Variant report

Variant	esv3445007
Chromosome Location	chr11:58638330-58709867
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1058)
CpG islands
(count:1407)
Chromatin interactive
region (count:12)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1058 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

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	ARID3A	chr11:58693760-58694429	HepG2	liver:	n/a	n/a
3	ATF1	chr11:58691061-58691064	K562	blood:	n/a	n/a
4	ATF2	chr11:58694851-58695251	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr11:58672951-58673767	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr11:58690792-58691378	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr11:58668343-58668597	K562	blood:	n/a	n/a
8	BHLHE40	chr11:58673515-58673655	K562	blood:	n/a	n/a
9	BHLHE40	chr11:58668390-58668584	HepG2	liver:	n/a	n/a
10	BHLHE40	chr11:58693810-58694128	HepG2	liver:	n/a	n/a
11	BRCA1	chr11:58673350-58673665	H1-hESC	embryonic stem cell:	n/a	n/a
12	CBX3	chr11:58684602-58685036	HCT-116	colon:	n/a	n/a
13	CBX3	chr11:58684635-58685102	HCT-116	colon:	n/a	n/a
14	CBX3	chr11:58684666-58684899	K562	blood:	n/a	n/a
15	CEBPB	chr11:58656689-58656951	HepG2	liver:	n/a	n/a
16	CEBPB	chr11:58648118-58648482	HepG2	liver:	n/a	chr11:58648287-58648300
17	CEBPB	chr11:58656085-58656389	Hela-S3	cervix:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
18	CEBPB	chr11:58648074-58648804	HepG2	liver:	n/a	chr11:58648287-58648300
19	CEBPB	chr11:58656127-58656438	K562	blood:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
20	CEBPB	chr11:58648024-58648392	HepG2	liver:	n/a	chr11:58648287-58648300
21	CEBPB	chr11:58656076-58656380	IMR90	lung:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
22	CEBPB	chr11:58648139-58648384	HepG2	liver:	n/a	chr11:58648287-58648300
23	CEBPB	chr11:58693679-58694509	IMR90	lung:	n/a	chr11:58694316-58694329
24	CEBPB	chr11:58656131-58656456	MCF-7	breast:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
25	CEBPB	chr11:58656078-58656414	A549	lung:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
26	CEBPB	chr11:58656150-58656434	MCF-7	breast:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
27	CEBPB	chr11:58693768-58694393	HepG2	liver:	n/a	chr11:58694316-58694329
28	CEBPB	chr11:58667853-58667861	A549	lung:	n/a	n/a
29	CEBPB	chr11:58695605-58695843	HepG2	liver:	n/a	chr11:58695719-58695730
30	CEBPB	chr11:58656053-58656436	HepG2	liver:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
31	CEBPB	chr11:58648183-58648434	A549	lung:	n/a	chr11:58648287-58648300
32	CHD1	chr11:58672850-58673135	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr11:58672403-58673216	IMR90	lung:	n/a	n/a
34	CHD2	chr11:58672662-58673757	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr11:58668301-58668501	GM12878	blood:	n/a	n/a
36	CHD2	chr11:58668323-58668505	K562	blood:	n/a	n/a
37	CHD2	chr11:58668027-58668642	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr11:58694884-58695809	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr11:58668271-58668693	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr11:58668219-58668775	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr11:58690800-58690950	GM12873	blood:	n/a	n/a
42	CTCF	chr11:58673540-58673690	WI-38	lung:	n/a	n/a
43	CTCF	chr11:58668280-58668430	A549	lung:	n/a	n/a
44	CTCF	chr11:58690100-58691258	SK-N-SH	brain:	n/a	n/a
45	CTCF	chr11:58687520-58687670	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr11:58690760-58690910	Caco-2	colon:	n/a	n/a
47	CTCF	chr11:58668380-58668530	WERI-Rb-1	eye:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
48	CTCF	chr11:58668460-58668610	BE2_C	brain:	n/a	n/a
49	CTCF	chr11:58690780-58690930	GM12875	blood:	n/a	n/a
50	CTCF	chr11:58673020-58673170	AG04449	skin:	n/a	n/a

