| Tag | Content |
|---|
EnhancerAtlas ID | HS133-08292 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:132665610-132666330 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr12:132666228-132666239 | GGAGGGTGTGG | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CAGCAACATG CAACAACCCC CTGACACACC TAACACACAC TCCCATCGCC AGTGCACACA 60
TAGCACACAT GTTTGCACAC TCACCCTGCA CAACTAATAT GGCACACTCA CCCAGCGCAC 120
GCTCACACCC AGCACAGGCT CAGCACATGC TCACACCCCA CACAACACAC ACAGCACACA 180
CACAATGCAC GCTCACACCC AGCACAGGCT CAGCACAGGC TCACACCCCA CACAACACAC 240
AGCACACACA CACACCTCAG TACACACATC CTGCACAACT CACACCGCAC ACACACATGC 300
TCAGCGCACG TTCACACCCC ACACAACTCA CACAGCACAC ACACGCACAG TACACACACC 360
CAACACAACT CAAACCACAC ACACACTCAG TACACACACC CAACACAACT CACACAGCAC 420
ACACACACAC ACTCGGTACA CACACCCAGC ACGCACACAT AGTACACACA CCCAGCACAA 480
CTCACACTCA GTACACACAC CCAGCACATG TACCCACCCA GCACACGTTC ACTCGCACCC 540
TGCACAGCCC AGCGCGCACA CACCCAGCAG ACAGCACATG CTCTCACATG CTGGCATCAG 600
CCGTCAGCCT CAGCTGCTGG AGGGTGTGGT GGAGGCGGGC GGTGAGCGCT GGGTGCTGGG 660
GTCCACGTCC TTCCAAGCCC CTGCATAGCG GCCGCCTTGG CTGGCGATGA CTGGAGGGGG 720
|
