Variant report

Variant	nsv916012
Chromosome Location	chr11:55084067-55622531
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:55425450-55425874	GM12878	blood:	n/a	n/a
2	BATF	chr11:55425431-55426129	GM12878	blood:	n/a	n/a
3	BATF	chr11:55426940-55427106	GM12878	blood:	n/a	chr11:55427071-55427081
4	BATF	chr11:55425468-55425815	GM12878	blood:	n/a	n/a
5	BCL11A	chr11:55425504-55425830	GM12878	blood:	n/a	n/a
6	BCL11A	chr11:55425496-55426197	GM12878	blood:	n/a	n/a
7	BHLHE40	chr11:55425502-55426161	GM12878	blood:	n/a	n/a
8	BHLHE40	chr11:55427039-55427080	GM12878	blood:	n/a	n/a
9	CCNT2	chr11:55598241-55598440	K562	blood:	n/a	n/a
10	CEBPB	chr11:55186537-55186742	HepG2	liver:	n/a	chr11:55186568-55186579
11	CEBPB	chr11:55567730-55568064	A549	lung:	n/a	chr11:55567868-55567879 chr11:55567908-55567919
12	CEBPB	chr11:55312931-55313225	HepG2	liver:	n/a	chr11:55313093-55313104
13	CEBPB	chr11:55436866-55437227	IMR90	lung:	n/a	chr11:55437045-55437056
14	CEBPB	chr11:55397950-55398078	A549	lung:	n/a	n/a
15	CEBPB	chr11:55479060-55479320	HepG2	liver:	n/a	chr11:55479150-55479161
16	CEBPB	chr11:55113743-55114014	HepG2	liver:	n/a	chr11:55113873-55113884
17	CEBPB	chr11:55268173-55268348	K562	blood:	n/a	n/a
18	CEBPB	chr11:55436869-55437201	A549	lung:	n/a	chr11:55437045-55437056
19	CEBPB	chr11:55237118-55237419	HepG2	liver:	n/a	chr11:55237275-55237286
20	CEBPB	chr11:55397893-55398090	HepG2	liver:	n/a	n/a
21	CEBPB	chr11:55225032-55225273	A549	lung:	n/a	n/a
22	CEBPB	chr11:55195070-55195304	IMR90	lung:	n/a	chr11:55195175-55195186
23	CEBPB	chr11:55397830-55398153	IMR90	lung:	n/a	n/a
24	CEBPB	chr11:55407058-55407336	A549	lung:	n/a	chr11:55407201-55407212
25	CEBPB	chr11:55113744-55114010	IMR90	lung:	n/a	chr11:55113873-55113884
26	CEBPB	chr11:55131841-55132160	HepG2	liver:	n/a	chr11:55131997-55132008 chr11:55131973-55131984
27	CEBPB	chr11:55460766-55460962	A549	lung:	n/a	n/a
28	CEBPB	chr11:55407077-55407277	HepG2	liver:	n/a	chr11:55407201-55407212
29	CEBPB	chr11:55535621-55535901	HepG2	liver:	n/a	chr11:55535727-55535738
30	CEBPB	chr11:55486845-55487046	A549	lung:	n/a	n/a
31	CEBPB	chr11:55436863-55437223	HepG2	liver:	n/a	chr11:55437045-55437056
32	CEBPB	chr11:55484570-55484826	K562	blood:	n/a	chr11:55484684-55484695 chr11:55484682-55484695 chr11:55484684-55484695 chr11:55484682-55484693 chr11:55484682-55484695
33	CEBPB	chr11:55290616-55290841	HepG2	liver:	n/a	chr11:55290662-55290673
34	CEBPB	chr11:55180617-55180678	HepG2	liver:	n/a	n/a
35	CEBPB	chr11:55407050-55407358	IMR90	lung:	n/a	chr11:55407201-55407212
36	CEBPB	chr11:55484586-55484848	HepG2	liver:	n/a	chr11:55484684-55484695 chr11:55484682-55484695 chr11:55484684-55484695 chr11:55484682-55484693 chr11:55484682-55484695
37	CEBPB	chr11:55567767-55568076	HepG2	liver:	n/a	chr11:55567868-55567879 chr11:55567908-55567919
38	CEBPB	chr11:55541048-55541310	A549	lung:	n/a	n/a
39	CEBPB	chr11:55436916-55437222	K562	blood:	n/a	chr11:55437045-55437056
40	CEBPB	chr11:55195039-55195318	HepG2	liver:	n/a	chr11:55195175-55195186
41	CEBPB	chr11:55237138-55237399	A549	lung:	n/a	chr11:55237275-55237286
42	CEBPB	chr11:55205280-55205382	HepG2	liver:	n/a	chr11:55205357-55205370 chr11:55205358-55205369
43	CEBPB	chr11:55591978-55592114	HepG2	liver:	n/a	chr11:55592043-55592056 chr11:55592042-55592059 chr11:55592043-55592056 chr11:55592043-55592054 chr11:55592044-55592055
44	CEBPB	chr11:55531894-55532015	HepG2	liver:	n/a	n/a
45	CEBPB	chr11:55217456-55217716	HepG2	liver:	n/a	chr11:55217582-55217595 chr11:55217582-55217595 chr11:55217582-55217595 chr11:55217583-55217594 chr11:55217582-55217593
46	CEBPB	chr11:55131951-55132124	A549	lung:	n/a	chr11:55131997-55132008 chr11:55131973-55131984
47	CEBPB	chr11:55143436-55143619	A549	lung:	n/a	n/a
48	CHD2	chr11:55425350-55426118	GM12878	blood:	n/a	n/a
49	CREB1	chr11:55461401-55461644	A549	lung:	n/a	n/a
50	CTCF	chr11:55482800-55482950	GM12867	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:55322753-55322803	SK-N-SH_RA	brain:	n/a
2	chr11:55563401-55563451	HNPCEpiC	eye:	n/a
3	chr11:55134268-55134318	A549	lung:	n/a
4	chr11:55561545-55561595	HCPEpiC	choroid plexus:	n/a
5	chr11:55587104-55587154	BE2_C	brain:	n/a
6	chr11:55227646-55227696	HPAEpiC	pulmonary alveolar:	n/a
7	chr11:55322753-55322803	SK-N-SH_RA	brain:	n/a
