| Tag | Content |
|---|
EnhancerAtlas ID | HS066-02696 |
Organism | Homo sapiens |
Tissue/cell | GM18516 |
Coordinate | chr19:8444510-8445690 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr19:8445064-8445078 | AGCTTCCGCTTTTC | - | 6.09 | | STAT3 | MA0144.2 | chr19:8444996-8445007 | TTTCTGGGAAG | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGAAGCTCTG TTCTTTCACT CTTCGCAATA AATCTTGCTG CTGCTCACTC TTTGGGTCCG 60
CACCACCTTT ATGAGCTGTA ACACTCACCG CAAAGATCTG CAGCTTCACT CCTGAAGTCA 120
GCGAGACCAC GAACCTACCA GAAGGAATAA ACTCCAGACA CATCCAAACA TCAGAAGGAA 180
CAAACTCCAG ACACACCATC TTTAAGAACT GTAACACTCA CCGTGAGGGT CCACAGCTTC 240
ATTCTTGAAG TCAGTGAGAC CAAGAACCCA CCAATACTGG ACACATTTTG GCGACCACGA 300
AGGGACTATC GCCTATCACC AAGCGGTGAG ACTATCGCCT ATCACCAAGC GGTGAGTACC 360
ATCGGACCCC TTTCGCTTGC TATTCGTCCT ATTTTTCCTT AGAATTTGGG GGCTAAATAC 420
CGGGCACCTG TCGGCCAGTT AAAAGCGACT AGCGCAGGTG CTGGACTAAA GACATGGGTG 480
TGAGGCTTTC TGGGAAGGGG CTCTCTAACA AACCCCGACT TTTTGGAGTT GGGAGCGTTA 540
GTTTGCCTGG AACCAGCTTC CGCTTTTCCT GTACTTCTGG GCTGAGTCGA GGGTTGACAG 600
GAAAGCCATT CAGCTCTGGG GTCTTGACAA CAAGTTGGTT GATCCTGTGG CCATGAGCAG 660
AACTCTCAAA GTCATGTCGC CCAAGTGAGA CTCGCCCATC TATCCTATCT GTCCTGACCC 720
TTGCCTCCTG GGTCCTAATG CCTGTCAGAC AAACTTCCTC TCGCCTCTCT TCTCCGAGGC 780
TAGTCCCACC TCTAAAAACC ACTCCCTGTC TCTGGTGCTT TTCTAGTTTC TCCTATAAGA 840
ATGACTTCTA GTATAAACTT CAGGACTCTG TTACCTTCTT TAGGCACCTA GGCTCACTAA 900
TCAGAAAGAC ATAATTTTTG CCCAAAGCCC TGTTGTAGGG GGGCTATCTG GAATTTTAGG 960
ATCCCTCCTC AGACAAGCAG GACTAATAAA AGCTATTCCT GAAGCTAGGA TATGGGGAGC 1020
CTCAGAAATT GTATTCTTCC TATTCATATA AGTGAGGACA AAAGGTGTCA CTCTTCCAAC 1080
CCTGGAGATC CCTTCCTTCC CTCATGGTAT GGCCCTCCAC TTCATTTTTG GGGCATAACA 1140
TCATTGTAGG AAATTGGTAA GGTCCCAATA CTAAAAGGAG 1180
|
