| Tag | Content |
|---|
EnhancerAtlas ID | HS105-38957 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr19:11189460-11190320 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr19:11189800-11189815 | CCTGACCTTGGCCTT | - | 6.41 |
|
| | 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 |
| GH19I011078 | chr19 | 11189661 | 11189810 |
|
Enhancer Sequence | CTGAGTATCT GGGATTACAG GTGCCTGTGA CCACGCCCGG CTGATTTTTG TATTTTTAGT 60
AGAGACGGGG TTTCACCACA TTGGTCAGGC TAGCCTCAAA CTCCTGACCC CGTGATCCTT 120
CCGCCTCAGC CTCCCAAAGT GCTGGGATTA CAGGACTCTG GCCCATCTTG GCTGCTGCCA 180
ATGTCCTTCC TTCTATCTTG GTTTTTCCAC AGTTACGCAC ATGCCAGATA ACGGCGAGTC 240
TGTTCCCCAG CAACTGCAAC GGATCTGCCC ACCACTGGGA AATGGAAGAC CTTGCAGCCC 300
AGGTCTTTGT AGACCAAGAT TAGATTGTGG TCAACAAACA CCTGACCTTG GCCTTTGGAA 360
CCATCAGCCA TGTCAGCTAA AATAAAAGCA GAATCTGGCT GGGCGCAGTG GCTCACGCCT 420
GTAATCCCAG CACTTTGGGG GGCTGAGGTG GGCAGACCAC CTGAGGTCCG GCGTTCTAGA 480
CCAGCCTGAC CAATATGATG AAACCCCGTC TCTACTAAAC ATACAAAAAT TAGCTGGGCA 540
TGGTGGCGGG CACCTGTAAT CCCAGCTACT CGGGAGGCTG AGGAAGGAGA ATTGCTTGAA 600
CCCTGGAGGC AGAGGTTGCA GTGAGCCGAG ATTGCGCCAC TGCACTCCAA CCTGGACTGC 660
AGAACAAGAC TCTGTCCCAA AAGCAGATAA ATAAAAATAA ATAAAAATAA AAATATGGCC 720
GGGCATGGTG GCTCACACCT GTAATCCCAA CACTGGGAAG ATGAGGCGGG CAGATCACGA 780
GGTCAGGGAT TCGAGACCAG CCTGGCCAAC ATGGTGAAAC CCCGTCTCTA CTAAAAATAC 840
AAAAATTAGC CGGGCATGAT 860
|
