Variant report

Variant	nsv1047073
Chromosome Location	chr11:36711638-36812910
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1358)
CpG islands
(count:184)
Chromatin interactive
region (count:52)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1358 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:36768584-36768987	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:36724165-36724519	HepG2	liver:	n/a	n/a
3	ATF1	chr11:36773162-36773181	K562	blood:	n/a	n/a
4	ATF1	chr11:36732716-36732720	K562	blood:	n/a	n/a
5	ATF1	chr11:36718932-36719015	K562	blood:	n/a	n/a
6	ATF1	chr11:36768697-36768952	K562	blood:	n/a	n/a
7	ATF2	chr11:36804861-36805225	GM12878	blood:	n/a	n/a
8	ATF2	chr11:36746340-36746858	GM12878	blood:	n/a	n/a
9	ATF2	chr11:36764611-36765015	GM12878	blood:	n/a	n/a
10	ATF2	chr11:36764570-36765073	GM12878	blood:	n/a	n/a
11	BACH1	chr11:36724237-36724550	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr11:36784758-36784973	GM12878	blood:	n/a	chr11:36784888-36784897
13	BATF	chr11:36724245-36724934	GM12878	blood:	n/a	n/a
14	BATF	chr11:36724568-36724931	GM12878	blood:	n/a	n/a
15	BATF	chr11:36764600-36764950	GM12878	blood:	n/a	n/a
16	BATF	chr11:36808891-36809216	GM12878	blood:	n/a	chr11:36809092-36809103
17	BATF	chr11:36784725-36785065	GM12878	blood:	n/a	chr11:36784888-36784897
18	BATF	chr11:36764552-36764919	GM12878	blood:	n/a	n/a
19	BCL11A	chr11:36724469-36724860	GM12878	blood:	n/a	n/a
20	BCL11A	chr11:36764548-36764961	GM12878	blood:	n/a	n/a
21	BHLHE40	chr11:36764524-36764996	GM12878	blood:	n/a	n/a
22	BHLHE40	chr11:36768556-36769024	GM12878	blood:	n/a	n/a
23	BRCA1	chr11:36724228-36724479	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr11:36768662-36768908	HepG2	liver:	n/a	n/a
25	CBX3	chr11:36766088-36766452	K562	blood:	n/a	n/a
26	CBX3	chr11:36766037-36766541	HCT-116	colon:	n/a	n/a
27	CEBPB	chr11:36724177-36724551	K562	blood:	n/a	chr11:36724360-36724371 chr11:36724360-36724373
28	CEBPB	chr11:36724177-36724551	IMR90	lung:	n/a	chr11:36724360-36724371 chr11:36724360-36724373
29	CEBPB	chr11:36761985-36762066	HepG2	liver:	n/a	n/a
30	CEBPB	chr11:36724230-36724575	MCF-7	breast:	n/a	chr11:36724360-36724371 chr11:36724360-36724373
31	CEBPB	chr11:36796124-36796526	Hela-S3	cervix:	n/a	chr11:36796326-36796337
32	CEBPB	chr11:36786966-36787126	HepG2	liver:	n/a	chr11:36787018-36787029
33	CEBPB	chr11:36785309-36785604	HepG2	liver:	n/a	chr11:36785452-36785461 chr11:36785450-36785461 chr11:36785450-36785463
34	CEBPB	chr11:36752696-36752811	HepG2	liver:	n/a	n/a
35	CEBPB	chr11:36724200-36724539	A549	lung:	n/a	chr11:36724360-36724371 chr11:36724360-36724373
36	CEBPB	chr11:36809711-36809761	IMR90	lung:	n/a	n/a
37	CEBPB	chr11:36745882-36746464	HepG2	liver:	n/a	n/a
38	CEBPB	chr11:36724175-36724559	HepG2	liver:	n/a	chr11:36724360-36724371 chr11:36724360-36724373
39	CEBPB	chr11:36724180-36724545	H1-hESC	embryonic stem cell:	n/a	chr11:36724360-36724371 chr11:36724360-36724373
40	CEBPB	chr11:36726324-36726607	HepG2	liver:	n/a	chr11:36726441-36726452
41	CEBPB	chr11:36796203-36796473	A549	lung:	n/a	chr11:36796326-36796337
42	CEBPB	chr11:36768670-36768966	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr11:36724181-36724547	Hela-S3	cervix:	n/a	chr11:36724360-36724371 chr11:36724360-36724373
44	CEBPB	chr11:36785309-36785570	IMR90	lung:	n/a	chr11:36785452-36785461 chr11:36785450-36785461 chr11:36785450-36785463
45	CEBPB	chr11:36785349-36785549	A549	lung:	n/a	chr11:36785452-36785461 chr11:36785450-36785461 chr11:36785450-36785463
46	CEBPB	chr11:36796189-36796500	IMR90	lung:	n/a	chr11:36796326-36796337
47	CEBPB	chr11:36796217-36796455	HepG2	liver:	n/a	chr11:36796326-36796337
48	CHD1	chr11:36768667-36768940	GM12878	blood:	n/a	n/a
49	CHD2	chr11:36768659-36769136	GM12878	blood:	n/a	n/a
50	CHD2	chr11:36768651-36768974	Hela-S3	cervix:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:36723640-36723690	HEEpiC	esophagus:	n/a
2	chr11:36723640-36723690	HEEpiC	esophagus:	n/a
3	chr11:36767011-36767061	HRCEpiC	kidney:	n/a
4	chr11:36767011-36767061	SK-N-SH	brain:	n/a
5	chr11:36807594-36807644	BE2_C	brain:	n/a
6	chr11:36723640-36723690	HCT-116	colon:	n/a
7	chr11:36723640-36723690	GM12878	blood:	n/a
8	chr11:36767011-36767061	PFSK-1	brain:	n/a
9	chr11:36767011-36767061	AG09309	skin:	n/a
10	chr11:36767011-36767061	BJ	skin:	n/a
11	chr11:36807594-36807644	AG10803	skin:	n/a
12	chr11:36767011-36767061	PrEC	prostate:	n/a
13	chr11:36723640-36723690	T-47D	breast:	n/a
14	chr11:36723640-36723690	AG10803	skin:	n/a
15	chr11:36767011-36767061	GM06990	blood:	n/a
