Variant report

Variant	nsv832072
Chromosome Location	chr11:15226843-15392190
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1234)
CpG islands
(count:488)
Chromatin interactive
region (count:47)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1234 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:15279992-15280281	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:15235422-15235795	HepG2	liver:	n/a	n/a
3	ATF1	chr11:15321576-15321629	K562	blood:	n/a	n/a
4	ATF1	chr11:15331806-15331953	K562	blood:	n/a	n/a
5	ATF1	chr11:15269085-15269109	K562	blood:	n/a	n/a
6	BCL3	chr11:15315524-15315976	GM12878	blood:	n/a	n/a
7	BCL3	chr11:15315514-15315854	GM12878	blood:	n/a	n/a
8	BHLHE40	chr11:15349302-15349371	K562	blood:	n/a	n/a
9	BHLHE40	chr11:15230205-15230498	GM12878	blood:	n/a	n/a
10	BHLHE40	chr11:15230233-15230409	K562	blood:	n/a	n/a
11	BHLHE40	chr11:15329459-15329501	GM12878	blood:	n/a	n/a
12	BRCA1	chr11:15230212-15230410	HepG2	liver:	n/a	n/a
13	BRCA1	chr11:15349375-15349575	H1-hESC	embryonic stem cell:	n/a	n/a
14	CBX3	chr11:15288582-15288882	K562	blood:	n/a	n/a
15	CBX3	chr11:15288577-15288907	K562	blood:	n/a	n/a
16	CEBPB	chr11:15228208-15228656	HepG2	liver:	n/a	chr11:15228349-15228360 chr11:15228510-15228521 chr11:15228510-15228523 chr11:15228510-15228521
17	CEBPB	chr11:15349300-15349563	H1-hESC	embryonic stem cell:	n/a	chr11:15349445-15349453
18	CEBPB	chr11:15330878-15331178	HepG2	liver:	n/a	chr11:15331003-15331014 chr11:15331001-15331012 chr11:15331001-15331014 chr11:15331003-15331012
19	CEBPB	chr11:15286931-15287157	A549	lung:	n/a	chr11:15287025-15287036
20	CEBPB	chr11:15329288-15329525	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr11:15330837-15331183	IMR90	lung:	n/a	chr11:15331003-15331014 chr11:15331001-15331012 chr11:15331001-15331014 chr11:15331003-15331012
22	CEBPB	chr11:15242125-15242398	IMR90	lung:	n/a	n/a
23	CEBPB	chr11:15310032-15310190	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr11:15279929-15280241	MCF-7	breast:	n/a	n/a
25	CEBPB	chr11:15273687-15273997	K562	blood:	n/a	n/a
26	CEBPB	chr11:15234481-15234745	K562	blood:	n/a	chr11:15234606-15234615 chr11:15234604-15234615 chr11:15234605-15234616
27	CEBPB	chr11:15230212-15230502	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr11:15228226-15228541	A549	lung:	n/a	chr11:15228349-15228360 chr11:15228510-15228521 chr11:15228510-15228523 chr11:15228510-15228521
29	CEBPB	chr11:15340416-15340736	IMR90	lung:	n/a	n/a
30	CEBPB	chr11:15286878-15287172	IMR90	lung:	n/a	chr11:15287025-15287036
31	CEBPB	chr11:15242079-15242343	A549	lung:	n/a	n/a
32	CEBPB	chr11:15340436-15340732	A549	lung:	n/a	n/a
33	CEBPB	chr11:15228262-15228602	Hela-S3	cervix:	n/a	chr11:15228349-15228360 chr11:15228510-15228521 chr11:15228510-15228523 chr11:15228510-15228521
34	CEBPB	chr11:15349356-15349536	HepG2	liver:	n/a	chr11:15349445-15349453
35	CEBPB	chr11:15234438-15234765	HepG2	liver:	n/a	chr11:15234606-15234615 chr11:15234604-15234615 chr11:15234605-15234616
36	CEBPB	chr11:15228183-15228554	IMR90	lung:	n/a	chr11:15228349-15228360 chr11:15228510-15228521 chr11:15228510-15228523 chr11:15228510-15228521
37	CEBPB	chr11:15345854-15346112	HepG2	liver:	n/a	n/a
38	CEBPB	chr11:15286913-15287084	Hela-S3	cervix:	n/a	chr11:15287025-15287036
39	CEBPB	chr11:15286881-15287199	K562	blood:	n/a	chr11:15287025-15287036
40	CEBPB	chr11:15330869-15331160	A549	lung:	n/a	chr11:15331003-15331014 chr11:15331001-15331012 chr11:15331001-15331014 chr11:15331003-15331012
41	CEBPB	chr11:15273707-15273946	A549	lung:	n/a	n/a
42	CEBPB	chr11:15280010-15280305	HepG2	liver:	n/a	n/a
43	CEBPB	chr11:15286923-15287183	HepG2	liver:	n/a	chr11:15287025-15287036
44	CEBPB	chr11:15280042-15280209	HepG2	liver:	n/a	n/a
45	CEBPB	chr11:15340442-15340713	HepG2	liver:	n/a	n/a
46	CEBPB	chr11:15228218-15228526	K562	blood:	n/a	chr11:15228349-15228360 chr11:15228510-15228521 chr11:15228510-15228523 chr11:15228510-15228521
47	CEBPB	chr11:15340468-15340669	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr11:15349303-15349666	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr11:15230171-15230458	H1-hESC	embryonic stem cell:	n/a	chr11:15230210-15230217
50	CTBP2	chr11:15329156-15329578	H1-hESC	embryonic stem cell:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:15230314-15230364	AG04450	lung:	fetal
2	chr11:15350125-15350175	HRCEpiC	kidney:	n/a
3	chr11:15230314-15230364	ProgFib	skin:	n/a
4	chr11:15258312-15258362	MCF10A-Er-Src	breast:	n/a
5	chr11:15229502-15229552	T-47D	breast:	n/a
6	chr11:15329459-15329509	MCF-7	breast:	n/a
7	chr11:15329459-15329509	BJ	skin:	n/a
8	chr11:15363270-15363320	CMK	blood:	n/a
