EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS101-08166 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr11:67232740-67234780 
Target genes
Number: 52             
NameEnsembl ID
PELI3ENSG00000174516
ZDHHC24ENSG00000174165
RBM4BENSG00000173914
SPTBN2ENSG00000173898
C11orf80ENSG00000173715
RP11ENSG00000213409
RCE1ENSG00000173653
LRFN4ENSG00000173621
PCENSG00000173599
C11orf86ENSG00000173237
SYT12ENSG00000173227
RHODENSG00000173156
KDM2AENSG00000173120
AP001885.1ENSG00000179038
ADRBK1ENSG00000173020
ANKRD13DENSG00000172932
SSH3ENSG00000172830
POLD4ENSG00000175482
7SKENSG00000201684
AP003419.11ENSG00000256514
CLCF1ENSG00000175505
RAD9AENSG00000172613
TBC1D10CENSG00000175463
CARNS1ENSG00000172508
PPP1CAENSG00000172531
RPS6KB2ENSG00000175634
AP003419.16ENSG00000255949
PTPRCAPENSG00000213402
CORO1BENSG00000172725
CABP4ENSG00000175544
GPR152ENSG00000175514
TMEM134ENSG00000172663
AIPENSG00000110711
PITPNM1ENSG00000110697
CDK2AP2ENSG00000167797
GSTP1ENSG00000084207
NDUFV1ENSG00000167792
DOC2GPENSG00000231793
NUDT8ENSG00000167799
TBX10ENSG00000167800
ACY3ENSG00000132744
ALDH3B2ENSG00000132746
RPL37P2ENSG00000239559
FAM86C2PENSG00000160172
UNC93B1ENSG00000110057
ALDH3B1ENSG00000006534
RP5ENSG00000255306
NDUFS8ENSG00000110717
TCIRG1ENSG00000110719
CHKAENSG00000110721
SUV420H1ENSG00000110066
C11orf24ENSG00000171067
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr11:67233269-67233280GGTGACTCATG+6.62
HNF4GMA0484.1chr11:67233014-67233029TGGACTTTGGGCTCT-6.25
JUNDMA0491.1chr11:67233269-67233280GGTGACTCATG+6.02
Spz1MA0111.1chr11:67234111-67234122AGGGTAGCAGC+6.02
Number of super-enhancer constituents: 4             
IDCoordinateTissue/cell
SE_27544chr11:67231042-67233407Esophagus
SE_27544chr11:67233804-67237383Esophagus
SE_42089chr11:67232247-67233368LNCaP
SE_42089chr11:67233829-67236754LNCaP
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr116723388067234455
Number: 1             
IDChromosomeStartEnd
GH11I067466chr116723373567234620
Enhancer Sequence
GGGAAGTGTG TGAAAGGAGA GATTTTTCTT TGTTCCTTGG GGTGGGCTTT TAGTCATTCA 60
GCAAACATTT ATGGAACACC TACTGCGTGC CTGGTACTGG GAATTCCGCC CTGAAGGGCA 120
GATAAGGTCC CTGCCCTCAT GGCCCGTCCT TAGTGGAGGA ACCAATAAGA ACCTGAAAGC 180
