| Tag | Content |
|---|
EnhancerAtlas ID | HS026-15398 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr18:43967200-43968360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr18:43967886-43967899 | GGCAGCTGTTCCT | + | 6.36 | | REL | MA0101.1 | chr18:43967948-43967958 | GGGGATTTCC | + | 6.02 |
|
| | 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 |
| GH18I046385 | chr18 | 43965757 | 43970208 |
|
Enhancer Sequence | AAGGCAGATA ACCAGGCCCC ACCTCCAGAG AGTCCCATTC AGCAAGTGGG TGAGGGGGTT 60
GGGGATCTGC ATTGAAACAA GCCCCCATCC TCCATGATTC CAGTGCAGAG CTTGGGGAAC 120
CACTCTGAAG TAAGGAAAGC AGCTTTTCCT TTGGACAGTG CAGGCCTTTG GGAGTGAATC 180
CAGTACAAAA ACAGCATTAG CTCTGAGGAC AAGAAATGTG TACAGAACTT GCAATATTCC 240
AGGACTAGGG GAGAAACTTG TCCCAACTTT AGTGCCAAAT TCCCCTCCAG GCTGTGCAAA 300
ATGTGGAAGT CCCTGTGCTT CCCGGCACCA CCTGGGTGTA GCTCTGGAGG GCATGAAGCA 360
AGAAAAACAT TCCCCACTTG GAAGAAGTCC AGAGCTGGGC ATACAGACCC GTGGAGGGTG 420
CAAGGGCCCC TGAATGGGAA CAGACCAGAA ACCACAGATA GCTTCAGTTT GGAAGTCAAA 480
CGCTGGGACG GGAGAAGCTT CTAGTCTTCA TCATCGAGGA CTGCTGAAAT CCCAGGGTCA 540
GCTCAGGGAT CTGTGTGCAC CCAAAGCAGC CTCTTGAAGC AGAAGCTGAC CTTAGGGGTT 600
ATTTAGTTAC AGGGACAGCC AGTGCAGGGC AACGCAGGCT GCCAGTCCAG CTCTTAGGAC 660
TGGGGCAGTC ACGCCTAATC AACCGTGGCA GCTGTTCCTT CAAGCCTACA GGCAGCATCA 720
GAATTCCTCT GAACAATCCC CACAGGCTGG GGATTTCCAA GATTCAAGCT GGCACTTGCG 780
TTCCAAGCAG GCCTCTTTGC CATTCCCCAT CTAGATGAAC ACCCTTATTT GACACACAAA 840
GAGTATAAAG CTGAGAGAGA GAAAGTGGCT TACTGAAGGT TACATGTTTA TTTGGGATTA 900
CAGCTGGGAG GTGAAGGGAG ATAGCTACAT AGTAAGATGG CATTTTCAAG GGGTGTTTGG 960
GTTCCCTGGC TAAGTAAGTT GGAGAAATCC TGTATGTAAT ACCACCTCTA ACTCGAAGAT 1020
TCACCACTCA TACAGTATGC AAAAGACTTG GAAAGGTTGC AAACCTGGAG AAGTTGGCAG 1080
GAAACAAAAC AAAACAAAAC AAAAACCTTG TTTAACTTTT TCAACTTTAT AATGTTTCCA 1140
TGCACTTCTT AGATACATTT 1160
|
