| Tag | Content |
|---|
EnhancerAtlas ID | HS105-16157 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr11:112434700-112435740 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr11:112435219-112435230 | AGTGACTCATG | + | 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 |
| GH11I112563 | chr11 | 112434580 | 112435878 |
|
Enhancer Sequence | CTAGCTGATA AAAAGTGTGT GGCACCTCCC ACTCTCTCTC TTGCTCCTGC TCTGGCCATG 60
TGATATGCCT AATCCTGTTT CTCTTTCCAC CATGAGTTAA AGCTCCCTGA GGCCTCCCCA 120
GAAGCCAAGC AGGTGCCAAT GTCAGGGTTG TACAGCCTGC AGAGCTGTGA GCCAATTAAA 180
TGTCTTTTGT TTACAAATTA CTCAGTCTCA AGTATTTCTT TATAGCAGTG CAAGAATGGA 240
TGAACACACA AGGAGACAGA AAAGCTTGCA GAGAGGGCAG TATATAGACA GGGCTTAAAA 300
GTGGCTGCTA AAATGGGACT GGACCGGTGC CTGTGAGCTC AAACACAAGT TCACATACTC 360
TCCTCAAGCA GGCCTAGCAT CCACCCCCCT CCCTAGGGTT CCAGTTTGGT TCTAAGTAGT 420
TTTTGGCTCA CAGCATCTTT TGTTGTTCTC TGCACTGCAG AGATATTTGC TGTCACTTTG 480
TTGTCAGACC CAGGAAACGT TGTCTGGCTC CCAGAGGTCA GTGACTCATG GACTCACGGT 540
AGACACACAG ATTGTTTGTG AGCTAGGGCT TGCTGGAGAG TATCTGGATA AACAAGAGAA 600
ACCCAAATCA GGCTGTCTCT CTGCCTGCTG AGAGCACTGT TTATTGTTCC AGCCTCAGTG 660
TTTGGAAATG TAAACCTCTG GCTGACTTTT CACTCCTCTG GCTTCACCAC AGAGTTCAGA 720
AATCCACTGT GGCCACAAAG GCTGTTTTGG AAGAGCTTTC TCTCTTTAGC TGTCTCTGCA 780
GTTTTAGGAT GCTGGAAGCC ATTTGCTTTT CTGATTTAAG AACATTTTTC CTGGAGTGAG 840
GGAGGGAAAG TCCAGGGTCT GATTGGTGAG GCTGCAGGGG TGGAACTGGG TCACCTGGAC 900
CTGGGATGCC TGCAACTTGT GGGCTGGCTG GTTAAACCAT GAGAGGGGAC AGGCCCCCCT 960
CTCTCAGGTA TGGTCCTGGC CTTTAGTCCT GGTCTTTCCC ACAACTAGGG CCCTTACCTG 1020
ATTGTTGGTG CCAGCTCAGA 1040
|
