| Tag | Content |
|---|
EnhancerAtlas ID | HS062-05442 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr15:40566540-40567580 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr15:40567040-40567059 | GGACGCCCCCTGCTGGCAG | - | 6.48 | | CTCF | MA0139.1 | chr15:40567082-40567101 | CACCGCCATCTGGTGGCCA | - | 8.63 |
|
| | 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 |
| GH15I040274 | chr15 | 40566801 | 40567401 |
|
Enhancer Sequence | ACCTGGGCTC CCAGCATCTC CCTTCCACTG AAGCCACAGG GTCTGGGCTC CTGGAAAAGG 60
CTCCTCTTTC CCCACACAAA ACCCGCACCT GGGTGTGGAG CCGCATCTAC GCACAAGTTC 120
GCATGTGCGC TCCGACAAGT CGCCTCCCAC GGCTGTGGCA GGAGAGTTGC TGCTTGGCAG 180
AAGGGTTGCT GCTTGGCAGG CACTGGTCGG AAGCCCAGTG GGGCCCATGA GCAGGGAAAG 240
CCAGGACACC AGCAATCCCT GCTGTCCAGG GAGGGATCCG GAGAAGCTTC ACTGAGCACA 300
AACCCTTCTA ACCCGTGTCG GGAGATCCAT ACCATGATTC GATGTCCCTG TCCATCACGG 360
CGAGTCGGCT CATGCTCCAT CGTTGCACAC CCCGACACAG CTAAGCCACA GCGTTCCCCT 420
TAAAGCCAGT ATAAGTGCAT GGAAGTGTAT ACATGTAACC CTTTTTGCCA AATCGGCCCC 480
AACCCCGCAG GCCTTACTGT GGACGCCCCC TGCTGGCAGG TCAGCACGGG GCTGCTAAGT 540
GGCACCGCCA TCTGGTGGCC AAAACAAGAA ATGTCTCAGA GGGCTGAAGC CTCTCCTCTA 600
AAATAGCAAA AAAACAAGAG TTCTGTGGCC CCAACACAAA GCTGGATGGG AGGACCAACA 660
GGAAACATCT TCCAAGACAA CTGGTCCTTG GAGCCCGCAC CGCTAACCCC AAAATTAGCA 720
TATAAAGATC TCCAGTTGGC TAATTCCTCA GAGGATGTAG CCTTCTGCCC AAGACTCAGC 780
CTCATCCCAA GATACTGGCT CAAAATGAAC CAAGATAAGC CCTTGCTTTA GACTCTTAAG 840
GCCTAGAGCA ACAAAGAAAT CTTCCTTTTC AGGTCTCACT TTATTTTCTA TTTTTCAGAG 900
TACTTCCTCA TCCTTGACTT GTTTGTTTCT GTTGTTGTTG GTTTTTTTTT TTTTTTTTTT 960
TTTGGAGATG GAGTCTCTCT CTGTTGCTCA GGCTGGAATG CAGTGGTGCG ATCTCAGCTC 1020
ACTGCAACCT CCGCCTCCTG 1040
|
