Variant report

Variant	esv3508599
Chromosome Location	chr11:23744425-23768884
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	CEBPB	chr11:23749404-23749739	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr11:23747309-23747636	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr11:23747390-23747532	A549	lung:	n/a	n/a
4	CTCF	chr11:23752440-23752590	GM12865	blood:	n/a	chr11:23752498-23752516 chr11:23752501-23752510 chr11:23752500-23752521
5	CTCF	chr11:23763049-23763156	Kidney_OC	kidney:	n/a	n/a
6	CTCF	chr11:23754060-23754210	HepG2	liver:	n/a	n/a
7	EP300	chr11:23749413-23749742	Hela-S3	cervix:	n/a	chr11:23749583-23749592 chr11:23749582-23749591 chr11:23749685-23749699
8	EP300	chr11:23747401-23747596	Hela-S3	cervix:	n/a	n/a
9	EP300	chr11:23749392-23749880	ECC-1	luminal epithelium:	n/a	chr11:23749759-23749769 chr11:23749583-23749592 chr11:23749582-23749591 chr11:23749685-23749699
10	EP300	chr11:23768679-23768696	K562	blood:	n/a	n/a
11	FOS	chr11:23747356-23747565	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr11:23749438-23749690	MCF10A-Er-Src	breast:	n/a	chr11:23749583-23749592 chr11:23749581-23749593 chr11:23749582-23749592 chr11:23749584-23749591 chr11:23749583-23749591
13	FOS	chr11:23749395-23749675	HUVEC	blood vessel:	n/a	chr11:23749583-23749592 chr11:23749581-23749593 chr11:23749582-23749592 chr11:23749584-23749591 chr11:23749583-23749591
14	FOS	chr11:23749400-23749744	Hela-S3	cervix:	n/a	chr11:23749583-23749592 chr11:23749581-23749593 chr11:23749582-23749592 chr11:23749584-23749591 chr11:23749583-23749591 chr11:23749724-23749736
15	FOS	chr11:23749399-23749766	MCF10A-Er-Src	breast:	n/a	chr11:23749583-23749592 chr11:23749581-23749593 chr11:23749582-23749592 chr11:23749584-23749591 chr11:23749583-23749591 chr11:23749724-23749736
16	FOS	chr11:23747417-23747574	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr11:23745596-23745749	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr11:23749407-23749740	MCF10A-Er-Src	breast:	n/a	chr11:23749583-23749592 chr11:23749581-23749593 chr11:23749582-23749592 chr11:23749584-23749591 chr11:23749583-23749591 chr11:23749724-23749736
19	FOS	chr11:23747398-23747569	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr11:23749403-23749756	MCF10A-Er-Src	breast:	n/a	chr11:23749583-23749592 chr11:23749581-23749593 chr11:23749582-23749592 chr11:23749584-23749591 chr11:23749583-23749591 chr11:23749724-23749736
21	FOS	chr11:23745545-23745831	MCF10A-Er-Src	breast:	n/a	n/a
22	FOXA1	chr11:23751774-23752080	T-47D	breast:	n/a	n/a
23	FOXA1	chr11:23751725-23752104	T-47D	breast:	n/a	n/a
24	GATA3	chr11:23763967-23764092	SH-SY5Y	brain:	n/a	n/a
25	JUN	chr11:23749399-23749756	Hela-S3	cervix:	n/a	chr11:23749583-23749592 chr11:23749581-23749593 chr11:23749582-23749592 chr11:23749584-23749591 chr11:23749583-23749591 chr11:23749724-23749736
26	JUND	chr11:23749502-23749747	H1-hESC	embryonic stem cell:	n/a	chr11:23749583-23749592 chr11:23749581-23749593 chr11:23749582-23749592 chr11:23749584-23749591 chr11:23749583-23749591 chr11:23749724-23749736
27	JUND	chr11:23749391-23749765	Hela-S3	cervix:	n/a	chr11:23749583-23749592 chr11:23749581-23749593 chr11:23749582-23749592 chr11:23749584-23749591 chr11:23749583-23749591 chr11:23749724-23749736
28	MAFF	chr11:23753643-23753863	HepG2	liver:	n/a	n/a
29	MAFK	chr11:23753618-23753993	IMR90	lung:	n/a	chr11:23753784-23753799
30	MAFK	chr11:23746415-23746590	HepG2	liver:	n/a	n/a
31	MAFK	chr11:23753723-23753923	HepG2	liver:	n/a	chr11:23753784-23753799
32	MYC	chr11:23747476-23747691	MCF10A-Er-Src	breast:	n/a	n/a
33	NFE2	chr11:23763908-23763921	GM12878	blood:	n/a	n/a
34	NFYB	chr11:23748952-23749220	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr11:23764685-23764703	MCF10A-Er-Src	breast:	n/a	n/a
36	POLR2A	chr11:23759963-23760117	MCF10A-Er-Src	breast:	n/a	n/a
37	POLR2A	chr11:23749557-23749577	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr11:23753832-23753973	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr11:23758065-23758153	MCF10A-Er-Src	breast:	n/a	n/a
40	RAD21	chr11:23754002-23754255	HepG2	liver:	n/a	n/a
41	RAD21	chr11:23749405-23749731	Hela-S3	cervix:	n/a	n/a
42	RAD21	chr11:23747462-23747585	A549	lung:	n/a	n/a
43	RCOR1	chr11:23749398-23749740	Hela-S3	cervix:	n/a	n/a
44	RFX5	chr11:23749401-23749882	Hela-S3	cervix:	n/a	n/a
45	SPI1	chr11:23745394-23745591	GM12891	blood:	n/a	n/a
46	STAT3	chr11:23761966-23762166	MCF10A-Er-Src	breast:	n/a	n/a
47	STAT3	chr11:23748385-23748613	MCF10A-Er-Src	breast:	n/a	n/a
48	STAT3	chr11:23749350-23749785	Hela-S3	cervix:	n/a	chr11:23749583-23749592 chr11:23749582-23749591
49	STAT3	chr11:23750406-23750423	MCF10A-Er-Src	breast:	n/a	n/a
50	TEAD4	chr11:23749326-23749789	ECC-1	luminal epithelium:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:23752469-23752519	HIPEpiC	eye:	n/a
2	chr11:23751628-23751678	GM12891	blood:	n/a
3	chr11:23752001-23752051	PrEC	prostate:	n/a
4	chr11:23752360-23752410	HRCEpiC	kidney:	n/a
5	chr11:23752222-23752272	AoSMC	blood vessel:	n/a
6	chr11:23752222-23752272	AG04449	skin:	fetal
7	chr11:23752001-23752051	HCM	heart:	n/a
8	chr11:23754485-23754535	ProgFib	skin:	n/a
9	chr11:23752469-23752519	HCM	heart:	n/a
10	chr11:23752469-23752519	HCT-116	colon:	n/a
