Variant report

Variant	nsv372
Chromosome Location	chr11:68311070-68340142
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:177)
CpG islands
(count:0)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:177 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr11:68323548-68323554	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr11:68314113-68314312	A549	lung:	n/a	n/a
3	CEBPB	chr11:68320068-68320422	A549	lung:	n/a	chr11:68320248-68320259
4	CEBPB	chr11:68320173-68320373	A549	lung:	n/a	chr11:68320248-68320259
5	CEBPB	chr11:68320134-68320340	HepG2	liver:	n/a	chr11:68320248-68320259
6	CEBPB	chr11:68320168-68320398	K562	blood:	n/a	chr11:68320248-68320259
7	CEBPB	chr11:68320084-68320408	Hela-S3	cervix:	n/a	chr11:68320248-68320259
8	CTCF	chr11:68318840-68318990	HBMEC	blood vessel:	n/a	n/a
9	CTCF	chr11:68318780-68318930	HPAF	blood vessel:	n/a	n/a
10	CTCF	chr11:68318873-68318891	HepG2	liver:	n/a	n/a
11	CTCF	chr11:68318800-68318950	HCPEpiC	choroid plexus:	n/a	n/a
12	CTCF	chr11:68318800-68318950	HPAF	blood vessel:	n/a	n/a
13	CTCF	chr11:68332831-68332839	Fibrobl	skin:	n/a	n/a
14	CTCF	chr11:68318760-68318910	HCM	heart:	n/a	n/a
15	CTCF	chr11:68330065-68330123	GM20000	blood:	n/a	n/a
16	CTCF	chr11:68318899-68319013	Pancreas_OC	pancreas:	n/a	n/a
17	CTCF	chr11:68330580-68330730	A549	lung:	n/a	n/a
18	CTCF	chr11:68318800-68318950	AG04450	lung:	n/a	n/a
19	CTCF	chr11:68318800-68318950	NHLF	lung:	n/a	n/a
20	CTCF	chr11:68318820-68318970	HVMF	connective:	n/a	n/a
21	CTCF	chr11:68318864-68318883	Pancreas_OC	pancreas:	n/a	n/a
22	CTCF	chr11:68318789-68318937	K562	blood:	n/a	n/a
23	CTCF	chr11:68318800-68318950	HPF	lung:	n/a	n/a
24	CTCF	chr11:68318820-68318970	MCF-7	breast:	n/a	n/a
25	CTCF	chr11:68311100-68311250	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr11:68322420-68322570	HepG2	liver:	n/a	n/a
27	CTCF	chr11:68332783-68332827	Fibrobl	skin:	n/a	n/a
28	CTCF	chr11:68318780-68318930	HPF	lung:	n/a	n/a
29	CTCF	chr11:68313280-68313430	Caco-2	colon:	n/a	n/a
30	CTCF	chr11:68318760-68318910	HVMF	connective:	n/a	n/a
31	CTCF	chr11:68318760-68318910	HMF	breast:	n/a	n/a
32	E2F4	chr11:68324153-68324353	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr11:68338039-68338339	MCF10A-Er-Src	breast:	n/a	chr11:68338323-68338332
34	EBF1	chr11:68337029-68337126	GM12878	blood:	n/a	n/a
35	ELF1	chr11:68311825-68312086	GM12878	blood:	n/a	chr11:68312013-68312025
36	ELF1	chr11:68314069-68314364	K562	blood:	n/a	chr11:68314172-68314185
37	EP300	chr11:68334835-68334901	GM12878	blood:	n/a	n/a
38	EP300	chr11:68337546-68337553	GM12878	blood:	n/a	n/a
39	EP300	chr11:68330310-68330445	K562	blood:	n/a	n/a
40	FOS	chr11:68314129-68314289	MCF10A-Er-Src	breast:	n/a	chr11:68314210-68314221
41	FOS	chr11:68327655-68328083	HUVEC	blood vessel:	n/a	n/a
42	FOS	chr11:68314053-68314409	HUVEC	blood vessel:	n/a	chr11:68314210-68314221
43	FOSL2	chr11:68314001-68314388	HepG2	liver:	n/a	n/a
44	FOXA1	chr11:68314085-68314434	HepG2	liver:	n/a	n/a
45	FOXA1	chr11:68314115-68314347	HepG2	liver:	n/a	n/a
46	FOXA1	chr11:68314058-68314329	HepG2	liver:	n/a	n/a
47	FOXA2	chr11:68314053-68314454	A549	lung:	n/a	n/a
48	FOXA2	chr11:68313906-68314434	A549	lung:	n/a	n/a
49	IRF1	chr11:68326518-68326532	K562	blood:	n/a	n/a
50	IRF1	chr11:68336795-68336888	K562	blood:	n/a	n/a

