| Tag | Content |
|---|
EnhancerAtlas ID | HS092-06629 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr10:70353910-70354730 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr10:70354463-70354474 | GGTGACTCATG | + | 6.62 | | HES2 | MA0616.2 | chr10:70354601-70354611 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr10:70354601-70354611 | GGCACGTGCC | - | 6.02 | | JUND | MA0491.1 | chr10:70354463-70354474 | GGTGACTCATG | + | 6.02 | | NKX2-5 | MA0063.2 | chr10:70354512-70354522 | ACCACTTGAG | + | 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 |
| GH10I068594 | chr10 | 70353850 | 70354660 |
|
Enhancer Sequence | GACCTCAAGT GATCCTCCCG CCTTGGCCTC CCAAAGTGCT GGGATTACAG GCATGAGGCA 60
CCATGCCCAG CCCTGTTATT GGATTTTTCT GTCCAAATTT TGAATCTAGA CACTGACACA 120
GGGAGTAGGC CTTCCAGTTT CTAGTTGGTA CAAAGAAGAG TTGAGAAATT TGAGAGAGGC 180
AATAATTTCA GCCCCATTCT TACAACAGTT TGTCTCAGTT GGTAACTGTT GAAGATTATT 240
CACCTACTTT TTCCTCAATT CTTGCTTTAG AAGAGCCATC AAGGAACAGC TATTACCAGC 300
AGAACTGCTG GAAGGAATCC AGTAGATCTG GCCCCTTGGG AGAGTGGGGG AAGAGCAAGA 360
GTAGCCTCAG GGAAAGGGGT CAGGGAGAGA TCCAGCAGGA AAGGCTCTTC TAGTGGACCA 420
ACCGCTTACA TCCGGACTAT TACTCCACCC AGTCTTCCAA GGAGATTCTC CAGTGTTAGC 480
CTTTCAGGTT CCTATGTGTC ACAGGAAATA AAACCAAACT AGCTTTTTTA AATCTATGAG 540
AGAGAACGGG CGCGGTGACT CATGTCTGTA CTCCCTGCAC TTTGGGAGGC TGAGGTAGGC 600
TGACCACTTG AGGTCAGGAG TTTAAGACCA GCCTGGCCAA CATAGTGAAA CCCTAACTCT 660
ATTGAAAATA CAAAAATTAG CCGGGCGTGG TGGCACGTGC CTGTAATCCC AGGTACTCAG 720
GAGCCTGAGG CAGGAGAATC CCTTGAACCC GGGAGGCGGA GGTTGCAGTG AGCAGAGATC 780
TCGCCATTGC ACTCCAGCCT GGGCAACAGT GCTCAAGACA 820
|