16	chr11:36723640-36723690	RPTEC	kidney:	n/a
17	chr11:36807594-36807644	NHDF-neo	bronchial:	n/a
18	chr11:36723640-36723690	HNPCEpiC	eye:	n/a
19	chr11:36723640-36723690	MCF10A-Er-Src	breast:	n/a
20	chr11:36807594-36807644	HCT-116	colon:	n/a
21	chr11:36807594-36807644	K562	blood:	n/a
22	chr11:36723640-36723690	NB4	blood:	n/a
23	chr11:36807594-36807644	PrEC	prostate:	n/a
24	chr11:36807594-36807644	GM19239	blood:	n/a
25	chr11:36767011-36767061	HIPEpiC	eye:	n/a
26	chr11:36807594-36807644	CMK	blood:	n/a
27	chr11:36767011-36767061	AG04449	skin:	fetal
28	chr11:36723640-36723690	K562	blood:	n/a
29	chr11:36767011-36767061	SK-N-SH_RA	brain:	n/a
30	chr11:36767011-36767061	CMK	blood:	n/a
31	chr11:36807594-36807644	MCF-7	breast:	n/a
32	chr11:36723640-36723690	ovcar-3	ovarian:	n/a
33	chr11:36723640-36723690	PANC-1	pancreas:	n/a
34	chr11:36723640-36723690	NT2-D1	testis:	n/a
35	chr11:36807594-36807644	GM06990	blood:	n/a
36	chr11:36807594-36807644	HL-60	blood:	n/a
37	chr11:36767011-36767061	HCM	heart:	n/a
38	chr11:36767011-36767061	HAEpiC	amniotic membrane:	n/a
39	chr11:36767011-36767061	ovcar-3	ovarian:	n/a
40	chr11:36807594-36807644	Jurkat	blood:	n/a
41	chr11:36807594-36807644	ovcar-3	ovarian:	n/a
42	chr11:36767011-36767061	GM19239	blood:	n/a
43	chr11:36767011-36767061	NHBE	bronchial:	n/a
44	chr11:36767011-36767061	LNCaP	prostate:	n/a
45	chr11:36767011-36767061	HNPCEpiC	eye:	n/a
46	chr11:36807594-36807644	HRE	kidney:	n/a
47	chr11:36807594-36807644	HMEC	breast:	n/a
48	chr11:36807594-36807644	SKMC	muscle:	n/a
49	chr11:36767011-36767061	SK-N-MC	brain:	n/a
50	chr11:36767011-36767061	HepG2	liver:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:36710108..36712201-chr11:36728263..36730385,2	K562	blood:
2	chr11:36778500..36779382-chr2:172367393..172368075,2	MCF-7	breast:
3	chr11:36722899..36725054-chr11:36764886..36767764,2	MCF-7	breast:
4	chr11:36724020..36724871-chr11:36765820..36767130,6	MCF-7	breast:
5	chr11:36723787..36725644-chr11:36767836..36769642,23	MCF-7	breast:
6	chr11:36724020..36724871-chr11:36765820..36767130,6	MCF-7	breast:
7	chr11:36724006..36724837-chr11:36767791..36768301,2	MCF-7	breast:
8	chr11:36723937..36724844-chr11:36768321..36769390,6	K562	blood:
9	chr11:36724006..36724837-chr11:36767791..36768301,2	MCF-7	breast:
10	chr11:36723701..36725897-chr11:36768513..36770363,2	K562	blood:
11	chr11:36588187..36588912-chr11:36768353..36769303,3	MCF-7	breast:
12	chr11:36723701..36725897-chr11:36768513..36770363,2	K562	blood:
13	chr11:36794916..36796666-chr11:36808832..36811328,2	K562	blood:
14	chr11:36760152..36763496-chr11:36764810..36767505,3	K562	blood:
15	chr11:36772270..36775146-chr11:36778042..36780979,2	MCF-7	breast:
16	chr11:36585872..36586620-chr11:36765861..36766774,5	MCF-7	breast:
17	chr11:36768324..36768860-chr16:67850405..67851033,2	MCF-7	breast:
18	chr11:36724082..36725333-chr11:36765913..36767362,6	MCF-7	breast:
19	chr11:36723925..36724827-chr11:36768344..36769277,7	MCF-7	breast:
20	chr11:36588028..36588693-chr11:36768352..36768969,2	MCF-7	breast:
21	chr11:36585768..36586611-chr11:36768401..36769196,4	K562	blood:
22	chr11:36531416..36532018-chr11:36768557..36769184,2	MCF-7	breast:
23	chr11:36784007..36786954-chr11:36790139..36792736,2	MCF-7	breast:
24	chr11:36723925..36724827-chr11:36768344..36769277,7	MCF-7	breast:
25	chr11:36724313..36724958-chr11:36765739..36766377,3	K562	blood:
26	chr11:36586002..36586650-chr11:36768339..36769255,5	MCF-7	breast:
27	chr11:36794916..36796666-chr11:36808832..36811328,2	K562	blood:
28	chr11:36723787..36725644-chr11:36767836..36769642,23	MCF-7	breast:
29	chr1:48802634..48803290-chr11:36761642..36762449,2	MCF-7	breast:
30	chr11:36536866..36537854-chr11:36768352..36769212,2	MCF-7	breast:
31	chr11:36585718..36586807-chr11:36768335..36769499,7	MCF-7	breast:
32	chr11:36772270..36775146-chr11:36778042..36780979,2	MCF-7	breast:
33	chr11:36723937..36724844-chr11:36768321..36769390,6	K562	blood:
34	chr11:36768499..36769405-chr7:29306639..29307162,2	MCF-7	breast:
35	chr11:36722899..36725054-chr11:36764886..36767764,2	MCF-7	breast:
36	chr11:36772768..36775100-chr11:36777744..36780242,2	K562	blood:
37	chr11:36710108..36712201-chr11:36728263..36730385,2	K562	blood:
38	chr11:36804091..36807084-chr11:36812047..36814004,2	MCF-7	breast:
39	chr11:36768357..36769346-chr11:36839767..36840522,2	MCF-7	breast:
40	chr11:36760152..36763496-chr11:36764810..36767505,3	K562	blood:
41	chr11:36724082..36725333-chr11:36765913..36767362,6	MCF-7	breast:
