| Tag | Content |
|---|
EnhancerAtlas ID | HS108-06991 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr11:12387760-12388340 |
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 | AAACTGTACA CTCCTGACCA AATACTGCGC TTTCTCCACA GTCTTAGCAA CTGGCAGACC 60
AGGAGATACC CTCCCATGCC TGGCTTAGTG GGTCCCACGC CCACGGAGCC TTGCTCACTG 120
CTAGCACAGC AGTCTGAGAT CGACCTGCGA TGCTGCAGAT TGGCGGGGGG AGGGGCGACT 180
GCCACTGCTG AGGCTTGAGT AGCTCACAGT GTAAACAAAG AGGCCAGGAA GCACGAATTG 240
GGTGGAGCCC ACTGCGGCTC AGCAAGGCCT ACTGCCTCTG TAGATTCCAC CTCTGGGGCA 300
GGGCATAATA GAACAAAAGG CAGCAGACAG CTTCTGCAGA CTTAAACATC CCAGTCTGAC 360
AGTTCTGAAG AGGGCAGTGG TTCTCTCAGC ATGGTGTTCG AGTTTCGAGA ACGGACAGAC 420
TGCCTCCTCA AGTGGGTTCC TGACCCCCGT GTAGCCTGAC TGGGAAACAT CTCCCAGTAG 480
GGGCCAACAG ACACCTCAAT CAGGCGGGTG CCCCTCTGGG ATGAAGCTTC CAGAGGAAGG 540
ATCAGGTAGC AATACTTGCT GTTCTGCAGC TTCCGCTGGT 580
|
