Tag | Content |
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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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