| Tag | Content |
|---|
EnhancerAtlas ID | HS061-00703 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr1:37979380-37980250 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX1 | MA0509.2 | chr1:37979571-37979587 | AGTTGCTATGGAAACC | + | 6.07 | | RFX1 | MA0509.2 | chr1:37979571-37979587 | AGTTGCTATGGAAACC | - | 6.09 | | RFX2 | MA0600.2 | chr1:37979571-37979587 | AGTTGCTATGGAAACC | - | 6.56 | | RFX2 | MA0600.2 | chr1:37979571-37979587 | AGTTGCTATGGAAACC | + | 6.57 | | RFX5 | MA0510.2 | chr1:37979571-37979587 | AGTTGCTATGGAAACC | - | 6.57 | | RFX5 | MA0510.2 | chr1:37979571-37979587 | AGTTGCTATGGAAACC | + | 6.63 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AATTTTGCAT ATACTTTAGA GGATTCACGG AAACCATGAG TCAAGAGCCC AGGCTAACGC 60
AGAACTTGGG CGATGTCCAC TCCCACGCAC AAAAGGTATC GCTACCAGGA GAGGGAAAGG 120
TGAGCAGCCT TTCAGCGTCA ACTCGCTCCC CTCCCCGCAG GCTCAAGAGA GGCCGCCGAC 180
ACCGGGCTGC CAGTTGCTAT GGAAACCTAG AAGGGCAGCT TCAGGTGAGA GGGGCCTCCC 240
GGGTGCCCAA GCCGAGACGC GGGGGCAGGA AGAGCTTAGC CACCAGAGTG CATTGGGCCT 300
TGGGTGCCTG TCACAATTCT GAATTCTCCG GAATGTGTTC TTCTCCCTCG CCTGTCACCT 360
TCTAGATGTT CCCAAACACA TCACAACCCT GTCTATCAAA AACCTCCATT CAACGGATCT 420
ACTCCCAGTA CCAAAAAGAA CACGCTCCCC ACCAGCCTCC AAAGTCCAGA CGGGGTGACT 480
GGGTCCCCCT CCCACACTAG CCTCCTTCCC CACCCCCTCC CCGCAAAGAT CACGGACTAG 540
CCCGCCTCGC CCACCCCCGC GGCTCACTGA CGCTCGCCCT TCCTAGCGCC CTCTCCCCGG 600
GCCCCGGCAC CGTCCTCCCT CCACGCCCCC TCCTGCGGCT GCCGCTTCCC CTCCCCCTCC 660
CGCGCTCCCG GCTCTCTCCC GGCTCCGGAT TCGCACAGCC GGGAAGCTGA ACCGCCGGCG 720
GGCCGCAGAA TGCGCACCCG GCCTCAGGCC GCCGAGCACC CGGCCCGCCG CGCCGCGCCC 780
CCGGAGTAAC AAACGGCCTA GCGCGGCCGG GCTTGGGGCC TGGAGGCGGG GCGGGCGCGG 840
AGCCCCATGC CGTGCAACCC CTGTCCTAGC 870
|
