| Tag | Content |
|---|
EnhancerAtlas ID | HS132-01183 |
Organism | Homo sapiens |
Tissue/cell | Melanocyte |
Coordinate | chr5:179604200-179604850 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr5:179604506-179604517 | CTGCAGCTGTC | - | 6.62 | | Tcf12 | MA0521.1 | chr5:179604506-179604517 | CTGCAGCTGTC | - | 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 |
| GH05I180176 | chr5 | 179603796 | 179605111 |
|
Enhancer Sequence | CCGAGTAGAG GATGCATTCA AACCATGTGC ACATCAGCCC CTCAGCCCCG AAGCCAGGGG 60
CTGCTTTCCC TTTCCGGCCC CACCTCCCCA CCCAGTGAAG GGGCTGGCCT GCCCGGCTCA 120
CCCAGCAGCT TCCCCAAAGA CACAGGCTGT TCATCGGCTC CATTTTTAAC CTTCCTTAGT 180
CCCAGCAGCC CCAGCAAAAG CTCTTCGGTG AGTGCCTGCG CAATCTGCCC GGCTGGGCCG 240
CAGCAGTCCA CGGGCAGGGC AGAGCCCCGG GCTTCCTTCC GGGACCCCTG CCAAGGCTCA 300
GCCCTGCTGC AGCTGTCCAA GGCCATGGCC TCTGCGGCTT CTGCCTGGCC AGCATCTGTT 360
CTTCCCTCTG AAAACAGAGC CCATTTGTCC TTCCTCTCCT GCCCGTGGTA GGAGGACATG 420
GCCCTGGTGC CACTTGGGGA AGGAGTTGCG TTGGTCTGTG ACAGTTGGGA TGGCATGTGA 480
TCCAGGCCCA GCCACTCAGT GCCTTTCATC TCCCTGGCCT CTGGGATAAA TCCATGGGCA 540
GGCATGTCAC CTGGGTGGGC CACCAGACTC AGTTCGTGGG ACATTTATTT GAACTGTCTG 600
AGCAGAGCCT CTCTCTCTGC TCAGGGCAAG GTAAGGACAG GAAGTAAGTA 650
|
