| Tag | Content |
|---|
EnhancerAtlas ID | HS105-33938 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr17:37270930-37271990 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr17:37270970-37270981 | GACAGCTGCAG | + | 6.62 | | NFE2L1 | MA0089.2 | chr17:37271540-37271555 | CAATGAGTCAGCAGA | + | 6.15 | | Tcf12 | MA0521.1 | chr17:37270970-37270981 | GACAGCTGCAG | + | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I039114 | chr17 | 37270806 | 37271498 |
|
Enhancer Sequence | TCTGAAGTCC AGGATAGGAT CATTTTACCA AACAAAGCAG GACAGCTGCA GATGCTAAAC 60
AGGTGCTCTC AGGTAAGTCT CAGAGTCAAC TGAATACAGC TTCCACCTGG GAACCTGAGC 120
GGGCCAGTGT TTAAGACGGT TGCTTTGAGG CTCGGAGAAA GGTCTGGTTT CAATCAGCCT 180
GCTTCCTGGG CCCCGCACAG CGAGAGCTTT CCCCAAACCT CCGGGCGTCT GAAATGAGTG 240
CCCGGGACAG AAGCCACGCT CTGCAGTTGT GAAGCCCAAA CAGATGCTGA CGTGTCTCTT 300
GCCGCCTCAG CTAAGACTGC AAAGCGTGAG CTTCCTGGGA ATGCATCTTC CTGGCCCGTT 360
GCTCGGAGTT CTCTGCTTCA CAGCAAAGAC AAGCAGTCTG ATCCAAACTA GTGCTGTTCT 420
GCAGAGAAAC CAGGCCCTGT GTCACGTGCC TCAGCTCTGA CACCTGGATG ATCCCTGGAC 480
TCATTCTTGG AGTTCCCGAT GACCCCTGCA ATGGCACCTC TTAACTGACA GAAAACTTCC 540
ATCTATTCTG ACTCAAGGAA AGTCAGAAAT GAAACGAGCT GCTGCCTCTA ACTCCTAAGC 600
TGATTCTCTC CAATGAGTCA GCAGATCCCA GGGAAGGCAA GAGCCTCGAA GCCTAACGAT 660
GCCCTACTCA GGCCAGCGAG GGTGAGGCCA AGCTCTGCTT CAGGCCTCAG AAGTGCCAAG 720
TACAGCTGGC CTGCCAGGGG GAGGACTGGC TCAAGGGCAA TGCCATGCAG AATCTGCTGC 780
AGGTCCCAAA CAGGCCCAAC AGACTGCCCT CCTGGCACAC CTGACTTTTA TTACTCCAGG 840
ACAGTGAAGC CAGGAGCCAT ATCTACTCAG CTCTGGCTGA GGGTGGCCAC ACAGTGATGG 900
GTGAGGCCAA ATTGCACCCT GGAGGGAGGG GGCGACTTGC AGGGGGATCA CTCCTGGGCA 960
GAGCCAAGCA CAAAGCCTGC AGGGGAGCAT TTGGGAGCGT GGGAGGAAGG AGAAGGGAAG 1020
CTGGCATTTG CTGAGTGGTG ATGGGAGAGT GCTGGGCATT 1060
|
