Variant report

Variant	nsv555101
Chromosome Location	chr11:56503728-56704042
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1167)
CpG islands
(count:734)
Chromatin interactive
region (count:20)
LncRNA
region (count:18)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1167 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr11:56517803-56518031	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF3	chr11:56700056-56700856	A549	lung:	n/a	n/a
3	ATF3	chr11:56700281-56700715	HCT-116	colon:	n/a	n/a
4	ATF3	chr11:56677422-56678255	A549	lung:	n/a	n/a
5	ATF3	chr11:56700116-56700807	A549	lung:	n/a	n/a
6	ATF3	chr11:56677375-56678070	A549	lung:	n/a	n/a
7	ATF3	chr11:56674119-56674737	A549	lung:	n/a	n/a
8	ATF3	chr11:56615453-56615997	A549	lung:	n/a	n/a
9	ATF3	chr11:56615460-56615977	A549	lung:	n/a	n/a
10	BACH1	chr11:56646070-56646184	K562	blood:	n/a	n/a
11	BCL3	chr11:56700090-56700807	A549	lung:	n/a	n/a
12	BCL3	chr11:56615380-56615997	A549	lung:	n/a	n/a
13	BCL3	chr11:56677223-56678627	A549	lung:	n/a	chr11:56678412-56678421 chr11:56678413-56678422
14	BCL3	chr11:56699810-56701075	A549	lung:	n/a	n/a
15	BCL3	chr11:56677385-56678346	A549	lung:	n/a	n/a
16	BCL3	chr11:56673648-56674760	A549	lung:	n/a	n/a
17	BCL3	chr11:56673973-56674803	A549	lung:	n/a	n/a
18	BCL3	chr11:56615347-56616338	A549	lung:	n/a	n/a
19	CBX3	chr11:56700195-56700768	HCT-116	colon:	n/a	n/a
20	CEBPB	chr11:56517620-56518023	HepG2	liver:	n/a	chr11:56517867-56517884
21	CEBPB	chr11:56678719-56679324	A549	lung:	n/a	n/a
22	CEBPB	chr11:56517634-56517959	IMR90	lung:	n/a	chr11:56517867-56517884
23	CEBPB	chr11:56677145-56679193	A549	lung:	n/a	chr11:56677154-56677166
24	CEBPB	chr11:56700255-56700726	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr11:56617323-56617647	A549	lung:	n/a	chr11:56617512-56617523
26	CEBPB	chr11:56568721-56568994	IMR90	lung:	n/a	chr11:56568834-56568843 chr11:56568834-56568843 chr11:56568834-56568843 chr11:56568832-56568845
27	CEBPB	chr11:56644885-56645198	HepG2	liver:	n/a	chr11:56645019-56645030
28	CEBPB	chr11:56617279-56617787	A549	lung:	n/a	chr11:56617512-56617523
29	CEBPB	chr11:56692200-56692499	A549	lung:	n/a	chr11:56692374-56692386 chr11:56692343-56692354
30	CEBPB	chr11:56594865-56595180	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr11:56517644-56518052	HepG2	liver:	n/a	chr11:56517867-56517884
32	CEBPB	chr11:56666303-56666724	A549	lung:	n/a	n/a
33	CEBPB	chr11:56700165-56700906	A549	lung:	n/a	n/a
34	CEBPB	chr11:56699438-56699655	A549	lung:	n/a	chr11:56699596-56699607
35	CEBPB	chr11:56517810-56517951	K562	blood:	n/a	chr11:56517867-56517884
36	CEBPB	chr11:56672226-56672606	HepG2	liver:	n/a	chr11:56672486-56672499 chr11:56672488-56672499 chr11:56672488-56672499
37	CEBPB	chr11:56700378-56700640	MCF-7	breast:	n/a	n/a
38	CEBPB	chr11:56568334-56568570	A549	lung:	n/a	chr11:56568406-56568417 chr11:56568405-56568416 chr11:56568405-56568418
39	CEBPB	chr11:56517717-56517991	A549	lung:	n/a	chr11:56517867-56517884
40	CEBPB	chr11:56617430-56617625	HepG2	liver:	n/a	chr11:56617512-56617523
41	CEBPB	chr11:56700358-56700682	IMR90	lung:	n/a	n/a
42	CEBPB	chr11:56689927-56690256	HepG2	liver:	n/a	chr11:56690086-56690097 chr11:56690086-56690099
43	CEBPB	chr11:56674000-56675226	A549	lung:	n/a	n/a
44	CEBPB	chr11:56653864-56654402	A549	lung:	n/a	chr11:56654140-56654153
45	CEBPB	chr11:56673532-56674712	A549	lung:	n/a	n/a
46	CEBPB	chr11:56565598-56565920	A549	lung:	n/a	n/a
47	CEBPB	chr11:56644870-56645190	A549	lung:	n/a	chr11:56645019-56645030
48	CEBPB	chr11:56616784-56617073	A549	lung:	n/a	n/a
49	CEBPB	chr11:56608674-56609010	A549	lung:	n/a	n/a
50	CEBPB	chr11:56615462-56616086	A549	lung:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:56545039-56545089	HIPEpiC	eye:	n/a
2	chr11:56587595-56587645	RPTEC	kidney:	n/a
3	chr11:56545039-56545089	HIPEpiC	eye:	n/a
4	chr11:56587595-56587645	RPTEC	kidney:	n/a
5	chr11:56512503-56512553	AG09309	skin:	n/a
6	chr11:56511965-56512015	GM12892	blood:	n/a
7	chr11:56615879-56615929	H1-hESC	embryonic stem cell:	embryo
8	chr11:56511965-56512015	HCF	heart:	n/a
9	chr11:56614928-56614978	SAEC	small airway:	n/a
10	chr11:56512503-56512553	HMEC	breast:	n/a
11	chr11:56615725-56615775	ProgFib	skin:	n/a
12	chr11:56615879-56615929	GM12878	blood:	n/a
13	chr11:56614928-56614978	HRCEpiC	kidney:	n/a
