Variant report

Variant	esv3351601
Chromosome Location	chr11:58979308-59052763
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1128)
CpG islands
(count:610)
Chromatin interactive
region (count:17)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1128 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:59040973-59041111	K562	blood:	n/a	n/a
2	ATF2	chr11:59051721-59052385	GM12878	blood:	n/a	n/a
3	ATF2	chr11:59051673-59052460	GM12878	blood:	n/a	n/a
4	ATF2	chr11:58980128-58981382	GM12878	blood:	n/a	n/a
5	ATF2	chr11:58983868-58985051	GM12878	blood:	n/a	n/a
6	ATF2	chr11:59034544-59035104	GM12878	blood:	n/a	n/a
7	ATF2	chr11:59026964-59027981	GM12878	blood:	n/a	n/a
8	ATF2	chr11:59034553-59035179	GM12878	blood:	n/a	n/a
9	ATF2	chr11:59040725-59041476	GM12878	blood:	n/a	n/a
10	ATF2	chr11:58980270-58981258	GM12878	blood:	n/a	n/a
11	ATF2	chr11:59040504-59041464	GM12878	blood:	n/a	n/a
12	ATF2	chr11:59027258-59027964	GM12878	blood:	n/a	n/a
13	ATF2	chr11:58983830-58984962	GM12878	blood:	n/a	n/a
14	BATF	chr11:59040781-59041398	GM12878	blood:	n/a	n/a
15	BATF	chr11:58983806-58984982	GM12878	blood:	n/a	n/a
16	BATF	chr11:59027333-59027902	GM12878	blood:	n/a	chr11:59027461-59027471 chr11:59027596-59027604
17	BATF	chr11:58987823-58988110	GM12878	blood:	n/a	n/a
18	BATF	chr11:59027365-59027874	GM12878	blood:	n/a	chr11:59027461-59027471 chr11:59027596-59027604
19	BATF	chr11:59034600-59035093	GM12878	blood:	n/a	n/a
20	BATF	chr11:59034671-59035066	GM12878	blood:	n/a	n/a
21	BATF	chr11:58980509-58981044	GM12878	blood:	n/a	n/a
22	BATF	chr11:58986379-58986914	GM12878	blood:	n/a	n/a
23	BATF	chr11:59051747-59052352	GM12878	blood:	n/a	n/a
24	BATF	chr11:58984024-58984785	GM12878	blood:	n/a	n/a
25	BATF	chr11:59027049-59027304	GM12878	blood:	n/a	n/a
26	BATF	chr11:59040862-59041178	GM12878	blood:	n/a	n/a
27	BCL11A	chr11:59040773-59041283	GM12878	blood:	n/a	n/a
28	BCL11A	chr11:58980517-58980930	GM12878	blood:	n/a	n/a
29	BCL11A	chr11:59034625-59035073	GM12878	blood:	n/a	n/a
30	BCL11A	chr11:58984030-58984800	GM12878	blood:	n/a	chr11:58984449-58984458
31	BCL11A	chr11:59051702-59052336	GM12878	blood:	n/a	n/a
32	BCL11A	chr11:58983913-58984830	GM12878	blood:	n/a	chr11:58984449-58984458
33	BCL11A	chr11:59027359-59027832	GM12878	blood:	n/a	chr11:59027372-59027381
34	BCL11A	chr11:59051822-59052117	GM12878	blood:	n/a	n/a
35	BCL11A	chr11:58980660-58980974	GM12878	blood:	n/a	n/a
36	BCL11A	chr11:59040876-59041255	GM12878	blood:	n/a	n/a
37	BCL3	chr11:58983982-58984768	GM12878	blood:	n/a	chr11:58984449-58984458
38	BCL3	chr11:59027441-59027879	GM12878	blood:	n/a	n/a
39	BCL3	chr11:59034749-59035148	GM12878	blood:	n/a	n/a
40	BCL3	chr11:58983927-58984751	GM12878	blood:	n/a	chr11:58984449-58984458
41	BCLAF1	chr11:59034616-59035170	GM12878	blood:	n/a	n/a
42	BCLAF1	chr11:58990135-58990614	GM12878	blood:	n/a	n/a
43	BCLAF1	chr11:58983977-58984746	GM12878	blood:	n/a	chr11:58984449-58984458
44	BCLAF1	chr11:59051846-59052479	GM12878	blood:	n/a	n/a
45	BCLAF1	chr11:58980303-58981308	GM12878	blood:	n/a	chr11:58981058-58981067
46	BCLAF1	chr11:59027494-59027869	GM12878	blood:	n/a	n/a
47	BCLAF1	chr11:59040788-59041378	GM12878	blood:	n/a	n/a
48	BCLAF1	chr11:59051782-59052436	GM12878	blood:	n/a	n/a
49	BCLAF1	chr11:58983847-58984902	GM12878	blood:	n/a	chr11:58984449-58984458
50	BHLHE40	chr11:59051705-59052380	GM12878	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58980157-58980207	H1-hESC	embryonic stem cell:	embryo
2	chr11:58984446-58984496	ovcar-3	ovarian:	n/a
3	chr11:58984544-58984594	A549	lung:	n/a
4	chr11:58981043-58981093	HRCEpiC	kidney:	n/a
5	chr11:58981043-58981093	ovcar-3	ovarian:	n/a
6	chr11:58980377-58980427	MCF10A-Er-Src	breast:	n/a
7	chr11:58980377-58980427	Jurkat	blood:	n/a
8	chr11:58980502-58980552	MCF-7	breast:	n/a
9	chr11:58980157-58980207	HRCEpiC	kidney:	n/a
10	chr11:59015338-59015388	HMEC	breast:	n/a
11	chr11:58981095-58981145	HPAEpiC	pulmonary alveolar:	n/a
12	chr11:59015338-59015388	HEK293	kidney:	embryo
