| Tag | Content |
|---|
EnhancerAtlas ID | HS040-00122 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr1:2468390-2469340 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| INSM1 | MA0155.1 | chr1:2468983-2468995 | TGCCTGGGGGCA | + | 6.04 | | Klf1 | MA0493.1 | chr1:2469056-2469067 | AGGGTGTGGCC | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 2468593 | 2468929 | | chr1 | 2469015 | 2469203 |
| Enhancer Sequence | GGCTCCTGTG TATACACCTG TGTGAGTGCA CCTGTGCGTG TGTGTGTGTG TGCCTGTATG 60
CATGTACTTA TGTGTGTGCA CTTGAGTACG TGTGTGTGCC TGTGTCTGTA CGAGTGTGTG 120
TGTGTGCCTG TGTCCCAGTG TGTGTGTGCG CTCATGTGTC TGTGTACCAG TGTGTGCGCT 180
TGTGTACGTG TGTGCCCATG TGTCTGTGTG TACCAGTGTG TGTGTGTGTG CATGTGTGCC 240
CATGTGTGTC TATGCATGCA TCTGCGTGCA TGTGCCCAGG AATGCTCACG CCTGCTCAGA 300
TGTCCTCAGC TGGGCCACCC GTCCCCACCC TGCCCCGCTG CCCTAACTCC CAGAGTACCC 360
GCATTGGCCG AGCACTGCTC TGTGCCACGT GAGCCCTGGG CCCTGGGGTG ACTGTGGGGA 420
AAAACCCTGA CAGGAGTGCC TCTGCCCTGC CCTGCCCAGT AGGAACGGTG CTCAACCAGG 480
CCCCTGGCGG CCCTCCGAGG CAGGTAAGTG CGTCCCTATC TGCAGGTGAG GGACAGAGGT 540
GCTGAGGGGC AAAATAACTT GCCAAGGTCT CACGGTCATG CCCCCCACCA CCATGCCTGG 600
GGGCAGGCCT TGGCAAGGGG CATGCTGCCA GTCAGTTGGC AGCAGAGCCA AGAAGGGACA 660
GAGCTCAGGG TGTGGCCCTC AGTGCTTAGG ACCAGCTGCT CCTCCCCTTG ACGCTGGCTT 720
CCCACAGGAG GTGCCGCTGT GTGCTGCTCA CACCCAGAAG AGGGGGTCAG GGCATGCAGA 780
GTCCAGTCGG GAAGCCGAGG CCCGAGGAAA GGTGGGCAGG GGCCAGAGCC TTCTCCTGGG 840
GTGGAGGTCA GGCTGCAGAC ACTGCTAGCC CTGTCCCACC ACAGCCCGGC TTCTCAGTTG 900
GGTCTCCACC GGCTGTGACA CTCCCACGTG ATGCCAACAG GTGTTATGAG 950
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