No data

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:68228323..68230365-chr11:68308958..68311493,2	K562	blood:
2	chr11:68322130..68324793-chr11:68337499..68339830,2	MCF-7	breast:
3	chr11:68227855..68229553-chr11:68312062..68313959,2	MCF-7	breast:
4	chr11:68233880..68236126-chr11:68339723..68341639,2	K562	blood:
5	chr11:68322674..68324269-chr11:68334762..68337571,2	MCF-7	breast:
6	chr11:68311501..68313206-chr11:68322676..68324188,2	MCF-7	breast:
7	chr11:68334224..68337075-chr11:68354866..68356879,2	K562	blood:
8	chr11:68311700..68314036-chr11:68318661..68320225,2	MCF-7	breast:
9	chr11:68312850..68315116-chr11:68319769..68322126,2	K562	blood:
10	chr11:68293951..68296055-chr11:68321896..68323728,2	MCF-7	breast:
11	chr11:68321048..68322861-chr11:68335454..68337526,2	K562	blood:
12	chr11:68311501..68313206-chr11:68322676..68324188,2	MCF-7	breast:
13	chr11:68335057..68338909-chr11:68339810..68344152,5	K562	blood:
14	chr11:68312589..68314305-chr11:68315878..68319333,3	K562	blood:
15	chr11:68324963..68327580-chr11:68329924..68332655,2	K562	blood:
16	chr11:68228084..68229879-chr11:68319760..68322370,2	MCF-7	breast:
17	chr11:68298372..68300264-chr11:68312543..68314090,2	MCF-7	breast:
18	chr11:68310824..68313673-chr11:68317930..68320124,2	MCF-7	breast:
19	chr11:68312589..68314305-chr11:68315878..68319333,3	K562	blood:
20	chr11:68330297..68331992-chr11:68334158..68336760,2	K562	blood:
21	chr11:68312850..68315116-chr11:68319769..68322126,2	K562	blood:
22	chr11:68311700..68314036-chr11:68318661..68320225,2	MCF-7	breast:
23	chr11:68332127..68334202-chr11:68341163..68343837,2	MCF-7	breast:
24	chr11:68322674..68324269-chr11:68334762..68337571,2	MCF-7	breast:
25	chr11:68315876..68319088-chr11:68319892..68321906,3	K562	blood:
26	chr11:68324963..68327580-chr11:68329924..68332655,2	K562	blood:
27	chr11:68310824..68313673-chr11:68317930..68320124,2	MCF-7	breast:
28	chr11:68321048..68322861-chr11:68335454..68337526,2	K562	blood:
29	chr11:68330314..68332415-chr11:68334560..68336909,2	MCF-7	breast:
30	chr11:68315876..68319088-chr11:68319892..68321906,3	K562	blood:
31	chr11:68227373..68229152-chr11:68311187..68313103,2	MCF-7	breast:
32	chr11:68259609..68262203-chr11:68317326..68319808,2	K562	blood:

No data

Variant related genes	Relation type
PPP6R3	TF binding region
ENSG00000110075	chromatin interactions

