| Tag | Content |
|---|
EnhancerAtlas ID | HS051-00256 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chr1:16405260-16406340 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:16405538-16405557 | TGGCCATCAGGGGGCAGCC | + | 6.46 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 16405357 | 16406103 | | chr1 | 16406117 | 16406245 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I016078 | chr1 | 16404981 | 16406456 |
| Enhancer Sequence | AGTGAGCCAA GATCACGCCA CTGCACTCCA GCCTGGGTGA CAGAGAGGGA CTCTGTCTCA 60
AAAAAAAAAA AAAAAAAAAA AAAAAGAGGC GCCCTGAGTT CATCTCTAAA ATGCCCGGCC 120
CTGTCCTGGC CCATGGTGGC TGCTATGTGA CAGGGTCCCT TCCTCAAGGT TCAGAGGGCT 180
GGTACTCCAA TTCCTAGATC TCAGGATCTC TGCAGGTAGA AGGAAGCCCC CCTGCTAGAA 240
CTGTTGCTTT TCCAGAGCTG TGAGTGTGAG GCAGCCGCTG GCCATCAGGG GGCAGCCTGA 300
GACAGCATCA TTCTCTGTTG CTTTCCTTTT CCTTCCTCCC GCCGTCTGCT GACCCAGAAA 360
GTACCCTGCT GGTAACTCAG CCCCAGCCAT GGCTCTGGGT GGTGCATGCT GCACCCTGCA 420
CAGAGGAGCC TGGCTGAGTG GGAGGGGACC AAAACCTGCC CGTGCTCTGG TCCCAAAGCC 480
CTGAGCTCTA CCGTTGTGTA GAGCTCTGTG TCTGCCCCAG GACAGGGAGG TTTTTTCCTA 540
GCACAAAGGT GTCACTTCCT CTAAGCTGTG CACTCACAGG GTGCATCTAC CCAGAGGGAA 600
GGCCTTTTAC AATTTTGCAC AAAGTCTCTG TATAGCCTAG CCAGGCTCCT GAAGTCAGAC 660
AACACGTGGT CCTGACCCCC ATTGTACAGA TGCGGAGACT GAACCCCAGG AAAGGAACCA 720
AGGCCAGTTA GGAGCACAGC TGGGACTGGA ACACCACAGC CAGCAGGACC CGCTGCTCCA 780
GTCTGGAGGA GTCAGGTGCT AGGTGTCACT TCTGGTGTCC TGGCCCCGCC TGGGGTTTCC 840
CCGGGGCTAG GACTTGGGGC CTTTCTGGGG AGCCTGAGAA AGTCACAGGC CGTTCTCGGA 900
ATATGCCTAC TCTCACTTCC AGGCTCCGAC TGGAATTGGA TGTTAGGTCA GAGCCCTCCC 960
CAGGAAAGCA GGCTGGACTA GGTGGGATAG GCCGAGACAG AAAGTTGAGC CCCTAGTCTG 1020
ATGGGGGAGA CAGAGCCCTT AGGGAATTCC AAGTCTGATG CAGGAGACAC AGCCATGCTG 1080
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