Variant report

Variant	nsv430387
Chromosome Location	chr11:58719050-58778643
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	BATF	chr11:58760001-58760259	GM12878	blood:	n/a	chr11:58760105-58760116
2	CEBPB	chr11:58719331-58719581	A549	lung:	n/a	chr11:58719485-58719496 chr11:58719485-58719498 chr11:58719487-58719498 chr11:58719485-58719498
3	CEBPB	chr11:58745445-58745663	HepG2	liver:	n/a	chr11:58745468-58745479
4	CEBPB	chr11:58774084-58774291	HepG2	liver:	n/a	chr11:58774243-58774254
5	CEBPB	chr11:58719356-58719620	HepG2	liver:	n/a	chr11:58719485-58719496 chr11:58719485-58719498 chr11:58719487-58719498 chr11:58719485-58719498
6	CEBPB	chr11:58719316-58719632	IMR90	lung:	n/a	chr11:58719485-58719496 chr11:58719485-58719498 chr11:58719487-58719498 chr11:58719485-58719498
7	CEBPB	chr11:58767565-58767768	HepG2	liver:	n/a	chr11:58767688-58767699 chr11:58767686-58767697
8	CEBPB	chr11:58767586-58767847	H1-hESC	embryonic stem cell:	n/a	chr11:58767688-58767699 chr11:58767686-58767697
9	CEBPB	chr11:58767676-58767679	K562	blood:	n/a	n/a
10	CEBPB	chr11:58767588-58767695	A549	lung:	n/a	n/a
11	CEBPB	chr11:58719355-58719662	K562	blood:	n/a	chr11:58719485-58719496 chr11:58719485-58719498 chr11:58719487-58719498 chr11:58719485-58719498
12	CEBPB	chr11:58767634-58767824	Hela-S3	cervix:	n/a	chr11:58767688-58767699 chr11:58767686-58767697
13	CEBPB	chr11:58747741-58747864	Hela-S3	cervix:	n/a	chr11:58747813-58747824 chr11:58747811-58747824
14	CEBPB	chr11:58747697-58747942	A549	lung:	n/a	chr11:58747813-58747824 chr11:58747811-58747824
15	CEBPB	chr11:58719387-58719568	H1-hESC	embryonic stem cell:	n/a	chr11:58719485-58719496 chr11:58719485-58719498 chr11:58719487-58719498 chr11:58719485-58719498
16	CEBPB	chr11:58745428-58745609	A549	lung:	n/a	chr11:58745468-58745479
17	CHD2	chr11:58730953-58731524	H1-hESC	embryonic stem cell:	n/a	n/a
18	CREB1	chr11:58725448-58725809	GM12878	blood:	n/a	n/a
19	CREB1	chr11:58725455-58725792	GM12878	blood:	n/a	n/a
20	CREB1	chr11:58735914-58736237	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr11:58726160-58726310	HCFaa	heart:	n/a	chr11:58726167-58726185 chr11:58726168-58726184 chr11:58726169-58726190 chr11:58726170-58726183 chr11:58726170-58726179
22	CTCF	chr11:58726084-58726193	A549	lung:	n/a	chr11:58726167-58726185 chr11:58726168-58726184 chr11:58726169-58726190 chr11:58726170-58726183 chr11:58726170-58726179
23	CTCF	chr11:58731260-58731410	HBMEC	blood vessel:	n/a	chr11:58731304-58731325 chr11:58731309-58731327
24	CTCF	chr11:58731160-58731310	HFF	foreskin:	n/a	n/a
25	CTCF	chr11:58731240-58731390	HPAF	blood vessel:	n/a	chr11:58731304-58731325 chr11:58731309-58731327
26	CTCF	chr11:58726057-58726269	HepG2	liver:	n/a	chr11:58726167-58726185 chr11:58726168-58726184 chr11:58726169-58726190 chr11:58726170-58726183 chr11:58726170-58726179
27	CTCF	chr11:58726015-58726353	IMR90	lung:	n/a	chr11:58726167-58726185 chr11:58726168-58726184 chr11:58726169-58726190 chr11:58726170-58726183 chr11:58726170-58726179
28	CTCF	chr11:58731260-58731410	HRE	kidney:	n/a	chr11:58731304-58731325 chr11:58731309-58731327
29	CTCF	chr11:58731154-58731415	K562	blood:	n/a	chr11:58731304-58731325 chr11:58731309-58731327
30	CTCF	chr11:58731260-58731410	HRPEpiC	eye:	n/a	chr11:58731304-58731325 chr11:58731309-58731327
31	CTCF	chr11:58725940-58726090	GM12870	blood:	n/a	n/a
32	CTCF	chr11:58731135-58731575	H1-hESC	embryonic stem cell:	n/a	chr11:58731304-58731325 chr11:58731309-58731327
33	CTCF	chr11:58731020-58731170	NHEK	skin:	n/a	n/a
34	CTCF	chr11:58731280-58731430	HCFaa	heart:	n/a	chr11:58731304-58731325 chr11:58731309-58731327
35	CTCF	chr11:58726094-58726296	GM12891	blood:	n/a	chr11:58726167-58726185 chr11:58726168-58726184 chr11:58726169-58726190 chr11:58726170-58726183 chr11:58726170-58726179
36	CTCF	chr11:58726072-58726244	GM10266	blood:	n/a	chr11:58726167-58726185 chr11:58726168-58726184 chr11:58726169-58726190 chr11:58726170-58726183 chr11:58726170-58726179
37	CTCF	chr11:58726080-58726230	AG04449	skin:	n/a	chr11:58726167-58726185 chr11:58726168-58726184 chr11:58726169-58726190 chr11:58726170-58726183 chr11:58726170-58726179
38	CTCF	chr11:58726100-58726250	HRE	kidney:	n/a	chr11:58726167-58726185 chr11:58726168-58726184 chr11:58726169-58726190 chr11:58726170-58726183 chr11:58726170-58726179
39	CTCF	chr11:58726040-58726190	GM12864	blood:	n/a	chr11:58726167-58726185 chr11:58726168-58726184 chr11:58726169-58726190 chr11:58726170-58726183 chr11:58726170-58726179