9	chr11:15363270-15363320	HPAEpiC	pulmonary alveolar:	n/a
10	chr11:15350125-15350175	HUVEC	blood vessel:	n/a
11	chr11:15229502-15229552	HRE	kidney:	n/a
12	chr11:15230314-15230364	ovcar-3	ovarian:	n/a
13	chr11:15258312-15258362	K562	blood:	n/a
14	chr11:15329459-15329509	HEK293	kidney:	embryo
15	chr11:15230314-15230364	PrEC	prostate:	n/a
16	chr11:15230314-15230364	SK-N-MC	brain:	n/a
17	chr11:15268469-15268519	SKMC	muscle:	n/a
18	chr11:15350125-15350175	Jurkat	blood:	n/a
19	chr11:15229502-15229552	HL-60	blood:	n/a
20	chr11:15363270-15363320	MCF-7	breast:	n/a
21	chr11:15363270-15363320	HCF	heart:	n/a
22	chr11:15268469-15268519	BE2_C	brain:	n/a
23	chr11:15279827-15279877	AG09309	skin:	n/a
24	chr11:15350125-15350175	ProgFib	skin:	n/a
25	chr11:15230314-15230364	AG09309	skin:	n/a
26	chr11:15279827-15279877	HepG2	liver:	n/a
27	chr11:15258312-15258362	HAEpiC	amniotic membrane:	n/a
28	chr11:15229502-15229552	U87	brain:	n/a
29	chr11:15350125-15350175	CMK	blood:	n/a
30	chr11:15350125-15350175	Caco-2	colon:	n/a
31	chr11:15279827-15279877	K562	blood:	n/a
32	chr11:15350125-15350175	GM12892	blood:	n/a
33	chr11:15329459-15329509	Hela-S3	cervix:	n/a
34	chr11:15230314-15230364	GM12878	blood:	n/a
35	chr11:15350125-15350175	AG09309	skin:	n/a
36	chr11:15350125-15350175	HEEpiC	esophagus:	n/a
37	chr11:15350125-15350175	LNCaP	prostate:	n/a
38	chr11:15279827-15279877	SAEC	small airway:	n/a
39	chr11:15350125-15350175	PFSK-1	brain:	n/a
40	chr11:15279827-15279877	ECC-1	luminal epithelium:	n/a
41	chr11:15230314-15230364	HCF	heart:	n/a
42	chr11:15329459-15329509	NH-A	brain:	n/a
43	chr11:15363270-15363320	Jurkat	blood:	n/a
44	chr11:15363270-15363320	RPTEC	kidney:	n/a
45	chr11:15350125-15350175	AG09319	gingival:	n/a
46	chr11:15363270-15363320	HIPEpiC	eye:	n/a
47	chr11:15268469-15268519	PANC-1	pancreas:	n/a
48	chr11:15279827-15279877	GM06990	blood:	n/a
49	chr11:15329459-15329509	NB4	blood:	n/a
50	chr11:15230314-15230364	NB4	blood:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:15296771..15299195-chr11:15299336..15301230,2	MCF-7	breast:
2	chr11:15349381..15349887-chr11:16009845..16010736,2	MCF-7	breast:
3	chr11:15362507..15364354-chr11:15365660..15367373,2	K562	blood:
4	chr11:15230303..15231896-chr11:15234367..15236672,2	K562	blood:
5	chr11:15122345..15123510-chr11:15229905..15230828,9	MCF-7	breast:
6	chr11:15321898..15323398-chr11:15324919..15326774,2	MCF-7	breast:
7	chr11:15321898..15323398-chr11:15324919..15326774,2	MCF-7	breast:
8	chr11:15236431..15237945-chr11:15241172..15243025,2	MCF-7	breast:
9	chr11:15238033..15238920-chr11:15246673..15247245,2	MCF-7	breast:
10	chr11:15122385..15123116-chr11:15238390..15238956,3	K562	blood:
11	chr11:15060394..15061162-chr11:15238309..15238839,2	MCF-7	breast:
12	chr11:15328820..15330429-chr11:15330814..15332523,2	K562	blood:
13	chr11:15230302..15230837-chr11:15238045..15239014,2	MCF-7	breast:
14	chr11:15279933..15280796-chr11:15636699..15637518,2	MCF-7	breast:
15	chr11:15280072..15281598-chr11:15284414..15286614,2	MCF-7	breast:
16	chr11:14929858..14930710-chr11:15230022..15230796,4	MCF-7	breast:
17	chr11:15121462..15122175-chr11:15230252..15230842,2	MCF-7	breast:
18	chr11:15337883..15340586-chr11:15346473..15348835,2	K562	blood:
19	chr11:15265846..15267612-chr11:15271655..15273612,2	K562	blood:
20	chr11:15230302..15230837-chr11:15238045..15239014,2	MCF-7	breast:
21	chr11:15362507..15364354-chr11:15365660..15367373,2	K562	blood:
22	chr11:14929842..14930739-chr11:15229981..15230831,5	K562	blood:
23	chr11:15280072..15281598-chr11:15284414..15286614,2	MCF-7	breast:
24	chr11:15122329..15123323-chr11:15229850..15230841,5	MCF-7	breast:
25	chr11:15303676..15305978-chr11:15318192..15319850,2	K562	blood:
26	chr11:15122346..15123401-chr11:15229849..15230871,9	K562	blood:
27	chr11:15238033..15238920-chr11:15246673..15247245,2	MCF-7	breast:
28	chr11:15265846..15267612-chr11:15271655..15273612,2	K562	blood:
29	chr11:15236431..15237945-chr11:15241172..15243025,2	MCF-7	breast:
30	chr11:15368518..15371257-chr11:15372733..15374518,2	MCF-7	breast:
31	chr11:15279933..15280768-chr11:15637018..15637550,2	MCF-7	breast:
32	chr11:15094886..15096748-chr11:15229663..15231358,2	MCF-7	breast:
33	chr11:15288180..15290335-chr11:15294752..15296796,2	K562	blood:
34	chr11:15230303..15231896-chr11:15234367..15236672,2	K562	blood:
35	chr11:15302123..15303920-chr11:15305908..15307725,2	K562	blood:
36	chr11:14991233..14992001-chr11:15230234..15230829,2	MCF-7	breast:
37	chr11:15288180..15290335-chr11:15294752..15296796,2	K562	blood:
38	chr11:15297897..15298552-chr11:16635311..16635851,2	MCF-7	breast:
39	chr11:15262063..15264369-chr11:15524628..15526995,2	K562	blood:
