| Tag | Content |
|---|
EnhancerAtlas ID | HS105-04189 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr1:109263380-109264520 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EGR1 | MA0162.3 | chr1:109264189-109264203 | GCTGCGTGGGCGTT | - | 6.18 | | EGR2 | MA0472.2 | chr1:109264191-109264202 | TGCGTGGGCGT | - | 6.62 | | EGR3 | MA0732.1 | chr1:109264189-109264204 | GCTGCGTGGGCGTTA | - | 6.19 | | EWSR1-FLI1 | MA0149.1 | chr1:109264379-109264397 | GACACCTTCCTTCCTTCC | - | 6.44 | | EWSR1-FLI1 | MA0149.1 | chr1:109264383-109264401 | CCTTCCTTCCTTCCTTTT | - | 7.95 |
|
| | 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 |
| GH01I108718 | chr1 | 109261592 | 109264524 |
|
Enhancer Sequence | AAATTTATTC TTTTAATAAG GAAATCAGCC ATATTGGATG AGGGCCCACC CTAATGATCT 60
CATCTTACCT GATTACATCT GCTATGACCC TATTTCCAAA TAAGGCTACA TTCTGAGAGT 120
ACTAGGGGCA AGAACTTCAA CATATGAACT TGGAGGGAAC TCAAGTCAAC TCATAACAGG 180
CTCTCACTAC TCTACCTATT TTTCCTAGTT CTCCCATGCT TCCTGTGGGA AAAGCAAGTT 240
GCCCTAAAAC ACTGCAGGCT ACCCCTACCA GCCCTGGGCC CAGCACTTCC CTAAAGCAGA 300
ACTGCCTCTG CAGACTAGCT GACCATGCAG TGGGAAGGGG CCTGTCAAGA TGGCCCACGG 360
GAAAATCATG GCAGATGCCT GCCTTACAGA GAATGAGTTA GGTCCTCATG TCCTCAAAGA 420
GGCCTTCCCG GCCGGGCACG GTAGCTCACG CCTGTAATCC CAGCACTTTG GGAGGCTGAG 480
GCGGGTGGAT CACGAGGTCA GGAGATCAAG AACATCCTGG CTAACATGGT GAAACCCCGT 540
CTCTACTAAA AATACAAAAA ATTAGCAGAG CATGGTGCCG GGCGCCTGTA GTCCCAGCTA 600
CTCAGGAGGC TGAGGCAGGA GAATGGCATG AACCCCGGAG GCGGAGTTTG CAGTAAGCCA 660
AGATTGCGAC ACTGCACTCC AGCCTGGGCG ACAGAGCGAG GCTCCGTCTC AAAAAAAAGA 720
AAAAAAAGAG GCCTTCCCTG TTTGTCCCAG ACATGTCCAG AGGATGCTGG TCTCTGCTCA 780
CAGACTGTTT AAGCAGTTTC CTAAGGCCTG CTGCGTGGGC GTTATTACAG TACAGATTCC 840
AAAGAACGGA GGCCAATTTC TCCCCTCCCC AGGCCAGGAC ACCTTCTTAC GCTTTTTTAA 900
TGCGGTAACT CTTAAGAAAG GAAGGTATAT TTACAAGAAT GTAGGGTTAA GTGTTTTGGA 960
GACACTAAAA GACTGCCTTA ATATGTATGC ATCACACTTG ACACCTTCCT TCCTTCCTTT 1020
TGATAATGAA TGGAAAGAAA ATCTGCTCCT CTAGAAACAA TTATGACCGA AAAGCTATTA 1080
CAGTAAAAGT TGTAGCAGAT GTCAAAAGTA ACGAAGGGAT ATGTTTAGTT TCATTGATCA 1140
|
