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

TagContent
EnhancerAtlas ID
HS101-07965 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr11:64951060-64953190 
Target genes
Number: 63             
NameEnsembl ID
FERMT3ENSG00000149781
PYGMENSG00000068976
SF1ENSG00000168066
MAP4K2ENSG00000168067
MEN1ENSG00000133895
CDC42BPGENSG00000171219
EHD1ENSG00000110047
AP001187.1ENSG00000203400
AP001187.9ENSG00000229719
ATG2AENSG00000110046
PPP2R5BENSG00000068971
BATF2ENSG00000168062
ARL2ENSG00000213465
SNX15ENSG00000110025
SAC3D1ENSG00000168061
NAALADL1ENSG00000168060
CDCA5ENSG00000146670
ZFPL1ENSG00000162300
C11orf2ENSG00000149823
AP003068.6ENSG00000187066
AP003068.9ENSG00000254501
TM7SF2ENSG00000149809
ZNHIT2ENSG00000174276
MRPL49ENSG00000149792
FAUENSG00000149806
SYVN1ENSG00000162298
PGAM1P8ENSG00000249251
AP003068.18ENSG00000255200
CAPN1ENSG00000014216
AP003068.23ENSG00000254614
SLC22A20ENSG00000197847
POLA2ENSG00000014138
CDC42EP2ENSG00000149798
DPF2ENSG00000133884
TIGD3ENSG00000173825
SLC25A45ENSG00000162241
FRMD8ENSG00000126391
NEAT1ENSG00000245532
AP000769.1ENSG00000173727
MALAT1ENSG00000251562
SCYL1ENSG00000142186
LTBP3ENSG00000168056
RP11ENSG00000260233
SSSCA1ENSG00000173465
FAM89BENSG00000176973
EHBP1L1ENSG00000173442
KCNK7ENSG00000173338
MAP3K11ENSG00000173327
PCNXL3ENSG00000197136
SIPA1ENSG00000213445
RELAENSG00000173039
KAT5ENSG00000172977
RNASEH2CENSG00000172922
AP001266.1ENSG00000175827
AP5B1ENSG00000254470
OVOL1ENSG00000172818
SNX32ENSG00000172803
EFEMP2ENSG00000172638
C11orf68ENSG00000175573
DRAP1ENSG00000175550
EIF1ADENSG00000175376
CST6ENSG00000175315
PACS1ENSG00000175115
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr11:64951948-64951959GCCCCGCCCCC+6.02
KLF4MA0039.3chr11:64951143-64951154CCACACCCTGT+6.14
KLF5MA0599.1chr11:64951948-64951958GCCCCGCCCC+6.02
Klf1MA0493.1chr11:64951141-64951152GGCCACACCCT+6.32
SP3MA0746.2chr11:64951947-64951960CGCCCCGCCCCCC+6.11
ZNF263MA0528.1chr11:64951837-64951858GCCCCCTTCCCTCGCTCCTCC-7.02
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_27499chr11:64947956-64952894Esophagus
SE_57890chr11:64951313-64951993VACO_503
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr116495114464951477
chr116495220064952800
Enhancer Sequence
CAGGTGAGGG CTCCCCTGGG GAGGAGGGGC AGCAGGCACT GGGGGAGATG CGGAAGGATG 60
ACCCACAATA CCTGCAGTTA GGGCCACACC CTGTGGGGCC AGCCCTCCCT CTAGCAGGTA 120