11	chr11:23752222-23752272	GM06990	blood:	n/a
12	chr11:23752469-23752519	PFSK-1	brain:	n/a
13	chr11:23752360-23752410	GM06990	blood:	n/a
14	chr11:23752138-23752188	A549	lung:	n/a
15	chr11:23752138-23752188	HRE	kidney:	n/a
16	chr11:23754485-23754535	Hepatocyte	liver:	n/a
17	chr11:23752001-23752051	HNPCEpiC	eye:	n/a
18	chr11:23752360-23752410	HNPCEpiC	eye:	n/a
19	chr11:23752222-23752272	HCT-116	colon:	n/a
20	chr11:23751628-23751678	NT2-D1	testis:	n/a
21	chr11:23752222-23752272	NB4	blood:	n/a
22	chr11:23752222-23752272	AG09319	gingival:	n/a
23	chr11:23754485-23754535	AG09309	skin:	n/a
24	chr11:23754485-23754535	NH-A	brain:	n/a
25	chr11:23752222-23752272	HMEC	breast:	n/a
26	chr11:23752222-23752272	HIPEpiC	eye:	n/a
27	chr11:23752360-23752410	HCPEpiC	choroid plexus:	n/a
28	chr11:23752360-23752410	PrEC	prostate:	n/a
29	chr11:23752360-23752410	RPTEC	kidney:	n/a
30	chr11:23752001-23752051	HEK293	kidney:	embryo
31	chr11:23752360-23752410	NHBE	bronchial:	n/a
32	chr11:23752360-23752410	Caco-2	colon:	n/a
33	chr11:23754485-23754535	ovcar-3	ovarian:	n/a
34	chr11:23752138-23752188	PFSK-1	brain:	n/a
35	chr11:23752001-23752051	GM12892	blood:	n/a
36	chr11:23752469-23752519	MCF-7	breast:	n/a
37	chr11:23754485-23754535	RPTEC	kidney:	n/a
38	chr11:23751628-23751678	HCM	heart:	n/a
39	chr11:23754485-23754535	MCF-7	breast:	n/a
40	chr11:23752222-23752272	T-47D	breast:	n/a
41	chr11:23754485-23754535	BE2_C	brain:	n/a
42	chr11:23752222-23752272	SKMC	muscle:	n/a
43	chr11:23751628-23751678	HepG2	liver:	n/a
44	chr11:23752360-23752410	HepG2	liver:	n/a
45	chr11:23752138-23752188	IMR90	lung:	fetal
46	chr11:23752222-23752272	Hepatocyte	liver:	n/a
47	chr11:23752469-23752519	ECC-1	luminal epithelium:	n/a
48	chr11:23751628-23751678	Hela-S3	cervix:	n/a
49	chr11:23754485-23754535	GM06990	blood:	n/a
50	chr11:23752222-23752272	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:23766902..23769192-chr6:80655556..80658439,2	MCF-7	breast:
2	chr11:23745761..23746467-chr2:67682721..67683342,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LUZP2-1	chr11:23753146-23753224	NONHSAT018426
2	lnc-LUZP2-1	chr11:23751855-23752432	NONHSAT018426
3	lnc-LUZP2-1	chr11:23756818-23757022	NONHSAT018426
4	lnc-LUZP2-1	chr11:23752134-23752432	ENSG00000255193
5	lnc-LUZP2-1	chr11:23753146-23753204	ENSG00000255193
6	lnc-LUZP2-1	chr11:23758946-23760526	NONHSAT018426

Variant related genes	Relation type
ENSG00000255193	TF binding region
ENSG00000255193	CpG island
ENSG00000118402	chromatin interactions

Extended variants
information (count: 560 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:560 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148256822	chr11:23744566-23744567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs373413686	chr11:23744583-23744584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs71458907	chr11:23744584-23744585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs61874536	chr11:23744585-23744586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs199787948	chr11:23744586-23744587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs75427032	chr11:23744587-23744588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs111714148	chr11:23744593-23744594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs71041724	chr11:23744600-23744601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs199806832	chr11:23744601-23744602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4323863	chr11:23744603-23744604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374050009	chr11:23744605-23744606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368224300	chr11:23744607-23744608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371951955	chr11:23744609-23744610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs543157083	chr11:23744611-23744612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139448619	chr11:23744613-23744614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372948131	chr11:23744622-23744623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs79348155	chr11:23744631-23744632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs74584901	chr11:23744645-23744646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs202225902	chr11:23744648-23744649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs61874537	chr11:23744649-23744650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs61874538	chr11:23744651-23744652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200882056	chr11:23744653-23744654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs201848849	chr11:23744655-23744656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201173096	chr11:23744657-23744658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201894418	chr11:23744659-23744660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112630557	chr11:23744660-23744661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113173825	chr11:23744661-23744662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs67690426	chr11:23744662-23744663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562930758	chr11:23744678-23744679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs115660357	