| Tag | Content |
|---|
EnhancerAtlas ID | HS040-00112 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr1:2312750-2313910 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:2313353-2313372 | GGCTGCCCCCTGGTGGATG | - | 6.92 |
| | | 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 |
| GH01I002381 | chr1 | 2313039 | 2313840 |
| Enhancer Sequence | AGGAGGAATG CCTGGAGAAG GCGCTGGAGG AGCAGGCAGC TCACTGGCCA TGGTCTGCCC 60
GTGCCTGCAG GTGTCAGCAG CGTGGACGAG GCCAGGGGAC TGCTGCCACC AGTGACACTG 120
CCCAGAGCAC CCCGTGGGGC AGCAAGCACC AGCACACAGC AGTGTCCCCA GGGAGCTCAA 180
GCCACGGGCC TGCCTGGGGA GGGTGTGCGG GCCTCGGTTG GCAGGCGGTC CCAGGGCCTG 240
CCCAGGTCTC CCAGTCCTCT GGGCCTGGAC GGCAGAGGAG TGGGGAGGTC ATGTTATAAC 300
CCCAGGGAAT GTAGGTCACG CGAAGGGTTT GGCACCAAGA CTCTCGCAGA AATCCTCTGC 360
AAAACCCTCT GCAGAATTCA AGGTTTTACC ACCAAGGGGA GAAACCATCC CAAGCAGAAA 420
GGCCTGGGGG GCCGCTTGGG GGCCCGGCTC TCAGGAGTAC CCAGCCAGCC CTTGGGCCCA 480
GTGGCCATCC CAGGCCATCC TCCCCCGTCC AAACTCATGG CTTGGGAATA AGCTCTGGGC 540
TCCCGGGGAG GAGCTGCCTC CCTCCAGCAA GGCCCGGGCC AGTGTGGTGC CGGGACAGGG 600
CTGGGCTGCC CCCTGGTGGA TGCGCTGAGC ACCCTGGTGC TGTCAGCCCA GGAGGGAGGG 660
CGCCGTCCCT TGCCTGGTCC TCTCTCTTGG CCCAGGGCGC TGGTGACCAG CAAGCAGTGT 720
GGACCCGAGT TGGCGCCTGG GTAGTAGCCA GGGGACCTGT GGGACAGAAC AGCCTCTGGG 780
GACAGGGCTA GGCTGGGAGT GGGGGTGGGG AGGACAAAGC TGTCCATGGT CCTCTGGAAG 840
AACAGGAGCT GCTTCTCGCC CGGCCCAGGC CGGAGGGGAT GGCCCTGTCT GGCAGCAGGC 900
GGCACCTCTG TGTCCCTGGG CCATGAGACA GGCCCTGACC AGGTCCTCCT GAATCTCAGG 960
GAACATGAGG ATTGGGTGAG TGGCTGGGGG CCCCCAGGGC TGTGTTGCCC TGGTGAGGGA 1020
GCCTGCCATC CTAGCACCTC AGCTTCCTCA CCTATGCCCT GCTCGGACTG GTGGGGATCA 1080
TGAGCCAATG CACCGAAAGG CTGACAGCAG CGCCTGGCAC CCAGGAAGTG AAACCACACA 1140
CCCGAGCCCA AGCTCCAGAG 1160
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