| Tag | Content |
|---|
EnhancerAtlas ID | HS051-00422 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr1:26002240-26003620 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr1:26002631-26002644 | AGAAACAGCTGCA | - | 6.29 | | Myog | MA0500.1 | chr1:26002634-26002645 | AACAGCTGCAG | + | 6.02 | | Tcf12 | MA0521.1 | chr1:26002634-26002645 | AACAGCTGCAG | + | 6.62 | | Znf423 | MA0116.1 | chr1:26002536-26002551 | TGCCCCCTGGGTGGC | - | 6.13 |
|
| | 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 |
| GH01I025675 | chr1 | 26002283 | 26003398 |
|
Enhancer Sequence | GCTGCTTTTT ATTGAGCACA TATTATATAC GAGCCATTGT GCTCAACACT TTACATCTGT 60
TATTTACTCT TAGGGTTATT CTAAGGATTA AGTATTTCTG TCCTTTTACA GATGAGGAAA 120
CTGAGACTTA CAGGGGTTAA GTCACTCACT CAAGGCCACA CAGCCAGTAA GGTGGCAGAG 180
CCCTAGAGCA GCCTCTCAAG CTTCAATGTG CGTTTGAATC ACCTGGGGCT CTTGTTAAAC 240
TGCTGCTACA GATTCAGCAG GTGGGAGAGT GGAACTGAGG TACTCTGTTT CTGACGTGCC 300
CCCTGGGTGG CCCTACTCCT GGTCCCTGGA GCACTTTGAG CAGCGAGAGT TTCTCTGCCT 360
GTATGGCCCA CACTCTCGAC CCTGATGCCT TAGAAACAGC TGCAGACAGG ATGCGATTCC 420
TGAGACTGCT CAAACCTGAA ACCCCATGGG CAGGATGTGG GTGAGCTGTC TGGACCTCAG 480
GTGGGTGGGA GTTGTATCAT ATGCTCATTT CCCACATTGG CCTTTCAATA GCTTGAGTAA 540
ACCCGAAACT GAGAGGGTTG GAGGCAGCAT CTCCCCTTCT ACTCCCCCGC TTCACCTCCC 600
CGGGCAACCA AACCCCACCC GTGCCCAGCT TCTGAGCGAT AGACCTGGGC TGTGTATTTG 660
CAGGAGCCTC ACTGGGGTCA CCAACCAGGT CATGTTGTGT TGCCCCAATA AATGGAACTG 720
GATCAGAAAA TCCAACGTGG ATAGTTTTTA GGTGCCAAGC TGTCAGCTCT TCCCTTGGAC 780
TGTGCTGAAA GTGGAAGAGG AGAAAAAAAT CAACCCAATG TTCTAAGCTC TCTGTCTACA 840
TAGTCATTAG ATCCCAGGAT CGTTAGAGAC CAAATCCCTT CCCACTTGGC CCCTGCAAAT 900
GGGGCCAGGT GTCACTGCTG GGAGACGCCA GTAAGGCTGC ACGTCATGGT GTGAGCACTT 960
GTCTTTAATG ACTGGGAAAA TCCATTTCCT TCCTTGGCAG CTTTGAATGT AGCAACTGTG 1020
GTTCTGGGTC ACTGCCAGAG CCAGCCTTGT GTGTATGTGT GTGATTTTTT AAAGTGGGGG 1080
AGAATGTCTC AATATTCAAT GCTCACCCCC TTCCTTCCAA GTTGTACCCC CAGAGAACTG 1140
TCCAACACAA ACTTTGGAGT TTTCCACTCT GGGAGTGGTC TGCTGGCACC CACGTGTCCT 1200
CCCCTCCTCT AATGCATCCT TTCTCTCTTG ATCTCATTGT TCTGGGGTCC TCAGCTGAGT 1260
GGGCATCTGT GCCTGGGTGA TCGATTCTAG TCTCTTTTCT GCAGGAGAGA ACTCTTGAGC 1320
TCTGAGACAG GTAGAAAGAA AATCTTAAAC CAAATAATAA TGTTCTGCCT CACACTAGTA 1380
|
