| Tag | Content |
|---|
EnhancerAtlas ID | HS080-13224 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr16:28543290-28544190 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr16:28543320-28543332 | TGCAGTGATTGC | - | 6.14 | | NFKB1 | MA0105.4 | chr16:28543618-28543631 | AGGGGGATCCCCC | + | 6.02 | | NFKB1 | MA0105.4 | chr16:28543618-28543631 | AGGGGGATCCCCC | - | 6.03 | | NFYA | MA0060.3 | chr16:28543830-28543841 | GGCCAATCAGA | + | 6.02 |
|
| | 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 |
| GH16I028531 | chr16 | 28543123 | 28546830 |
|
Enhancer Sequence | AATTTAAAAA TTAGCCCAGG AGGTCAAGGC TGCAGTGATT GCACCACTCC ACCCCAGCCT 60
GGGTGATAGA CTGAAACCCT GTCTCAAAAA GGAGAAAACT GAGGGTGATT CTGAAATTTA 120
AAAATGTACT CCTGTATCTG TGAGCTGGCC TTTGAGAAAG GGGAAGGTGG AAGAGAATCA 180
GGTTGCTTGC AGAACAGACA GACAACCCCA TGGTGAGTTT CTCAGTTCTC TGCAAGGAGT 240
CGGGAGTCCT TTGAGTTACA GAAGCCTGAC AGGGCCAATT CTGTAAGCCC CTGGGGTAGG 300
ACAGAGGTCA GTGATTTCTC TAGTTCTCAG GGGGATCCCC CCAAAATGGG GAAACAGACA 360
TGCAACCAGA AGAAAAAGAA AGGGTTTAGG AAAGGGGATG GAGACAGAAG AGGAAGAGTC 420
TGGGTAGGAT CCTTTCGGAT CCAAAAATTC TGCAATTCCA AGAATTGCCT TAATTCCCAG 480
AACAGCCACT TAAAGGCCTC TCAGGCAGAG GCTGTGCCAG GCGAGGGCGA GGCCAGGAAA 540
GGCCAATCAG AGGCCAGGAG GGAGGGGCAG TGTGTGAGGA CTCCTGGCTG GTGTCAAAGG 600
ACCCAGGACA GGGAGTGGCC ATTCCAGCTA GGGACACAGT GCTTCCCAGC CTTCATTTTC 660
TCTTTTGACA GAAGAGAGGC CAGTCTCACC ATTTGACAGG TGAGGAAACC CAGGCCCAGA 720
GGAGTAATTG ACCAGAAATT AACGAGAGTT TAGGATTCTT CATTGTCAAT ACATGGTTCT 780
TCCCAGGCAT GTAGCAAAGG GGGAAAAATC CAGGCTTTAA AATTCAGATA GACCTGAGTT 840
CATAATTCCA AGTCCTACAG GATGTGGCTG TGTGACTTTA GGCAAATTAC TTAATGTCTC 900
|