14	chr11:56511248-56511298	NB4	blood:	n/a
15	chr11:56615879-56615929	U87	brain:	n/a
16	chr11:56587595-56587645	NH-A	brain:	n/a
17	chr11:56587256-56587306	Hela-S3	cervix:	n/a
18	chr11:56587212-56587262	HRE	kidney:	n/a
19	chr11:56615725-56615775	HCF	heart:	n/a
20	chr11:56511965-56512015	CMK	blood:	n/a
21	chr11:56545039-56545089	HRCEpiC	kidney:	n/a
22	chr11:56587212-56587262	LNCaP	prostate:	n/a
23	chr11:56587595-56587645	LNCaP	prostate:	n/a
24	chr11:56512503-56512553	H1-hESC	embryonic stem cell:	embryo
25	chr11:56512503-56512553	ovcar-3	ovarian:	n/a
26	chr11:56587212-56587262	HEK293	kidney:	embryo
27	chr11:56614928-56614978	BJ	skin:	n/a
28	chr11:56614928-56614978	GM12891	blood:	n/a
29	chr11:56587212-56587262	BJ	skin:	n/a
30	chr11:56587595-56587645	PFSK-1	brain:	n/a
31	chr11:56643145-56643195	ECC-1	luminal epithelium:	n/a
32	chr11:56587595-56587645	H1-hESC	embryonic stem cell:	embryo
33	chr11:56510971-56511021	K562	blood:	n/a
34	chr11:56545039-56545089	HCPEpiC	choroid plexus:	n/a
35	chr11:56587256-56587306	NT2-D1	testis:	n/a
36	chr11:56512503-56512553	HIPEpiC	eye:	n/a
37	chr11:56511248-56511298	SAEC	small airway:	n/a
38	chr11:56587595-56587645	HCPEpiC	choroid plexus:	n/a
39	chr11:56511965-56512015	RPTEC	kidney:	n/a
40	chr11:56510971-56511021	HEEpiC	esophagus:	n/a
41	chr11:56614928-56614978	SKMC	muscle:	n/a
42	chr11:56643145-56643195	HL-60	blood:	n/a
43	chr11:56615725-56615775	SK-N-MC	brain:	n/a
44	chr11:56615879-56615929	GM06990	blood:	n/a
45	chr11:56545039-56545089	HPAEpiC	pulmonary alveolar:	n/a
46	chr11:56511965-56512015	PANC-1	pancreas:	n/a
47	chr11:56510971-56511021	SKMC	muscle:	n/a
48	chr11:56545039-56545089	HMEC	breast:	n/a
49	chr11:56615725-56615775	HRCEpiC	kidney:	n/a
50	chr11:56615725-56615775	HMEC	breast:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:56562414..56565346-chr11:56565920..56568664,2	K562	blood:
2	chr11:56562414..56565346-chr11:56565920..56568664,2	K562	blood:
3	chr11:56618059..56620569-chr11:56629242..56631002,2	K562	blood:
4	chr11:56640294..56642115-chr11:56642674..56646805,4	K562	blood:
5	chr11:56391852..56392531-chr11:56550628..56551135,2	MCF-7	breast:
6	chr11:56640294..56642115-chr11:56642674..56646805,4	K562	blood:
7	chr11:56664007..56666719-chr11:56666908..56669064,2	K562	blood:
8	chr11:56646465..56649384-chr11:56653182..56655132,3	K562	blood:
9	chr11:56628427..56630548-chr11:56631596..56633931,2	K562	blood:
10	chr11:56604071..56605908-chr11:56606591..56609227,2	K562	blood:
11	chr11:56608476..56609545-chr11:57016926..57017835,4	K562	blood:
12	chr11:56608365..56609372-chr11:57017133..57018075,3	MCF-7	breast:
13	chr11:56288968..56289520-chr11:56550857..56551450,2	MCF-7	breast:
14	chr11:56608383..56609306-chr11:57016176..57017128,2	MCF-7	breast:
15	chr11:56664007..56666719-chr11:56666908..56669064,2	K562	blood:
16	chr11:56646465..56649384-chr11:56653182..56655132,3	K562	blood:
17	chr11:56628427..56630548-chr11:56631596..56633931,2	K562	blood:
18	chr11:56608400..56609354-chr11:57016455..57017401,5	MCF-7	breast:
19	chr11:56604071..56605908-chr11:56606591..56609227,2	K562	blood:
20	chr11:56618059..56620569-chr11:56629242..56631002,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR5AK2-1	chr11:56643073-56645554	XLOC_009132
2	lnc-OR5AK2-1	chr11:56638567-56638727	NR_110136
3	lnc-OR5AK2-1	chr11:56616044-56616091	ENSG00000255433
4	lnc-OR5AK2-1	chr11:56615954-56616091	ENSG00000255433
5	lnc-OR5AK2-1	chr11:56638567-56638727	ENSG00000255433
6	lnc-OR5AK2-1	chr11:56615954-56616091	XLOC_009132
7	lnc-OR9G4-1	chr11:56570001-56570030	NONHSAT021395
8	lnc-OR5AK2-1	chr11:56642200-56642319	ENSG00000255433
9	lnc-OR9G4-1	chr11:56569552-56569670	NONHSAT021395
10	lnc-OR5AK2-1	chr11:56638567-56638727	ENSG00000255433
11	lnc-OR5AK2-1	chr11:56643073-56645554	NR_110136
12	lnc-OR5AK2-1	chr11:56643073-56644687	ENSG00000255433
13	lnc-OR5AK2-1	chr11:56638567-56638727	XLOC_009132
14	lnc-OR5AK2-1	chr11:56642200-56642319	NR_110136
15	lnc-OR9G4-1	chr11:56570184-56570284	NONHSAT021395
16	lnc-OR5AK2-1	chr11:56643073-56645554	ENSG00000255433
17	lnc-OR9G4-1	chr11:56587057-56587123	NONHSAT021395
18	lnc-OR5AK2-1	chr11:56615954-56616091	NR_110136

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6128	chr11:56511419-56511437	MIMAT0024611

No data

Variant related genes	Relation type
OR5G1P	TF binding region
OR9G2P	TF binding region
