Variant report

Variant	nsv897134
Chromosome Location	chr11:25592935-25674033
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:101)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:101 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr11:25630449-25630466	K562	blood:	n/a	n/a
2	BACH1	chr11:25623762-25623935	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr11:25654801-25655170	MCF-7	breast:	n/a	chr11:25654930-25654941
4	CEBPB	chr11:25654759-25654990	H1-hESC	embryonic stem cell:	n/a	chr11:25654930-25654941
5	CEBPB	chr11:25654767-25655104	IMR90	lung:	n/a	chr11:25654930-25654941
6	CEBPB	chr11:25654846-25655049	MCF-7	breast:	n/a	chr11:25654930-25654941
7	CEBPB	chr11:25654797-25655096	A549	lung:	n/a	chr11:25654930-25654941
8	CEBPB	chr11:25636635-25637011	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr11:25654764-25655080	HepG2	liver:	n/a	chr11:25654930-25654941
10	CEBPB	chr11:25607889-25608194	HepG2	liver:	n/a	n/a
11	CEBPB	chr11:25654755-25655103	Hela-S3	cervix:	n/a	chr11:25654930-25654941
12	CTCF	chr11:25623780-25623930	HPF	lung:	n/a	n/a
13	CTCF	chr11:25672614-25672668	GM13976	blood:	n/a	n/a
14	CTCF	chr11:25650075-25650115	GM10248	blood:	n/a	n/a
15	CTCF	chr11:25632967-25633016	LNCaP	prostate:	n/a	n/a
16	CTCF	chr11:25606896-25606899	GM20000	blood:	n/a	n/a
17	CTCF	chr11:25606859-25606882	GM20000	blood:	n/a	n/a
18	E2F4	chr11:25616132-25616392	MCF10A-Er-Src	breast:	n/a	n/a
19	EP300	chr11:25614816-25615134	SK-N-SH_RA	brain:	n/a	n/a
20	FOS	chr11:25618375-25618587	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr11:25609170-25609433	MCF10A-Er-Src	breast:	n/a	chr11:25609317-25609326 chr11:25609317-25609325 chr11:25609318-25609325 chr11:25609316-25609326
22	FOS	chr11:25618279-25618545	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr11:25609155-25609369	MCF10A-Er-Src	breast:	n/a	chr11:25609317-25609326 chr11:25609317-25609325 chr11:25609318-25609325 chr11:25609316-25609326
24	FOS	chr11:25618316-25618516	MCF10A-Er-Src	breast:	n/a	n/a
25	FOXA1	chr11:25646723-25647073	T-47D	breast:	n/a	chr11:25646955-25646970
26	FOXA1	chr11:25646701-25647094	T-47D	breast:	n/a	chr11:25646955-25646970
27	FOXA2	chr11:25670576-25671009	A549	lung:	n/a	n/a
28	FOXA2	chr11:25670762-25670975	A549	lung:	n/a	n/a
29	GATA2	chr11:25616883-25617244	SH-SY5Y	brain:	n/a	n/a
30	GATA2	chr11:25633662-25634223	SH-SY5Y	brain:	n/a	n/a
31	GATA3	chr11:25633758-25633881	SH-SY5Y	brain:	n/a	n/a
32	GATA3	chr11:25617089-25617252	SH-SY5Y	brain:	n/a	n/a
33	GATA3	chr11:25615099-25615162	SH-SY5Y	brain:	n/a	n/a
34	JUN	chr11:25623924-25623969	H1-hESC	embryonic stem cell:	n/a	n/a
35	JUN	chr11:25662228-25662238	H1-hESC	embryonic stem cell:	n/a	n/a
36	JUND	chr11:25618424-25618457	H1-hESC	embryonic stem cell:	n/a	n/a
37	JUND	chr11:25623841-25624041	H1-hESC	embryonic stem cell:	n/a	n/a
38	JUND	chr11:25654885-25655167	HepG2	liver:	n/a	chr11:25655028-25655037
39	MAFF	chr11:25607548-25607819	K562	blood:	n/a	chr11:25607677-25607695
40	MAFF	chr11:25625677-25625793	HepG2	liver:	n/a	n/a
41	MAFF	chr11:25607532-25607858	HepG2	liver:	n/a	chr11:25607677-25607695
42	MAFK	chr11:25664518-25664740	HepG2	liver:	n/a	n/a
43	MAFK	chr11:25607623-25607757	K562	blood:	n/a	n/a