40	chr11:15302123..15303920-chr11:15305908..15307725,2	K562	blood:
41	chr11:15368518..15371257-chr11:15372733..15374518,2	MCF-7	breast:
42	chr11:15349014..15349930-chr11:15670842..15672081,7	MCF-7	breast:
43	chr11:15296771..15299195-chr11:15299336..15301230,2	MCF-7	breast:
44	chr11:15337883..15340586-chr11:15346473..15348835,2	K562	blood:
45	chr11:15303676..15305978-chr11:15318192..15319850,2	K562	blood:
46	chr11:15328820..15330429-chr11:15330814..15332523,2	K562	blood:
47	chr11:15122594..15123314-chr11:15279666..15280219,2	MCF-7	breast:

No data

Variant related genes	Relation type
INSC	TF binding region
INSC	CpG island
ENSG00000175868	chromatin interactions
ENSG00000110680	chromatin interactions

Extended variants
information (count: 5400 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:5400 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559501073	chr11:15226868-15226869	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs575391677	chr11:15226944-15226945	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543942103	chr11:15226945-15226946	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs116517147	chr11:15226998-15226999	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs115780150	chr11:15226999-15227000	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557441306	chr11:15227017-15227018	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs151146276	chr11:15227032-15227033	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs531450831	chr11:15227065-15227066	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549714846	chr11:15227105-15227106	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs141077975	chr11:15227120-15227121	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189299862	chr11:15227134-15227135	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs146960629	chr11:15227143-15227144	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs181054537	chr11:15227186-15227187	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116845195	chr11:15227200-15227201	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs187276094	chr11:15227210-15227211	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372135494	chr11:15227222-15227223	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs537095497	chr11:15227248-15227249	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577272991	chr11:15227261-15227262	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192071318	chr11:15227263-15227264	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs541380733	chr11:15227278-15227279	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs559971655	chr11:15227286-15227287	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577659257	chr11:15227323-15227324	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs142205752	chr11:15227332-15227333	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs183286090	chr11:15227378-15227379	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs75017516	chr11:15227418-15227419	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376183506	chr11:15227462-15227463	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs185744447	chr11:15227526-15227527	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111353050	chr11:15227540-15227541	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs369957107	chr11:15227560-15227561	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs529063740	chr11:15227635-15227636	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547409296	chr11:15227653-15227654	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190506041	chr11:15227706-15227707	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565970295	chr11:15227725-15227726	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539485681	chr11:15227786-15227787	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542457530	chr11:15227815-15227816	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569628450	chr11:15227816-15227817	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs113374393	chr11:15227855-15227856	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560063428	chr11:15227931-15227932	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs182388619	chr11:15227941-15227942	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555410026	chr11:15227946-15227947	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574177403	chr11:15227960-15227961	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs1945628	chr11:15227989-15227990	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs4316495	chr11:15227992-15227993	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs76922923	chr11:15228037-15228038	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577922499	chr11:15228049-15228050	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs4343008	chr11:15228054-15228055	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs138674394	chr11:15228093-15228094	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs575207262	chr11:15228104-15228105	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs1945629	chr11:15228188-15228189	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs561418286	chr11:15228194-15228195	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