42	chr11:36531321..36532055-chr11:36768370..36769234,2	K562	blood:
43	chr11:36772768..36775100-chr11:36777744..36780242,2	K562	blood:
44	chr11:36784007..36786954-chr11:36790139..36792736,2	MCF-7	breast:
45	chr11:36805719..36807919-chr11:36809523..36812018,2	K562	blood:
46	chr11:36805719..36807919-chr11:36809523..36812018,2	K562	blood:
47	chr11:36724313..36724958-chr11:36765739..36766377,3	K562	blood:
48	chr11:36804091..36807084-chr11:36812047..36814004,2	MCF-7	breast:
49	chr11:36773100..36776427-chr11:36776879..36779629,3	K562	blood:
50	chr11:36778255..36778775-chr8:120867803..120868704,2	HCT-116	colon:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C11orf74-9	chr11:36719309-36719417	NONHSAT018837
2	lnc-C11orf74-9	chr11:36717867-36718640	NONHSAT018837

No data

Variant related genes	Relation type
ENSG00000254498	TF binding region
ENSG00000254498	CpG island
ENSG00000136982	chromatin interactions
ENSG00000175104	chromatin interactions
ENSG00000166349	chromatin interactions

Extended variants
information (count: 3808 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:3808 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545112566	chr11:36711643-36711644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553066473	chr11:36711655-36711656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs60804169	chr11:36711672-36711673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185314026	chr11:36711702-36711703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12276154	chr11:36711714-36711715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542767141	chr11:36711718-36711719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs373990706	chr11:36711720-36711721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530250690	chr11:36711724-36711725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs377490741	chr11:36711727-36711728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570990194	chr11:36711728-36711729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs5791114	chr11:36711729-36711730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs375383326	chr11:36711808-36711809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549809835	chr11:36711810-36711811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs569693687	chr11:36711830-36711831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs1039205	chr11:36711834-36711835	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs558299986	chr11:36711839-36711840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs534833653	chr11:36711860-36711861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534881562	chr11:36711906-36711907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554926496	chr11:36711925-36711926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115141113	chr11:36711965-36711966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543651583	chr11:36711990-36711991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs145644059	chr11:36712000-36712001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs114158618	chr11:36712049-36712050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545363321	chr11:36712052-36712053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs116319482	chr11:36712101-36712102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572310156	chr11:36712118-36712119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs77903151	chr11:36712139-36712140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563041857	chr11:36712141-36712142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531709947	chr11:36712142-36712143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs397849493	chr11:36712153-36712154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs7116141	chr11:36712172-36712173	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs145189390	chr11:36712191-36712192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190155660	chr11:36712238-36712239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs561248000	chr11:36712337-36712338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs571271147	chr11:36712347-36712348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs77000213	chr11:36712357-36712358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs34836113	chr11:36712359-36712360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs143612856	chr11:36712387-36712388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs149178164	chr11:36712398-36712399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs143279463	