| Tag | Content |
|---|
EnhancerAtlas ID | HS040-00895 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:22458770-22459490 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr1:22459297-22459310 | AGCAGCTGTCCCC | + | 7.04 | | Myog | MA0500.1 | chr1:22459296-22459307 | CAGCAGCTGTC | - | 6.14 | | Tcf12 | MA0521.1 | chr1:22459296-22459307 | CAGCAGCTGTC | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65544 | chr1:22451883-22461737 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I022134 | chr1 | 22458693 | 22458894 | | GH01I022132 | chr1 | 22459101 | 22459250 |
|
Enhancer Sequence | TCTGCTCCCA CAGCATGCAG CCAAGAAGGC TGCATCTGGC TGTGCTGGGC CCTGGGCTCT 60
GGTCAAGGGA GGCACCCAAG GGCAGGGGTT CTCTGGGCAG GGGGGGCAGC CTCTGACCCA 120
CCATGACCTT GGGCAAGTCC CTGCCATACT TGGAGCCTGT CTCCTTATGG GTACAGTAAA 180
CCGGTGGGTC CATATGGCCT TTCCCACTGT CGGAGTTGGT GGGCCTCCTT CTACTGGCAG 240
GGTGGGGAGT GGCCGGGCCT CAGGGGCCTG CTGGCCCCAT GCCAGGCTGA TAGATGTGTC 300
TCTGCCATTG AATAAGTAGT AAGATGGACC AGGGGAGCCA CCTGCATCCC CCCACCCAGG 360
CTCAGAACTC AGCAAGGGGA GACTGGCTGA ATGACAGTCG CAGGGGCTTA GGGTGAGCTG 420
CTGGGCTGCC GTGGCCGTGA GTCACTGGGC CAGCTTCCAG GAAGGAGCTG AGCAACCTCT 480
TCCGTTGGCA CCAGTGCCCA CCCCCAGCCC CTGCCTTCAT CTGGCACAGC AGCTGTCCCC 540
TTCCGTACAC ACGAGGCCCA GCCCCATCCC CACCCCTGTT CCCCCAGACC CCAGGGTCTC 600
GCCCGGGCAG GGCTGGGTGC CAGGGCTGGA AATGGAACCG GGCACCGGCT CTAGAGAGTG 660
AGAACCCCAG GCATTACAGG CCCTCATCCA CAATGTTTCT GCTTGCCCGT TTCAGTATCC 720
|
