| Tag | Content |
|---|
EnhancerAtlas ID | HS105-16887 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr11:129620210-129621160 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr11:129620874-129620893 | CGGCGCCCCCTGGCGGCAG | - | 6.95 |
|
| | 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 |
| GH11I129750 | chr11 | 129620200 | 129621180 |
|
Enhancer Sequence | AGAATTCTCC GAGAGAAAAC AAGCTTTGCA GACTCTCAAA GGGAATGTCT GGCCATGGTG 60
GAACGCGGGC CCTTGGAGGA CTGGCCGGGG CTATGACTCT GGAAGCAGCA AGGGAGGCAA 120
GTGCGCAAGC CTCACCGAGA AGGGAAGACC AGGCTGCTCT CAGCTCTCGG CCGGGCTCCT 180
CACACACCGG AGTGGGCCTA AAGTTCGAGG AGCTTCTTTC TCCTTTTCTC CCCGCAGTGC 240
TTAACGTCTC GGGCCACGGG CTGCCAGCAC TCACCTTCTG CCGAGGCCGC CCTGCGGCCT 300
CCCTGTTCTG AGGCCCCTGC CCCTCCCTGA TGAAACTTCC TCGGTGCTAA CTTGGCAAGA 360
ACAGGCAAAC GCTGCTGTGC TTCCCTTTGC CCATGAAAAG AATGAGGTTT AGGGGAGGCT 420
CTGCACAGTC CTGTGCTGCC CGGGAGAGCT GAGCAGAAGC TGTTGAAGCC GGCCTCCTGG 480
ACTGAGCTTG GTCCAGCAGC CTATCCACGT GAGAGCCCTG GCTGTCTGGA GGCACAGGGA 540
GCGGCTGGGC CTGCAGCGTC CCACCTGGAG GGAAAGGACG CACCGCGACG GAGGCGTGGG 600
CCCTGCGCCG GTGCTGGGCA GGCGGCGGCC GCGCGCCCGG GAGCCACGCT TCTCCGGCGG 660
AACGCGGCGC CCCCTGGCGG CAGAACGCTT GTGGCCGCCG TTACGCTCGT GTGGAAACAG 720
CGCCATCTGC CGAACGTTCT GTCACATTGC TGATTGGCCC ACACAGATTT TGTAAGGATT 780
TTTCCTTCTG CTTGCTTAAA TCAGGCCGTC CTGAGCCTAT TCAAAGTGTA CTTTTGAAAT 840
GAAAAAAGAA ACTGACTGTA CAAGATGTTT TGCTCGCTGG AAAAACGAGG ATGAAAGGAA 900
AATGGGTAGC GATTATCTGA ATAACATGTG CTTCCTGTCT GTAGTGAGGT 950
|