44	MAFK	chr11:25625682-25625872	HepG2	liver:	n/a	chr11:25625699-25625710 chr11:25625688-25625705
45	MAFK	chr11:25607593-25607839	HepG2	liver:	n/a	n/a
46	MAFK	chr11:25607619-25607709	Hela-S3	cervix:	n/a	n/a
47	MAFK	chr11:25625602-25625874	HepG2	liver:	n/a	chr11:25625699-25625710 chr11:25625688-25625705
48	MAFK	chr11:25607531-25607866	HepG2	liver:	n/a	n/a
49	MAFK	chr11:25622010-25622185	HepG2	liver:	n/a	chr11:25622059-25622074
50	MAFK	chr11:25621890-25621907	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:25623877-25623927	T-47D	breast:	n/a
2	chr11:25623877-25623927	AoSMC	blood vessel:	n/a
3	chr11:25623877-25623927	ProgFib	skin:	n/a
4	chr11:25623877-25623927	HCPEpiC	choroid plexus:	n/a
5	chr11:25623877-25623927	HPAEpiC	pulmonary alveolar:	n/a
6	chr11:25623877-25623927	HepG2	liver:	n/a
7	chr11:25623877-25623927	H1-hESC	embryonic stem cell:	embryo
8	chr11:25623877-25623927	HNPCEpiC	eye:	n/a
9	chr11:25623877-25623927	NT2-D1	testis:	n/a
10	chr11:25623877-25623927	NH-A	brain:	n/a
11	chr11:25623877-25623927	ECC-1	luminal epithelium:	n/a
12	chr11:25623877-25623927	Hela-S3	cervix:	n/a
13	chr11:25623877-25623927	CMK	blood:	n/a
14	chr11:25623877-25623927	HUVEC	blood vessel:	n/a
15	chr11:25623877-25623927	Hepatocyte	liver:	n/a
16	chr11:25623877-25623927	RPTEC	kidney:	n/a
17	chr11:25623877-25623927	IMR90	lung:	fetal
18	chr11:25623877-25623927	SKMC	muscle:	n/a
19	chr11:25623877-25623927	AG09319	gingival:	n/a
20	chr11:25623877-25623927	AG04450	lung:	fetal
21	chr11:25623877-25623927	NHDF-neo	bronchial:	n/a
22	chr11:25623877-25623927	HL-60	blood:	n/a
23	chr11:25623877-25623927	ovcar-3	ovarian:	n/a
24	chr11:25623877-25623927	A549	lung:	n/a
25	chr11:25623877-25623927	NHBE	bronchial:	n/a
26	chr11:25623877-25623927	Jurkat	blood:	n/a
27	chr11:25623877-25623927	PFSK-1	brain:	n/a
28	chr11:25623877-25623927	GM12878	blood:	n/a
29	chr11:25623877-25623927	HCF	heart:	n/a
30	chr11:25623877-25623927	PANC-1	pancreas:	n/a
31	chr11:25623877-25623927	GM12892	blood:	n/a
32	chr11:25623877-25623927	AG09309	skin:	n/a
33	chr11:25623877-25623927	GM12891	blood:	n/a
34	chr11:25623877-25623927	HIPEpiC	eye:	n/a
35	chr11:25623877-25623927	PrEC	prostate:	n/a
36	chr11:25623877-25623927	HAEpiC	amniotic membrane:	n/a
37	chr11:25623877-25623927	BE2_C	brain:	n/a
38	chr11:25623877-25623927	MCF10A-Er-Src	breast:	n/a
39	chr11:25623877-25623927	AG10803	skin:	n/a
40	chr11:25623877-25623927	LNCaP	prostate:	n/a
41	chr11:25623877-25623927	SK-N-SH	brain:	n/a
42	chr11:25623877-25623927	MCF-7	breast:	n/a
43	chr11:25623877-25623927	HMEC	breast:	n/a
44	chr11:25623877-25623927	HEK293	kidney:	embryo
45	chr11:25623877-25623927	BJ	skin:	n/a
46	chr11:25623877-25623927	SK-N-MC	brain:	n/a
47	chr11:25623877-25623927	AG04449	skin:	fetal
48	chr11:25623877-25623927	SK-N-SH_RA	brain:	n/a
49	chr11:25623877-25623927	Caco-2	colon:	n/a
50	chr11:25623877-25623927	HRPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:25619794..25621822-chr11:25698109..25699950,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MUC15-3	chr11:25610021-25610389	NONHSAT018447
2	lnc-LUZP2-2	chr11:25652266-25652587	NONHSAT018449
3	lnc-MUC15-3	chr11:25609916-25610413	NONHSAT018446
4	lnc-MUC15-3	chr11:25609802-25609808	NONHSAT018446
5	lnc-MUC15-3	chr11:25610021-25610341	NONHSAT018448

