Variant report

Variant	esv1824025
Chromosome Location	chr11:58626835-58669877
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	chr11:58648155-58648546	HepG2	liver:	n/a	n/a
2	BATF	chr11:58634982-58635318	GM12878	blood:	n/a	n/a
3	BHLHE40	chr11:58668390-58668584	HepG2	liver:	n/a	n/a
4	BHLHE40	chr11:58668343-58668597	K562	blood:	n/a	n/a
5	CEBPB	chr11:58648139-58648384	HepG2	liver:	n/a	chr11:58648287-58648300
6	CEBPB	chr11:58648024-58648392	HepG2	liver:	n/a	chr11:58648287-58648300
7	CEBPB	chr11:58627346-58627618	HepG2	liver:	n/a	chr11:58627487-58627498
8	CEBPB	chr11:58648118-58648482	HepG2	liver:	n/a	chr11:58648287-58648300
9	CEBPB	chr11:58656085-58656389	Hela-S3	cervix:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
10	CEBPB	chr11:58648183-58648434	A549	lung:	n/a	chr11:58648287-58648300
11	CEBPB	chr11:58656053-58656436	HepG2	liver:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
12	CEBPB	chr11:58648074-58648804	HepG2	liver:	n/a	chr11:58648287-58648300
13	CEBPB	chr11:58667853-58667861	A549	lung:	n/a	n/a
14	CEBPB	chr11:58656131-58656456	MCF-7	breast:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
15	CEBPB	chr11:58656076-58656380	IMR90	lung:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
16	CEBPB	chr11:58656150-58656434	MCF-7	breast:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
17	CEBPB	chr11:58656127-58656438	K562	blood:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
18	CEBPB	chr11:58656689-58656951	HepG2	liver:	n/a	n/a
19	CEBPB	chr11:58656078-58656414	A549	lung:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
20	CEBPB	chr11:58627355-58627619	A549	lung:	n/a	chr11:58627487-58627498
21	CHD2	chr11:58668323-58668505	K562	blood:	n/a	n/a
22	CHD2	chr11:58668301-58668501	GM12878	blood:	n/a	n/a
23	CHD2	chr11:58668027-58668642	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr11:58668271-58668693	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr11:58668219-58668775	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr11:58668400-58668550	BJ	skin:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
27	CTCF	chr11:58668400-58668550	K562	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
28	CTCF	chr11:58668174-58668600	K562	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
29	CTCF	chr11:58668318-58668587	K562	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
30	CTCF	chr11:58668328-58668595	Pancreas_OC	pancreas:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
31	CTCF	chr11:58668400-58668550	GM12878	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
32	CTCF	chr11:58668167-58668218	GM19240	blood:	n/a	n/a
33	CTCF	chr11:58668420-58668570	GM06990	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
34	CTCF	chr11:58668239-58668678	H1-hESC	embryonic stem cell:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
35	CTCF	chr11:58668263-58668560	T-47D	breast:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
36	CTCF	chr11:58668380-58668530	GM12864	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
37	CTCF	chr11:58668310-58668593	MCF-7	breast:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
38	CTCF	chr11:58668420-58668570	GM12872	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
39	CTCF	chr11:58668680-58668830	AoAF	blood vessel:	n/a	n/a
40	CTCF	chr11:58668359-58668567	GM10248	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
41	CTCF	chr11:58668304-58668689	H1-hESC	embryonic stem cell:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
42	CTCF	chr11:58668820-58668970	HMEC	breast:	n/a	n/a
43	CTCF	chr11:58668380-58668530	Hela-S3	cervix:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
44	CTCF	chr11:58668400-58668550	GM12866	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
45	CTCF	chr11:58668340-58668490	GM12868	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
46	CTCF	chr11:58668400-58668550	AG09319	gingival:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
47	CTCF	chr11:58668400-58668550	GM12870	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
48	CTCF	chr11:58668400-58668550	HepG2	liver:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
49	CTCF	chr11:58668175-58668675	MCF-7	breast:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
50	CTCF	chr11:58668364-58668503	SK-N-SH_RA	brain:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58668068-58668118	ProgFib	skin:	n/a
2	chr11:58668488-58668538	GM12892	blood:	n/a
3	chr11:58668068-58668118	ProgFib	skin:	n/a
4	chr11:58668488-58668538	GM12892	blood:	n/a
5	chr11:58668977-58669027	AG04450	lung:	fetal
6	chr11:58651984-58652034	ProgFib	skin:	n/a
7	chr11:58668488-58668538	HPAEpiC	pulmonary alveolar:	n/a
8	chr11:58651984-58652034	HNPCEpiC	eye:	n/a
9	chr11:58668345-58668395	BJ	skin:	n/a
10	chr11:58668345-58668395	ECC-1	luminal epithelium:	n/a
11	chr11:58668068-58668118	HNPCEpiC	eye:	n/a
12	chr11:58668488-58668538	HAEpiC	amniotic membrane:	n/a
13	chr11:58668068-58668118	SKMC	muscle:	n/a
14	chr11:58651984-58652034	ovcar-3	ovarian:	n/a
15	chr11:58668068-58668118	HPAEpiC	pulmonary alveolar:	n/a
16	chr11:58668488-58668538	Hepatocyte	liver:	n/a
17	chr11:58651984-58652034	GM06990	blood:	n/a
18	chr11:58667964-58668014	AG04449	skin:	fetal
19	chr11:58668977-58669027	AG09319	gingival:	n/a
20	chr11:58668345-58668395	HEK293	kidney:	embryo
21	chr11:58667964-58668014	SK-N-MC	brain:	n/a
22	chr11:58667964-58668014	HRE	kidney:	n/a
23	chr11:58651984-58652034	GM19239	blood:	n/a
