| Tag | Content |
|---|
EnhancerAtlas ID | HS003-24148 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr19:49091930-49093100 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:49092315-49092334 | CGGCGCCCTCTGGCGGTCA | - | 7.08 | | ZNF263 | MA0528.1 | chr19:49092577-49092598 | AGGGGAGCAGGCGGGGGAGGA | + | 6.05 | | ZNF263 | MA0528.1 | chr19:49092565-49092586 | AGGGGAGGAGGGAGGGGAGCA | + | 6.56 | | ZNF263 | MA0528.1 | chr19:49092580-49092601 | GGAGCAGGCGGGGGAGGAAGA | + | 7.84 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27310 | chr19:49091844-49093429 | Esophagus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr19 | 49092038 | 49092197 | | chr19 | 49092379 | 49092800 | | chr19 | 49092091 | 49092636 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I048588 | chr19 | 49091858 | 49093070 |
|
Enhancer Sequence | AGAGGGCTGG AGATAGAGTT AGAGGTGGGT GTGGGGCTGC AATTATAAAT AAGGAGGTCA 60
AGGGGGCCCC CAGTGAGTAA AAACCCGGGA GGTGATGGTG GGAGCCACAG AGGTTTCTAG 120
AGGAAGAGCA TTTCAGGCAA GAGGGAAAAG CAGGTGCAAA GGCCCTGAGG TGGGTGTATC 180
TGAGGTGCAA GAGGGAGGTC GGTGTGGCCG GAGCCAAGTG AGCAAGTGGG GAAAGGAGTG 240
GAGATGAGGT CCGGGTGGGG AGGCAACAGG GGCCAAAATG TGCAGGGCCG CGTGGGCCCG 300
GTGCGGACTT GAGCTCTGAC CGAGTGACGA GGCAGCGCGG CAGGGATCGC AGCAGAGGAG 360
GAGCCCGAGC GGGCTTAGGC TTCACCGGCG CCCTCTGGCG GTCAGATGGG GACCGACTGT 420
CGAGAGAGCA GAAGCCGGGA AGCCCGAGAG GCGGCGCTGG CCGGGGTCCA GGGGAGGGGA 480
CGGTGGCTGG ACTAGGGTGA TGGTCACGGA GGTATTTTGA AGGTGAGACC GGGAGGATTT 540
GCTGACAGAC TGGATGTGGG TGTGAGAGAA GGGGATGAGT CAAGGGTGAC TCCAAGGTTT 600
CGGCGGAAGC AACTGTCAGG GTGGGGCAAC TGGGAAGGGG AGGAGGGAGG GGAGCAGGCG 660
GGGGAGGAAG ACACGGGCTC TGCGGCGGCC CATCCCACGT CCAGCAGAGG CTGCCGGTGG 720
GCACAGAAAT GCACCCATCG GGATCTGAGG GGAGAGACTT GGGCTGACAC GTCCATTTGC 780
AATTCCTTGG CACATATATT CTGTAATTAA TCGAAGCTCC AGGACTGGGT GATATCGCCA 840
AGGAATTGAG CGTGGACAGA GCAGAGAGGG GGGGCTGCAA TCAGGAAGTC CCCAAGACCA 900
CCCTCAGGCT CAACGACTTA GCAAAACTCA TAGTGTTCAG CAAAGCTGCT GGACTCCCGG 960
GTTATAGTCA ATTACAATGA AAGCAAACGT GAAAATCAGG CAAGGGGGCC GGGCGCGGTG 1020
GCTCACGCCT GAAATCCCAG CACTTTCAGA GGCCAAGGTG AGCAGTTGAT TGAGCCCAGG 1080
AGTTCAAGAC CAGCTGGGCA ACTTAGAAAC ACCCATCTCT ACAAAAAAGT TTAAAAATTC 1140
GTCACGTGTA GTGGCATACA CCTGTAGTCC 1170
|
