| Tag | Content |
|---|
EnhancerAtlas ID | HS176-05588 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr10:79702770-79703700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN | MA0488.1 | chr10:79703562-79703575 | ATGACATCATCAT | - | 7.52 | | JUND(var.2) | MA0492.1 | chr10:79703561-79703576 | CATGACATCATCATT | - | 7.2 | | Myod1 | MA0499.1 | chr10:79702934-79702947 | AGCAGCTGTCTCC | + | 6.21 | | Myog | MA0500.1 | chr10:79702933-79702944 | CAGCAGCTGTC | - | 6.14 | | Tcf12 | MA0521.1 | chr10:79702933-79702944 | CAGCAGCTGTC | - | 6.02 |
|
| | 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 |
| GH10I077941 | chr10 | 79701561 | 79704826 |
|
Enhancer Sequence | GGCAAAACCT GAATTTTTAA CTAGCATGCT GGGTGAATTT TATCAGGACA GTGAACCAGG 60
ACTCTCTGAA ATCCCTTCCC CGGGATAGTC AACGAGGCTT TCAATTTAAA CTTGCATTTG 120
AAGCTTGCAG AGACTCACAC TGACTTACCC AGGCCCTAAC ACACAGCAGC TGTCTCCATG 180
GTTGCGCCAG GTAGTGAAGG ATACAGGGCA GCAGGAAACG AGTCCCGGTT CTCAGGTGGA 240
TCCCGTGCTT CCACCTCTGT TAGAGCCCAG GCCCTGAGGG CATAGGGCCA AATTGCCACA 300
GAGCTCCAGA GAAATCTGTC TCTCCCGTCC CCCACCCTAA GACTGAGCTG CTGGAGGAAA 360
GAGGCCAGGT TTGTTTCCTT TTATTGGTTA ACTCTCTTCA GTCGCCCCTT TCTCCTGCAG 420
ACACCTTGGG GACTTTTAGT AATTGTCAGC TGAATGAATA AATTAATGAC AGAGGGAGAC 480
AGACGTGTTA ACAGCTAACA GTAATTCAAG CAGAATGGAG TAAGTGCTAA ATAGTGGTGG 540
AATGAGTCAT GAATGCTGAC AGGGAAGGAA GAGGGAAAAA GGCATTCATT CTCTCCCCCT 600
CCACTGTCAA AACAGTGCCT TCACTCTTCC TCCCTCCATC TCTCTTACAG GCACCAGAGA 660
GCAGAAAATG TATGTGTATA GTTTCAAGAA CAGTTCCAAA GCAAACACCC ATATAGTCAC 720
CCCCATGTGC TGGCCCCCAG GATAAGAAAT AGAACCTTGC CAGAACCTCA GAAGCCTTTC 780
CTGGCCCCCT CCATGACATC ATCATTCCCC GCCTCTTGCC CTCATCTAAC TTCTAATCTG 840
ATTCTGAGGG GAATCATTTT CTTACTTTTC TTTTTTTTTT CTCCTTCTTT TTTTTTTTTT 900
TTTTGAGACA GAGTCTTTCG CTCGGTCACC 930
|
