| Tag | Content |
|---|
EnhancerAtlas ID | HS187-04157 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr11:12387500-12388410 |
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 | GAAAAAAGGG CGCTTTTAAG ATGGCCAAAT AAGAACAGCT CCGGTTTGCA GCTCCTAGCG 60
AGATCGATAC AGAAGACAGG TGATTCTTGC ATTTCAAACT GAGGTATCTG GTTCCTCTCA 120
TTGGGACTGG TTGGACAGTG GATGCAGCCC ATGGAGGGCG AGCTGAAGCA GGGCAGGGCA 180
TCGCCTCACC CAGGAAGTGC AAGGGGTCAG GGGACTTCCC TTTCCTAGCC AAGGGAAGCC 240
ATGGCAGACT GTACCTGGAG AAACTGTACA CTCCTGACCA AATACTGCGC TTTCTCCACA 300
GTCTTAGCAA CTGGCAGACC AGGAGATACC CTCCCATGCC TGGCTTAGTG GGTCCCACGC 360
CCACGGAGCC TTGCTCACTG CTAGCACAGC AGTCTGAGAT CGACCTGCGA TGCTGCAGAT 420
TGGCGGGGGG AGGGGCGACT GCCACTGCTG AGGCTTGAGT AGCTCACAGT GTAAACAAAG 480
AGGCCAGGAA GCACGAATTG GGTGGAGCCC ACTGCGGCTC AGCAAGGCCT ACTGCCTCTG 540
TAGATTCCAC CTCTGGGGCA GGGCATAATA GAACAAAAGG CAGCAGACAG CTTCTGCAGA 600
CTTAAACATC CCAGTCTGAC AGTTCTGAAG AGGGCAGTGG TTCTCTCAGC ATGGTGTTCG 660
AGTTTCGAGA ACGGACAGAC TGCCTCCTCA AGTGGGTTCC TGACCCCCGT GTAGCCTGAC 720
TGGGAAACAT CTCCCAGTAG GGGCCAACAG ACACCTCAAT CAGGCGGGTG CCCCTCTGGG 780
ATGAAGCTTC CAGAGGAAGG ATCAGGTAGC AATACTTGCT GTTCTGCAGC TTCCGCTGGT 840
GATACCCAGG CGAACAGCAT CTGGAGTGGA CCTCCAGCAA ACTCCAACAG ACCTGCAGCT 900
GAGGGGTCTG 910
|
