| Tag | Content |
|---|
EnhancerAtlas ID | HS080-23644 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr3:45379350-45380170 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MSC | MA0665.1 | chr3:45379866-45379876 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr3:45379866-45379876 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr3:45379866-45379876 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr3:45379866-45379876 | AACAGCTGTT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AAAATCTAGG TTTCCACGGA AGACCAGCTG GCCTTCTAAT TTGAGCAGAA TTTGCAACCG 60
ATTATAAAGT CAAAGATCAA TGTTTAACAA AAATCAAGTC AGCCTGGAAA TCTTTTATTC 120
TCCTGAGCTG TGTAGGCGGC TTTTCTGATA GGGAACGCTC ACTCTGCGTT GGCGTTTTGG 180
AGGTGTTCTG CATTTGAAAA GCACCCTGCA ATCTGCTTTC CCCCCCAACA CCCAGGCAAA 240
GTTGACGGCA TTTTCCCCTC AGTCCTTTCT ATTAGTGCCG CAGGACAAAG GTTGGTCACA 300
AAGCTCCAGA TTCACTATAT CCATCCAGCT CTGCCAAATG CAGATCACAG TTTAACAATC 360
TAACTTCTCG AGAGAGGTCT GCACTCCAGG CCCTGTGCTA AATGGGGAGG AACAGAAATG 420
AATAACGTAT GGTCTTGGCA CCGAGGACTT AGAATTGTGG AGGCAGAAAC AGACACACAA 480
ACAAAAACAT ATGACAGTAT TATGGGAGCC ACCAGGAACA GCTGTTGGAA TCCAGTTGGG 540
CACAAGGAAG GGAATGGTCC CTTCTCCTCA GTGTTATTCA GCTGGCTGTA AGTCGTGGGG 600
CTTTCCAAAG GATGGAAAAG AGGGATCTGG GACCAGCATC TCAACACACG CACTTTGTAC 660
CAAAGCTCCC AGCCCACCCA CCTTTTCCCA GGCATCTCTG CTTCCTGAGG TTTCTCTGGC 720
ACCTCTATTA CTGTGTTATC TCCAGGTTTC GGGGTCTGCT CACCCAAACC CTAGAAAGAA 780
AAGCCCAGTA CTTTCTGTGA AAGCCAGGTA GTGATGTAGA 820
|
