| Tag | Content |
|---|
EnhancerAtlas ID | HS052-37933 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr8:141506210-141507100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr8:141506603-141506614 | CTGAGTCATCC | - | 6.32 | | FOXA1 | MA0148.4 | chr8:141506824-141506840 | CTTTATGTAAATAAAG | + | 6.14 | | JUNB | MA0490.1 | chr8:141506603-141506614 | CTGAGTCATCC | - | 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 |
| GH08I140496 | chr8 | 141506119 | 141506884 |
|
Enhancer Sequence | GCCAGGATGG TCTCGATCTC CTGACCTCAT GATCCACCCG CCTCAGCCTC CCAAAGTGCT 60
GGGATTACAG GCGTGAGCCA CCGCGCCCGG CCAACAGGGC CTTTTCTTTT AAATCAACTT 120
CATTATGACA TAATTTCATA GAGTAAAAGG CATCCCTTTT AAGTGTACAA TGTAATGAGT 180
TTTGACAAGT GTATACACCC TTATAACCAC TTTCACAATC AAAATAGAGA CATTTCCACC 240
CTGCCCCTTG GCAGTCAGCC CCATCCCCAC CCTGGCAGGC AACCGGGGGT CTGTTTCCTG 300
TCACTGTGAA CGTGCTCAGC CTGATCTAGA ATTTCATGTA ACGCGGTCCT GCAGGAAGTG 360
CGCTTCTGTC TGGCTTGCCT CGGCACAGTG CTTCTGAGTC ATCCAGGCGA CTGTGTGTAC 420
CCGTTGCTTC TCCCACTGTT GGTGTTCCAT GCAGGGATGT GCCATGGTTT GTGAACAGTC 480
TCTCTGCTCA TGGGTGTTTG AGTTGTTTCC ACCCATAGTT ATCATGAATA AAGCTGAAAT 540
GAACATTCAG GGACAATCTT GTGTGGACAT ACCTGTTTGT TTCTTTGGGT AAATAACAGA 600
AGTAAAGTTA TTTACTTTAT GTAAATAAAG TAATTTATGG GAGTAAGCTG GCTCCCATGG 660
TAAGAGGATG TTTAGCTTTT TAAGAACTGT AACCTATTTT CCAAAGTGTT TGGAACATAT 720
AGCATTGCCA CCAGCAGTGT GTGAGGGCAG CAGTTGGGGC CACACCTCAC TCTCTAACAT 780
GGGGTACCAC TGCATCATGA GTCTTGTAGA GCGTACATCC TGGCTCCTGG CCCAGTGCTG 840
GCCACTGTGG GTGCCCATTC TATTTTTTTT TGAGACGGAG TCTCATTCTT 890
|
