| Tag | Content |
|---|
EnhancerAtlas ID | HS040-01362 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr1:38579390-38580820 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mafb | MA0117.2 | chr1:38580083-38580095 | AGTCAGCAGTTT | - | 6.22 | | PLAG1 | MA0163.1 | chr1:38579912-38579926 | GGGGCCCTAGGGAG | + | 6.11 | | ZNF263 | MA0528.1 | chr1:38580292-38580313 | CTCTCTTTTTCTTTCTCCTTC | - | 6.64 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATCGACTCTG CTCAACGAAT TGCTCAAGGT GCTTTCTCTG AATCTCATGT TGGGCTGGGG 60
CACTGAGGCC GATCAATCAG GAAGAGCCCA CTCTCTAAGC TCACAGGTCA GGGGAGGAAG 120
CAGTCATGGG CCAGAAAGGG CTGGGATCAA AGGAAGCTAT CAGGACTGGG GTGTGCAGAG 180
GACACAGAGA CTGACTCTGT CTTGGTGACA GGGAATCTGG GAAGATGTCT TGGAATAAGA 240
GATAGTAGGA TTGGGCCTTG GAAGTGTGTA TGACCCTGCA GTTGGTGATC CCTTCTGCAA 300
AATGGGGCCA AGGAAAACTT CCAGGCCCCA AAGTGACATC TGGTTTGTCC CCTTGCTTCC 360
TGGTCCCTAG TAACAACCTG GGACTCATGA GGATCCTCTT GAGGTTTCTT TAAGGCAGTC 420
CTGAGCATGG GGCTCGCAGC TGGAGCCAGC CTGGAACCTG GGCCCTTGGT GGTTGGCCAG 480
GGTGGGTGCC CTGGAAGAGT CAGCTTTGAG CCTGTCTTCA GAGGGGCCCT AGGGAGGGCT 540
GTGGCCTAGG CGCTCTGCCC ACCAGGCTTC CTGTGGGTGG CAAGTGAAAC TTTTCCTCTT 600
GGTTCTCTCC CAGAAGCCAG CTTCATTCCC CCAGCCCCAA GTGGCGGCTC CTTGGGCCGG 660
AAACAATGTG CTTTCTCCAC GCCTTAGAGT GGAAGTCAGC AGTTTGGCAC CGTCTGGCTG 720
GCAGCCTCCA CCGGCTTCCT TTGGCACTTT ATTGGCAAAG GCGGTGACAT TTCTTTCAGT 780
TGGGTGGGTG GAGCTGTTAT GCAAACTCCC GCTCTCCTCA TTCGCCAGAT GAATATTCAT 840
GACTCAGGCA ATCTGTACCA GCCAGACTTT CCTGAGGGCG GCAGCTTTTC TTCTCTTCCT 900
CTCTCTCTTT TTCTTTCTCC TTCTCTCCTT CCCAGCTCTT TGGAAAGCTG AAGTGCAGCT 960
ATATTTAATT TACAAATACA GAGCCATTTA GCTTGCCTTT TGAGATGCAG GCACTGGGGA 1020
GGAGGTGCTG GGGAATGGGA ACAGTGGTTG AGGAGTTTGG TCCTGACCCT GTGCCTCTAA 1080
GCTCCAGTGT CCAGCCCCTG GGCCCTAGAT CCTGGGAAGC TTTGGGAGTC TGGAGCTTCT 1140
TTGAGCTTGG CCTCTTGGGG CCTTCAGGGA TGAAGGTACA GCAGCTCACG CCACCCCATT 1200
CCACACTGGC CTCTGAGGTC AACATGGAAA TTCTCAGGCA ATGATGGTTT CCTGCAATTC 1260
ATGGCCTGGG ACCCACCAAT ACATCTTCTC CCGCTCTGCT CTCCCGTTTG TCAAGGCCCA 1320
CCCAGATCCT GCTCCAAGCT CTAGGTGGAA GCCCAGAAGG CACTGGAGCA TTTGCTAGTC 1380
ATTGGCTTTC CGGGGAAAGA AATAATCCTT GTTTGGGGTC CAATTCCTTG 1430
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