8	chr11:55563401-55563451	HNPCEpiC	eye:	n/a
9	chr11:55134268-55134318	A549	lung:	n/a
10	chr11:55561545-55561595	HCPEpiC	choroid plexus:	n/a
11	chr11:55587104-55587154	BE2_C	brain:	n/a
12	chr11:55227646-55227696	HPAEpiC	pulmonary alveolar:	n/a
13	chr11:55371077-55371127	HUVEC	blood vessel:	n/a
14	chr11:55134268-55134318	IMR90	lung:	fetal
15	chr11:55593465-55593515	HEK293	kidney:	embryo
16	chr11:55431584-55431634	LNCaP	prostate:	n/a
17	chr11:55135331-55135381	AG10803	skin:	n/a
18	chr11:55586264-55586314	HUVEC	blood vessel:	n/a
19	chr11:55417018-55417068	AG04450	lung:	fetal
20	chr11:55338135-55338185	GM19239	blood:	n/a
21	chr11:55431584-55431634	MCF-7	breast:	n/a
22	chr11:55606216-55606266	Jurkat	blood:	n/a
23	chr11:55110562-55110612	HCPEpiC	choroid plexus:	n/a
24	chr11:55406191-55406241	PANC-1	pancreas:	n/a
25	chr11:55109885-55109935	AG09319	gingival:	n/a
26	chr11:55593465-55593515	GM12891	blood:	n/a
27	chr11:55593465-55593515	SKMC	muscle:	n/a
28	chr11:55109885-55109935	PANC-1	pancreas:	n/a
29	chr11:55321480-55321530	PANC-1	pancreas:	n/a
30	chr11:55417018-55417068	BE2_C	brain:	n/a
31	chr11:55227718-55227768	Hepatocyte	liver:	n/a
32	chr11:55339961-55340011	SK-N-SH_RA	brain:	n/a
33	chr11:55586264-55586314	HIPEpiC	eye:	n/a
34	chr11:55109885-55109935	Caco-2	colon:	n/a
35	chr11:55541269-55541319	MCF10A-Er-Src	breast:	n/a
36	chr11:55135046-55135096	SK-N-MC	brain:	n/a
37	chr11:55605161-55605211	LNCaP	prostate:	n/a
38	chr11:55587764-55587814	MCF10A-Er-Src	breast:	n/a
39	chr11:55586293-55586343	U87	brain:	n/a
40	chr11:55593465-55593515	Jurkat	blood:	n/a
41	chr11:55109885-55109935	HRPEpiC	eye:	n/a
42	chr11:55321480-55321530	NHBE	bronchial:	n/a
43	chr11:55110233-55110283	MCF10A-Er-Src	breast:	n/a
44	chr11:55586293-55586343	BJ	skin:	n/a
45	chr11:55606216-55606266	AG04449	skin:	fetal
46	chr11:55587764-55587814	NB4	blood:	n/a
47	chr11:55593465-55593515	ovcar-3	ovarian:	n/a
48	chr11:55586293-55586343	AG04449	skin:	fetal
49	chr11:55577775-55577825	HIPEpiC	eye:	n/a
50	chr11:55338135-55338185	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:55569608..55571383-chr11:55587513..55589076,2	K562	blood:
2	chr11:55087931..55090092-chr11:55095019..55097450,2	K562	blood:
3	chr11:55599784..55601500-chr11:55669222..55671222,2	K562	blood:
4	chr11:55087931..55090092-chr11:55095019..55097450,2	K562	blood:
5	chr11:55575230..55577016-chr11:55600877..55602678,2	K562	blood:
6	chr11:55569608..55571383-chr11:55587513..55589076,2	K562	blood:
7	chr11:55491735..55492235-chr19:6736783..6737284,2	NB4	blood:
8	chr11:55575230..55577016-chr11:55600877..55602678,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4C11-1	chr11:55451617-55451701	ENSG00000254804
2	lnc-OR4C11-1	chr11:55453377-55453636	ENSG00000254804

Variant related genes	Relation type
OR4A11P	TF binding region
OR4S2	TF binding region
OR4A13P	TF binding region
OR4A9P	TF binding region
OR5D13	TF binding region
OR5D15P	TF binding region
OR4A21P	TF binding region
OR9M1P	TF binding region
OR4P4	TF binding region
OR4A50P	TF binding region
OR4A14P	TF binding region
OR5D17P	TF binding region
OR4C1P	TF binding region
OR5D14	TF binding region
OR4A10P	TF binding region
OR4A17P	TF binding region
OR4A16	TF binding region
OR4C6	TF binding region
ENSG00000254804	TF binding region
OR4C11	TF binding region
OR5L1	TF binding region
OR5L2	TF binding region
OR4X7P	TF binding region
ENSG00000255493	TF binding region
OR5D2P	TF binding region
OR5D18	TF binding region
OR4C16	TF binding region
OR4C15	TF binding region
OR4A12P	TF binding region
OR4A15	TF binding region
OR5D16	TF binding region
OR4C14P	TF binding region
OR4V1P	TF binding region
OR4P1P	TF binding region
OR5D3P	TF binding region
OR4A11P	CpG island
OR4S2	CpG island
OR4A13P	CpG island
OR4A9P	CpG island
OR5D13	CpG island
OR5D15P	CpG island
OR4A21P	CpG island
OR9M1P	CpG island
OR4P4	CpG island
OR4A50P	CpG island
OR4A14P	CpG island
OR5D17P	CpG island
OR4C1P	CpG island
OR5D14	CpG island
OR4A10P	CpG island
OR4A17P	CpG island
OR4A16	CpG island
OR4C6	CpG island
ENSG00000254804	CpG island
OR4C11	CpG island
OR5L1	CpG island
OR5L2	CpG island
OR4X7P	CpG island
ENSG00000255493	CpG island
OR5D2P	CpG island
OR5D18	CpG island
OR4C16	CpG island
OR4C15	CpG island
OR4A12P	CpG island
OR4A15	CpG island
OR5D16	CpG island
OR4C14P	CpG island
OR4V1P	CpG island
