Variant report

Variant	nsv971949
Chromosome Location	chr11:56126625-56344170
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	BACH1	chr11:56138124-56138366	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr11:56147615-56147939	Hela-S3	cervix:	n/a	chr11:56147786-56147799 chr11:56147786-56147797 chr11:56147786-56147799 chr11:56147788-56147797 chr11:56147788-56147797 chr11:56147788-56147797
3	CEBPB	chr11:56299193-56299386	A549	lung:	n/a	chr11:56299319-56299332 chr11:56299319-56299330
4	CEBPB	chr11:56147604-56147937	HepG2	liver:	n/a	chr11:56147786-56147799 chr11:56147786-56147797 chr11:56147786-56147799 chr11:56147788-56147797 chr11:56147788-56147797 chr11:56147788-56147797
5	CEBPB	chr11:56292462-56292582	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr11:56172033-56172106	H1-hESC	embryonic stem cell:	n/a	chr11:56172088-56172099
7	CEBPB	chr11:56199056-56199115	A549	lung:	n/a	n/a
8	CEBPB	chr11:56147604-56147989	IMR90	lung:	n/a	chr11:56147786-56147799 chr11:56147786-56147797 chr11:56147786-56147799 chr11:56147788-56147797 chr11:56147788-56147797 chr11:56147788-56147797
9	CEBPB	chr11:56298482-56298726	IMR90	lung:	n/a	chr11:56298562-56298573 chr11:56298561-56298574
10	CEBPB	chr11:56240213-56240354	HepG2	liver:	n/a	chr11:56240268-56240279
11	CEBPB	chr11:56138128-56138346	A549	lung:	n/a	chr11:56138266-56138277
12	CEBPB	chr11:56298548-56298677	K562	blood:	n/a	chr11:56298562-56298573 chr11:56298561-56298574
13	CEBPB	chr11:56156453-56156716	HepG2	liver:	n/a	n/a
14	CEBPB	chr11:56147598-56147982	H1-hESC	embryonic stem cell:	n/a	chr11:56147786-56147799 chr11:56147786-56147797 chr11:56147786-56147799 chr11:56147788-56147797 chr11:56147788-56147797 chr11:56147788-56147797
15	CEBPB	chr11:56138112-56138329	HepG2	liver:	n/a	chr11:56138266-56138277
16	CEBPB	chr11:56213754-56213902	A549	lung:	n/a	n/a
17	CEBPB	chr11:56147589-56147981	K562	blood:	n/a	chr11:56147786-56147799 chr11:56147786-56147797 chr11:56147786-56147799 chr11:56147788-56147797 chr11:56147788-56147797 chr11:56147788-56147797
18	CEBPB	chr11:56171906-56172267	HepG2	liver:	n/a	chr11:56172088-56172099
19	CEBPB	chr11:56332491-56332492	A549	lung:	n/a	n/a
20	CEBPB	chr11:56289541-56289703	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr11:56171929-56172241	A549	lung:	n/a	chr11:56172088-56172099
22	CEBPB	chr11:56173447-56173559	A549	lung:	n/a	n/a
23	CEBPB	chr11:56298468-56298699	HepG2	liver:	n/a	chr11:56298562-56298573 chr11:56298561-56298574
24	CEBPB	chr11:56292494-56292630	A549	lung:	n/a	n/a
25	CEBPB	chr11:56147618-56147932	A549	lung:	n/a	chr11:56147786-56147799 chr11:56147786-56147797 chr11:56147786-56147799 chr11:56147788-56147797 chr11:56147788-56147797 chr11:56147788-56147797
26	CEBPB	chr11:56156547-56156579	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr11:56128420-56128570	GM12878	blood:	n/a	n/a
28	CTCF	chr11:56163620-56163770	GM12874	blood:	n/a	chr11:56163712-56163730 chr11:56163707-56163728
29	CTCF	chr11:56163558-56163856	GM12878	blood:	n/a	chr11:56163712-56163730 chr11:56163707-56163728
30	CTCF	chr11:56289032-56290037	A549	lung:	n/a	chr11:56289575-56289593 chr11:56289577-56289598 chr11:56289578-56289591
31	CTCF	chr11:56141680-56141830	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr11:56289460-56289610	GM12865	blood:	n/a	chr11:56289575-56289593 chr11:56289577-56289598 chr11:56289578-56289591
33	CTCF	chr11:56289460-56289610	NHEK	skin:	n/a	chr11:56289575-56289593 chr11:56289577-56289598 chr11:56289578-56289591
34	CTCF	chr11:56289462-56289716	A549	lung:	n/a	chr11:56289575-56289593 chr11:56289577-56289598 chr11:56289578-56289591
35	CTCF	chr11:56289515-56289628	Lung_OC	lung:	n/a	chr11:56289575-56289593 chr11:56289577-56289598 chr11:56289578-56289591
36	CTCF	chr11:56163607-56163820	LNCaP	prostate:	n/a	chr11:56163712-56163730 chr11:56163707-56163728
37	CTCF	chr11:56289520-56289670	GM12867	blood:	n/a	chr11:56289575-56289593 chr11:56289577-56289598 chr11:56289578-56289591
38	CTCF	chr11:56163640-56163790	WERI-Rb-1	eye:	n/a	chr11:56163712-56163730 chr11:56163707-56163728
39	CTCF	chr11:56289495-56289622	Medullo	brain:	n/a	chr11:56289575-56289593 chr11:56289577-56289598 chr11:56289578-56289591
40	CTCF	chr11:56168356-56168512	MCF-7	breast:	n/a	n/a
41	CTCF	chr11:56287880-56288030	RPTEC	kidney:	n/a	n/a
