Tag | Content |
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EnhancerAtlas ID | HS138-40410 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr8:30932250-30933680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr8:30933493-30933505 | ATGTAAACAGTA | + | 6.11 | ONECUT1 | MA0679.1 | chr8:30933664-30933678 | AATATTGATTTTTT | - | 7.31 | ONECUT2 | MA0756.1 | chr8:30933664-30933678 | AATATTGATTTTTT | - | 7.25 | ONECUT3 | MA0757.1 | chr8:30933664-30933678 | AATATTGATTTTTT | - | 7.47 |
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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: 2 | ID | Chromosome | Start | End |
GH08I031075 | chr8 | 30932641 | 30932790 | GH08I031076 | chr8 | 30932814 | 30933483 |
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Enhancer Sequence | GAGGGAAGAG CAAAGGAGTT GAGAGTATAG ATACAAAGGA ATGATTACTG TAATGTGGGT 60 AAGAGAGGAA TGGAAGGCTC AGTGGGCAGT GGGAGTAGGG ATGTTGATAG GTAAGGAAAA 120 GGTGATAGGA TCAATGCATT TGGTTCTGCA AGTGTCAAAG TATTGTTGGG GAAAGCATGC 180 TGGAAGGAAA GATAGGGATG CTGGTGTTCT CAGGGTGGAA GGCTTACAGT TGTAGTCTGG 240 AAGTGGTGAT TTTATTGGCA ATTATAAGGT CAACGGTATG ACTATGGAAT TGAGTGGCTA 300 AGGTCTGTTG AAGAAAAGAT TGTCGGAAAT GCAGGGGTCA AGGAACTGGC CTGTGGATGT 360 TGAACTCACT GGCAGTGATC AAGGAATAGT AGTGGAGTGA AAGTAGTTAA TGAATCAGGC 420 ACTAAGATCT CCAAGGGATG AAAGGATGCA GTTTGGAGAT GACAAGATAA CTGTAGTAAT 480 CAGGAATAGC AGGTTTTGTA GCTCTGTCTC ATAGGCCTCA GAGGAGATGG GCTTTTGAAG 540 GACAAGAGAA ATGATGATGA ATAAATTCTA AGCAGGGGAA GTGTTTGGGA AAGCAGGGCA 600 GGCTTTGTGC TGTTGATGGC AAATGATGTA CCAGACAGGA TGAAGTTGAG AATTTGGAAG 660 TTGATCACTG ATTAGAAAGG CTTACATTTT ATTTTGGCCG GGGGTGGCAG CTCATGCCTG 720 TAATCCCAGC ACTTTGGGAG GCCAAGGTGG GCGGATCCCT TAGGCCAGAA GTTGGAGACC 780 AGCCTGGCCA CCATTGCGAA ACACTGTCTC TACTAGAAAT ACAAAAAAAA AAAAAATTAG 840 CTGGTCGTGG TGGCACATGC CTGTAGTCCC AGCTACTCCG GGGGCTAGGG AATGAGAATA 900 GCTTGAAGCC GGGAGGTGGA GGTTGCAGTG AGCCGAGATT GCGCCACTGC ATTCCAGCCT 960 GGGTGACAGA GTGAGACTCT GTCTCAAAAA AAAAAAAAAG GAAGGGCTTA CATTTTATTT 1020 TGGTGCTGAC TGGGAATGAA GGCAATGAGG GATGACTGTT GGAGAAGGCT GTGCTTACTA 1080 AACAGTATTA TTAAGTAGCA GCATACATGG TGTTATACTG ACTTCTGATT TTGCAATAGT 1140 ACAGACAGGT TCAGATTCTC ATTTCCACCT TCTCCTTCTG CCTAGGTGAA TAACTGCTGG 1200 GTTATAGTAC AGATGACTGC AGATCATTTG GAATTTACTT TAAATGTAAA CAGTAAAAAT 1260 TTGAAAGAGA GGGAAAGTGA TTGAGGCAAT TTGGGGATTG AATAAGAAGG TCTTTTTGTT 1320 GGAATTCATT TAAGGAAAGA AAATGAAAAT TTGATCCCTA ATATTATTTA ATGAAGTGGC 1380 TAAATGAATA TCTCTGCTTT GTGGTTTGAA AATTAATATT GATTTTTTTT 1430
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