| Tag | Content |
|---|
EnhancerAtlas ID | HS051-28741 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chrX:153755030-153756150 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chrX:153755557-153755567 | GCCCCGCCCC | + | 6.02 |
| | | 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 |
| GH0XI154525 | chrX | 153753688 | 153756371 |
| Enhancer Sequence | TCTTGCTGTG TGGCCCAGGC TGGAGTGCAA TGGTGTGATC ATGGCCCAAG TGAACCTCCC 60
ACCTCAGTCT CCTGAGTAGC TAGGACTACA GGCATGTGCC AACATGCCCG GCTAATTTTT 120
GTATTATTGT AGAAACAGGG TTTCATCATG TTGCTCTGCT GGTCTGGAAC TCTTGGGCTC 180
AAGCAAAATG CCCAAAGTGC TGGGATTACA GGAGTGAGAC ACTGTGTCCA GCCATAGAGT 240
CTCACTGTCC TTACAGAAAG CCAGAATTCA GTCTGCTTCT TGTTCCCTCA AAGCTTCCTC 300
GAAGTGTTCT AGTGGAGGCG AGCAGTGAAG CTCTAGGAGG CAAGAGGCCT TCTCAGGGAC 360
CCCAGCTTTG GCCTGTATGT CTGGGTGTCG TCCTGGACTA GTCTGATCAC GTCTCACAGC 420
TGAGTTTCTC AGCTTCTCCT CCTGCAGTAC AGGAAGGACA ATCCCTTCCG ACTGCTTCTC 480
ACAGGGAGAG GGCAGTGGTG AGCCTAGAAA ATAAAGGCCC GAAGCCAGCC CCGCCCCATT 540
TGTGCCTCTC CCTCCTCTCC TTTTCTGCTT CGCAGAGCAG ACAATGCAAC AGTCGCCCCC 600
GCCCAGCTCA GCCTGAAGAC CCCTTCTCCA CTCCCATCCC TTTCTGGCTC AGCCACCCGG 660
CAGTGGGCCA GGTTCGGATG GAGGGAGGGA GAGGAGCTGG AGAGAGTTTT AAGTACTCTC 720
TGGGCTTCTC ACATTGCTGG CTTCAGTGGT TGCTGGACGC AAATTGATGT GATGTCAGAC 780
ACCGGCAGCA GAGAAGGAAG CTAAGGCATT TGGGTCTGTG CTGCTGTGGC ACCTGGGACT 840
CAGTGTGAAG GGATCAGGCT AGGTTTGAAA TTCTCTTCCG GCTTAATAAT TTGCAGGTCT 900
GGGCTGGGAG GTAAAGCTCT GAGTACACTG CGAGTGTCAG GGGTCCGGCA GGGGGGCTCT 960
TTCCAGCTCC TACCCACTCC CGCGTGGGGT GAAACCTTGA GAGATGAGAC ACCAATCCAG 1020
GGCCTCTGAA GACCCACGAG GTAGAGTGCA CTTAACAGTA AATTGTGGGC TGGGTGCGGT 1080
GGCTCTTGCC TGTAATCCCA GCACTTTGAG AAGCCTAGGC 1120
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