OR4P1P	CpG island
OR5D3P	CpG island
ENSG00000125734	chromatin interactions

Extended variants
information (count: 3743 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3743 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538492678	chr11:55107497-55107498	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs61918407	chr11:55107504-55107505	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs556418761	chr11:55107523-55107524	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs368540818	chr11:55107541-55107542	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs372038114	chr11:55107558-55107559	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs182754619	chr11:55107559-55107560	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs546474781	chr11:55107580-55107581	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs146290080	chr11:55107589-55107590	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs573516903	chr11:55107593-55107594	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs540826683	chr11:55107600-55107601	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs574942577	chr11:55107607-55107608	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs112266150	chr11:55107609-55107610	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs574458247	chr11:55107634-55107635	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs187512702	chr11:55107648-55107649	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs142846642	chr11:55107650-55107651	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs544187503	chr11:55107651-55107652	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs545389217	chr11:55108132-55108133	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs558080132	chr11:55109912-55109913	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs78976577	chr11:55109921-55109922	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs117442637	chr11:55109922-55109923	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs74832906	chr11:55109932-55109933	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs571580369	chr11:55110234-55110235	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs193168148	chr11:55110249-55110250	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs10750871	chr11:55110277-55110278	Inactive region	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs565777810	chr11:55110282-55110283	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs75919730	chr11:55110440-55110441	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs531400410	chr11:55110562-55110563	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs77343615	chr11:55110566-55110567	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs571214028	chr11:55110572-55110573	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs60999778	chr11:55110577-55110578	Inactive region	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs547423295	chr11:55110592-55110593	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs565943239	chr11:55110594-55110595	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs536092057	chr11:55110596-55110597	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs75213121	chr11:55110598-55110599	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs80074384	chr11:55110601-55110602	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs77977511	chr11:55110604-55110605	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs202202418	chr11:55110804-55110805	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs200076303	chr11:55110806-55110807	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs142814072	chr11:55110807-55110808	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs147394509	chr11:55110809-55110810	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs201128700	chr11:55110817-55110818	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs370400176	chr11:55110825-55110826	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs200751761	chr11:55110826-55110827	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs139771656	chr11:55110837-55110838	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs199644874	chr11:55110843-55110844	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs200889979	chr11:55110845-55110846	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs201845728	chr11:55110847-55110848	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs199939319	chr11:55110849-55110850	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs144092380	chr11:55110856-55110857	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs200705953	chr11:55110861-55110862	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21990379	CNVD
