Tag | Content |
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EnhancerAtlas ID | HS042-29949 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr22:26338050-26339510 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr22:26338797-26338810 | AGCAGCTGTCTCC | + | 6.21 | Myog | MA0500.1 | chr22:26338796-26338807 | CAGCAGCTGTC | - | 6.14 | Tcf12 | MA0521.1 | chr22:26338796-26338807 | CAGCAGCTGTC | - | 6.02 |
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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 |
GH22I025941 | chr22 | 26337259 | 26339725 |
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Enhancer Sequence | CCATGTATCC TGCAGACATC CTGTGATGGA ACCATCCCTA TTTTATAGAG GAGGAAAACT 60 GAGGCATAGC AAGACGGTGC TGCTGGCAGA AGCAGACTGC CTCAGGTCTG GCTCCAGTGC 120 CCAAGCTCTG AACCACACAC ACAGTGAAAT CTGGCACTTA GTGTTGGTAA CGTTGGTTTC 180 CTTCCTCTGT CCTTCGGAAT GAATGTGTTC ATCCCTGGCA GGTTCCAGGA ATGATGCATA 240 TTTCCACCAC ATTTGCTCAA ACTCCGAGTT CTGTCATTTT ACAGACTCCC AACTTAGTCC 300 AGGCTCTCCT GATGCTGCCT AAGAGGTTTC CGTTATAGCA CGAAACCACT GAGCTGTTTT 360 CTCTGCAACA GAGCTCTCTC TTTATTTTGA TCCATTCCGT CTGTGTGGTC AGACCTCCCA 420 GTGAGTGGCT TTCTATGAGG GGCAGTGAAG CTCAGTAGTT AAGAGCTTGG GCTCTGGCGT 480 TGGAGCAAGC AGGCTCTCCA CAGACCAGCT CTGTGATGGT GAACAAGTCA CTTCCCCTCT 540 GTGTGTCTCA GAGTCCGCCT TTATCAAAAG GTCCTAATGG TGGCACCTTT CTCCTAGAGG 600 TGCTGTGGGG CTGTCATGAA GCAAGGCAGA GAAAGCACAG TGCCTTGAAC ATGGTCCCCA 660 AGCAACAGTA GCAGGTGGGA CTGCTAATGC CAAAACCATC AGGGCCAAGA TAATCCTATC 720 TCCAGCCCAG TATGAGCTAA GAAGGCCAGC AGCTGTCTCC ATTGACTGCT GTCTGTGTTC 780 ATCTCTCTCT GGGGATAAGT CGTCCCTCTC TCTGCTTGCT CCAAGGAAAG AAGGGAAAGG 840 AAAGAGCATT TCTGGATCAT GCACCATTAT GCCATCTATA AAATGGGGAT AAAAATAGAG 900 TCTCCTTTCT CCAGGGGCTC CGAGGACTGG CGGGATCATG CTGCTGAAAC CCTCTGCTGA 960 AGTAGGGGCT GGGCAGATGG GAACTGTGTC ATCGTGTTCT GCTTTGCCCT GTTGCTTTAT 1020 TTACAATGAC TCTCTCTTGC CTCCTGGCTC CCAGCCCAGC TCCTTGGCCT GGCAGAGGGG 1080 CCCTGCGTGA GGCCTCCTCT TCCACCATTA GTTATCTGAC ATCATCTCCC TTGATGGCCC 1140 ATCTGCTCCT GCCGCCCAGA CCTTTTGTTG TTTGCATGCC CTGCTGTGCC GATTCTTCCA 1200 TTTCTTTCCA CTTCCACCCC TTCCACCCCG GCTGGAGCAC CTCCACCGCC TCCTTCCTGC 1260 AGGACCATGG CGATCCCCTC ACTGGCTGCC CTATTTGCAA TCTGGTCCCA CCCTCCCCAC 1320 AGCAGCCAGA GGGAGATTAG GCCACCTACC TCCTTAGAAA CCATCCATGG CTTCCTGGCA 1380 GACTGAAATA AAATCTAAGC TTTGTAGCCC AGCTCACAAG CCTCAGAGAT GTGACCCGCG 1440 TCCACATCTT CAGCATCTCC 1460
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