TTTGACCTCT CAGTGCCATC TCGGGTCTGT CATGTGTGAA GTGACTGGGC TGGGCAGGTA 180
TTTCGGCTGG CAGTTTTCCT AGGTGGTTGT ATGTATCAGG TGGAAAGTGC TTGAAAGAAC 240
AGAAAGACTT TTGTGTTATA TCCTGTGGGA CAAATTCCAC TCCTCCCGGA GGTCGGTCTC 300
AGTTGCCCCA TCTGAGAAAG GAGTGTTCGC TGGGGAAAAC AGATCAGCAC GTGTGGCCTT 360
CTCCACGTGT CAAGCCTCCT ATCCCCCAAC TCCTCCTGCG CTTTGGCAAG GTCTGACTGA 420
GCCCAGCAGA AAAGAAAGAC TCGGGATTAA GTCTACGTAA ACCAGCTTTT CCTGACGGTG 480
TGCCCAGGGC CCATTTTTCA AGTCACACCA ATCAATTCTC AATGAGCTGC CTTTGGGAGG 540
GACATGCCCA GCAACCCTGG ATGAGACTCT CCAGCCTTGG AGGCCCCAGC CCTGCCCGAA 600
GGACTCTTGG GTGTTCCCTC CTTCTGCCTG GTTAGAGAGC CCCTTACCCT ACTCTGTCCT 660
TGCCCGCCTT GCGCGGGTGG AGGTGGCCCT CGGAACCCAG GGTGCGGAAC CCACAGTGCG 720
GATCCACTTT GGCCCAGCGC CACACCCACC TGCTCCAGTC TGCAGGGGCG CAGTCTCGCC 780
CCCTTCCCTC GCTCCTCCAA TCCGCTCCTC CCTGGCCTCC GATTGGCCAG TTCAGTACCC 840
GCCACCCACA CTCTCCGCAA CCTGGGCTCC TAGGGCCGCC TCCACCCCGC CCCGCCCCCC 900
GTTGTCCTGG CCCCGACCCC TCAGATGGTA CCTCGAGTCC TTGGTCGCTT CTGACCCCAG 960
ACGCCTTCGG CCCCGACCCT GCCCTGGGAA ACGTGGCCTT TGTGGCATCT CAGAAACAAA 1020
GCCCGTGATT GTGAGAACCA GTCCTGCCCA TCTTGTGGTT GTAGGATCTG GATGCCACAT 1080
TTTCACTGCT CATCCAATGA CACAGGTGCC CCTAACCCCC TTGAATAGGG AGGGAAGAGC 1140
CAGGGGGCCA TGGCCTAAAA GGGGGCTAGT TCCGGAAAGC CCAGGCCCCA GAGCTTTTCC 1200
ACCTCTCCGT GCCTGAGGAG GAACCCTGTT TGTTCAGTGA CTCCCTAAAG GCTTTGCCTG 1260
TGCTCTTGTT TAAGTCTTCC GTGAAGAAGG CACCGCTGCT CCTTTTTATG GATAGGGAAA 1320
CTGAGGCTCA GAGGCGATAA CTTTTCCAGG ATCATGTAGC TAGTATGTCT CGAGCATACA 1380
TGTACATATC AAGTATACAC ATGTCTATAT GTGGTATGCA TGTATTAGTA TACAGCAAAT 1440
ATGCAGGTAT CTAGTATACA TTGTACAGGC AAAGGAAAGC ATCCCCTTAG CCCTCTGAAG 1500
GTTCACTGAA AAATCAACTC ACAAAAGGAG GTTAGTAGGA GAAATGGCAT ACAAATTGAT 1560
TAGCCTGCAG CGTGGGGTCG GGAACCACAG AGTGTTCACC CCAGCCCCAC AATGGGTACA 1620
GAAGCCTATA TACCATCCTG AGGTTACAGG AAGAATGGGG GCTCGAACAT GGCCAAAACC 1680
AGTTTCTGGT GGTAAATCAG GTTATAGTGG CAAGACAGAC TATGGAAGGG GGAGAAAAGG 1740
GGGCCTGGGT AGCAAAGGCA GTCTTGTTAT GTAGATGAAA CCTCACAGGT AGCAGCCCTC 1800
AGAGGGAATA GATGGTAATT GTTTCGTTCA GACCTTTAAA GGGTGTCAGG CTCTCAGTCT 1860
GACAAGGGAA GGCCTTAGAG AAAGCCTGGC TACATCAATG CAGATTTTCT CTACAGATGC 1920
AAATCTCCCC CACAAAAGAC AGTATTACAG GGCTACTTCT GTTTGCAGAC CCTCTGAACA 1980
GCTATCTCAA AATATGTTGA AGAAGTATAT TTCAGGGTGA AATACTTTGA TTTCCTTCAA 2040
TACCTAGATA CATGTATCTA GTATATCTGT AGCATACATG TATCTAGAGG TACACATGCA 2100
TCTAGTATGT ATCTAGTATA TGTGATTTAG 2130