24	chr11:58651984-58652034	AG04450	lung:	fetal
25	chr11:58667964-58668014	H1-hESC	embryonic stem cell:	embryo
26	chr11:58668634-58668684	GM19239	blood:	n/a
27	chr11:58667964-58668014	U87	brain:	n/a
28	chr11:58668977-58669027	K562	blood:	n/a
29	chr11:58668977-58669027	ECC-1	luminal epithelium:	n/a
30	chr11:58668345-58668395	H1-hESC	embryonic stem cell:	embryo
31	chr11:58667960-58668010	HRPEpiC	eye:	n/a
32	chr11:58668977-58669027	SK-N-SH	brain:	n/a
33	chr11:58668068-58668118	ovcar-3	ovarian:	n/a
34	chr11:58667960-58668010	HRCEpiC	kidney:	n/a
35	chr11:58668488-58668538	HCM	heart:	n/a
36	chr11:58667960-58668010	GM12878	blood:	n/a
37	chr11:58668634-58668684	HEK293	kidney:	embryo
38	chr11:58651984-58652034	SK-N-SH_RA	brain:	n/a
39	chr11:58668488-58668538	H1-hESC	embryonic stem cell:	embryo
40	chr11:58668488-58668538	SKMC	muscle:	n/a
41	chr11:58668488-58668538	PANC-1	pancreas:	n/a
42	chr11:58668488-58668538	GM12891	blood:	n/a
43	chr11:58651984-58652034	A549	lung:	n/a
44	chr11:58668977-58669027	GM19239	blood:	n/a
45	chr11:58668068-58668118	H1-hESC	embryonic stem cell:	embryo
46	chr11:58667960-58668010	AG04450	lung:	fetal
47	chr11:58667964-58668014	AG09319	gingival:	n/a
48	chr11:58668488-58668538	BE2_C	brain:	n/a
49	chr11:58668488-58668538	AG09319	gingival:	n/a
50	chr11:58668488-58668538	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:58667985..58668808-chr11:58825960..58826578,4	MCF-7	breast:
2	chr11:58345930..58347450-chr11:58657978..58660327,2	K562	blood:
3	chr11:58346639..58348965-chr11:58654113..58656554,2	K562	blood:
4	chr11:58668032..58668917-chr11:58825619..58826508,3	K562	blood:
5	chr11:58661995..58664743-chr11:58668611..58670936,2	K562	blood:
6	chr11:58661995..58664743-chr11:58668611..58670936,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLYATL1-1	chr11:58660135-58660266	NONHSAT021485
2	lnc-GLYAT-1	chr11:58659760-58660337	l_477_chr11:58656260-58660325_ovary
3	lnc-GLYATL1-1	chr11:58645775-58645854	ENSG00000254717
4	lnc-GLYATL1-1	chr11:58652379-58652497	ENSG00000254717
5	lnc-GLYAT-1	chr11:58656261-58656370	l_477_chr11:58656260-58660325_ovary
6	lnc-GLYATL1-1	chr11:58660135-58660445	ENSG00000254717
7	lnc-GLYAT-1	chr11:58656394-58657698	l_477_chr11:58656260-58660325_ovary
8	lnc-GLYAT-1	chr11:58657761-58659741	l_477_chr11:58656260-58660325_ovary
9	lnc-GLYATL1-1	chr11:58652424-58652497	NONHSAT021485
10	lnc-GLYAT-1	chr11:58664013-58664214	l_477_chr11:58656260-58660325_ovary

Variant related genes	Relation type
GLYATL1P2	TF binding region
ENSG00000224130	TF binding region
GLYATL1	TF binding region
GLYATL1P2	CpG island
ENSG00000224130	CpG island
GLYATL1	CpG island
ENSG00000255240	chromatin interactions
ENSG00000186660	chromatin interactions
ENSG00000255073	chromatin interactions

Extended variants
information (count: 1628 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1628 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564228687	chr11:58631000-58631001	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs587953	chr11:58631001-58631002	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs492802	chr11:58631023-58631024	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs113040048	chr11:58631078-58631079	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs493659	chr11:58631089-58631090	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs550276403	chr11:58631149-58631150	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs569873535	chr11:58631181-58631182	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs116573974	chr11:58631185-58631186	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs144334796	chr11:58631190-58631191	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs559199100	chr11:58631252-58631253	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs561197502	chr11:58631272-58631273	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573063727	chr11:58631289-58631290	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs530039996	chr11:58631307-58631308	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs534999503	chr11:58631361-58631362	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553428482	chr11:58631390-58631391	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs148360785	chr11:58631397-58631398	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs141673318	chr11:58631420-58631421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs557501963	chr11:58631421-58631422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs496601	chr11:58631443-58631444	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs497348	chr11:58631476-58631477	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs191419986	chr11:58631479-58631480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs117610125	chr11:58631490-58631491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540434600	chr11:58631552-58631553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs11229669	chr11:58631592-58631593	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs519256	chr11:58631593-58631594	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs150542258	chr11:58631598-58631599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs519310	chr11:58631607-58631608	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs183947636	chr11:58631608-58631609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs682780	chr11:58631624-58631625	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs139795946	