| Tag | Content |
|---|
EnhancerAtlas ID | HS177-10978 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr19:33925900-33926760 |
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 | chr19:33926310-33926321 | AGTGACTCATC | + | 6.02 | | Gabpa | MA0062.2 | chr19:33926333-33926344 | GTCACTTCCGG | - | 6.14 | | JUN(var.2) | MA0489.1 | chr19:33926306-33926320 | AGAGAGTGACTCAT | + | 6.6 | | JUND | MA0491.1 | chr19:33926310-33926321 | AGTGACTCATC | + | 6.32 | | POU4F2 | MA0683.1 | chr19:33926245-33926261 | ATGAATAATAAATGTA | + | 6.22 | | SOX10 | MA0442.2 | chr19:33926105-33926116 | TCCTTTGTTTT | - | 6.32 | | Sox3 | MA0514.1 | chr19:33926106-33926116 | CCTTTGTTTT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCCCAGGGAC TCGGGAAAGA TCAAAGTGTG AGCCGGAATG CGATGCCAGA GGAAGACGAG 60
GGATGGAAGA GGCAGAGAAC CTTGGGCGCT GGGGAGGCCA AATGAGGTGG CTGAGACGGT 120
AGCTCCCTCA TCCATCCGGC ATCTCCAGGC AGAGGAGAGC AAAGGCCTGG CCACCCGCGG 180
CTGCCCGAAA GCCACCAGGA TGGGATCCTT TGTTTTCATT TCCAAACCCA AAGGCCCCTC 240
GGCTGGGCCG GCGTCTGATC CCGACTCAAA GCCACAGGGA GCCTCAGCTG GGACGCAACC 300
TGAGGGCTTG GAAAATGGAG GACCCAGAGC CAGTTTTAGC AGTTGATGAA TAATAAATGT 360
AATTAACATG ATGGAAAACA GAAGCTGGAG GCCCGGCTGA GGCCCCAGAG AGTGACTCAT 420
CAGCTGCCTC CCTGTCACTT CCGGCTGCCC GGGCCCCTCG GCAGGGACAG GTGCCAGGAG 480
GTGAGGGGCG CCGAGCCCAG ACGAAGGACA ACTGGGGCAG GTCTGGCTGG GGACAACAGC 540
CCCTCCAGAA CCAACCCCCC TCGTTCGGTC CCAGCAGGGC CTGCCCTGGT GCTGGGGTCC 600
CTGGGCCCTG CAGCACGCCT CTCTGGCCTC AGGTGCTGCG CTTGTAAAGT GGGAGTGACA 660
GCCACGCTTT GGCTGTTGTC CTCTGGGCAC TGTGTGAGAA TCTGCTGATG CTCGTATGGC 720
CGTTAGTTCT CAATCACGAC AGGACTGGGT GTCAGAACCT CCCAGGGCCA TGGGCAGAGG 780
CCGTGCAGCC CAACCCACGC TCCCATGGCG TCCCTGGATT GGTCACTGGG ATGCTCAGGT 840
GAGTCTGAGG CCAGGGGGTG 860
|
