| Tag | Content |
|---|
EnhancerAtlas ID | HS110-01505 | Organism | Homo sapiens | Tissue/cell | KATO3 | Coordinate | chr16:811180-812670 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr16:812078-812088 | GCCCCGCCCC | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AACAACCTTT GAGCTCTTCC TGTTGTGGTG TGGATGGAAT CTGCACCTTC CATCTGGAGA 60
ACTGGGGCCG CCCCAGGCCG GGCTTCCAGC ACCAGAGCGA TGGTCAGGCT TCAGCTGGAC 120
GCAGATTTCA CCCCGCAGGG CACACGCAGA CCCATTTGTT TGGAAGCGGC AGTCCTAAGG 180
CAGTGCAGGT GCCTCCACGG CCCCAGCCCA GCTCTCCTGC AGGTGTAAAG GATGCAGATT 240
CCAGGGCCCC CCATGGCCTG CAGAGGCCCC TCAGAGCAGG AAGGGCCGGG CTCTCGGGGA 300
GCCCCCATCC CAGGTGCTGA GGTCCTTGGG TCACATGGAG CTGGGGTGGG GAGTGCCCAG 360
GTCCCCTGTG ATCCGATGGC CACGTTTCCC TCCTGGCTTC ACGCACCCCA AGGGCTGGGG 420
GTCCCACTCA CTGCCCATTT TCTGGCTGTG GGGGGGGTCT GTTTTCTTCC ACCTTCTCAA 480
GGTGTTCAGA GCCTCAGGGG CCTCCCCACT TCCTCTGGGG CCTGGGGGAG TAGAGTCTGT 540
CACCCGGAGG CTGTGTGCCT CCCCGCGACA TTCCCCAGTG GCCGGGCCGA CCAGGCAGGC 600
TCTGCCTGTG GATGGGGCTG CTGAGCATGA GCGTGTGACC CCCATTTCTG AGCTGTGGGT 660
GGACCCACCG GGCCTGGGCC AAGGTTTTCA GGAGGCAGCT CTATTCTACT CCGCCATGGT 720
GGCCTCCCTG AAAGGGGTGA GTGTAGAAGC CAGTTCCCTC TTCTGCGAGC CCCACCCCTA 780
CCCCAGGAGG ACAATTCTTG TTCAGGGAGG GTCTCCCCAC CCACTTCCCC ACCCCACAGT 840
GGCCCACAGG CCCCACCCTA GAGAGTACAA GGGGCTCCCC AGGCTGCTCA CTGGCCCAGC 900
CCCGCCCCAC CTGGACTGCA CCTGAAAATG GGCTCAGAGA GGCCAAGTGG CCCAAAAAGA 960
CGCTGCTGGG TGGGAAGGGG CGGTGGCCTC TGTGCCCGCA GTGCCCCTCC TGCCTCAAGG 1020
GTGTTGTCTG CCTGGCAGAG CCTGGGGTGT TCACAAAGCC CAGGCACCTG CAGCTGAGGG 1080
CAGGGGAGAG GGAAGGGAGC CACATCCAGG CGACGGGGCT GCTCGTCCTC CTGTGCGAGA 1140
GTGGGGAGAC TCAGGCCAGC CCAAGTGGGC GGCGGCCCCG GTTGCTTGAT CTAAGCTCTG 1200
CTCACACTGC CCTGCCCTTC TGGGAGAGGG GTGGGCGCCA ACTGACTCCT GGGCTGTCTG 1260
GGCTGGGGAC CGGGATCTCA GACCCAGCCC CTCCCCTGGA CAGGAGGAGC CAGTCCAGGG 1320
GACAGAGGGC TCAGTGGCTG GAGGGCAGGG CCAGGGTGCG GACACAAGCT GCAGGTACCA 1380
CAGAAGTTTG CTCTGGGAGC CCCTCCTGGG CCCATGTGGC CCCAGGCTGG CCCAGGACAG 1440
AGGCGTGGGG TGGGAGCAGG GGGTCCCATC CTGAGTCACT GCCCTCCACA 1490
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