chr11:58631628-58631629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571100425	chr11:58631645-58631646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs535305243	chr11:58631646-58631647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs553721484	chr11:58631669-58631670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs78656302	chr11:58631693-58631694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs682357	chr11:58631714-58631715	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs536556487	chr11:58631757-58631758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs143179429	chr11:58631795-58631796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189754646	chr11:58631807-58631808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557696623	chr11:58631827-58631828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs56001071	chr11:58631836-58631837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs202026188	chr11:58631840-58631841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs573016041	chr11:58631848-58631849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs76907161	chr11:58631934-58631935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192746597	chr11:58631942-58631943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs573297132	chr11:58631945-58631946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573402234	chr11:58631982-58631983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs680976	chr11:58632016-58632017	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs565839010	chr11:58632036-58632037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs562586357	chr11:58632046-58632047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs146259738	chr11:58632056-58632057	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:230 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58631000-58631400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:58631000-58631400	ZNF genes & repeats	Thymus	Thymus
3	chr11:58631200-58631400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr11:58631400-58635000	Enhancers	Thymus	Thymus
5	chr11:58631600-58632400	Enhancers	Fetal Thymus	thymus
6	chr11:58632400-58632800	Weak transcription	Fetal Thymus	thymus
7	chr11:58632800-58634600	Enhancers	Fetal Thymus	thymus
8	chr11:58633800-58634000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr11:58634000-58634800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr11:58634000-58635800	Enhancers	NHEK	skin
11	chr11:58634200-58634600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr11:58634200-58635600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr11:58634400-58635000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr11:58634400-58635600	Enhancers	HMEC	breast
15	chr11:58634800-58635400	Enhancers	NHDF-Ad	bronchial
16	chr11:58634800-58635600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr11:58635000-58635600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr11:58635000-58636000	Weak transcription	Thymus	Thymus
19	chr11:58635000-58668000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr11:58635600-58637600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr11:58636000-58636200	Enhancers	Thymus	Thymus
22	chr11:58637600-58638200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr11:58638200-58638400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr11:58643600-58644800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
25	chr11:58645400-58645600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
26	chr11:58645400-58646400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
27	chr11:58645600-58652400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr11:58647600-58649000	Enhancers	Liver	Liver
29	chr11:58647600-58649000	Enhancers	HepG2	liver
30	chr11:58647800-58648000	Enhancers	Fetal Intestine Small	intestine
31	chr11:58648000-58654400	Weak transcription	Fetal Lung	lung
32	chr11:58648000-58655000	Weak transcription	Fetal Intestine Small	intestine
33	chr11:58651000-58671200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr11:58651400-58660200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr11:58652400-58653200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr11:58652600-58653400	ZNF genes & repeats	Fetal Stomach	stomach
37	chr11:58653200-58661400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr11:58654400-58654800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
39	chr11:58658000-58667600	Weak transcription	Brain Germinal Matrix	brain
40	chr11:58658400-58668000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr11:58659000-58661400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr11:58659000-58668000	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr11:58659400-58661600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr11:58659400-58667600	Weak transcription	Fetal Brain Female	brain
45	chr11:58659400-58671000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr11:58660200-58660800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr11:58660600-58666000	Weak transcription	Fetal Muscle Trunk	muscle
48	chr11:58660800-58665600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr11:58661000-58661800	Enhancers	H1 Cell Line	embryonic stem cell
50	chr11:58661200-58662000	Enhancers	HUES64 Cell Line	embryonic stem cell

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