Variant report

Variant	nsv949575
Chromosome Location	chr11:27005687-27233359
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2340)
CpG islands
(count:1285)
Chromatin interactive
region (count:60)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2340 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:27076369-27077106	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:27196470-27196721	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:27223146-27223932	K562	blood:	n/a	n/a
4	ARID3A	chr11:27223258-27223908	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:27231128-27231495	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:27231119-27231533	K562	blood:	n/a	n/a
7	ARID3A	chr11:27228793-27228803	K562	blood:	n/a	n/a
8	ARID3A	chr11:27046863-27047194	HepG2	liver:	n/a	n/a
9	ARID3A	chr11:27180369-27180629	HepG2	liver:	n/a	n/a
10	ATF1	chr11:27223031-27223468	K562	blood:	n/a	n/a
11	ATF1	chr11:27231138-27231527	K562	blood:	n/a	n/a
12	ATF2	chr11:27231055-27231481	GM12878	blood:	n/a	n/a
13	ATF3	chr11:27223124-27223791	A549	lung:	n/a	n/a
14	ATF3	chr11:27180266-27180705	K562	blood:	n/a	n/a
15	ATF3	chr11:27180379-27180595	K562	blood:	n/a	n/a
16	ATF3	chr11:27231115-27231574	K562	blood:	n/a	n/a
17	ATF3	chr11:27179905-27180741	A549	lung:	n/a	n/a
18	ATF3	chr11:27230975-27231596	A549	lung:	n/a	n/a
19	ATF3	chr11:27180331-27180589	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF3	chr11:27230945-27231544	A549	lung:	n/a	n/a
21	ATF3	chr11:27179915-27180632	A549	lung:	n/a	n/a
22	ATF3	chr11:27180365-27180557	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr11:27231415-27231480	K562	blood:	n/a	n/a
24	BATF	chr11:27231094-27231569	GM12878	blood:	n/a	n/a
25	BATF	chr11:27230352-27230602	GM12878	blood:	n/a	n/a
26	BATF	chr11:27180294-27180574	GM12878	blood:	n/a	n/a
27	BCL3	chr11:27230856-27231631	A549	lung:	n/a	n/a
28	BCL3	chr11:27223194-27223948	A549	lung:	n/a	n/a
29	BCL3	chr11:27226670-27227327	A549	lung:	n/a	n/a
30	BCL3	chr11:27204270-27204518	GM12878	blood:	n/a	n/a
31	BCL3	chr11:27230837-27231612	A549	lung:	n/a	n/a
32	BCL3	chr11:27226624-27227279	A549	lung:	n/a	n/a
33	BDP1	chr11:27180003-27180578	Hela-S3	cervix:	n/a	n/a
34	BHLHE40	chr11:27231242-27231386	GM12878	blood:	n/a	n/a
35	BHLHE40	chr11:27223103-27223970	K562	blood:	n/a	n/a
36	BHLHE40	chr11:27226242-27226243	K562	blood:	n/a	n/a
37	BHLHE40	chr11:27180438-27180713	GM12878	blood:	n/a	n/a
38	BHLHE40	chr11:27076685-27077064	HepG2	liver:	n/a	n/a
39	BHLHE40	chr11:27230953-27231523	K562	blood:	n/a	n/a
40	BRCA1	chr11:27140734-27140760	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr11:27223419-27223896	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr11:27180331-27180690	Hela-S3	cervix:	n/a	n/a
43	CBX3	chr11:27163163-27163370	K562	blood:	n/a	n/a
44	CBX3	chr11:27223068-27223510	K562	blood:	n/a	n/a
45	CBX3	chr11:27231050-27231533	K562	blood:	n/a	n/a
46	CBX3	chr11:27228645-27229083	K562	blood:	n/a	n/a
47	CCNT2	chr11:27231027-27231443	K562	blood:	n/a	n/a
48	CCNT2	chr11:27227724-27227925	K562	blood:	n/a	n/a
49	CCNT2	chr11:27228695-27228915	K562	blood:	n/a	n/a
50	CEBPB	chr11:27180303-27180665	Hela-S3	cervix:	n/a	n/a

