| Tag | Content |
|---|
EnhancerAtlas ID | HS041-03606 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr11:12387530-12388440 |
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 | AAGAACAGCT CCGGTTTGCA GCTCCTAGCG AGATCGATAC AGAAGACAGG TGATTCTTGC 60
ATTTCAAACT GAGGTATCTG GTTCCTCTCA TTGGGACTGG TTGGACAGTG GATGCAGCCC 120
ATGGAGGGCG AGCTGAAGCA GGGCAGGGCA TCGCCTCACC CAGGAAGTGC AAGGGGTCAG 180
GGGACTTCCC TTTCCTAGCC AAGGGAAGCC ATGGCAGACT GTACCTGGAG AAACTGTACA 240
CTCCTGACCA AATACTGCGC TTTCTCCACA GTCTTAGCAA CTGGCAGACC AGGAGATACC 300
CTCCCATGCC TGGCTTAGTG GGTCCCACGC CCACGGAGCC TTGCTCACTG CTAGCACAGC 360
AGTCTGAGAT CGACCTGCGA TGCTGCAGAT TGGCGGGGGG AGGGGCGACT GCCACTGCTG 420
AGGCTTGAGT AGCTCACAGT GTAAACAAAG AGGCCAGGAA GCACGAATTG GGTGGAGCCC 480
ACTGCGGCTC AGCAAGGCCT ACTGCCTCTG TAGATTCCAC CTCTGGGGCA GGGCATAATA 540
GAACAAAAGG CAGCAGACAG CTTCTGCAGA CTTAAACATC CCAGTCTGAC AGTTCTGAAG 600
AGGGCAGTGG TTCTCTCAGC ATGGTGTTCG AGTTTCGAGA ACGGACAGAC TGCCTCCTCA 660
AGTGGGTTCC TGACCCCCGT GTAGCCTGAC TGGGAAACAT CTCCCAGTAG GGGCCAACAG 720
ACACCTCAAT CAGGCGGGTG CCCCTCTGGG ATGAAGCTTC CAGAGGAAGG ATCAGGTAGC 780
AATACTTGCT GTTCTGCAGC TTCCGCTGGT GATACCCAGG CGAACAGCAT CTGGAGTGGA 840
CCTCCAGCAA ACTCCAACAG ACCTGCAGCT GAGGGGTCTG ACTGTTAGAA AACTAACAAA 900
CAGAAAGGAA 910
|
