| Tag | Content |
|---|
EnhancerAtlas ID | HS098-26772 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr19:2488600-2489650 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr19:2488824-2488842 | TACGCCTTCCTTCCTTCC | - | 6.45 | | EWSR1-FLI1 | MA0149.1 | chr19:2488828-2488846 | CCTTCCTTCCTTCCACCT | - | 6.56 | | NR2C2 | MA0504.1 | chr19:2488602-2488617 | GGAGGGCAGAGTTCA | + | 6.03 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_24383 | chr19:2488019-2489749 | Colon_Crypt_2 | | SE_25170 | chr19:2487722-2489940 | Colon_Crypt_3 | | SE_27369 | chr19:2488366-2489529 | Esophagus | | SE_31940 | chr19:2488633-2489386 | Gastric | | SE_43297 | chr19:2487788-2489849 | Lung | | SE_50943 | chr19:2488184-2490012 | Sigmoid_Colon | | SE_54295 | chr19:2488527-2489543 | Spleen | | SE_65706 | chr19:2488397-2489169 | Pancreatic_islets |
|
| | 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 |
| GH19I002487 | chr19 | 2487747 | 2490069 |
|
Enhancer Sequence | AGGGAGGGCA GAGTTCAGGC CCTACAGGGA GGAAAAGGGA GGGGCGGAGG CCTGGCTTTA 60
GGTTTGAATC TCCGCGGCTT ACTAGCTCCA GCAGCTCAGC AAAAGCGTGA CTCAGTTTCC 120
CTCGTCCATA AAAGGGAAAG CCGAATCGCC CTCCCACGTG TCGAGGTGAA ACTAGACAGT 180
GCACTAAGGC ACTTAGCAAA ACGCGCTGCC TTGAGAACCC TTATTACGCC TTCCTTCCTT 240
CCACCTCACC CCCTGGCCAG ACACTCTGGG GGTGGAGAGG GGCGCTGACC CAGGCCCCAG 300
ACGCCCCTCC CGTCCGCCCT CCCTAGCAGG CAGGAGTCCC GGCTTTCCCG TTCCTTAAAT 360
TGGATAATTG GAGACAGAGG CGGGTGCTCG AGACGGAGAA ATCCCCAAGT GGGCGAAAGG 420
CAAGGGGCCT GTCCTAGTTT CCCTGCACTG GGGGCCCCCA CCCTCGCCAG CGCTCCCTCC 480
GGTGCGCCCT GGGCGCGCAG TCTGTGCGCT CGGGAGCCCC CAGCGCCGGC TGTCGACCCC 540
CTCCAGAGCC CGGCGGTGCC AGCCTCCCTC TGTTGCCCGC CAGGCGCGGT GTCTGCGGCC 600
GCCCCGGCAG GAGGGGTTGG GGGGTCCGGG CCGGCGGCAG CTCCGGCGGC GTCTCCCTCC 660
TCCAAGCCCC TGGCGGCGGG CGGCCGGGCC GAGGGCGGGG CGTCTGCACA GACCCTCCTT 720
TTGTGAGCGG CGCCTTCCCC GGGCGGCCTG GCGCGCAGGG CTCGGGCACT GCGCCAGGGC 780
CCGGAATAGC CTCCCTGCCC GGCCGCCCGC CCCACGCCCC GGCGGAGCCG CCTGACCTGC 840
CCGGTCGGGC GCAGAAGAGC CTGGGGCCGC GGTGGCACAG GAACCGGGTG CGTGCTCAGC 900
TGCACGGGGC TGCAGCCGCT ACTCTCCGCT GGGCCGGCAC TGGACGCGTG CAGCCGGGCC 960
TACTGTGCGC AGCCCGTCTT TTGTGTGAAA ACGCCCGCTG TGTGCAGATC TCCGTCTTCG 1020
TGCAGGGCCT ACTGTGCGCC GCACCCCCCT 1050
|