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
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
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Myelofibrosis	22110671	CNVD
Cancer	24489367	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Neuroblastoma	19435921	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:15218600-15229400	Weak transcription	Gastric	stomach
2	chr11:15219200-15234600	Weak transcription	Fetal Intestine Small	intestine
3	chr11:15221600-15227600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr11:15222200-15244600	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr11:15222600-15230000	Weak transcription	Fetal Brain Male	brain
6	chr11:15226000-15227000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr11:15226800-15227200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr11:15226800-15227200	Weak transcription	Liver	Liver
9	chr11:15226800-15231600	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr11:15227000-15228400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr11:15227200-15227600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr11:15227200-15228800	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr11:15227200-15230800	Enhancers	Liver	Liver
14	chr11:15227600-15227800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr11:15227600-15230000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr11:15227800-15229000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr11:15228200-15230800	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr11:15228400-15228600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr11:15228400-15229200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr11:15228600-15229800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr11:15228800-15229800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr11:15229000-15229200	Enhancers	Fetal Muscle Leg	muscle
23	chr11:15229200-15230200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr11:15229600-15233000	Weak transcription	Right Atrium	heart
25	chr11:15229800-15230000	Enhancers	Fetal Muscle Leg	muscle
26	chr11:15229800-15230200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr11:15229800-15230200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
28	chr11:15229800-15231200	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr11:15230000-15230200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr11:15230000-15230400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
31	chr11:15230000-15230400	Enhancers	Colonic Mucosa	Colon
32	chr11:15230000-15230400	Enhancers	Fetal Brain Male	brain
33	chr11:15230200-15230400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
34	chr11:15230200-15231400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr11:15230800-15232200	Weak transcription	Primary neutrophils fromperipheralblood	blood
36	chr11:15231200-15246800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr11:15231400-15231600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr11:15231600-15232600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr11:15231600-15241000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr11:15231800-15232400	Enhancers	HSMMtube	muscle
41	chr11:15232200-15241800	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr11:15232400-15232600	Enhancers	Fetal Intestine Large	intestine
43	chr11:15232600-15234400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr11:15232800-15234800	Weak transcription	Fetal Intestine Large	intestine
45	chr11:15234400-15272000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr11:15234600-15235800	Enhancers	Fetal Intestine Small	intestine
47	chr11:15234800-15235000	Enhancers	Primary B cells from cord blood	blood
48	chr11:15234800-15235200	Enhancers	Duodenum Mucosa	Duodenum
49	chr11:15234800-15235400	Enhancers	Rectal Mucosa Donor 29	rectum
50	chr11:15234800-15235600	Enhancers	Fetal Intestine Large	intestine

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