| Tag | Content |
|---|
EnhancerAtlas ID | HS093-13975 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr18:9173690-9174740 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr18:9174642-9174653 | CCACACCCTGC | + | 6.62 | | NFE2L1 | MA0089.2 | chr18:9173840-9173855 | AAGGCTGAGTCATTC | - | 6.14 |
|
| | 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 |
| GH18I009173 | chr18 | 9173902 | 9174798 |
|
Enhancer Sequence | TTAGGAGGTC TCACCCAATC AGGAGGGACA GGATCAGGGA CCTGCTTAAA GATGCAGTCT 60
GGTTGCTTTT TGGTAGATCA GGTGTGCTGA ATTGGGGGTA ACCGTTCCTT GCCCAGACTG 120
CCTGGACTCT CCAGAGCCAG CCCGCTTAGA AAGGCTGAGT CATTCGTGTA CCCTAAAACT 180
TAAAGTATAA AAAAATAATA AGAAGAAGAA AGGCTTAGTC AACTGAACCG CAGAGACATT 240
GGGCACTCCT CCCCCTAGGG GCTTGTCCCA GGGAGAGATC AGAGTACTGT TCATATAACC 300
TTGGCTGGAG TTGCTGAAAT TCCCTCAGGG AGGCCCCACC CAGTGAGGAG GGATGGATTG 360
GGGTCCCACT TAAAAGAGCA GTCTGGCCAC GATCTGGCAC AGCAGCTGTG CTGCCCTGTG 420
AGGGACTCCT CCTCATCAGG ACCACCTGGA TTCTTGGGAG CAGGCTAGAA CAGCTGGGTC 480
AACTGAACTG CAGAAATGGC AGCCGCCCCT CCCCCTGAAA ACTCATCCAT TTTAGGCAGT 540
CTCTAGCCTG TTGCACTGGC TGGCTAGAAT TCAAAGCCAG TGGGTTGAGG TGCCATGGAA 600
GTGAGGCCCG CAGAATGACA CTGCTTGGTT CCCAGGATTC AGCCCTCTTC CTAGGGGAGG 660
ATACGGATGG ATTTCTCACC TTGTTGGGAT TCCCAAGGGT GGAGTCTGTA AAACTCCTGG 720
GTTTACGTGT GAGCCTGAGC AACTGCTCTG CCAAGACTCC GCACAGCTCT GTATGTTGGA 780
CCTAAGTAAG GCCCTGGTGG CCTGGGTTCA TGAGGGGATC TCCTGATCCA TGGTTGCAAA 840
GATCCGTAGG AGAAGTGTGG TTTCCTGAGT GGGGTTACAC AATCACTCAC TGCTTCCCTT 900
GGCTGGGGGT GGGGGTTCCT TTGGCTCCCC AGTGCTCCTG GGTGGGCCAT TGCCACACCC 960
TGCTTTTTTT GTTGTCTGTG GGTCATGCCA TCCTCCTAAT CAGTCCCAGT GTGAGAACCT 1020
GGACATTTCA TTTGAAGGTG CTGAATTCAC 1050
|
