| Tag | Content |
|---|
EnhancerAtlas ID | HS052-02942 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:178971400-178972670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:178972412-178972430 | GGCAGGCAGGCAGGCAGG | + | 6.1 | | FOXH1 | MA0479.1 | chr1:178971625-178971636 | TGTGGATTGGG | - | 6.14 | | HSF1 | MA0486.2 | chr1:178972506-178972519 | GAATTTTCTAGAA | - | 6.34 | | PAX6 | MA0069.1 | chr1:178971973-178971987 | AACTCAAGCATGAA | - | 6.55 | | TEAD1 | MA0090.2 | chr1:178972431-178972441 | ATGGAATGTG | - | 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 |
| GH01I179002 | chr1 | 178971429 | 178973891 |
|
Enhancer Sequence | CAAGACCCTA TCTCAAAAAA TAATTTTTAA AAACCCAGGC ATGGTGGCGC ATGCCTACAG 60
TCCCAGCTAC TCGGGAGGCT GAGGCCTGCT TGAGCCTGGG AAGCCGAGGC TGCAGTGAGC 120
TGTGATCATC CCACTGCACT CCAGCCTGGG TGACAGAGCA ATACCCCATC TCCAAAACAA 180
AAACAAAAAC AAAAACAAAA AACAGGACCA GCAGGAATAG TCTGCTGTGG ATTGGGACCC 240
CTGAATGTTC CAGAGGGATT TAAGTGTGCG GAATTCAGAC GTCTTCCCTG TTGTGGCTGG 300
CCTTCCCGCC TCCCCAGCCG TCTGCCCGAA TGAGTGCTTA CTAATGAGCC AGAGAGCTCT 360
GAGCCGGCCT GTGTAGGGCA TCCATGCAGG GCTCCAGGGG CCCCTCTCAG TGAAACAACA 420
TGACTGTGAA AACAATCTGC TGCTCTTCTT CTTCACCCTG ACCTTGGGTC ATTCTGGCGT 480
AAAAGATTAC TTTGCTCCCA GCCTCGGGGA AGTTTTTGTA CAATTAGCTA CAACTCGGCA 540
GAAAGACCCT GCAGAGAGAG CCCTGGGGTC ACCAACTCAA GCATGAAAGG ACACTGACCC 600
CGTGTGGTCA TGTTTGGAGG TGCAGCACGG GGAGAGAGGA AAGGCCCCGG CACGGTCCTT 660
TGGCCAAACG ACCCCTGCAG GCCCTCCCTG ACCGACCTTG CTCTGTCCCT GCTCACTTCA 720
CAAGACCCTG GGGAGAGGAC CTGGCCCTAT CAGGGCCTGC TGACTCGTTC TCCCCTGGCG 780
AAATGTCCCC ACCAGGTGCT CTCAACTCTG GGGTATGACT TCACAGGCCA TTTGAGTTCA 840
GATGGGTAAG GCGTGTAGGA AATGAGCTCA AAGGGTAGGA TGGATTTTGA TGGGGTAAGA 900
AGAGAGTGTT TCTCACTCAC CCAAAGCACT GAGCACAGTG TCCCAAACAT AATGTGGAGT 960
AAACACGCGC ATGCACACGT GCACTTCAGG TGCAGGAGAC AGCCTAAGCA GGGGCAGGCA 1020
GGCAGGCAGG TATGGAATGT GCATGGAGGG CTGGAGAGTG GAGCTGCTTT TCTGCGGAGA 1080
TTTCAGGTTA GGTGGAGCAC TGAGCTGAAT TTTCTAGAAG CTGGATTCCT AAGCCCCAGT 1140
TCTGGGCTCT TTCTCTGACC ACACAGCTGT GTAGAAGGAA AGGGGCCTGA GTTCTGCCAT 1200
CTGGGCTAGG AGTCGGTATA GAGCCAGCCA GTTGTAGCAT TTCTGATTCC ATCTGAATTC 1260
CTAACACATC 1270
|