42	CTCF	chr11:56289560-56289710	GM12872	blood:	n/a	chr11:56289575-56289593 chr11:56289577-56289598 chr11:56289578-56289591
43	CTCF	chr11:56289501-56289670	LNCaP	prostate:	n/a	chr11:56289575-56289593 chr11:56289577-56289598 chr11:56289578-56289591
44	CTCF	chr11:56289500-56289650	SK-N-SH_RA	brain:	n/a	chr11:56289575-56289593 chr11:56289577-56289598 chr11:56289578-56289591
45	CTCF	chr11:56289304-56289801	SK-N-SH	brain:	n/a	chr11:56289575-56289593 chr11:56289577-56289598 chr11:56289578-56289591
46	CTCF	chr11:56163653-56163782	MCF-7	breast:	n/a	chr11:56163712-56163730 chr11:56163707-56163728
47	CTCF	chr11:56163600-56163750	HepG2	liver:	n/a	chr11:56163712-56163730 chr11:56163707-56163728
48	CTCF	chr11:56289541-56289637	NHEK	skin:	n/a	chr11:56289575-56289593 chr11:56289577-56289598 chr11:56289578-56289591
49	CTCF	chr11:56289480-56289630	WERI-Rb-1	eye:	n/a	chr11:56289575-56289593 chr11:56289577-56289598 chr11:56289578-56289591
50	CTCF	chr11:56289539-56289645	ProgFib	skin:	n/a	chr11:56289575-56289593 chr11:56289577-56289598 chr11:56289578-56289591

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:56259243-56259293	RPTEC	kidney:	n/a
2	chr11:56259243-56259293	HCF	heart:	n/a
3	chr11:56259243-56259293	RPTEC	kidney:	n/a
4	chr11:56259243-56259293	HCF	heart:	n/a
5	chr11:56258485-56258535	HMEC	breast:	n/a
6	chr11:56309888-56309938	HCPEpiC	choroid plexus:	n/a
7	chr11:56128137-56128187	PrEC	prostate:	n/a
8	chr11:56264782-56264832	HRPEpiC	eye:	n/a
9	chr11:56259243-56259293	HRCEpiC	kidney:	n/a
10	chr11:56259268-56259318	SAEC	small airway:	n/a
11	chr11:56259268-56259318	AG04449	skin:	fetal
12	chr11:56309888-56309938	AoSMC	blood vessel:	n/a
13	chr11:56143818-56143868	GM12891	blood:	n/a
14	chr11:56239108-56239158	HCT-116	colon:	n/a
15	chr11:56239108-56239158	GM12891	blood:	n/a
16	chr11:56258485-56258535	AG10803	skin:	n/a
17	chr11:56264637-56264687	NB4	blood:	n/a
18	chr11:56264637-56264687	ProgFib	skin:	n/a
19	chr11:56259268-56259318	HEK293	kidney:	embryo
20	chr11:56258856-56258906	HCPEpiC	choroid plexus:	n/a
21	chr11:56259268-56259318	HCF	heart:	n/a
22	chr11:56259268-56259318	ECC-1	luminal epithelium:	n/a
23	chr11:56143818-56143868	U87	brain:	n/a
24	chr11:56185737-56185787	NHBE	bronchial:	n/a
25	chr11:56309888-56309938	BE2_C	brain:	n/a
26	chr11:56264782-56264832	CMK	blood:	n/a
27	chr11:56128137-56128187	ProgFib	skin:	n/a
28	chr11:56237629-56237679	Caco-2	colon:	n/a
29	chr11:56141839-56141889	HUVEC	blood vessel:	n/a
30	chr11:56258856-56258906	AG04449	skin:	fetal
31	chr11:56259243-56259293	LNCaP	prostate:	n/a
32	chr11:56259268-56259318	AG10803	skin:	n/a
33	chr11:56310671-56310721	SK-N-MC	brain:	n/a
34	chr11:56143818-56143868	HCPEpiC	choroid plexus:	n/a
35	chr11:56128137-56128187	HCPEpiC	choroid plexus:	n/a
36	chr11:56309888-56309938	A549	lung:	n/a
37	chr11:56143818-56143868	HRPEpiC	eye:	n/a
38	chr11:56185737-56185787	ovcar-3	ovarian:	n/a
39	chr11:56239108-56239158	A549	lung:	n/a
40	chr11:56311179-56311229	MCF10A-Er-Src	breast:	n/a
41	chr11:56143818-56143868	AG04450	lung:	fetal
42	chr11:56258485-56258535	Hepatocyte	liver:	n/a
43	chr11:56264782-56264832	HUVEC	blood vessel:	n/a
44	chr11:56185737-56185787	MCF10A-Er-Src	breast:	n/a
45	chr11:56309888-56309938	HCF	heart:	n/a
46	chr11:56311179-56311229	HIPEpiC	eye:	n/a
47	chr11:56259243-56259293	H1-hESC	embryonic stem cell:	embryo
48	chr11:56264782-56264832	LNCaP	prostate:	n/a
49	chr11:56143818-56143868	Hepatocyte	liver:	n/a
50	chr11:56259243-56259293	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:56288968..56289520-chr11:56550857..56551450,2	MCF-7	breast:
2	chr11:56127160..56128874-chr11:56130489..56132638,2	K562	blood:
3	chr11:56181160..56181939-chr6:137746651..137747385,2	MCF-7	breast:

Variant related genes	Relation type
OR5M7P	TF binding region
OR5M3	TF binding region
OR5M2P	TF binding region
OR8U1	TF binding region
OR5M8	TF binding region
OR5M4P	TF binding region
OR5M11	TF binding region
OR8L1P	TF binding region
OR5M6P	TF binding region
OR5R1	TF binding region
OR5M5P	TF binding region
ENSG00000272987	TF binding region
OR5AL2P	TF binding region
ENSG00000254411	TF binding region
OR8J1	TF binding region
ENSG00000254660	TF binding region
OR5AL1	TF binding region
OR5M9	TF binding region
OR5M7P	CpG island
OR5M3	CpG island
OR5M2P	CpG island
OR8U1	CpG island
OR5M8	CpG island
OR5M4P	CpG island
OR5M11	CpG island
OR8L1P	CpG island