40	CTCF	chr11:58726020-58726170	MCF-7	breast:	n/a	n/a
41	CTCF	chr11:58726100-58726250	GM12869	blood:	n/a	chr11:58726167-58726185 chr11:58726168-58726184 chr11:58726169-58726190 chr11:58726170-58726183 chr11:58726170-58726179
42	CTCF	chr11:58726180-58726330	HepG2	liver:	n/a	n/a
43	CTCF	chr11:58726080-58726230	AoAF	blood vessel:	n/a	chr11:58726167-58726185 chr11:58726168-58726184 chr11:58726169-58726190 chr11:58726170-58726183 chr11:58726170-58726179
44	CTCF	chr11:58726120-58726270	HPAF	blood vessel:	n/a	chr11:58726167-58726185 chr11:58726168-58726184 chr11:58726169-58726190 chr11:58726170-58726183 chr11:58726170-58726179
45	CTCF	chr11:58726080-58726230	HMF	breast:	n/a	chr11:58726167-58726185 chr11:58726168-58726184 chr11:58726169-58726190 chr11:58726170-58726183 chr11:58726170-58726179
46	CTCF	chr11:58731240-58731390	HRE	kidney:	n/a	chr11:58731304-58731325 chr11:58731309-58731327
47	CTCF	chr11:58726160-58726310	Hela-S3	cervix:	n/a	chr11:58726167-58726185 chr11:58726168-58726184 chr11:58726169-58726190 chr11:58726170-58726183 chr11:58726170-58726179
48	CTCF	chr11:58726140-58726290	K562	blood:	n/a	chr11:58726167-58726185 chr11:58726168-58726184 chr11:58726169-58726190 chr11:58726170-58726183 chr11:58726170-58726179
49	CTCF	chr11:58731260-58731410	BJ	skin:	n/a	chr11:58731304-58731325 chr11:58731309-58731327
50	CTCF	chr11:58726100-58726250	GM12864	blood:	n/a	chr11:58726167-58726185 chr11:58726168-58726184 chr11:58726169-58726190 chr11:58726170-58726183 chr11:58726170-58726179

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58731433-58731483	SK-N-SH_RA	brain:	n/a
2	chr11:58736000-58736050	SK-N-SH	brain:	n/a
3	chr11:58730897-58730947	HUVEC	blood vessel:	n/a
4	chr11:58736104-58736154	GM19239	blood:	n/a
5	chr11:58731433-58731483	HCPEpiC	choroid plexus:	n/a
6	chr11:58728533-58728583	HAEpiC	amniotic membrane:	n/a
7	chr11:58730897-58730947	LNCaP	prostate:	n/a
8	chr11:58731505-58731555	ECC-1	luminal epithelium:	n/a
9	chr11:58736081-58736131	AG04449	skin:	fetal
10	chr11:58731505-58731555	Hepatocyte	liver:	n/a
11	chr11:58736081-58736131	GM12878	blood:	n/a
12	chr11:58728533-58728583	AoSMC	blood vessel:	n/a
13	chr11:58731634-58731684	HAEpiC	amniotic membrane:	n/a
14	chr11:58728533-58728583	ovcar-3	ovarian:	n/a
15	chr11:58731505-58731555	AG09319	gingival:	n/a
16	chr11:58731505-58731555	GM12892	blood:	n/a
17	chr11:58731104-58731154	A549	lung:	n/a
18	chr11:58730897-58730947	AG04450	lung:	fetal
19	chr11:58736000-58736050	HRE	kidney:	n/a
20	chr11:58731104-58731154	NH-A	brain:	n/a
21	chr11:58735304-58735354	HAEpiC	amniotic membrane:	n/a
22	chr11:58736081-58736131	GM19239	blood:	n/a
23	chr11:58735304-58735354	HRCEpiC	kidney:	n/a
24	chr11:58736000-58736050	AG04450	lung:	fetal
25	chr11:58731104-58731154	Hela-S3	cervix:	n/a
26	chr11:58731433-58731483	HCT-116	colon:	n/a
27	chr11:58731104-58731154	Hepatocyte	liver:	n/a
28	chr11:58724252-58724302	PANC-1	pancreas:	n/a
29	chr11:58736000-58736050	AG10803	skin:	n/a
30	chr11:58731505-58731555	LNCaP	prostate:	n/a
31	chr11:58731433-58731483	A549	lung:	n/a
32	chr11:58735304-58735354	AG09319	gingival:	n/a
33	chr11:58731357-58731407	SAEC	small airway:	n/a
34	chr11:58731357-58731407	NHDF-neo	bronchial:	n/a
35	chr11:58728533-58728583	H1-hESC	embryonic stem cell:	embryo
36	chr11:58731357-58731407	MCF10A-Er-Src	breast:	n/a
37	chr11:58735304-58735354	NHBE	bronchial:	n/a
38	chr11:58730897-58730947	NHBE	bronchial:	n/a
39	chr11:58731634-58731684	HRE	kidney:	n/a
40	chr11:58731634-58731684	HIPEpiC	eye:	n/a
41	chr11:58731104-58731154	HCM	heart:	n/a
42	chr11:58730897-58730947	A549	lung:	n/a
43	chr11:58731433-58731483	HRCEpiC	kidney:	n/a
44	chr11:58736104-58736154	AG04450	lung:	fetal
45	chr11:58730897-58730947	GM12878	blood:	n/a
46	chr11:58736104-58736154	AG09319	gingival:	n/a
47	chr11:58724252-58724302	HEEpiC	esophagus:	n/a
48	chr11:58735304-58735354	SK-N-MC	brain:	n/a
49	chr11:58724252-58724302	SK-N-MC	brain:	n/a
50	chr11:58730897-58730947	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:58726086..58726653-chr11:58902781..58903961,3	K562	blood:
2	chr11:58721468..58724070-chr11:58726713..58729457,3	K562	blood:
3	chr11:58729566..58731391-chr11:58732930..58735906,2	K562	blood:
4	chr11:58721468..58724070-chr11:58726713..58729457,3	K562	blood:
5	chr11:58762969..58764487-chr11:58768997..58771127,2	K562	blood:
6	chr11:58762969..58764487-chr11:58768997..58771127,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLYATL2-4	chr11:58735069-58735764	NONHSAT021495