Extended variants
information (count: 1179 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1179 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571958936	chr11:68311070-68311071	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
2	rs535045776	chr11:68311118-68311119	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs539375250	chr11:68311121-68311122	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
4	rs149687539	chr11:68311132-68311133	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs569179273	chr11:68311134-68311135	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs34420448	chr11:68311140-68311141	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs144482356	chr11:68311189-68311190	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs554769897	chr11:68311190-68311191	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs185469117	chr11:68311205-68311206	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs534500509	chr11:68311212-68311213	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs139713540	chr11:68311274-68311275	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs144359459	chr11:68311287-68311288	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs544926779	chr11:68311297-68311298	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs545169527	chr11:68311313-68311314	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs146637073	chr11:68311320-68311321	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs189883736	chr11:68311338-68311339	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs141425093	chr11:68311399-68311400	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs142294055	chr11:68311422-68311423	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs79964044	chr11:68311449-68311450	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs151243884	chr11:68311459-68311460	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs140513663	chr11:68311485-68311486	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs182600904	chr11:68311513-68311514	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs551310159	chr11:68311576-68311577	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs569186164	chr11:68311588-68311589	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs371373785	chr11:68311688-68311689	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs530039233	chr11:68311711-68311712	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs78014180	chr11:68311733-68311734	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs566837291	chr11:68311764-68311765	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs534058787	chr11:68311765-68311766	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs542374563	chr11:68311787-68311788	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs17149166	chr11:68311796-68311797	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs538506267	chr11:68311804-68311805	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs556976362	chr11:68311809-68311810	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs575540075	chr11:68311850-68311851	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs542247356	chr11:68311906-68311907	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs187676631	chr11:68311923-68311924	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs572952307	chr11:68311927-68311928	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs540351161	chr11:68311936-68311937	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs565443497	chr11:68311937-68311938	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs532761115	chr11:68311975-68311976	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs113781374	chr11:68311976-68311977	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs150434316	chr11:68311980-68311981	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs115794993	chr11:68311988-68311989	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs530459629	chr11:68311996-68311997	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs367827774	chr11:68311997-68311998	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs116292300	chr11:68312003-68312004	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs370255391	chr11:68312016-68312017	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs566882469	chr11:68312027-68312028	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs527748964	chr11:68312038-68312039	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs7935578	chr11:68312060-68312061	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Acute myeloid leukemia	20729466	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
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	22860045	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	21399695	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21373257	CNVD
speech delay	21373257	CNVD
small cell lung cancer	17426248	CNVD
Gastric cancer	18160780	CNVD
Lung cancer	21569311	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1215 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:68277600-68336000	Strong transcription	Dnd41	blood
2	chr11:68283000-68358200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr11:68296600-68316800	Strong transcription	Primary B cells from peripheral blood	blood
4	chr11:68299200-68384000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr11:68300600-68313800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr11:68301000-68313400	Strong transcription	Primary T cells from cord blood	blood
7	chr11:68301200-68312800	Weak transcription	Stomach Mucosa	stomach
8	chr11:68301600-68316800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr11:68302800-68313400	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr11:68303800-68317000	Strong transcription	Liver	Liver
11	chr11:68303800-68317400	Strong transcription	Primary B cells from cord blood	blood
12	chr11:68304000-68384400	Strong transcription	Rectal Mucosa Donor 29	rectum
13	chr11:68304400-68317000	Weak transcription	Small Intestine	intestine
14	chr11:68304800-68313200	Strong transcription	Primary monocytes fromperipheralblood	blood
15	chr11:68305000-68317000	Strong transcription	Duodenum Mucosa	Duodenum
16	chr11:68305200-68313200	Strong transcription	Primary neutrophils fromperipheralblood	blood
17	chr11:68305200-68316600	Strong transcription	Rectal Mucosa Donor 31	rectum
18	chr11:68305200-68316800	Strong transcription	Fetal Intestine Large	intestine
19	chr11:68305200-68317000	Strong transcription	Thymus	Thymus
20	chr11:68305400-68316800	Strong transcription	Fetal Muscle Leg	muscle
21	chr11:68305600-68312400	Strong transcription	Fetal Brain Female	brain
22	chr11:68306000-68312000	Genic enhancers	HUES6 Cell Line	embryonic stem cell
23	chr11:68306000-68312000	Strong transcription	Brain Germinal Matrix	brain
24	chr11:68306200-68312200	Strong transcription	Fetal Intestine Small	intestine
25	chr11:68306200-68313800	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr11:68306800-68318200	Genic enhancers	Skeletal Muscle Female	skeletal muscle
27	chr11:68307000-68311600	Genic enhancers	Primary T helper cells PMA-I stimulated	--
28	chr11:68307400-68326600	Weak transcription	Fetal Brain Male	brain
29	chr11:68307600-68312800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr11:68307600-68313000	Weak transcription	HSMMtube	muscle
31	chr11:68307600-68338800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr11:68307800-68319400	Weak transcription	Fetal Kidney	kidney
33	chr11:68308600-68311200	Enhancers	Left Ventricle	heart
34	chr11:68308600-68311600	Genic enhancers	Skeletal Muscle Male	skeletal muscle
35	chr11:68308600-68311800	Enhancers	Colon Smooth Muscle	Colon
36	chr11:68308600-68312000	Genic enhancers	H1 Cell Line	embryonic stem cell
37	chr11:68308600-68312000	Genic enhancers	Primary T cells fromperipheralblood	blood
38	chr11:68308600-68313200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr11:68308600-68324200	Strong transcription	GM12878-XiMat	blood
40	chr11:68308800-68311600	Genic enhancers	Placenta	Placenta
41	chr11:68308800-68327200	Strong transcription	Hela-S3	cervix
42	chr11:68309000-68311200	Enhancers	Brain Hippocampus Middle	brain
43	chr11:68309000-68312000	Enhancers	Placenta Amnion	Placenta Amnion
44	chr11:68309200-68311400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr11:68309200-68311800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr11:68309200-68312000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr11:68309200-68312000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr11:68309200-68312200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr11:68309200-68313600	Strong transcription	HepG2	liver
50	chr11:68309200-68315400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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