(count:1407 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58695093-58695143	GM06990	blood:	n/a
2	chr11:58651984-58652034	GM12892	blood:	n/a
3	chr11:58694950-58695000	AG04450	lung:	fetal
4	chr11:58673615-58673665	HAEpiC	amniotic membrane:	n/a
5	chr11:58695093-58695143	GM06990	blood:	n/a
6	chr11:58651984-58652034	GM12892	blood:	n/a
7	chr11:58694950-58695000	AG04450	lung:	fetal
8	chr11:58673615-58673665	HAEpiC	amniotic membrane:	n/a
9	chr11:58673615-58673665	AoSMC	blood vessel:	n/a
10	chr11:58694950-58695000	NB4	blood:	n/a
11	chr11:58696069-58696119	HEK293	kidney:	embryo
12	chr11:58694219-58694269	HCPEpiC	choroid plexus:	n/a
13	chr11:58667960-58668010	GM19239	blood:	n/a
14	chr11:58668068-58668118	BJ	skin:	n/a
15	chr11:58667964-58668014	GM12892	blood:	n/a
16	chr11:58667960-58668010	Hepatocyte	liver:	n/a
17	chr11:58651984-58652034	HMEC	breast:	n/a
18	chr11:58668345-58668395	AoSMC	blood vessel:	n/a
19	chr11:58668634-58668684	NT2-D1	testis:	n/a
20	chr11:58673167-58673217	HL-60	blood:	n/a
21	chr11:58673167-58673217	SK-N-MC	brain:	n/a
22	chr11:58675749-58675799	NHDF-neo	bronchial:	n/a
23	chr11:58668488-58668538	HepG2	liver:	n/a
24	chr11:58667960-58668010	GM06990	blood:	n/a
25	chr11:58696069-58696119	BE2_C	brain:	n/a
26	chr11:58667960-58668010	T-47D	breast:	n/a
27	chr11:58673477-58673527	SK-N-SH_RA	brain:	n/a
28	chr11:58673577-58673627	PFSK-1	brain:	n/a
29	chr11:58667964-58668014	GM19239	blood:	n/a
30	chr11:58667964-58668014	HEEpiC	esophagus:	n/a
31	chr11:58694950-58695000	Caco-2	colon:	n/a
32	chr11:58673453-58673503	GM12891	blood:	n/a
33	chr11:58668977-58669027	PFSK-1	brain:	n/a
34	chr11:58668634-58668684	CMK	blood:	n/a
35	chr11:58673477-58673527	A549	lung:	n/a
36	chr11:58673087-58673137	AoSMC	blood vessel:	n/a
37	chr11:58709394-58709444	HRCEpiC	kidney:	n/a
38	chr11:58673453-58673503	AG09319	gingival:	n/a
39	chr11:58673453-58673503	CMK	blood:	n/a
40	chr11:58673453-58673503	SK-N-MC	brain:	n/a
41	chr11:58668488-58668538	Jurkat	blood:	n/a
42	chr11:58672702-58672752	HCM	heart:	n/a
43	chr11:58667964-58668014	GM06990	blood:	n/a
44	chr11:58672888-58672938	HCM	heart:	n/a
45	chr11:58673453-58673503	Hepatocyte	liver:	n/a
46	chr11:58696069-58696119	K562	blood:	n/a
47	chr11:58673453-58673503	MCF10A-Er-Src	breast:	n/a
48	chr11:58667964-58668014	HUVEC	blood vessel:	n/a
49	chr11:58696069-58696119	GM06990	blood:	n/a
50	chr11:58695093-58695143	ProgFib	skin:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:58345930..58347450-chr11:58657978..58660327,2	K562	blood:
2	chr11:58677524..58679024-chr6:58777164..58778728,2	K562	blood:
3	chr11:58346639..58348965-chr11:58654113..58656554,2	K562	blood:
4	chr11:58667985..58668808-chr11:58825960..58826578,4	MCF-7	breast:
5	chr11:58678524..58679504-chr6:58776958..58777672,3	MCF-7	breast:
6	chr11:58668032..58668917-chr11:58825619..58826508,3	K562	blood:
7	chr11:58421165..58421796-chr11:58687413..58688096,2	MCF-7	breast:
8	chr11:58671775..58674615-chr11:58675003..58676520,2	K562	blood:
9	chr11:58678524..58679504-chr6:58777166..58777745,2	MCF-7	breast:
10	chr11:58661995..58664743-chr11:58668611..58670936,2	K562	blood:
11	chr11:58669175..58672165-chr11:58677460..58679347,2	K562	blood:
12	chr11:58661995..58664743-chr11:58668611..58670936,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLYAT-1	chr11:58659760-58660337	l_477_chr11:58656260-58660325_ovary
2	lnc-GLYATL1-1	chr11:58660135-58660445	ENSG00000254717
3	lnc-GLYATL1-1	chr11:58660135-58660266	NONHSAT021485
4	lnc-GLYATL2-1	chr11:58695790-58696162	ENSG00000255523.1
5	lnc-GLYATL1-3	chr11:58672343-58672709	NONHSAT021486
6	lnc-GLYATL2-2	chr11:58701116-58703171	NR_033853
7	lnc-GLYAT-1	chr11:58656394-58657698	l_477_chr11:58656260-58660325_ovary
8	lnc-GLYATL1-1	chr11:58645775-58645854	ENSG00000254717
9	lnc-GLYAT-1	chr11:58656261-58656370	l_477_chr11:58656260-58660325_ovary
10	lnc-GLYAT-1	chr11:58664013-58664214	l_477_chr11:58656260-58660325_ovary
11	lnc-GLYATL1-1	chr11:58652424-58652497	NONHSAT021485
12	lnc-GLYATL2-2	chr11:58701116-58703171	ENSG00000255240.1
13	lnc-GLYATL2-1	chr11:58684488-58684757	ENSG00000255523.1
14	lnc-GLYATL1-1	chr11:58652379-58652497	ENSG00000254717
15	lnc-GLYAT-1	chr11:58657761-58659741	l_477_chr11:58656260-58660325_ovary