2	lnc-GLYATL2-2	chr11:58746601-58746758	ENSG00000255240.1
3	lnc-GLYATL2-2	chr11:58761476-58761524	ENSG00000255240.1
4	lnc-GLYATL2-2	chr11:58725690-58726293	ENSG00000255240.1
5	lnc-GLYATL2-2	chr11:58746601-58746798	ENSG00000255240.1
6	lnc-GLYATL2-2	chr11:58746601-58746798	NR_033853
7	lnc-GLYATL2-2	chr11:58736415-58736546	ENSG00000255240.1
8	lnc-GLYATL2-2	chr11:58761476-58761524	NR_033853
9	lnc-GLYATL2-2	chr11:58736426-58736546	ENSG00000255240.1

Variant related genes	Relation type
ENSG00000254786	TF binding region
GLYATL1P1	TF binding region
ENSG00000255240	TF binding region
ENSG00000254877	TF binding region
ENSG00000254786	CpG island
GLYATL1P1	CpG island
ENSG00000255240	CpG island
ENSG00000254877	CpG island
ENSG00000254877	chromatin interactions

Extended variants
information (count: 2358 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2358 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531424	chr11:58719050-58719051	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs527805698	chr11:58719058-58719059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571948615	chr11:58719059-58719060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs370810774	chr11:58719074-58719075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547468447	chr11:58719105-58719106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs200944121	chr11:58719130-58719131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542678764	chr11:58719142-58719143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182711304	chr11:58719164-58719165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574264338	chr11:58719197-58719198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544867168	chr11:58719327-58719328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541763235	chr11:58719331-58719332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185974279	chr11:58719344-58719345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1783530	chr11:58719374-58719375	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs545383682	chr11:58719385-58719386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368732357	chr11:58719434-58719435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560511886	chr11:58719450-58719451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191267291	chr11:58719508-58719509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116714393	chr11:58719510-58719511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs141998912	chr11:58719522-58719523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs5792142	chr11:58719530-58719531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370617970	chr11:58719531-58719532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368693804	chr11:58719533-58719534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371422707	chr11:58719534-58719535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567681059	chr11:58719546-58719547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371582206	chr11:58719601-58719602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531396262	chr11:58719632-58719633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187184273	chr11:58719723-58719724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191998819	chr11:58719753-58719754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183001830	chr11:58719759-58719760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376054222	chr11:58719771-58719772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs524821	chr11:58719779-58719780	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs553801943	chr11:58719820-58719821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528752783	chr11:58719846-58719847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187602101	chr11:58719854-58719855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535898014	chr11:58719857-58719858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551684556	chr11:58719861-58719862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571770402	chr11:58719864-58719865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs117295698	chr11:58719909-58719910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146910805	chr11:58719921-58719922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs578231039	chr11:58719951-58719952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374156152	