(count:1285 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:27145585-27145635	NH-A	brain:	n/a
2	chr11:27016671-27016721	NB4	blood:	n/a
3	chr11:27097023-27097073	MCF10A-Er-Src	breast:	n/a
4	chr11:27015991-27016041	PFSK-1	brain:	n/a
5	chr11:27145585-27145635	NH-A	brain:	n/a
6	chr11:27016671-27016721	NB4	blood:	n/a
7	chr11:27097023-27097073	MCF10A-Er-Src	breast:	n/a
8	chr11:27015991-27016041	PFSK-1	brain:	n/a
9	chr11:27016671-27016721	LNCaP	prostate:	n/a
10	chr11:27061756-27061806	HCPEpiC	choroid plexus:	n/a
11	chr11:27017005-27017055	PFSK-1	brain:	n/a
12	chr11:27224020-27224070	GM12892	blood:	n/a
13	chr11:27105814-27105864	HCT-116	colon:	n/a
14	chr11:27015991-27016041	NHDF-neo	bronchial:	n/a
15	chr11:27160935-27160985	U87	brain:	n/a
16	chr11:27015872-27015922	T-47D	breast:	n/a
17	chr11:27105814-27105864	HAEpiC	amniotic membrane:	n/a
18	chr11:27160935-27160985	NHDF-neo	bronchial:	n/a
19	chr11:27015872-27015922	GM12878	blood:	n/a
20	chr11:27224020-27224070	Hepatocyte	liver:	n/a
21	chr11:27015813-27015863	HepG2	liver:	n/a
22	chr11:27015592-27015642	HEK293	kidney:	embryo
23	chr11:27062963-27063013	HAEpiC	amniotic membrane:	n/a
24	chr11:27015813-27015863	HRPEpiC	eye:	n/a
25	chr11:27016671-27016721	BJ	skin:	n/a
26	chr11:27015656-27015706	NT2-D1	testis:	n/a
27	chr11:27015519-27015569	AG09309	skin:	n/a
28	chr11:27160935-27160985	AG09309	skin:	n/a
29	chr11:27015592-27015642	Jurkat	blood:	n/a
30	chr11:27015991-27016041	A549	lung:	n/a
31	chr11:27015519-27015569	BE2_C	brain:	n/a
32	chr11:27016671-27016721	NHBE	bronchial:	n/a
33	chr11:27062416-27062466	NHDF-neo	bronchial:	n/a
34	chr11:27105814-27105864	HMEC	breast:	n/a
35	chr11:27226988-27227038	ovcar-3	ovarian:	n/a
36	chr11:27224020-27224070	HRCEpiC	kidney:	n/a
37	chr11:27015813-27015863	HNPCEpiC	eye:	n/a
38	chr11:27015872-27015922	AG10803	skin:	n/a
39	chr11:27062963-27063013	CMK	blood:	n/a
40	chr11:27015813-27015863	NHDF-neo	bronchial:	n/a
41	chr11:27015872-27015922	HIPEpiC	eye:	n/a
42	chr11:27224020-27224070	PANC-1	pancreas:	n/a
43	chr11:27061756-27061806	K562	blood:	n/a
44	chr11:27062416-27062466	AG10803	skin:	n/a
45	chr11:27062963-27063013	HRCEpiC	kidney:	n/a
46	chr11:27061899-27061949	PrEC	prostate:	n/a
47	chr11:27097023-27097073	MCF-7	breast:	n/a
48	chr11:27062963-27063013	IMR90	lung:	fetal
49	chr11:27015813-27015863	HCT-116	colon:	n/a
50	chr11:27160935-27160985	BJ	skin:	n/a

