EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS197-03882 
Organism
Homo sapiens 
Tissue/cell
ZR75-30 
Coordinate
chr11:65148100-65149040 
Target genes
Number: 45             
NameEnsembl ID
SF1ENSG00000168066
MEN1ENSG00000133895
EHD1ENSG00000110047
ARL2ENSG00000213465
SNX15ENSG00000110025
SAC3D1ENSG00000168061
NAALADL1ENSG00000168060
CDCA5ENSG00000146670
ZFPL1ENSG00000162300
C11orf2ENSG00000149823
AP003068.6ENSG00000187066
AP003068.9ENSG00000254501
TM7SF2ENSG00000149809
AP003068.12ENSG00000255173
ZNHIT2ENSG00000174276
MRPL49ENSG00000149792
FAUENSG00000149806
SYVN1ENSG00000162298
AP003068.17ENSG00000255058
SPDYCENSG00000204710
AP003068.18ENSG00000255200
CAPN1ENSG00000014216
AP003068.23ENSG00000254614
SLC22A20ENSG00000197847
POLA2ENSG00000014138
CDC42EP2ENSG00000149798
DPF2ENSG00000133884
TIGD3ENSG00000173825
SLC25A45ENSG00000162241
FRMD8ENSG00000126391
NEAT1ENSG00000245532
MIR612ENSG00000207727
AP000769.1ENSG00000173727
MALAT1ENSG00000251562
SCYL1ENSG00000142186
LTBP3ENSG00000168056
RP11ENSG00000260233
SSSCA1ENSG00000173465
FAM89BENSG00000176973
EHBP1L1ENSG00000173442
MAP3K11ENSG00000173327
PCNXL3ENSG00000197136
SIPA1ENSG00000213445
RELAENSG00000173039
RNASEH2CENSG00000172922
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NR2C2MA0504.1chr11:65148377-65148392TGAGGTCAAAGGTGA+6.3
Nr2f6MA0677.1chr11:65148378-65148392GAGGTCAAAGGTGA+6.59
RxraMA0512.2chr11:65148378-65148392GAGGTCAAAGGTGA+6.65
ZNF263MA0528.1chr11:65148137-65148158GCTTCTCCCCTCCCCTCCACC-6.16
Number of super-enhancer constituents: 14             
IDCoordinateTissue/cell
SE_06631chr11:65145999-65161052Brain_Hippocampus_Middle
SE_15241chr11:65148147-65155374CD4_Memory_Primary_7pool
SE_19864chr11:65148895-65155106CD4p_CD25-_Il17p_PMAstim_Th17
SE_20457chr11:65148872-65151186CD56
SE_22846chr11:65148732-65154998CD8_primiary
SE_27990chr11:65144554-65154911Fetal_Intestine
SE_28982chr11:65144537-65154947Fetal_Intestine_Large
SE_34935chr11:65147086-65155327HeLa
SE_41444chr11:65147327-65155112Left_Ventricle
SE_43022chr11:65146897-65153444Lung
SE_47549chr11:65146153-65151062Pancreas
SE_52899chr11:65146765-65153405Small_Intestine
SE_53834chr11:65148822-65154999Spleen
SE_65492chr11:65144518-65155720Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr116514820065148400
chr116514840065148600
Enhancer Sequence
GCCCTGATGG GGGTCATGCC TGGGCACCTG CAGAGGAGCT TCTCCCCTCC CCTCCACCTG 60
CCCACTGCCT AGCCCTGCCC TCCACAGCAG AGGCTGGTTC TGGAGTTTGG GGGAGGTCGC 120
ACCCCCAGGA GGCAGGTTCA GAACGTCCCT CTCTTTCTCC TAAGAGGAAT GCCACCCAGA 180
AGCTGGGCTG GGACCACAGC ACAACAGGCC TCAGGGCCCG GGACTGCGGC CCACAGCCAG 240
GTGGGGCAGA GGCCCAGAGG GGACTCAGGA CAGCAGGTGA GGTCAAAGGT GAACTTCCTT 300
TGTAAGCCCA ACAGGGTGGG CCTGGAGAGC AGGGCTCAAG GTATAGGGTG CTCACCTGGC 360
TCTCCCGCCC TCTGCAGGTG TCAGGCAGAG TGGCCTTGGA AGGCAGAGGC AGCACCCTCC 420
CACCTGTGCC TTCCTCTCTT CTTCCCATCG GCCACTCCCC AGAGGACTGG GGACAGCTGG 480
CTCTGGGGTG CTCCACGGAA CCCAGACTTT TTTTTTTTGA CACAGGGTCT TGCTGGTGTT 540
GTCCAGGCTG GAGTGCAGTG GCATGATCAT GGCTCATTGC AGCTTCAACC TCCTGAGCTT 600
AAGGGCTCCT TCCACCTCAG CCTCTGGAGT AGTTGGGACC ACAGGCGTGC GCCACCGCGC 660
CTGGCTAATT TTTGTATTTT TAGTAGAGAC GGGGTTTCAC CATGTTGGCC AGCCTGGTCT 720
CGAAATCTTG ACCTCATGAT CCACCTACCT CAGCCTCCCA AAGTGCTGGG CTTACAGGCA 780
TGAGCCACCG CGCCCAGCCT CTCATTTCTT ATAAAGACAG GGTCTTCCTA TGTTGCCCAG 840
GCTGGTCTCA AACTCCTGGC CCCAAGTGAT CCTCCTACCT CAGCCTCGCA AAGTGCTGGG 900
ATTACAGGTG TGAGCCACCA TGCCCTGATT CTTTTTTTTT 940