Variant report

Variant	nsv1053528
Chromosome Location	chr11:48086151-48125731
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:497)
CpG islands
(count:183)
Chromatin interactive
region (count:42)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:497 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:48118839-48119112	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:48114969-48116284	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:48095041-48095124	K562	blood:	n/a	n/a
4	ARID3A	chr11:48123329-48123998	HepG2	liver:	n/a	n/a
5	ATF2	chr11:48094862-48095450	GM12878	blood:	n/a	n/a
6	BACH1	chr11:48119683-48119696	K562	blood:	n/a	n/a
7	BACH1	chr11:48110331-48110562	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr11:48094903-48095273	GM12878	blood:	n/a	n/a
9	BATF	chr11:48115348-48115634	GM12878	blood:	n/a	n/a
10	BCL11A	chr11:48115355-48115560	GM12878	blood:	n/a	n/a
11	BCL3	chr11:48115343-48115664	GM12878	blood:	n/a	n/a
12	BCLAF1	chr11:48094857-48095248	GM12878	blood:	n/a	n/a
13	BCLAF1	chr11:48115236-48115686	GM12878	blood:	n/a	n/a
14	BHLHE40	chr11:48103167-48103191	K562	blood:	n/a	n/a
15	BHLHE40	chr11:48115378-48115650	K562	blood:	n/a	n/a
16	BRCA1	chr11:48093751-48093761	HepG2	liver:	n/a	n/a
17	CEBPB	chr11:48096050-48096341	Hela-S3	cervix:	n/a	chr11:48096193-48096206
18	CEBPB	chr11:48096132-48096309	K562	blood:	n/a	chr11:48096193-48096206
19	CEBPB	chr11:48122314-48122514	K562	blood:	n/a	n/a
20	CEBPB	chr11:48090968-48091162	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr11:48118713-48119122	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr11:48104258-48104526	HepG2	liver:	n/a	chr11:48104338-48104349 chr11:48104335-48104352
23	CEBPB	chr11:48091014-48091149	K562	blood:	n/a	n/a
24	CEBPB	chr11:48115956-48116106	HepG2	liver:	n/a	n/a
25	CEBPB	chr11:48122463-48122467	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr11:48094837-48094838	GM12878	blood:	n/a	n/a
27	CREB1	chr11:48125459-48125829	A549	lung:	n/a	n/a
28	CTCF	chr11:48102540-48102690	GM12864	blood:	n/a	n/a
29	CTCF	chr11:48118600-48118750	GM12870	blood:	n/a	chr11:48118677-48118686
30	CTCF	chr11:48102760-48102910	AG10803	skin:	n/a	chr11:48102792-48102805
31	CTCF	chr11:48118500-48118650	HAc	cerebellar:	n/a	n/a
32	CTCF	chr11:48102820-48102847	ProgFib	skin:	n/a	n/a
33	CTCF	chr11:48116393-48116398	K562	blood:	n/a	n/a
34	CTCF	chr11:48118640-48118790	HCT-116	colon:	n/a	chr11:48118677-48118686
35	CTCF	chr11:48118440-48118590	NHEK	skin:	n/a	n/a
36	CTCF	chr11:48118655-48118716	MCF-7	breast:	n/a	chr11:48118677-48118686
37	CTCF	chr11:48118620-48118770	HEEpiC	esophagus:	n/a	chr11:48118677-48118686
38	CTCF	chr11:48102720-48102870	AG09309	skin:	n/a	chr11:48102792-48102805
39	CTCF	chr11:48102660-48102810	AG09309	skin:	n/a	chr11:48102792-48102805
40	CTCF	chr11:48118640-48118790	AG09319	gingival:	n/a	chr11:48118677-48118686
41	CTCF	chr11:48102680-48102830	HCFaa	heart:	n/a	chr11:48102792-48102805
42	CTCF	chr11:48118620-48118770	NHEK	skin:	n/a	chr11:48118677-48118686
43	CTCF	chr11:48118540-48118690	AoAF	blood vessel:	n/a	chr11:48118677-48118686
44	CTCF	chr11:48118640-48118790	HBMEC	blood vessel:	n/a	chr11:48118677-48118686
45	CTCF	chr11:48118603-48118767	H1-hESC	embryonic stem cell:	n/a	chr11:48118677-48118686
46	CTCF	chr11:48118664-48118729	MCF-7	breast:	n/a	chr11:48118677-48118686
47	CTCF	chr11:48118638-48118729	MCF-7	breast:	n/a	chr11:48118677-48118686
48	CTCF	chr11:48118600-48118750	MCF-7	breast:	n/a	chr11:48118677-48118686
49	CTCF	chr11:48118660-48118810	HRE	kidney:	n/a	chr11:48118677-48118686
50	CTCF	chr11:48118620-48118770	GM12871	blood:	n/a	chr11:48118677-48118686

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48118041-48118091	K562	blood:	n/a
2	chr11:48110045-48110095	HRE	kidney:	n/a
3	chr11:48118041-48118091	BE2_C	brain:	n/a
4	chr11:48110045-48110095	HRCEpiC	kidney:	n/a
5	chr11:48112253-48112303	SK-N-SH	brain:	n/a
6	chr11:48110045-48110095	AoSMC	blood vessel:	n/a
7	chr11:48112253-48112303	NT2-D1	testis:	n/a
8	chr11:48112253-48112303	HNPCEpiC	eye:	n/a
9	chr11:48118041-48118091	SAEC	small airway:	n/a
10	chr11:48118041-48118091	AoSMC	blood vessel:	n/a
11	chr11:48118041-48118091	A549	lung:	n/a
12	chr11:48112253-48112303	ECC-1	luminal epithelium:	n/a
13	chr11:48112253-48112303	ProgFib	skin:	n/a
14	chr11:48110045-48110095	K562	blood:	n/a
15	chr11:48112253-48112303	HRE	kidney:	n/a