OR5M6P	CpG island
OR5R1	CpG island
OR5M5P	CpG island
ENSG00000272987	CpG island
OR5AL2P	CpG island
ENSG00000254411	CpG island
OR8J1	CpG island
ENSG00000254660	CpG island
OR5AL1	CpG island
OR5M9	CpG island
ENSG00000172487	chromatin interactions

Extended variants
information (count: 2113 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:2113 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539761923	chr11:56126888-56126889	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs1945204	chr11:56126922-56126923	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs117801944	chr11:56130504-56130505	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs187864770	chr11:56130518-56130519	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs142034497	chr11:56130533-56130534	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs564581159	chr11:56130555-56130556	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs150691121	chr11:56130588-56130589	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs568620695	chr11:56130595-56130596	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs139059858	chr11:56130602-56130603	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs149870061	chr11:56130609-56130610	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs145973782	chr11:56130612-56130613	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs139843057	chr11:56130658-56130659	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs192300542	chr11:56130695-56130696	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs576528935	chr11:56130698-56130699	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs143377470	chr11:56130712-56130713	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs146739916	chr11:56130761-56130762	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574674928	chr11:56130840-56130841	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs183340715	chr11:56130842-56130843	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs550761803	chr11:56130886-56130887	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs542091288	chr11:56130964-56130965	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs188349189	chr11:56130967-56130968	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs114127412	chr11:56131006-56131007	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs148876053	chr11:56131070-56131071	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs34913154	chr11:56131100-56131101	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs369065764	chr11:56131101-56131102	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs71055593	chr11:56131111-56131112	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs564134082	chr11:56131112-56131113	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs201720825	chr11:56131118-56131119	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs528105364	chr11:56131120-56131121	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs192557190	chr11:56131174-56131175	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs367816953	chr11:56131210-56131211	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs1945231	chr11:56131233-56131234	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs540906983	chr11:56131281-56131282	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs536573878	chr11:56131499-56131500	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs562288375	chr11:56131590-56131591	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs34093872	chr11:56131598-56131599	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs529398389	chr11:56131604-56131605	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs550769569	chr11:56131664-56131665	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs562605546	chr11:56131666-56131667	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs7126732	chr11:56131667-56131668	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs551612122	chr11:56131673-56131674	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs566842958	chr11:56131686-56131687	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs77394740	chr11:56131723-56131724	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs142720475	chr11:56131741-56131742	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs151005993	chr11:56131742-56131743	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs76507737	chr11:56131744-56131745	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs184486415	chr11:56131803-56131804	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs78526397	chr11:56131807-56131808	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs557819819	chr11:56131814-56131815	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs578056688	chr11:56131839-56131840	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

