| Tag | Content |
|---|
EnhancerAtlas ID | HS187-00376 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:25174330-25175630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:25174752-25174770 | GCCTCCTTCCCTCCTTCC | - | 7.61 | | Myog | MA0500.1 | chr1:25174635-25174646 | GACAGCTGCAG | + | 6.62 | | PLAG1 | MA0163.1 | chr1:25175091-25175105 | CCCCCGGGGGCCCC | - | 6.24 | | Sox6 | MA0515.1 | chr1:25175584-25175594 | CCATTGTTTT | + | 6.02 | | Tcf12 | MA0521.1 | chr1:25174635-25174646 | GACAGCTGCAG | + | 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 |
| GH01I024847 | chr1 | 25173986 | 25175722 |
|
Enhancer Sequence | CTCAAGCAAT CCTCCTGTCG TAGCCTCCGA AACTGTTGGG ATTTCAGGCG TGAGCCACCG 60
CGCCCGGCCA AGAGCACGTT TGGTTGGTTT GTCCTGAGGG GCAGGTCTCT CGCACCAAGC 120
AGGAGGTAGA GGTCTCGGGC CCAGAGGGGC CCTGCATCCC CCACCTCCTG CTGCGAGAGG 180
CATCAGCCGG CCTTGTCCCT AAAGCCCCTG CTCGCTTTCC TGTCACCACT CGGGTGCGGT 240
TCCGAAGTGG CCAGCAGGGG CCGCGGTTCC CCTCCTTTCG GCGCCACTTC TGCAAGCAGG 300
GCTGGGACAG CTGCAGGACC TCGTCAGTTT GGGGAGCTGC CAGACCCGAT CAGCAGCGTT 360
GTCGGCTTCC TTCCTCTTTA TCAGATCTGT CAGGGCTGCT GCGCGCTGCG AAGGCGCCTC 420
CGGCCTCCTT CCCTCCTTCC TGTGTCGAAC GGACGCTCCC CGGCGCCGCT GCGAACCGAC 480
ACCTCCGCGC CTCCCCCGGC GGGGCAGGGC AGGGACCCGC TCACACCCTA GGTGGGGTGG 540
GGTGGGAAGT GCCAGCGGTC TGGGTGTGAC GGAGCCAGCC AATGTCCACG CGAGGTCAGG 600
TCGCACGTGG GCCTCGACGC TGGCACTTCT GCATGTCCCT GGTTCTCGGC CGGCCACCGG 660
CAGCTAGAGG AAGCGCTTCG CCCGCGAACC ACAGGGCTGG GCGGCGGTTG GGTCGCGGCA 720
GGGCGAGGGC TCCGCTGCGG TTGGCCCCGA GCGGCGTCCT TCCCCCGGGG GCCCCCGATC 780
ACTGCCTGGG GACTCGAGAG CGTCCCCGCC GCCGCGCCAG GCGCCAGTTC CCTGCTTCTG 840
AGAGCGCGCA CGGGAGCCCG AGCGAGCCCT CCTGGACGCC CGGCACAGGC CGGAGCGCCG 900
ACCGCGGGAG GGGCCACCTG GGCACTAGGA AAAGGGGCCA CGGTTCCAGG CGGGGCGGTC 960
CCCGCTCTGC TGACTCGGAC GGGCCTCACT TCCCCGCCAG AAGAAGCGGC ACCCATCCAC 1020
GGGGAGGGAC GGCCTCGGGA CATCCTTTGG GGAAGCCAGT GACACATTTC TGATCCAATT 1080
TCTTATAAGA AATAGATAAA CCTCAGTTTC TTCCTGTGCT TCCTTTCTCT AATTTCCTCA 1140
GTCAGATAAT AATTGTCATT AAACTCGATG TACCAGTTAT TGTGCTAAAG TTTTTAAAAT 1200
GTTTCAAGTC TCTTCATATT CTCAAGTCTA TTAGAGGAGG GACTATTCTT GTCCCCATTG 1260
TTTTATATAA AGAAACTTAA ACCTAGAGAG GTTAAATAAT 1300
|