chr11:23744710-23744711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4274196	chr11:23744711-23744712	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs551235603	chr11:23744727-23744728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs73437833	chr11:23744740-23744741	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs530198612	chr11:23744744-23744745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546312370	chr11:23744809-23744810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566186107	chr11:23744827-23744828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549199060	chr11:23744892-23744893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538259282	chr11:23744960-23744961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551928200	chr11:23744982-23744983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75198714	chr11:23744996-23744997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537783519	chr11:23745102-23745103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554812199	chr11:23745138-23745139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs574703881	chr11:23745173-23745174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533924611	chr11:23745182-23745183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553513969	chr11:23745223-23745224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376262488	chr11:23745326-23745327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545479793	chr11:23745352-23745353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558707106	chr11:23745376-23745377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575580997	chr11:23745472-23745473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs144321676	chr11:23745482-23745483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:23742000-23754600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr11:23745400-23745600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr11:23745400-23745600	Enhancers	NH-A	brain
4	chr11:23745600-23748600	Weak transcription	NH-A	brain
5	chr11:23746200-23749000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr11:23746800-23747400	Enhancers	HSMMtube	muscle
7	chr11:23746800-23750200	Enhancers	HSMM	muscle
8	chr11:23747000-23747200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr11:23747000-23747400	Enhancers	Muscle Satellite Cultured Cells	--
10	chr11:23747000-23747400	Enhancers	Osteobl	bone
11	chr11:23747000-23748400	Enhancers	Placenta Amnion	Placenta Amnion
12	chr11:23747400-23747600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr11:23747400-23748200	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr11:23747400-23749400	Weak transcription	HSMMtube	muscle
15	chr11:23747600-23748600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr11:23748200-23748400	Enhancers	Muscle Satellite Cultured Cells	--
17	chr11:23748200-23750800	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr11:23748400-23749000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr11:23748600-23749400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr11:23748600-23750000	Enhancers	NH-A	brain
21	chr11:23749000-23749200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr11:23749000-23750000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr11:23749000-23750000	Enhancers	Muscle Satellite Cultured Cells	--
24	chr11:23749000-23750000	Enhancers	Hela-S3	cervix
25	chr11:23749200-23753200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr11:23749400-23749800	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr11:23749400-23749800	Enhancers	HSMMtube	muscle
28	chr11:23749400-23751000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr11:23749600-23750000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr11:23750000-23750600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr11:23750000-23750800	Weak transcription	NH-A	brain
32	chr11:23750200-23750600	Weak transcription	HSMM	muscle
33	chr11:23750600-23751000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr11:23750600-23751000	Enhancers	HSMM	muscle
35	chr11:23750800-23751000	Enhancers	NH-A	brain
36	chr11:23750800-23751200	Enhancers	Fetal Kidney	kidney
37	chr11:23751000-23752600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr11:23751000-23753200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr11:23751000-23753600	Weak transcription	NH-A	brain
40	chr11:23752000-23752200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr11:23752000-23753800	ZNF genes & repeats	Dnd41	blood
42	chr11:23752200-23754800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr11:23752800-23753600	Enhancers	Fetal Stomach	stomach
44	chr11:23753200-23754400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr11:23753200-23754400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr11:23753400-23754200	Enhancers	Fetal Intestine Large	intestine
47	chr11:23753400-23754200	Enhancers	Fetal Intestine Small	intestine
48	chr11:23753600-23753800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr11:23753600-23754000	Enhancers	HepG2	liver
50	chr11:23753600-23754200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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