16	chr11:48112253-48112303	HEEpiC	esophagus:	n/a
17	chr11:48118041-48118091	NH-A	brain:	n/a
18	chr11:48118041-48118091	GM12892	blood:	n/a
19	chr11:48112253-48112303	Caco-2	colon:	n/a
20	chr11:48118041-48118091	ovcar-3	ovarian:	n/a
21	chr11:48110045-48110095	MCF10A-Er-Src	breast:	n/a
22	chr11:48112253-48112303	HRPEpiC	eye:	n/a
23	chr11:48110045-48110095	A549	lung:	n/a
24	chr11:48110045-48110095	BE2_C	brain:	n/a
25	chr11:48110045-48110095	HNPCEpiC	eye:	n/a
26	chr11:48112253-48112303	HCT-116	colon:	n/a
27	chr11:48110045-48110095	BJ	skin:	n/a
28	chr11:48118041-48118091	HEK293	kidney:	embryo
29	chr11:48110045-48110095	HCM	heart:	n/a
30	chr11:48112253-48112303	AG09319	gingival:	n/a
31	chr11:48110045-48110095	ovcar-3	ovarian:	n/a
32	chr11:48110045-48110095	Hepatocyte	liver:	n/a
33	chr11:48112253-48112303	SKMC	muscle:	n/a
34	chr11:48112253-48112303	HCPEpiC	choroid plexus:	n/a
35	chr11:48118041-48118091	HIPEpiC	eye:	n/a
36	chr11:48110045-48110095	SAEC	small airway:	n/a
37	chr11:48110045-48110095	HPAEpiC	pulmonary alveolar:	n/a
38	chr11:48110045-48110095	HEK293	kidney:	embryo
39	chr11:48118041-48118091	HCF	heart:	n/a
40	chr11:48112253-48112303	GM12892	blood:	n/a
41	chr11:48110045-48110095	RPTEC	kidney:	n/a
42	chr11:48112253-48112303	AG04449	skin:	fetal
43	chr11:48112253-48112303	HMEC	breast:	n/a
44	chr11:48112253-48112303	NHDF-neo	bronchial:	n/a
45	chr11:48112253-48112303	HepG2	liver:	n/a
46	chr11:48118041-48118091	SK-N-SH	brain:	n/a
47	chr11:48112253-48112303	HRCEpiC	kidney:	n/a
48	chr11:48112253-48112303	NH-A	brain:	n/a
49	chr11:48112253-48112303	HL-60	blood:	n/a
50	chr11:48112253-48112303	BJ	skin:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:48082980..48084917-chr11:48096551..48099093,2	K562	blood:
2	chr11:47970432..47972132-chr11:48121699..48124423,2	K562	blood:
3	chr11:48101649..48104254-chr11:48106713..48109745,3	MCF-7	breast:
4	chr11:48105031..48106761-chr11:48108023..48109885,2	MCF-7	breast:
5	chr11:48087146..48090054-chr11:48094817..48096585,2	MCF-7	breast:
6	chr11:48097619..48099123-chr11:48100995..48103478,2	MCF-7	breast:
7	chr11:48099180..48102059-chr11:48102708..48105162,2	K562	blood:
8	chr11:48086913..48088924-chr11:48093954..48095544,2	K562	blood:
9	chr11:48086913..48088924-chr11:48093954..48095544,2	K562	blood:
10	chr11:48125100..48126917-chr11:48129444..48131504,2	MCF-7	breast:
11	chr11:48047876..48049953-chr11:48109269..48111434,2	MCF-7	breast:
12	chr11:48107721..48110377-chr11:48121800..48123863,2	MCF-7	breast:
13	chr11:48098800..48100999-chr11:48104120..48106582,2	MCF-7	breast:
14	chr11:47869473..47872069-chr11:48119800..48121931,2	MCF-7	breast:
15	chr11:48120614..48123449-chr11:48129423..48131714,2	MCF-7	breast:
16	chr11:48121014..48122957-chr11:48124539..48127155,2	K562	blood:
17	chr11:48109181..48111732-chr11:48113222..48115393,2	K562	blood:
18	chr11:48001457..48003735-chr11:48105234..48107341,2	K562	blood:
19	chr11:48092743..48095466-chr11:48097566..48099297,2	K562	blood:
20	chr11:48109181..48111732-chr11:48113222..48115393,2	K562	blood:
21	chr11:48105031..48106761-chr11:48108023..48109885,2	MCF-7	breast:
22	chr11:48081883..48084532-chr11:48088077..48090811,2	MCF-7	breast:
23	chr11:48098800..48100999-chr11:48104120..48106582,2	MCF-7	breast:
24	chr11:18993520..18994020-chr11:48120012..48120966,2	MCF-7	breast:
25	chr11:48093831..48096549-chr11:48096756..48099477,2	MCF-7	breast:
26	chr11:48101649..48104254-chr11:48106713..48109745,3	MCF-7	breast:
27	chr11:48087146..48090054-chr11:48094817..48096585,2	MCF-7	breast:
28	chr11:48108133..48109846-chr11:48110400..48112858,3	MCF-7	breast:
29	chr11:48092743..48095466-chr11:48097566..48099297,2	K562	blood:
30	chr11:48119543..48121197-chr11:48126844..48128670,2	K562	blood:
31	chr11:48099180..48102059-chr11:48102708..48105162,2	K562	blood:
32	chr11:48112031..48113821-chr11:48114417..48116008,2	K562	blood:
33	chr11:48108133..48109846-chr11:48110400..48112858,3	MCF-7	breast:
34	chr11:48083070..48085451-chr11:48088899..48092016,4	K562	blood:
35	chr11:48121014..48122957-chr11:48124539..48127155,2	K562	blood:
36	chr11:48097619..48099123-chr11:48100995..48103478,2	MCF-7	breast:
37	chr11:47868317..47870983-chr11:48125503..48128104,3	K562	blood:
38	chr11:48112031..48113821-chr11:48114417..48116008,2	K562	blood:
39	chr11:48081533..48083185-chr11:48091579..48093994,2	MCF-7	breast:
40	chr11:48093831..48096549-chr11:48096756..48099477,2	MCF-7	breast:
41	chr11:48107721..48110377-chr11:48121800..48123863,2	MCF-7	breast:
42	chr11:48077645..48080175-chr11:48086953..48089270,2	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3161	chr11:48118343-48118365	MIMAT0015035

No data

Variant related genes	Relation type
MIR3161	TF binding region
MIR3161	CpG island
ENSG00000149177	chromatin interactions
ENSG00000030066	chromatin interactions

Extended variants
information (count: 1346 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1346 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs58452311	chr11:48086151-48086152	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs368346668	chr11:48086194-48086195	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs61914730	chr11:48086217-48086218	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs184819348	chr11:48086234-48086235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188715615	chr11:48086242-48086243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534956650	chr11:48086250-48086251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572235187	chr11:48086265-48086266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs56020868	chr11:48086305-48086306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564121398	chr11:48086309-48086310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs532930542	chr11:48086315-48086316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs77559567	chr11:48086316-48086317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181553267	chr11:48086353-48086354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs527739649	chr11:48086376-48086377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546489189	chr11:48086380-48086381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563169982	chr11:48086392-48086393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs61914731	chr11:48086409-48086410	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs549238571	chr11:48086417-48086418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs151185169	chr11:48086448-48086449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538577221	chr11:48086451-48086452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140402339	chr11:48086452-48086453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150369251	chr11:48086464-48086465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571713860	chr11:48086465-48086466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537192667	chr11:48086468-48086469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs538633178	chr11:48086483-48086484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs557310628	chr11:48086492-48086493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185987855	chr11:48086516-48086517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs200226996	chr11:48086529-48086530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs146698354	chr11:48086530-48086531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35387232	chr11:48086532-48086533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs190831660	chr11:48086553-48086554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs12798259	chr11:48086557-48086558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs61139660	chr11:48086580-48086581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs181923255	chr11:48086692-48086693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs555657481	chr11:48086756-48086757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs372934705	chr11:48086794-48086795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs185976866	chr11:48086813-48086814	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541223237	chr11:48086815-48086816	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs61914732	chr11:48086845-48086846	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs190800191	chr11:48086857-48086858	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs543180184	chr11:48086858-48086859	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183007621	chr11:48086931-48086932	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs528849872	chr11:48086951-48086952	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546913439	chr11:48086955-48086956	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs542224331	chr11:48086983-48086984	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs554288416	chr11:48087082-48087083	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs76583296	chr11:48087089-48087090	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528809160	chr11:48087099-48087100	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs551553833	chr11:48087119-48087120	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187964717	chr11:48087216-48087217	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs531015129	chr11:48087307-48087308	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Glioblastoma multiforme	21390271	CNVD