ENSG00000255433	TF binding region
OR5G3	TF binding region
ENSG00000254953	TF binding region
OR9G3P	TF binding region
OR9G4	TF binding region
OR5G5P	TF binding region
OR5G4P	TF binding region
OR5G1P	CpG island
OR9G2P	CpG island
ENSG00000255433	CpG island
OR5G3	CpG island
ENSG00000254953	CpG island
OR9G3P	CpG island
OR9G4	CpG island
OR5G5P	CpG island
OR5G4P	CpG island

Extended variants
information (count: 4842 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:4842 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568919709	chr11:56503917-56503918	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs149807199	chr11:56504833-56504834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538004927	chr11:56504913-56504914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs146809124	chr11:56504920-56504921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571619337	chr11:56504951-56504952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539099705	chr11:56504982-56504983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553911016	chr11:56505003-56505004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115573559	chr11:56505008-56505009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs534126474	chr11:56505031-56505032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs485424	chr11:56505055-56505056	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs573890541	chr11:56505068-56505069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187272200	chr11:56505080-56505081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs600778	chr11:56505081-56505082	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs544471699	chr11:56505108-56505109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577693692	chr11:56505112-56505113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190117468	chr11:56505124-56505125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559935700	chr11:56505129-56505130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs140687722	chr11:56505147-56505148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs145782967	chr11:56505153-56505154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561209256	chr11:56505167-56505168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531806005	chr11:56505168-56505169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs138484791	chr11:56505185-56505186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144128348	chr11:56507527-56507528	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs544083385	chr11:56507528-56507529	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs576754830	chr11:56507561-56507562	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs535388115	chr11:56507593-56507594	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs190470325	chr11:56507598-56507599	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs575096872	chr11:56507612-56507613	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs148724186	chr11:56507635-56507636	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs527960803	chr11:56507638-56507639	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs181726215	chr11:56507639-56507640	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs575723855	chr11:56507675-56507676	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs61741400	chr11:56507716-56507717	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs564549997	chr11:56507728-56507729	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs528427048	chr11:56507738-56507739	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs547297399	chr11:56507742-56507743	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs559187102	chr11:56507789-56507790	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs529867305	chr11:56507790-56507791	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs473032	chr11:56507812-56507813	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs200224092	chr11:56507816-56507817	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs74219940	chr11:56507838-56507839	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs74213568	chr11:56507852-56507853	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs75498336	chr11:56507902-56507903	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs537158643	