chr11:36712400-36712401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181441689	chr11:36712440-36712441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs144057524	chr11:36712446-36712447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184052351	chr11:36712498-36712499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532145512	chr11:36712510-36712511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs552266145	chr11:36712526-36712527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs565651107	chr11:36712550-36712551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs4316481	chr11:36712583-36712584	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs548465047	chr11:36712606-36712607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188391366	chr11:36712616-36712617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs568403335	chr11:36712707-36712708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
WAGR syndrome	19222835	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Non-small cell lung cancer	21829676	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:398 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:36707800-36713600	Weak transcription	Fetal Lung	lung
2	chr11:36708000-36715200	Enhancers	Dnd41	blood
3	chr11:36710600-36713200	Weak transcription	Fetal Stomach	stomach
4	chr11:36711400-36718000	Enhancers	Thymus	Thymus
5	chr11:36711400-36719600	Enhancers	Fetal Thymus	thymus
6	chr11:36713200-36714400	Enhancers	Fetal Stomach	stomach
7	chr11:36713600-36718400	Enhancers	Fetal Lung	lung
8	chr11:36714000-36714600	Enhancers	Fetal Kidney	kidney
9	chr11:36714400-36714800	Weak transcription	Fetal Stomach	stomach
10	chr11:36714600-36715000	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr11:36714800-36715000	Enhancers	Fetal Stomach	stomach
12	chr11:36715000-36716200	Weak transcription	Fetal Stomach	stomach
13	chr11:36715200-36715400	Bivalent Enhancer	Primary T cells from cord blood	blood
14	chr11:36715200-36716000	Flanking Active TSS	Dnd41	blood
15	chr11:36716000-36720400	Enhancers	Dnd41	blood
16	chr11:36716200-36718400	Enhancers	Fetal Stomach	stomach
17	chr11:36718000-36718400	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr11:36718000-36718400	Bivalent Enhancer	Thymus	Thymus
19	chr11:36718400-36719600	Enhancers	Thymus	Thymus
20	chr11:36718400-36721600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr11:36718400-36729000	Weak transcription	Fetal Stomach	stomach
22	chr11:36719600-36720400	Weak transcription	Fetal Thymus	thymus
23	chr11:36719600-36720600	Weak transcription	Thymus	Thymus
24	chr11:36720400-36722200	Flanking Active TSS	Dnd41	blood
25	chr11:36720400-36725400	Enhancers	Fetal Thymus	thymus
26	chr11:36720600-36721000	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr11:36720600-36721200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr11:36720600-36721200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr11:36720600-36721200	Enhancers	HMEC	breast
30	chr11:36720600-36721200	Enhancers	NHEK	skin
31	chr11:36720600-36724200	Enhancers	Thymus	Thymus
32	chr11:36720800-36721000	Enhancers	Fetal Intestine Small	intestine
33	chr11:36720800-36721200	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr11:36720800-36721200	Enhancers	Duodenum Mucosa	Duodenum
35	chr11:36721000-36721800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr11:36721000-36723000	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr11:36721600-36721800	Enhancers	Fetal Kidney	kidney
38	chr11:36721600-36722200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr11:36721600-36722800	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr11:36721800-36722800	Enhancers	H1 Cell Line	embryonic stem cell
41	chr11:36721800-36722800	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr11:36721800-36724000	Weak transcription	Fetal Kidney	kidney
43	chr11:36721800-36724400	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr11:36721800-36725200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr11:36722000-36722200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr11:36722000-36722800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr11:36722000-36723000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr11:36722000-36723000	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr11:36722200-36723000	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr11:36722200-36724000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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