Variant report

Variant	nsv897063
Chromosome Location	chr11:23723766-23940407
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	ARID3A	chr11:23808741-23808892	HepG2	liver:	n/a	n/a
2	BACH1	chr11:23878232-23878445	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr11:23895497-23895518	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr11:23924606-23925059	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr11:23791141-23791164	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr11:23878299-23878513	A549	lung:	n/a	chr11:23878381-23878392
7	CEBPB	chr11:23723663-23723849	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr11:23921929-23922263	A549	lung:	n/a	chr11:23922112-23922125 chr11:23922112-23922123
9	CEBPB	chr11:23794359-23794613	HepG2	liver:	n/a	chr11:23794482-23794495 chr11:23794482-23794493
10	CEBPB	chr11:23924606-23925075	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr11:23921978-23922264	HepG2	liver:	n/a	chr11:23922112-23922125 chr11:23922112-23922123
12	CEBPB	chr11:23921942-23922265	IMR90	lung:	n/a	chr11:23922112-23922125 chr11:23922112-23922123
13	CEBPB	chr11:23918963-23919709	IMR90	lung:	n/a	chr11:23919170-23919181
14	CEBPB	chr11:23887287-23887522	MCF-7	breast:	n/a	n/a
15	CEBPB	chr11:23891315-23891609	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr11:23883174-23883477	IMR90	lung:	n/a	chr11:23883330-23883341 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883329-23883340 chr11:23883331-23883340
17	CEBPB	chr11:23844250-23844479	IMR90	lung:	n/a	chr11:23844394-23844405
18	CEBPB	chr11:23829094-23829349	A549	lung:	n/a	chr11:23829233-23829244
19	CEBPB	chr11:23887264-23887584	MCF-7	breast:	n/a	n/a
20	CEBPB	chr11:23747309-23747636	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr11:23878304-23878551	ECC-1	luminal epithelium:	n/a	chr11:23878381-23878392
22	CEBPB	chr11:23883286-23883491	K562	blood:	n/a	chr11:23883330-23883341 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883329-23883340 chr11:23883331-23883340
23	CEBPB	chr11:23777380-23777595	HepG2	liver:	n/a	n/a
24	CEBPB	chr11:23924608-23925038	A549	lung:	n/a	n/a
25	CEBPB	chr11:23749404-23749739	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr11:23829111-23829319	K562	blood:	n/a	chr11:23829233-23829244
27	CEBPB	chr11:23777366-23777662	IMR90	lung:	n/a	n/a
28	CEBPB	chr11:23829064-23829390	IMR90	lung:	n/a	chr11:23829233-23829244
29	CEBPB	chr11:23878214-23878526	MCF-7	breast:	n/a	chr11:23878381-23878392
30	CEBPB	chr11:23876059-23876251	IMR90	lung:	n/a	n/a
31	CEBPB	chr11:23808790-23808947	HepG2	liver:	n/a	chr11:23808906-23808917
32	CEBPB	chr11:23878204-23878582	Hela-S3	cervix:	n/a	chr11:23878381-23878392
33	CEBPB	chr11:23883263-23883345	H1-hESC	embryonic stem cell:	n/a	chr11:23883330-23883341 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883329-23883340 chr11:23883331-23883340
34	CEBPB	chr11:23883188-23883494	HepG2	liver:	n/a	chr11:23883330-23883341 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883329-23883340 chr11:23883331-23883340
35	CEBPB	chr11:23876110-23876208	HepG2	liver:	n/a	n/a
36	CEBPB	chr11:23891244-23891591	HepG2	liver:	n/a	n/a
37	CEBPB	chr11:23883192-23883491	A549	lung:	n/a	chr11:23883330-23883341 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883329-23883340 chr11:23883331-23883340
38	CEBPB	chr11:23878241-23878611	A549	lung:	n/a	chr11:23878381-23878392
39	CEBPB	chr11:23747390-23747532	A549	lung:	n/a	n/a
40	CEBPB	chr11:23829075-23829384	HepG2	liver:	n/a	chr11:23829233-23829244
41	CEBPB	chr11:23891244-23891619	IMR90	lung:	n/a	n/a
42	CEBPB	chr11:23820766-23821130	IMR90	lung:	n/a	chr11:23821104-23821117
43	CEBPB	chr11:23878236-23878516	MCF-7	breast:	n/a	chr11:23878381-23878392
44	CEBPB	chr11:23891235-23891626	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr11:23878199-23878609	IMR90	lung:	n/a	chr11:23878381-23878392
46	CEBPB	chr11:23878225-23878534	HepG2	liver:	n/a	chr11:23878381-23878392
47	CEBPB	chr11:23844303-23844514	HepG2	liver:	n/a	chr11:23844394-23844405
48	CEBPB	chr11:23878231-23878550	A549	lung:	n/a	chr11:23878381-23878392
49	CEBPB	chr11:23723649-23723934	HepG2	liver:	n/a	n/a
