| Tag | Content |
|---|
EnhancerAtlas ID | HS091-22925 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:4266680-4267620 |
Target genes | | Number: 30 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:4267192-4267211 | CAGCCAGCAGAGGGCACTG | + | 7.65 |
|
| | 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 |
| GH19I004269 | chr19 | 4267101 | 4267290 |
|
Enhancer Sequence | TAAAACAGAT TGAAGAGGCT AGATGCAGTG GCTCACGCCT GTCATCCCAG CTCTTTGGGA 60
CGCTGAGACG GGAGGATCGC TTGAGCCAGG AGTTTGAGAC CAGCCTGGGC AACATAGCGA 120
GATCCCGTCT CTACAAAAAT TAAAAATGTT AGCCTGCCAT GGTGGCGTGC ACCTGCAGGA 180
GGCTGAGGCA GGAGAATCGC TTGAGCCCAG GAGTTCGAGG CTGCAGTGAG CTATGATTGC 240
ACCACTGCAC TCCAGCCTGG GCAATAGAGT GAGACCTTCC CCCCAAAAAA ATTTTTTTAA 300
TAATATAGAT TAAAGGGTCC CTTCTGTTGC AGTTAAGGAG CTGGAGGCCT TTTCTACCTG 360
CCCCTAACTC TTTCTCAAGG CGGCTTCCTC CATTTTCACT CGTTCTCTCA AGTACATTGA 420
GCACCTCCTT GTGCCAGGAA CTGTTTGTGG CACCGCAGAG CCAGCAGTGG GGAAGACAGG 480
AGCTCACGGC AGAGTTGGGG AGAGAGTTAT AACAGCCAGC AGAGGGCACT GTGAGCGTGG 540
ACATGCAGCC TGCATGTGAG CTTGAACCAT GATGGGCTTC TCAGAGGAGG GGTGTCTTGT 600
GTTGGGTATT GAAGGGTGAG TAGGAGTTCA CCAAGCGAGT GCATGGAAAA GGGGGCATCC 660
CTGGTGAAGG GAATAGCATG GGTAAAGGCG TGGAGATGAG AAGCCATGGT GTGACTCAGG 720
AAGTGCCAGA CCAGGCTATG TGGGATGGAG AATGGGCAGA GGCCTTGAGT GCCAAGCCTA 780
GGGCAGTGGG GAGCCATAGA GGAGTTTAGA GCAGAGGAGG AATGTGGTCA GTGCAGCAGT 840
GGAAGAGTGG GCATGGGGCA GTGAGCAGGG GTTGTGGCGA GGGGCCAGAC TGGGCCCTGG 900
ATCCGGGCCA GACCCCCACA TGTGTCCCCA TCACCTGCAG 940
|