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
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
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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:56143200-56143800	Active TSS	Brain Substantia Nigra	brain
2	chr11:56156200-56157000	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr11:56161200-56162800	Enhancers	Fetal Intestine Small	intestine
4	chr11:56161200-56163000	Enhancers	Fetal Intestine Large	intestine
5	chr11:56163600-56164000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr11:56169600-56170000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr11:56171000-56172400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr11:56171600-56172400	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr11:56173600-56173800	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr11:56173800-56175400	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr11:56200400-56200800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr11:56210000-56210800	Enhancers	Fetal Intestine Large	intestine
13	chr11:56210800-56211000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:56210800-56211200	Weak transcription	Fetal Intestine Large	intestine
15	chr11:56211200-56211600	Enhancers	Fetal Intestine Large	intestine
16	chr11:56220800-56221800	Enhancers	Fetal Brain Male	brain
17	chr11:56222400-56222800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr11:56223400-56224200	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr11:56241400-56243600	Enhancers	Fetal Intestine Large	intestine
20	chr11:56241800-56243600	Enhancers	Fetal Intestine Small	intestine
21	chr11:56250200-56250400	Weak transcription	Fetal Intestine Large	intestine
22	chr11:56250400-56251000	Enhancers	Fetal Intestine Small	intestine
23	chr11:56250400-56251200	Enhancers	Fetal Intestine Large	intestine
24	chr11:56251000-56253200	Weak transcription	Fetal Intestine Small	intestine
25	chr11:56251200-56253600	Weak transcription	Fetal Intestine Large	intestine
26	chr11:56253200-56256200	Enhancers	Fetal Intestine Small	intestine
27	chr11:56253600-56256400	Enhancers	Fetal Intestine Large	intestine
28	chr11:56260400-56261200	Enhancers	Fetal Brain Male	brain
29	chr11:56261200-56261600	Weak transcription	Fetal Brain Male	brain
30	chr11:56261600-56261800	Enhancers	Fetal Brain Male	brain
31	chr11:56261800-56263200	Weak transcription	Fetal Brain Male	brain
32	chr11:56263200-56263600	Enhancers	Fetal Brain Male	brain
33	chr11:56269400-56271000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr11:56271200-56271800	Enhancers	Fetal Brain Male	brain
35	chr11:56271800-56273000	Weak transcription	Fetal Brain Male	brain
36	chr11:56273000-56273600	Enhancers	Fetal Brain Male	brain
37	chr11:56279800-56281400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr11:56292400-56293000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr11:56292600-56293000	Enhancers	Fetal Intestine Large	intestine
40	chr11:56292600-56293400	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr11:56293000-56298400	Weak transcription	Fetal Intestine Large	intestine
42	chr11:56295200-56295600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr11:56298200-56298400	Enhancers	Fetal Intestine Small	intestine
44	chr11:56298400-56299400	Weak transcription	Fetal Intestine Small	intestine
45	chr11:56298400-56302000	Enhancers	Fetal Intestine Large	intestine
46	chr11:56299400-56301200	Enhancers	Fetal Intestine Small	intestine
47	chr11:56299800-56300600	Enhancers	Colonic Mucosa	Colon
48	chr11:56299800-56300600	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr11:56299800-56301000	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr11:56300400-56300800	Enhancers	Sigmoid Colon	Sigmoid Colon

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