| Tag | Content |
|---|
EnhancerAtlas ID | HS133-26021 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr5:179603840-179605080 |
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 | | ZNF263 | MA0528.1 | chr5:179604095-179604116 | GGAGGAGGACCAGGGTGAGAG | + | 6.51 |
|
| | 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 | CCACCGCGCC TGGTCCCGGG GCTAATACTT TTTTCCAGAA AGATTCAGCC ACAGCAGAAG 60
CTATGAAAGC ATGACTGCTG CGTGGTGCCA GCCGTCAGGG TTGGGCAGTG GTCAGTCCTG 120
CCCATGTCTC CCCCTGGCAT AACCCAAGAC AGGGCCCCTG GCCTGGCCTC CAACTCCCAC 180
CCAACCTTGG TCAACCTCCC AGAGGAGAGG GCTGCAGACG AGGGGTTTCC AAGGGACGGC 240
AACTTTTGCC AGCATGGAGG AGGACCAGGG TGAGAGGTGA GACTCTCAGA GCCTGACGGA 300
GGGGCTGGAT GAGGGGCAGT GGGATGGGGG GCTGGCTGGG CTACTTCCAG AAACGTCCAG 360
CCGAGTAGAG GATGCATTCA AACCATGTGC ACATCAGCCC CTCAGCCCCG AAGCCAGGGG 420
CTGCTTTCCC TTTCCGGCCC CACCTCCCCA CCCAGTGAAG GGGCTGGCCT GCCCGGCTCA 480
CCCAGCAGCT TCCCCAAAGA CACAGGCTGT TCATCGGCTC CATTTTTAAC CTTCCTTAGT 540
CCCAGCAGCC CCAGCAAAAG CTCTTCGGTG AGTGCCTGCG CAATCTGCCC GGCTGGGCCG 600
CAGCAGTCCA CGGGCAGGGC AGAGCCCCGG GCTTCCTTCC GGGACCCCTG CCAAGGCTCA 660
GCCCTGCTGC AGCTGTCCAA GGCCATGGCC TCTGCGGCTT CTGCCTGGCC AGCATCTGTT 720
CTTCCCTCTG AAAACAGAGC CCATTTGTCC TTCCTCTCCT GCCCGTGGTA GGAGGACATG 780
GCCCTGGTGC CACTTGGGGA AGGAGTTGCG TTGGTCTGTG ACAGTTGGGA TGGCATGTGA 840
TCCAGGCCCA GCCACTCAGT GCCTTTCATC TCCCTGGCCT CTGGGATAAA TCCATGGGCA 900
GGCATGTCAC CTGGGTGGGC CACCAGACTC AGTTCGTGGG ACATTTATTT GAACTGTCTG 960
AGCAGAGCCT CTCTCTCTGC TCAGGGCAAG GTAAGGACAG GAAGTAAGTA TGGAGCTGGT 1020
GGGGGCTTTC TTGTGAAAGG GGCCCACATG GAGGAAACGG AGCCAAGACT CACAGAGACC 1080
GAGACCATGT CCCACATCCA GCCATGCCTG AAGCCCACCT TGGGCTTTTT TTTTTTTTCT 1140
TTTTGAGGTG GAGTCTCGCT CTGTTGCCCA GGCTGGAGTG CAGTGGCATG ATCTCGGCTC 1200
ACCGCAACTT TCGCCTCCCA GGTTCAAGTG ATTCTCCTGC 1240
|
