| Tag | Content |
|---|
EnhancerAtlas ID | HS076-09404 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr11:12387510-12388380 |
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 | CGCTTTTAAG ATGGCCAAAT AAGAACAGCT CCGGTTTGCA GCTCCTAGCG AGATCGATAC 60
AGAAGACAGG TGATTCTTGC ATTTCAAACT GAGGTATCTG GTTCCTCTCA TTGGGACTGG 120
TTGGACAGTG GATGCAGCCC ATGGAGGGCG AGCTGAAGCA GGGCAGGGCA TCGCCTCACC 180
CAGGAAGTGC AAGGGGTCAG GGGACTTCCC TTTCCTAGCC AAGGGAAGCC ATGGCAGACT 240
GTACCTGGAG AAACTGTACA CTCCTGACCA AATACTGCGC TTTCTCCACA GTCTTAGCAA 300
CTGGCAGACC AGGAGATACC CTCCCATGCC TGGCTTAGTG GGTCCCACGC CCACGGAGCC 360
TTGCTCACTG CTAGCACAGC AGTCTGAGAT CGACCTGCGA TGCTGCAGAT TGGCGGGGGG 420
AGGGGCGACT GCCACTGCTG AGGCTTGAGT AGCTCACAGT GTAAACAAAG AGGCCAGGAA 480
GCACGAATTG GGTGGAGCCC ACTGCGGCTC AGCAAGGCCT ACTGCCTCTG TAGATTCCAC 540
CTCTGGGGCA GGGCATAATA GAACAAAAGG CAGCAGACAG CTTCTGCAGA CTTAAACATC 600
CCAGTCTGAC AGTTCTGAAG AGGGCAGTGG TTCTCTCAGC ATGGTGTTCG AGTTTCGAGA 660
ACGGACAGAC TGCCTCCTCA AGTGGGTTCC TGACCCCCGT GTAGCCTGAC TGGGAAACAT 720
CTCCCAGTAG GGGCCAACAG ACACCTCAAT CAGGCGGGTG CCCCTCTGGG ATGAAGCTTC 780
CAGAGGAAGG ATCAGGTAGC AATACTTGCT GTTCTGCAGC TTCCGCTGGT GATACCCAGG 840
CGAACAGCAT CTGGAGTGGA CCTCCAGCAA 870
|
