Tag | Content |
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EnhancerAtlas ID | HS092-13383 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:113477750-113479170 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYC | MA0147.3 | chr12:113478853-113478865 | GGCCACGTGCTC | + | 6.92 | Myod1 | MA0499.1 | chr12:113478485-113478498 | TGCAGCTGTCTCT | + | 6.36 |
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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 |
GH12I113039 | chr12 | 113477778 | 113479408 |
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Enhancer Sequence | GAGTGGGACT CCATCTCAAA AAATAAAATA AAATGAAGAT CCCAGTCTAA TTACTGTAAT 60 ACTTCAAAGC AGTGATGAGT AAAAGCAATA TATTTTGAGA CAGCACCAAC AAGTGAAATG 120 TAATAGGAAA CTATAGGATT CTATTCATGA CACAGTCAGA CGCTACTCAC ACCATTGTGG 180 TTTGTTGCCT ATGTTCATAG TAGAAGGAAA TGCTGTCTTT CAATTCACAG TTAATGAGAA 240 TAAAGATATC ACTTTCCCCA TCCAAGTTCA AAGGAGTCTG TGATCCCCAG GCTGAGAACC 300 CCAGCCAAGA GATTCTTCGC TATCTTCTAG GCTAGGGTTT TGGGATCTGA ATGTGTCAGG 360 GTAATGTCTC CTGGGTCCGC CAAATCCTCA ATGAATCACC CAGTTCTACC CCCATCCTTC 420 TTTCTCAAGG GTCATCTCCC ATCTCAAGAT AATCCAGATA CAGCCCTTCT ACTCTCTGCA 480 TCTATGAATT TGACTCTTAG ATTTCGCTTA CTAGTGAGAT CCTGCAGTGT TTTTCTTTTT 540 GTGTTTGGCT TATTTCACTT AGCATAATGT CCTCCAAGTT CATCAAGGTT GTTGTAAATG 600 GCAGAGTTTC CCTTTTTGGA AGGCTGAATA ATCTTTGTGT ATATACCACG GTTTCGTTAT 660 CCATCGTCTG CCATGAACAC CTGGGTTGTT TCCGTATCTT GGTTATTGTG AATAATGATG 720 GAATGAGCAT TGGAGTGCAG CTGTCTCTAG ATATCCAGAT TTAGTTTCTC ACCCTGAATG 780 TTGAAACCTT AATCTCCTGC AGGGTTTATC CCAGGACCAC ACCCAGGATT GTCCTAGGCA 840 AGTTCCTGTT CAAGCTTCGA GTTAGTCATC ACTTCCTCCC TGAGGCCTCC CTGACTCCAT 900 GGTTTGCATT AGTGATTCCT CTGTCCCAGG CTCCACCTCC CCAACCCAGC ACTGACCACC 960 TCATCCCTGC CTCCACTGAC CTAGTTCCTG GGCTGGAACT GGAGTGAGAC TGACATGTGA 1020 CTTTGGGAGT TAAGGCAATG GAGAGCTGGT GTTGTGAAAT GGAGCAGCCC CACCGCTCTC 1080 TTGCCCTGCC ACAGTGACCC CGAGGCCACG TGCTCTCTCT GGGGAAGGGC TGCCCTCCTC 1140 CTTAGAAGAG CGAGAAGCAA GCCTTGATTG TGTTTCGCCA CTGCAAGTCC AGGGTTTGTC 1200 TGTTGTGGCA GCTGGCATTA AACGCCCTGG CACACTCAGA CCTCAAAGCC CAAGCCTAGA 1260 AGACAGTGAA GCAACCTGGT AGATGGTAAA TGATGAAATA TTCTGCTTTT AATAATTTTT 1320 TTTGAGACAG AGTCTGGCTC TGTCACCCGG CTAGAGTGTA GTGGTGAGAT CTCGGCTCAC 1380 TGCAACCTCC ACCCCCCCCG GGCTCAAGCA ATTCTCATGC 1420
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