chr11:58719956-58719957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545650854	chr11:58719959-58719960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560658452	chr11:58719961-58719962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527661672	chr11:58719996-58719997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542700022	chr11:58720014-58720015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs193119997	chr11:58720047-58720048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531650470	chr11:58720090-58720091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549865911	chr11:58720108-58720109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs80059489	chr11:58720109-58720110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139212503	chr11:58720185-58720186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58713400-58721800	Weak transcription	Fetal Intestine Small	intestine
2	chr11:58718000-58720200	Weak transcription	Liver	Liver
3	chr11:58720200-58723400	Strong transcription	Liver	Liver
4	chr11:58721800-58722000	Enhancers	Fetal Intestine Small	intestine
5	chr11:58721800-58723400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr11:58721800-58723400	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr11:58722200-58722600	Enhancers	H9 Cell Line	embryonic stem cell
8	chr11:58722200-58722800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr11:58722200-58722800	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr11:58722200-58723000	Enhancers	H1 Cell Line	embryonic stem cell
11	chr11:58722400-58722800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr11:58723000-58723400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr11:58723000-58726800	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr11:58723200-58723400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr11:58723400-58724000	Genic enhancers	Liver	Liver
16	chr11:58723400-58731000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr11:58723400-58731000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr11:58724000-58724200	Enhancers	Liver	Liver
19	chr11:58724200-58725000	Weak transcription	Liver	Liver
20	chr11:58725000-58726000	Enhancers	Liver	Liver
21	chr11:58725000-58728400	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr11:58725400-58726000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr11:58726000-58726200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr11:58726000-58730600	Weak transcription	Liver	Liver
25	chr11:58726200-58726600	Enhancers	Primary B cells from peripheral blood	blood
26	chr11:58726200-58730800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr11:58726600-58740000	Weak transcription	Primary B cells from peripheral blood	blood
28	chr11:58726800-58727000	Enhancers	H1 Cell Line	embryonic stem cell
29	chr11:58727000-58727400	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr11:58727400-58727800	Enhancers	H1 Cell Line	embryonic stem cell
31	chr11:58728400-58730000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr11:58730000-58730200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr11:58730000-58730600	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr11:58730200-58730600	Weak transcription	NHEK	skin
35	chr11:58730200-58739400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr11:58730400-58730600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr11:58730400-58730600	Active TSS	Fetal Intestine Small	intestine
38	chr11:58730400-58730800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
39	chr11:58730600-58730800	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr11:58730600-58730800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr11:58730600-58730800	Enhancers	Liver	Liver
42	chr11:58730600-58730800	Enhancers	NHEK	skin
43	chr11:58730600-58730800	Enhancers	Osteobl	bone
44	chr11:58730600-58731000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
45	chr11:58730600-58731000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr11:58730600-58731000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
47	chr11:58730600-58731000	Flanking Active TSS	Fetal Intestine Small	intestine
48	chr11:58730600-58731200	Bivalent Enhancer	Fetal Muscle Leg	muscle
49	chr11:58730600-58731800	Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr11:58730800-58731000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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