(count:60 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:27199374..27201790-chr11:27208479..27210287,2	K562	blood:
2	chr11:27226865..27228689-chr11:27238688..27241396,2	MCF-7	breast:
3	chr11:27217202..27219718-chr11:27226989..27229921,2	MCF-7	breast:
4	chr11:27205289..27206114-chr11:27232993..27233660,2	MCF-7	breast:
5	chr11:27205266..27206256-chr11:27507177..27508122,4	MCF-7	breast:
6	chr11:27015097..27016903-chr11:27033368..27035440,2	K562	blood:
7	chr11:27222741..27229054-chr11:27229384..27235549,8	K562	blood:
8	chr11:27226401..27228305-chr11:27239224..27240810,2	K562	blood:
9	chr11:26774919..26776345-chr11:27179975..27180962,4	MCF-7	breast:
10	chr11:27195294..27197746-chr11:27526620..27528329,2	MCF-7	breast:
11	chr11:27227128..27229012-chr11:27229843..27232341,2	K562	blood:
12	chr11:27222710..27225256-chr11:27227598..27230568,2	K562	blood:
13	chr11:27231561..27233849-chr11:27237662..27241564,3	K562	blood:
14	chr11:27204301..27206366-chr11:27223714..27225288,2	MCF-7	breast:
15	chr11:27223288..27224844-chr11:27234778..27236414,2	MCF-7	breast:
16	chr11:27212584..27215226-chr11:27218417..27220419,2	K562	blood:
17	chr11:27226003..27226803-chr11:27507005..27507695,2	K562	blood:
18	chr11:27217663..27219197-chr11:27221701..27223639,2	MCF-7	breast:
19	chr11:27222741..27229054-chr11:27229384..27235549,8	K562	blood:
20	chr11:26775214..26776083-chr11:27180054..27180898,5	MCF-7	breast:
21	chr11:27050228..27052948-chr11:27053328..27055109,2	MCF-7	breast:
22	chr11:27016139..27017650-chr11:27021439..27023753,2	K562	blood:
23	chr11:27217663..27219197-chr11:27221701..27223639,2	MCF-7	breast:
24	chr11:27205192..27206125-chr11:27317809..27318532,3	MCF-7	breast:
25	chr11:27215715..27217258-chr11:27219758..27222636,2	K562	blood:
26	chr11:27046527..27047233-chr8:129115547..129116417,2	MCF-7	breast:
27	chr11:27217202..27219718-chr11:27226989..27229921,2	MCF-7	breast:
28	chr11:26307690..26308295-chr11:27180273..27180978,2	K562	blood:
29	chr11:27205070..27206237-chr11:27507034..27508588,8	MCF-7	breast:
30	chr11:27206362..27207013-chr11:27317950..27318581,2	MCF-7	breast:
31	chr11:27204301..27206366-chr11:27223714..27225288,2	MCF-7	breast:
32	chr11:27199374..27201117-chr11:27208388..27209979,2	K562	blood:
33	chr11:26353203..26353841-chr11:27180057..27180963,2	K562	blood:
34	chr11:27205289..27206114-chr11:27232993..27233660,2	MCF-7	breast:
35	chr11:27231045..27234560-chr11:27492364..27494838,3	MCF-7	breast:
36	chr11:27199374..27201790-chr11:27208479..27210287,2	K562	blood:
37	chr11:27228075..27231004-chr11:27492695..27495157,2	MCF-7	breast:
38	chr11:27199376..27201905-chr11:27487180..27488680,2	MCF-7	breast:
39	chr11:27205188..27206173-chr11:27507158..27508421,10	K562	blood:
40	chr11:27222753..27224767-chr11:27527380..27529573,2	K562	blood:
41	chr11:27232539..27234716-chr11:27503664..27505854,2	K562	blood:
42	chr11:27173133..27174774-chr11:27180444..27183032,2	K562	blood:
43	chr11:27212584..27215226-chr11:27218417..27220419,2	K562	blood:
44	chr11:27227128..27229012-chr11:27229843..27232341,2	K562	blood:
45	chr11:27173133..27174774-chr11:27180444..27183032,2	K562	blood:
46	chr11:27050228..27052948-chr11:27053328..27055109,2	MCF-7	breast:
47	chr11:26775142..26776062-chr11:27146200..27147224,6	MCF-7	breast:
48	chr11:27230911..27232790-chr11:27234631..27237421,2	MCF-7	breast:
49	chr11:27231059..27233774-chr11:27527025..27529396,3	MCF-7	breast:
50	chr11:27016139..27017650-chr11:27021439..27023753,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC34-1	chr11:27172597-27172699	ENSG00000254560.1
2	lnc-CCDC34-1	chr11:27084530-27084607	ENSG00000254560.1
3	lnc-FIBIN-2	chr11:27148999-27149235	NONHSAT018479
4	lnc-CCDC34-1	chr11:27068733-27068859	ENSG00000254560.1
5	lnc-FIBIN-1	chr11:27062418-27062566	NONHSAT018464
6	lnc-FIBIN-1	chr11:27062763-27063025	NONHSAT018464
7	lnc-CCDC34-1	chr11:27172597-27172699	ENSG00000254560.1
8	lnc-CCDC34-1	chr11:27088039-27088209	ENSG00000254560.1
9	lnc-FIBIN-1	chr11:27067789-27067833	NONHSAT018464

No data

Variant related genes	Relation type
FIBIN	TF binding region
BBOX1	TF binding region
FIBIN	CpG island
BBOX1	CpG island
ENSG00000205213	chromatin interactions
ENSG00000148943	chromatin interactions
ENSG00000254862	chromatin interactions
ENSG00000245573	chromatin interactions
ENSG00000134343	chromatin interactions
ENSG00000254560	chromatin interactions
ENSG00000176971	chromatin interactions
ENSG00000242527	chromatin interactions

Extended variants
information (count: 8384 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:8384 , 50 per page) page: 1 2 3 4 5 6 7 ... 168