No data

Variant related genes	Relation type
ENSG00000255454	TF binding region
RPL36AP40	TF binding region
ENSG00000255454	CpG island
RPL36AP40	CpG island

Extended variants
information (count: 1859 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1859 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17242363	chr11:25592935-25592936	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs148615432	chr11:25592963-25592964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185357623	chr11:25592983-25592984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371089703	chr11:25593051-25593052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555991968	chr11:25593079-25593080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs11028769	chr11:25593246-25593247	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs188919922	chr11:25593248-25593249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142688274	chr11:25593276-25593277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs77506895	chr11:25593310-25593311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373068543	chr11:25593345-25593346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147385278	chr11:25593356-25593357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557768194	chr11:25593357-25593358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542317397	chr11:25593370-25593371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572831214	chr11:25593389-25593390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560290866	chr11:25593420-25593421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181293708	chr11:25593434-25593435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561536763	chr11:25593468-25593469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564282298	chr11:25593503-25593504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370600764	chr11:25593515-25593516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs16914158	chr11:25593596-25593597	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs562664708	chr11:25593622-25593623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545868206	chr11:25593666-25593667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375567016	chr11:25593673-25593674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372529231	chr11:25593727-25593728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533325728	chr11:25593731-25593732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73431318	chr11:25593744-25593745	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs185890142	chr11:25593745-25593746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs72888534	chr11:25593747-25593748	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs527775910	chr11:25593788-25593789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10767409	chr11:25593808-25593809	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs188644597	chr11:25593831-25593832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538463031	chr11:25593833-25593834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs55753339	chr11:25593848-25593849	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs571830670	chr11:25593876-25593877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539346920	chr11:25593880-25593881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540190093	chr11:25593893-25593894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs139553073	chr11:25593918-25593919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572546865	chr11:25593919-25593920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529741888	chr11:25593929-25593930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376785559	chr11:25593936-25593937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533602532	chr11:25593943-25593944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374248915	chr11:25594062-25594063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs60336566	chr11:25594087-25594088	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs559629155	chr11:25594137-25594138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565060122	chr11:25594173-25594174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs58805544	chr11:25594205-25594206	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs577854222	chr11:25594212-25594213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145092797	chr11:25594244-25594245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs60595797	chr11:25594277-25594278	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs368533859	chr11:25594279-25594280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:25590400-25598000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:25592800-25599200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr11:25596600-25599600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr11:25596600-25600000	Enhancers	NHEK	skin
5	chr11:25597200-25599600	Enhancers	HMEC	breast
6	chr11:25598000-25599600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr11:25598000-25603000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr11:25598200-25600600	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr11:25598800-25599800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr11:25598800-25599800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr11:25598800-25600800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr11:25598800-25600800	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr11:25598800-25601200	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr11:25599200-25599400	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr11:25599200-25600600	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr11:25599400-25599600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr11:25599400-25599600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr11:25599400-25601800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr11:25599600-25601800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr11:25599600-25608600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr11:25599800-25600200	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr11:25600200-25600600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr11:25600600-25601000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
24	chr11:25600600-25601000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
25	chr11:25600600-25601000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
26	chr11:25600600-25601400	Enhancers	H9 Cell Line	embryonic stem cell
27	chr11:25600800-25601000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
28	chr11:25600800-25601000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr11:25600800-25602200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr11:25601000-25601200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr11:25601000-25601200	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr11:25601000-25601200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr11:25601000-25601200	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr11:25601000-25601200	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr11:25601200-25601400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
36	chr11:25601200-25601400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
37	chr11:25601200-25601400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
38	chr11:25601200-25601600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
39	chr11:25601200-25601600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
40	chr11:25601200-25601600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr11:25601200-25602200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:25601200-25602400	Enhancers	H1 Cell Line	embryonic stem cell
43	chr11:25601400-25603000	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr11:25601400-25603200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr11:25601400-25603200	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr11:25601600-25602800	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr11:25601600-25603000	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr11:25601600-25603200	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr11:25601800-25603000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr11:25601800-25603000	Enhancers	Breast Myoepithelial Primary Cells	Breast

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