| Tag | Content |
|---|
EnhancerAtlas ID | HS108-17086 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:45078440-45079200 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:45078668-45078687 | TGCTGTCCTCTAGTGGCCA | - | 6.89 | | ETV6 | MA0645.1 | chr17:45078720-45078730 | AGCGGAAGTG | + | 6.02 | | SPI1 | MA0080.4 | chr17:45078716-45078730 | AAAAAGCGGAAGTG | + | 7.73 | | SPIB | MA0081.2 | chr17:45078718-45078730 | AAAGCGGAAGTG | + | 6.92 | | SPIC | MA0687.1 | chr17:45078716-45078730 | AAAAAGCGGAAGTG | + | 6.15 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH17I047002 | chr17 | 45078367 | 45078967 | | GH17I047001 | chr17 | 45079167 | 45079366 |
|
Enhancer Sequence | GCAGTGAGCC GAGATGGTGC CACAGAACTC CAGTCTGGGC GACCTTCCTG CACTCCCGGT 60
GTTCGGGGAC CAACAAGGCG TAATAAGGAG CCAGAGACCA AGGCCCAAGT CTCAGCTCTA 120
ACTGAGTATT ATGGGGGTAT TAATGTCCAC CTCCCAGGAT AGGGAGCACA GAGCAAGGAA 180
TACTAAGTAT TGAAGCCCTG AAACGCCCAC TTCCTGTACC TGAGTCGCTG CTGTCCTCTA 240
GTGGCCACTG GATAAATTGC ACAGCACGCC GGCCTGAAAA AGCGGAAGTG AGAGATGCTT 300
TTCCCCACTT CTGAATCTAC CAGATGCTGG GGGGTTCTCA ACCATGCTCC ACTCATGACT 360
TCCTTTTTAT AAAATGTATT TTGTGTAATT ACAGTAATTT TTGAACATTT TAGGCAGATT 420
TATTGAGGTA TTGACATATA ATAAACTGCC TAGAGATTAC AATTTGATAA TATCTGAGCC 480
TTAGTATACA GCTGAAATCA TTATCACAAT CAAGATAGTG AAGAAAGCCA TCCTCCCAAA 540
AAATTTCCTT GTTGCCCCTT GGTGATCCTG CTTCCTGCCC TTTCTACTTC CCTCTCACCC 600
CCAAGCAACT ACTGATCTGC TTTCTTTCTC TTCTCTTTTT TCCTTTTTTT TTTTTTTTTT 660
TTTTTTGAGA TGGAGTTTCA CTCTGTCACC AGGCCGGAGT GCAGTGGTGA GATCTCGGCT 720
CACTGCAACC TCCGCCTCCC AGGTTCAACA GATTCTCCTG 760
|
