EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS012-01961 
Organism
Homo sapiens 
Tissue/cell
Caco-2 
Coordinate
chr11:819910-821620 
Target genes
Number: 45             
NameEnsembl ID
HRASENSG00000174775
ANO9ENSG00000185101
TSPAN4ENSG00000214063
PTDSS2ENSG00000174915
POLR2LENSG00000177700
RNH1ENSG00000023191
DEAF1ENSG00000177030
CD151ENSG00000177697
EFCAB4AENSG00000177685
SIGIRRENSG00000185187
PNPLA2ENSG00000177666
C11orf35ENSG00000185522
RPLP2ENSG00000177600
PIDDENSG00000177595
RASSF7ENSG00000099849
PHRF1ENSG00000070047
IRF7ENSG00000185507
PSMD13ENSG00000185627
AP2A2ENSG00000183020
BET1LENSG00000177951
CHID1ENSG00000177830
ATHL1ENSG00000142102
IFITM2ENSG00000185201
IFITM1ENSG00000185885
IFITM3ENSG00000142089
B4GALNT4ENSG00000182272
PKP3ENSG00000184363
AP006621.1ENSG00000177236
SNORA52ENSG00000199785
TALDO1ENSG00000177156
RP13ENSG00000254739
RP11ENSG00000254815
MIR210HGENSG00000247095
MIR210ENSG00000199038
AP006621.6ENSG00000255142
TMEM80ENSG00000177042
EPS8L2ENSG00000177106
AP006621.8ENSG00000255108
RIC8AENSG00000177963
AC138230.1ENSG00000243562
SLC25A22ENSG00000177542
CEND1ENSG00000184524
AP006621.5ENSG00000255284
PDDC1ENSG00000177225
MUC6ENSG00000184956
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr11:820074-820085GGGGGCGGGGC-6.02
KLF5MA0599.1chr11:820075-820085GGGGCGGGGC-6.02
SP1MA0079.4chr11:820073-820088TGGGGGCGGGGCCTG-6.56
SP4MA0685.1chr11:820071-820088CCTGGGGGCGGGGCCTG-6.14
ZfxMA0146.2chr11:820074-820088GGGGGCGGGGCCTG+6.19
Number of super-enhancer constituents: 20             
IDCoordinateTissue/cell
SE_25263chr11:818399-822086Colon_Crypt_3
SE_41667chr11:818954-822806LNCaP
SE_65923chr11:818226-830100Pancreatic_islets
SE_68140chr11:795581-863109TC32
SE_68141chr11:795581-863109TC32
SE_68142chr11:795581-863109TC32
SE_68143chr11:795581-863109TC32
SE_68144chr11:795581-863109TC32
SE_68145chr11:795581-863109TC32
SE_68146chr11:795581-863109TC32
SE_68147chr11:795581-863109TC32
SE_68148chr11:795581-863109TC32
SE_68453chr11:795673-860573TC71
SE_68454chr11:795673-860573TC71
SE_68455chr11:795673-860573TC71
SE_68456chr11:795673-860573TC71
SE_68457chr11:795673-860573TC71
SE_68458chr11:795673-860573TC71
SE_68459chr11:795673-860573TC71
SE_68460chr11:795673-860573TC71
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr11820655821200
chr11820387820489
Enhancer Sequence
CGGGGCCGGG GGCGGCAGGC GGGGGGCTGG CGGGAAGGCC GTGCGGGGCC GGGGGATGGT 60
CTCCGTGAGC GGAGGGGCCC CGCGGCGAGT CGGTGGGTAC CGTGGGGAGG GTTCCGGTCC 120
GCGCCTGGGG AACCCGGCGA GGATCCAATC CGGGTCGCTG GCCTGGGGGC GGGGCCTGGT 180
TTGTTTTGCT CCGAGGGTGC CCGGGGCCCG CCTGTCTGGC GCAAAGGTTT GGGGGCGGGC 240
AGGTGCAGCA AAAGCTGCTT AATTGGACAG AAAAAGTAAC TCGTGGGCGG GACCGTGAGA 300
ATCCGAGGAG GGACCTAAGT CACCCCGTGG CCCTGGATAT TACAACCGGT GCCAGCGATC 360
GGTCACAGTG TCCTGGGCTT CCGCAGTTGC AGGCTGCTAT CAGGGGGCCT GGCATGGGGG 420
TAGCCTCTTG AGAGGCGTCT GGGAACCGTG ACCTGGTCCT TCCCAAGGGC CCGGAGGAGG 480
AGCCCCGCTG AGGTCAGGGC TGGGCGCGAA GGGGCTCTCC TGCCCTCTCC TTGCACACGG 540
TGCCCTGTGG CCTGGCTCCC CGCTGCGGCC CACCGCGTTT GCACACTTCA TGGGTGAGGG 600
TGCTTCTGGG CTCTGGTGCC TGGGTCAGGA GTGGATGGGT CTCTGTGTGC TGGGCTGGCC 660
TCGGCTCGCA CCATCGGCTG CCATGAGGGA GTGATGTTTA CAGCACACGA CTTCAGGAGC 720
CTGTGAGGAC ACCCAAGATG ACAGGGGCAC TCTGCTCAGC AGGAGCCTGT CCGGGGCTCA 780
CCCCTGCCCT CTTCCTCTGA ACTTTGTCCT GGGAGGGAGG GGGCTGGACC ACAGAAGTGA 840
ACCTCTCAGG TCCCAATAAC TAGAGCTATT ATTGGGAACA GCCCCCTCCA GCCCCCTCCC 900
TCTCATGGAG GCCTTCAGAC AAGCGCCTCA GTCGGCCCCC TGGCTTCAAG ATACATCAAG 960
GTCCCTGCTA CCCGAGCCAA GGACACCTCT CCCACAGTGC TTCCCCACCC TGCTCCCAAC 1020
AAGACTCCTT CTCACGGGTG GTCTTGCACA GCTGGAGCCC ATAGTGCAGC AGGTGCTGGC 1080
TGAAGAGCCC CTGGCTCCAC ACTGCCCCAC TCCTGACCAG GGTGATGCAC TGGAGGAGGG 1140
CTTGGACCTC AGCTCCTCCC TCAGTGCTCC CGACCACTTC CAGGGACTAT CCCCAAGCTG 1200
GCCAGCACTC CTGCGCCCCA AGAGGAGTGT TTGGGGTGCT TCCTCTTGGC TGCAGTGGGA 1260
CACAGGTGTG CCTTCCTAGG AACTGGGCCC TGACTACTTC CAGCCCAACA CTCCCGGGCC 1320
TGTGAACTGT GACCTGTGTG CCGGGATGGG TTTTGTGGGT CTGCCCCATC CCCGCACTGC 1380
TGGATCTGGC CAAGTGGGTG AAGGCTAAGG CCGGTCAGAG TTGAGTTTCT GCCTTGTCCC 1440
CTCTCCTGGG CTAGATGCCA CACCAGGCCC AGTGACTCAT AGGGCAGGCA GTTGGGAAAT 1500
ACCAGGCAGA GGGCAGGTCC TGGTCTCAGC TGGCCAGCCT CTGCTGTCTG CCATCCCAGG 1560
GGAGGTGGCC AAAGTCCCAA CTGTGAGCCA GGCCCCACAT TCACTGGGCC TCCTCCAGGG 1620
TCTGTATGCC ATGGAACCCT GGACATGGGG CTATGAAGGA AGGTGGGTGT TGCTAAGCCC 1680
AGGAGCATGG GCCCCTAACC TTGGCCCTGT 1710