50	CEBPB	chr11:23820809-23821124	HepG2	liver:	n/a	chr11:23821104-23821117

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:23752469-23752519	GM12891	blood:	n/a
2	chr11:23752469-23752519	GM12891	blood:	n/a
3	chr11:23752138-23752188	AG04450	lung:	fetal
4	chr11:23752469-23752519	NT2-D1	testis:	n/a
5	chr11:23811425-23811475	NB4	blood:	n/a
6	chr11:23754485-23754535	HCPEpiC	choroid plexus:	n/a
7	chr11:23752001-23752051	HPAEpiC	pulmonary alveolar:	n/a
8	chr11:23751628-23751678	GM19239	blood:	n/a
9	chr11:23752360-23752410	AG10803	skin:	n/a
10	chr11:23895772-23895822	NT2-D1	testis:	n/a
11	chr11:23752469-23752519	GM06990	blood:	n/a
12	chr11:23752138-23752188	HRPEpiC	eye:	n/a
13	chr11:23752222-23752272	AG09319	gingival:	n/a
14	chr11:23811425-23811475	U87	brain:	n/a
15	chr11:23754485-23754535	HEEpiC	esophagus:	n/a
16	chr11:23919652-23919702	AG04450	lung:	fetal
17	chr11:23811425-23811475	ProgFib	skin:	n/a
18	chr11:23751628-23751678	Hepatocyte	liver:	n/a
19	chr11:23752138-23752188	HNPCEpiC	eye:	n/a
20	chr11:23752469-23752519	HCM	heart:	n/a
21	chr11:23919652-23919702	GM19239	blood:	n/a
22	chr11:23895772-23895822	AoSMC	blood vessel:	n/a
23	chr11:23895772-23895822	ovcar-3	ovarian:	n/a
24	chr11:23752138-23752188	MCF-7	breast:	n/a
25	chr11:23811425-23811475	HRPEpiC	eye:	n/a
26	chr11:23752001-23752051	U87	brain:	n/a
27	chr11:23752360-23752410	HIPEpiC	eye:	n/a
28	chr11:23895772-23895822	ProgFib	skin:	n/a
29	chr11:23752001-23752051	HRCEpiC	kidney:	n/a
30	chr11:23752360-23752410	HRCEpiC	kidney:	n/a
31	chr11:23752001-23752051	HCF	heart:	n/a
32	chr11:23752360-23752410	SK-N-MC	brain:	n/a
33	chr11:23752001-23752051	PFSK-1	brain:	n/a
34	chr11:23752469-23752519	HRPEpiC	eye:	n/a
35	chr11:23752222-23752272	HIPEpiC	eye:	n/a
36	chr11:23752001-23752051	HIPEpiC	eye:	n/a
37	chr11:23919652-23919702	GM12892	blood:	n/a
38	chr11:23895772-23895822	Caco-2	colon:	n/a
39	chr11:23754485-23754535	GM19239	blood:	n/a
40	chr11:23895772-23895822	HRE	kidney:	n/a
41	chr11:23752138-23752188	HAEpiC	amniotic membrane:	n/a
42	chr11:23752469-23752519	AG09319	gingival:	n/a
43	chr11:23754485-23754535	NHDF-neo	bronchial:	n/a
44	chr11:23751628-23751678	NH-A	brain:	n/a
45	chr11:23926945-23926995	AG04449	skin:	fetal
46	chr11:23752001-23752051	SK-N-SH	brain:	n/a
47	chr11:23926945-23926995	H1-hESC	embryonic stem cell:	embryo
48	chr11:23751628-23751678	NHBE	bronchial:	n/a
49	chr11:23752469-23752519	HCPEpiC	choroid plexus:	n/a
50	chr11:23926945-23926995	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:23712261..23714812-chr11:23726962..23729358,2	K562	blood:
2	chr11:23798376..23799116-chr5:32449587..32450235,2	MCF-7	breast:
3	chr11:23745761..23746467-chr2:67682721..67683342,2	MCF-7	breast:
4	chr11:23822728..23824994-chr11:23830826..23833587,2	K562	blood:
5	chr11:23766902..23769192-chr6:80655556..80658439,2	MCF-7	breast:
6	chr11:23822728..23824994-chr11:23830826..23833587,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-17A1.2.1-5	chr11:23817463-23817487	NONHSAT018430
2	lnc-RP11-17A1.2.1-2	chr11:23789323-23789362	XLOC_009394
3	lnc-RP11-17A1.2.1-6	chr11:23877391-23877541	NONHSAT018433
4	lnc-RP11-17A1.2.1-2	chr11:23782876-23783176	ENSG00000254861
5	lnc-LUZP2-1	chr11:23818254-23818516	ENSG00000255193
6	lnc-LUZP2-3	chr11:23908634-23908905	NONHSAT018434
7	lnc-LUZP2-1	chr11:23753146-23753224	NONHSAT018426
8	lnc-RP11-17A1.2.1-2	chr11:23829736-23829778	XLOC_009395
9	lnc-RP11-17A1.2.1-6	chr11:23874839-23875216	NONHSAT018433
10	lnc-LUZP2-1	chr11:23756818-23757022	NONHSAT018426
11	lnc-RP11-17A1.2.1-2	chr11:23802334-23802418	ENSG00000254861
12	lnc-LUZP2-1	chr11:23758946-23760526	NONHSAT018426
13	lnc-LUZP2-1	chr11:23751855-23752432	NONHSAT018426
14	lnc-LUZP2-3	chr11:23911055-23911129	NONHSAT018434
15	lnc-RP11-17A1.2.1-2	chr11:23826000-23826222	XLOC_009395
16	lnc-LUZP2-1	chr11:23816369-23816430	ENSG00000255193
17	lnc-RP11-17A1.2.1-5	chr11:23818256-23819005	NONHSAT018430
18	lnc-RP11-17A1.2.1-2	chr11:23826025-23826144	ENSG00000254861
19	lnc-RP11-17A1.2.1-2	chr11:23782899-23783176	XLOC_009394
20	lnc-LUZP2-1	chr11:23753146-23753204	ENSG00000255193
21	lnc-LUZP2-1	chr11:23752134-23752432	ENSG00000255193

