetal Heart	heart
19	chr11:56861800-56862400	Enhancers	HMEC	breast
20	chr11:56861800-56862400	Enhancers	HSMM	muscle
21	chr11:56861800-56862600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr11:56861800-56864800	Weak transcription	Fetal Stomach	stomach
23	chr11:56862000-56862200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr11:56862000-56862600	Enhancers	NHEK	skin
25	chr11:56862000-56863200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr11:56862000-56863200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr11:56862000-56865400	Weak transcription	Fetal Heart	heart
28	chr11:56862200-56862600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr11:56862600-56863000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr11:56863000-56863200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr11:56863400-56863600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr11:56864600-56865000	Enhancers	Placenta	Placenta
33	chr11:56864600-56866600	Enhancers	Ovary	ovary
34	chr11:56864800-56866200	Enhancers	Fetal Lung	lung
35	chr11:56864800-56866400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr11:56864800-56866400	Enhancers	Fetal Stomach	stomach
37	chr11:56865400-56865800	Enhancers	Fetal Heart	heart
38	chr11:56866000-56866200	Enhancers	Lung	lung
39	chr11:56866000-56866200	Enhancers	Right Atrium	heart
40	chr11:56866200-56867200	Weak transcription	Lung	lung
41	chr11:56866200-56868200	Weak transcription	Fetal Lung	lung
42	chr11:56866200-56871800	Weak transcription	Right Atrium	heart
43	chr11:56866400-56869400	Weak transcription	Fetal Stomach	stomach
44	chr11:56866600-56867000	Weak transcription	Ovary	ovary
45	chr11:56867000-56868600	Enhancers	Ovary	ovary
46	chr11:56867200-56867400	Enhancers	Brain Germinal Matrix	brain
47	chr11:56867200-56867400	Enhancers	Lung	lung
48	chr11:56867200-56867800	Enhancers	Spleen	Spleen
49	chr11:56867400-56868600	Weak transcription	Brain Germinal Matrix	brain
50	chr11:56867600-56868200	Enhancers	HUVEC	blood vessel

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