Acute lymphoblastic leukemia	20699438	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21990379	CNVD

Chromatin state (count:1578 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48077400-48088600	Weak transcription	Right Atrium	heart
2	chr11:48077800-48088800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:48078200-48090600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr11:48078600-48086400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr11:48078600-48088600	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr11:48078800-48093000	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr11:48079200-48088800	Weak transcription	Esophagus	oesophagus
8	chr11:48079200-48102800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr11:48080600-48100800	Weak transcription	Spleen	Spleen
10	chr11:48081200-48094600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr11:48081600-48097200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr11:48081800-48101600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr11:48082000-48096000	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr11:48082200-48087600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr11:48082200-48088600	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr11:48082400-48086600	Enhancers	Placenta	Placenta
17	chr11:48083200-48088200	Weak transcription	Gastric	stomach
18	chr11:48083200-48088600	Weak transcription	Lung	lung
19	chr11:48083400-48087600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr11:48083400-48088200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr11:48083400-48088400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr11:48083600-48086600	Enhancers	Fetal Muscle Leg	muscle
23	chr11:48084000-48086200	Enhancers	Placenta Amnion	Placenta Amnion
24	chr11:48084000-48089200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr11:48084000-48090200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr11:48084200-48086400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr11:48084200-48086400	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr11:48084200-48089800	Enhancers	Brain Hippocampus Middle	brain
29	chr11:48084400-48086200	Enhancers	Primary T helper cells fromperipheralblood	blood
30	chr11:48084400-48086200	Enhancers	Liver	Liver
31	chr11:48084400-48087000	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr11:48084800-48086200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr11:48084800-48089200	Enhancers	Fetal Stomach	stomach
34	chr11:48085000-48086200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr11:48085000-48086200	Enhancers	Brain Anterior Caudate	brain
36	chr11:48085000-48086200	Enhancers	Brain Substantia Nigra	brain
37	chr11:48085000-48086200	Enhancers	Fetal Lung	lung
38	chr11:48085000-48086200	Enhancers	Left Ventricle	heart
39	chr11:48085000-48086200	Enhancers	Psoas Muscle	Psoas
40	chr11:48085000-48086200	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr11:48085000-48086200	Enhancers	HUVEC	blood vessel
42	chr11:48085000-48086400	Enhancers	Brain Cingulate Gyrus	brain
43	chr11:48085200-48086200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr11:48085200-48086200	Enhancers	Adipose Nuclei	Adipose
45	chr11:48085400-48086200	Flanking Active TSS	Osteobl	bone
46	chr11:48085400-48087800	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr11:48085600-48086200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr11:48085600-48086200	Enhancers	Primary T cells fromperipheralblood	blood
49	chr11:48085600-48086200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr11:48085600-48086200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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