Tag | Content |
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EnhancerAtlas ID | HS101-04007 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:222012220-222013640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr1:222013277-222013288 | CATGAGTCACT | - | 6.14 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_35982 | chr1:222011920-222015308 | HMEC | SE_52249 | chr1:222012660-222016056 | Skeletal_Muscle_Myoblast | SE_55946 | chr1:222012458-222014856 | u87 | SE_64045 | chr1:222012660-222016056 | HSMM |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I221838 | chr1 | 222012115 | 222015694 |
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Enhancer Sequence | AGCAAGACCT CCTTGTTCAG ATTCTTCCTG GCCTCTGTGT CTTTGAGGAT AAGGATGTTC 60 CTTTCCTCTA GGTATAGAGA TGGCACCTTT TTTTTTTTTT GAGACTGAGT CTCTTTCTGT 120 CACCCAGGCT GGAGTGCAGT GGTGTGATCT CAGCTCACTT CAACCTCTGC CTCCCGGGTT 180 CAAGTGATTC TCCTGCCTCA GCCTCCCAAG TAGCTGGGAC TACAGGTGTG TGCCACCACG 240 CCTGGCTAAT TTTTTGTGTT TTTAGTAGAG ACAGGGGTTT CACCTTGTTA GCCAGGATGG 300 TCTCGATCTC CTGACCTCAT GATCTGCCCA CCTCGGCCTC CCAAAGCGCT GGGATTACAG 360 GCATGAGCCA CTGCACCCGG CCTGAAGGCA CCTCTTGAAT GAGGATCTTG TGGTCTCTTT 420 CAGGTGGTCA GAAAATTCTG TCTAGGTTTG ATAGTCTGCT TTAGGGGAGA AGGGCAAGAG 480 GAGGTCAGAG AGTGTCCTTA CTGCTTCTGC TGTTTTCTAA AATGCCAAGG GGCCATATTT 540 TGGAGCAGCC TGTCCTGAAC TCCAACAGCA AAGGTAGAAC AGGGCAGAGT GATAGCCTGG 600 TCAGGAAGTG AATGAATGGG ACTCACAGCC ACACTGATTG TCTCTAGTGA CACCAAGAGC 660 TCAGGTGAGG CTAAATCAGC CAGGAACCCC CAGGGGCCCA AAGAGGATGG TCAGGAGTAG 720 GAGGAAGACA TCACAAGTCA TAGAAAAGAG ATAGGAGGGC CGTTTTCTCT GCATATGCCA 780 GTTATAACAG TTGAATTTGC ACTCCCCAGT ACTCCTAGAG ACTCTAACAT TGTGAGAAAG 840 CCAATTCTTT CAGAATGTGG AAGACTCGTC AGTTGGACCT GCCAAATCCA CCTGTATACT 900 TTGCTATAGT ATCAGAAATG ATTCTTTTTT ATTTTCTCTC TCCCCAAGGA CCAAGATGGA 960 TTTCCAGCCT GGATGTTTTG GCGGGGATTC TACCCAGCGG TGGGGGGAAG AACCACGTGC 1020 CCTTCCAACC TTGCGTCAGC AATCCCATGA GGCCCGCCAT GAGTCACTGC CAGTGGCCCA 1080 GACTCAGTTG TGTGGAGTCT CACACCCTGG GGCGAAACTA GCTAAGTTCA TGGGTCTTTC 1140 CTGTCTGTGT TCTCAGTGAC TCACCCGAAA CAGATAATAA CAGTGAGGTT GGGCACACCA 1200 TGTGACTGGT GCCAGCCAGA ACAGGTCATG CTGTTAACCC TTGGATCCCA GGCCACCAAC 1260 TGCTGACTCC CAGGCCCTGG GACAGGCCCA TGACACACTT GAGTGGTATC TCCTTCCTAT 1320 CTCTCTGGGA TACTTGGTCA AGGTTTCAGT TTTGGAAATA TGACCTTCCC TTGTAAAGGA 1380 TCTCAAACTT GGGGTGGTTA CTGATAGAGA CTGCATCAAT 1420
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