| Tag | Content |
|---|
EnhancerAtlas ID | HS012-12410 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr12:133170210-133171080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr12:133170736-133170750 | AGGTGGGCGTGGCA | - | 7.14 | | SP3 | MA0746.2 | chr12:133170737-133170750 | GGTGGGCGTGGCA | - | 7.12 | | SP4 | MA0685.1 | chr12:133170735-133170752 | AAGGTGGGCGTGGCAAC | - | 6.33 | | SP8 | MA0747.1 | chr12:133170737-133170749 | GGTGGGCGTGGC | - | 6.62 | | ZNF263 | MA0528.1 | chr12:133170577-133170598 | GAAGGAAGAGGAAATGGGAAA | + | 6.12 |
|
| | 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 |
| GH12I132593 | chr12 | 133170057 | 133171053 |
|
Enhancer Sequence | TTCAGGGTCA GCCCGCAGCC AGGGGTCCCA GAGCAGGCAA GGGCTTGAGG AGGGCCTCCC 60
GGGGCTGGGG CACCTGCCTT TCAGGTGAAA TATCAGAGTG TTCAACCCAG ACCATACCAA 120
TGGCACCCGC GCGGAGTGCA GTCACCAGGG AACCGCCCTG CGGCGATGGC CCCGGCGGGG 180
AGAGGGTGGG TGACGTGCGC TGCGGAGCAT CTGCCCTGGT GGAGGTGCAG CCCCACTCAA 240
AAAGGTTCAC CGTGTGAGTT AAAGATGTTT ACTGTGAACC CTGAAGCAAC CACTAAAACA 300
ACAAAACAAA ATTCTGGCTC ATAAGCCAAC AACTGCAATC AAACAGGATC ATCAAACAGA 360
ATCCAAGGAA GGAAGAGGAA ATGGGAAAGG GAGAGCCGGT GACAGCAGCG GGAGCAGAGA 420
GCAGGACGGC GGGCGTGGCC TCTACACAGT GAGACCAATG GGAGCAGAGA ACAGGATGGC 480
AGGCGTGGCC TCTGCATAGT GAGACCAAAG GGAGCAGAGA ACAGGAAGGT GGGCGTGGCA 540
ACTGCACACT GAGACCAATG GGAACAGAGC AGGACAGCAG GCGTGGCCTC CACGCAGCCA 600
CAGCCACACC GGAGCAAGTG GTCAGACAGC CCCAGTTAAG AGCAGAGATT GCCAGGGAGG 660
GTAGGACAGC AAAACCCAAC GCTAAACTGC TCATGAGAAA TGCACTTTAG ATATGGACAC 720
CAATAAGTCA AAAGGACAGG AAAAGCTATG CCATGCAAAC AAAAATTTTT AAAACCTGCA 780
GTGACTATGT CAATATCAAA GTAACTTCAG GGGCCGAGCA CGGTGGCTCA CGCCTGTAAT 840
CCCAACACTT TGGGAAGCTG AGGCGGGCAG 870
|
