| Tag | Content |
|---|
EnhancerAtlas ID | HS037-05981 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr11:12387450-12388200 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr11:12387964-12387980 | CACAGTGTAAACAAAG | + | 6 |
|
| | 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 |
| GH11I012366 | chr11 | 12387548 | 12388368 |
|
Enhancer Sequence | TGCACTCCAG CCTGGGCAAC AGAGTGAGAC TCAGTCTAAA AAAAAAAAAA GAAAAAAGGG 60
CGCTTTTAAG ATGGCCAAAT AAGAACAGCT CCGGTTTGCA GCTCCTAGCG AGATCGATAC 120
AGAAGACAGG TGATTCTTGC ATTTCAAACT GAGGTATCTG GTTCCTCTCA TTGGGACTGG 180
TTGGACAGTG GATGCAGCCC ATGGAGGGCG AGCTGAAGCA GGGCAGGGCA TCGCCTCACC 240
CAGGAAGTGC AAGGGGTCAG GGGACTTCCC TTTCCTAGCC AAGGGAAGCC ATGGCAGACT 300
GTACCTGGAG AAACTGTACA CTCCTGACCA AATACTGCGC TTTCTCCACA GTCTTAGCAA 360
CTGGCAGACC AGGAGATACC CTCCCATGCC TGGCTTAGTG GGTCCCACGC CCACGGAGCC 420
TTGCTCACTG CTAGCACAGC AGTCTGAGAT CGACCTGCGA TGCTGCAGAT TGGCGGGGGG 480
AGGGGCGACT GCCACTGCTG AGGCTTGAGT AGCTCACAGT GTAAACAAAG AGGCCAGGAA 540
GCACGAATTG GGTGGAGCCC ACTGCGGCTC AGCAAGGCCT ACTGCCTCTG TAGATTCCAC 600
CTCTGGGGCA GGGCATAATA GAACAAAAGG CAGCAGACAG CTTCTGCAGA CTTAAACATC 660
CCAGTCTGAC AGTTCTGAAG AGGGCAGTGG TTCTCTCAGC ATGGTGTTCG AGTTTCGAGA 720
ACGGACAGAC TGCCTCCTCA AGTGGGTTCC 750
|