13	chr11:58980377-58980427	HRPEpiC	eye:	n/a
14	chr11:58981043-58981093	K562	blood:	n/a
15	chr11:58981095-58981145	Jurkat	blood:	n/a
16	chr11:58980157-58980207	HCT-116	colon:	n/a
17	chr11:58980157-58980207	NHBE	bronchial:	n/a
18	chr11:58990439-58990489	GM12878	blood:	n/a
19	chr11:58980502-58980552	GM19239	blood:	n/a
20	chr11:58984446-58984496	AoSMC	blood vessel:	n/a
21	chr11:58990439-58990489	HL-60	blood:	n/a
22	chr11:58984544-58984594	PrEC	prostate:	n/a
23	chr11:58980665-58980715	BJ	skin:	n/a
24	chr11:58981043-58981093	AG04449	skin:	fetal
25	chr11:58984544-58984594	PFSK-1	brain:	n/a
26	chr11:58981043-58981093	A549	lung:	n/a
27	chr11:58990439-58990489	T-47D	breast:	n/a
28	chr11:59015338-59015388	ovcar-3	ovarian:	n/a
29	chr11:58990439-58990489	NHBE	bronchial:	n/a
30	chr11:58981043-58981093	U87	brain:	n/a
31	chr11:58980377-58980427	K562	blood:	n/a
32	chr11:58980157-58980207	Hela-S3	cervix:	n/a
33	chr11:58980157-58980207	Jurkat	blood:	n/a
34	chr11:58980377-58980427	SK-N-MC	brain:	n/a
35	chr11:58980157-58980207	Hepatocyte	liver:	n/a
36	chr11:58984544-58984594	GM12878	blood:	n/a
37	chr11:58980502-58980552	HEEpiC	esophagus:	n/a
38	chr11:58980377-58980427	HUVEC	blood vessel:	n/a
39	chr11:58984446-58984496	AG09319	gingival:	n/a
40	chr11:58984446-58984496	Caco-2	colon:	n/a
41	chr11:58980502-58980552	NT2-D1	testis:	n/a
42	chr11:58981095-58981145	K562	blood:	n/a
43	chr11:58980502-58980552	AG09309	skin:	n/a
44	chr11:58984544-58984594	Hepatocyte	liver:	n/a
45	chr11:58980502-58980552	AG10803	skin:	n/a
46	chr11:59015338-59015388	MCF-7	breast:	n/a
47	chr11:58990439-58990489	SAEC	small airway:	n/a
48	chr11:58980502-58980552	BE2_C	brain:	n/a
49	chr11:58980502-58980552	GM12892	blood:	n/a
50	chr11:58980157-58980207	GM12891	blood:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:59032632..59035314-chr11:59038415..59042026,3	MCF-7	breast:
2	chr11:58985014..58986524-chr11:58989804..58992131,2	K562	blood:
3	chr11:59030502..59031404-chr11:59051922..59052691,3	MCF-7	breast:
4	chr11:58975142..58976053-chr11:58985350..58986017,2	MCF-7	breast:
5	chr11:58985014..58986524-chr11:58989804..58992131,2	K562	blood:
6	chr11:58990211..58992297-chr11:58995837..58998568,2	K562	blood:
7	chr11:59022960..59025371-chr11:59027303..59028814,2	K562	blood:
8	chr11:58996924..58998524-chr11:59001703..59003947,2	K562	blood:
9	chr11:59015910..59019299-chr11:59020414..59023026,3	K562	blood:
10	chr11:59020470..59022310-chr11:59023811..59025321,2	K562	blood:
11	chr11:58996924..58998524-chr11:59001703..59003947,2	K562	blood:
12	chr11:59020470..59022310-chr11:59023811..59025321,2	K562	blood:
13	chr11:58938664..58939165-chr11:59051489..59052229,2	K562	blood:
14	chr11:58990211..58992297-chr11:58995837..58998568,2	K562	blood:
15	chr11:58937186..58939247-chr11:58980596..58982199,2	K562	blood:
16	chr11:59032632..59035314-chr11:59038415..59042026,3	MCF-7	breast:
17	chr11:59022960..59025371-chr11:59027303..59028814,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MPEG1-1	chr11:59036349-59039081	ENSG00000214797
2	lnc-MPEG1-3	chr11:58981880-58982172	NONHSAT021517
3	lnc-MPEG1-1	chr11:59051435-59051506	ENSG00000214797

No data

Variant related genes	Relation type
SLC25A47P1	TF binding region
MPEG1	TF binding region
RN7SL42P	TF binding region
ENSG00000225802	TF binding region
ENSG00000214797	TF binding region
SLC25A47P1	CpG island
MPEG1	CpG island
RN7SL42P	CpG island
ENSG00000225802	CpG island
ENSG00000214797	CpG island
ENSG00000110042	chromatin interactions
ENSG00000225802	chromatin interactions
ENSG00000254799	chromatin interactions
RBL2	miRNA target sites
GATA6	miRNA target sites

Extended variants