TAACAGTACA GGTGATTGGG ATATAGGGGG TAAGAACAGG GCAGTGCAGG AGTCCTGGGT 240
CCCCAGTTAG AAGAGTGATG GGGGAATGAG GAGCTGGACT TTGGGCTCTG CAACAAGGGG 300
GGTAGTAAGC CTGGGGGACT GGGGGGCCAC CATGGACTGC TTTGTGCATT GCCCAGACTA 360
CTTCAAAAAG GGTGGGCCAG GTGTGGTGGC TCATGCCTGT AATCCCAGTG CTTCAGGGAG 420
CCAAGGCAGG AAGATCGCTT GAGGCCAGGA GTTTGAAGCC AGCCTGGGCA ACATACCAAG 480
ATCCCCATCT CTATAAAAGG TTAAAAAAAA ATTAGCCCAG CCCAGGCGTG GTGACTCATG 540
GCTGTAATCC TAGCACTTTG GGAGGCTGAG GCAGGAGGAT CACTTGAGTT CAGGAGTTCA 600
AGACCAGCCT GGGCAACATA GTGAGACCTT GTCTCTATTA TTATTTTAAA AAAAAAAAAA 660
TTAGCTGAGC ATGGTGGTAC ATGCCTGTAG TCCCAGCTAC TAGGGAGGCT CAGCTGGGAG 720
GATGGCTTGA GTCCAAGAGT TTGAGGCTGC AGTGATCATA CCACAGCTCT CCAGCTTGGG 780
CAACAGAACA AGACCCTGTC TCTAAAAAAT AAAAAGGGCT GGGCGTGGTG GCTCACGCCT 840
GTAATCCCAA CACTTTGGGA AGCTGAGGTG GGTGGATCAC CTGAGGCCAA CATGGTGAAA 900
CCCCATCTCT ACTAAAAAAA TACAAAAAAT TAGCCAGGTG TGGTGGCGCG CGCCTGTAAT 960
CCCAGCTACT CTGGAGGCTA AGGCATGAAA ATCCCTTGAA CCCAGGAGGC AGAGGTTGCA 1020
GTGAGCCGAG ATTGCGCCAC TACACTCCTG CCTGGGCGAC AGAGCAAGAC TCCTCCTCAA 1080
AAAATAAATA AATAAAAATA AAGGGGTATA GGGTATGATG GGGGCTGAAA CTCACTCCCT 1140
GCACCCTACA AAGGCCCTCT AAGGCGCTCT GGTAGCCCCA GGCTTGCCTT GCTGGGTTGA 1200
GGGGAAAAAT GAAAGAACTT GGCAGCACTA CCAGGGCCAG TGTACAGCGG TGCTGGGAAG 1260
TGGCAGCCCC CTCCCCCACA CTCAAACACC CTGAGCAGAG GCCAGACTCT GTGCCAGGGG 1320
CCTGGCTGGC TGGGGAGCCT TGGCCTTCCT GGAGAAGCGG AGAGATGAGC CAGGGTAGCA 1380
GCCACAGTTA GTCCCTTCTT ATGGATCACT CGTGACCCCA ACCCTGGATC CTTTCTGGGG 1440
ACTCTGCCTC CTCTACCCCA AAGAACGAGG TGCCTGGGAG CCAAAGAACA CCTGGTGTGA 1500
GATCTGCCTG CTCTGGACCA AAAGTTCCCC CATCTGAGCA ATGGGTAGGA GAGGGGTGCT 1560
TGTCAGTGCT TAGATGCCAG ACAAGGGGAA GTGCCAGGTG CCCTGCGGCT CTGCACTGGC 1620
TGGGCACTCG GCATCCCTGA GCCCCTACAC GTGGCTTCTG GGCACCACCT CACTTGTAGG 1680
ACTTCTGTAA GATGGGAAAA TAAAACTGCC CTGCACCTTG CCCAGAGTAG ACACAGAATA 1740
AATGGTAGCT GCTACTCTTC TGTCCTCTAA TGGATTTAAA CAGGTTAAAT TTTTTAAAAA 1800
AGGAAAAGTC TTTGCAGTGA TAAGCCAGGT TCCATTTTCA GCTATGTGTG ATTTCCTGGC 1860
TGTGTGCCCA GGTCACAAGG CCTCTGTCTC CTCACCTGTA AAATGGGAGT GTGATGATGG 1920
CAGCCAGCTG CCTCCTCAGG ATGCTGGGAG GCTCAGTGTC AAGGGGGAGG CAGAGCCTGT 1980
ACAAAAGGAG GGCAGAGCCT CCCACGGGGC CCCTCTTGAC CCCAACCCTC AGGGCCACTC 2040