Variant related genes	Relation type
ENSG00000255193	TF binding region
RNU6-783P	TF binding region
ENSG00000254861	TF binding region
ENSG00000255193	CpG island
RNU6-783P	CpG island
ENSG00000254861	CpG island
ENSG00000118402	chromatin interactions

Extended variants
information (count: 5213 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:5213 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4922665	chr11:23723766-23723767	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs6483980	chr11:23723781-23723782	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs539476036	chr11:23723833-23723834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116575982	chr11:23723850-23723851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs539634915	chr11:23723868-23723869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs180912811	chr11:23723888-23723889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs10767108	chr11:23723891-23723892	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs555732391	chr11:23723894-23723895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs12419260	chr11:23723985-23723986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs11027453	chr11:23730227-23730228	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs192679201	chr11:23730284-23730285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541407509	chr11:23730382-23730383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558407697	chr11:23730416-23730417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116701235	chr11:23730436-23730437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570492277	chr11:23730470-23730471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544004841	chr11:23730551-23730552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563376411	chr11:23730590-23730591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528957467	chr11:23730592-23730593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs137967652	chr11:23730615-23730616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185070032	chr11:23730627-23730628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs559133684	chr11:23730637-23730638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528069479	chr11:23730726-23730727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs576132854	chr11:23732400-23732401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs7126806	chr11:23732511-23732512	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs78761479	chr11:23732538-23732539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573349263	chr11:23732539-23732540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185837044	chr11:23732550-23732551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192085202	chr11:23732563-23732564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527582725	chr11:23732570-23732571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10767111	chr11:23732593-23732594	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs564085660	chr11:23732598-23732599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543771418	chr11:23732621-23732622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs368692620	chr11:23732640-23732641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373706519	chr11:23732646-23732647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs139850521	chr11:23732651-23732652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574634711	chr11:23732652-23732653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs116622762	chr11:23732701-23732702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560340586	chr11:23732705-23732706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375925832	chr11:23732708-23732709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141903117	chr11:23732710-23732711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111386539	chr11:23732740-23732741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531302433	chr11:23732780-23732781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376825314	chr11:23732784-23732785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs77237866	