| Tag | Content |
|---|
EnhancerAtlas ID | HS105-00124 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr1:1874980-1876020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP1 | MA0079.4 | chr1:1875862-1875877 | ATGGCCACGCCCACG | + | 6.22 | | SP3 | MA0746.2 | chr1:1875864-1875877 | GGCCACGCCCACG | + | 6.04 |
|
| | 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 |
| GH01I001942 | chr1 | 1873910 | 1876089 |
|
Enhancer Sequence | CAGCCTCGCC GTCCCTCTGC GCTTTCCCAC CGGCGTGGCT GTTCAGGGCA GGCTGCTTGC 60
TCTGATGTCT GGAGCCCTTG CCAAACCCTG CAAGTGGAGG CTTCCTCCTC CAGGCTCACC 120
CTGCCTGTGT CCACGAGGGG CTGAGGACTC TGGCCGGGCC CAGGCGGGCA GTGCGTTTCC 180
TGTGGCTGCT GAAAGGATTT GCCCCAAGCT TAGGGGCCCC ACAACACAGA GGCACATTCA 240
TTCTCTCCAC GTCCTGGAGG TCAGAAGCCA AGACGGAGCT AAGGCCAAGG TGCGGGCAGG 300
GCCGTGCCCT TGTGGCTCTA CGGGACAGGT TTCTCCTCTC CTTTCACAGC CTCTAGAAGC 360
TGCAGTGTCC CCGGGCTCGG GGCCCTTCCT CCATCTTGGA AGCCGACAGT GCAGTGTCTT 420
CAAATCGGCC TGACTCTGAC CCTCCTGCCT CCCTGTGACG CCTCCCGTGA TGACACTGGC 480
GCCTCCCAGA TGATCCTGGA TCACCCCCCA CCAAGGTCCC TCTCCCCAAC CATGTCTGCT 540
AAGCCCCCTG CTTGCCACAC AGGATGCCGT TCAGGGCCTG GACAGCAGCC GTGGCAGCCC 600
CAGGTGCCAT GTCCCCGCTG GCCACTGGGG GGCTCACCGC GTGTGCACAG GCAGGCAGCG 660
GCTCACCCCG TGTGCGTGGG TCACCCCGTG TGCGTGGACA GGAGGGGGCT CACCGCGTGT 720
GCACAGGCAG GCAGCGGCTC ACCCCGTGTG CGTGGGTCAC CCCGTGTGCA TGGACAGGAG 780
GGGGCTCACC GCGTGTGCAC GAGCACAGAG TCCTGGTAGA GCCGGTCATA CATGCAGATC 840
TTCAGGTCCA CGCTGGGCTT CGGCACCCAG ACCGGCACAT CGATGGCCAC GCCCACGACC 900
CTGAAATGCA GCTGCATATG GACACAGGAG CTCAGCAACA GGAGTTCCTT GGGCACAGCA 960
GGCATTGTTG GTGAGCACTG ACACAGCTCC CAGGAGGAAC GTTTCATGGG CTTGAGTTTT 1020
CTAACTCTTT GGGACGGCTG 1040
|