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11029765	chr11:27005687-27005688	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576384604	chr11:27005761-27005762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143704917	chr11:27005818-27005819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs146772452	chr11:27005829-27005830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201075514	chr11:27005875-27005876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs56216114	chr11:27005956-27005957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148934399	chr11:27006054-27006055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs559959688	chr11:27006055-27006056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs202015168	chr11:27006069-27006070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567324360	chr11:27006085-27006086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534950425	chr11:27006113-27006114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531224408	chr11:27006158-27006159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374465895	chr11:27006170-27006171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571257361	chr11:27006181-27006182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs112901792	chr11:27006207-27006208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532280918	chr11:27006219-27006220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554113082	chr11:27006282-27006283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142200999	chr11:27006319-27006320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs10835090	chr11:27006346-27006347	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs192882451	chr11:27006348-27006349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184612402	chr11:27006385-27006386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546269097	chr11:27006451-27006452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537056261	chr11:27006499-27006500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs151217875	chr11:27006514-27006515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs557980352	chr11:27006538-27006539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189549441	chr11:27006635-27006636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541161444	chr11:27006673-27006674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553529912	chr11:27006728-27006729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs576534322	chr11:27006750-27006751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545022375	chr11:27006751-27006752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534757278	chr11:27006772-27006773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs542481435	chr11:27006786-27006787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs180692148	chr11:27006846-27006847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs148252905	chr11:27006871-27006872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs186472449	chr11:27006909-27006910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs552995470	chr11:27006943-27006944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140418029	chr11:27007047-27007048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs147851486	chr11:27007087-27007088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs1445327	chr11:27007113-27007114	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs532091257	chr11:27007120-27007121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs547541034	chr11:27007136-27007137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566246445	chr11:27007141-27007142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs117879578	chr11:27007194-27007195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs548854484	chr11:27007260-27007261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs12362707	chr11:27007293-27007294	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs1838617	chr11:27007329-27007330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs558668368	chr11:27007353-27007354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs189438981	chr11:27007458-27007459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534767124	chr11:27007498-27007499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs138125177	chr11:27007502-27007503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
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
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
Congenital diaphragmatic hernia	21525063	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Neuroticism	17667963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
early-passage human iPS cells	21368824	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:1701 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:26998200-27008600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:27004800-27010400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr11:27005400-27005800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr11:27006000-27006200	Enhancers	Duodenum Smooth Muscle	Duodenum
5	chr11:27006200-27014800	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr11:27006400-27009400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr11:27006600-27008000	Enhancers	NHDF-Ad	bronchial
8	chr11:27007000-27007200	Enhancers	Rectal Smooth Muscle	rectum
9	chr11:27007000-27008200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr11:27007000-27009600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr11:27007200-27007800	Weak transcription	Rectal Smooth Muscle	rectum
12	chr11:27007200-27008000	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr11:27007200-27008000	Enhancers	Osteobl	bone
14	chr11:27007200-27010400	Enhancers	Fetal Lung	lung
15	chr11:27007400-27008000	Enhancers	Aorta	Aorta
16	chr11:27007800-27008000	Enhancers	Rectal Smooth Muscle	rectum
17	chr11:27008000-27012200	Weak transcription	NHDF-Ad	bronchial
18	chr11:27008000-27012800	Weak transcription	Aorta	Aorta
19	chr11:27008000-27013000	Weak transcription	Osteobl	bone
20	chr11:27008000-27013400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr11:27008000-27015400	Weak transcription	Rectal Smooth Muscle	rectum
22	chr11:27008200-27012800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr11:27008600-27010200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr11:27008800-27009600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr11:27008800-27009600	Enhancers	Muscle Satellite Cultured Cells	--
26	chr11:27008800-27010000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr11:27009400-27012800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr11:27009600-27012800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr11:27009600-27013000	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr11:27009600-27013200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr11:27010000-27013000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr11:27010200-27010600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr11:27010400-27010600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr11:27010400-27010600	Flanking Active TSS	Fetal Lung	lung
35	chr11:27010600-27010800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr11:27010600-27011200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr11:27010800-27013000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr11:27011000-27011800	Weak transcription	Fetal Lung	lung
39	chr11:27011200-27011400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr11:27011400-27015200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr11:27011800-27012000	Enhancers	Fetal Lung	lung
42	chr11:27012000-27012200	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr11:27012000-27012800	Weak transcription	Fetal Lung	lung
44	chr11:27012200-27012400	Enhancers	NHDF-Ad	bronchial
45	chr11:27012400-27012800	Weak transcription	NHDF-Ad	bronchial
46	chr11:27012600-27014400	Enhancers	Colon Smooth Muscle	Colon
47	chr11:27012800-27013200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr11:27012800-27013200	Enhancers	Aorta	Aorta
49	chr11:27012800-27013400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr11:27012800-27013600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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