chr11:23732799-23732800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182906142	chr11:23732802-23732803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs567971522	chr11:23732811-23732812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7933415	chr11:23732826-23732827	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs186699541	chr11:23732828-23732829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190633503	chr11:23732847-23732848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139151647	chr11:23732848-23732849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Renal cell carcinoma	18194544	CNVD
Myelofibrosis	22110671	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Autism	22102821	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:23723600-23724000	Enhancers	Dnd41	blood
2	chr11:23730200-23730600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr11:23730400-23730800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:23732400-23733600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr11:23733200-23733600	Enhancers	Dnd41	blood
6	chr11:23733600-23733800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr11:23733600-23733800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr11:23733600-23734000	Enhancers	H1 Cell Line	embryonic stem cell
9	chr11:23733600-23734000	Flanking Active TSS	Dnd41	blood
10	chr11:23734000-23736000	Active TSS	Dnd41	blood
11	chr11:23738000-23738400	Weak transcription	Dnd41	blood
12	chr11:23741400-23742000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
13	chr11:23742000-23754600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr11:23745400-23745600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr11:23745400-23745600	Enhancers	NH-A	brain
16	chr11:23745600-23748600	Weak transcription	NH-A	brain
17	chr11:23746200-23749000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr11:23746800-23747400	Enhancers	HSMMtube	muscle
19	chr11:23746800-23750200	Enhancers	HSMM	muscle
20	chr11:23747000-23747200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr11:23747000-23747400	Enhancers	Muscle Satellite Cultured Cells	--
22	chr11:23747000-23747400	Enhancers	Osteobl	bone
23	chr11:23747000-23748400	Enhancers	Placenta Amnion	Placenta Amnion
24	chr11:23747400-23747600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr11:23747400-23748200	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr11:23747400-23749400	Weak transcription	HSMMtube	muscle
27	chr11:23747600-23748600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr11:23748200-23748400	Enhancers	Muscle Satellite Cultured Cells	--
29	chr11:23748200-23750800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr11:23748400-23749000	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr11:23748600-23749400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr11:23748600-23750000	Enhancers	NH-A	brain
33	chr11:23749000-23749200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr11:23749000-23750000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr11:23749000-23750000	Enhancers	Muscle Satellite Cultured Cells	--
36	chr11:23749000-23750000	Enhancers	Hela-S3	cervix
37	chr11:23749200-23753200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr11:23749400-23749800	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr11:23749400-23749800	Enhancers	HSMMtube	muscle
40	chr11:23749400-23751000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr11:23749600-23750000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:23750000-23750600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr11:23750000-23750800	Weak transcription	NH-A	brain
44	chr11:23750200-23750600	Weak transcription	HSMM	muscle
45	chr11:23750600-23751000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr11:23750600-23751000	Enhancers	HSMM	muscle
47	chr11:23750800-23751000	Enhancers	NH-A	brain
48	chr11:23750800-23751200	Enhancers	Fetal Kidney	kidney
49	chr11:23751000-23752600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr11:23751000-23753200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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