| Tag | Content |
|---|
EnhancerAtlas ID | HS105-77057 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr8:26297640-26299120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr8:26297783-26297794 | AAAACAAAGAA | + | 6.62 | | ZNF263 | MA0528.1 | chr8:26298556-26298577 | CCCTCCTCTGCCTCCTGCTCT | - | 6.58 |
|
| | 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 |
| GH08I026436 | chr8 | 26294140 | 26300315 |
|
Enhancer Sequence | GTAATCCCAG CTACTCAGGA GGCTGAGGCA GGACAATCAC TTGAACCCGG GAGGCGGAGG 60
TTTCAGTGAG CCAAGATCAC TCCATTGCAT TCCAGCCTGA GTGACAGAGC AAGACTCTGT 120
TTAAAAAAGA CAACGAAAAC CGAAAAACAA AGAACAGGTG GAGTCTACTG ACTTGCATGA 180
GTCAGGTAAT TCATTGACCG GGGCTGGTCA AAAAGATGGG TTGATCCTTA CTGTGGAAGC 240
TCTCAGCTGC CCTGCAATAC TTTGGAAATA AACCAGGCAA AACACTGCTC AGTGTGCTGC 300
ACTCCAGACA CAAACAGGAA GCTGCTCTTT CTCTGCTTCC CTCCCCCACA ATCAGACTCT 360
TGTAACTCTC TTTTCTTCTT TTTCTAAAAT GAATCTGGGA GTTTCCTTTA GCCCCTGTTT 420
TGTGGTCGCC TCCCATACAC GTTTTATCTG TCCGTGGCAT TTTCTTTTAT TTATTGAAAG 480
CACCGTGTCT TAGATCAAGT CTTGAGAAAC AGAACCTGAG ACAAACATGA ATGTGGTTAA 540
TTGAACGAGC GCTGTGCAGG AAAAGCTGTA CTGGAGAGAG GTAAGCGGAC AGATACGGGG 600
AAGAGCTGGG CCCAGCAAAG ATGAGGTCTC AAGTAAAGCT TATGTTTGGC TTAATCCACC 660
GGGGACGGTT CTGGAACATA AGCCACACCG CAGAGCTGTG ATGTCACACC TTGAGGCGAG 720
GGCCTTGCCT CCTGGTATCA GTCAGTCCTG GCTGTGGGGA GCAAGGTGGC TCCACTCAGT 780
GCAAGGCCAT CCTGGGCAAG GGGCAGCCCC CCTCACCGCA GTGGCCTGGC AGTGGGGCCC 840
TGGGTCCGGC ACAGCTCCTC CTTCGCACAG TGCTGTCTGC TCGCCCGGTG TCTTTCATGC 900
CGTTTCCCAC CAACTTCCCT CCTCTGCCTC CTGCTCTGCA TTGCACAGTG CAGCGAGGTT 960
GCCAATTCCA TAGTTGTAGC GGCTGTGGGG GAAGGGGCAG GCGGGACAGG GGAGGCAGCC 1020
ATCTAACTTT TGTCCTGACT CACGCAGGCC TGGCCTGGTG TTCAGAACAC AAATGTGAAA 1080
AATCAGACCG GGAAGATCAC GGGAGGCAGG AAGCATCTGG TTTGCAGGTA GGGAAGTGAC 1140
AGACCCCGCG GATGCCATGC ACAAGGGTAC ACAGTGGAGT GGGGATGAAA TCAGGGCGGA 1200
AGTGCAGGGC TCCTGAGCCC GGGGCTGGGG CTGTTTCCCC AACTGTCCGC TGCCTCTGCT 1260
GCCTCCTGAG ATCGTCTCCT TCTGCTGTCT GCCCGCTGGA ACTTATTTTT AGTTTTAATT 1320
TTTTCGAGAC AGGGTTTTAA TCTGTCACCT GGGCTGGAGT GTAGTGTCGT GATCAGGGCT 1380
GACTGCAGCT TCAACCTCTC GGGCTCAAGT GATCCTCCCA CCTTAGTTTC CCAAACAACC 1440
AGGACTACAG ATGCATGCCA CCAAGCCTGC CTAATTTATT 1480
|
