| Tag | Content |
|---|
EnhancerAtlas ID | HS040-20707 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr2:129030440-129031750 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr2:129030651-129030664 | AGGGACAGCTGCT | - | 7.52 | | Myog | MA0500.1 | chr2:129030654-129030665 | GACAGCTGCTG | + | 6.14 | | Tcf12 | MA0521.1 | chr2:129030654-129030665 | GACAGCTGCTG | + | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_06274 | chr2:129029235-129031282 | Brain_Hippocampus_Middle | | SE_27025 | chr2:129030702-129031772 | Esophagus | | SE_65419 | chr2:129029936-129030740 | Pancreatic_islets | | SE_68818 | chr2:129029877-129030873 | H9 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I128271 | chr2 | 129029236 | 129031772 |
|
Enhancer Sequence | CTTTACTGCC CCAGGCCTGG CTCTCTCCTC TGCCAAGGCC TTCTGTGCAC AGGAGGTCTA 60
GCAGGCACCA ACAGGGGCAA CGGCAGGGGA AAGGGGCACC TGAGCCAGCG AAAGCCCTCA 120
TGGTCCCTGG AATGACCAAG CCTGTCAGCC TCACCTGTCC TTCCTGCGCC CATGTCCCAC 180
ATAACCCTTC TGGACCAAGG CCTCCCGCTG CAGGGACAGC TGCTGGGGAA CCACACCAGG 240
GAGGCGGGTG TGTTCAAAGA TATTAGCAGT GCTGGCCCAG CGGCTCTGCG TCTTGTAATA 300
AAATGGCGCA ACGGACACTG CACCTGGGGG AGCCTTAGGA GCTGACCGAG GCCCCTGCCC 360
TAAGGCCCAA TGGCTTACGC TGTCCCCACG GCTCCCTGTG CACCTTCTCT GCTCAGAACA 420
TTGCCATGCC CTGGGTCCCC TTGTTCTGTC CCCTAGACAC GGCCTGTGGT ATAGACAAAG 480
GGCCAGCCAG ACTCTAGAAG CTGCCTGTGA GGCCAGCAGC CAAATGTGGG TGTTCCTGCC 540
CCTTTCTGCA GATGTGACAG CTGATCCAGG CAGGGTGACC TGCCCTTGGC CACCGTCCAG 600
TTCCTACCTA CACCTGCCTG AACGGTATGG AAGCCACTAC CTGGCACGCC CCTCCATAGC 660
CGGTGGGACT CTTTAGGAGC CAGAGGCGTC CAGTCCCATG CCCAACACGC AGAGCCCTCC 720
CCTCCCCTCT GCCTTGTCCC CTTCCCTCTG CCAAACACTG CAGGCACTGC TGGCCACAGG 780
CACGTCCTGG CCATCCTCTG GTCTGGTGCC CCAGCTGCGC CTTGCCCTGT CCCACCTCCT 840
GTGCTCCGTC CTCTTTCCTC CATTGCATGC GTTGCCAGAC GCATCTGCTG TTTACTCTCC 900
AGTCTGTCAT CTGCCAAAAG GCGGGGTGGA GGTGTCAAAC AGAAGCAGGA AGAGGGCGGG 960
GTGTGGCGAG GTGCAGAGGA CTCCCCAAAT GGCCCACCCC AGATCTAGGC AGCTCTCTGA 1020
CATGTGCTCT CTGGAGGTGC CAAGGGGGCG GCTCATGGCT CAGAGGTTTG AGGAATGGTC 1080
TGCACACTCA CGGTGGTCCC CAGCCCCTGC CCTCAGGAGC CCAGGCTCAT CTAATCCCTG 1140
CCTCGCACCC CCTGCTGAAG GGTCTGTGCC CCAGAGCAGT CTTCCCTGCA CTGACACCTG 1200
GGACCCCACA AAGCAGGGGC TTTGTGCCTA TCACTATCCA GCAGGGTCTA TCCATTCAGG 1260
TGCTCCAAGT GCCTGCCAGC AAGGCTTCCA GAAAGAGGGG AGAGAGAAAA 1310
|
