| Tag | Content |
|---|
EnhancerAtlas ID | HS195-05665 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr5:138897230-138898180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NHLH1 | MA0048.2 | chr5:138897574-138897584 | CGCAGCTGCG | + | 6.02 | | NHLH1 | MA0048.2 | chr5:138897574-138897584 | CGCAGCTGCG | - | 6.02 |
|
| | 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 |
| GH05I139517 | chr5 | 138896810 | 138898710 |
|
Enhancer Sequence | TGGCCATCCA GCCTGGAGTC GATGTTGGCA TGAATGAAGA CACAGGCAGT TGGGACAGAG 60
AGAAGCGAGT GGGATGTGGA GGTGACCCGA TGAAATACTG GCCCGGAGAT ATGAGGCATG 120
AGGCGGGGAG CACGAGGGTG TCGAAGGGCC AAAATGTGGT AAGAGAAGCC GGAGGAGTGT 180
GAGGACAGGT GGAAGGGATC CAATGTGGGA TCTAAGGGGT CTGAGACCAC CGTGGCCGCG 240
GGAGGCAGGA GAAGGTACCG CAGAGCTCCC GGTGATGTGT CAGGAGGCCC TACACTCGCG 300
CGTGCACTGG CTCGCAGTTT GGACAGAGAC CCTACAGGCC AGGCCGCAGC TGCGCCCAGA 360
CCACCCCCAG CGGGTGAAGA CTGCCGCGGC GGCGCAGTTC CCGGCATGCC TCCGGCCGGT 420
GACTTCATCC GGCCCGGGGC CAAGGCCCGG CCTCCGCTAG AGGGCGCTGC TCTCAGCAGC 480
CGCGCCGCCC GGATGGACTC GCGCCAGAGT AGGACAAGAG AGGCAGGCGG CGGCTGCTCC 540
GTGCGGCTCC CACGCCTCTC GGGCGGCAGG TCCTGCCTCG GACCTGGGAC CACTGGCTGG 600
CGCCTGTGGC TCACATCTCC ACGCCTTTGC CCGCTCCTCC CAGGAGCCCG AGTCAGAAAC 660
CTGTGCTTCA CCCTCGAGAG CGCTGCCATC CTCCCCCTCA ACCAGACGGG CATGGCGTCT 720
GGTTGTCCGT CCTGTCTTCT CATCGTCTCA GAGCCCTTCC CTGACCCCTA CCCTCTCTCA 780
GACCAACAGG ATGATGACAG GAAGAGGATC CAGGACCAAC TCCTAGCGGT GACCTTGAGA 840
AAACAATCTC ATACCCCAGT TTCCCTTACA ATGCAATGGA AATAATACTA ACAACCCTGG 900
AAGAGTGTTG GAAGGACTAA ACGAAATCAT CTTTTTCAGT ACTAAGCAGA 950
|
