| Tag | Content |
|---|
EnhancerAtlas ID | HS133-13873 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:80287960-80289300 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZEB1 | MA0103.3 | chr17:80288312-80288323 | CCCACCTGCCC | + | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 80287992 | 80288104 | | chr17 | 80288129 | 80289095 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I082328 | chr17 | 80285936 | 80289111 |
|
Enhancer Sequence | ACAAGGAGAC CCCAGGGGGC CTGGGTCCGG CTCCCTCACC CCACGCTCCA CGATGCCAGC 60
TCAGCCACCC ACCTTGGAAC CGTGCAGATG GACAGCAGGG AGGGTCGGGG CTGCTGGGGG 120
CTCCCCCACT GCTCTCCGCA CCACCCCGCC GACCGTGTCC GGGAGGGGAT GCCCTGCTGC 180
TCTCCCCAGG CTGCTCTGGG GAGTCCTGCC CTCACCTGGA GCCTGGAGGC CATCTGAGTC 240
TGTTTCACAA ATGCTTCCAG GGACTGCCCC TGCCATGTGT TAGGGGTGGG AATTCTGGGC 300
ACACAGCCAA AGGTCACAGA TCCCCAGAGA GCCCCGACAG CGCTGCGTCC ACCCCACCTG 360
CCCACCCAGG TGCTGGCTCT GCCACCCGTC TGTGTCCTGA GTCAGCCCTG ACTCGGCAGA 420
GAGCTGCACC CTGAGCCAGA CCTCAGCAGC TGGGTCCTGG AGGCCCCCAA GGGCCAGCTG 480
CACGCACCTG GCTTCATGCC AAGCTCCTCC CGCCTGGCAG TGGCTGCATC TGCCTCCCCT 540
CCACCCTGAG TGTCCCAAGT CTGCCCGCTG TGCATTCCAT GGGGCCAGCA GCTCGGTGGA 600
GCCTCTGCTC TCGGGGGCTA CAGCTGCTCC TAGATGCCTC TGCCACCGAG GGTGGACCCT 660
GCAGTGCTGG CTCCTAGCCT CCCTGCCGAT TGCTTCCTGA AGACCTGGGG CCCTGGGCTG 720
CAGTGGTTGG GGAGAGGGGG GTGGGAGTGA GAAGCTGGCA CTGTCCGTCT TTCTGGCCTC 780
ATCCTCTCCA TGGTCTCAGC CCCTGGCGGC CTGGACTGCA CCGTTCCGGA GATGCTGCCT 840
CCCCACCAAG TCCCTTTAGC CCAACTGTGG TGGCGGCCGC TGCTTCTCAC ACGCGGGTCC 900
TCTCACTGCC TCTCCCCGGT CCTCCCTTCC TCCCAGCACC TTCACCAGCT CCCCACTGAG 960
TGCCCTCCAA TGTTGGCGAC CCTGACCCTT GTCCAGCCAG GGGTGAAGGG CGGCAAGGGA 1020
TGGGCTGGAG GGTACTAGGA GCAGGTGGCG GTGCCCTTCC TGTCGGTCCA CACCCGGCAA 1080
GTGGCGGGAA AGGTGTGGAA TGAGTCAGCC GTGGAGGGGA GCCCTGGGCC TGGAAGACCC 1140
CTGTCTTTGG CTTGAGAATG ACTTTGAAGG GCTCAGGGGG TAGGGAGCTG GGGGGAGACC 1200
GGGAGGAGAG CGGCAGGTCT GGCTCTACCC CGAGGCTTCA GGCTGCGGAC CATGCGTGGC 1260
CCCAGCTCTG TCTGGGCAGC AGGTGTCAGC GACTTTGGGT TGCTGTGGGA ATTTGCTCCG 1320
TTTATCAGAA GAAAACGCAC 1340
|