information (count: 2501 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:2501 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200150659	chr11:58979320-58979321	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs540845788	chr11:58979321-58979322	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs182852785	chr11:58979322-58979323	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs529935404	chr11:58979329-58979330	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs370919527	chr11:58979349-58979350	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs377757190	chr11:58979368-58979369	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs551486642	chr11:58979380-58979381	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs371318082	chr11:58979389-58979390	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs11229878	chr11:58979393-58979394	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs562894677	chr11:58979412-58979413	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs367733685	chr11:58979413-58979414	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs370268323	chr11:58979425-58979426	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs374800011	chr11:58979445-58979446	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs374105942	chr11:58979520-58979521	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs397832527	chr11:58979530-58979531	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs368175940	chr11:58979553-58979554	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs367999964	chr11:58979562-58979563	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs372079624	chr11:58979565-58979566	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs375135198	chr11:58979568-58979569	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs4084080	chr11:58979587-58979588	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs551823490	chr11:58979597-58979598	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs372290102	chr11:58979598-58979599	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs186806583	chr11:58979599-58979600	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs191524398	chr11:58979606-58979607	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs200053414	chr11:58979633-58979634	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs369015266	chr11:58979634-58979635	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs200732824	chr11:58979641-58979642	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs138151828	chr11:58979643-58979644	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs555005923	chr11:58979644-58979645	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs576469915	chr11:58979659-58979660	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs199564440	chr11:58979668-58979669	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs559035712	chr11:58979672-58979673	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs566154687	chr11:58979673-58979674	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs369379839	chr11:58979682-58979683	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs577249718	chr11:58979690-58979691	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs373577741	chr11:58979693-58979694	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs142542166	chr11:58979709-58979710	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs370837054	chr11:58979712-58979713	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs76683796	chr11:58979722-58979723	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs377486743	chr11:58979726-58979727	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs78500826	chr11:58979739-58979740	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs370351139	chr11:58979748-58979749	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs201984349	chr11:58979762-58979763	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs541679679	chr11:58979779-58979780	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs200143926	chr11:58979794-58979795	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs370491206	chr11:58979797-58979798	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs146004268	chr11:58979810-58979811	