small cell lung cancer	20016488	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	15273396	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
Multiple myeloma	16616336	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Alcoholism	21790672	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Incontinentia Pigmenti	22033527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD
Breast cancer	20369283	CNVD
Bipolar disorder	19214233	CNVD
early-passage human iPS cells	21368824	CNVD
Obesity	21131291	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:55110800-55112400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
2	chr11:55120800-55121800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:55120800-55122200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr11:55121200-55121600	Enhancers	Brain Hippocampus Middle	brain
5	chr11:55124200-55124400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
6	chr11:55149400-55149800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
7	chr11:55168200-55169000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr11:55170600-55173200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
9	chr11:55190600-55191200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
10	chr11:55215800-55222400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
11	chr11:55225400-55225800	Active TSS	HSMMtube	muscle
12	chr11:55225800-55227600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
13	chr11:55227400-55227800	Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr11:55243200-55243600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
15	chr11:55260600-55262800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
16	chr11:55263400-55263600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
17	chr11:55268600-55270400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
18	chr11:55269600-55277400	Weak transcription	Pancreas	Pancrea
19	chr11:55277400-55277800	ZNF genes & repeats	Pancreas	Pancrea
20	chr11:55277400-55278000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
21	chr11:55282000-55282400	Active TSS	Fetal Heart	heart
22	chr11:55312200-55315800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
23	chr11:55325800-55326000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
24	chr11:55337800-55338200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr11:55338000-55338400	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr11:55340200-55340400	Bivalent Enhancer	Aorta	Aorta
27	chr11:55353800-55354600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
28	chr11:55366800-55367200	ZNF genes & repeats	Esophagus	oesophagus
29	chr11:55395800-55397000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
30	chr11:55411800-55412000	Active TSS	Fetal Brain Male	brain
31	chr11:55412000-55421200	Weak transcription	Fetal Brain Male	brain
32	chr11:55414600-55415000	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
33	chr11:55415000-55416200	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr11:55416200-55416400	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
35	chr11:55421200-55421600	Active TSS	Fetal Brain Male	brain
36	chr11:55425800-55426600	Enhancers	GM12878-XiMat	blood
37	chr11:55426200-55426400	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr11:55451200-55453000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
39	chr11:55453400-55454000	Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr11:55500200-55500800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr11:55508400-55508600	Enhancers	Esophagus	oesophagus
42	chr11:55508400-55508600	ZNF genes & repeats	Pancreas	Pancrea
43	chr11:55545600-55547200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
44	chr11:55589400-55590400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell

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