| Tag | Content |
|---|
EnhancerAtlas ID | HS047-17871 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr19:49091940-49092980 |
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 | AGATAGAGTT AGAGGTGGGT GTGGGGCTGC AATTATAAAT AAGGAGGTCA AGGGGGCCCC 60
CAGTGAGTAA AAACCCGGGA GGTGATGGTG GGAGCCACAG AGGTTTCTAG AGGAAGAGCA 120
TTTCAGGCAA GAGGGAAAAG CAGGTGCAAA GGCCCTGAGG TGGGTGTATC TGAGGTGCAA 180
GAGGGAGGTC GGTGTGGCCG GAGCCAAGTG AGCAAGTGGG GAAAGGAGTG GAGATGAGGT 240
CCGGGTGGGG AGGCAACAGG GGCCAAAATG TGCAGGGCCG CGTGGGCCCG GTGCGGACTT 300
GAGCTCTGAC CGAGTGACGA GGCAGCGCGG CAGGGATCGC AGCAGAGGAG GAGCCCGAGC 360
GGGCTTAGGC TTCACCGGCG CCCTCTGGCG GTCAGATGGG GACCGACTGT CGAGAGAGCA 420
GAAGCCGGGA AGCCCGAGAG GCGGCGCTGG CCGGGGTCCA GGGGAGGGGA CGGTGGCTGG 480
ACTAGGGTGA TGGTCACGGA GGTATTTTGA AGGTGAGACC GGGAGGATTT GCTGACAGAC 540
TGGATGTGGG TGTGAGAGAA GGGGATGAGT CAAGGGTGAC TCCAAGGTTT CGGCGGAAGC 600
AACTGTCAGG GTGGGGCAAC TGGGAAGGGG AGGAGGGAGG GGAGCAGGCG GGGGAGGAAG 660
ACACGGGCTC TGCGGCGGCC CATCCCACGT CCAGCAGAGG CTGCCGGTGG GCACAGAAAT 720
GCACCCATCG GGATCTGAGG GGAGAGACTT GGGCTGACAC GTCCATTTGC AATTCCTTGG 780
CACATATATT CTGTAATTAA TCGAAGCTCC AGGACTGGGT GATATCGCCA AGGAATTGAG 840
CGTGGACAGA GCAGAGAGGG GGGGCTGCAA TCAGGAAGTC CCCAAGACCA CCCTCAGGCT 900
CAACGACTTA GCAAAACTCA TAGTGTTCAG CAAAGCTGCT GGACTCCCGG GTTATAGTCA 960
ATTACAATGA AAGCAAACGT GAAAATCAGG CAAGGGGGCC GGGCGCGGTG GCTCACGCCT 1020
GAAATCCCAG CACTTTCAGA 1040
|