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs530399719	chr11:58979830-58979831	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs368341399	chr11:58979843-58979844	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs200830689	chr11:58979848-58979849	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:728 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58973400-58983200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr11:58973600-58982000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr11:58973800-58979600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr11:58973800-58984000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr11:58974800-58980200	Weak transcription	Brain Germinal Matrix	brain
6	chr11:58975000-58980400	Weak transcription	Fetal Brain Female	brain
7	chr11:58975200-58980000	Weak transcription	Lung	lung
8	chr11:58975400-58980000	Active TSS	Duodenum Mucosa	Duodenum
9	chr11:58975400-58986600	Weak transcription	Gastric	stomach
10	chr11:58975600-58980200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr11:58975800-58980000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr11:58975800-58980400	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
13	chr11:58975800-58980400	Active TSS	Fetal Intestine Large	intestine
14	chr11:58975800-58980800	Active TSS	Adipose Nuclei	Adipose
15	chr11:58975800-58981800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr11:58976000-58980400	Active TSS	Placenta	Placenta
17	chr11:58976000-58989400	Weak transcription	Stomach Mucosa	stomach
18	chr11:58976200-58980400	Active TSS	Duodenum Smooth Muscle	Duodenum
19	chr11:58976200-58980400	Active TSS	Fetal Muscle Leg	muscle
20	chr11:58976400-58981000	Active TSS	Rectal Mucosa Donor 29	rectum
21	chr11:58976600-58980400	Active TSS	Liver	Liver
22	chr11:58977000-58980400	Active TSS	Rectal Mucosa Donor 31	rectum
23	chr11:58977000-58981000	Flanking Active TSS	Primary B cells from cord blood	blood
24	chr11:58977200-58980200	Active TSS	Primary monocytes fromperipheralblood	blood
25	chr11:58977200-58981200	Active TSS	Rectal Smooth Muscle	rectum
26	chr11:58977400-58980200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr11:58977400-58981000	Weak transcription	HSMMtube	muscle
28	chr11:58977400-58981400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:58977600-58981600	Flanking Active TSS	GM12878-XiMat	blood
30	chr11:58977600-58984000	Weak transcription	Fetal Lung	lung
31	chr11:58977800-58980400	Active TSS	Spleen	Spleen
32	chr11:58977800-58980600	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
33	chr11:58978000-58980000	Weak transcription	Fetal Kidney	kidney
34	chr11:58978000-58980400	Active TSS	Left Ventricle	heart
35	chr11:58978000-58980400	Active TSS	Skeletal Muscle Female	skeletal muscle
36	chr11:58978200-58980000	Weak transcription	Primary hematopoietic stem cells	blood
37	chr11:58978200-58981000	Flanking Active TSS	Primary B cells from peripheral blood	blood
38	chr11:58978400-58980400	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
39	chr11:58978600-58979800	Active TSS	Pancreas	Pancrea
40	chr11:58978600-58980000	Weak transcription	Fetal Thymus	thymus
41	chr11:58978600-58984000	Weak transcription	Colon Smooth Muscle	Colon
42	chr11:58978800-58979600	Weak transcription	Fetal Muscle Trunk	muscle
43	chr11:58978800-58980200	Active TSS	Brain Substantia Nigra	brain
44	chr11:58979000-58979400	Active TSS	Fetal Stomach	stomach
45	chr11:58979000-58980200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr11:58979200-58979400	Active TSS	Brain Hippocampus Middle	brain
47	chr11:58979200-58979800	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr11:58979200-58980400	Active TSS	Fetal Intestine Small	intestine
49	chr11:58979200-58989600	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr11:58979400-58980000	Weak transcription	Brain Hippocampus Middle	brain

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