chr11:56507905-56507906	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs551938203	chr11:56507950-56507951	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs374306166	chr11:56507951-56507952	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs112145881	chr11:56507986-56507987	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs113842427	chr11:56507987-56507988	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs77233504	chr11:56507988-56507989	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs112487069	chr11:56508013-56508014	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Breast cancer	17142309	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:435 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:56504800-56505200	Enhancers	Fetal Brain Male	brain
2	chr11:56519000-56519200	ZNF genes & repeats	Spleen	Spleen
3	chr11:56520000-56520400	Enhancers	Dnd41	blood
4	chr11:56520400-56524600	Weak transcription	Dnd41	blood
5	chr11:56521600-56521800	Enhancers	H1 Cell Line	embryonic stem cell
6	chr11:56521800-56522800	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr11:56521800-56523600	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr11:56522000-56523600	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr11:56522400-56522800	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr11:56522400-56523400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr11:56522600-56522800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
12	chr11:56522600-56523000	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr11:56522800-56523000	Enhancers	H1 Cell Line	embryonic stem cell
14	chr11:56522800-56523200	Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr11:56523000-56523600	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr11:56523600-56523800	Enhancers	H1 Cell Line	embryonic stem cell
17	chr11:56523800-56525200	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr11:56524600-56525800	Enhancers	Dnd41	blood
19	chr11:56525200-56525400	Enhancers	H1 Cell Line	embryonic stem cell
20	chr11:56532400-56533000	Enhancers	A549	lung
21	chr11:56541800-56542200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr11:56543600-56544200	Enhancers	Fetal Intestine Small	intestine
23	chr11:56543800-56544400	Enhancers	Fetal Intestine Large	intestine
24	chr11:56544200-56545200	Weak transcription	Fetal Intestine Small	intestine
25	chr11:56544400-56544800	Weak transcription	Fetal Intestine Large	intestine
26	chr11:56544800-56545200	Enhancers	Fetal Intestine Large	intestine
27	chr11:56545200-56545400	Enhancers	Fetal Intestine Small	intestine
28	chr11:56545200-56546200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr11:56545400-56546200	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr11:56545600-56546200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr11:56546200-56550200	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr11:56546200-56550600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr11:56550000-56551000	Enhancers	GM12878-XiMat	blood
34	chr11:56550200-56551000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr11:56550600-56551000	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr11:56550600-56551200	Active TSS	A549	lung
37	chr11:56550800-56551000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr11:56550800-56551000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr11:56550800-56551200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr11:56550800-56551200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr11:56550800-56551200	Active TSS	Pancreatic Islets	Pancreatic Islet
42	chr11:56550800-56551200	Active TSS	Rectal Mucosa Donor 29	rectum
43	chr11:56550800-56551200	Active TSS	Rectal Mucosa Donor 31	rectum
44	chr11:56558000-56558400	Enhancers	Spleen	Spleen
45	chr11:56558200-56558400	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
46	chr11:56559400-56559800	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr11:56565200-56566200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr11:56565600-56565800	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr11:56565600-56566000	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr11:56567600-56568000	Enhancers	iPS-15b Cell Line	embryonic stem cell

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