| Tag | Content |
|---|
EnhancerAtlas ID | HS184-01413 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:150185680-150186420 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NRF1 | MA0506.1 | chr1:150185928-150185939 | CGCGCATGCGC | - | 6.02 | | NRF1 | MA0506.1 | chr1:150185929-150185940 | GCGCATGCGCA | + | 6.32 | | SPI1 | MA0080.4 | chr1:150185878-150185892 | GCAAAGCGGAAGTA | + | 6.04 | | SPIB | MA0081.2 | chr1:150185880-150185892 | AAAGCGGAAGTA | + | 6.37 | | SPIC | MA0687.1 | chr1:150185878-150185892 | GCAAAGCGGAAGTA | + | 6.11 | | USF2 | MA0526.2 | chr1:150186010-150186026 | GGACCACGTGACTGGG | - | 6.06 |
|
| | 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 |
| GH01I150213 | chr1 | 150185372 | 150186896 |
|
Enhancer Sequence | GCTTGAGCCC AAGAATTCGA GACCAACCTG GGCAACAGGA CAAGACTCCA TGTGTATTAA 60
AAAAAAAAAA TTAAGAAAAC AAAAGCTTTG TTAATCGTTA AGTAAGGATT GCAAAATGGA 120
AGACAGTAAA GAAAAGGAAG GTCCTAAGAA TCTGACCCAC GAGTTTCAGT CCAAGTAACC 180
TGGACCTGCC CAGAGGAAGC AAAGCGGAAG TAGGATCCAA AACGCTTTCA GCAGGCCGCC 240
TGCGCCCCCG CGCATGCGCA GGTCTCTGAC TTTGACCGTT TTGGCGGGTG CGCGCCAGCC 300
CTAGTTTATC TAGAGGGGAA GGGCGGTGCG GGACCACGTG ACTGGGGTTG CGGCATTTCT 360
GGCCCAATCC GAGACGGTTT CGTAGAGCGC CCTGTAGAGC AATTCGGGTT GCCCGGGTCC 420
TTTCCGAGTC TTGACCTCCT CTTTTGCTTC TGGCTTTTCG ACTCTGCTCT CGAATCTAAA 480
AATTTGCCTT GGCAGAAGTT TTTCCCTGTG TTCCAGGAAT TACATTAGGG ACACACTCTA 540
AAGTGATCAG CACTTTTTAT TTTTTTCCTT CATCAACTAA AATAACATTG CTGTCTCCCC 600
AAGACGCTCG AATTCTGTTC TATTGCTTGA GATTCCAGAA TCGCTGGAGG GCGCCCTGTT 660
GTAAAAATAG CACTCCCCAC AAAAAGAGAG AGAAAGTTTT ATCTATATCA GGGGGTTGAG 720
GATTGGAGAA ATAAAGATGA 740
|