No data

Variant related genes	Relation type
GLYATL1P2	TF binding region
ENSG00000224130	TF binding region
GLYATL2	TF binding region
ENSG00000255523	TF binding region
GLYATL1	TF binding region
GLYATL1P2	CpG island
ENSG00000224130	CpG island
GLYATL2	CpG island
ENSG00000255523	CpG island
GLYATL1	CpG island
ENSG00000166840	chromatin interactions
ENSG00000186660	chromatin interactions
ENSG00000156689	chromatin interactions
ENSG00000255073	chromatin interactions
ENSG00000255240	chromatin interactions
ENSG00000224130	chromatin interactions

Extended variants
information (count: 2736 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2736 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547309310	chr11:58638471-58638472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540157902	chr11:58638605-58638606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561312946	chr11:58638629-58638630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76297697	chr11:58638645-58638646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562437751	chr11:58638649-58638650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546574616	chr11:58638733-58638734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs116561991	chr11:58638737-58638738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371060157	chr11:58638745-58638746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554561628	chr11:58638748-58638749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564900748	chr11:58638764-58638765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187909367	chr11:58638795-58638796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191791816	chr11:58638805-58638806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184245593	chr11:58638844-58638845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564746432	chr11:58638868-58638869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528769388	chr11:58638878-58638879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373340136	chr11:58638885-58638886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs12421313	chr11:58638888-58638889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547335517	chr11:58638891-58638892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568325880	chr11:58638907-58638908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546902541	chr11:58638915-58638916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs187438649	chr11:58638918-58638919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550793659	chr11:58638930-58638931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530236588	chr11:58639053-58639054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs12799196	chr11:58639105-58639106	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs140527019	chr11:58639106-58639107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566343550	chr11:58639107-58639108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533795759	chr11:58639135-58639136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs12804928	chr11:58639144-58639145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376624295	chr11:58639223-58639224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563130854	chr11:58639247-58639248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145793065	chr11:58639283-58639284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552952451	chr11:58639330-58639331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192346653	chr11:58639335-58639336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538475469	chr11:58639336-58639337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577694059	chr11:58639339-58639340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138448301	chr11:58639343-58639344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141622255	chr11:58639357-58639358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs145379061	chr11:58639374-58639375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540881910	chr11:58639474-58639475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562454571	chr11:58639506-58639507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529265177	chr11:58639514-58639515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550989388	chr11:58639564-58639565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569232886	chr11:58639570-58639571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533217708	chr11:58639594-58639595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551467482	chr11:58639607-58639608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566280623	chr11:58639643-58639644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10792203	chr11:58639655-58639656	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs555363994	chr11:58639663-58639664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567584994	chr11:58639676-58639677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537420604	chr11:58639681-58639682	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1020 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58635000-58668000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:58638200-58638400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr11:58643600-58644800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
4	chr11:58645400-58645600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
5	chr11:58645400-58646400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
6	chr11:58645600-58652400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr11:58647600-58649000	Enhancers	Liver	Liver
8	chr11:58647600-58649000	Enhancers	HepG2	liver
9	chr11:58647800-58648000	Enhancers	Fetal Intestine Small	intestine
10	chr11:58648000-58654400	Weak transcription	Fetal Lung	lung
11	chr11:58648000-58655000	Weak transcription	Fetal Intestine Small	intestine
12	chr11:58651000-58671200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr11:58651400-58660200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr11:58652400-58653200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr11:58652600-58653400	ZNF genes & repeats	Fetal Stomach	stomach
16	chr11:58653200-58661400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr11:58654400-58654800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
18	chr11:58658000-58667600	Weak transcription	Brain Germinal Matrix	brain
19	chr11:58658400-58668000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr11:58659000-58661400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr11:58659000-58668000	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr11:58659400-58661600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr11:58659400-58667600	Weak transcription	Fetal Brain Female	brain
24	chr11:58659400-58671000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr11:58660200-58660800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr11:58660600-58666000	Weak transcription	Fetal Muscle Trunk	muscle
27	chr11:58660800-58665600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr11:58661000-58661800	Enhancers	H1 Cell Line	embryonic stem cell
29	chr11:58661200-58662000	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr11:58661400-58661800	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr11:58661400-58661800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr11:58661400-58662400	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr11:58661400-58662400	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr11:58661400-58663000	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr11:58661600-58661800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr11:58661600-58662000	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr11:58661800-58667800	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr11:58662400-58667800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr11:58662800-58663600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr11:58663000-58664000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr11:58663600-58668000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr11:58664000-58665200	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr11:58664000-58668000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr11:58665000-58668800	Enhancers	Primary hematopoietic stem cells	blood
45	chr11:58665200-58665800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr11:58665200-58667800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr11:58665200-58667800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr11:58665200-58671600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr11:58665600-58666000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr11:58665600-58667800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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